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BS-240 Chemistry Analyzer

Service Manual
IVD Global Technical Support Dept

Preface

© 2017-2020 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights Reserved.
For this Service Manual, the issue date is 2020-12.

This manual contains the instructions necessary to operate the product safely and in accordance with its function
and intended use. Please read this manual thoroughly before using the product. Observance of this manual is
a prerequisite for proper performance and correct operation, and it ensures patient and operator safety. All
graphics including screens and printouts in this manual are for illustration purpose only and must not be used
for any other purposes. The screens and printouts on the actual product should prevail.
This manual is used for models: BS-240.
Manual introduction
Intellectual Property Statement
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray) owns the
intellectual property rights to this Mindray product and this manual. This manual may refer to information
protected by copyright or patents and does not convey any license under the patent rights or copyright of
Mindray, or of others.

, , , , , , , ,RealTF,
TrackWB,TrueTCR,Q-pick,AutoOLC,iVision,DBF,DRF,RDA,DRA,DFS、SyncNavi、GQ-Ana、One-
touchIP、Holo-IS、Opt-VRA、SuperVE-Cine、NFP-DSC、iTouch、iStation、BeneView、SmarTemp are the
trademarks, registered or otherwise, of Mindray in China and other countries. All other trademarks that appear
in this manual are used only for informational or editorial purposes. They are the property of their respective
owners.
Statement
All information contained in this manual is believed to be correct. Mindray shall not be liable for errors contained
herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this
manual.
Mindray is responsible for the effects on safety, reliability and performance of this product, only if:
◼ All installation operations, expansions, changes, modifications and repairs of this product are
conducted by Mindray authorized personnel.
◼ All repairs involving replacement parts and associated accessories and consumables are original
(original) or approved by Mindray.
◼ The electrical installation of the relevant room complies with the applicable national and local
requirements.
◼ The product is used in accordance with the instructions for use.

Warning
It is important for the hospital or organization that employs this equipment to carry out a reasonable
service/maintenance plan. Neglect of this may result in machine breakdown or personal injury.

Note
This equipment must be operated by skilled/trained clinical professionals.

Warranty
THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESSED OR
IMPLIED, INCLUDING WARRANTIES OF MERCHANTABILITY OR FITNESS FOR ANY PARTICULAR

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PURPOSE.
Exemptions
Mindray's obligation or liability under this warranty does not include any transportation or other charges or
liability for direct, indirect or consequential damages or delay resulting from the improper use or application of
the product or the use of parts or accessories not approved by Mindray or repairs by people other than Mindray
authorized personnel.
This warranty shall not extend to:
▪ Malfunction or damage caused by improper use or man-made failure.
▪ Malfunction or damage caused by unstable or out-of-range power input.
▪ Malfunction or damage caused by force majeure such as fire and earthquake.
▪ Malfunction or damage caused by improper operation or repair by unqualified or unauthorized service
people.
▪ Malfunction of the instrument or part whose serial number is not legible enough.
▪ Others not caused by instrument or part itself.
Customer service department
Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Address: Mindray Building, Keji 12th Road South, High-tech
industrial park, Nanshan, Shenzhen 518057,P.R.China
Website: www.mindray.com
E-mail Address: [email protected]
Tel: +86 755 81888998
Fax: +86 755 26582680
EC - Representative
EC-Representative: Shanghai International Holding Corp. GmbH(Europe)
Address: Eiffestraβe 80, 20537 Hamburg, Germany
Tel: 0049-40-2513175
Fax: 0049-40-255726

Product introduction
The instrument is a computer-controlled fully-automated chemistry analyzer, intended for quantitative
determination of clinical chemistries in serum, plasma, urine, cerebrospinal fluid (CSF), and other human body
fluids. It can fulfill auto dispensing, reaction, colorimetric measurement, process monitoring, and result
calculation. It is one of the necessary tools for laboratory automation.

Safety information
This chapter provides you with safety symbols used in this manual and their meanings, summarizes the safety
hazards and operating precautions that should be considered seriously when the instrument is being operated,
and lists the labels and silkscreens that have been applied to the instrument and their indications.
Safety symbols
Safety symbols are used in this manual in order to remind you of the instructions necessary to operate the
product safely and in accordance with its function and intended use. A safety symbol and text constitutes a
warning as shown in the table below:
Symbol Meaning
Caution

Biological risks

Summary of hazards
This section lists hazards of the instrument itself. The hazards of specific operation are included in the warning
information of each operation task.
Observe the following safety precautions when using the product. Ignoring any of them may lead to personal

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injury or equipment damage.

WARNING
If the product is used in a manner not specified by our company, the protection provided by the product may be
impaired.

Electric shock hazards

WARNING
When the MAIN POWER is turned on, users other than the servicing personnel authorized by our company
must not open the rear cover or side cover.
Spillage of reagent or sample on the product may cause equipment failure and even electric shock. Do not place
sample and reagent on the product. In case of spillage, Switch off the power immediately, remove the spillage
and contact our Customer Service Department or your local distributor.

Moving Parts Hazards

WARNING
Do not touch such moving parts as sample/reagent carousel, reaction carousel, probe, mixer, and cuvette wash
station, when the system is in operation.
Exercise caution while using the ISE module Prevent your hair, legs or other parts of your body from being hurt
by the driving parts.
Do not put your fingers or hands into any open part when the system is in operation.

Photometer lamp hazards

WARNING
Eye injury could occur from light emission from the photometer lamp. Do not stare into the lamp when the system
is in operation.
If you want to replace the photometer lamp, first switch off the MAIN POWER and then wait at least 5 minutes
for the lamp to cool down before touching it. Do not touch the lamp before it cools down, or you may get burned.

Sample, calibrator and control hazards

BIOHAZARD
Inappropriately handling samples, controls and calibrators may lead to biohazardous infection. Do not touch
samples, controls, calibrators, mixtures, or waste with your bare hands. Wear gloves and lab coat and, if
necessary, goggles.
In case your skin contacts the sample, control or calibrator, follow the standard laboratory safety procedure and
consult a doctor.
The serum samples remaining in the electrodes may contain a great number of viruses. Wear gloves to prevent
infection while operating around the electrodes.

Reagent and wash solution hazards

WARNING
Reagents, diluted wash solution and concentrated wash solution are corrosive to human skins. Exercise caution
when using reagents and concentrated wash solution. In case your skin or clothes contact them, wash them off

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with soap and clean water. If reagents or wash solution spills into your eyes, rinse them with much water and
consult an oculist.

Waste hazards

BIOHAZARD
Some substances contained in reagent, control, calibrator, concentrated wash solution, and waste are subject
to regulations of contamination and disposal. Dispose of the waste in accordance with your local or national rule
for biohazard waste disposal and consult the manufacturer or distributor of the reagents for details.
Wear gloves and lab coat and, if necessary, goggles.

System disposal hazards

WARNING
Materials of the analyzer are subject to contamination regulations. Dispose of the waste analyzer in accordance
with your local or national rule for waste disposal.

Fire and explosion hazards

WARNING
Ethanol is flammable substance. Please exercise caution while using ethanol around the instrument in order to
prevent fire and explosion.

Removal of analyzer from use for repair or disposal

WARNING
When the analyzer is not in use, for example, in repair, transportation or disposal process, please clean and
sterilize the parts that may cause biohazards(probe, mixer, etc.) and remind the person who handles the device
of the related hazards.

Cleaning and Decontamination

CAUTION
Appropriate decontamination is carried out if hazardous material is spilled onto or into the equipment.
No decontamination or cleaning agents are used which could cause a HAZARD as a result of a reaction with
parts of the equipment or with material contained in it. Strong acid or alkaline solutions are forbidden to clean
the equipment.
If there is any doubt about the compatibility of the decontamination or cleaning agents with parts of the
equipment or with material contained in it, please contact our customer service department or the local
distributor.

Summary of precautions
This section lists precautions to be understood during instrument operation. The precautions of specific
operation are included in the warning information of each operation task.
To use the product safely and efficiently, pay attention to the following operating precautions.

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Intended use

WARNING
The instrument is an automated chemistry analyzer for in vitro diagnostic use in clinical laboratories and
designed for in vitro quantitative determination of clinical chemistries in serum, plasma, urine and cerebrospinal
fluid samples.
Please consult us before you use the instrument for other purposes.
When drawing a clinical conclusion, please also refer to patients' clinical symptoms and other test results.

Installation Precautions

NOTE
The safety of any system incorporating the equipment is the responsibility of the assembler of the system.

Environment precautions

CAUTION
Please install and operate the system in an environment specified by this manual. Installing and operating the
system in other environment may lead to unreliable results and even equipment damage.
To relocate the system, please contact our Customer Service Department or your local distributor.

Electromagnetic noise precautions

CAUTION
Electromagnetic noise may interfere with operations of the system. Do not install devices generating excessive
electromagnetic noise around the system. Do not use such devices as radio transmitters in the room housing
the system. Do not use other CRT displays around the system.
Do not use other medical instruments around the system that may generate electromagnetic noise to interfere
with their operations.
Do not use this device in close proximity to sources of strong electromagnetic radiation (e.g. mobile phones or
radio transmitters), as these may interfere with the proper operation.
The electromagnetic environment should be evaluated prior to operation of the device.
This device has been designed and tested to CISPR 11 Class A, and in a domestic environment may cause
radio interference, in which case, you may need to take measures to mitigate the interference.

NOTE
It is the manufacturer's responsibility to provide equipment electromagnetic compatibility information to the
customer or user.
It is the user's responsibility to ensure that a compatible electromagnetic environment for the equipment can be
maintained in order that it will perform as intended.

Operating precautions

CAUTION
Take the clinical symptoms or other test results of the patient into considerations when making diagnosis based
on the measuring results produced by the system.
Operate the system strictly as instructed by this manual. Inappropriate use of the system may lead to unreliable

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test results or even equipment damage or personal injury.


When using the system for the first time, run calibrations and QC tests to make sure the system is in proper
state.
Be sure to run QC tests every time when you use the system, otherwise the result may be unreliable.
Start the operating software again when the analyzing unit is powered off.
Do not uncover the reagent carousel when the system is in operation. Keep the reagent carousel cover closed.
The RS-232 port on the analyzing unit is used for connection with the operation unit only. Do not use it for other
connections. Use the cables provided by our company or your local distributor for the connection.
The operation unit is a personal computer with the operating software installed. Installing other software or
hardware on the computer may interfere with the system operation. Do not run other software when the system
is working.
Computer virus may destroy the operating software or test data. Do not use the computer for other purposes or
connect it to the Internet. If the computer is infected by virus, please install anti-virus software to check for and
clear virus.
Do not touch the display, mouse or keyboard with wet hands or hands with chemicals.
Do not place the MAIN POWER to ON again within 10 seconds after placing it to OFF; otherwise the system
may enter the protection status. If it does so, place the MAIN POWER to OFF and place it to ON again.

Chemistry parameter configuration precautions

CAUTION
To define such parameters as sample volume, reagent volume and wavelength, follow the instructions in this
manual and the instructions of reagents.

ISE module precautions

CAUTION
To prevent ISE electrodes from being damaged due to water scarcity, if the system, when equipped with an ISE
module will be powered off for a long time, perform the electrode storage maintenance.

Sample precautions

CAUTION
Use samples that are completely free of insoluble substances like fibrin or suspended matter; otherwise the
probe may be clogged.
Medicines, anticoagulants or preservative in the samples may lead to unreliable results.
Hemolysis, icterus or lipemia in the samples may lead to unreliable test results; running a serum index test
therefore, is recommended.
Store the samples properly. Improper storage may change the compositions of samples and lead to unreliable
results.
Sample volatilization may lead to unreliable results. Do not leave the sample open for a long period.
Prepare sufficient sample volume before analysis.
Load samples to correct positions on the sample carousel before the analysis begins; otherwise reliable results
may not be obtained.

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Reagent, calibrator and control precautions

CAUTION
Use proper reagents, calibrators and controls on the system.
Select appropriate reagents according to the performance characteristics of the system. Consult the reagent
suppliers, our company or our authorized distributor for details, if you are not sure about your reagent choice.
Store and use the reagents, calibrators and controls strictly as instructed by the suppliers; otherwise, reliable
results or best performance of the system may not be obtained. Improper storage of reagents, calibrators and
controls may lead to unreliable results and bad performance of the system even in validity period.
Perform calibration after changing the reagents, otherwise reliable results may not be obtained.
Contamination caused by carryover among reagents may lead to unreliable test results. Consult the reagent
suppliers for details.

ISE calibration precautions

BIOHAZARD
The calibrators contain preservatives. In case your skin contacts calibrators, wash them off with soap and water.
In case the calibrators spill into your eyes, rinse them with water and consult an oculist. If you swallow them by
mistake, see a doctor.

CAUTION
Use the calibrators specified by our company. Use of other reagents or calibrators may result in unreliable
results, or damage the Hydropneumatic system, or even shorten the electrodes life span.
Prior to using the calibrators, check if they are within the expiration date.
Place them correctly; otherwise, it may cause unreliable results, or leak, or module damage.

ISE wash solution biohazards

BIOHAZARD
The ISE wash solution is sodium hypochlorite. Use the ISE wash solution carefully to prevent it from contacting
your skins or eyes. If your skins or eyes contact the ISE wash solution, rinse them off with fresh water and
consult a doctor.

Data archiving precautions

NOTE
The system automatically stores the data to the built-in hard disk. Data loss, however, is still possible due to
mis-deletion or physical damage of the hard disk. You are recommended to regularly archive the data to such
medium as CDs.
To avoid the data loss caused by unexpected power failure, UPS (uninterrupted power supply) is recommended.

External equipment precautions

WARNING
For operating instructions and precautions of the computer and printer, please refer to their operation manuals.
External equipment connected to the analogue and digital interfaces must be authorized and complied with
relevant safety and EMC standards (e.g., IEC 60950 Safety of Information Technology Equipment Standard
and CISPR 22 EMC of Information Technology Equipment Standard (CLASS B)). Any person, who connects

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additional equipment to the signal input or output ports and configures an IVD system, is responsible for
ensuring that the system works normally and complies with the safety and EMC requirements. If you have any
questions, consult the technical services department of your local representative.

Maintenance and Servicing Precautions

CAUTION
Maintain the system strictly as instructed by this manual. Inappropriate maintenance may lead to unreliable
results, equipment damage or personal injury.
To wipe off dust from the system surface, use a soft, clean and wet (not too wet) cloth soaked with soap water
rather than organic solvents such as ethanol. After cleaning, wipe the surface dry with dry cloth.
Switch off all the powers and disconnect the power plug before cleaning. Take necessary measures to prevent
water ingression, otherwise equipment damage or personal injury may be caused.
Replacement of such major parts as photometer lamp, probe, mixer and syringe assembly must be followed by
a calibration.
Replacement of the photometer lamp should be done when the system power has been switched off for at least
5 minutes.
If the system fails and needs servicing, contact our Customer Service Department or the local distributor. The
system may need to be stopped or transported during servicing, which will probably cause biohazards, electric
shock hazards and moving part hazards. Exercise caution when prepare the system for servicing.
Wear gloves and lab coat and, if necessary, goggles.

NOTE
Check the safe state of the equipment after repair. Make sure the equipment is safe and then offer it to the
customer.

Tube and liquid container precautions

WARNING
When the tube or the part that contain liquid become aged or damaged, please stop its use immediately and
contact our customer service department or your local distributor to check and replace it.

Labels and silkscreen


The following labels and silkscreen are used on the product for system identification and operating instruction.

For the label marked with , please consult the related documentations in order to find out the nature of the
potential HAZARDS and any actions which have to be taken to avoid them.
Check the labels regularly for cleanliness and integrity. If any of the labels becomes vague or peels off, contact
our Customer Service Department or your local distributor for replacement.
Labels and silkscreen list
Symbol Meaning
Serial Number

Date of Manufacture

Manufacturer

CE marking

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Symbol Meaning
Authorized Representative in the European
Community

The following definition of the WEEE label applies


to EU member states only: The use of this
symbol indicates that this product should not be
treated as household waste. By ensuring that
this product is disposed of correctly, you will help
prevent bringing potential negative
consequences to the environment and human
health. For more detailed information with
regard to returning and recycling this product,
please consult the distributor from whom you
purchased the product.
In Vitro diagnostic medical device

Biological risks

Caution

Caution: hot surface

“ON” (Power)

“OFF” (Power)

“ON” for a part of equipment

“OFF” for a part of equipment

Serial interface

Protective conductor terminal

Fuse(for models powered by 220V-240V~ or


220V/230V~ supply voltage)
Fuse(for models powered by 110V/115V~ supply
voltage)

Instrument Labels and Silkscreen


The positions on the sample /reagent carousel
This symbol indicates the positions on the sample/reagent carousel. Middle ring: 1~40. Inner ring: 41~80

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Wash Station bracket


This symbol indicates wash station bracket

Interfaces for fluid connection


This symbol located on the fluid connection interfaces indicates the connection of fluid tubing.

ISE tube installation location


This symbol indicates the specific tubes of ISE module.

Humidity range
This symbol indicates the humidity requirement under normal working condition.

Atmospheric pressure
This symbol indicates the atmospheric pressure requirement under normal working condition.

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Temperature limit
This symbol indicates the temperature requirement under normal working condition.

Warning labels
Biohazard warning
This label indicating the risk of biohazardous infection is located in the following positions:
▪ Probe
▪ Waste outlet
▪ Waste tank

Moving parts warning


This symbol and text indicating the hazardous moving parts is located in the following positions:
▪ Probe
▪ Mixer
▪ Wash station

Photometer lamp warning


This symbol and text located on the lamp housing reminds you of not touching the lamp before it gets cool.

Probe collision warning


This symbol and text located near the sample/reagent carousel and reaction carousel reminds you of not
opening the cover to prevent from damaging the probe.

ISE module
This symbol and text located on the left side panel of the analyzer. Please turn off the main power before opening
the small door.

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Liquid level floater


This symbol and text is located near the liquid level floater of the DI water tank and the wash solution tank,
Please do not take out the liquid level floater during test.

Cuvette replacement window


This symbol and text is located on the cuvette replacement window.

Risk of injury when replacing the lamp


This label is located close to the door of the lamp. Do not touch the moving parts when replacing the lamp.

Chemical hazard
This label is applied on the diluted wash solution tank. Please take protective measures to prevent chemical
hazard.

Cabinet
This label is applied at the middle of the cabinet back. If you want to relocate your analyzer, contact our
Customer Service Department or your local distributor. When relocating it, do not carry it with the cabinet. Only
when the cabinet is supported by the anchors, can the analyzer be placed on the cabinet.

User Permissions
◼ Engineer username: serviceuser
◼ Password: #BS8A#SEU
Note: After logging into the analyzer using the engineer on a client, remember to switch back to the
account of engineer.
Revision history
Chapter History Version
1.Added revision history
Preface V1.0
2. Added description about user permission

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Chapter 1 1. Rearranged V1.0


1.Rearranged
Chapter 2 V1.0
2. Changed FRU
1. Rearranged
2. Changed FRU
Chapter 3 V1.0
3. Changed wrong description
4. Added ISE
1. Rearranged
2. Changed FRU
Chapter 4 V1.0
3. Changed PCB picture
4. Added 4.5.4
Chapter 5 1. Rearranged V1.0
1. Rearranged
2. Added 6.2
3. Added 6.3
Chapter 6 V1.0
4. Added 6.6.2
5. Added 6.7
6. Added6.8
1. Rearranged
Chapter 7 2. Changed picture. V1.0
3. Added7.9
1. Rearranged
Chapter 8 2. Added 8.1 V1.0
3. Added 8.6-8.8
Chapter 9 1. Rearranged V1.0
1. Rearranged
Chapter 10 2. Added 10.1~10.3 V1.0
3. Changed 10.4
Chapter 11 1. Added chapter V1.0
Chapter 12 1. Added chapter V1.0
Chapter 13 1. Added chapter V1.0
Chapter 14 1. Added chapter V1.0
Added :
1. Installation Acceptance Report
2. Moving Parts Position Confirmation Guide (No Alignment
Tooling)
Appendices V1.0
3. Tool list
4. Error Information Feedback Form
5. Series Recovery Checklist
6. Maintenance log sheet
Chapter 11 1. Added Assembly Explosive Views V3.0

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Table of Contents

Preface ................................................................................................................................................................. I
Manual introduction ....................................................................................................................................... I
Intellectual Property Statement .............................................................................................................. I
Statement ............................................................................................................................................... I
Warranty ................................................................................................................................................. I
Exemptions............................................................................................................................................ II
Customer service department ............................................................................................................... II
EC - Representative .............................................................................................................................. II
Product introduction .............................................................................................................................. II
Safety information ................................................................................................................................. II
Summary of hazards ............................................................................................................................. II
Summary of precautions ...................................................................................................................... IV
Labels and silkscreen ......................................................................................................................... VIII
Instrument Labels and Silkscreen ........................................................................................................ IX
User Permissions ....................................................................................................................................... XII
Revision history .......................................................................................................................................... XII
Table of Contents .................................................................................................................................................. I
1 System Description ................................................................................................................................... 1-1
1.1 Overview ......................................................................................................................... 1-1
1.2 Components of Analyzing Unit ....................................................................................... 1-1
1.3 Functions of Analyzing Unit ............................................................................................ 1-2
2 System Performance and Workflow .......................................................................................................... 2-3
2.1 Major Specifications ....................................................................................................... 2-3
2.1.1 General Specifications .............................................................................................................. 2-3
2.2 Sample Specifications .................................................................................................... 2-4
2.2.1 Reagent Specifications ............................................................................................................. 2-5
2.2.2 Specifications of Reaction System ............................................................................................ 2-5
2.2.3 Specifications of Operation Unit ................................................................................................ 2-6
2.2.4 Typical Test Procedure .............................................................................................................. 2-6
2.2.5 Startup Procedure ..................................................................................................................... 2-7
2.2.6 Shutdown Procedure ................................................................................................................. 2-7
2.2.7 Workflow Descriptions ............................................................................................................... 2-7
2.2.8 Measuring Points ...................................................................................................................... 2-8
3 Modules and Units .................................................................................................................................... 3-8
3.1 Shell Assembly ............................................................................................................... 3-8
3.1.1 Module Functions ...................................................................................................................... 3-8
3.1.2 Component Locations and FRU Details .................................................................................... 3-8
3.1.3 Removing and Reinstalling Shielding Cover ........................................................................... 3-10
3.1.4 Removing and Reinstalling Left and Right Panels .................................................................. 3-10
3.1.5 Removing and Reinstalling Front Panel .................................................................................. 3-10
3.1.6 Removing and Reinstalling Panels ......................................................................................... 3-11
3.1.7 Replacing Air Spring ................................................................................................................ 3-11
3.1.8 Remove the dust from the fans ............................................................................................... 3-11
3.2 Frame Assembly ........................................................................................................... 3-12

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3.2.1 Module Functions .................................................................................................................... 3-12


3.2.2 Component Locations and FRU Details .................................................................................. 3-13
3.2.3 Replacing Front and Rear Dust Screens ................................................................................ 3-13
3.3 Reaction Carousel Assembly ....................................................................................... 3-14
3.3.1 Main functions ......................................................................................................................... 3-14
3.3.2 Locations and FRU details ...................................................................................................... 3-14
3.3.3 Replacing the cables of the reaction carousel cover .............................................................. 3-15
3.3.4 Replacing the cable of the heat insulation chamber ............................................................... 3-16
3.3.5 Replacing Home Position Sensor and Coder Sensor ............................................................. 3-18
3.3.6 Replacing motor assembly and synchronous belt .................................................................. 3-20
3.3.7 Replacing Reaction Cuvette ................................................................................................... 3-21
3.4 Sample/Reagent carousel cover assembly .................................................................. 3-21
3.4.1 Module Functions .................................................................................................................... 3-21
3.4.2 Locations and FRU details ...................................................................................................... 3-21
3.4.3 Replacing Sample/Reagent Carousel Body Assembly ........................................................... 3-23
3.4.4 Replacing Reagent Temperature Sensor ................................................................................ 3-24
3.4.5 Replacing cooler(Peltier) and sealing ring .............................................................................. 3-26
3.4.6 Replacing Home Position Sensor and Coder Sensor ............................................................. 3-27
3.4.7 Replacing Sample/Reagent Carousel Motor Assembly .......................................................... 3-28
3.4.8 Replacing the synchronous belt .............................................................................................. 3-30
3.4.9 Replacing cooling fan of reagent refrigeration ........................................................................ 3-31
3.4.10 Replacing Bar Code Reader ................................................................................................. 3-32
3.4.11 Replacing Reagent Anti-fogging Heating Assembly .............................................................. 3-33
3.5 Probe assembly ............................................................................................................ 3-34
3.5.1 Module Functions .................................................................................................................... 3-34
3.5.2 Locations and FRU details ...................................................................................................... 3-35
3.5.3 Replacing the optical coupler of horizontal and vertical movement ........................................ 3-37
3.5.4 Replacing probe assembly,Anti-collision spring and powder screws ................................... 3-38
3.5.5 Replacing Reagent Preheating Assembly............................................................................... 3-38
3.5.6 Replacing liquid level detection board .................................................................................... 3-40
3.5.7 Replacing horizontal rotational synchronous belt ................................................................... 3-40
3.5.8 Replacement of Horizontal Motor Assembly ........................................................................... 3-41
3.5.9 Replacement of Vertical Motor Assembly ............................................................................... 3-42
3.5.10 Replacing Probe Drive Assembly .......................................................................................... 3-43
3.6 Mixer Assembly ............................................................................................................ 3-45
3.6.1 Module Functions .................................................................................................................... 3-45
3.6.2 Component Locations and FRU Details .................................................................................. 3-45
3.6.3 Replacing the optical coupler of horizontal and vertical movement ........................................ 3-46
3.6.4 Replacing horizontal rotational synchronous belt ................................................................... 3-47
3.6.5 Replacement of Horizontal Motor Assembly ........................................................................... 3-48
3.6.6 Replacing DC motor, mixer and powder screws ..................................................................... 3-49
3.6.7 Replacement of Vertical Motor Assembly ............................................................................... 3-50
3.6.8 Replacement of Mixer Drive Assembly ................................................................................... 3-51
3.7 Cuvette Wash Station ................................................................................................... 3-53
3.7.1 Module Functions .................................................................................................................... 3-53
3.7.2 Locations and FRU details ...................................................................................................... 3-53
3.7.3 Replacing Wash Probes Assembly ......................................................................................... 3-54
3.7.4 Replacing Wash Station .......................................................................................................... 3-55
3.7.5 Replacing Wash Probe Drive Assembly.................................................................................. 3-56
3.7.6 Replacing Wash Probe Drive Motor ........................................................................................ 3-58
3.7.7 Replacing Zero Position Photocoupler .................................................................................... 3-59
3.8 Syringe Assembly ......................................................................................................... 3-60
3.8.1 Module Functions .................................................................................................................... 3-60
3.8.2 Component Locations and FRU Details .................................................................................. 3-60
3.8.3 Replacing 2.5ml syringe and 10ml syringe ............................................................................. 3-60
3.9 Photometer Unit............................................................................................................ 3-61
3.9.1 Functions and Parameters ...................................................................................................... 3-61
3.9.2 Composition and Structure of Optical Assembly ..................................................................... 3-61
3.9.3 Replacing Lamp ...................................................................................................................... 3-63
3.9.4 Disassembling/Assembling Optical Assembly ........................................................................ 3-63

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3.9.5 Replacing Filter ....................................................................................................................... 3-65


3.9.6 Replacing Preamplifier Board ................................................................................................. 3-66
3.9.7 Replacing lamp fan ................................................................................................................. 3-66
3.9.8 Replacing Reaction Cuvette ................................................................................................... 3-67
3.9.9 Replacing AD collection board ................................................................................................ 3-68
3.10 ISE Unit (Optional) ....................................................................................................... 3-68
3.10.1 Module Functions .................................................................................................................. 3-68
3.10.2 Structure and FRU List.......................................................................................................... 3-72
3.10.3 Unclogging Waste Tubes ...................................................................................................... 3-75
3.10.4 Replacing Pump Tube ........................................................................................................... 3-76
3.10.5 Replacing Calibrator Tube .................................................................................................... 3-76
3.10.6 Replacing ISE electrode........................................................................................................ 3-77
3.10.7 Removing reagent pack(ISE) ................................................................................................ 3-78
3.10.8 Storing electrodes(ISE) ......................................................................................................... 3-78
3.10.9 Inventory Calculation of Reagent Pack ................................................................................. 3-79
4 Hardware Circuits...................................................................................................................................... 4-1
4.1 Overview ......................................................................................................................... 4-1
4.2 Hazards .......................................................................................................................... 4-1
4.3 Summary of PCBAs ....................................................................................................... 4-1
4.4 Functions of PCBA ......................................................................................................... 4-3
4.4.1 Control Structure ....................................................................................................................... 4-3
4.4.2 Main Board ................................................................................................................................ 4-4
4.4.3 Power driver board .................................................................................................................... 4-8
4.4.4 AD collection board ................................................................................................................. 4-13
4.4.5 Pre-amplification Board ........................................................................................................... 4-15
4.4.6 Liquid Level Detection Board (LLD Board) ............................................................................. 4-16
4.4.7 Reagent Refrigeration Board .................................................................................................. 4-18
4.5 Power Supply System .................................................................................................. 4-22
4.5.1 Power Supply System of Whole Unit ...................................................................................... 4-22
4.5.2 Performance Indices ............................................................................................................... 4-23
4.5.3 Power supply board ................................................................................................................ 4-23
4.5.4 Replacing Power switch .......................................................................................................... 4-28
4.6 Wiring Diagram of Analyzer .......................................................................................... 4-31
5 Fluidic system ........................................................................................................................................... 5-1
5.1 Overview ......................................................................................................................... 5-1
5.2 Fluidic Diagram............................................................................................................... 5-1
5.3 Principles of Hydropneumatic System ........................................................................... 5-1
5.3.1 Probe wash module .................................................................................................................. 5-1
5.3.2 Cuvette Wash Module ............................................................................................................... 5-2
5.3.3 Inlet/outlet module ..................................................................................................................... 5-3
5.3.4 Interfaces for fluid connection ................................................................................................... 5-4
5.4 Introduction of Fluidic Actions ......................................................................................... 5-5
5.4.1 Fluidic Initialization .................................................................................................................... 5-5
5.4.2 Priming Wash Station ................................................................................................................ 5-5
5.5 Removing and Reinstalling Hydropneumatic Components ............................................ 5-5
5.5.1 Overview ................................................................................................................................... 5-5
5.5.2 Probe and mixer wash module ................................................................................................. 5-6
5.5.3 Cuvette Wash Module ............................................................................................................. 5-11
5.5.4 External Modules .................................................................................................................... 5-14
6 Software .................................................................................................................................................... 6-1
6.1 Software Installation ....................................................................................................... 6-1
6.1.1 Introduction of Installation Package .......................................................................................... 6-1
6.1.2 Analyzer Software Version Information ..................................................................................... 6-1
6.1.3 Folder Structure ........................................................................................................................ 6-2
6.1.4 Log Files .................................................................................................................................... 6-3
6.2 Computer Settings .......................................................................................................... 6-4
6.2.1 Computer Requirements (for International Customers) ............................................................ 6-4
6.2.2 Hard disk defragment ................................................................................................................ 6-5
6.2.3 Application Software .................................................................................................................. 6-5
6.2.4 Remove Screen Saver and System Standby............................................................................ 6-5

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6.2.5 Disable Automatic Synchronization with Internet Time Server ................................................. 6-6
6.2.6 Turn off Automatic Updates ....................................................................................................... 6-7
6.2.7 Resolution Setting ..................................................................................................................... 6-7
6.2.8 Confirmation of Administrator Permission and UAC ................................................................. 6-8
6.2.9 SQL Version Check ................................................................................................................. 6-10
6.2.10 Check the installation. ........................................................................................................... 6-10
6.2.11 Firewall Whitelist Setting ....................................................................................................... 6-11
6.3 Installation of Operating Software ................................................................................ 6-11
6.3.1 Preparation before Installation ................................................................................................ 6-11
6.3.2 Software Installation ................................................................................................................ 6-11
6.3.3 Confirm the configuration file .................................................................................................. 6-14
6.4 Software Upgrading ...................................................................................................... 6-15
6.4.1 Preparation before Upgrading ................................................................................................. 6-15
6.4.2 Upgrading of Operating Software ........................................................................................... 6-17
6.4.3 Upgrading Control System ...................................................................................................... 6-18
6.4.4 Confirmation after Upgrading .................................................................................................. 6-20
6.5 Software startup process and autostart settings .......................................................... 6-20
6.5.1 Normal Startup Procedure ...................................................................................................... 6-20
6.5.2 Software antostart settings...................................................................................................... 6-20
6.6 Software and SQL Database Uninstallation ................................................................. 6-22
6.6.1 Remove the software .............................................................................................................. 6-22
6.6.2 SQL Database Uninstalling ..................................................................................................... 6-22
6.7 Data backup and recovery ........................................................................................... 6-23
6.7.1 Data backup ............................................................................................................................ 6-23
6.7.2 Database Recovery................................................................................................................. 6-23
6.7.3 Unit parameter Backup ........................................................................................................... 6-23
6.7.4 Parameter Configuration ......................................................................................................... 6-24
6.8 Demo Software Setup .................................................................................................. 6-25
6.9 upgraded to V24.00.06 instructions ............................................................................. 6-26
7 Alignment .................................................................................................................................................. 7-1
7.1 Basic Operation .............................................................................................................. 7-1
7.1.1 Utility - Maintenance .................................................................................................................. 7-1
7.1.2 Alignment fixtures ...................................................................................................................... 7-1
7.1.3 Mechanical Reset ...................................................................................................................... 7-2
7.2 Alignment Procedure ...................................................................................................... 7-4
7.3 Photometric Unit ............................................................................................................. 7-5
7.3.1 Signal Collecting Position Adjustment....................................................................................... 7-5
7.3.2 Photoelectric Gain Adjustment .................................................................................................. 7-6
7.4 Sample/Reagent carousel unit ....................................................................................... 7-7
7.4.1 Reaction Carousel Circumferential Position Adjustment .......................................................... 7-8
7.4.2 Sample/Reagent Carousel Outer Ring Circumferential Position ............................................ 7-10
7.4.3 Sample/Reagent Carousel Middle Ring Circumferential Position .......................................... 7-12
7.4.4 Sample/Reagent Carousel Inner Ring Circumferential Position ............................................. 7-12
7.5 Probe unit ..................................................................................................................... 7-13
7.5.1 Probe to Horizontal Position on Reaction Carousel ................................................................ 7-13
7.5.2 Probe to Horizontal and Vertical Positions on Wash Well ....................................................... 7-15
7.5.3 Probe to Sample/Reagent Carousel Outer Ring ..................................................................... 7-16
7.5.4 Probe to Sample/Reagent Carousel Middle Ring ................................................................... 7-16
7.5.5 Probe to Sample/Reagent Carousel Inner Ring ..................................................................... 7-17
7.5.6 Probe to Vertical Limit Position on Reaction Carousel ........................................................... 7-17
7.5.7 Probe to Vertical Limit Position in Reagent Bottle .................................................................. 7-17
7.5.8 Probe to Horizontal Position on ISE Part (Optional) ............................................................... 7-18
7.5.9 Probe to Vertical Position on ISE Part (Optional) ................................................................... 7-19
7.6 Mixer Unit ..................................................................................................................... 7-20
7.6.1 Mixer to Horizontal Position on Reaction Carousel ................................................................ 7-20
7.6.2 Mixer to Horizontal Wash Position .......................................................................................... 7-21
7.6.3 Mixer to Vertical Position on Reaction Carousel ..................................................................... 7-22
7.7 Alignment of Cuvette Wash Unit .................................................................................. 7-23
7.7.1 Setting Parameters of Best Alignment Position ...................................................................... 7-24
7.7.2 Cuvette Wash Station Home ................................................................................................... 7-24

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7.7.3 Cuvette Wash Station Height .................................................................................................. 7-26


7.8 Bar Code Unit (Optional) .............................................................................................. 7-26
7.8.1 Bar Code Sticking Requirements ............................................................................................ 7-26
7.8.2 Bar code Unit .......................................................................................................................... 7-27
7.8.3 Bar Code reader model Adjustment ........................................................................................ 7-28
7.8.4 Bar Code Reader Position Adjustment ................................................................................... 7-29
7.8.5 Bar Code Stability Test ............................................................................................................ 7-30
7.9 Hydropneumatic Unit .................................................................................................... 7-31
7.9.1 Preparations before Alignment ................................................................................................ 7-32
7.9.2 Checking Floater and Valve Status ......................................................................................... 7-33
7.9.3 Syringe Check ......................................................................................................................... 7-34
7.9.4 Fluidic Prime ........................................................................................................................... 7-34
7.9.5 the volume of the reaction liquid during cuvette washing process ......................................... 7-36
7.10 Pyrology Unit ................................................................................................................ 7-37
7.10.1 Configuration of Sensor Parameters ..................................................................................... 7-37
7.10.2 Observe Temperature Curve ................................................................................................. 7-38
7.10.3 Wash Solution Temperature Control ..................................................................................... 7-39
7.11 ISE Unit ........................................................................................................................ 7-40
7.11.1 Module Initialization ............................................................................................................... 7-40
7.11.2 ISE Error Codes .................................................................................................................... 7-41
8 Installation ............................................................................................................................................... 8-42
8.1 Installation Procedure ................................................................................................... 8-42
8.1.1 Installation Procedure ............................................................................................................. 8-42
8.1.2 Installation Time Consumption ................................................................................................ 8-43
8.2 Check before Installation .............................................................................................. 8-43
8.2.1 Installation Environment .......................................................................................................... 8-43
8.2.2 Configuration Check ................................................................................................................ 8-43
8.3 Installation Requirements ............................................................................................. 8-44
8.3.1 Space and Accessibility Requirements for Installation ........................................................... 8-44
8.3.2 Power Supply and Noise ......................................................................................................... 8-44
8.3.3 Water Supply and Drainage .................................................................................................... 8-44
8.3.4 Computer Requirements ......................................................................................................... 8-45
8.4 Installing the Analyzer .................................................................................................. 8-45
8.4.1 Unpacking ............................................................................................................................... 8-45
8.4.2 Removing Packaging .............................................................................................................. 8-47
8.4.3 Installing Accessories .............................................................................................................. 8-48
8.4.4 Connect the pipeline ............................................................................................................... 8-51
8.4.5 Connecting the Overall System .............................................................................................. 8-54
8.4.6 Setting the PC ......................................................................................................................... 8-54
8.4.7 Software Installation ................................................................................................................ 8-54
8.4.8 Starting up the System ............................................................................................................ 8-54
8.4.9 Aligning the Analyzer ............................................................................................................... 8-56
8.4.10 Aligning the ISE (Optional) .................................................................................................... 8-56
8.4.11 Prime the fluidic system ........................................................................................................ 8-57
8.4.12 Initial Maintenance Record ................................................................................................... 8-57
8.4.13 Startup Initialization ............................................................................................................... 8-57
8.4.14 Importing and Configuring Chemistry Parameters of Mindray Reagents ............................. 8-58
8.4.15 Running Water Test ............................................................................................................... 8-59
8.5 Verifying Basic Performance ........................................................................................ 8-65
8.5.1 Checking System Status ......................................................................................................... 8-65
8.5.2 Testing Movement Positioning Performance ........................................................................... 8-65
8.5.3 Testing Optical Performance ................................................................................................... 8-65
8.5.4 Testing Bar Code Performance ............................................................................................... 8-65
8.5.5 Testing Clinical Performance................................................................................................... 8-65
8.6 LIS Connection ............................................................................................................. 8-67
8.7 Backing Up Data........................................................................................................... 8-67
8.8 Handling Exceptions in Installation............................................................................... 8-67
8.9 List of accessories and functions ................................................................................. 8-67
9 Preventive maintenance ........................................................................................................................... 9-1
9.1 Overview ......................................................................................................................... 9-1

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9.1.1 Preventive maintenance............................................................................................................ 9-1


9.1.2 Biochemistry maintenance commands ..................................................................................... 9-1
9.1.3 ISE maintenance commands .................................................................................................... 9-3
9.2 Maintenance Tools.......................................................................................................... 9-4
9.3 Maintenance Procedure ................................................................................................. 9-5
9.3.1 Procedure .................................................................................................................................. 9-5
9.3.2 Steps ......................................................................................................................................... 9-6
9.4 Post-maintenance Check ............................................................................................. 9-13
10 Troubleshooting ............................................................................................................................... 10-1
10.1 Overview ....................................................................................................................... 10-1
10.1.1 Classification of logs ............................................................................................................. 10-1
10.1.2 Viewing and handling logs .................................................................................................... 10-2
10.1.3 Error Troubleshooting............................................................................................................ 10-3
10.2 Common Troubleshooting ............................................................................................ 10-4
10.2.1 Database initializing failed..................................................................................................... 10-4
10.2.2 Database backup failed......................................................................................................... 10-5
10.2.3 Database Version Is Higher Than the Current Software Version .......................................... 10-5
10.2.4 Unmatched Operating Software VersionA22039 .................................................................. 10-7
10.2.5 Water Residues Exist in the Cuvette A02027 ....................................................................... 10-7
10.2.6 Bar Code Scanning Faults .................................................................................................... 10-8
10.2.7 Cuvette Blank Out of Range C07004 .................................................................................... 10-9
10.2.8 Light Intensity Is Too Weak C07003.................................................................................... 10-10
10.2.9 Water Blank Out of Range (10X) C07009 ........................................................................... 10-10
10.2.10 Lamp Is Not Turned On C07005 ....................................................................................... 10-12
10.2.11 Light Intensity Is Too Strong C07006 ................................................................................ 10-13
10.2.12 Analyzer cannot be connected .......................................................................................... 10-13
10.2.13 Sample Probe Fails to Detect the Level of the Wash Well A01028 .................................. 10-15
10.2.14 Sample Probe Fails to Detect the Level on the Reaction Carousel when Dispensing A01033
....................................................................................................................................................... 10-17
10.2.15 Dark current is too high C07007 ....................................................................................... 10-18
10.2.16 Clinical Result Problems ................................................................................................... 10-19
10.3 Data alarms ................................................................................................................ 10-21
10.4 Error messages and corrective actions ...................................................................... 10-30
11 Assembly Explosive Views...................................................................................................................... 11-1
11.1 Overview ....................................................................................................................... 11-1
11.2 Instrument Panels Exploded ........................................................................................ 11-1
11.2.1 Front Right Panels ................................................................................................................. 11-1
11.2.2 Back Left Panels ................................................................................................................... 11-2
11.2.3 Top Panels ............................................................................................................................. 11-3
11.2.4 Front Left Panels ................................................................................................................... 11-4
11.3 ISE Unit ........................................................................................................................ 11-5
11.3.1 ISE Unit Position ................................................................................................................... 11-5
11.3.2 ISE Unit Exploded ................................................................................................................. 11-6
11.4 S/R Probe Unit.............................................................................................................. 11-7
11.4.1 S/R Probe Unit Position ......................................................................................................... 11-7
11.4.2 S/R Probe Unit Exploded ...................................................................................................... 11-8
11.4.3 S/R Probe Drive Assembly Exploded .................................................................................... 11-9
11.5 Reagent/sample Disk ................................................................................................. 11-10
11.5.1 Reagent/sample Disk Position ............................................................................................ 11-10
11.5.2 Reagent/sample Disk Exploded ........................................................................................... 11-11
11.5.3 Reagent Refrigeration Unit Exploded .................................................................................. 11-12
11.6 Barcode Scanner Unit ................................................................................................ 11-13
11.6.1 Barcode Scanner Unit Position ........................................................................................... 11-13
11.6.2 Barcode Scanner Unit Exploded ......................................................................................... 11-14
11.6.3 Reagent Disk Antifogging Assembly Exploded ................................................................... 11-15
11.7 Reaction Disk Unit ...................................................................................................... 11-16
11.7.1 Reaction Disk Unit Position ................................................................................................. 11-16
11.7.2 Reaction Disk Unit Exploded ............................................................................................... 11-17
11.7.3 Heat Insulation Chamber of Reaction Carousel Exploded .................................................. 11-18
11.7.4 Heater cables above and under Reaction Carousel Exploded ........................................... 11-19

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11.8 Wash Well................................................................................................................... 11-20


11.8.1 Wash Well Positions ............................................................................................................ 11-20
11.9 Photometer Unit Exploded ......................................................................................... 11-21
11.9.1 Optical Assembly Position ................................................................................................... 11-21
11.9.2 Optical Assembly(BA24) Exploded ..................................................................................... 11-22
11.10 Mixer Assembly .......................................................................................................... 11-23
11.10.1 Mixer Assembly Position ................................................................................................... 11-23
11.10.2 Mixer Assembly Exploded ................................................................................................. 11-24
11.10.3 Mixer Drive Assembly Exploded ........................................................................................ 11-25
11.11 Wash Station Assembly .............................................................................................. 11-26
11.11.1 Wash Station Assembly Position ....................................................................................... 11-26
11.11.2 Wash Station Assembly Exploded ..................................................................................... 11-27
11.12 Rear Frame Part ......................................................................................................... 11-28
11.12.1 Rear Frame Part Exploded................................................................................................ 11-28
11.12.2 Power Supply Assembly Exploded .................................................................................... 11-29
11.12.3 10ml Syringe Module Exploded ........................................................................................ 11-30
11.12.4 2.5ml Syringe Drive Assembly Exploded .......................................................................... 11-31
11.12.5 PCB Bracket Exploded ...................................................................................................... 11-32
11.12.6 Communication and Power Joint Exploded ...................................................................... 11-33
11.12.7 Valve Assembly Exploded ................................................................................................. 11-33
11.13 Front Right Frame Part ............................................................................................... 11-34
11.13.1 S/R Syringe Assembly Position ......................................................................................... 11-34
11.13.2 S/R Syringe Assembly Exploded ....................................................................................... 11-35
11.13.3 Drive Assembly of Syringe Exploded ................................................................................ 11-36
11.13.4 Front Right Frame Part Exploded ..................................................................................... 11-37
11.13.5 Wash Station Preheater Assembly Exploded .................................................................... 11-38
11.13.6 Fluidic Joint Bracket Exploded .......................................................................................... 11-38
11.14 Optional Module ......................................................................................................... 11-39
11.14.1 Drainage Unit (BA40-30-61346) ........................................................................................ 11-39
12 LIS Connection Setting and Troubleshooting .................................................................................. 12-1
12.1 Overview of LIS ............................................................................................................ 12-1
12.2 LIS Networking ............................................................................................................. 12-1
12.2.1 Querying State of RS232 Serial Port Card and Network Card ............................................. 12-1
12.2.2 Checking Network Status ...................................................................................................... 12-2
12.3 LIS Parameter Setup .................................................................................................... 12-4
12.3.1 Introduction to Protocols ....................................................................................................... 12-4
12.3.2 Parameter Setup on a Workstation Computer ...................................................................... 12-5
12.3.3 Basic Concept of Unidirectional/Bidirectional LIS Communication ....................................... 12-5
12.3.4 Channel ID Setup .................................................................................................................. 12-6
12.4 Operation Guidance of Test Tool .................................................................................. 12-8
12.4.1 Operation Procedure of Test Tool.......................................................................................... 12-8
12.5 Common Problems and Corrective Measures ........................................................... 12-11
12.5.1 LIS cannot be connected .................................................................................................... 12-11
12.5.2 LIS communication interrupted suddenly ............................................................................ 12-12
12.5.3 Issues with firewall .............................................................................................................. 12-13
12.5.4 Invalid LIS response ............................................................................................................ 12-13
12.5.5 ISE response time out ......................................................................................................... 12-14
12.5.6 LIS communication result slowly transmitted ...................................................................... 12-15
12.5.7 Part of item results missed during LIS communication ....................................................... 12-15
12.6 Bidirectional LIS communication interaction log ......................................................... 12-15
13 Instrument Relocation and Emptying .............................................................................................. 13-1
13.1 Overview ....................................................................................................................... 13-1
13.1.1 Short-Term Suspension......................................................................................................... 13-1
13.1.2 Long-Term Suspension ......................................................................................................... 13-1
13.1.3 Analyzer Relocation .............................................................................................................. 13-1
13.2 Emptying Fluidic Tubes ................................................................................................ 13-2
13.2.1 Empty ISE Tube (optional) .................................................................................................... 13-2
13.2.2 Emptying Wash Tube ............................................................................................................ 13-4
13.2.3 Emptying Waste Tubes ......................................................................................................... 13-1
13.2.4 Use Count of Emptying Pump and Syringe .......................................................................... 13-2

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13.2.5 Confirmation after emptying .................................................................................................. 13-2


13.3 Clearing Data................................................................................................................ 13-3
13.4 Packing ......................................................................................................................... 13-5
13.4.1 Removing the Tubes ............................................................................................................. 13-5
13.4.2 Removing the Accessories .................................................................................................... 13-5
13.4.3 Securing the Assemblies by Tape and Foam ........................................................................ 13-5
13.4.4 Securing and Packing the Main Unit ..................................................................................... 13-5
13.4.5 Packing the Accessories ....................................................................................................... 13-6
13.4.6 Packing the Main Unit and Display of the PC ....................................................................... 13-6
14 Optional Modules............................................................................................................................. 14-1
14.1 Overview ....................................................................................................................... 14-1
14.2 ISE Module ................................................................................................................... 14-1
14.2.1 Overview of ISE Module........................................................................................................ 14-1
14.2.2 Installing the ISE Module ...................................................................................................... 14-1
14.2.3 Alignment of the ISE module ................................................................................................. 14-7
14.2.4 Precautions for ISE ............................................................................................................... 14-8
14.3 Bar Code Scanning Module ....................................................................................... 14-10
14.3.1 Overview of Bar Code Scanning Module ............................................................................ 14-10
14.3.2 Installing the Barcode Scanner ........................................................................................... 14-10
Appendices ........................................................................................................................................................... I
A.1 BS-240 Installation Acceptance Report .................................................................................................. I
A.2 BS-240 Moving Parts Position Confirmation Guide (No Alignment Tooling)........................................... I
A.3 Tool list .................................................................................................................................................... I
A.4 BS-240_Error Information Feedback Form_V1.0_EN ............................................................................ I
A.5 BS-240 Series Recovery Checklist ......................................................................................................... I
A.6 Maintenance log sheet ............................................................................................................................ I
A.7 Fluidic Diagram ..................................................................................................................................... III

No.HSH-19021-BS-240 Version: 4.0 VIII


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1 System Description
1.1 Overview
The BS-240 is a fully automated and computer-controlled chemistry analyzer designed for the in vitro
determination of clinical chemistries in serum, plasma, urine, and cerebrospinal fluid (CSF) samples. This
product consists of Analyzing Unit and Operation Unit.

Figure 1-1 Chemistry analyzer

The throughput of the analyzer is at most 200 tests/hour.


Throughput of the ISE module:
300 tests/hour for serum and plasma (Na+, K+ and Cl-)
198 tests/hour for urine (Na+, K+, Cl-)
Maximum throughput of biochemistry and ISE: 400 tests/hour
1.2 Components of Analyzing Unit
The Chemistry Analyzer consists of the analyzing unit (analyzer), operation unit (computer), and output unit
(printer).
▪ The analyzing unit performs all operations of sample analysis, which include dispensing sample and
reagent, mixing, reaction and measurement, auto washing of cuvettes, ISE analysis, etc.
▪ The operation unit is a computer installed with the operating software, which controls operation of the
analyzer and processes the test data.
▪ The printer is used to print test results.
▪ The operation unit and the analyzing unit are independent structurally and communicate with each other
through the serial port. The operation unit sends data and instructions to the analyzing unit and acquires
the data and status information from the analyzing unit.

Analyzing
unit

PC(Operating software)
Main unit
Printer

Figure 1-2 System structure

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The instrument is composed of the following components: one reaction carousel, one sample/reagent carousel,
one probe, one mixer, one automatic cuvette wash station, one photometric detection system, one ISE module
(optional). The optical measurement system performs photometric measurement to the reaction cuvettes that
hold "sample+reagent" mixture. After testing, the cuvette wash station performs 4-phase auto wash to the
reaction cuvettes.

(5)

(1)
(4)
(2)
(3)

Figure 1-3 Layout of the analyzer’s operation panel

(1) Probe (2) Sample/reagent carousel


(3)Mixer (4) Reaction carousel
(5) Cuvette wash station
1.3 Functions of Analyzing Unit
The working procedure of the system is described as follows.
1) The system resets to initialize all mechanical units and wash the exterior and interior of the probe and mixer.
2) Reaction cuvettes are washed through 8 phases(Two 4-phase), and run water blank test after phase-6.
Note: The phase-6 here is actually the 2nd phase of the wash station (facing the analyzer, from right to
left), and the 240 wash station has only four phases.
3) The reagent carousel rotates to the R1 position, from which the probe aspirates reagent.
4) The reaction cuvettes are carried to the reagent dispense position after the 4-phase washing. Then rotate
the probe with R1 added to the reaction carousel and dispense R1 into the reaction cuvette;
5) R1 is incubated in the cuvette.
6) The sample carousel rotates to the specified aspirating position, and the probe lowers down to aspirate
specified amount of sample.
7) The reaction cuvette with R1 added is carried to the sample dispense position, to which the probe rotates
to dispense sample after aspirating from the sample/reagent carousel.
8) The reaction cuvettes with sample added are carried to the sample mixing position for stirring.
9) For double-reagent tests, the reagent carousel rotates to the R2 position after a fixed period, and the probe
lowers down to aspirate R2.
10) The reaction cuvette is carried to the R2 dispense position. Then rotate the probe with R2 added to the
reaction carousel and dispense R2 into the reaction cuvette;
11) With R2 added, the reaction cuvette rotates to the mixing position for stirring.
12) During each period, the reaction cuvette experiences photometric measurement (absorbance data
collecting) when passing by the photometric unit.
13) The reaction cuvette in which reaction is finished will be washed automatically when passing by the wash
station.
Table 1-1 Functions of system units

Unit Name Functions


Probe unit Performs aspiration and dispensing for all biochemistries and ISE tests.
Performs aspiration and dispensing of reagents for all biochemistry tests.

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Sample/Reagent The outer ring can hold 40 sample containers.


carousel unit The middle ring supports 40ml and 20ml reagent bottles and can hold 40 sample
containers with adapter.
The inner ring supports 20ml reagent bottles.
The sample/reagent carousel provides a refrigerating environment which is constant
within 2°C-12°C for 24 hours a day.
The outer and middle rings support barcode scanning.
Reaction 40 positions are available for plastic cuvettes.
Carousel Unit
Mixer Unit Mixes the reaction liquid.
Photometric unit Reversed optics with gratings, supporting 8 wavelength: 340nm, 405nm, 450nm,
510nm, 546nm, 578nm, 630nm, 670nm
Cuvette Wash 4-phase automatic washing of reaction cuvettes
Station
ISE Unit Provides the function of ISE measurement
(Optional)

2 System Performance and Workflow


2.1 Major Specifications
2.1.1 General Specifications
Table 2-1 General Specifications

System Random selection, multi-channel, multi-chemistry, capable to pause test and


adding new tests
System structure Analyzing unit + computer + printer
Sample type Serum, urine, plasma, CSF (cerebrospinal fluid), full blood, etc.
Maximum number of 39 double-reagent tests/78 single-reagent tests
tests run simultaneously
Throughput At most 200 tests/hour (single/double-reagent), and at most 400 tests/hour
(with ISE module)
Reaction type Endpoint, Kinetic and Fixed-time; supporting single-/double-reagent tests,
and single-/double-wavelength tests
Reaction time The longest reaction time is 20 minutes for single-reagent test, and 10
minutes for double-reagent test
Reaction temperature 37±0.3℃
Test type Clinical chemistries, immunoturbidimetry, Therapeutic Drug Monitoring (TDM)
Predilution Dilution is conducted in reaction cuvette at the ratio of 1:3~1:125
Operation mode Chemistries are defined one by one via the operating software; panels and
calculation tests are supported
Calibration math model Single-point linear, two-point linear, multi-point linear, Logit-Log 4P, Logit-Log
5P , Spline, Exponential, Polynomial, and Parabola.
QC Westgard multi rules, cumulative sum check, and twin-plot
Data processing Capable of storing and outputting various types of data and charts, and
calculating among different chemistries.
Dimensions Analyzing unit: 690mm (length) *580mm (depth) *595mm (height)
Weight Analyzing unit: 79 kg
STAT sample Emergent samples can be analyzed at any time with highest priority

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Networking Capable to connect with a LIS (Laboratory Information Management System)

2.2 Sample Specifications


Sample loading
Samples are loaded via sample carousel.
Sample cuvette type
Table 2-2 Sample tube volume and dead volume

Sample Container Specification


Sample tube Φ14×25mm,0.5ml ( Beckman, ISE test
not supported)
Sample tube Φ14×25mm,2ml ( Beckman, ISE test not
supported)
Sample tube Φ12×37mm,2ml ( Hitachi, ISE test not
supported)
Primary tube/Plastic Φ12×68.5 mm
tube
Primary tube or plastic Φ12×99 mm
tube
Primary tube or plastic Φ12.7×75 mm
tube
Primary tube or plastic Φ12.7×100 mm
tube
Primary tube or plastic Φ13 X 75 mm
tube
Primary tube or plastic Φ13 X 95 mm
tube
Primary tube or plastic Φ13 X 100 mm
tube
For the tests of the whole blood(centrifuged), onlyΦ12×68.5mm, Φ12×99mm, Φ12.7×75mm,
Φ12.7×100 mm, Φ13×75 mm, Φ13×95 mm, Φ13×100 mm anticoagulation tubes can be used. The sample
height in the tube should be no higher than 55mm and the blood cell level should be no lower than 10mm.
Microcups are not allowed. To ensure the clinical performance and avoid the system alarm, EDTA
anticoagulation tubes are recommended.
Sample carousel
One carousel is shared for holding sample and reagent and the outer and middle ring supports bar code
scanning.
Sample positions on sample carousel
The outer ring can hold 40 samples and the middle ring can hold 40 sample with sample position adapter. In
total, up to 80 samples can be placed on the outer and inner ring.
STAT sample
Emergent samples can be analyzed at any time with highest priority.
Sample volume
2μl ~ 45μl, with an increment of 0.1μl
ISE: 70μl for serum and 140μl for urine
Sample probe
One probe is shared for adding sample and reagent with liquid level sense, featuring level detection (vertical
collision detection) and level tracking.
Sample probe cleaning
The exterior and interior of the sample probe is washed with carryover rate no more than 0.05%.
Sample input mode (bar code)
Table 2-3 Sample bar code

Name Value
Symbology Codabar, ITF, code128, code39, UPC/EAN, Code93
Minimum bar code Outer ring 0.19mm~0.5mm
density Middle ring 0.25mm~0.5mm

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Data bits 3-27


Format and content Defined by user
Maximum width 55mm
Minimum height 10mm
Maximum ±5°
inclination angle
Print quality No less than Class C according to the ANSI MH10.8M
Print Quality Specification.
Width and 2.5-3.0:1
narrowness
2.2.1 Reagent Specifications
Reagent loading
Reagents are loaded through reagent carousel.
Reagent refrigeration
Reagent refrigeration temperature: 2~12℃.
Reagent addition approach
Reagent is aspirated and dispensed precisely by syringe, which is capable of detecting fluid level and checking
reagent volume.
Supported reagent types
R1, R2.
Reagent volume
R1:100μl~250μl,with an increment of 0.5μl and R2:10μl~250μl,with an increment of 0.5μl.
Reagent Carousel
One carousel is shared for holding sample and reagent. The reagents can be placed on the middle ring and
inner ring. All positions on the middle ring support scanning by a built-in reagent bar code reader.
Number and volume of reagent bottle
The reagent positions support Mindray reagent bottles, which include: middle ring 40ml and middle ring 20ml;
inner ring 20 ml.
Reagent carousel positions
Middle ring supports 40 40ml or 20ml reagent bottles and inner ring supports 40 20ml reagent bottles. When
middle ring is used to hold 40ml reagent bottles, 20ml reagent bottles cannot be placed on the inner ring.
Reagent bar code
Table 2-4 Reagent bar code

Name Value
Symbology Codabar, ITF, code128, code39, UPC/EAN,
Code93
Minimum bar code density 0.25mm~0.5mm
Data bits 13-30
Format and content Defined by user
Maximum width 55mm
Minimum height 10mm
Maximum inclination angle ±5°
Print quality Class A (ANSI MH10.8M)
Width and narrowness 2.5:1
Reagent probe
One probe is shared for adding sample and reagent with liquid level sense, featuring level detection (vertical
collision detection) and level tracking.
Reagent probe cleaning
Both interior and exterior of the probe are washed.
Prevention of reagent cross contamination
Users are allowed to perform carryover settings, e.g. washing interior and exterior of probe and inserting special
wash between tests.
2.2.2 Specifications of Reaction System
Table 2-5 Specifications of Reaction System

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Optical pathlength of reaction 5mm


cuvette
Material of reaction cuvette 5mm*5mm*29.5mm. Plastic cuvette: Cuvette segments with 5
cuvettes each segment.
Number of reaction cuvettes 40
Mixing method Mixing after sample and R2 are added.
Reaction liquid volume 100μl~360μl;
Optical measurement method Forward splitting filter system, detecting each wavelength
through a photodiode
Wavelength 8 wavelengths: 340nm, 405nm, 450nm, 510nm, 546nm,
578nm, 630nm, 670nm
Light source 12v/20W tungsten-halogen lamp
Wavelength accuracy ±2nm
Photometric measurement Measuring through a photodiode
method
Number of wavelengths Supporting one or two wavelengths
simultaneously measured for each
test
Absorbance range 0-4.0A, optical path: 10mm

2.2.3 Specifications of Operation Unit


Table 2-6 Specifications of Operation Unit

Display Monitor Screen resolution of 1280×1024


Operating system Supporting Window 8 (64 bit)/Window 10 (64 bit)
Communication interface RS232, compatible with TCP/IP
Printer Supporting three types of printer: inkjet printer, laser (black and white) printer
and stylus printer.
Data input Keyboard, mouse and barcode reader, LIS: HL7, ASTM1394 (TCP/IP or serial
interface)
Data output Display monitor, printer, LIS system
Data storage Hard disk and USB interface

2.2.4 Typical Test Procedure


Wait for
steadiness
of lamp and Mixer
Add
balance of perfor
Double Reagent R2 to
reaction ms Available
probe
Mixer performs mixing

Chemistries
Complete absorbency

Shutdown Procedure

carousel mixing
Add sample to probe

chemistrie
Startup Initialization

Add R1 to probe

temperatur s are
measurement

Wash Cuvette
Wash Cuvette
Procedure

e finished
Single Reagent
Chemistries

Next test

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Figure 2-1 Test flowchart

2.2.5 Startup Procedure


1) The analyzer is powered on.
2) The operating software is run and starts checking the running environment.
3) The software checks the status of the middle-/low- layer units.
4) The software checks the parameters and status of the analyzer, and inquires the key
parameters and status of all the units.
5) The system communicates with the bar code reader, if it is configured.
6) Fluidic Initialization is performed: 1) the pumps and valves are powered off for resetting;
2) the floaters of the water tank, diluted wash solution tank, and high-concentration
waste tank are checked.
7) The system resets all mechanical units.
8) The reaction carousel temperature control is turned on.
9) The lamp is turned off and the dark current and maximum luminance value of the
reaction carousel lamp are inquired. The lamp is turned on (it takes 5 minutes for the
lamp to become steady. When 5 minutes are not reached and the system finishes its
home procedure, the system enters incubation status.
10) The whole unit is reset.
11) The probe is specially washed.
12) The preheating of cuvette wash solution, cleaning water and reagent is turned on.
13) The reagent carousel is scanned (when the built-in reagent bar code reader is
configured.)
14) The ISE module is initialized, if configured.
15) If the conditions of entering Standby status are met, the system enters into Standby
status.
2.2.6 Shutdown Procedure
1) When the system is in Standby status, it can be shut down.
2) The power of lamp, reaction carousel temperature control and the preheating of cuvette
wash solution, cleaning fluid and reagent are turned off.
3) Pumps and valves are powered off for resetting.
4) 10 cycles of ISE MANT are performed to discharge the ISE waste into the ISE reagent
pack, if ISE module is configured.
5) The database is shut down. If the operation fails, the system gives a warning, and
continues the shutdown after confirmation.
6) The system exits.
2.2.7 Workflow Descriptions
Sequential actions of the probe in each period (adding sample for biochemistry test)
Wash> raise to “home” position vertically ->rotate to sample carousel->lower into the sample tube-> aspirate
sample -> raise to “home” position vertically -> rotate to reaction carousel -> lower into the reaction carousel ->
dispense sample -> raise to the vertical home position -> rotate to wash well -> lower into the wash well->
wash -> go to next period

Sequential actions of the probe in period (dispensing R1 and R2)


Wash > raise to “home” position vertically ->rotate to reagent carousel->lower into the reagent bottle-> aspirate
reagent -> raise to “home” position vertically -> rotate to reaction carousel -> lower into the reaction carousel ->
dispense reagent -> raise to the vertical home position -> rotate to wash well -> lower into the wash well ->
wash -> go to next period.

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Sequential actions of the probe in each period (dispensing ISE sample)


Wash > raise to “home” position vertically ->rotate to sample carousel->lower into the sample tube-> aspirate
sample -> raise to “home” position vertically -> Rotate to above the ISE sample injection port -> lower into the
ISE sample injection port -> dispense sample -> raise to the vertical home position -> rotate to wash well ->
lower into the wash well -> wash -> go to next period

Sequential actions of the probe in each period (dispensing whole blood sample)
Wash > raise to “home” position vertically ->rotate to sample carousel->lower into the sample tube-> aspirate
sample->raise to vertical home position->Rotate to wash well->Lower to the position for special wash -> Special
wash the exterior of the probe -> raise to “home” position vertically -> rotate to reaction carousel -> dispense
sample->Raise to vertical home position->rotate to wash well -> lower into the wash well -> wash -> lower to
position for special wash ->special wash the exterior of the probe-> raise to “home” position vertically -> wash
->go to next period.

Sequential actions of mixer in each period


Sequential actions: Lower to wash well ->wash-> raise to the wash well(vertical home position) -> rotate to
reaction carousel->lower to reaction carousel->mixing->raise to above the reaction carousel->go to next period.
2.2.8 Measuring Points
Set the
R1 R1 incubates for S MixS incubation time R2 MixR2 Maximum reaction time of double Reaction end
180 seconds of R2 arbitrarily reagent is over 10 min

T1 T11
Maximum reaction time of single reagent is over 20 min

Figure 2-2 Measuring points for BS-240 single-/double-reagent test

3 Modules and Units


3.1 Shell Assembly
3.1.1 Module Functions
The shells assembly indicates the apparent structures of the whole analyzer and is designed for protecting the
internal assemblies. It provides interfaces for each module, and is also a representation of industrial design.
3.1.2 Component Locations and FRU Details
The shells assembly consists of the shielding cover, top panel, desk panel, left and right panels, front panel,
doors, middle panel and rear panel.

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Shielding cover hinge


assembly
Syringe cover assembly

Auto wash tube sleeve

Shielding cover Wash station desk panel


assembly
Air spring holder
Middle baffle (BA24)

Reaction carousel panel


Air spring
assembly (BA24)
ISE port plug for panel Lamp panel

Sample/reagent panel Screw plug for panel


Front cover
Sample/reagent carousel
assembly (BA24)
cover assembly
Left panel assembly

Top cover

Rear panel

Right panel assembly

Figure 3-1 Shells assembly

Table 3-1 List of materials

No FRU No. Part Name Remarks


1 115-036569-00 Shielding cover assembly
3 042-016861-01 Middle baffle (BA24)
4 M6T-010005--- Air spring
5 BA40-20-72908 ISE port plug for panel
6 043-006892-00 Sample/reagent panel
7 115-036339-00 Sample/reagent carousel cover
assembly
8 115-036338-00 Left panel assembly
9 115-036337-00 Front cover assembly (BA24)
10 BA40-20-72907 Screw plug for panel (Mould MR72907)
11 043-006894-00 Lamp panel
12 115-036340-00 Reaction carousel panel assembly
(BA24)
13 042-018183-00 Air spring holder

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No FRU No. Part Name Remarks


14 043-006896-00 Wash station desk panel
15 043-006897-00 Wash tube sleeve
16 BA10-30-78156 Syringe skylight cover assembly
17 BA10-20-77801 Top cover
18 115-036570-00 Right panel assembly
19 042-016863-00 Rear panel
3.1.3 Removing and Reinstalling Shielding Cover
When to do
Replace the shielding cover when it is damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Flathead screwdriver(small) / 1
How to do
1) Switch off the main power of the analyzer to ensure all moving assemblies are not in working status.
2) Open the shielding cover, and use a flathead screwdriver to insert into the gap of circlip and the bulb
on the air spring to push outwards the circlip to the degree that it will not be dropped.
3) Hold the shielding cover and pull out the air spring from the bulb and restore the air spring to its original
position.
4) Use a cross screwdriver to remove the four M4*12 powder screws on the hinge of the shielding cover,
and then remove the shielding cover assembly.
5) To restore the shielding cover assembly, follow the steps mentioned above in the reversed order.
Alignment and confirmation
After restoring the shielding cover assembly, check the gap with the panels, and if the gap is uneven or the
shielding cover interferes with the panels, adjust the hinges.
3.1.4 Removing and Reinstalling Left and Right Panels
When to do
When the left and right panels need to be removed to repair the internal assemblies
Tools
Name Code Quantity
Cross screwdriver / 1
How to do
1) Unscrew the three screws at the rear of the left (right) panel.
2) Push the left or right panel backward until the panel falls out of the two positioning pins at the front of
the panel. Remove the left or right panel.
3) Install back the left and right panel according to the reversed order above.
Alignment and confirmation
When installing back the left and right panel, make sure the hook on the panel inserted into the square holes
on the frame in order to maintain the gap between the left (right) panel and the frame.
3.1.5 Removing and Reinstalling Front Panel
When to do
This operation is performed when an inner component of the instrument needs repair and the front panel need
to be removed.
Tools
Name Code Quantity
Cross screwdriver / 1
How to do
1) Remove the left and right panel first.
2) Loosen the 2 screws (without removing) in the front of the sample/reagent panel, and then remove the
lamp panel.
3) Loosen (without removing) a retaining screw of the front panel and the front beam of the frame to the
maximum extent
4) Remove the retaining screws located on both sides of the front panels and used for fastening to the
frame.
5) Pull out the panel assembly towards the front of the instrument.

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6) To restore the front panel assembly, follow the steps mentioned above in the reversed order.
Alignment and confirmation
When restoring, if the gap between the front panel and the sample/reagent panel and the lamp panel is not
proper, you can remove the lamp panel, and adjust the gap by adjusting the retaining screw that fastens the
front panel and the frame beam.
3.1.6 Removing and Reinstalling Panels
When to do
This operation is performed when an inner component of the instrument needs repair and the front panel need
to be removed.
Tools
Name Code Quantity
Cross screwdriver / 1
How to do
Removing and Reinstalling BS-240 Reaction Carousel Panel
1) Remove the panel screws on the wash station panel, the reaction carousel panel, the lamp panel first,
unscrew the retaining screws on the 3 parts, and remove the wash station panel and the lamp panel.
2) Loosen the knurled screws on the wash probe assembly, and remove the wash probe assembly.
Handle carefully to protect the probe assembly against bending and contamination.
3) Remove the probe arm cover and the mixer arm cover.
4) Remove the reaction carousel panel assembly. Note that the panel needs to tilt at a specific angle so
that it can be taken out. Handle carefully to protect the sample probe and the mixer.
5) To restore the reaction carousel panel assembly, follow the steps mentioned above in the reversed
order.
Removing/Reinstalling Sample/Reagent disk panel
1) Remove the panel screws on the reaction carousel panel and the lamp panel, and unscrew the
retaining screw.
2) Remove the sample/reagent carousel cover assembly from the sample/reagent carousel panel.
3) Remove the sample/reagent panel.
4) To restore the reaction carousel panel assembly, follow the steps mentioned above in the reversed
order.
Alignment and confirmation
To restore the reaction carousel panel, adjust the gap evenly before tightening the screw.
3.1.7 Replacing Air Spring
When to do
Replace the air spring if it loses elasticity or fails.
Tools
Name Code Quantity
Flathead screwdriver(small) / 1
How to do
1) Open the shielding cover, and use a flathead screwdriver to insert into the gap of circlip and the bulb
on the air spring to push outwards the cir clip to the degree that it will not be dropped.
2) Hold the air spring and pull it out. If the bulb of the air spring is not damaged, keep using it.
3) Install the new air spring (Only air spring cylinder needs to be replaced.)
Alignment and confirmation
The cylinder of the air spring should be at the side of the shielding cover. Open and close the shielding cover
several times to make the air spring cylinder lubricated.
3.1.8 Remove the dust from the fans
When to do
When much dust is accumulated on the fans, or it has been 1 year since the last maintenance
Maintenance Tools
Name Code Quantity
Cross screwdriver / 1
Suction cleaner/ hair brush / 1
Maintenance Procedure
1) Place the analyzing unit power to the OFF position.

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2) If the reagent refrigeration fan and PCB fan need cleaning, remove the left panel.
3) If the cooling fans for the whole unit and the power supply need cleaning, remove the rear panel.
4) If the lamp fan needs cleaning, remove the right panel.
5) Manually rotate the fan and remove the dust on it.
6) Install the removed panels.
7) Switch on the analyzing unit power.
Alignment and confirmation
Check if the fans work normally.
3.2 Frame Assembly
3.2.1 Module Functions
The frame assembly is a basic unit for installing and supporting the components of the analyzer.
Sample Probe Movement Assembly Mixer Movement Assembly

Shielding Cover Warning

Sample/reagent carousel cover


Wash station desk
Sample/reagent panel panel

Reagent bar code Reaction


assembly carousel panel

Lamp panel

Frame
Assembly

Reaction Carousel
Assembly

Sample/reagent
Left panel assembly
carousel assembly
Reagent refrigeration
Front cover assembly
board and the bracket

Figure 3-2 Locations of components on the instrument

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3.2.2 Component Locations and FRU Details

Dust screen
retaining screw

BA24 rear dust screen

BA24 front dust screen

Dust screen retaining screw

Figure 3-3 Frame assembly

Table 3-2 List of materials

No. FRU Part Name Remarks


1 048-006111-00 BA24 front dust screen
2 048-006112-00 BA24 rear dust screen
3.2.3 Replacing Front and Rear Dust Screens
When to do
The front and rear dust screens need to be replaced when they need cleaning or are damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Exploded view for installation
See the figure of Frame assembly
How to do
1) Switch off the power supply of the whole unit.
2) Remove the right panel assembly.
3) Use a cross head screwdriver to loosen the dust screen retaining screw M3×10 and cross recessed
pan head screw.
4) Remove the dust screens.
5) Replace or clean the dust screens.
6) Restore the assembly in the reversed order.
Alignment and confirmation
Make sure that the dust screen completely covers the air inlet.

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3.3 Reaction Carousel Assembly


3.3.1 Main functions
Reaction carousel assembly is situated at the right front side of the analyzer, including the body of the reaction
carousel, reaction carousel drive assembly, reaction carousel chamber, reaction carousel sensor, and the
reaction carousel motor assembly. It is used to complete various actions, such as carrying and rotating the
reaction cuvette to the specified position, adding sample/reagent to the cuvette, mixing and washing, together
with the probe, the mixer and the 4-phase wash probes. It, as well as, provides a constant temperature for the
reaction cuvette for analysis.
Temperature Sensor Wire of Reaction Disk is Honeywell's high-precision temperature sensor. It is a positive
temperature coefficient, the resistance increases with increasing temperature.
temperature Resistance
0°C 1058 Ω
37°C 1140 Ω
100°C 1375 Ω
3.3.2 Locations and FRU details
The reaction carousel assembly is located in the right front side of the instrument.

Upper cover assembly

Optical
assembly

Reaction carousel Sensor Reaction carousel heat


motor assembly assembly chamber assembly

Figure 3-4 Reaction carousel assembly

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Temperature protection switch wire


Heater cable above (for reaction carousel)
reaction carousel
Cuvettes
Cover

Reaction Carousel
Body Assembly

M2.5×8 cross countersunk


head screw
M3× cross pan head
combination screw
Temperature control fan cable M5×20 hexagon screw
M3×14 cross recessed pan
head screw
Reaction carousel
temperature sensor
Stand bar of fan cable
Reaction chamber

Heater cable under


Thermal Guard 60C 2Lead15.6mm
reaction carousel
M3×6 cross recessed pan head screw

Heater baffle plate


M4×8 cross pan head screw

Reaction carousel Reaction carousel support


motor assembly

Reaction Carousel Sensor Assembly

Figure 3-5 Reaction carousel explosion diagram

Table 3-3 List of materials

No FRU Part Name Remark


1 009-006306-00 Reaction carousel temperature sensor
cable
2 115-038798-00 Motor assembly
3 BA10-20-78144 Temperature control fan cable

4 BA10-21-78143 Heater cable under reaction carousel


5 BA10-21-78142 Heater cable above reaction carousel
6 Temperature protection switch wire
BA10-21-78147
(for reaction carousel)
7 009-002204-00 Correlative photocoupler (S)
8 M6C-020007--- Synchronous cog belt, TBN180XL037
3.3.3 Replacing the cables of the reaction carousel cover
When to do
When the temperature of the reaction chamber is abnormal due to the connection problem of the heater cable
or temperature protection switch cable.
Tools
Name Code Quantity
Cross screwdriver / 1
Exploded view for installation

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M4×12 cross pan head screw

M4×8 cross
countersunk head
screw

Reaction carousel anchor plate

Temperature protection switch


wire (for reaction carousel)

Heater cable above


reaction carousel

Cover

Figure 3-6 Replacing reaction carousel cover cables

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, loosen the knurled screws on the wash probe assembly, remove the wash
probe assembly, and place the probe properly against bending. Remote the probe to the reagent
aspirating port position, remote the mixer to the wash well position, unscrew the M4×8 cross recessed
pan head padded screw, remove the reaction carousel panel, lamp panel, wash panel, unscrew the 3
M4×8 cross recessed pan head screws for fastening the right panel assembly, and remove the right
panel assembly.
3) Use a cross head screwdriver to unscrew the 4 M4×12 cross recessed combination screws that fasten
the upper cover assembly, unplug the heater connection cable on the reaction carousel and the
temperature protection switch cable of the reaction carousel, and remove the upper cover assembly.
4) Unscrew the 4 M4×8 cross pan head combination screws that fasten the anchor plate of the reaction
carousel, and remove the anchor plate of the reaction carousel.
5) Remove the faulty heater cable on the reaction carousel or the faulty temperature protection switch
cable of the reaction carousel.
6) To replace the heater cable on the reaction carousel, apply thermal paste evenly on the heater cable
of the reaction carousel, and apply a small amount of hot melt adhesive at the outlet of the heater
cable on the reaction carousel to fasten the lead-out cable.
7) To replace the temperature protection switch cable of the reaction carousel, apply thermal paste evenly
in the installation slot on the panel, and apply a small amount of hot melt adhesive at the outlet of the
temperature protection switch cable of the reaction carousel to fasten the lead-out cable.
8) Restore the components in the reversed order.
Alignment and confirmation
After replacing the cable of reaction carousel upper heater or the cable of temperature protection switch, perform
the heat insulation performance test.For reaction carousel temperature test, see 7.10.2 .
3.3.4 Replacing the cable of the heat insulation chamber
When to do
When the temperature of the heat insulation chamber is abnormal due to the cable of lower heater, Thermal
Guard 60C 2Lead15.6mm, the cable of temperature sensor or the cable of the fan of heat insulation chamber
is damaged or disconnected.
Tools
Name Code Quantity
Cross screwdriver / 1

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Hexagon wrench / 1
Exploded view for installation

Reaction carousel cover


M2.5*8 cross countersunk
head screw
M3*14 cross pan head
screw
Reaction carousel
Reaction carousel temperature temperature sensor cable
control 60 fan cable
M3*6 cross pan head Bracket of temperature
combination screws sensor
M5*20 hexagon socket cap
Fan bracket head screws with spring and
flat washer

Reaction chamber

Thermal Guard 60C


2Lead15.6mm
Silicone
heating film M3*6 hexagon socket cap head
screw

Press plate of
lower heater M4*8 cross pan head
combination screws

Supporting rod

Figure 3-7 Replacing the cable of the heat insulation chamber of reaction carousel

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, loosen the knurled screws on the wash probe assembly, remove the wash
probe assembly, and place the probe properly against bending. Remote the probe to the reagent
aspirating port position, remote the mixer to the wash well position, unscrew the M4×8 cross recessed
pan head padded screw, remove the BA24 reaction carousel panel, lamp panel, wash panel, unscrew
the 3 M4×8 cross recessed pan head screws for fastening the right panel assembly, and remove the
right panel assembly.
3) Use a cross head screwdriver to unscrew the 4 M3×14 cross recessed combination screws that fasten
the upper cover assembly, unplug the heater connection cable on the reaction carousel and the
temperature protection switch cable of the reaction carousel, and remove the upper cover assembly
and place it properly
4) Disassemble the BS-240 reaction carousel assembly: Loose the anchor plate of the reaction cuvette,
remove the reaction cuvette segment, and place them properly. Loosen the 3 M3×12 hexagon screws
that fasten the reaction carousel assembly, and remove the reaction carousel assembly, as shown in
the following diagram:

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Reaction cuvette Reaction cuvette


segment anchor plate Fan and Reaction carousel
bracket temperature sensor cable

M3×12 hexagon screw Reaction Carousel Body Assembly

Figure 3-8 Removing Reagent carousel body assembly

5) To replace the temperature sensor cable of the reaction carousel, use a cross head screwdriver to
loosen the M3×8 cross countersunk head screw, unplug the temperature sensor cable of the reaction
carousel, remove the temperature sensor cable of the reaction carousel directly, and replace it with a
new temperature sensor cable of the reaction carousel and plug it properly.
6) To replace the heat chamber fan cable, unplug the heat chamber fan cable, use a cross head
screwdriver to unscrew 2 M3×6 cross recessed pan head combination screws, remove the stand bar
of the fan together with the fan, and install a new fan onto the stand bar and plug it properly. (Note:
When installing the fan, please make sure that the label faces the stand bar, and the cable of the fan
is led out from the lower right side)
7) To change the heater cable under the reaction carousel or the Thermal Guard 60C 2Lead15.6mm,
remove 1 M4×12 screw and two M4×16 hexagon screws that fasten the optical assembly, unplug the
cable that connects the motor and the sensor, loosen the 3 M5X20 hexagon screws that fasten the
reaction chamber, unplug the related cables, and remove the reaction chamber.
8) To replace the Thermal Guard 60C 2Lead15.6mm, put the reaction chamber upside down, and loosen
the 2 M3×6 cross recessed pan head screws directly to perform replacement.
9) To replace the heater cable under the reaction carousel, loosen 10 M4×8 cross recessed pan head
combination screws that fasten the baffle plate of the heater, remove the baffle plate of the heater, and
replace the heater cable under the reaction carousel. Apply thermal paste evenly on the heater cable
under the heater of the reaction carousel, and apply a small amount of hot melt adhesive at the outlet
of the heater cable under the reaction carousel to fasten the lead-out cable.
10) Restore the assembly in reserved order. Try to align the heat chamber with the rotor of the reaction
carousel when installing the heat chamber.
Alignment and confirmation
After replacing silicone heating film, Thermal Guard 60C 2Lead15.6mm and the reaction carousel temperature
sensor cable, reconfigure the related sensor parameters on the software and perform the heat insulation
performance test. For sensor parameter configuration, see7.10.1 Configuration of Sensor Parameters; for
reaction carousel temperature test and reaction carousel temperature curve, see7.10.2 Observe Temperature
Curve.
If replacing the Optical measure assembly, refer to 7.3.1 Signal Collecting Position Adjustment to adjust
photoelectric signal collecting position; Refer to 7.3.2 Photoelectric Gain Adjustment to adjust photoelectric gain.
3.3.5 Replacing Home Position Sensor and Coder Sensor
When to do
When the Home Position Sensor and Coder Sensor failed
Tools
Name Code Quantity

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Cross screwdriver / 1
Hexagon wrench / 1
Exploded view for installation
Cross pan head Coded disk
screw with Home sensor
sensor
washerM3*6

Mounting
plate

The sensor
installed on the
Sensor left of the
Hexagon socket cap Cross pan head
bracket bracket.
head screws M3*8 screw M3*6

Figure 3-9 Replacing Home Position Sensor and Coder Sensor

Note:
Install the sensors according to the identifications on the cable connectors and the instrument connectors:
"RCD--PHO-C" for coder sensor and "RCD--PHO-O" for home position sensor.
Do not tighten the sensor screws with excessive torque force, in order to avoid damaging the sensors.
Make sure to install the home position sensor in the correct position.
How to do
Replacing coder sensor assembly
1) Switch off the main power of the whole unit.
2) Unscrew 3 M4×8 cross recessed pan head screws that fasten the right panel assembly, remove the
right panel assembly, and then unscrew 2 M4×8 cross recessed pan head combination screws that
fasten the AD bracket assembly, and put the AD bracket assembly aside (without removing the cable
of the AD box).
3) Unplug the connector of the reaction carousel coder sensor.
4) Unscrew the two M3*6 cross pan head combination screws on the sensor’s mounting plate and
remove the coder sensor cable with the sensor.
5) Loosen the two cross pan head screws on the coder sensor, and remove the coder sensor from the
mounting plate.
6) Fix the new coder sensor on the mounting plate using two M3×6 cross pan head screws.
7) Use two M3*6 cross pan head combination screws to fix the sensor mounting plate to the bracket of
the sensor. Adjust the height of the mounting plate of the sensor to keep the coder in the middle of the
coder sensor, and then tighten the retaining screws of the mounting plate.
8) Connect the connector of the reaction carousel coder sensor.
9) After aligning the sensor assembly, restore the components in the reversed order.
Replacing home position sensor assembly
1) Switch off the main power of the whole unit.
2) Unscrew 3 M4×8 cross recessed pan head screws that fasten the right panel assembly, remove the
right panel assembly, and then unscrew 2 M4×8 cross recessed pan head combination screws that
fasten the AD bracket assembly, and put the AD bracket assembly aside (without removing the cable
of the AD box).
3) Unplug the connectors of the reaction carousel home position sensor and coder sensor.
4) Loosen the three M3*8 hexagon socket cap head screws with spring and flat washers on the sensor
assembly, and then remove the sensor assembly. Pay attention not to drop the screws into the
instrument.
5) Unscrew the two M3*6 cross pan head screws on the cables of carousel home position sensor to
remove it from the bracket of the sensor.
6) Fix the new cables of carousel home position sensor onto the sensor bracket using two M3*6 cross

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pan head screws.


7) Fix the sensor assembly of the reaction carousel onto the big bottom plate with three M3*8 hexagon
socket cap head screws with spring and flat washers. Manually rotate the reaction carousel and
check that the zero position stopper of the coded disk does not interfere with the zero position sensor.
8) Connect the home position sensor and the coded disk sensor.
9) After aligning the sensor assembly, restore the components in the reversed order.
Alignment and confirmation
1) Refer to 7.3.1 Signal Collecting Position Adjustment to adjust photoelectric signal collecting position.
2) Refer to 7.4 Sample/Reagent carousel unit to adjust reaction carousel circumferential position,
sample/reagent carousel circumferential position,
3) Refer to 7.5.1 Probe to Horizontal Position on Reaction Carousel and 7.6.1 Mixer to Horizontal Position
on Reaction Carousel and 7.7.2 Cuvette Wash Station Home to adjust the probe and mixer to
horizontal position on reaction carouse.
3.3.6 Replacing motor assembly and synchronous belt
When to do
Replace the reaction carousel motor or synchronous belt when they are damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Exploded view for installation
M4×10 hexagon socket head
cap screw + spring washer

Motor

Motor shock pad

M5×12 hexagon
socket head cap screw
+ spring/flat washer

Figure 3-10 Reaction carousel motor assembly

WARNING
During removing and installation, avoid dropping screws and washers into the analyzer.
How to do
Replacing the motor
1) Switch off the power of the analyzer.
2) Unscrew 3 M4×8 cross recessed pan head screws that fasten the left panel assembly and those that
fasten the right panel assembly, remove the left and right panel assemblies, unscrew M4×8 cross
countersun head screws that fasten the front housing, and remove it.
3) Disconnect the motor cable, unscrew the 4 M5×12 hexagon socket head screws with spring washer
on the reaction carousel motor assembly, remove the motor assembly and avoid dropping screws into
the analyzer.
4) Fix a new motor assembly to the large bottom plate using 4 M5×12 hexagon socket head cap screws
with spring washer. Tighten the belt and screws and connect the cable of the motor.
5) Restore the components in the reversed order.

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Replacing the synchronous belt


1) Switch off the power of the analyzer.
2) Open the shielding cover, loosen the knurled screws on the wash probe assembly, remove the wash
probe assembly, and place the probe properly against bending. Remote the probe to the reagent
aspirating port position, remote the mixer to the wash well position, unscrew the M4×8 cross recessed
pan head padded screw, remove the reaction carousel panel, lamp panel, wash panel, unscrew the 3
M4×8 cross recessed pan head screws for fastening the left panel assembly and those for fastening
the right panel assembly, and remove the left and right panel assemblies. Unscrew the M4×8 cross
countersunk head screw that fastens the front housing and remove it
3) Use a cross head screwdriver to unscrew the 4 M4×12 cross recessed combination screws that fasten
the upper cover assembly, unplug the heater connection cable on the reaction carousel and the
temperature protection switch cable of the reaction carousel, and remove the upper cover assembly
and place it properly
4) Loose the anchor plate of the reaction cuvette, remove the reaction cuvette segment, and place them
properly. Loosen the 3 M3×12 hexagon screws that fasten the reaction carousel assembly, and
remove the reaction carousel assembly.
5) Remove 1 M4×12 screw and two M4×16 hexagon screws that fasten the optical assembly, unplug the
cable that connects the motor and the sensor, loosen the 3 M5X20 hexagon screws that fasten the
reaction chamber, unplug the related cables, and remove the reaction chamber.
6) Disconnect the motor cable, unscrew the 4 M5×12 hexagon socket head screws with spring washer
on the reaction carousel motor assembly, remove the motor assembly and avoid dropping screws into
the analyzer.
7) Install a new synchronous belt.
8) Fix a reaction carousel motor assembly to the large bottom plate using 4 M5×12 hexagon socket head
cap screws with spring washer. Tighten the belt and screws and connect the cable of the motor.
9) Restore the assembly in reserved order. Try to align the heat chamber with the rotor of the reaction
carousel when installing the heat chamber.
Alignment and confirmation
The belt tension needs to be adjusted to ensure that the tension is the same as before the replacement.
3.3.7 Replacing Reaction Cuvette
Refer to 3.9.8 Replacing Reaction Cuvette.
3.4 Sample/Reagent carousel cover assembly
3.4.1 Module Functions
Sample/Reagent carousel assembly is located at the left front of the analyzer, including the carousel body,
refrigeration assembly, drive assembly, motor assembly, coded disk optical coupler and the reagent bar code
reader (Optional). It is used to complete various actions, such as carrying and rotating the reagent bottle or
sample tube to the specified position with sampling assembly. It provides a refrigerating environment, and the
reagents stored in such environment can be kept stable with little volatilization. For details, please refer to the
following contents.
◼ Load sample/reagent. Place some reagent bottles with reagent and sample tubes with sample on the
carousel. Let the probe aspirate sample and reagent and dispense them into the cuvettes.
◼ Refrigerating reagent: Provide 24-hour refrigeration and constant temperature environment (2-12°C)
to keep the reagent stable with little volatilization.
◼ Sequential feeding: The drive assembly drives the carousel to carry certain reagent and sample in the
given order to the aspirate position for aspiration.
◼ Input reagent and sample data automatically: Bar code reader (optional).
Reagent Temperature Sensor: It is a Negative temperature coefficient, the resistance decreases with
increasing temperature.
temperature Resistance
2°C About 11KΩ
25°C About 5KΩ
3.4.2 Locations and FRU details
Sample/Reagent carousel assembly is located at the left front of the analyzer

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Sample Probe Movement Assembly

Sample/reagent carousel cover

Sample/reagent panel

Reagent bar code assembly

Sample/reagent
Left panel assembly
carousel assembly

Figure 3-11 Locations of sample/reagent carousel on the instrument

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11

10

9 2

3
4
5

6
8
7
Figure 3-12 Sample/Reagent carousel assembly

Table 3-4 List of materials

No FRU Part Name Remarks


1 115-036341-00 Sample/reagent carousel body
assembly
2 024-000110-00 Sensor temperature 5Kohm B3470K
with threads
3 082-000855-00 O-shaped 48.7X2.65 silicon rubber
black A70
4 049-001224-00 Square seal ring
5 BA40-21-61655 Semi-conductive Peltier cable
6 009-002204-00 Correlative photocoupler (S)
7 115-036317-00 Sample/reagent carousel motor
assembly
8 M6C-020007--- Synchronous cog belt, TBN180XL037
9 BA10-20-78146 Cables of reagent refrigeration and
radiating fan
10 115-036320-00 Reagent carousel anti-fogging heater
assembly
11 023-000738-00' Built-in bar code reader MS-3 High
density laser D-Sub
12 BA20-20-75214 Cuvette holder base 1
13 115-036342-00 Handle assembly
14 BA30-20-15100 Rubber pad 1
15 BA30-20-15210 Transparent shield rubber pad
16 041-023325-00 Sample tube adapter
3.4.3 Replacing Sample/Reagent Carousel Body Assembly
When to do
When the sample/reagent carousel body is damaged.
Tools

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Name Code Quantity


Cross screwdriver / 1
Medical rubber gloves / 1 pair
Exploded view for installation
Sample/reagent
carousel
body assembly

Figure 3-13 Sample/Reagent carousel body assembly

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, rotate the probe to the reaction carousel side, and remove the
sample/reagent carousel cover assembly.
3) Lift the handlebar to remove the sample/reagent carousel body assembly.
4) Align the locating holes on the new sample carousel body with the stop bolt, and pinch the handlebar
flat.
5) Restore the sample/reagent carousel cover, and close the shielding cover.
Alignment and confirmation
N/A
3.4.4 Replacing Reagent Temperature Sensor
When to do
When the temperature sensor fails.
Tools
Name Code Quantity
Cross screwdriver / 1
Flathead screwdriver / 1
Hexagon wrench / 1
Glue gun / 1
Medical rubber gloves / 1 pair
Exploded view for installation

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Sample/reagent
carousel body assembly

M3×10 cross countersunk


head screw
Refrigeration sleeve
M4×10 hexagon socket cap head screw
Rubber pad 1
Abrasion-resistant pad

Reagent refrigeration chamber

Rubber cushion

Temperature sensor

Figure 3-14 Reagent temperature sensor assembly

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove the left panel
assembly, front cover assembly, lamp panel, reaction carousel panel, wash panel, and sample/reagent
panel. Protect the probe from colliding during the deatching.
3) Lift the handlebar to remove the sample/reagent carousel body assembly.
4) Remove the reagent refrigeration board and bracket, disconnect the drain tube of the reagent
refrigeration compartment from the reagent refrigeration compartment, remove the temperature
sensor connector, and remove the reagent bar code assembly if the bar code is configured.
5) Use a cross head screwdriver to remove 6 M3×10 cross countersunk head screws that fasten the
refrigeration sleeve, and remove the refrigeration sleeve and the rubber pad 1.
6) Use the hexagon wrench to remove the 8 M4×10 hexagon socket head cap screws that fasten the
reagent refrigeration compartment, remove the abrasion-resistant pad, and remove the reagent
refrigeration compartment.
7) Clear the sealing glue in the installation position of the temperature sensor, and remove the
temperature sensor and the rubber pad.
8) Sheathe the rubber pad into a new temperature sensor, load them into the reagent refrigeration
compartment, and seal the installation hole with the sealing glue.
9) Apply thermal paste on the installation surface of the reagent refrigeration compartment and the
refrigeration aluminum block, apply the sealing glue on the abrasion-resistant pad, and use 8 M4×10
hexagon socket head cap screws to install the reagent refrigeration compartment onto the refrigeration
aluminum block. Try to align the reagent refrigeration compartment with the rotor.
10) Sheathe the rubber pad 1 into the refrigeration sleeve, apply the sealing glue to the fitting surface of
the reagent refrigeration compartment, and use 6 M3×6 cross countersunk head screws to fix the
refrigeration sleeve.
11) Install the disassembled parts in reversed order of steps 2~4.

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Note
When filling the installation hole of the temperature sensor with the sealing glue, completely fill the cable hole
with glue. Wipe off overflowing glue when filling the abrasion-resistant pad.
Alignment and confirmation
1) Re-align Probe to outer ring, middle ring and inner ring positions, see 7.5.3 ~7.5.5 .
2) Re-align barcode scanning position, see 7.8.4 Bar Code Reader Position Adjustment.
3.4.5 Replacing cooler(Peltier) and sealing ring
When to do
When the cooler(Peltier) failed
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Glue gun / 1
Medical rubber gloves / 1 pair
Exploded view for installation

Sample/reagent
M3×10 cross carousel body
countersunk head screw assembly

M4×10 hexagon socket


Refrigeration sleeve cap head screw
Rubber pad 1
Abrasion-resistant
pad
Reagent
refrigeration
chamber

Refrigeration aluminum block


M4×8 cross countersunk M4×8 cross countersunk
head screw head screw
O-shaped 48.7×2.65 sealing ring
Refrigeration aluminum block
M5×20 hexagon socket head cap
O-shaped 48.7×2.65 sealing ring
screws and spring/flat washer
Refrigeration fixing base Refrigeration fixing base
O-shaped 65×2 sealing ring O-shaped 65×2 sealing ring
Peltier Peltier

Figure 3-15 Removing cooler and sealing ring

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove the left panel
assembly, front cover assembly, lamp panel, reaction carousel panel, wash panel, and sample/reagent
panel. Protect the probe from colliding during the deatching.

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3) Lift the handlebar to remove the sample/reagent carousel body assembly.


4) Remove the reagent refrigeration board and bracket, disconnect the drain tube of the reagent
refrigeration compartment from the reagent refrigeration compartment, detach the temperature sensor
connector, and detach the reagent bar code assembly if the bar code is configured.
5) Use a cross screwdriver to remove 6 M3×10 cross countersunk head screws that fasten the
refrigeration sleeve, and remove the refrigeration sleeve and the rubber pad 1.
6) Use the hexagon wrench to remove the 8 M4×10 hexagon socket head cap screws that fasten the
reagent refrigeration compartment, remove the abrasion-resistant pad, and remove the reagent
refrigeration compartment.
7) Remove the 2 M5×20 hexagon socket head cap screws, the elastomer and the flat washer that are
used to fasten the refrigeration base on the Peltier to be replaced, and remove the refrigeration base
that carry a refrigeration aluminum block, so that the Peltier and the O-shaped 65×2 sealing ring can
be replaced.
8) To replace the O-shaped 48.7×2.65 sealing ring, remove the 4 M4×8 cross countersunk head screws
that fasten the refrigeration aluminum block, and replace the O-shaped 48.7×2.65 sealing ring.
9) Apply thermal pate on both sides of the substitute Peltier, install the Peltier according to the direction
before disassembling, and plug the cable. Install the substitute sealing ring.
10) Use 4 M4×8 cross countersunk head screws to fix the refrigeration aluminum block onto the
refrigeration base, and then use 2 M5×20 hexagon socket head cap screws, the elastomer and the
flat washer to fix the refrigeration base onto the Peltier. The direction needs to be consistent with the
direction before disassembling.
11) Apply thermal paste on the installation surface of the reagent refrigeration compartment and the
refrigeration aluminum block, apply the sealing glue on the abrasion-resistant pad, and use 8 M4×10
hexagon socket head cap screws to install the reagent refrigeration compartment onto the refrigeration
aluminum block. Try to align the reagent refrigeration compartment with the rotor.
12) Sheathe the rubber pad 1 into the refrigeration sleeve, apply the sealing glue to the fitting surface of
the reagent refrigeration compartment, and use 6 M3×6 cross countersunk head screws to fix the
refrigeration sleeve.
13) Install the disassembled parts in reversed order of steps 2~4.

Note
When filling the installation hole of the temperature sensor with the sealing glue, completely fill the cable
hole with glue. Wipe off overflowing glue when filling the abrasion-resistant pad.
Alignment and confirmation
1) Re-align Probe to outer ring, middle ring and inner ring positions,see7.5.3 ~7.5.5 .
2) Re-align barcode scanning position, see 7.8.4 Bar Code Reader Position Adjustment.
3.4.6 Replacing Home Position Sensor and Coder Sensor
When to do
When the Home position sensor and coded disk sensor of the reagent carousel failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Medical rubber gloves / 1 pair
Exploded view for installation

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M3*6 cross pan head screw M3*6cross pan


with washer head screw
Sensor mounting plate Coded disk
M3*6 Hexagon socket cap
optical coupler
screw with washer
M3*6cross pan
head screw
M3*6 hexagon
socket cap head
screw with spring
and flat washers
Bracket of the
Home position sensor
optical coupler

Figure 3-16 Removing Correlative optical coupler wire (S)

How to do
1) Switch off the power of the analyzer.
2) Remove the left panel assembly and the front panel assembly.
3) Remove the reagent refrigeration board and bracket, and unplug home position photocoupler of the
reagent carousel and the coder photocoupler.
4) Unscrew the 3 M3×6 hexagon socket head cap screws and the spring/flat washer that are used to
fasten the coder photocoupler assembly, and remove the coder photocoupler assembly.
5) Loosen the 2 M3×6 cross pan head combination screws on the photocoupler mounting plate, and then
remove the photocoupler mounting plate together with the coder photocoupler.
6) Loosen the 2 M3×6 cross pan head screws that fasten the coder photocoupler, and remove the coder
photocoupler from the sensor mounting plate.
7) Use 2 M3×6 cross pan head screws to fix the new coder photocoupler onto the sensor mounting plate.
8) Use 2 M3×6 cross recessed pan head combination screws to fix the sensor with the coder
photocoupler onto the photocoupler bracket, without tightening them.
9) Unscrew the 2 M3×6 cross recessed pan head screws of the photocoupler in the home position of the
reagent carousel, and remove the photocoupler from photocoupler bracket.
10) Use 2 M3×6 cross recessed pan head screws to fix a new photocoupler cable in the home position of
the reagent carousel onto the photocoupler bracket
11) Use 3 M3×6 hexagon socket head cap screws to fix the coder photocoupler assembly onto a large
bottom plate, push the photocoupler bracket to a stop position of the two hexagon screws, fit the
bracket closely, and tighten the retaining screws. Adjust the sensor mounting plate to make the coder
lie in the middle of the coder photocupler, and then tighten the screws on the mounting plate.
12) Plug the connectors of the photocoupler in the home position of the reagent carousel and the coder
photocoupler.
13) After aligning the position of the coder photocoupler assembly, restore the assembly in the reversed
order.

Note
• To replace only the coder photocoupler, omit steps 9 and 10.
• To replace only the photocoupler in the home position of the reagent coupler, omit steps 5 to 8.
Alignment and confirmation
After the sample/reagent carousel home sensor and coded disk sensor, refer to 7.4.2 ~ 7.4.4 to align
sample/reagent carousel circumferential position.
Refer to 7.5.3 ~7.5.5 to align probe to horizontal position on the sample/reagent carouse.
Refer to 7.8.4 Bar Code Reader Position Adjustment.
3.4.7 Replacing Sample/Reagent Carousel Motor Assembly
When to do
When motor failed.
Tools

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Name Code Quantity


Hexagon wrench / 1
Cross screwdriver / 1
M3*20 hexagon socket cap head / 1
screws with spring and flat washers
Medical rubber gloves / 1 pair
Exploded view for installation

Synchronous belt
M3×20 hexagon socket cap
M4×10 hexagon socket head screw hole
head cap screws and
Sample/reagent carousel motor assembly
spring/flat washer

Figure 3-17 Removing Sample/Reagent Carousel Motor Assembly

How to do
1) Switch off the power of the analyzer.
2) Remove the left panel assembly and the front panel assembly.
3) Unplug the motor cable, use a hand to check the tension of the synchronous belt and keep a record.
4) Use the hexagon wrench to remove the 4 M4×10 hexagon socket head cap screws and spring/flat
washer that are used to fasten the sample/reagent carousel motor assembly, and remove the
assembly from the synchronous belt.
5) Replace the assembly with a new sample/reagent carousel motor assembly, sheathe the pulley of the
assembly into the synchronous belt, and then tighten the M4×10 hexagon socket head cap screws
and spring/flat washer. Pay attention to the motor direction.
6) Pass 1 M3×20 hexagon socket head cap screw with a washer (either spring or flat washer, depending
on requirements) through a tension hole, fasten the screw into the motor mounting plate, strain the
belt to the original status, and tighten the motor assembly screw. Remove the M3×20 hexagon socket
screw, and plug the motor cable.
7) Assemble and reset the front panel assembly and the left panel assembly.

Note
Note: Do not mistaken the direction of the motor.
Alignment and confirmation
1) Align the position before fixing the air vent.
2) Re-align Probe to outer ring, middle ring and inner ring positions, see 7.5.3 ~7.5.5 .
3) Re-align barcode scanning position,see7.8.4 Bar Code Reader Position Adjustment.

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3.4.8 Replacing the synchronous belt


When to do
When it is damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Glue gun / 1
Medical rubber gloves / 1 pair
M3*20 hexagon socket cap head / 1
screws with spring and flat washers
Exploded view for installation

Sample/reage
nt carousel
body
assembly
M3×10 cross
Refrigeration
countersunk
sleeve
Rubber pad 1 head screw

Rotor

Gap
Reagent
refrigeration
chamber
Synchronou
s belt

M3×20 hexagon
screw hole

Sample/reagent carousel
motor assembly Synchronous
belt replacing
M4×10 hexagon socket space
cap head screw

Figure 3-18 Removing synchronous belt

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove the left panel
assembly, front cover assembly, lamp panel, reaction carousel panel, wash panel, and sample/reagent
panel. Protect the probe from colliding during the deatching.
3) Lift the handlebar to remove the sample/reagent carousel body assembly.
4) Remove the reagent refrigeration board and the bracket.
5) Use a cross screwdriver to remove 6 M3×10 cross countersunk head screws that fasten the
refrigeration sleeve, and remove the refrigeration sleeve and the rubber pad 1.
6) Draw an aligned mark line on the motor mounting plate and the large bottom plate (in the tension
direction of the motor assembly to facilitate use after the synchronous belt is replaced), loosen the 4
M4×10 hexagon socket head cap screws that fasten the motor assembly of the sample/reagent
carousel until the motor assembly can move, without taking out the screws.
7) Remove the synchronous belt. If the belt is broken or can be cut off, remove the belt. If the belt is not
broken and needs to keep the current status, remove the belt from the gap between the reagent

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refrigeration compartment and the rotor.


8) Sheathe a new synchronous belt into the rotor, and feed the belt slowly into the gap between the
reagent refrigeration compartment and the rotor. At the belt replacing operation space and at the motor
end, sheathe the belt into the motor pulley and rotor pulley.
9) Pass 1 M3×20 hexagon socket head cap screw with a washer (either spring or flat washer, depending
on requirements) through a tension hole, fasten the screw into the motor mounting plate, strain the
belt until it is aligned with the mark line drawn before the motor mounting plate is loosened, and tighten
the motor assembly screw. Remove the M3×20 hexagon screw.
10) Sheathe the rubber pad 1 into the refrigeration sleeve, apply the sealing glue to the fitting surface of
the reagent refrigeration compartment, and use 6 M3×6 cross countersunk head screws to fix the
refrigeration sleeve.
11) Install the disassembled parts in reversed order of steps 2~4.

NOTE
Pass the synchronous belt through the gap between the reagent refrigeration compartment and the rotor
slowly, and avoid applying a large force.
Alignment and confirmation
The belt tension needs to be adjusted to ensure that the tension is the same as before the replacement.
3.4.9 Replacing cooling fan of reagent refrigeration
When to do
When cooling fan failed.
Tools
Name Code Quantity
Hexagon wrench / 1
Medical rubber gloves / 1 pair
Cross screwdriver / 1
Exploded view for installation

M4×45 cross recessed


pan head screw and
flat washer
φ92 fan screen cover
Reagent refrigeration/radiating fan

Figure 3-19 Replacing cooling fan of the reagent refrigeration assembly

How to do

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IVD Global Technical Support Dept

1) Switch off the power of the analyzer.


2) Remove the left panel assembly and the front panel assembly.
3) Remove the connector of the fan that needs to be replaced.
4) Remove the 4 M4×45 cross recessed pan head screws and the flat washer of the fan that needs to
be replaced, and remove the fan screen and the fan.
5) Install a new fan. The installation direction of the fan needs to be consistent with the original direction,
and tidy the cable and the connector.
6) Install the front panel assembly and the left panel assembly.
Alignment and confirmation
After powering on the instrument, check that the cooling fan is blowing wind outwards,
3.4.10 Replacing Bar Code Reader
When to do
When the bar code reader failed.
Tools
Name Code Quantity
Hexagon wrench / 1
Medical rubber gloves / 1 pair
Cross screwdriver / 1
Exploded view for installation
M3×10 hexagon socket head cap screws
and spring washer and big flat washer Small bracket for bar code reader

Bar code reader

Figure 3-20 Removing bar code reader

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove the left panel
assembly, front cover assembly, lamp panel, reaction carousel panel, wash panel, and sample/reagent
panel. Protect the probe from colliding during the deatching.

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3)Remove the connector of the bar code reader.


4)Remove the 2 M3×10 hexagon socket head cap screws, the spring washer, and the big flat washer,
and remove the bar code reader.
5) Install a new bar code reader into a small bracket mounting position of the bar code reader. Pre-tighten
the screw, and plug the cable of the bar code reader.
6) Power on the bar code reader, re-align the bar code scan position, and use an adjustment tool of the
bar code scan light of the BA24-J03 BA24 to perform alignment according to steps described on the
software. After the light of the bar code reader is adjusted, tighten the retaining screw.
7) Assemble and reset the panel removed in step 2.
Alignment and confirmation
Re-align barcode scanning position,see7.8.4 Bar Code Reader Position Adjustment.
3.4.11 Replacing Reagent Anti-fogging Heating Assembly
When to do
Replace the anti-fogging heater assembly when the glass is damaged or the assembly does not work.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Medical rubber gloves / 1 pair
M3×10 hexagon socket
Small bracket for
head cap screws and Reagent carousel anti-fogging heater assembly
bar code reader
spring washer and big flat
Anti-fogging mounting plate
washer M2×8 cross recessed pan head screw
Dust shield Antifogging M3×8 cross recessed
and sponge heater pan head screw
Heat
Temperature
conductive
switch
plate

Bar code
reader

Switch
Rubber
anchor plate
M3×6 cross recessed Glass cushion
M3×12 hexagon socket
pan head screw cap head screw window

Figure 3-21 Replace the anti-fogging heater assembly

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove the left panel
assembly, front cover assembly, lamp panel, reaction carousel panel, wash panel, and sample/reagent
panel. Protect the probe from colliding during the deatching.
3) Remove the 2 M3×10 hexagon socket head cap screws, the spring washer, and the big flat washer,
and remove the bar code reader.
4) Remove the 4 M3×6 cross recessed pan head screws, and remove the dust shield with sponge.
5) Remove the connectors of the temperature switch and the antifogging heater, unscrew the 4 M3×8
cross pan head screws, and remove the antifogging heating assembly of the reagent carousel.
6) Remove 1 M3×12 hexagon socket head cap screws, and remove the anchor plate of the switch, the
temperature protection switch, and the antifogging heater.
7) Remove 4 M2×8 cross recessed pan head screws, remove the thermal conductive aluminum plate
and the damaged glass pane, and clear the broken glass in the slot of the mounting plate. Replace

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IVD Global Technical Support Dept

the rubber pad when necessary.


8) Place a new glass pane onto the silicone pad in the slot of the mounting plate of the antifogging
apparatus. Ensure that the glass is not cracked or dirty.
9) Use 4 M2×8 cross recessed pan head screws to fasten the thermal conductive aluminum plate into
the mounting position.
10) Apply thermal paste onto the fitting surface between the antifogging heater (if the heater is damaged,
use a new antifogging heater) and the thermal conductive aluminum plate, and place the heater in the
mounting position.
11) Apply thermal paste onto the fitting surface between the temperature switch (if the temperature switch
is damaged, use a new temperature switch) and the antifogging heater, and place switch in a middle
position. Place the anchor plate of the switch in the mounting position, and fasten it with 1 M3×12
hexagon socket head cap screw.
12) Use 4 M3×8 cross recessed pan head screws to install the reagent carousel antifogging assembly into
the mounting position of the reagent refrigeration compartment.
13) Plug the cable of the temperature switch and the antifogging heater, use 4 M3×6 cross pan head
screws to fasten the dust shield with sponge onto the mounting plate of the antifogging apparatus.
14) Install the bar code reader into a small bracket of the bar code reader, and pre-tighten the screw (plug
the cable of the bar code reader).
15) Power on the bar code reader, re-align the bar code scan position, and use an adjustment tool of the
bar code scan light of the BA24-J03 BA24 to perform alignment according to steps described on the
software. After the light of the bar code reader is adjusted, tighten the retaining screw.
16) Assemble and reset the panel removed in step 2.
Alignment and confirmation
Re-align barcode scanning position,see7.8.4 Bar Code Reader Position Adjustment.
3.5 Probe assembly
3.5.1 Module Functions
The probe assembly consists of probe drive assembly, arm assembly and the probe. The probe assembly can
move in horizontal and vertical direction, featuring fluid level detection, vertical obstruction detection. The probe
assembly has other functions, such as limiting of mechanical position, self-lock during power interruption, etc.
Horizontal direction: Probe moving to wash well→aspirating sample position→reaction carousel/ISE
aspirating position→wash well→aspirating reagent position→dispensing reagent position on the reaction
carousel→wash well.
Vertical direction: The probe moves in vertical direction among the positions of reagent bottle, sample tube,
cuvette, wash well and ISE sample injection port.
Reagent Preheating temperature sensor: It is a Negative temperature coefficient, the resistance decreases
with increasing temperature.
Resistance at 25℃ of temp sensor: 2252Ω±20.
Heater 24V/24W, Resistance = 24.6 ~ 28.5 Ω

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3.5.2 Locations and FRU details


Probe Movement Assembly Mixer Movement Assembly

Shielding Cover
Sample/reagent carousel cover
Wash station desk
Sample/reagent panel panel

Reagent bar code assembly Reaction carousel panel

Lamp panel

Frame Assembly

Reaction Carousel Assembly

Sample/reagent
Left panel
carousel assembly Reagent refrigeration
assembly Front cover assembly
board and the bracket

Figure 3-22 Locations of probe assembly on the instrument

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IVD Global Technical Support Dept

10

6
3 11

7
2

8
1

12

Figure 3-23 Probe movement assembly

Table 3-5 List of FRU materials

No FRU Part Name Remarks


1 009-002204-00 Correlative photocoupler (S)
2 115-037085-00 BA24 HbA1c sample probe
assembly
3 Guide rod and anti-collision
115-016462-00
spring
4 115-037552-00 Reagent preheating
assembly
5 051-002479-00 Liquid level detection board
PCBA
6 041-009179-00 Hardened power screw
(M3×6)
7 BA30-10-06619 Synchronous belt
B123MXL6.4
8 115-038796-00 probe drive horizontal motor
assembly
9 115-036662-00 Probe drive assembly
10 044-000263-00 130mm arm base
11 043-002344-00 130mm arm cover
12 probe drive vertical motor
115-038797-00
assembly

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IVD Global Technical Support Dept

3.5.3 Replacing the optical coupler of horizontal and vertical movement


When to do
When the optical coupler of horizontal and vertical movement failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Medical rubber gloves / 1 pair
Exploded view for installation

M3×6 cross recessed pan head screw


M3×6 cross recessed pan head screw

Horizontal Horizontal movement


sensor bracket photocoupler

Vertical movement photocoupler

M3×6 cross recessed pan head screw

Figure 3-24 Replacing the optical coupler of horizontal and vertical movement

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover and remove the lamp panel, the reaction carousel panel, and the wash panel.
Protect the probe from colliding during the disassembling.
3) When replacing the vertical movement optical coupler, disconnect the cable and remove the M3*6
cross pan head screw to remove the optical coupler. Replace it with new optical coupler, fix it and
connect the cable.
4) When replacing the horizontal movement optical coupler, disconnect the cable, remove one M3*6
cross pan head screw to remove the bracket and then remove one M3*6 screw to remove the
horizontal movement optical coupler. Replace it with new optical coupler and fix the optical coupler
and its bracket with M3*6 screws. Connect the cable.
5) Install back the panels.
Alignment and confirmation
After replacing the horizontal movement optical coupler, align the horizontal positions: probe to reaction carousel,
wash well, sample/reagent carousel and ISE sample injection port.
After replacing the vertical movement optical coupler, align the vertical positions: probe to reaction carousel,

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IVD Global Technical Support Dept

wash well, sample/reagent carousel and ISE sample injection port.


Refer to 7.5 Probe unit.
3.5.4 Replacing probe assembly,Anti-collision spring and powder
screws
When to do
When probe assembly is damaged or anti-collision spring failed or cosmetic defect of the powder screw occurs.
Tools
Name Code Quantity
Cross screwdriver / 1
Flathead screwdriver / 1
Medical rubber gloves / 1 pair
Exploded view for installation

probe arm cover

Spring guide
post

Anti- Hardened powder


collision screw(M3*6)
spring

Probe

Figure 3-25 Replacing probe assembly-collision spring and powder screws

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover.
3) Remove the two hardened powder screws (M3*6) and the probe arm cover. At this time, you can
replace the hardened powder screw.
4) Use Flathead screwdriver to remove the spring guide post and anti-collision spring. At this time, you
can replace the anti-collision spring.
5) Disconnect the cable of the anti-collision sensor and the wash tubes.
6) Remove the probe assembly and replace it with new one. Connect the cable and tubes.
7) Restore the instrument in the reversed order of step 2~4.
Alignment and confirmation
N/A
3.5.5 Replacing Reagent Preheating Assembly
Reagent Preheating temperature sensor: It is a Negative temperature coefficient, the resistance decreases
with increasing temperature.
Resistance at 25℃ of temp sensor: 2252Ω±20.

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IVD Global Technical Support Dept

Heater 24V/24W, Resistance = 24.6 ~ 28.5 Ω

When to do
When Reagent Preheating Assembly failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Medical rubber gloves / 1 pair
Exploded view for installation

probe arm cover

Reagent
Preheating
Assembly
Heat
insulation
pad

M3*6
cross pan
head
M3*8 screw
cross pan
head
screw

Hardened powder
screw(M3*6)

Figure 3-26 Replacing Reagent preheating assembly

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover.
3) Remove the two hardened powder screws (M3*6) and the probe arm cover (DS193).
4) Remove the cable of reagent preheating assembly. Remove the connector of the wash tubes from the
probe.
5) Remove one M3*8 cross pan head screw and one M3*6 cross pan head screw. Remove the two
heating insulation pad. Lay down the reagent preheating assembly. Remove the cover of the reagent
preheating assembly and then remove the wash tube.
6) Install new reagent preheating assembly and route the wash tube.
7) Install the two heating insulation pads and fix the reagent preheating assembly with one M3*8 and one
M3*6 cross pan head screw.
8) Connect the cable and the wash tube.
9) Use the sealing glue to seal the inlet and outlet of the wash tube and the cable.
10) Restore the instrument in the reversed order of step 2~3.
Alignment and confirmation
N/A

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IVD Global Technical Support Dept

3.5.6 Replacing liquid level detection board


When to do
When liquid level detection board failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Medical rubber gloves / 1 pair
Exploded view for installation

probe arm cover

Level sense
board

M3*6 cross pan


head screw

Hardened
power
screws(M3X6)

Figure 3-27 Removing liquid level detection board

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover.
3) Remove the two hardened powder screws (M3*6) and the probe arm cover.
4) Disconnect the connector of the liquid level detection board.
5) Remove the two M3*6 cross pan head screws to remove the liquid level detection board.
6) Replace it with new one and restore the instrument.
Alignment and confirmation
N/A
3.5.7 Replacing horizontal rotational synchronous belt
When to do
When horizontal rotational synchronous belt failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Medical rubber gloves / 1 pair
Exploded view for installation

No.HSH-19021-BS-240 Version: 4.0 3-40


IVD Global Technical Support Dept

Horizontal
rotational
synchronous belt

M3*8 hexagon
socket cap screw

Figure 3-28 Replacing horizontal rotational synchronous belt

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover and remove the lamp panel, the reaction carousel panel, and the wash panel.
Protect the probe from colliding during the disassembling.
3) Draw an arc along the flat washers under the two M3×8 hexagon socket head cap screws that fasten
the outside of the motor.
4) Loosen 4 M3×8 hexagon socket head cap screws that fasten the motor, and remove the synchronous
belt.
5) Sheathe a new synchronous belt slowly from the tip into two pulleys.
6) Move the motor. When the flat washers under the two outside screws basically overlap the arc drawn
in step 3, tighten the 4 screws to fasten the motor.
7) Reset the panel disassembled in step 2.
Alignment and confirmation
The belt tension needs to be adjusted to ensure that the tension is the same as before the replacement.
3.5.8 Replacement of Horizontal Motor Assembly
When to do
When Horizontal Motor Assembly failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Medical rubber gloves / 1 pair
Exploded view for installation

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IVD Global Technical Support Dept

Horizontal
rotational
synchronous belt

M3*8 hexagon
socket cap screw

Horizontal motor
Figure 3-29 Replacing Horizontal motor assembly

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover and remove the lamp panel, the reaction carousel panel, and the wash panel.
Protect the probe from colliding during the disassembling.
3) Draw an arc along the flat washers under the two M3×8 hexagon socket head cap screws that fasten
the outside of the motor.
4) Remove the motor cable connector, remove 4 M3×8 hexagon socket head cap screws and the
spring/flat washers that are used to fasten the motor, and remove the horizontal motor assembly.
5) Use 4 M3×8 hexagon socket head cap screws and spring/flat washers to pre-tighten a new horizontal
motor, and move the motor until the flat washers under the two outside screws basically overlap the
arc drawn in step 3. Tighten the 4 screws to fasten the motor, and plug the motor cable connector.
6) Reset the panel disassembled in step 2.
Alignment and confirmation
N/A
3.5.9 Replacement of Vertical Motor Assembly
When to do
When vertical Motor Assembly failed
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Diagonal pliers / 1
Exploded view for installation

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Probe movement
assembly

Synchronous
belt

Fixing plate B

Fixing plate A Vertical motor

M4*16 hexagon socket cap head screw

Figure 3-30 Replacing vertical motor assembly

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover. Unscrew all the M4*8 cross pan head screw with washer on the desk panels.
Remove the cover of the sample/reagent carousel, sample/reagent desk panel, reaction carousel desk
panel and auto wash desk panel. Protect the probe from being collided during the dismantling.
3) Disconnect the connectors of the vertical and horizontal motor. Disconnect the connector of the optical
coupler.
4) Remove 3 M6×16 hexagon socket head cap screws(see Figure 3-31 Replacing probe drive
assembly ) and spring/flat washers, and take out the probe drive assembly from the instrument.
5) Mark a line at the place where the upper surfaces of fixing plate A and B contact the bracket. Remove
the three M4*16 hexagon socket cap head screws with spring washers to remove the fixing plate A
and B.Remove the synchronous belt from the pulley and finally remove the motor.
6) Install new motor and sleeve the synchronous belt onto the pulley. Connect the motor with its fixing
plate A and B with three M4*16 hexagon socket cap head screws with spring washers and move the
motor till the fixing plates align with the line. Tighten the screws to fix the motor.
7) Restore the instrument in the reversed order of step 2~4.
Alignment and confirmation
Refer to 7.5.1 ~7.5.9 to align the positions: probe to reaction carousel, wash well, sample/reagent carousel and
ISE sample injection port.
3.5.10 Replacing Probe Drive Assembly
When to do
When Probe Drive Assembly failed
Tools

No.HSH-19021-BS-240 Version: 4.0 3-43


IVD Global Technical Support Dept

Name Code Quantity


Cross screwdriver / 1
Hexagon wrench / 1
Diagonal pliers / 1
Exploded view for installation
Probe arm cover

Sample probe arm


assembly

M3×10 hexagon socket


head cap screws and
spring washer Hardened power
screw (M3×6)

Probe drive
assembly

M6×16 hexagon socket


head cap screws and
spring/flat washer

Figure 3-31 Replacing probe drive assembly

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove the left panel
assembly, front cover assembly, rear panel, lamp panel, reaction carousel panel, wash panel, and
sample/reagent panel. Protect the probe from colliding during the disassembling.
3) Remove the cable and wash tube that pass through the precision shaft, remove all the cables and
tube terminals, and take out the braided hose.
4) Remove vertical and horizontal motor connectors, and remove 2 photocoupling connectors.
5) Remove 2 hardened power screws (M3×6) to take out the arm cover.
6) Remove 2 M3×10 hexagon socket head cap screws and spring washers to take out the probe arm
assembly, and move the cable out of the precision shaft. Prevent probe collision.
7) Remove 3 M6×16 hexagon socket head cap screws and spring/flat washers, and take out the probe
drive assembly from the instrument.
8) Place a new probe drive assembly into the mounting position, and use 3 M6×16 hexagon socket head
cap screws and spring/flat washers to fasten the assembly.

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9) Thread the cable and tube on the probe arm assembly from the top of the precision shaft, and use 2
M3×10 hexagon socket head cap screws and spring washers to pre-tighten the arm assembly onto
the precision shaft.
10) Sheathe the braided hose into the cable and the tube, reinstall connectors of the cable, and insert the
cable into the corresponding slot. Screw the tube mounting terminals and the quick connector into the
corresponding port.
11) Connect the motor cable and the photocoupler cable.
12) Refer to 7.5.1 ~7.5.9 to align the positions: probe to reaction carousel, wash well, sample/reagent
carousel and ISE sample injection port. Tighten two M4*16 hexagon socket cap screws to fix the arm
assembly. Use two hardened powder screws (M3*6) to install the arm cover.
13) Install back the panels.
Alignment and confirmation
Refer to 7.5.1 ~7.5.9 to align the positions: probe to reaction carousel, wash well, sample/reagent carousel and
ISE sample injection port.
3.6 Mixer Assembly
3.6.1 Module Functions
Mixer assembly consists of drive assembly and arm assembly. The mixer can move in horizontal and vertical
direction and mix the reaction liquid after sample is dispensed and after the reagent is dispensed.
Horizontal direction: mixer can move to wash well and reaction carousel.
Vertical direction: The mixer moves in vertical direction among the positions of cuvette and wash well.
3.6.2 Component Locations and FRU Details
Mixer is located at the front of the instrument.

Sample Probe Movement Mixer Movement Assembly


Assembly
Shielding Cover
Sample/reagent
carousel cover Wash station desk
Sample/reagent panel panel

Reagent bar code Reaction


assembly carousel panel

Lamp panel

Frame
Assembly

Reaction Carousel
Assembly

Sample/reagent
Left panel
carousel assembly Reagent refrigeration
assembly Front cover
assembly board and the bracket

Figure 3-32 Locations of mixer assembly on the instrument

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IVD Global Technical Support Dept

9
2

1
10

Figure 3-33 Mixer movement assembly

Table 3-6 List of materials

No FRU Part Name Remarks


1 009-002204-00 Correlative photocoupler
(S)
2 BA30-10-06619 Synchronous belt.
B123MXL6.4
3 115-038796-00 Horizontal motor
assembly (BA24)
4+5 801-BX50-00012-00 Mixer assembly
6 BA30-10-15052 DC motor WRF-130CH
Changzhou Weite Motor
General Factory
7 043-003064-00 Mixer arm cover
8 044-000333-00 mixer arm base
9 115-036665-00 Mixer drive assembly
10 115-038797-00 Vertical motor assembly
3.6.3 Replacing the optical coupler of horizontal and vertical movement
When to do
When the optical coupler of horizontal and vertical movement failed
Tools

Name Code Quantity


Cross screwdriver (long and short) / each respectively
Adjustable wrench / 1

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IVD Global Technical Support Dept

Diagonal pliers / 1
Medical rubber gloves / 1 pair

Exploded view for installation


Mixer Movement Assembly
Wash well support
shaft

M3×6 cross recessed pan


head screw

Horizontal
movement
photocoupler

Horizontal sensor
bracket
M3×6 cross recessed
pan head screw

Vertical movement
photocoupler
M3×6 cross recessed
pan head screw

Figure 3-34 Replacing the optical coupler of horizontal and vertical movement

Replacement steps:
1) Switch off the power of the analyzer.
2) Open the shielding cover and remove the lamp panel, the reaction carousel panel, and the wash panel.
Protect the mixer from colliding during the disassembling.
3) When replacing the vertical movement photocoupler, remove the wash well support shaft, remove the
photocoupler cable, use a short crosshead screwdriver to take out 1 M3×6 cross recessed pan head
screw and take out the vertical movement photcoupler, use 1 M3×6 cross recessed pan head screw
to fasten a new photocoupler, and plug the cable. Install the wash well support shaft.
4) When replacing the horizontal movement photocoupler, remove the photocoupler cable, remove 1
M3×6 cross recessed pan head screw to take out the horizontal sensor bracket with the photocoupler,
remove 1 M3×6 cross recessed pan head screw to take out the horizontal movement photcoupler, use
1 M3×6 cross recessed pan head screw to fasten a new photocoupler onto the horizontal sensor
bracket, use 1 M3×6 cross recessed pan head screw to fasten the horizontal sensor bracket in the
mounting position, and plug the photocoupler cable.
5) Install the panel that is disassembled in step 2.
Alignment and confirmation
Refer to 7.6.2 Mixer to Horizontal Wash Position to align mixer rotary to wash well.
3.6.4 Replacing horizontal rotational synchronous belt
When to do
When horizontal rotational synchronous belt failed
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Medical rubber gloves / 1 pair
Exploded view for installation

No.HSH-19021-BS-240 Version: 4.0 3-47


IVD Global Technical Support Dept

M3*8 hexagon socket cap


head screws with spring
and flat washer
Horizontal motor
assembly

Horizontal
rotational
synchronous belt

Figure 3-35 Replacing horizontal rotational synchronous belt

Replacement steps:
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove lamp panel,
reaction carousel panel, wash panel, and sample/reagent panel. Protect the mixer from colliding during
the disassembling.
3) Draw an arc along the flat washers under the two M3×8 hexagon socket head cap screws that fasten
the outside of the motor.
4) Loosen 4 M3×8 hexagon socket head cap screws that fasten the motor, and remove the synchronous
belt.
5) Sheathe a new synchronous belt slowly from the tip into two pulleys.
6) Move the motor. When the flat washers under the two outside screws basically overlap the arc drawn
in step 3, tighten the 4 screws to fasten the motor.
7) Reset the panel disassembled in step 2.
Alignment and confirmation
Refer to 7.6.1 and 7.6.2 to align Reagent Mixer Rotary to Cuvette and mixer rotary to wash well.
3.6.5 Replacement of Horizontal Motor Assembly
When to do
When Horizontal Motor Assembly failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Medical rubber gloves / 1 pair
Exploded view for installation

No.HSH-19021-BS-240 Version: 4.0 3-48


IVD Global Technical Support Dept

M3*8 hexagon socket cap


head screws with spring
and flat washer
Horizontal motor

Horizontal
rotational
synchronous belt

Figure 3-36 Replacing horizontal motor assembly

Replacement steps:
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove lamp panel,
reaction carousel panel, wash panel, and sample/reagent panel. Protect the mixer from colliding during
the disassembling.
3) Draw an arc along the flat washers under the two M3×8 hexagon socket head cap screws that fasten
the outside of the motor.
4) Remove the motor cable connector, remove 4 M3×8 hexagon socket head cap screws and the
spring/flat washers that are used to fasten the motor, and remove the horizontal motor assembly.
5) Use 4 M3×8 hexagon socket head cap screws and spring/flat washers to pre-tighten a new horizontal
motor, and move the motor until the flat washers under the two outside screws basically overlap the
arc drawn in step 3. Tighten the 4 screws to fasten the motor, and plug the motor cable connector.
6) Reset the panel disassembled in step 2.
Alignment and confirmation
Refer to 7.6.1 and 7.6.2 to align Reagent Mixer Rotary to Cuvette and mixer rotary to wash well.
3.6.6 Replacing DC motor, mixer and powder screws
When to do
When DC motor failed, mixer is damaged or twisted or cosmetic defect of the powder screw occurs.
Tools
Name Code Quantity
Cross screwdriver / each respectively
(big and small)
Medical rubber gloves / 1 pair
Exploded view for installation

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Mixer arm cover

DC motor

M2*4 cross pan


head screw
with the flat
washer

Retaining nut

Mixer

Hexagon socket cap


screws(M3*6)

Figure 3-37 Replacing DC motor, mixer and powder screws

Replacement steps:
1) Switch off the power of the analyzer.
2) Open the shielding cover and remove the lamp panel. When necessary, remove the left panel
assembly and the front panel assembly.
3) Remove 2 hardened power screws (M3×6) to take out the mixer arm cover. The powder screw may
be replaced directly.
4) Loosen the retaining nut and remove the mixer. When repairing the mixer, replace the mixer with a
new mixer, and insert the mixer into the motor shaft and tighten the retaining nut.
5) Remove the motor cable, remove 2 M2×4 cross countersunk head screw and flat washers, take out
the DC motor, replace the motor with a new DC motor, and use 2 M2×4 cross countersunk head
screws and flat washers to pre-tighten the motor. Plug the motor cable.
6) Install the mixer, tighten the retaining nut and install the mixer arm cover.
7) Install the cover that is disassembled in step 2.
Alignment and confirmation
Refer to 7.6.1 and 7.6.2 to align Reagent Mixer Rotary to Cuvette and mixer rotary to wash well.
3.6.7 Replacement of Vertical Motor Assembly
When to do
When vertical Motor Assembly failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Diagonal pliers / 1
Exploded view for installation

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Vertical
Probe movement
motor
assembly
Synchronous
belt
Motor fixing
plate B

Motor fixing M4*16hexagon socket cap


plate A head screws with spring and
flat washer

Figure 3-38 Replacing vertical motor assembly

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover. Unscrew all the M4*8 cross pan head screw with washer on the desk panels.
Remove the cover of the sample/reagent carousel, sample/reagent desk panel, reaction carousel desk
panel, auto wash desk panel, left panel, right panel and front panel. Remove the bracket of the wash
well together with the wash well. Protect the mixer from being collided during the dismantling.
3) Disconnect the connectors of the vertical and horizontal motor. Disconnect the connector of the optical
coupler.
4) Remove 3 M6×16 hexagon socket head cap screws(see Figure 3-39 Exploded view of mixer drive
assembly) and spring/flat washers, and take out the mixer drive assembly from the instrument.
5) Mark a line at the place where the upper surfaces of fixing plate A and B contact the bracket. Remove
the three M4*16 hexagon socket cap head screws with spring washers to remove the fixing plate A
and B.Remove the synchronous belt from the pulley and finally remove the motor.
6) Install new motor and sleeve the synchronous belt onto the pulley. Connect the motor with its fixing
plate A and B with three M4*16 hexagon socket cap head screws with spring washers and move the
motor till the fixing plates align with the line. Tighten the screws to fix the motor.
7) Restore the instrument in the reversed order of step 2~4.
Alignment and confirmation
Refer to 7.6.1 ~ 7.6.2 to align positions: Mixer Rotary to Cuvette and mixer rotary to wash well.
3.6.8 Replacement of Mixer Drive Assembly
When to do
When mixer Drive Assembly failed
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Diagonal pliers / 1

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Medical rubber gloves / 1 pair


Exploded view for installation
Mixer arm cover

Mixer arm
assembly

M3×10 hexagon socket


Hardened power
head cap screws and
screw (M3×6)
spring washer

Mixer drive
assembly

M6×16 hexagon
socket head cap
screws and
spring/flat washer

Figure 3-39 Exploded view of mixer drive assembly

Replacement steps:
1) Switch off the power of the analyzer.
2) Open the shielding cover, remove the sample/reagent carousel cover, and remove the left panel
assembly, front cover assembly, rear panel, lamp panel, reaction carousel panel, wash panel, and
sample/reagent panel. Protect the mixer from colliding during the disassembling.
3) Remove the cable that passes through the precision shaft, remove all the cables and terminals, and
take out the braided hose.
4) Remove vertical and horizontal motor connectors, and remove 2 photocoupling connectors.
5) Remove 2 hardened power screws (M3×6) to take out the arm cover.
6) Remove 2 M3×10 hexagon socket head cap screws and spring washers to take out the mixer arm
assembly, and move the cable out of the precision shaft. Prevent mixer collision.
7) Remove 3 M6×16 hexagon socket head cap screws and spring/flat washers, and take out the mixer
drive assembly from the instrument.
8) Place a new mixer drive assembly into the mounting position, and use 3 M6×16 hexagon socket head
cap screws and spring/flat washers to fasten the assembly.
9) Thread the cable on the mixer arm assembly from the top of the precision shaft, and use 2 M3×10
hexagon socket head cap screws and spring washers to pre-tighten the arm assembly onto the
precision shaft.
10) Sheathe the braided hose into the cable, reinstall connectors of the cable, and insert the cable into
the corresponding slot.
11) Connect the motor cable and the photocoupler cable.

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12) Refer to 7.6.1 ~ 7.6.2 to align the positions: mixer to reaction carousel and wash well. Tighten two
M3*10 hexagon socket cap screws to fix the arm assembly. Use two hardened powder screws (M3*6)
to install the arm cover.
13) Install back the panels.
Alignment and confirmation
Refer to 7.6.1 ~ 7.6.2 to align positions: Mixer Rotary to Cuvette and mixer rotary to wash well.
3.7 Cuvette Wash Station
3.7.1 Module Functions
The cuvette wash unit, located in the rear right of the whole unit, consists of the wash probes assembly and
wash probe drive assembly. It provides 4-phase auto wash for non-disposable reaction cuvettes so that they
can be used repeatedly without influencing the test effects. The first three phase wash probes inject wash
solution to wash the cuvettes and the fourth phase probe wipes the cuvettes.

3.7.2 Locations and FRU details


Sample Probe Reaction
Sample/reagent Movement Auto Wash Carousel
Assembly Assembly
carousel assembly
Assembly

Frame Mixer Optical


Assembly Movement assembly
Assembly
Figure 3-40 Location of the cuvette wash assembly

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Wash probes assembly


Knurled screw

Wash Station
Wash probes
optical coupler
PCBA
Wipe block

Wash probe
drive assembly

OPtical coupler
wire (S)

Figure 3-41 Cuvette wash assembly

Table 3-7 List of materials

No FRU Part Name Remarks


1 115-045543-00 Wash probes assembly
2 051-001147-00 BA48 wash station
photocoupler PCBA
3 115-045542-01 Wash probe drive
assembly
4 009-002204-00 Photocoupler (S) Zero position
photocoupler
5 BA38-30-88154 Wash-phase probe
assembly
6 BA40-30-61934 Wipe-phase probe
assembly
7 041-001845-00 Wipe block
8 024-000908-00 Motor
9 041-031405-00 Support pole
3.7.3 Replacing Wash Probes Assembly
When to do
Replace the wash probes when they are bent or damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Exploded view for installation

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Wash probes assembly


Knurled screw

Wash support
plate

Figure 3-42 Wash probe

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover. Unscrew all the M4*8 cross pan head screw with washer on the desk panels.
Remove the cover of the sample/reagent carousel and auto wash desk panel.
3) Unplug the cable connector of the wash station photocoupler.
4) Unplug the tubes and cables on the wash probes assembly, and manually loosen the knurled screw
to remove the wash probes assembly.
5) Install the new wash probes assembly, manually tighten the knurled screw, and restore the tubes and
cables according to their numbers.
6) Restore the components in the reversed order.

Note:
Reinstall the tubes and cables on the wash probes assembly according to the number marking.
Alignment and confirmation
Check the wash probes' vertical position in reaction cuvettes according to 7.7.3 Cuvette Wash Station Height.
3.7.4 Replacing Wash Station
When to do
Replace the wash station photocoupler when it is damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Exploded view for installation

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Cable anchor
plate

M2.5×4 cross
wash station recessed pan
photocoupler head screw

Figure 3-43 Wash station photocoupler

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover assembly, unscrew 8 M4×8 cross pan head combination screws to remove
the rear panel.
3) Unplug the cable connector of the wash station photocoupler.
4) Remove the M2.5*4 cross pan head screw to remove the anchor plate.
5) Remove the M2.5*4 cross pan head screw to remove the optical coupler of the wash station.
6) Replace it with new one and tighten the M2.5*4 cross pan head screw.
7) Restore the components in the reversed order.
Alignment and confirmation
N/A
3.7.5 Replacing Wash Probe Drive Assembly
When to do
Replace the wash probe drive assembly when it is damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Exploded view for installation

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Knurled
screw

Position adjusting
plate

M4×16 hexagon
socket head cap screw
+ spring washer

Zero position
photocoupler

M3×8 cross recessed


pan head screw

M4×12 hexagon socket head


cap screw + spring washer
Motor support
block

Figure 3-44 Wash probe drive assembly

How to do
1) Switch off the power of the analyzer.
2) Open the shielding cover, loosen the knurled screws on the wash probe assembly, remove the wash
probe assembly, and place the probe properly against bending. Remote the probe to the reagent
aspirating port position, remote the mixer to the wash well position, unscrew the M4X8 cross recessed
pan head padded screw, remove the reaction carousel panel (basic part), lamp panel, wash panel,
unscrew the 3 M4X8 cross recessed pan head screws for fastening the right panel assembly, and
remove the right panel assembly.
3) Unplug the zero position photocoupler and the motor, loosen 4 M4×12 hexagon socket head cap
screws with spring washer on the motor supporting block, replace the wash probe drive assembly with
a new one, and then fix it with 4 M4×12 hexagon socket head cap screws with spring washer. Do not
tighten the 2 M4×16 hexagon socket head cap screws with spring washer on the wash probe drive
assembly, till you finish the alignment.
4) Restore the components in the reversed order.
Alignment and confirmation
Check the wash probes' vertical and horizontal positions in reaction cuvettes according to 7.7.2 ~ 7.7.3 .

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3.7.6 Replacing Wash Probe Drive Motor


When to do
When the wash probe drive motor is damaged
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Exploded view for installation

M3*8 cross pan


head combination
screw

Damper
pad

Motor

Figure 3-45 Wash probe drive motor assembly

How to do
1) Switch off the main power of the whole unit.
2) Open the shielding cover. Loosen the knurled screw on the wash probes assembly with your hand to
remove the wash probes assembly. Take caution not to collide the wash probes. Rotate the probe to
the aspirating reagent position and rotate the mixer to the wash well position. Unscrew all the M4*8
cross pan head screws with washers on the desk panels to remove the reaction carousel desk panel
and auto wash desk panel. Loosen the three M4*8 cross pan head screws holding the right panel to
remove the right panel.
3) Unplug the connectors of the zero position photocoupler and the motor. Unscrew the four M4*12
hexagon socket screws and washers to remove the wash probe drive assembly (115-045542-01).
4) Unscrew the two M3*8 cross pan head screws holding the damper pad. Loosen the two M3*5 retaining
screws holding the screw rod to remove the motor and the damper pad. Then the two M3*8 cross pan
head screws holding the motor to remove it.
5) Fix the new motor and damper pad with two M3*8 cross pan head screws, and mount it onto the
wash motor bracket with two more M3*8 cross pan head screws. The motor axis must reach the bottom
of the lead screw hole. Apply a moderate amount of thread glue to tighten the two M3*5 retaining
screws, one of which is against the flat position on the motor axis. Make sure the outlet of the damper
pad and the motor is in the right direction so that the entire mechanism can move smoothly.
6) Restore the components according to the reversed order of Steps 1-3.
Alignment and confirmation

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Check the wash probes' vertical and horizontal positions in reaction cuvettes according to 7.7.2 ~ 7.7.3 .
3.7.7 Replacing Zero Position Photocoupler
When to do
Replace the zero position photocoupler on the wash probe drive assembly when it is damaged.
Tools
Name Code Quantity
Cross screwdriver / 1
Exploded view for installation
Knurled screw

Position adjusting plate

M4×16 hexagon socket


head cap screw + spring
washer

Zero position
photocoupler

M3×8 cross recessed


pan head screw

M4×12 hexagon socket head


cap screw + spring washer

Motor support block

Figure 3-46 Zero position photocoupler on the wash probe drive assembly

How to do
1) Switch off the power of the analyzer.
2) Unscrew the 8 M4×8 cross pan head combination screws on the rear panel. Remove the syringe drive
assembly when removing the rear panel.
3) Unplug the connector of the zero position photocoupler.
4) Loosen 1 M3×8 cross pan head screw on the wash probe drive assembly, replace the zero position
photocoupler with a new one, and then fix it with 1 M3×8 cross pan head screw.
5) Restore the components in the reversed order.
Alignment and confirmation
Check the wash probes' vertical and horizontal positions in reaction cuvettes according to 7.7.2 ~ 7.7.3 .

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3.8 Syringe Assembly


3.8.1 Module Functions
Syringe assembly consists of one 500ul sampling syringe and two wash syringes, of which 2.5ml syringe is
used to inject the wash solution and 10ml syringe is used to inject the cleaning fluid.
3.8.2 Component Locations and FRU Details

Frame

Syringe
bracket weld
Syringe
module
Syringe left
bracket
2.5ml
syringe
assembly

Syringe left bracket

10 ml screw rod Power supply


driving syringe
assembly
assembly

Syringe lower
bracket

Figure 3-47 Location of the syringe assemblies


Table 3-8 List of materials

No FRU Part Name Remarks


1 10 ml screw rod driving syringe
115-011901-00
assembly
2 115-031800-00 2.5ml syringe assembly
3 011-000297-00 Photoelectric position sensor
4 115-036403-00 BA25 syringe assembly
3.8.3 Replacing 2.5ml syringe and 10ml syringe
When to do
When the syringe functions abnormally.
Tools
Name Code Quantity
Cross screwdriver / 1
Hexagon wrench / 1
Exploded view for installation
See Figure 3-48.
How to do

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1) Switch off the power supply of the whole unit.


2) Pull out the tube and lines on the syringe, and use a hexagon socket wrench for loosening. Fasten the
2.5ml syringe to the 4 hexagon screws of the left bracket and lower bracket of the syringe, so that the
2.5ml syringe assembly can be taken out.
3) Pull out the tube and lines on the syringe, and use a hexagon socket wrench for loosening. Fasten the
10ml screw rod driving syringe to the 4 hexagon screws of the right bracket and lower bracket of the
syringe, so that the 10ml screw rod driving syringe assembly can be taken out.
4) After replacing the syringe with a new syringe, restore the assembly in the reversed order.
3.9 Photometer Unit
3.9.1 Functions and Parameters
The BS-240 has inherited the mature filter light-splitting technology of Mindray's BS series. The photoelectric
detection unit uses a light source to illuminate directly. After passing through the interference filter, composite
light becomes monochromatic light of a specific bandwidth. After being absorbed by a solution, the
monochromatic beam is received by a photodetector. The photodetector converts the optical signal with light
intensity into an electric signal. A microprocessing unit calculates the concentration of the solution by calculating
the change of the light intensity. Multiple monochromatic wavelengths required in a photometric system are
implemented by using a filter wheel apparatus. During measurement, filters are sequentially shifted into the
optical path to implement colorimetric measurement of each wavelength.
Table 3-9 Technical Parameters

Optical system filter wheel forward-splitting system, optical-to-electric conversion of


silicon photodiode.
Wavelength 8 wavelengths: 340nm, 405nm, 450nm, 510nm, 546nm, 578nm, 630nm, and
670nm
Wavelength accuracy ±2nm
Light source 12V/20W, tungsten-halogen lamp, transmitting light through fiber bundle
Minimum reaction volume 100μL
Absorbance range 0-4A, 10mm light pathlength
Cuvette Light pathlength of cuvette:5mm
Number of cuvettes: 40 cuvettes, 5mm*5mm*29.5mm
Cuvette material plastic

Table 3-10 Terms of Optics

AD value the value converted from photoelectric signal (voltage) through AD converter.
Water blank the AD value of a cuvette measured when the wash station dispenses water in phase-6.
Water blank is the base point for calculation absorbance, that is, the 0 point of absorbance.
Note: The phase-6 here is actually the 2nd phase of the wash station (facing the analyzer,
from right to left), and the 240 wash station has only four phases.
Cuvette means the water blank of phase-6 is less than the light intensity low limit. This alarm is
blank out of used to monitor the energy level of the optical system to ensure normal signal-to-noise
range ratio.
Cuvette means the relative change of continuous phase-6 water blanks for 10 cuvettes is greater
blank out of than 3% comparing with the history data. This alarm is used to prevent light fluctuation or
range (10X) erroneous result due to cuvette overflowing and to remind the operator of this
phenomenon.

3.9.2 Composition and Structure of Optical Assembly


The BS-240 optical assembly uses a filter wheel plus a PD for photometric measurement. See the figure below.
The light source illuminates directly, and the beam is converged by the lens 1 and then split by the filter. A
monochromatic beam is shaped by the lens 2 and then passes through the cuvette. After being absorbed by
the solution, the beam is converged by the lens 3. Finally, the optical signal is received by the photodiode and

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converted into an electric signal for outputting. The whole optical path is from the reaction carousel inwards.
Light source Lens 1 Filter Cuvettes Lens 3

Photodiode

Lens 2 Optical base

Figure 3-49 Optical path

Optical assembly

Figure 3-50 Locations of light source assembly and optical measurement assembly

The optical assembly consists of a light source assembly and a measurement assembly.
Table 3-11 List of materials

No FRU Part Name Remarks


1 115-038466-00 20W lamp assembly (FRU)
2 041-001143-00 Lamp base retaining screw
3 BA10-20-78211 Patch cord for lamp housing
fan
4 801-BA10-00099-00 Preamplifier board
PCBA(FRU/C)
5 115-036571-00 Cuvette (Surface processed)
6 801-BA10-00041-00 Filter 340 (C)
7 801-BA10-00042-00 Filter 405 (C)
8 801-BA10-00043-00 Filter 450 (C)
9 801-BA10-00044-00 Filter 510 (C)
10 801-BA10-00045-00 Filter 546 (C)
11 801-BA10-00046-00 Filter 578 (C)
12 801-BA10-00047-00 Filter 630 (C)
13 801-BA10-00048-00 Filter 670 (C)
14 801-BA10-00004-00 AD collection board (C)

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3.9.3 Replacing Lamp


When to do
Replace the lamp when an alarm is triggered indicating that the lamp has insufficient intensity, or not turned on,
or has been used for over 2000 hours, or used more than 6 months,
or has cuvette blank out of range (10X).
Tools
Cross screwdriver
Exploded view for installation

Figure 3-51 Exploded view of lamp and fiber bundle for installation

Note:
Replace the lamp according to the instructions on the screen.
Please wait for at least 5 minutes (if the lamp fan works properly) after turning off the lamp to avoid
injury.
Do not touch the bulb when installing the new lamp. In case of touching, please clean the bulb with
fibre cloth or ethanol-moistened gauze.
How to do
1) Select Utility -> Maintenance -> Maintenance -> Biochemistry Maintenance, and select Replace
Lamp.
2) Follow the instructions prompted by the software and wait for 10 minutes until the lamp cools down.
3) Use a cross screwdriver to loosen the screws of the lamp panel, and remove the panel.
4) Unscrew the cable connectors and the lamp base retaining screws with hands, to remove the lamp.
5) Install the lamp and panel in a reversed order. Before installing the panel, ensure that the lamp has
been installed properly in the right place and there is no gap between the lamp and the lamp base.
6) Select "Continue" and wait for 5 minutes for the new lamp to get steady. Select "Photometer Check"
to check if the lamp can work normally.
Alignment and confirmation
Refer to 7.3.2 Photoelectric Gain Adjustment to adjust the Photoelectric Gain.
3.9.4 Disassembling/Assembling Optical Assembly
When to do
Remove the optical assembly before replacing the filter, preamplifier board, and lamp radiating fan.
Tools
Cross screwdriver and hexagon wrench
Exploded view for installation

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Figure 3-52 Exploded view of optical assembly

NOTE:
Do not touch the optical surface of the filter with a hand during disassembling/assembling.
During disassembling, please wait for at least 5 minutes (if the lamp fan works properly) after turning off the
lamp, so as to avoid burn.
Do not lose the adjustment washer under the assembly during disassembling.
How to do
1) Switch off the power supply of the instrument.
2) Use a cross screwdriver to loosen the screws of the lamp panel, and remove the panel and the panel
on the top of the reaction carousel.
3) Refer to the Section about the reaction carousel unit maintenance to remove the upper cover of the
reaction chamber and remove the reaction carousel.
4) Remove the right cover.
5) Unplug the power cord of the lamp radiating fan.
6) Unplug the cable between the preamplifier board and the AD collection board.
7) Use a hand to unscrew off the nuts on the cable terminals, and then remove the lamp power cord
terminal from the terminals.
8) Use a cross screwdriver to loosen the 2 screws that fasten the wiring terminal bracket, and remove
the wiring terminal bracket together with the wiring terminal from the optical assembly.
9) Unscrew the screws that fasten the fiber baffle plate, and remove the fiber baffle plate.
10) Use a hexagon wrench to remove the 3 M4 hexagon screws that fasten the optical assembly.
11) Extract the optical assembly upwards. Adjustment washes may exist under the assembly, which
should not be lost and shall be restored after installation. The positions of the washers are shown in
the following figure, and the semicircle of the washer clasps the positioning pin.
12) Install the optical assembly in reserved order of the foregoing steps.

Figure 3-53 Exploded view of optical assembly

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Alignment and confirmation


Refer to 7.3 Photometric Unit to adjust signal collecting position and the photoelectric gain.
3.9.5 Replacing Filter
When to do
Replace the filter when an alarm indicates that the light intensity is low and when energy of a wavelength channel
is confirmed weak.
Tools
Hexagon wrench, cross screwdriver
How to do
1) Remove the optical assembly according to the method described in the previous section.
2) According to the following figure and the following table, find the holes of the filter of the corresponding
wavelength. Use a cross screwdriver to loosen the retaining screws and washers on both ends of the
filter that needs to be replaced, and remove the filter. The outer cylinder surface of the filter has filter
center wavelength silkscreen, which may be used to check again whether the filter is expected to be
replaced.

Filter retaining
screw

Filter retaining
washer

Filter retaining
washer

Filter hole No.

Filter wavelength Filter direction


(nm)

Filter hole NO.

Figure 3-54 Exploded view for replacing filter

Hole 1 2 3 4 5 6 7 8
Filter wavelength (nm) 340 405 546 670 450 510 578 630
3) Install a new filter in reversed order of the foregoing steps.
4) Install the optical assembly in reserved order of the foregoing steps.
5) Select "Maintenance"->"Alignment" -> " Signal Collecting Position Adjustment " and
"Photoelectric Gain Adjustment".Refer to 7.3 Photometric Unit.

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NOTE:
Do not touch the optical surface of the filter with a hand during disassembling/assembling.

3.9.6 Replacing Preamplifier Board


When to do
The preamplifier board may need to be replaced when no photoelectric signal is output or a dark current is
abnormal.
Tools
Cross screwdriver and hexagon wrench
How to do
1) Remove the optical assembly according to the method.
2) See the following figure. Use a screwdriver to remove the retaining screws of the shielding cover, and
remove the shielding cover.
3) Use a cross screwdriver to remove the retaining screws of the preamplifier board, and gently take out
the preamplifier board.
4) Install the preamplifier board in reversed order. Use water as sample or reagent to request test, the
reaction curve must be flat and straight.
Retaining
Optical base screws on the Leaf spring Lens Lens
shielding cover

Washer

Preamplifier

Preamplifier board
retaining screw

Shielding cover

Figure 3-55 Exploded view for installing related parts on preamplifier board side on optical
base

NOTE:
The parts such as the lens and the lens base in the holes on the preamplifier board in the optical base are fixed
by using only the preamplifier board, and are not fixed by other means. Therefore, the preamplifier board should
be taken out upwards. When placing the optical assembly after the preamplifier board is taken out, the mounting
holes should face upwards to prevent dropping of the parts in the holes.
Alignment and confirmation
Select "Maintenance"->"Alignment" -> " Signal Collecting Position Adjustment " and "Photoelectric Gain
Adjustment".Refer to 7.3 Photometric Unit.
3.9.7 Replacing lamp fan
When to do
Replace the lamp radiating fan when it fails.
Tools
Flathead screwdriver, hexagon wrench

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How to do
1) Remove the optical assembly according to the method.
2) See the following figure. Use a screwdriver to remove 4 screws that fasten the fan, and remove the
fan.
3) Install a new fan, and fasten it with screws.

NOTE:
The fan radiates heat towards the lamp base. During installation, the fan surface that bears characters faces
the optical base, and the surface without characters faces outwards.

Lamp Light source


base radiating
fan

Fan retaining
screws

Figure 3-56 Exploded view of lamp radiating fan

3.9.8 Replacing Reaction Cuvette


When to do
Replace a cuvette if,
▪ it is detected abnormal through the Cuvette Check procedure; or
▪ scratches or cracks are found on the optical surface of the cuvette.

WARNING
While installing the reaction cuvettes, exercise caution to avoid scratching them. Do not touch the optical surface
of the reaction cuvettes. If the optical surface is polluted, the obtained absorbance may be inaccurate.
Wear gloves free of fiber and powder to avoid polluting the optical surface of the reaction cuvettes.

BIOHAZARD
Wear gloves and lab coat, and if necessary, goggles during the maintenance process.
Tools
Cross screwdriver, fiber-free gloves, dry cloth or gauze, reaction cuvettes, and concentrated wash solution
manufactured by our company
How to do
1) Select Utility-Maintenance-Maintenance- Biochemistry Maintenance.
2) Choose Replace Cuvette.
3) Select Next.
4) Type in the position number of the cuvette segment you want to replace.
The input range is 1-8. Only one position number can be entered each time.
5) Select Replace.
6) Push open the cuvette window cover. Loosen the cuvette anchor plate screw with a hand, flip the anchor
plate screw rightward, and take out the reaction cuvette.
7) Install a new reaction cuvette, flip back the reaction cuvette anchor plate, and tighten it with a hand.
Note: If all or many segments need to be replaced, the analyzing unit or the mains supply may be turned

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off first. Push open the cuvette window. Rotate the reaction carousel with a hand to replace the reaction
cuvette.
8) After completion of replacing the cuvette, close the cuvette window cover.
9) Select Utility->Maintenance->Maintenance->Biochemical Maintenance Instruction->Reaction
Cuvette Detection to check whether the new cuvette meets the requirements.
Note: If the cuvette detection is not performed, the water blank of the new cuvette may be too big to use,
or an alarm "Water blank out of range (10X)" appears.
3.9.9 Replacing AD collection board
When to do
The AD collection board may need to be replaced when no photoelectric signal is output or a dark current is
abnormal.
Tools
Cross screwdriver and antistatic gloves
How to do
1) Power off the analyzing unit or the instrument.
2) Use a cross screwdriver to remove the right cover of the instrument.
3) See the following figure. Use a cross screwdriver to remove the screws that fasten the upper cover of
the AD box, and remove the upper cover of the AD box.
4) Unplug the signal cable between the AD collection board and the Main board.
5) Use a cross screwdriver to remove the screws that fasten the AD collection board, and remove the AD
collection board.
6) Install a new AD collection board in reversed order of the foregoing steps.

Signal cable interface

AD collection board

AD box upper cover

Figure 3-57 Exploded view of AD collection board

NOTE:
Wear ESD gloves when replacing the AD collection board.

Alignment and confirmation


Select "Maintenance"->"Alignment" -> "Photoelectric Gain Adjustment".Refer to 7.3 Photometric Unit.
3.10 ISE Unit (Optional)
3.10.1 Module Functions
The ISE module is an optional module for the fully-automated chemistry analyzer and designed to measure the
concentration of K+, Na+ and Cl- in serum, plasma and diluted urine. The sample volume for measurement is:
70µl for serum and plasma, 140µl for urine diluted at the ratio of 1:9 (1 for urine and 9 for diluent).

Work principle
The ISE Module measures sodium, potassium, lithium and chloride in biological fluids,

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using ion selective electrode technology. The flow-through of each electrode uses selective membrane
tubing, specially formulated to be sensitive to corresponding ions. The potential of each electrode is
Measured relative to a fixed, stable voltage established by the double-junction silver/silver chloride
Reference electrode. an ion selective electrode develops a voltage that varies with the concentration
of the ion to which it responds.
The relationship between the voltage and the concentration can be expressed by Nernst equation
ENa ERef

ENa − ERe f = S log Na +

Na
Ref

Two-points Calibration

→factor S

Figure 3-58 ISE Work principle

Calibrator Calibrator
B A
Pump Pump Pump ISE
Waste tank B A W

Figure 3-59 Fluidic system of ISE Unit

Two-points calibration
1) Adding Calibrant A
2) Locating
3) Draining
4) Adding Calibrant B
5) Locating
6) Draining
One-point Calibration(serum sample test)
1) Adding serum sample
2) Locating
3) Draining
4) Adding Calibrant A
5) Locating
6) Draining

Parameters
Table 3-12 ISE Parameters

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Item Features

Sample Serum,Plasma,Urine
Sample volume Serum, plasma 70uL, diluted urine 140uL
(10-fold dilution)
Method Direct method

Time 35s/cycle(Serum)

Speed 300Test/hour(Serum)/198 Test/hour(Urine)


Power 24VDC ,1A

Communication RS232C
Maximum ambient 32℃
temperature

composition
ISE module
There are five kinds of electrodes with Na+, K+, Cl-, reference and spacer electrodes. The sample is added by
the addition port of the ISE module, and the sample is analyzed and measured.

Spacer

Figure 3-60 ISE module

Peristaltic pump

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–Pump W:Draining the wasted liquid, and locating the liquid in the tubing
–Pump A:Controlling adding calibrator A.
–Pump B:Controlling adding calibrator B.
Reagent module
The reagent module integrates calibrator A, calibrator B, waste container, and a chip used for monitoring reagent
inventory. It provides reagent for sample analysis and stores the liquid waste herein..
–Calibrant A: Two point and single-point calibration,Pump calibration,Bubble calibration,
Washing after each test.
–Calibrant B:Two point and single-point calibration for urine sample.
–waste container,:storage waste.

Figure 3-61 Peristaltic pump and Reagent module

Auxiliary reagent
–Cleaning solution: It is used once every 50 samples to prevent protein buildup, 100uL of
cleaning solution will be used.
–Urine Diluent: It is used for urine samples. Urine samples must be diluted to perform
urine measurement: 1 part urine specimen to 9 parts Urine Diluent

Urine diluent

Cleaning solution

Figure 3-62 Cleaning solution and Urine diluent

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3.10.2 Structure and FRU List

SP3.5*8 screw

ISE shielding box

ISE module

ISE shield

M4*8 screw

Figure 3-63 Exploded view for installation of ISE module

Pump bracket

Pump
M2.5*6 screw

M2.5*6 screw

Figure 3-64 Exploded view for installation of pump module

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Figure 3-65 Exploded view for installation of reagent module

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16 13

1-5

17 10 14 15

8 18 12

Table 3-13 List of materials

No FRU Part Name Remarks


1 115-004626-00 K electrode

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No FRU Part Name Remarks


2 115-004627-00 Na electrode
3 115-004630-00 Cl electrode
4 115-004625-00 Reference electrode
5 115-004628-00 Spacer
6 BA34-10-63657 Main control board of the ISE
module
7 BA34-10-63659 Pre-amplification board of the ISE
module
8 BA34-10-63658 Compression plate
9 801-BA34-00104-00 ISE module bubble detector
10 801-BA34-00103-00 Sample tube of ISE module
11 BA34-10-63663 O ring of ISE module(3)
12 BA34-10-63668 O ring of ISE electrode
13 082-000684-00 Peristaltic Pump
14 801-BA34-00105-00 The peristaltic pump tube(3 pcs)
15 BA34-10-63666 ISE waste tube connector
16 BA34-10-63667 Tube connector of ISE (4)
17 801-BA34-00106-00 ISE module plastic tube for A ,B and
W liquid
18 BA34-10-63812 ISE module wand

3.10.3 Unclogging Waste Tubes


When to do
If the sample contains insoluble substances like fibrin or other substances, they can be accumulated in the
waste tube after long time use, causing clogging of the waste tube.
Maintenance Tools
Name Code Quantity
Unclogging tool for ISE 115-023372-00 1

WARNING
Do not spill liquid on the analyzer. Liquid ingression may cause equipment damage.

Biohazards
Wear gloves and lab coat, and if necessary, goggles during the maintenance process.

Note
Excessive bleach and DI water flushed into the ISE reagent pack waste bag may cause waste bag over
expansion and clog the Cal A & Cal B reagent flow.
To prevent this problem, connect to an old used-up reagent pack or use the connector of the used-up reagent.
How to do
1) Ensure the analyzer is in idle (standby) status. Open the ISE window on the right side panel of
the analyzer.
2) Connect the waste tube fitting to a syringe and unclogging tool with 5mL of undiluted household
bleach.
3) Press the wand release button to remove the wand from the current in use ISE reagent pack and
keep it in a save place. Engage the wand to an old used-up reagent pack.

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4) Inject bleach into the ISE waste tube and soak the tube for 5 minutes. Discharge the waste into
the reagent pack.
Note: When the bleach cannot be injected into the ISE pack, remove the wand and push down to open the
waste valve manually with a sharp object, and then inject again. If bleach can go through this time, the waste
bag was clogged and cannot be used. If bleach still cannot be injected, replacing the ISE wand is recommended.
5) Repeat this step with 5mL of DI water without the 5 minutes of soaking time.
6) Remove the wand from the old use-up pack and re-install it back to the current in use ISE pack.
Re-install the waste tube fitting back to the ISE electrode housing right angle adapter and waste
peri-pump tube back to the pump bracket. Re-install the housing cover.
Alignment and confirmation
Perform ISE pump calibration and if it succeeds, the tube has been successfully unclogged.
3.10.4 Replacing Pump Tube
When to do
Replace the pump tube when it is aged or leaking or has not been maintained for a half year.
Maintenance Tools
Cross screwdriver, pump tube.
Precautions:

Biohazards
Wear gloves and lab coat, and if necessary, goggles during the maintenance process.
How to do
1) Ensure the analyzer is on idle (standby) condition. Open the ISE cover on the right side analyzer
panel.
2) Select Utility-Maintenance-Maintenance-ISE-Remove Reagent Pack.
3) Select Utility -> Maintenance -> Maintenance -> ISE -> Replace Pump Tube and Calibrator Tube.
4) Select Pump Tube.
5) Replace it with new one. Make sure the connectors and tubes are correctly connected; otherwise
ISE module failure may occur.
6) Load the reagent pack and the procedure is completed.
7) Install back the right side panel.
8) Record the maintenance log.
Alignment and confirmation
Perform ISE pump calibration and if it succeeds, the tube has been successfully replaced.
3.10.5 Replacing Calibrator Tube
When to do
Replace the calibrator tube when it is aged or leaking or has not been maintained for over one year.
Maintenance Tools
Cross screwdriver, calibrator tube
Precautions:

Biohazards
Wear gloves and lab coat, and if necessary, goggles during the maintenance process.
How to do
1) Ensure the analyzer is on idle (standby) condition. Open the ISE cover on the right side analyzer
panel.
2) Select Utility-Maintenance-Maintenance-ISE-Remove Reagent Pack.
3) Select Utility -> Maintenance -> Maintenance -> ISE -> Replace Pump Tube and Calibrator Tube.
4) Select Calibrator Tube.
5) Replace it with new one. Make sure the connectors and tubes are correctly connected; otherwise
ISE module failure may occur.
6) Load the reagent pack and the procedure is completed.
7) Install back the right side panel.
8) Record the maintenance log.
Alignment and confirmation
Perform ISE pump calibration and if it succeeds, the tube has been successfully replaced.

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3.10.6 Replacing ISE electrode


ISE electrodes are consumables and have a limited life span. When used for a long period or after measuring
a large number of samples, the ISE electrodes may have their performance degraded and should be replaced
immediately.
Purpose
To replace the ISE electrodes to ensure the optimal measurement performance.
When to do
▪ Reference electrode: Every 6 months
Other electrodes:
When 10,000 ISE tests are performed.
When the ISE electrodes are used for 6 months since installation.
▪ When calibration fails or quality control is abnormal as the result of degraded electrode performance.
Materials required
Reference electrode, ISE electrode
System status
Make sure that the status of the ISE module is Standby or Stopped
Precautions

BIOHAZARD
⚫ Wear gloves and lab coat, and if necessary, goggles.

NOTE
⚫ After performing this procedure, recalibrate the ISE electrodes prior to starting analysis.
How to do
1) To remove the electrodes
a) Select Utility > Maintenance > Maintenance > ISE Maintenance.
b) Choose Replace Electrode.
c) Select desired electrodes, and enter the lot number and expiration date.
d) Select Add and then select OK.
e) Select Continue.
f) Open the ISE side door and remove the cover of the shielding box.
g) Open the electrode case, take out the electrode, remove the tapes around its inside, and then
use clean tissue to wipe it.

NOTE
⚫ Take out the insert from the reference electrode, and ensure no crystallized salt exists in and around it. If
needed, clean the electrode with warm water.
⚫ Make sure the red ball of the reference electrode floats on the internal fluid. Make sure the O rings of all
electrodes remain intact.
h) Remove all electrodes from the ISE module.
2) To install the new electrodes
a) To install a new reference electrode:
Place the reference electrode at the bottom of the ISE module and make the rear part of the electrode contact
closely with the internal wall of the ISE module.
Loosen the compressor and ensure the electrodes are fixed tightly.
b) Install other electrodes in the order of Cl, K, Na, and spacer from bottom to top.
c) If the O ring is lost, install a new one. There are two more O rings in each electrode case.
d) Check if the electrode positions are correct:
▪ The Na, K and Cl electrodes are of the same size and shape. Ensure that the electrodes are inserted in
the correct order.
▪ If one of the electrodes cannot be easily pushed into the housing, check the electrode first and then repeat
the installation process.
▪ Check if the 5 electrodes are relatively on the same straight line; otherwise, liquid cannot flow through the
electrode tubes smoothly.

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e) Select Continue. The system primes the tubes with calibrators A and B.
f) Select Done.
g) Restore the cover of the shielding box and close the side door of the ISE module.
h) Run ISE calibration.
i) If the calibration fails, perform the following operations:
▪ Run ISE calibration for multiple times so that the electrodes can get steady quickly.
▪ Or, drip little serum sample in the electrode channel, and leave it for 10-30 minutes, and then run calibration
again.

NOTE
⚫ The new electrode can be calibrated successfully only after certain time period.

3.10.7 Removing reagent pack(ISE)


When powering off the analyzer for a long time, or storing the electrodes, or replacing the electrode tubes,
remove the reagent pack first.
When to do
Perform this maintenance procedure when powering off the analyzer for a long time (over 3 days), or storing
the electrodes, or replacing the electrode tubes
System status
Make sure that the status of the ISE module is Standby or Stopped
How to do
1) Select Utility > Maintenance > ISE Maintenance, and choose Remove Reagent Pack.
2) Remove the tube of pump A and then reinstall the tube by switching the connectors of
the tube.
3) Handle pump B in the same way.
4) Select Continue. The system executes purge A and B each for 30 times.
5) Restore the reversed pump tubes.
6) Install the three red caps on the tube connectors of the reagent pack, and keep the
reagent pack at room temperature away from sunshine.
7) Select Done.
3.10.8 Storing electrodes(ISE)
Before the analyzer is powered off for a long time or after the reagent pack is removed, the ISE electrodes
cannot be moistened by regular prime, and may be damaged due to lack of water. It is necessary to store the
electrodes properly before powering off the analyzer for a long period.
Purpose
To store the electrodes separately to prevent them from being damaged due to lack of water while the analyzer
is powered off.
Materials required
Electrode cases and tapes
When to do
Perform this procedure when the analyzer is going to be powered off for over 3 days. If it will be powered off for
no more than 3 days, prime the ISE electrodes to protect them from being damaged.
System status
Make sure that the status of the ISE module is Standby or Stopped
Precautions

BIOHAZARD
Wear gloves and lab coat, and if necessary, goggles during the maintenance process

note
Make sure that the storage temperature is below 40℃.

How to do

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1) Remove the reagent pack, see 3.10.7 Removing reagent pack(ISE).


2) Open the ISE side door and remove the cover of the shielding box.
3) Remove all electrodes from the ISE module.
4) To save the reference electrode:
a) Put back the insert to the cell of the reference electrode and prevent the crystallized salt
from clogging the cell.
b) Store the electrode in an electrode case at the room temperature in a sun-shielding place.
5) To save the Na, K and Cl electrodes:
a) Take out a little calibrator A from the reagent pack, inject it into the cell of the electrode and
seal it with tape. Make sure proper amount of calibrator is injected into the cell of the
electrode.
b) Store the capped electrodes in an electrode case at the room temperature in a sun-shielding
place.
6) Restore the cover of the shielding box and close the side door of the ISE module.
3.10.9 Inventory Calculation of Reagent Pack
Reagent pack as one part of the ISE module should be installed as instructed by this manual. You should
install reagent pack while the analyzer is powered off, and then check the reagent inventory and prime the ISE
module with Calibrator A and B. If the reagent pack is not properly installed, error may be produced in inventory
calculation, and the actual volume may differ from that displayed on the screen.

The following operations may result in the actual inventory of the ISE reagent pack
less than the displayed one.
1) When the analyzer is turned on and the ISE module is in failure status, the reagent pack is changed, without
recovering the module failure or checking the inventory immediately.
Operation explanation: When the ISE module is in Stopped status, the software will stop writing volume
information into the reagent pack chip. However, the analyzer will automatically execute the sip action of the
ISE module during startup to consume certain amount of reagent. Therefore, when the reagent pack is replaced,
but the ISE module is not restored or the screen display refreshed, the software will not calculate the reagent
consumption volume until reading the new reagent pack. At this moment, the actual reagent volume =
displayed volume - consumption of Sip after replacing the reagent pack, which means that the actual reagent
volume is less than the displayed volume on the screen.
2) When the analyzer is powered on but the software is closed or the computer is shut down, the reagent
pack is changed.
Operation explanation: During shutdown, the analyzer will automatically execute the sip action of the ISE
module to consume certain amount of reagent. When the analyzer is started up, the software will detect a new
reagent pack and zero the consumption that is not written into the reagent pack chip, and then display the
volume read from the reagent pack chip. At this moment, the actual reagent volume = displayed volume -
consumption of Sip after replacing the reagent pack, which means that the actual reagent volume is less than
the displayed volume on the screen.
3) When the analyzer is powered on but the software is closed or the computer is shut down, the reagent
pack is switched to another analyzer and then installed back after use.
Operation explanation: During shutdown process, the analyzer cannot detect if the reagent pack is normal.
If the reagent pack is installed on the current instrument after being used on another one, the analyzer, when
started up, will detect that the recorded reagent volume on the chip is less than the original one, and the software
will zero the reagent consumption of Sip during shutdown and display the read volume on the screen. At this
moment, the actual reagent volume = displayed volume - consumption of Sip during shutdown (with reagent
pack installed), which means that the actual reagent volume is less than the displayed volume on the screen.
1) The ISE module is de-configured, but the reagent pack is still on the instrument.
Operation explanation: Though the ISE module is de-configured, the original reagent pack information is not
cleared from the database. When the ISE module is configured again with the same reagent pack, the Sip
period without ISE module will be included in calculation of the reagent consumption.
Note:
▪ In condition 1, restore the ISE module and check the reagent inventory immediately to minimize or eliminate
the calculation error.
▪ In condition 2 and 3, before running the operating software to start up the analyzer, remove the reagent
pack and then run the operating software. After the startup procedure is complete, re-install the reagent
pack and inquire the reagent volume immediately to minimize or eliminate the calculation error.
▪ In condition 4, remove the reagent pack and then de-configure the ISE module.

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The following operations may result in the actual inventory of the ISE reagent pack
more than the displayed one.
1) When the analyzer is turned on and the ISE reagent pack is changed, without checking the inventory
immediately.
Operation explanation: The analyzer will automatically refresh the ISE reagent consumption, by subtracting
the consumption of calibrator A or B from the known volume (of the original reagent pack) and writing it into the
reagent pack chip, when calibrator A or B is consumed for 1%. The written volume is based on the original
reagent pack before replacement, and the volume of a used reagent pack is often less than that of a new one.
So the volume recorded on the chip of the new reagent pack is less than the actual volume, and the actual
volume is greater than the displayed volume on the screen.
2) When the analyzer is powered on but the software is closed or the computer is shut down, the reagent
pack is removed for storage, and re-installed before the operating software is run.
Operation explanation: During shutdown process, the analyzer cannot detect if the reagent pack is normal.
If the reagent pack is loaded before the analyzer is started up, the analyzer, when started up, will detect that the
reagent volume recorded on the chip is same as that recorded by the software, but the software will confirm by
mistake the reagent consumption of sip during shutdown. (Actually, no reagent is consumed.) Therefore, after
calculating the reagent consumption, the software will write the new volume information onto the chip and
display it on the screen. At this moment, the actual reagent volume = displayed volume + consumption of Sip
during shutdown (with reagent pack installed), which means that the actual reagent volume is greater than the
displayed volume on the screen.
3) The analyzer is powered off after the operating software is closed, and it is powered on again before the
operating software is run.
Operation explanation: When closed normally, the operating software cannot detect if the ISE module is
working. When powered on before the software is run, the analyzer, when started up, will detect that the reagent
volume recorded on the chip is same as that recorded by the software, but the software will confirm by mistake
the reagent consumption of sip during shutdown. (Actually, no reagent is consumed because the ISE module is
not working while the analyzer is powered off.) Therefore, after calculating the reagent consumption, the
software will write the new volume information onto the chip and display it on the screen. At this moment, the
actual reagent volume = displayed volume + consumption of Sip during shutdown (with reagent pack installed),
which means that the actual reagent volume is greater than the displayed volume on the screen.
Note:
▪ In condition 1, inquire the ISE reagent volume immediately to minimize or eliminate the calculation error.
▪ In condition 2 and 3, before running the operating software to start up the analyzer, remove the reagent
pack and then run the operating software. After the startup procedure is complete, re-install the reagent
pack and inquire the reagent volume immediately to minimize or eliminate the calculation error.

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4 Hardware Circuits
4.1 Overview
This chapter describes the functions of the printed circuit board assemblies (PCBAs) used on the BS-240.
4.2 Hazards

Note:
• While the instrument is working, do not touch the hardware circuit boards with your hands or other objects.
• Before removing a circuit board, disconnect the instrument from the (AC) power supply. Please wear a pair
of anti-static gloves or take other measures to prevent static electricity prior to removing a circuit board.

4.3 Summary of PCBAs


The table bellows provides a summary of the PCBAs used on the BS-240 Chemistry Analyzer and briefly
describes their functions.
Table 4-1 Summary of PCBAs

PCBA(PCB) Functions ID
Main board The main board is the control center of the #1
051-002414-00 instrument. It is mainly used to fulfill the
following tasks: 1) communicating with a
computer through the RS232 serial port to
transmit data and instructions; 2)
communicating with the smart modules,
including the ISE module, through the
extended serial ports to transmit data and
instructions; and 3) controlling digital
potentiometer adjustment and photoelectric
data collection of the AD collection board
and receiving the photoelectric data.
Power driver board The power drive board drives and controls #2
051-002413-00 the probe, mixer, sample/reagent carousel,
reaction carousel, wash station and wash
syringe and other related components. After
EBJ485, the code of board PCB changes
from BA10-20-77756 to 050-003059-01.
Reagent refrigeration board The reagent refrigeration board is used to #3
BA20-30-75227 drive the reagent refrigeration circuit
(including heatsinks), fans, and demisting
circuit of the reagent bar code reader.
Integration Liquid Detecting Board The board detects the level of samples and #4
051-002479-00 reagents, and detect/convert the signals of
the vertical obstruct detection sensor.
AD collection board The AD collection board adjusts the #5
BA10-30-77759 photoelectric signals output by the pre-
amplification board and controls it for AD
conversion. It provides an SPI interface for
connecting with the Main board.
Pre-amplifying board The pre-amplification board converts the #6
BA10-30-77760 signals of the discrete photodiode array
from analog to digital.

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Power supply board It is used for power the whole unit, #7


051-002404-00 outputting the A12V, A5V digital,
D12V/E12V analog, C12V power, B24V
power, and the B12V power for partial
Peltiers
ISE power PCBA It is used for powering the ISE module. #8
BA34-30-63624
The locations of the PCBA on the instrument.

Power drive
board

Main Board
ISE power PCBA
Power supply

Figure 4-1 Locations of the PCBA on the instrument 1

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Level sense
board

Reagent
refrigeration board
AD collection
Pre-amplification Board board

Figure 4-2 Locations of the PCBA on the instrument 2

4.4 Functions of PCBA


4.4.1 Control Structure
The BS-240 Chemistry Analyzer consists of the analyzing unit (analyzer), operation unit (computer), and output
unit (printer).
The analyzing unit (analyzer) is composed of the temperature control system, reaction system (including ISE
module), photometric system, sample/reagent handling system, mixer system, and cuvette wash station.
The control diagram is as follows:

Optical System

Photoelectric signal
Control signal
Temperature
control signal
Temperature control
PC RS232 Hardware System
system
Control signal
Control signal

Position signal

Drive and execute


system

Figure 4-3 General functions

The hardware system has the following functions:


• Communicating with a computer through the serial port, and receiving/sending commands, responses, and
data.
• Controlling data collection of the photometric system.
• Controlling movement and status signal collection of execution units.
• Controlling working and temperature control signal collection of the temperature control system.

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4.4.2 Main Board


Functions and Principles
• Communicating with computer through the serial port to transmit data and instructions and update its
application program.
• Communicating with the smart modules, including the ISE module, through the extended serial ports to
transmit data and instructions.
• Controlling digital potentiometer adjustment and photoelectric data collection of the AD collection board
and receiving the photoelectric data.
• Detecting position signal and horizontal obstruct signal.
• Detecting level sense signal and vertical obstruct signal through the interface for the liquid level detection
board.
The figure below shows the relation between the main board and other PCBAs.
Power
supply
board

Reagent
Power drive
refrigeration Main Board
board
board

AD collection
board

Preamplifier
board

Figure 4-4 Relation between main board and other PCBAs

The functional diagram of the control board is as shown below.

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Drive clock/direction sign al


Injection unit
Probe wash pump valve signal
Location sensor

Drive clock/direction sign al


Level floater Mixer Unit
Wash p ump valve signal

Reaction Unit Drive clock/direction sign al


PC

FPGA Drive clock/direction signal

Cuvette Wash Unit

Wash p ump valve signal

Reaction carou sel heater control signal


Temperature
Cont rol signal of d eionized w ater heater
Control Unit
Cont rol signal of w ash solution heater

Main Control Unit

Main Board
Figure 4-5 Functional diagram of main board

Description
PCB
The PCB layout of the main board is as shown below.

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Figure 4-6 Main board PCB

Connectors

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The main board includes the following connectors.


Power supply:
Power supply input (J2): 6-pin, providing +12V analog and +5V digital for PCBAs.
Pin No. Signal Reference Value
1 +5V 4.75~5.25V
2 GND /
3 / /
4 / /
5 12V 11.4~-12.6V
6 GND /
Connectors for sending/receiving communication signals:
▪ Serial port (J7) for PC: 10-pin, RS232, used for communication with a computer.
▪ Drive signal interface (J1):40 PIN, TTL used to transmit control signal to power drive board.
▪ Connector (J39) for AD collection board: DB25, used for communication with the AD collection board and
providing power supply for it.
▪ Connector (J6) for ISE module: 8-pin, RS232, used for communication with the ISE module.
▪ Connector (J5) for bar code reader: 8-pin, RS232, used for communication with the bar code reader.
▪ Connector for optical coupler (J12):36 PIN, used for the input of the sensors of moving parts.
▪ Connector for optical coupler (J13):36 PIN, used for the input of the sensors of moving parts.
▪ Connector for optical coupler (J14):10 PIN, used for the input of the liquid floater sensor.
▪ Connector of temperature sensor (J18):4PIN, used for the input of temperature sensor of the reaction
carousel.
▪ Connector of temperature sensor (J21):4PIN, used for the input of temperature sensor of cleaning fluid.
▪ Connector of temperature sensor (J22):4PIN, used for the input of temperature sensor of wash solution.
▪ Connector of temperature sensor (J23):4PIN, used for the input of temperature sensor of reagent
preheating.
▪ Connector of the liquid level detection board (J11):4PIN, for power supply and signal output of liquid level
detection board: 4-pin, used to input a level signal and an anti-collision signal into and provide a power
supply for the liquid level detection board.
Connectors for debugging:
▪ JTAG connector (J8): 10-pin, used for debugging the FPGA.
Indicators
The main board contains the following indicators.
• +12V power supply indicator (D8): green. It is lit when the analyzer power switch is turned on, indicating
that the +12V power supply has been connected.
• +5V power supply indicator (D7): green. It is lit when the analyzer power switch is turned on, indicating that
the +5V power supply has been connected.
• +3.3V power supply indicator (D9): green. It is lit when the analyzer power switch is turned on, indicating
that the +3.3V power supply has been connected.
• Analog +12V power supply indicator (D20): green. It is lit when the analyzer power switch is turned on,
indicating that the analog +12V power supply has been connected.
• Analog -12V power supply indicator (D21): green. It is lit when the analyzer power switch is turned on,
indicating that the analog -12V power supply has been connected.
• D19: orange FPGA configuration indicator. On indicates FPGA is successfully configured.
• D14: Green FPGA working status indicator. LED is flashing every second, indicating FPGA works normally.
• D23: Green. When communication with the lower layer unit is interrupted, the indicator is lit.
Test points
In the following positions of the main board can signal tests be performed.
• 12V: +12V power supply input. Normal range: 11.4 - 12.6V.
• P12V: analog +12V power supply input. Normal range: 11.4 - 12.6V.
• N12V: analog -12V power supply input. Normal range: -11.4 - -12.6V.
• 5V: +5V power supply input. Normal range: 4.75 - 5.25V.
• VDD: +3.3V power supply. It is secondary power supply used to power the major digital circuits of the PCBA.
Normal range: 2.97 - 3.63V.
• 2.5V: +2.5V power supply. It is secondary power supply used for FPGA downloading. Normal range: 2.25
- 2.75V.
• 1.2V: +1.2V power supply. It is secondary power supply used to power the FPGA core. Normal range: 1.14
- 1.26V.

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Installation Methods and Precautions


Steps:
1) Before replacing, you need to confirm the closed channel configuration of the current main board of
the instrument.
2) Before replacing the main board, you need to back up the unit parameters in advance. Refer to 6.7.3
Unit parameter Backup.
3) Power off, and remove the back cover.
4) Disconnect all the connectors on the main board (it is recommended to take pictures before
disconnecting to avoid subsequent wiring errors)
5) Replace the new main board and connect all the connectors.
6) Need to brush the control system software after replacement, refer to 6.4.3 Upgrading Control System.
7) After brushing the control system software, you need to confirm the parameters. If there is any change,
you need to configure the parameters according to Section 6.7.4 Parameter Configuration.

Note
• Prior to removing the PCBA, disconnect the instrument from the power supply and wear a pair of anti-static
gloves or wrist straps.
• Make sure that the connectors are inserted properly into the PCBA.
• Check the connectors with locks and ensure they have been locked properly.
• Check other connectors and ensure that they are inserted into the end of the slots.
• It requires great force to plug/unplug the J1,J12~J13 connectors. Hold the PCBA by its edge while
plugging/unplugging the connectors to prevent it from being deformed or damaged.
• After connecting J39 connector (DB25), tighten the retaining screws on two sides of it.
• Save the parameters before removing the PCBA in order to load the parameters after the PCBA is removed.

4.4.3 Power driver board


Functions and Principles
▪ It is used to control the step motor, DC motor and Valve.
▪ It receives the signal from the Main Board through the connector for the control board.
▪ It control and drive the wash station, syringe, sample/reagent carousel, sample/reagent probe, mixer,
reaction carousel valve.
The functional diagram of the power drive board is as shown below.
The PCB layout of the power drive board is as shown below.

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Power drive board


Drive clock/direction sign al
Injection unit
Probe vertical motor
Probe wash pump valve signal

Location sensor Probe horizontal motor

Probe syringe motor

Drive clock/direction sign al Motor


Level floater Mixer Unit drive
Wash p ump valve signal A3985/A3
CPLD
979

Reaction Unit Drive clock/direction sign al


PC Wash syringe motor

FPGA Drive clock/direction sign al

Cuvette Wash Unit


Pump/
Wash p ump valve signal Valve Pump/ valve
Drive

Pump/Valve
Drive
Reaction carou sel heater control signal
Temperature 220V heater drive Reaction Carousel Heat er
Cont rol signal of d eionized w ater heater
Control Unit 220V heater drive Deionized Water Heat er
Cont rol signal of w ash solution heater
220V heater drive Wash Solu tion Heater

Main Control Unit Power supply board

Main Board

Figure 4-7 Power drive board

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BA10-20-77756(before EBJ485)

No.HSH-19021-BS-240 Version: 4.0 4-10


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050-003059-01(after EBJ485)

Figure 4-8 Power drive board PCB

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Connectors:
The power drive board contains the following connectors.
Power supply:
Power supply input (J17): 8-pin, providing 24V, 12V analog and +5V digital for PCBAs.
Pin No. Signal Reference Value
1 +24V 23.5~26V
2 +24V 23.5~26V
3 +5V 4.75~5.25V
4 +12V 11.4~12.6V
5 GND /
6 GND /
7 GND /
8 GND /
Connectors for sending/receiving communication signals:
• Connector (J20) for transmitting control signal of main control board: 40-pin, TTL, used for transmitting a
control signal.
Connectors for debugging:
• JTAG connector (J2): 10-pin, used for debugging the FPGA.
Connectors for drive and control:
• Valve driving connector (J6): 8-pin, used for driving interior pump and interior wash valve of the probe.
• Valve driving connector (J9): 8-pin, used for driving phase-1\2\3\4 waste pump, deionized water and wash
solution dispense valves, and mixer exterior valve.
• Sample/reagent carousel motor driving connector (J15): 4-pin, used for driving the sample/reagent
carousel motor.
• Reaction carousel motor driving connector (J16): 4-pin, used to drive reaction carousel motor.
• Sample/reagent horizontal motor driving connector (J5): 4-pin, used for driving the sample/reagent
horizontal motor.
• Sample/reagent vertical motor driving connector (J13): 4-pin, used for driving the sample/reagent vertical
motor.
• Sample/reagent syringe motor driving connector (J8): 4-pin, used for driving the sample/reagent syringe
motor.
• Deionized water syringe motor driving connector (J11): 4-pin, used for driving the deionized water syringe
motor.
• Wash solution syringe motor driving connector (J12): 4-pin, used for driving the wash solution syringe motor.
• Wash station motor driving connector (J4): 4-pin, used for driving the wash station motor.
• Sample/reagent mixer horizontal motor driving connector (J10): 4-pin, used for driving the sample/reagent
mixer horizontal motor.
• Sample/reagent mixer vertical motor driving connector (J14): 4-pin, used for driving the sample/reagent
mixer vertical motor.
• Mixer motor driving connector (J22): 2-pin, used to drive the mixer motor.
• Reagent preheating driving connector (J24): 2-pin, used for driving the reagent preheater.
Indicators
The power drive board contains the following indicators.
Power supply:
• +12V power supply indicator (D3): green. It is lit when the analyzer power switch is turned on, indicating
that the +12V power supply has been connected.
• +5V power supply indicator (D2): green. It is lit when the analyzer power switch is turned on, indicating that
the +5V power supply has been connected.
• +24V power supply indicator (D1): green. It is lit when the analyzer power switch is turned on, indicating
that the +24V power supply has been connected.
Test points
In the following positions of the power drive board can signal tests be performed.
• 12V: +12V power supply input. Normal range: 11.4 - 12.6V.
• 24V: 24V power supply input. Normal range: 23.5 - 26V.
• 5V: +5V power supply input. Normal range: 4.75 - 5.25V.

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Installation Methods and Precautions

Note
• Prior to removing the PCBA, disconnect the instrument from the power supply and wear a pair of anti-static
gloves or wrist straps.
• Make sure that the connectors are inserted properly into the PCBA.
• Check the connectors with locks and ensure they have been locked properly.
• Check other connectors and ensure that they are inserted into the end of the slots.
• It requires great force to plug/unplug the J20 and J17 connectors. Hold the PCBA by its edge while
plugging/unplugging the connectors to prevent it from being deformed or damaged.

4.4.4 AD collection board


Functions and Principles
• Adjusting gains of 8 photoelectric signals via a digital potentiometer.
• Controlling the channel selection switch to switch among 8 channel signals at different time.
• Converting photoelectric analog signals into digital signals via an AD converter and then outputting the
signals.
The figure below shows the relation between the AD collection board and other PCBAs.
Preamplifier
board

AD collection
board

Main Board

The functional diagram of the AD collection board is as shown below.


Preamplifier
board

Single analog signal gain


adjustment

Main Board

AD

Description
PCB
The PCB layout of the AD collection board is as shown below.

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Figure 4-9 Preamplifying AD PCB

Connectors
The AD collection board includes the following connectors.
Power supply:
• Power supply output connector (J1): 6-pin, used to provide +12V and -12V power supplies for the
preamplifier board and receive optical and electric signals from the preamplifier board.
Pin No. Signal Reference Value
1 Signal 0.25V-2.5V (water blank condition)
2 +12V 11.4~12.6V
3 GND /
4 GND /
5 GND /
6 -12V -11.4~-12.6V
• Main board connector (P1): 25-pin, used for communication with the main control board.
Indicators
The AD collection board contains the following indicators.
Power supply:
• +12V power supply indicator (D5): green. When it is lit, it indicates that the +12V power supply has been
connected.
• -12V power supply indicator (D4): green. When it is lit, it indicates that the -12V power supply has been
connected.
• +5V power supply indicator (D3): green. When it is lit, it indicates that the +5V power supply has been
connected.
Test points
In the following positions of the AD collection board can signal tests be performed.
• VIN: Optical/electric signal output Normal range: varies with the signal strength and lies between 0-5V.
• VPP: +12V power supply input. Normal range: 12V±5%, that is, 11.4 - 12.6V.
• VSS: -12V power supply input. Normal range: -12V±5%, that is, -11.4 - -12.6V.
• VCC: +5V power supply input. Normal range: 5V±5%, that is, 4.75 - 5.25V.
• AVCC: analog +5V power supply. Normal range: 5V±5%, that is, 4.75 - 5.25V.
• DVCC: digital +5V power supply. Normal range: 5V±5%, that is, 4.75 - 5.25V.

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Installation Methods and Precautions


Refer to 3.9.9 Replacing AD collection board.

Note
• Prior to removing the PCBA, disconnect the instrument from the power supply and wear a pair of anti-static
gloves or wrist straps.
• Make sure that the connectors are inserted properly into the PCBA.
• Check the connectors with locks and ensure they have been locked properly.
• Check other connectors and ensure that they are inserted into the end of the slots.
• It requires relatively great force to plug/unplug connectors J1. Hold the PCBA by its edge while
plugging/unplugging these connectors to prevent it from being deformed or damaged.
• After connecting P1 connector (DB25), tighten the retaining screws on two sides of it..

4.4.5 Pre-amplification Board


Functions and Principles
• Converting optical signals into electric signals via a photodiode array.
• With the help of the back circuit, filtering signals and transmitting them to the AD collection board after
amplification.
The figure below shows the relation between the pre-amplification board and other PCBAs.

Optical signal
AD collection
Preamplifier board
board

Figure 4-10 Relation between pre-amplification board and other PCBAs

The functional diagram of the pre-amplification board is shown below.

Optical signal

PDA

Signal filtering and amplification

AD collection
board

Figure 4-11 Functional diagram of preamplifier board

Description
PCB layout
The preamplifier board layout of the main board is shown below.

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Figure 4-12 PCB layout of preamplifier board

Connectors
The pre-amplification board includes the following connectors.
Power supply:
• Power supply input connector (2): 1-pin, used to provide +12V power supplies for the preamplifier board.
• Power supply input connector (6): 1-pin, used to provide -12V power supplies for the preamplifier board.
• Power supply input connector (3): 1-pin, used to ground the preamplifier board.
Connectors for sending/receiving communication signals:
• Preamplifier board signal output connector (1): 1-pin, used to transmit 1 optical/electric analog signal.
Installation Methods and Precautions
Refer to 3.9.6 Replacing Preamplifier Board.
4.4.6 Liquid Level Detection Board (LLD Board)
Functions and Principles
The BS-240 liquid level detection board is used to sense the sample/reagent fluid level, and primarily
implements the following functions:
• Sensing the reagent/sample levels; detecting the fluid level steadily and reliably, especially allowing the
sample/reagent probe to correctly detecting the fluid level inside reaction cuvettes.
• Outputting level sense signals to the main control board when the probe contacts the fluid level.
• Detecting vertical collision, and outputting the detection signal to the main control board.
The functional diagram of the liquid level detection board is shown below.

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Vertical
collision
circuit

probe Capacity Connect


Main
detection CPU or
Board
chip circuit

Figure 4-13 Functional diagram of liquid level detection board

Description
PCB layout
The top layer of the liquid level detection board is shown below.

图 1.1 Figure 4-14 Liquid level detection board PCB


Connectors
The liquid level detection board contains the following connectors.
Probe connector (J1): 2-pin, used for connecting the sample/reagent probe with related circuit.
Pin No. Signal
1 GND
2 Probe capacitor signal input
Power supply and signal output connector (J2): 4-pin, used to provide power supply for the liquid level detection
board and output the level sense signal and vertical obstruction signal.
Pin No. Signal Reference Value
1 GND /
2 Vertical High level (about 4V) is output when no vertical
obstruction obstruction occurs, and low level (about 0V) is output
signal output when vertical obstruction happens.
3 Level sense Low level (about 0V) is output when the probe fails to
signal output detect the fluid level, and high level (about 4V) is output
when the probe detects the fluid level.
4 +12V 11.4~12.6V
Reserved port: serial port communication cable connector (J3): 3-pin, used for communication between the
liquid level detection board and the control drive board.
Pin No. Signal

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1 RXD
2 RST
3 TXD
Indicators
The liquid level detection board contains the following indicators.
▪ Level sense indicator (D5): green. It is extinguished when the probe fails to detect the fluid level, and vice
versa.
▪ Vertical obstruction indicator (D1): redid is extinguished when no vertical obstruction occurs, and vice versa.
▪ Level detection system working indicator (D2): yellow. When level detection system works normally, it is
flashing. If strong obstruction signal is detected, the indicator is constantly lit.
Test points
In the following positions of the liquid level detection board can signal tests be performed.
▪ LEVEL: level sense signal output. Normal condition: Low level (about 0V) is output when the probe fails to
detect the fluid level, and high level (about 4V) is output when the probe detects the fluid level.
▪ GND: grounding terminal of the liquid level detection board.
▪ 5V:5V power for the level detection board. Normal range: 4.75~5.25V.
▪ 3.3V:3.3V power for the level detection board. Normal range: 2.97~3.63V.
▪ RAM: vertical obstruction signal output. Normal condition: High level (about 4V) is output when no vertical
obstruction occurs, and low level (about 0V) is output when vertical obstruction happens.

Installation Methods and Precautions

Note
• Prior to removing the PCBA, disconnect the instrument from the power supply and wear a pair of anti-static
gloves or wrist straps.
• Make sure that the connectors are inserted properly into the end of the slots on the PCBA.
• It requires great force to plug/unplug the connectors. Hold the PCBA by its edge while plugging/unplugging
the connectors to prevent it from being deformed or damaged.

4.4.7 Reagent Refrigeration Board


Functions and Principles
• Refrigeration control and drive: controlling the switch of the heatsinks and refrigerating the reagent
compartment to keep the temperature within certain range.
• Control of cooling fans and demisting.
The functional diagram of the reagent refrigeration board is shown below.

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Temperature sen sor

Reagent
Temperature
refrigeration Refrigeration
indication 2 Pelt iers
board control circuit
circuit

2 Pelt ier radiat ing fan s

6 reserved system radiating


Voltage conversion fan s
12V circuit

1 lamp radiating fan


12VFAN
1 power drive board
rad iatin g fan
Antifogging circuit
1 reserved radiating fan

Reaction carousel fan


Photoelectric 4 reaction carousel
Main Board feedback signal
coupling temp erature c on trol fans
processing circuit

Figure 4-15 Functional diagram of reagent refrigeration board

Description
PCB layout
The PCB layout of the reagent refrigeration board is shown below.

Figure 4-16 Reagent refrigeration board PCB

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Connectors
The reagent refrigeration board includes the following connectors.
Power supply:
Power supply input connectors (J86): providing refrigeration F12V and refrigeration B12V for the PCBAs.
Pin No. Signal Reference Description
Value
1 F12V 11.4~12.6V 12V power supply input for cooling fans.
4 GND 0
2, 3 B12V 11.4~12.6V Refrigeration power supply input: used
5, 6 FGND / for loading the corresponding Peltiers
J89_1 and J89_2.
Peltier connectors (J4-J7): providing power supply for the Peltiers.
Connector Pin No. Signal Reference Value
J89_1 1 1 Peltier 0V for ON and 12V for OFF.

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2 12V

Connector Pin No. Signal Reference Value


J89_2 1 2 Peltier 0V for ON and 12V for OFF.
2 12V

Demisting circuit connector (J15): providing power supply for the demisting heater.
Connector Pin No. Signal Reference Value
J9 1 1 demisting 11.4~12.6V
2 heaters /
3 /
4 0

Reagent refrigeration fan connectors (J84, J85): providing a power supply for the reagent refrigeration 12V fan.
Connector Pin No. Signal Reference Value
J84 1 GND /
2 FAN 11.4~12.6V
J85 1 GND /
2 FAN 11.4~12.6V
Temperature sensor connector (J88): checking temperature of the refrigeration compartment and refrigeration
board.
Connector Pin Signal Reference
No. Value
J88 1 GND 0V
2 Temperature sensor signal of the /
refrigeration compartment
PCBA radiating fan connector (J75): providing a 12V power supply for the PCBA radiating fan.
Connector Pin No. Signal Reference Value
J75 1 GND /
2 FAN 11.4~12.6V

Whole unit radiating fan connector (J81): providing a 12V power supply for the whole unit radiating fan.
Connector Pin No. Signal Reference Value
J81 1 GND /
2 FAN 11.4~12.6V

Lamp radiating fan connector (J73): providing a 12V power supply for the lamp radiating fan.
Connector Pin No. Signal Reference Value
J73 1 GND /
2 FAN 11.4~12.6V

Reaction carousel constant-temperature fan connectors (J76, J77): providing a 12V power supply for the fan
that keeps temperature of the reaction carousel.
Connector Pin No. Signal Reference Value
J76 1 GND /

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2 FAN 11.4~12.6V
J77 1 GND /
2 FAN 11.4~12.6V
Indicators
The reagent refrigeration board includes the following indicators.
Power supply:
No. Description Color Introduction
D45 C24V Green When it is lit, it indicates that the power supply works normally.
D48 VCC Green When it is lit, it indicates that the power supply works normally.
D47 B12V Green When it is lit, it indicates that the power supply works normally.
D49 VDD Green When it is lit, it indicates that the power supply works normally.
D46 F12V Green When it is lit, it indicates that the power supply works normally.
Indicators to indicate PCBA functions:
No. Description Color Introduction
D15 Fan power supply indicator Green When it is lit, it indicates that the
refrigeration board is working.
D3 Refrigeration power supply Green When it is lit, it indicates that the
indicator refrigeration board is working.
D4 Indicating the reagent Red When the reagent compartment
compartment temperature temperature exceeds the high limit
D6 Indicating the reagent Green When the reagent compartment
compartment temperature temperature is within the target range
D5 Indicating the reagent Yellow When the reagent compartment
compartment temperature temperature is lower than the low limit
D7 Indicating status of the peltier Green When it is lit, it indicates that the peltier is
working.

Installation Methods and Precautions

NOTE:
• Prior to removing the PCBA, disconnect the instrument from the power supply and wear a pair of anti-static
gloves or wrist straps.
• Make sure that the connectors are inserted properly into the end of the slots on the PCBA.
• It requires great force to plug/unplug the connectors. Hold the PCBA by its edge while plugging/unplugging
the connectors to prevent it from being deformed or damaged.

4.5 Power Supply System


4.5.1 Power Supply System of Whole Unit
Connected
E yellow to housing Analyzer Switch
green Main Power Switch
L brown L brown L
Power jack Power
N light blue N light blue supply
N
board

Figure 4-17 Power supply system of the whole unit

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Power Supply System


The power supply board, as the major part of the entire power supply system, provides power supply for the
lamp, DC power supply for major control boards, and power supply for refrigeration modules. For details, see
the figure below:

A12V/2A Lamp

5V Analog +/-12V Analog +/-12V


Power supply board

Analog Power
5V/4A AD collection Preamplifier
Main Board Supply C onversion
board board
Board

12V/5A

Power drive board

24V/6A

ISE Pow er Board ISE module

12V/11A
Reagent
refrigeration
board

Figure 4-18 Power Supply System


4.5.2 Performance Indices
Power supply input
• AC voltage input: 220-240V, 220/230V, and 110/115V.
• AC voltage frequency: 50/60±1Hz
• AC input power: 1KVA
Power supply output
No Name Rated Output Usage Control Description
1 5V 5V/4A 5V digital Controlled by analyzer power switch
2 12V 12V/2A Lamp Controlled by operating software
3 12V 12V/11A Reagent refrigeration Controlled by main power switch
4 12V 12V/5A 12V drive Controlled by analyzer power switch
5 24V 24V/6A 24V drive and heater Controlled by analyzer power switch
NOTE:
• Control by operating software means that the lamp voltage is controlled by the operating software while
the main power switch and analyzer power switch are turned on.
• Control by analyzer power switch means that the power supply is controlled by the analyzer power switch
with the prerequisite that the main power switch is turned on.
• Control by main power switch means that the power supply works normally when the analyzer power switch
is turned on, and vice versa.
4.5.3 Power supply board
Functions and principles are described below.
The PCB layout of the power supply board is shown below.

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Figure 4-19 Layout of power supply board

Indication of voltage outputs:


LED Indication Status Controlled By
L12V When L12V is lit, it indicates that the Controlled by operating
lamp outputs a 12V power. software
D5V When D5V is lit, it indicates that the Controlled by analyzer
PCBA outputs a 5V power. power switch
B12V When B12V is lit, it indicates that the Controlled by main
reagent refrigerator outputs a 12V power switch
power.
P12V When P12V is lit, it indicates that the Controlled by analyzer
lamp outputs a 12V power. power switch

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P24V When P24V is lit, it indicates that the Controlled by analyzer


PCBA outputs a 24V power. power switch
NOTE:
• Control by operating software means that the lamp is controlled by the operating software while the main
power switch and analyzer power switch are turned on.
• Control by analyzer power switch means that the power supply is controlled by the analyzer power switch
with the prerequisite that the main power switch is turned on.
• Control by main power switch means that the power supply works normally when the analyzer power switch
is turned on, and vice versa
Output connectors:
No. Pins Output Description
J1 1 AC input L
3 AC input N
J2 1 12VOUT
2 Analyzer Switch
3 Ground (Analyzer Switch)
J3 1 deionized water Heater (220V)
12
2 Wash solution heater (220V)

5
3 Upper heater of reaction carousel (220V)
10
7 Lower heater of reaction carousel (220V)
9
4 /
6 /
8 /
11 /
J4 1 Lamp ground
2 Ground
3 Ground
4 Ground
5 Ground
6 Ground
7 Ground
8 Ground
9 Ground
10 Ground
11 12V output of lamp
12 12V output of reagent refrigeration
13 12V output of reagent refrigeration
14 24V output of driving

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No. Pins Output Description


15 24V output of driving
16 12V output of driving
17 12V output of driving
18 12V output of driving
19 5V output
20 5V output
J5 1 Control input of deionized water heater
2 Control input of wash solution heater
3 Control input of reaction carousel heater
4 Ground
5 Control input of inlet valve
6 Ground
7 Control input of SV07 dispense valve
8 Ground
9 Reserved

10 Ground

11 Lamp control input

12 Ground

J6 1 Driving output of inlet valve


2
3 Driving output of SV07 dispense valve
4
5 Reserved
6
J7 1 Radiating fan
2
3 Radiating fan
4

Installation Methods and Precautions


1) Turn off main switch and remove the back cover.
2) Remove 4 screws of disassemble Power Box, then Pull out top cover.

No.HSH-19021-BS-240 Version: 4.0 4-26


IVD Global Technical Support Dept

4 screws

Top cover

Figure 4-20 Replacing power board 1

3) Draw out 10cm and disconnect AC 110/220 cable.


4) Rotate power box 90 degrees clockwise. Disconnect all cables left.

AC
110/220
cable

cables

Figure 4-21 Replacing power board 2

No.HSH-19021-BS-240 Version: 4.0 4-27


IVD Global Technical Support Dept

NOTE:
• Prior to removing the PCBA, disconnect the instrument from the power supply and wear a pair of anti-static
gloves or wrist straps.
• Make sure that the connectors are inserted properly into the end of the slots on the PCBA.
• It requires great force to plug/unplug the connectors. Hold the PCBA by its edge while plugging/unplugging
the connectors to prevent it from being deformed or damaged.
• Because the connector J6 is in the middle of the board, it is easy to loosen and causes the valve SV07 to
not work.

4.5.4 Replacing Power switch


Replacing Main Power Switch
1) Turn off the power, remove the cable, and remove the back cover of the instrument
2) Disassemble the two screws on the fixing bracket shown in the figure below.

Figure 4-22 Main Power Switch position

3) Disconnect the power cord from the main power switch. Note that the line and switch are marked. To
avoid errors, it is recommended to take a picture.
4) Replace the main power switch.
5) Connect the wire, pay attention to the corresponding , cables can not be connected wrong, the joint
should be tightly inserted, can not be loose. If the metal piece is loose, refer to the middle picture in
the figure below and squeeze the metal piece slightly.
6) Connect the power cord and turn on the main power switch.
7) After the power-on test is normal (the main switch will light), restore and replace the bracket and the
rear case.

No.HSH-19021-BS-240 Version: 4.0 4-28


IVD Global Technical Support Dept

Figure 4-23 Replace the main power switch

Replacing rocker switch


1) Turn off the power.
2) Remove the left side panel.

Figure 4-24 rocker switch Position

3) Remove the two screws that secure the switch support plate. Take the picture for the switch wiring.

No.HSH-19021-BS-240 Version: 4.0 4-29


IVD Global Technical Support Dept

Figure 4-25 The rocker switch wiring

4) Remove the rocker switch wiring.


5) Remove the switch from the bracket and replace it with a new one.
6) Wiring in order, note: there are corresponding signs on the wire and switch (1a, 1b, etc.), please
connect accordingly, and compare according to the picture, not connected.
7) Replace the bracket.
8) After the power-on test is normal (the switch will light),replacing the shell.

No.HSH-19021-BS-240 Version: 4.0 4-30


IVD Global Technical Support Dept

4.6 Wiring Diagram of Analyzer


1 2 3 4 5 6 7 8
RE APPR
ECN DESCRIPTION DRAW CHECHK
V DATE

D D

Power
Heater voltage
supply
selection board
board

C C

Reagent
Power drive
refrigeration Main Board
board
board

AD collection
board
B B

MINDRAY
APPROVALS DATE
DESIGN
CHECK
A TITLE Host (220V) cabling A
CHECK diagram
File: Bytes: CONFIDENTIAL DISCLOSURE: This set of drawing(s) and all it's intellectual property rights (including copyright) CHECK
subsisting herein are property of Shenzhen Mindray Bio-medical Electronics Co.,Ltd. No use, copies or reproductions
should be made of this drawing or any part(s) thereof for whatever purpose nor shall any information, data, DWG NO. BA10 REV 1.1
Date: Time:
calculations, or other contents contained in this drawing be disseminated without prior written permission of Shenzhen R&D
Mindray Bio-medical Electronics Co.,Ltd.
Software & Rev: Microsoft office Visio 2003 CHIEF ENG. SHEET 1 OF 9 SIZE A4
1 2 3 4 5 6 7

No.HSH-19021-BS-240 Version: 4.0 4-31


IVD Global Technical Support Dept

1 2 3 4 5 6 7 8

BA33-21-35191

Wash Solution Heater

protection switch on
Heater temperature

Heater temperature
Power socket and connector

Heater on reaction
protection switch

protection switch

protection switch
Deionized Water

reaction carousel

reaction carousel
Dionized water

Water inlet valve


Wash solution

under reaction

Reserved pump
Heater under
temperature

temperature

Reserved valve
E yell ow green

carousel

carousel
Housing ground

Heater
Main Power
Power jack Switch
M07-00061S---
D
Main control board N light blue D

Bump and valve wire of ACDB


Thermal protector switch power wire
Reactor top heater connector
009-006301-00

Reactor lower heater connector


ACDB communication wire L brown
J16 J5

12

BA10-21-78142
2
5
J3

10
5 bl ue

7
9
1 PV1CTRL

009-006303-00
1 2 3 4 5 6

BA10-21-78147
2 PV2CTRL 7 bl ack 5 1

BA10-21-78143
1

J14
3 PV3CTRL 9 yellow
6 2 J1
3

4 GND 4 red 1 brown L


1
5

7 3
5 220VCTRL1 1 bl ue
AC power supply cables from
7

6 220VCTRL2 2 bl ack 8 4 2 power switch to PFC board


and 24V board
34
33

7 GND 6 yellow
9 10 3 3 light blue N
8 220VCTRL3 3 red
009-006302-00
15 GND 8 yellow 11 12
AC input power wire (BA24)
20 GND 10 red

9 LAMPCTRL 11 yellow
12 GND 12 bl ack J4

Main control board


12V&5V power cord
J2 12GND 6 8 bl ue 11 1 Power supply board
4 1 GND 4 10 bl ack
12V 3 18 yellow
C 5 2 C
5V 1 20 red
6 3 12 2 1 1 12Vout NO
Drive board power cord J2 2
Power drive board BA10-20-78108
3 3 bl ue C
13 3
5V 3 19 red
J17
GND 7 9 bl ack + Analyzer Switch
2 6
12V 4 17 yellow
14 4
12GND 8 7 bl ue
1 5 2 bl ack GND
24V 1 15 orange

3 4 24V 2 14 orange 15 5 009-006299-00


GND 6 5 white Wire for Analyzer Switch
8 GND 5 4 white
7
16 6

Refrigeration board 12V


power patch cord Refrigeration board 12V power cord
17 7
J86
6 B12V 3 12 yellow
5 B12V 2 13 yellow 8 B
B 18
4 GND 6 3 bl ue
GND 5 2 bl ue
3
GND 4 6 white 19 9
2
C12V 1 16 orange
1

ISE power supply PCBA


ISE module

3 yellow 12V
1 24V 3
1
2 GND 2
2 1 bl ue GND
1

J1 J2

M32: lamp 20 10
1 bl ack

MINDRAY
2 bl ack
12VGND

11 red
1 red
LAMP12V A
A
Power Supply System Cabling
TITLE: Diagram
File: Bytes:

DWG NO. REV 1.1


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No.HSH-19021-BS-240 Version: 4.0 4-32


IVD Global Technical Support Dept

1 2 3 4 5 6 7 8

C31: Sample probe

PROBE
GND
1 black

2 red
D
D

Sam ple probe level


BA40-20-61774

BA30-20-06546
detection cable
Power supply board

1 black
J5

2 red
J4
BNC BNC BNC
Power drive

10
1

4
2

1
J66 1 2
board
Dionized water blank sensor

J20
Diluted wash solution blank

9
(Sample probe) level

High-concentration
waste sensor
sense board PCBA

11

18 17

28 27

31

38 37

42 41
22 21

48 47
14 13

16 15

20 19

24 23

26 25

30 29

34 33

36 35

40 39

44 43

46 45

50 49
1

9
sensor

2 black
5 yellow

4 red

1 black

8 yellow
3 blue

7 yellow
J65

6 red
8 yellow

11 red
9 bl ue

11 red
3 yellow

1 blue
4 red

2 black
12

32
2

4
Wire for main board level sensor

1 2 3 4

Main control board control signal


4 NC
5 NC

7 NC
2 NC
3 NC

6 NC

22

44
1

3
Cables from m ain control board to

12V&5V power cord


Main control board
009-006304-00

(BA24)

BA10-20-78115

40 DIR_ RESERVED_MOTOR3
power drive board

39 CLK_RESERVED_MOTOR3

cable
31 DIR_ RESERVED_MOTOR2
26 CLK_RESERVED_MOTOR1

30 CLK_RESERVED_MOTOR2
27 DIR_RESERVED_MOTOR1
11 VALVE_WASH_INJECT1
12 VALVE_WASH_INJECT2

38 DIR_ SYR_MOTOR2
36 DIR_ SYR_MOTOR1
37 CLK_SYR_MOTOR2
35 CLK_SYR_MOTOR1
16 PWR_PV_WASH1
17 PWR_PV_WASH2
10 PUMP_FILL_OUT

13 PREHEAT_REAG

25 CLK_ WASH_UP
24 DIR_WASH_UP

44 DIR_ FILL _UP


45 CLK_FILL_SYR
9 VAVLE_FILL_IN

43 CLK_FILL_UP
8 PUMP_FILL_IN

46 DIR_FILL_SYR
32 CLK_STIR_UP
33 DIR_STIR_UP
2 yellow LEVEL1

15 LAMP_CTRL

41 CLK_FILL_R
42 DIR_FILL_R
23 DIR_ STIR_R

5 220VCTRL1
6 220VCTRL2

8 220VCTRL3
22 CLK_STIR_R

28 CLK_FILL_T
29 DIR_FIIL_T
20 REAC-CLK
21 REAC-DIR
4 red LEVEL2

14 STIR_DC

3 PV3CTRL
2 PV2CTRL
1 PV1CTRL
18 RELAY_T
1 white GND
3 blue GND

6 12GND
4 GND
19 GND

34 GND

47 GND

4 GND
1 VCC
3 12V

7 GND
50 VCC
48 VCC
49 VCC

33 5V
34 5V
33 5V
1 GND

34 5V
4 NC
5 NC

7 NC
3 NC

6 NC
2 NC
NC
NC

NC

NC

22

44
NC

NC

3
J14 10 9 8 7 6 5 4 3 2 1 1 2 3 4

4
6

5
11

18 17

28 27

31

38 37

42 41
22 21

48 47
14 13

16 15

20 19

24 23

26 25

30 29

34 33

36 35

40 39

44 43

46 45

50 49
2 4 6
1

9
8 34
J1

J16
C C

12

32
1 3 5 33
2

4 7

1
3

2
J11
J2

Main board

J39

J5 J6 J7
13 12 11 10 9 8 7 6 5 4 3 2 1
J23 J22 J21
2 4 6 8 10 12 14 16 20 22 24 26 J18
18 28 30 32 34 2 4 6 8 10 12 14 16 18 20 22 24 26 28 30 32 34 2 4 6 8 2 4 6 8 2 4 6 8 10
J12 1 3 5 7 9 11 13 15 17 19 21 23 25 27 29 31 33 J13 13 15 19 23 25 25 24 23 22 21 20 19 18 17 16 15 14
1 3 5 7 9 11 17 21 27 29 31 33 1 3 5 7 1 3 5 7 1 3 5 7 9
3 2 1

3
2 bl ack
3 red

Reagent preheating sensor patch


009-006309-00 PC communications

3 PRTD_T1
009-006309-00

2 PRTD_REF
Cable 1 from main control board to position sensor Cable 2 from main control board to position sensor
BA10-20-78117 patch cord

SENSOR

SENSOR
Reaction carousel temperature

Wire for wash temperature sensor


SHIELD

SHIELD
1 red VCC 1 Patch cord from main control board to ISE
+ 4 white PHO_REAC_T 2 1 red VCC 1 module
BA10-20-78212

REF

REF
C13: reaction carousel C 2 bl ack C16:sample/reagent + 4 white PHO_FILL_T 2 009-000880-00 1 NC NC 1

009-006306-00
home position sensor - GND 3
carousel C 2 bl ack GND 3 BA10-20-78206
3 green GND 4 PC COM

sensor cable
- Connection wire for main

cord
E 3

009-006308-00
1 red VCC 5 home position sensor 3 green GND 4 RXD 2 1 Cable between m ain control board
+ E board and bar code module
4 white PHO_REAC_TC 6 1 red VCC 5 2 TXD 3 NC and AD board
Reaction Carousel Coder C C15:sample/reagent +
2 bl ack GND 7 4 white PHO_FILL_TC 6 2
Sensor - C 4 NC NC 4
3 green GND 8 carousel - 2 bl ack GND 7 RXD232
E 1 VCC Red 1
1 red VCC 9 coder sensor 3 green GND 8 ISE module 5 GND 5 3

Black1
+ E

Red 2
4 whitePHO_FILTER_MOTOR 10 1 red VCC 9 TXD232

10 DCP_CLK
+

Black
C

11 DCP_DIN
2 RXD Green 3

18 AD_BUSY

Red
C40: filter whe el PHO_WASH_UP 6 NC NC 6

19 AD_CLK
2 bl ack GND 11 4 white 10

9 DCP_EN
4

6 AD_DIN
- C

20 AD_RC

22 CH_A2

23 CH_A1

24 CH_A0
home position sensor B

21 CH_A3
17 15GND
3 TXD Blue 2

4 15GND
B E 3 green GND 12 Standby - 2 bl ack GND 11 8 RTS 7 NC

14 +15V

12 GND
25 GND
13 GND
1 +15V

5 GND
15 -15V
1 red VCC

16 VCC

7 GND

8 GND
2 -15V
13 3 green 12

3 VCC
+ E GND 5 GND Black 4 5
C18: sample vertical 4 white PHO_FILL_UP 14 1 red VCC 13 7 CTS 8
C + GND
moveme nt motor 4 white PHO_WASH_SUCKSYR 14 6 RTS White 10
- 2 bl ack GND 15

Preheating Sensor
C 9 NC 6

3
temperature sensor
Standby 2 bl ack GND 15
Reagent bar code reader

home position sensor 3 green GND 16

M29: Reagent
E - 7 CTS Yel low 6 NC carousel
1 red VCC 17 E 3 green GND 16
C17: sample probe rotation + 4 white PHO_FILL_R 7 C29: reaction
18 1 red VCC 17 8 TRIG Orange 9
motor C + ISP_RESET
- 2 bl ack GND 19 Cuvette wash station 4 white PHO_WASH_EJECT 18
home position sensor C 9 NC NC 5 8 14 15 16 17 18 19 20 21 22 23 24 25

Deionized water temperature sensor cable


E 3 green GND 20 anti-collision - 2 bl ack GND P1

Wash solution tem perature sensor cable


1 red VCC 21 3 green GND 20 NC 7 NC
+ E 4 NC
C19: sample syringe m otor C 4 white PHO_FILL_SYR 22 1 red VCC 21 9
+ NC 8
4 white PHO_RESERVED1 22 NC 1 2 3 4 5 6 7 8 9 10 11 12 13
home position sensor - 2 bl ack GND 23
Wash Station Hom e Position C
2 bl ack GND 23 10
E 3 green GND 24 - NC 11
VCC 25 E 3 green GND 24 NC
+ NC 12
C28: mixer vertical 4 white PHO_STIR_UP 26 + VCC 25 AD collection board BA10-30-77759
C SHIELD
- 2 bl ack 27 4 white PHO_RESERVED2 26
syring

GND
water
positi

NC 13
home

Dioni

movement motor C
zed
on

E 3 green 28 2 bl ack GND 27


e

home position sensor GND -


1 red VCC 29 3 green GND 28 NC 14
+ E
C27: mixer rotation motor 4 white PHO_STIR_R 30 1 red VCC 29
C + NC 15
4 white PHO_RESERVED3 30
home position sensor - 2 bl ack GND 31 Wash Solution Syringe C
2 bl ack GND 31
E 3 green GND 32 Home Position -
33 NC E 3 green GND 32
34 NC 33 NC
34 NC

MINDRAY
A A

TITLE: Main board cabling diagram

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DWG NO. BA10 REV 1.1
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SHEET 3 OF 9 SIZE A2
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No.HSH-19021-BS-240 Version: 4.0 4-33


IVD Global Technical Support Dept

1 2 3 4 5 6 7 8

1
1

2
2

1
1

2
2

1
M19: Mixer DC motor

2
phase 2/3 aspiration pump
phase 1 aspiration pump
preheating block

P04: phase 4 aspiration


SV05: Dionized water

SV03: Sample Probe

SV02: interior valve


SV04: Mixer Exterior

P01: interior pump


SV06: Wash Solution
M29: Reagent

Exterior Valve
Dispense Valve

dispense valve
Power supply board

Valve

P02:

pump
P03:
J4

D D
- +

Power drive board power cord


2 white

1 white
4 orange

3 orange
1 of drive board

2 bl ack
2

1 bl ue

4 red
1
1

3 yellow
2

Wire 2 of drive board


Patch cord from drive board
Patch cord from drive board
to three-probe board mixer

to three-probe board

009-006311-00

009-006310-00
preheater
motor

pump valve
pump valve

Wire

24V 1

24V 2

12V 4
12GND 8

VCC 3
GND 5

GND 6

GND 7
1 black
yellow
5 blue
6 red

2 red
4 red

3
2 red
1 blue

1 blue

2 red
Syringe motor cabl e 1 2 1 2 7 5 3 1 7 5 3 1 1 2 3 4

6 white 4 white 8 6 4 2 8 6 4 2 J17 8


6 5 6 7

1
J22 J24
BA10-20-78115
4 yellow 3 yellow J9 J6
4 Cables from main control 1 2
2

DGND 12V
1 2 board to power board

GND 24V

GND 24V
Bla
ck

GND 5V
J8
3 3 blue 2 blue 3 3 4
R

d
2 e

1 GND 1GND
3 4
1

1 1 red 1 red 2 NC 2 NC 5 6
3 NC 3 NC
4

Reagent probe vertical 5 6 4 NC 4 NC 7 8


movement motor cable 5 NC 5 NC
C 7 8 6 NC 6 NC C
6 white 4 white 7 NC 7 NC 9 4
1

6
9 4 8 PUMP_FILL_IN 8
4 yellow 3 yellow 9 VAVLE_FILL_IN 9 11 12
4
2

10 PUMP_FILL_OUT 10
J13

11 12 11 VALVE_WASH_INJECT1 11 13 14
3 3 blue 2 blue 12 VALVE_WASH_INJECT2 12
3

13 14 13 PREHEAT_REAG 13
14 STIR_DC 14 15 16
1 red 1 red 15 LAMP_CTRL 15
1 15 16
4

16 CLK_WASH_SYR 37 17 18
17 DIR_WASH_SYR 38
Filter wheel motor 17 18 18 RELAY_T 18 19 20
patch cord 19 GND 19
19 20 20 REAC-CLK 20 J40
6 white 00 4 white 21 22
1

Main control board


6 Power drive board 21 REAC-DIR 21
21 22 22 CLK_STIR_R 22
5 yellow 3 yellow 23 DIR_ STIR_R 23 23 24
4
2

J20 23 24 24 CLK_RESERVED_MOTOR1 24
25 DIR_RESERVED_MOTOR1 25 25 26
J7

3 2 blue 2 blue 26 CLK_WASH_UP 26


25 26
3

27 DIR_WASH_UP 27 27 28
1 red 28 CLK_FILL_T 28
1 1 red 27 28 29 DIR_FIIL_T 29
4

30 CLK_RESERVED_MOTOR2 30 29 30
Reagent probe rotation motor 29 30 31 DIR_ RESERVED_MOTOR2 31
cable 32 CLK_STIR_UP 32 31 32
6 white 4 white 31 32 33 DIR_STIR_UP 33
1

6 34 GND 34 33 34
35 CLK_SYR_MOTOR1 35
4 yellow 3 yellow 33 34 36 DIR_ SYR_MOTOR1 36
4 35 36
2

37 CLK_RESERVED_MOTO4 16
J5

3 blue 35 36 38 DIR_RESERVED_MOTO4 17
3 2 blue 39 CLK_RESERVED_MOTOR3 39 37 38
3

37 38 40 DIR_ RESERVED_MOTOR3 40
1 1 red 1 red 41 CLK_FILL_R 41 39 40 B
B 42 DIR_FILL_R 42
4

39 40 43 CLK_FILL_UP 43
44 DIR_ FILL _UP 44 41 42
Exterior Wash Syringe 41 42 45 CLK_FILL_SYR 45
46 DIR_FILL_SYR 46 43 44
6 white 4 white
1

6 43 44 47 GND 47
48 VCC 48 45 46
4 yellow 3 yellow 49 VCC 49
45 46
2

4 50 VCC
J11

47 48
3 3 blue 2 blue 47 48
3

49 50
1 red 49 50
1 1 red
4

J12 J15 J4 J10 J16 J14

4 3 2 1 4 3 2 1 4 3 2 1 4 3 2 1 4 3 2 1 4 3 2 1
Reagent carousel motor cable

009-006834-00

3 yellow
3 yellow

4 white
3 yellow

4 white

3 yellow
4 white
4 white

3 yellow

4 white
3 yellow

2 blue

2 blue
4 white

1 red
2 blue

1 red
2 blue

2 blue

1 red
1 red

movement motor cable


2 blue
1 red
Wash solution syringe

BS-240motor cable
1 red

Reaction carousel
motor patch cord

Mixer rotation

Mixer vertical
motor cable

motor cable
station motor
Cuvette wash

MINDRAY
4 yellow
6 white
4 yellow

4 yellow

4 yellow

4 yellow
3 blue
6 white

6 white

6 white
4 yellow
1 red

6 white

6 white
3 blue

3 blue

3 blue
1 red

1 red

1 red
3 blue

1 red

3 blue

1 red
A A
6

1
3
6

3
6

1
TITLE:

1
Power drive board connection diagram

File: Bytes:
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1 2 3 4 5 6 7 8

D D

Preamplifier board
BA10-30-77760

AGND_SHILED
340nm

AGND
AGND
+15V

-15V
6
1
2
3
4
5
preamplifier board
collection board to
Cables from AD
BA10-20-78126
C C

2 4 6
J1
1 3 5

AD collection board

14 15 16 17 18 19 20 21 22 23 24 25
P1
1 2 4 5 6 7 8 9 10 11 12 13

3
B B

BA10-20-78206
Cable between main board and AD
board

10 DCP_CLK
18 AD_BUSY

11 DCP_DIN
19 AD_CLK

9 DCP_EN
6 AD_DIN

20 AD_RC

22 CH_A2

23 CH_A1

24 CH_A0
17 15GND

21 CH_A3
4 15GND
14 +15V

12 GND
25 GND
13 GND
1 +15V

5 GND
15 -15V

16 VCC

7 GND

8 GND
2 -15V

3 VCC

14 15 16 17 18 19 20 21 22 23 24 25
J39
1 2 3 4 5 6 7 8 9 10 11 12 13

A
Main Board 051-002414-00 MINDRAY A
TITLE: AD collection board cabling diagram
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1 2 3 4 5 6 7 8

M42-M43: refrigeration 92 fan


C35:试剂制冷温度传感器

D Demisting
Demisting temperature
D

GND
GND

GND

12V
12V

12V
GND
protection

temperature sensor patch cord


heater

12V
sw itch

Rear panel fan patch cord

refrigeration/radiati

Demisting heater cable


Reagent refrigeration

BA10-20-78203
1 GND BA10-20-78209

ng fan cable

009-006314-00
Reagent

reserved
1 GND

4 +5V
1 GND

1 GND
2 12V

2 12V

2 12V

3
J88 1 2 J81 1 2 J79 1 2 J80 1 2 J78 1 2 J82 1 2 J83 1 2 J84 1 2 J85 1 2 J15 1 2 3 4
J89
J86
PELTIER cable 1 6 3
C 1 12V yellow C
1

Power supply board


12V 12VFANGNDFAN

11 12
1 4

1
5 2
M30-M31:PELTIER

yellow
2

2
GND 2 6

J4
COOLER Reagent 5 4
12V GND 2 blie
PELTIER cable 2 1 refrigeration 3 12
12V blue
12V board 3 6

19
9
1 12V GND 2 13
white
2

10
20
GND 16
COOLER 1
009-006313-00 2 orange
Reagent refrigeration sheet
cable

J74 1 2 3 J73 1 2 3 J72 1 2 3 J71 1 2 3 J75 1 2 J76 1 2 J77 1 2 J87 1 2 3

GND

FAN
2 12V

5V
1 GND
Temperature control chamber fan

1 GND
Cable between reagent refrigeration

1 GND

2 12V
2 12V
FAN4
12VFAN

FAN3
GNDFAN

GNDFAN

12VFAN

主控板至制冷板风扇
Lamp fan patch cord

board and PCB fan


B

009-006315-00
B

反馈转接线
patch cord
009-006316-00

12V
12V
GND

GND
GND

12V

12V
GND

GND
GND

GND
12V
12V

12V
FAN

FAN

J10
Power drive Temperature control chamber
Lamp box radiating fan fan cable
Main board
board radiating BA30-30-77755
patch cord fan

A
MINDRAY A
TITLE: Reagent refrigeration board cabling diagram
File: Bytes:
DWG NO. BA24 REV 1.1
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No.HSH-19021-BS-240 Version: 4.0 4-36


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5 Fluidic system
5.1 Overview
The major function of the fluidic system is:
• To provide deionized water for washing interior/exterior of probes and mixers via the water supply unit.
• To provide deionized water and wash solution for washing cuvettes via the cuvette wash station.
• To provide the whole unit with deionized water via the deionized water tank and to discharge waste liquid
via the drainage module.
This chapter describes the working principles and repairing methods of the BS-240's hydropneumatic system.
5.2 Fluidic Diagram
See A.7 Fluidic Diagram.
5.3 Principles of Hydropneumatic System
The hydropneumatic system is composed of the probe wash module, cuvette wash station, and water
supply/drainage module. See the figures below:
Hydropneumatic
System

Probe and Mixer Cuvette Wash Inlet/outlet


Wash Module Module module
Reaction cuvette
Reaction cuvette

Waste drainage
Mixer cleaning
Probe Wash

dispensing

aspiration

Inlet

Figure 5-1 Principles of Hydropneumatic System

5.3.1 Probe wash module


The probe/mixer wash module consists of: 1 probe, 1 mixer, 2 syringes, and 1 diaphragm pump. The sample
syringe SY03 is 500μl. The probe exterior is washed by a 10ml syringe SY01. The probe interior is washed by
the diaphragm pump P01.
This module is used for fixed-quantity sampling and two-probe cleaning.
• Fixed-quantity sampling is realized through cooperation of the syringes, the sampling solenoid valve SV02
and the probe NS with the aim of delivering fixed-quantity reagent and sample.
• The probe interior is washed by a diaphragm pump.
• The probe and the mixer exterior are both washed by a 10ml syringe. The start and end of the wash action
are controlled by the exterior wash solenoid valve. A deionized water T-valve controls the dispensing of the
syringe. The volume limiter of the syringe controls the volume of the syringe.
The schematic diagram of the probe wash module is shown below.

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SV02 T10
D06 D07
6
T103 T104 T10
7 NS MIX
SY03
T105

D05
SV03 T222

T221 D32 D33 D34

SV04

T211 D22 D23 T212 D24


D31

D21 W01

P01

T204
D04

D16

ZZ11
T203

D11 T202 D12


T10
SV01
2
D15 T201 D14 D13

D03

SY0
1

Panel
D02 T101
FL01

Figure 5-2 Schematic diagram of probe wash module

5.3.2 Cuvette Wash Module


The cuvette wash unit is divided into dispense module and aspirate module, which cooperate with each other
to clean the reaction cuvettes for 4 phases, making repeated use of cuvettes possible.
The dispense module uses a cuvette wash syringe SY02 (2.5ml) to provide diluted wash solution (alkaline) in
phase 1. In phases 2 to 3, the cuvette wash syringe SY01 (10ml) provides deionized water. In phase 4, no liquid
is injected.
The diluted wash solution provided for phase 1 is obtained by diluting the concentrated wash solution with
deionized water at the ratio of 1:10. Samples are diluted manually. The dispense action is controlled by the
exterior wash solenoid valve and adjusted by the syringe volume limiter. The dispensed volume is the same in
phase 1 to phase 3.
A diaphragm pump is used to aspirate waste, so as to discharge waste fluid and wipe the cuvettes after cleaning.
High-concentration waste is generated in phase 1, and low-concentration waste during phases 2-4. Wipe blocks
are provided to absorb the remaining wash solution inside cuvettes during phase 4.
When aspirating fluid, the phase-4 wash probe assembly lowers into reaction cuvettes, and then waste pump
is opened so that the waste is aspirated into the external waste container.
The schematic diagram of the module is shown below.

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ZQ01
ZQ11
ZQ21
ZQ31

T613

ZQ12
SI1 SI2 SI3 SI4
T611 T612 T702

ZQ32 ZQ13 ZQ02

P04 P03 P02


T312
ZZ33 ZZ34
ZZ24
SV05 ZZ23 T305
SV07 ZZ08
ZZ32 ZQ33 ZQ14 ZQ03
ZZ22
T311
T304
ZZ21 T404 T405
ZZ31
1 2 3
T303
ZZ05
ZZ07 T602
SV06
ZZ12
ZZ04

CAN02 ZZ06
ZQ15

T203 T301 T302

T202 D12
SY02
SV01 T403
T402
D15 T201 D14 D13 CAN01

W03

SY01
ZZ03

Figure 5-3 Schematic diagram of cuvette wash unit

5.3.3 Inlet/outlet module


The water supply/drainage module includes the water supply part and waste drainage part.
Inlet deionized water is provided from the outside of the instrument, and is conveyed by the interior wash pump
and the deionized water syringe to other modules. Inlet diluted wash solution is provided by an external diluted
wash solution tank outside the instrument, and is conveyed by the wash solution syringe to phase 1 of wash,
as detailed below:
• detecting deficient fluid level of deionized water, and alarming.
• detecting deficient fluid level of diluted wash solution, and alarming.
• filtering deionized water and diluted wash solution, and performing filtering before the inlet deionized water
and the inlet diluted wash solution outside the whole unit are distributed to each unit.
The drainage module allows discharging high-/low-concentration waste separately. The high-concentration
waste is discharged by the waste pump to the external high-concentration waste tank; the low-concentration
waste is discharged by the waste pump of the low-concentration waste tank outside the instrument (and may
be discharged via sewers directly). The high-concentration waste tank is capable of detecting the fluid level.
The high-concentration waste is produced during cuvette cleaning in phase 1.
Low-concentration waste comes from the following sources:
• Cleaning interior/exterior of probe
• Cleaning exterior of sample mixer and reagent mixer
• Auto cuvette cleaning in phase 2-4
• Condensate water of the reagent carousels
• Overflowed fluid of the reaction carousel
The first three are the major sources and account for over 99% of low-concentration waste.
The fluidic diagram of the module is shown below.

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Reagent Reaction
NS MIX Carouse Carouse

T602

W21 W31
W01 W11

ZQ15

T521 T511
W02 W22

T502

W03

ZZ03

D02 T101 ZZ02 T401 T501 T601 T701


FL01 W04 ZQ16 ZQ04
FL02
D01 ZZ01 FS03
FS01 FS02
V01 V02 V03(选配) V04

Figure 5-4 Fluidic diagram of water supply/drainage module

5.3.4 Interfaces for fluid connection


The Hydropneumatic system of BS-240 contains 8 external interfaces, as shown in the figure below.
• fluidic outlets: used for discharging high-concentration waste, low-concentration waste 1, and low-
concentration waste 2.
• fluidic inlets: used for supplying deionized water and diluted wash solution.
• control cable connectors: used for connecting the high-concentration waste level sensor, deionized water
level sensor, and diluted wash solution level sensor.

Interfaces for fluid connection

No. Name 8
1 dionized water
4
2 diluted wash solution
3 high concentration waste
4 low concentration waste 1
5 dionized water sensor
6 diluted wash solution sensor 7 3
7 high concentration waste sensor
8 low-concentration waste 2

6 2
Water Waste

Legend
Wash
Sensor
solution
5 1

Figure 5-5 External fluidic interfaces of the instrument

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5.4 Introduction of Fluidic Actions


5.4.1 Fluidic Initialization
The specific procedure is described below:
• Power off all the pump and valve and they return to the home position.
• The waste pump discharges waste.
• The floater status of the deionized water tank, diluted wash solution tank, and high concentration waste
tank are checked. If related alarm is removed, the system moves to the next step. If not, the system
gives out the alarm and the fluidic initialization fails.
• Cleaning Probes/Mixers Exterior is performed.
• The probe and mixer exterior wash syringe is reset; and phase1 wash syringe is reset.
NOTE:
The fluidic initialization is one part of the startup , system recovery and system wakeup procedure.
5.4.2 Priming Wash Station
• The specific procedure is described below:
• Open wash waste pump P02~P04.
• Let the wash station move down to the cuvette bottom.
• Prime the wash station cyclically 3 times.
• After completion of priming, close the wash solenoid valve, reset the wash syringe, let the wash station
move to the home position, and close the waste pump P02~P04.
5.5 Removing and Reinstalling Hydropneumatic Components
This section describes removing and installation methods of the Hydropneumatic components, and provides
schematic diagrams and pictures of components for service engineers to refer.
5.5.1 Overview
When an alarm is displayed on the operating software of BS-240, service engineers can analyze the instrument
status and finally locate the failure source, and if necessary, replace the failed part or component. Generally,
service engineers are not recommended to remove the electric devices, such as pumps, solenoid valves,
syringes, etc. Only when both hardware and software are confirmed normal but the Hydropneumatic alarm still
remains are service engineers suggested to remove the relevant device and then analyze or replace it.
Prior to removing Hydropneumatic components, make sure that all pumps and solenoid valves of the
Hydropneumatic system have been turned off, and both the analyzer power switch and main power switch have
been placed to the OFF position.
Table 5-1 Necessary tools for removing/installing Hydropneumatic components

Name Quantity
Cross screwdriver 1
Hexagon screwdriver 1
Flathead screwdriver 1
Cable tie Several
Diagonal pliers 1
Tube cutter 1

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5.5.2 Probe and mixer wash module


Sample probe 500μl syringe Mixer

Probe wash well

Mixer wash well

Figure 5-6 Assembly drawing of whole unit -- Probe and mixer wash module-front view

No.HSH-19021-BS-240 Version: 4.0 5-6


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Probes exterior
Deionized water inlet T-valve Mixer Exterior Wash valve
wash valve

Deionized Water Syringe

Probe interior wash valve

Probes Interior wash pump

Figure 5-7 Assembly drawing of whole unit -- Probe wash module-rear view

Table 5-2 List of materials

No. FRU Part Name Remarks


1 801-BA23- Syringe 500ul(ZDV) FRU
00025-00
2 082-002435-00 Two-position two-way valve FRU/probe interior
wash valve
3 BA30-21-15311 KNF diaphragm pump assembly FRU/probe interior
wash pump
4 115-011901-00 10 ml screw rod driving syringe FRU/deionized water
assembly (FRU) Syringe
5 082-002373- Three-way valve of LVMK/WTB-3R-N4E FRU/ deionized water
00/801-BA38- three-way EM valve wire inlet valve
00011-00
6 082-002273- EM valve LVMK21-6J wire/wire for FRU/probe exterior
00/082-002720- solenoid valve wash valve
00
7 M6G-020049--- Rubber FRU
hose .PTFEID1.5mmXOD2.5mm×100M
8 0040-10-32301 Rubber hose .PTFE,0.040"IDX0.066"OD FRU
9 082-002374-00 Rubber hose .3.2*6.4mm TPU polyether FRU
10 801-BA80- Wash well shell FRU
00009-00
11 801-BA40- Wash well (mould MR61463) FRU
00221-00

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Removing/Reinstalling Wash Syringe Assembly


When to do
Analyze or replace the wash syringe when it has abnormal sound, worse precision, leaking, or other failures.
How to do
1) Switch off the power supply of the whole unit.
2) Open the rear panel.
3) Remove the 4 M4×8 cross pan head screws used to fix the syringe shield and remove the shield.
4) Disconnect the syringe motor cable and sensor cable.
5) Remove the tube from the barbed connector of the syringe.
6) Remove the four M3×12 hexagon socket head cap screws with spring washer and remove the syringe.
Installation Procedure
1) Install the 4 M3×12 hexagon socket head cap screws with spring washer and do not miss the shock
pad .
2) Cut off a little from the tube's end and insert the tube to the barbed connector of the syringe. If a strap
has been applied, restore it.
3) Connect the syringe motor cable and sensor cable.
4) Use 4 M4×8 cross pan head screws to fix the syringe shield on the right side plate.
5) Power on the analyzer, log on the software with service user account, and then select Utility ->
Maintenance -> Maintenance -> Engineer -> Clear. If the interior wash syringe is replaced, select
the "Replace Interior Wash Syringe" item. If the cuvette wash syringe is replaced, select the "Replace
Cuvette Wash Syringe" item. Click OK to zero the use count of the relevant syringe.

Connector of wash
Connector of cleaning
solution syringe tube
fluid syringe tube

Screw

Wash solution syringe

Cleaning fluid syringe

Figure 5-8 Replacing wash syringe.

Removing/Installing Solenoid Valves


When to do
When a solenoid valve cannot be turned on or has leaks, it needs to be removed and then analyzed or replaced.
Removing Steps
1) Switch off the power supply of the whole unit.
2) Open the rear panel.
3) Disconnect the solenoid valve’s power cord connector.
4) Mark the installation direction of the valve and the connection mode of the inlet and outlet tubes to

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prevent them from being confused.


5) Remove the tubes and apply strap on their openings to prevent liquid spraying.
6) Loosen the screws on the solenoid valve and then remove the solenoid valve.
Installation Procedure
1) Check the installation direction according to the marks, connect the inlet and outlet tubes, and then
tighten the tube clamps or straps.
2) Tighten the retaining screws to fix the solenoid valve.
3) Make sure that the power cord is connected to the correct positive and negative ends.
Verification steps
Refer to 7.9 Hydropneumatic Unit.

Figure 5-9 Details of wash solenoid valve assembly

Note
• The tubes must be connected in correct order otherwise the analyzer may not work normally. Do not
confuse the inlet tube with the outlet tube.
• Take caution not to spill the liquid onto other parts.
• The positive and negative of the cable of the solenoid valve must be correctly connected.
• After replacement or reparation, conduct fluidic prime in case the air bubbles in the tube affect the
performance of the analyzer.

Replacing interior wash pump


When to do
The pump does not work, that is, there is no flow or pressure.
The pump flow and pressure is low.
The pump has leaks.
Noise is produced when the pump is working.
Removing Steps
1) Switch off the power supply of the whole unit.
2) Open the rear panel.
3) Disconnect the pump’s power cord connector.
4) Mark the connection mode of the inlet and outlet tubes and prevent them from being confused.

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5) Remove the tubes and apply straps on their openings or use a tank to hold water, so as to prevent
liquid from entering the instrument.
6) Loosen the screws fixing the pump and then remove the pump.
Installation Procedure
1) Connect the inlet and outlet tubes according to the marks and then tighten the tube clamps.
2) Tighten the retaining screws to fix the pump.
3) Make sure that the power cord is connected correctly.
Verification steps
Refer to 7.9 Hydropneumatic Unit.

Note
• The tubes must be connected in correct order otherwise the analyzer may not work normally. Take caution
not to spill the liquid onto other parts.
• Make sure that the power cord of the pump is connected to the correct positive and negative ends. After
replacement or reparation, conduct fluidic prime in case the air bubbles in the tube affect the performance
of the analyzer.

bracket

screw

Phase 4 waste
pump
Phase 2/3 waste
pump
Phase 1 waste
pump
Probe interior
wash/mixer wash
pump

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Figure 5-10 Structure of pump

5.5.3 Cuvette Wash Module


See Figure 5-6 Assembly drawing of whole unit -- Probe and mixer wash module-front view and Figure 5-7
Assembly drawing of whole unit -- Probe wash module-rear view.
Table 5-3 List of materials

No. FRU FRU name Remarks


1 801-BA34- Rotational diaphragm pump Phase 1-3 Wash Waste
00001-00/ 082- assembly/diaphragm pump of Pump/ Phase 4 Wash
002426-00 P02&P03 Waste Pump
2 082-002273- Phase 2-3 cuvette wash
EM valve LVMK21-6J wire/wire for solenoid valve
00/082-002720-
solenoid valve
00
3 082-002373- Three-way valve of LVMK/WTB-3R- Phase 1 cuvette wash
00/801-BA38- N4E three-way EM valve wire solenoid valve
00011-00
4 115-011901-00 10 ml screw rod driving syringe Cuvette wash syringe
assembly assembly
5 115-020528-00 Preheating assembly FRU
6 043-000422-00 Filter FRU
7 115-036353-00 Wash probe assembly FRU
8 041-005591-00 Wipe block FRU
9 BA38-30-88154 Wash phase probe assembly FRU
10 BA40-30-61934 Wipe phase probe assembly FRU

Removing/Reinstalling Wash Syringe Assembly


See Figure 5-8 Replacing wash syringe.
When to do
Analyze or replace the wash syringe when it has abnormal sound, worse precision, leaking, or other failures.
Removing Steps
1) Switch off the power supply of the whole unit.
2) Open the rear panel.
3) Disconnect the syringe motor cable and sensor cable.
4) Remove the tube from the barbed connector of the syringe. Take caution not to spill the liquid onto
other parts.
5) Remove the four M3*12 hexagon socket cap head screws with spring washer and remove the syringe.
Installation Procedure
1) Install the four M3*12 hexagon socket cap head screws with spring washer and do not miss the shock

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pad.
2) Insert the tube deeply into the connector of the syringe and use the cable tie to fix the tube on the joint.
Take caution not to spill the liquid onto other parts.
3) Connect the syringe motor cable and sensor cable.
4) Power on the analyzer, log on the software with service user account, and then select Utility ->
Maintenance -> Maintenance -> Engineer -> Clear. If the cuvette wash syringe is replaced, select the
"Replace Cuvette Wash Syringe" item. Click OK to zero the use count of the relevant syringe.
Verification steps
Refer to7.9 Hydropneumatic Unit.

Replacing Waste Pump


See Figure 5-10 Structure of pump.
When to do
When waste pump fails such as no liquid or insufficient liquid aspirated, leakage or abnormal noise.
Removing Steps
1) Switch off the power supply of the whole unit.
2) Open the rear panel.
3) Disconnect the pump’s power cord connector.
4) Mark the connection mode of the inlet and outlet tubes and prevent them from being confused.
5) Remove the tubes and apply straps on their openings or place a container under it to prevent liquid
from entering the instrument.
6) Remove the tubes and apply straps on their openings or place a container under it to prevent liquid
from entering the instrument.
Installation Procedure
1) Connect the tubes according to the marks and then tighten the tube clamps or cable tie. For the
severely twisted tube, cut about 5mm off its end.
2) Install the pump on its bracket and fix the bracket.
3) Make sure that the power cord is connected correctly.
Verification steps
Refer to 7.9 Hydropneumatic Unit.

Note
• The tubes must be connected in correct order otherwise the analyzer may not work normally. Take caution
not to spill the liquid onto other parts.
• Make sure that the power cord of the pump is connected to the correct positive and negative ends.
• After replacement or reparation, conduct fluidic prime in case the air bubbles in the tube affect the
performance of the analyzer.

Removing/Reinstalling Cuvette Wash Preheating Assembly


When to do
▪ The heater is damaged.
▪ The temperature sensor is damaged.
▪ The temperature protection switch is damaged.
▪ The canister has leaks.
▪ The connectors are leaking.
Removing Steps
1) Switch off the power supply of the whole unit.
2) Open the rear panel.
3) Mark the connection modes of the following parts: inlet/outlet tubes, heaters, sensors and temperature
protection switches for wash solution and deionized water.
4) Disconnect the connectors of the heater, sensor and protection switch.
5) Loosen the two hexagon socket head screws fixing the cuvette wash preheating assembly.
6) Apply cable tie on the tube openings to prevent liquid from flowing out.
7) Disconnect the inlet and outlet tubes. Take caution not to spill the liquid onto other parts. Because
the tube connection is very tight, exercise caution not to damage the connector.
Installation Procedure

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1) Prepare a new wash preheating assembly.


2) Connect the connectors according to the marks.
3) Connect the tubes according to the marks and then tighten the tube clamps or cable tie. For the
severely twisted tube, cut about 5mm off its end.
4) Use two M4*8 hexagon socket head screws to fix the preheating assembly.
5) Check if the configurations are complete.
6) Restore the instrument.
7) Connect the power supply and perform fluidic prime before starting test.
Verification steps
Refer to 7.9 Hydropneumatic Unit.

Note
• Cleaning fluid temperature Sensor and Wash solution temperature Sensor: Negative temperature
coefficient, the resistance decreases with increasing temperature.
temperature Resistance
2°C About 11KΩ
25°C About 5KΩ
• Take caution not to spill the liquid onto other parts.
• Connect the connectors of the tubes and cables correctly otherwise the components or the instrument may
be damaged.
• After the tubes are connected, make sure the tubes are tightly connected to the deep of the connector.
• After the washing preheater is replaced, prime it first otherwise the instrument may not work normally.

Wash solution Wash solution Wash solution heater


Wash solution inlet
outlet Heating sensor
Heating
temperature
switch

Heating
temperature
switch Of
cleaning fluid

Cleaning fluid Cleaning fluid


Cleaning fluid heater
inlet screw outlet
Heating sensor

Figure 5-11 Structure of cuvette wash preheating assembly

Removing/Reinstalling Filter
When to do
▪ The filter used for more than 1 year.
▪ The filter damage.
Removing Steps
1) There are one filter respectively on the cleaning fluid and wash solution inlet tubes. The filters are
installed on the tubes between the fluidic interfaces and the DI water tank and wash solution tank.
2) Disconnect the tubes at the two ends of the filter and remove the filter.
Installation Procedure
1) Install the new filter and fix it with clamp or cable tie. For the severely twisted tube, cut about 5mm off
its end. Make sure the tubes are tightly connected to the deep of the connector.

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2) After the filter is replaced, prime it first otherwise the instrument may not work normally.
Verification steps
Refer to 7.9 Hydropneumatic Unit.

Figure 5-12 Assembly drawing of whole unit -- Acetabular filter

Removing/Reinstalling Wash Probes Assembly


When to do
When fluid overflows the cuvettes or the dispensed cleaning fluid is less than the normal volume, probably a
wash probe is clogged and needs to be removed and unclogged.
Removing Steps
1) Manually loosen the retaining screws on the wash station. See Figure 3-42 Wash probe.
2) Remove the wash station with tubes not connected, put the wash probes in a container.
3) Inject cleaning fluid and wash solution to find the place where the probe is clogged.
4) Use a needle to unclog the probe.
Installation Procedure
1) Align the locating holes on the wash station with the stop studs on the bracket, and then slightly tighten
the retaining screws.
2) Lower the wash probes assembly, use an alignment tool or visually check the phase 4 wipe block in
the cuvette. The wipe block must not contact the interior of the cuvette.
3) After finishing the second step, completely tighten the retaining screws on the wash station.
Verification steps
Refer to 7.9 Hydropneumatic Unit.

Note
• Operate carefully to prevent liquid from dropping into the reaction carousel and cuvettes.

5.5.4 External Modules


Cap assembly of External high-concentration waste tank
The cap assembly of external high-concentration waste tank contains one FRU.
Table 5-4 High-concentration waste tank cap assembly FRU

No FRU Part Name Remarks


1 115-037348-00 waste cap module

Cap assembly of the external diluted wash solution tank


The cap assembly of external diluted wash solution tank contains one FRU.
Table 5-5 Cap assembly of the diluted wash solution tank FRU

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No FRU Part Name Remarks


1 115-037347-00 washing barrel cap module

Cap assembly of DI water tank


The cap assembly of external DI water tank contains one FRU.
Table 5-6 Cap assembly of DI water tank FRU

No FRU Part Name Remarks


1 115-037347-00 washing barrel cap module

10L water tank


The high-concentration waste tank and diluted wash solution tank contains one FRU.
Table 5-7 10L water tank FRU

No FRU Part Name Remarks


1 043-002159-00 10L water tank 10L

The DI water tank and low-concentration waste tank contains one FRU.
Table 5-8 15L water tank FRU

No FRU Part Name Remarks


1 043-000491-00 15L water tank 15L

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6 Software
6.1 Software Installation
6.1.1 Introduction of Installation Package
The installation package of the operating software contains three folders: Setup, SetupGuide, and Thirdparty.

Figure 6-1 Folders in operating software installation package

Setup folder: includes the operating software installation file setup.exe and the KillBsLog tool that can end the
Bslog service.

Figure 6-2 Setup folder

Bslog: a service run automatically when the operating software is started, and used to record the logs of the
software. When started, the software checks if the service is started, and if it is not started, the software gives
an alarm indicating startup failure. When logging on the software, you are allowed to end this process, and this
action will not be recorded in the logs.
SetupGuide folder: includes the software installation and upgrading guide.
Thirdparty folder: includes dotnetfx and SQLExp installation packages. The former contains the installation
program of Microsoft .net Framework and is the running environment assembly of SQL; while the latter is
database software.
6.1.2 Analyzer Software Version Information
The software version can be viewed from the software package. Open the Setup folder in the software package,
right-click the ModVersion.dll file to select Properties, and view the software version in Version of the Details
tab page.

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Figure 6-3 View Software Version

6.1.3 Folder Structure


The default installation path of the operating software is: D:\Mindray\BS240
After installation, the folder structure is like the following:

Figure 6-4 BS-240 folder

The OperationSoft folder is relatively important and expanded as follows:

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Figure 6-5 OperationSoft folder

Important folders include:


AbsData stores reaction curve files.
AlarmFile stores alarm log messages.
Database database file, which contains all parameters, test results,
calibration and QC data, etc.
BA80_DATA.MDF:database storage file
BA80_LOG.LDF: database boot file
The Backup folder contains BA80.bak, a database backup, see
Figure 6-37 Database location
ExceptionLog records address segment for error analysis when the software
collapses abnormally. (Note: There are two ExceptLog files, and the
other one is in Instrument_1 folder.)
Help online help in .chm format.
Instrument_1 log file.
PrintTemplate Print template
Item Mindray's chemistry parameter file.
Language Software Language

6.1.4 Log Files


The BsLog process records in real-time mode the communication and action information of the software and
analyzer, which includes but not limited to the following:
• Keyboard input
• Error log, operation log and maintenance log of the software
• Communication instructions between the PC and analyzer
• Action instructions of the analyzer
• Floater and photocoupler statuses of the analyzer (real-time)
• Pump and valve powering statuses of the analyzer (real-time)

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• Photoelectric data (real-time)


• ……
Separate log files are produced every day and stored in the following addresses:
1) In the WorkstationLOG folder of D:\Mindray\ BS240\OperationSoft.
2) In the InstrumentLOG folder of D:\Mindray\ BS240\OperationSoft\Instrument_1
The folder structure is shown below:

Figure 6-6 InstrumentLOG folder

Important folders include:


Perio the water blank data.
Lislog LIS communication data.
RPC (short form of Remote Procedure Call)
basic control command data.
ISEAdapterSrv ISE command and test data.
Workdata Instrument work instruction record

6.2 Computer Settings


6.2.1 Computer Requirements (for International Customers)
CPU At least Intel Dual Core, 2.6GHz
Memory At least 2GB for each RAM
Network Adapter If you are going to connect the computer with the LIS or Internet, you should
prepare another network adapter (Intel gigabit network adapter)
Serial Port The computer should provide an RS232 serial port, which is used to connect
with the analyzer.
USB USB2.0 and above, no less than 2
Other built-in speakers (instrument alarm sound prompt)
Operating System Windows 10 Home 1803 Chinese(64bit)

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6.2.2 Hard disk defragment


Install the operating system in the C drive and the operating software of the instrument in the D drive. Make
sure that the C drive is over 30G and D drive over 100G, and the disk file system is of NTFS format. Deselect
the two options at the bottom of the disk properties window: “Compress drive to save disk space” and “Allow
Indexing Service to index this disk for fast file searching”.

Figure 6-7 Hard disk defragment

6.2.3 Application Software


Except for the operating system, other application software must not be installed or reserved on the computer.
If anti-virus application has been installed, remove the automatic scheduled scanning and add Workstation (BS-
240) and BSLOG to the trust list.
6.2.4 Remove Screen Saver and System Standby
To remove the screen saver and system standby, select None in the Screen saver pull-down list box of the
Screen Saver Settings window, and then select Change power settings -> Change plan settings to go to the
Edit plan settings window. Perform the settings as shown in the figures below.

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Figure 6-8 Remove screen saver

Select None in the Turn off the display and Put the computer to sleep pull-down list boxes.

Figure 6-9 Standby settings

6.2.5 Disable Automatic Synchronization with Internet Time Server


Double click the time icon on the lower-right corner of the task bar. The Date and Time Properties window is
displayed.

Figure 6-10 Disable automatic synchronization with Internet time server-1

Select the Internet Time tab, and then deselect the checkbox in front of Synchronize with an Internet time server.

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Figure 6-11 Disable automatic synchronization with Internet time server-2

6.2.6 Turn off Automatic Updates


Turn off the automatic updates on the Windows Update window.

Figure 6-12 Turn off the automatic updates

6.2.7 Resolution Setting


Determine whether the screen resolution is 1280*1024.
Procedure:
On the PC desktop, right-click and select Display > Advanced display setting, set the resolution to 1280*1024,
and click OK, as shown in the following figure:

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Figure 6-13 Set Resolution

6.2.8 Confirmation of Administrator Permission and UAC


1. Confirming that the current account is the Administrator
1) Open the command prompt. Enter windows+X, and click Command Prompt (Administrator) (A), shown
as the following figure.

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Figure 6-14 Open Command Prompt

2) Enter the net user administrator /active: yes command to activate the administrator account (pay
attention to the space in the command), and press Enter. The "Command(s) completed successfully"
is displayed, as shown in the following figure:

Figure6-15 Enter command to Activate the Administrator Account


2. Logging in using the administrator account
Press Ctrl+Alt+Delete, click Log Off to enter the login screen, and click Administrator to enter the OS using
the Administrator account.
3. Modifying UAC setting
1) Enter regedit to run the registry, as shown in the following figure:

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Figure 6-16 Run Registry

2) Find the EnableLUA item (0 indicates to disable UAC) in the following path of the
registry.[HKEY_LOCAL_MACHINE\SOFTWARE\Microsoft\Windows\CurrentVersion\Policies\System
]
3) Check the EnableLUA item. If the value is 1, change it to 0 (0 indicates to disable UAC).
6.2.9 SQL Version Check
Check the database version in the installation software directory and confirm that the database software is not
installed in the computer. If there is, refer to 6.6.2 SQL Database Uninstalling.
6.2.10 Check the installation.
On the Customize Format window, ensure that the decimal point "." has been chosen in the Decimal symbol
pull-down list box.
Note: Customize Format is configured according to the actual conditions of the countries which purchase the
analyzer. For example, the decimal point in Spain is "," so "," should be set as the decimal point (".") in this
country.

Figure 6-17 Special character setting

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6.2.11 Firewall Whitelist Setting


Add the program of the operating software into the whitelist to ensure that the instrument and PC communicate
normally and avoid instrument disconnection.
Set relevant program to Allow programs to communicate through Windows Firewall. Specific operation is
as follows:
1) Choose Control Panel > Windows Firewall, and click Allow programs to communicate through
Windows Firewall.
2) In the program list, select the program with operating software, and tick it.
6.3 Installation of Operating Software
6.3.1 Preparation before Installation
1) Download the corresponding version of the software on the TDP.
2) Complete the computer settings, refer to 6.2 Computer Settings.
6.3.2 Software Installation
Please refer to the “UpgradeGuide_EN” in the “SetupGuide” folder of the installation package, see Figure 6-1
Folders in operating software installation package ,which will be updated with the software update.
The following are the detailed installation steps:
1) Run setup.exe in the Setup folder.
Note: If it is the first time the software has been installed, the system will prompt you to reboot the computer.
The SQL Server will be installed automatically after the computer is rebooted.
If the software has been installed and is uninstalled, the PC will not restart.
2) Click Next to enter the installation screen.

Figure 6-18 Installation Wizard Screen

3) The following screen is displayed. Wait for the third-party program to install. Then, the PC will
automatically restart.

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Figure 6-19 Installing SQL Software

Note: During database installation, the DOS dialog box is displayed. Do not close this dialog box. It will
automatically disappear after the database is installed. It takes about 20 minutes to install the database. As
shown in the following figure:

Figure 6-20 DOS Dialog Box During SQL Installation

Note: If the DOS dialog box is closed by mistake, the installation fails. Follow the steps below to handle
the problem:
▪ Uninstall the SQL database, and reinstall the software. (For details about database uninstalling,
see section 6.6.2 SQL Database Uninstalling )
▪ If the installation fails again, restore the system, and reinstall the software.
3) Select the path for installing the software.
Select the path for installing the software, and click Next, as shown in the following figure:

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Figure 6-21 Select a Path to Install the Software

4) Wait till the language selection window pops up.

Figure 6-22 Software installing

5) Choose a language that is used to display the software screens and printed reports, and then select
Next.

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Figure 6-23 Select Language for the Operating Software

6) Select Finish. The installation is complete.

Figure 6-24 Installation Finished Screen

7) Confirm the configuration file, refer to 6.3.3 Confirm the configuration file.
6.3.3 Confirm the configuration file
Note:
1) After the installation is complete, the default serial port connecting the analyzer is COM1. If the
software can not be run due to the serial port configuration, please refer to 3).
2) The configuration file is located in the installation directory by default. If the path has been changed

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during software installation, find the configuration file in the new directory.
3) The serial port in the configuration file should be set as the one used by the instrument.
Step 1: Open the configuration file COMMUNICATION_USE.INI in the default directory:
D:\Mindray\ BS240\OperationSoft\COMMUNICATION_USE.INI
Step 2: Check if the configurations in the COMMUNICATION_USE.INI file are the same with the following
examples. If they are different, change them according to relevant instructions.
[INSTRUMENTS]
HasTestInstrumentsNum=1
; Note: Number of Instrument
HasSDM=0
; Note: Is SDM configured
IsUseInstrument1=1
IsUseInstrument2=1
IsUseInstrument3=1
IsUseInstrument4=1
NameOfInstrument1 = 240
NameOfInstrument2 = 240
NameOfInstrument3 = 240
NameOfInstrument4 =240
[SAMPRACK_COMM_USE]
SAMPRACK_COMM_TYPE=SERIALPORT
SAMPRACK_COMM_NAME=SIM
; Note: Serial port of SDM
[BAUDRATE_SEC]
Baudrate=38400
; Note: Baud rate of SDM
[Demo]
ComPort=COM1
Step 3: Open the configuration file InstrServerConfig.ini in the default directory:
D:\Mindray\ BS240 \OperationSoft\Instrument_1\ InstrServerConfig.ini
Step 4: Check if the configurations in the InstrServerConfig.ini file are the same with the following examples. If
they are different, change them according to relevant instructions.
[INSTR]
INSTRNO=1
SERVER_IP=127.0.0.1
SERVER_PORT=7001
CLIENT_IP=127.0.0.1
CLIENT_PORT=8001
[SERIALPORT]
COMPORT=COM1
; Note: Serial port
BAUDRATE=38400
; Note: Baud rate
6.4 Software Upgrading
The software upgrade is divided into two parts, operating software upgrades and control system upgrades.
Please refer to the “UpgradeGuide_EN” in the “SetupGuide” folder of the installation package, see Figure 6-1
Folders in operating software installation package ,which will be updated with the software update.
Note: After the upgrade is complete, be sure to turn off the analyzer's power and restart to configure the
instrument parameters
6.4.1 Preparation before Upgrading
When it comes to upgrading V30.00.06 software, be sure to check the 6.9 upgraded to V24.00.06 instructions
first.

Check the software version


Enter the current operating software system on the operating computer to confirm the current software version
information, as follows:
Steps:
Enter the main screen of the operating software, select Utility > System Setup > Instrument Setup > Software

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Version, and confirm the current software version information.

Figure 6-25 Operating Software Version

LIS Setting backup


If the customer uses the LIS, the LIS setup information needs to be backed up.
Steps:
1) Select Utility > System Setup > LIS Setup.

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Figure 6-26 Host Communication Parameters window

Note: Take pictures of this LIS setting interface, Channel number content also needs to take full. Make sure no
Settings related are lost.
2) If the customer uses TCP/IP for LIS connection, you need to take a screenshot of the operating
computer network settings.
In the lower right corner of the desktop taskbar, right click, pop up "Network Settings", select the
network settings used by the LIS, screenshot IP settings information

Figure 6-27 IP setting information

Data Backup
Upgrading the software may result in database loss, so please make a backup before upgrading. Please refer
to 6.7.1 Data backup.

Backup system parameters


During the process of upgrading the control system, the unit parameters may change, so you need to back up
in advance,refer to 6.7.3 Unit parameter .
6.4.2 Upgrading of Operating Software
1) Use the engineer username and password to quit the operating software to the desktop.
2) Access the Windows Task Manager window.Workstation.exe 、 BsLog.exe 、 BsLog1.exe 、
Instrument.exe Check if relevant processes of the Workstation and Upgrade have been ended. If
not, select the process and click End Process.
The processes include:
Workstation.exe, BsLog.exe,BsLog1.exe,Instrument.exe .

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Figure 6-28 Task Manager Window

3) Select programs on the menu on the lower right corner; Then select programs and features and
double click the BS240 program to remove it.
4) Reboot the computer.
5) Install the new operating software. Refer to 6.3.2 Software Installation.
6) After finishing the installation, do not reboot the computer or run the BS-240 operating software.
Please executive upgrade control system upgrade.
6.4.3 Upgrading Control System
1) Confirm again that the instrument unit parameters have been backed up, refer to 6.7.3 Unit
parameter Backup.
2) Re-confirm that the new version of the software has been installed, the instrument's main power
switch and analysis unit power switch are turned on.
3) Run the upgrading tool UpgradeEntry:
D:\Mindray\BS240\UpgradeTool\UpgradeEntry.exe

Figure 6-29 Screen of UpgradeEntry

4) Select a serial port used for the analyzer from "Uart name". The default setting is COM1. Note: If
the service engineer changes the serial port during instrument installation, the actual one used

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for PC communication should prevail. Select the target units to write the program. "All Units"
should be selected when the first time to upgrade.

Figure 6-30 UpgradeEntry 1

5) The burning file is under the installation directory and the default installation
directory :D:\Mindray\BS240\AnalyzeSoft. Any burning file can be selected when the "All Unit"
selected.

Figure 6-31 UpgradeEntry 2

6) The control units will be download from the "Main Unit" After "Start" button clicked.

Figure 6-32 UpgradeEntry 3

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7) Click the "Exit" button when the upgrade completed.

Figure 6-33 Upgrade completed

8) Power off, and power it on again after 10 seconds.


9) 10 seconds later, Reboot the computer to run the operating software.
10) Check according to 6.4.4 Confirmation after Upgrading.
6.4.4 Confirmation after Upgrading
1) Refer to 6.3.3 Confirm the configuration file, Confirm that the configuration file has no errors,
otherwise modify it.
2) Check the software version information after entering the software to check whether the upgrade
is successful,refer to Figure 6-25 Operating Software Version.
3) Check whether the database information is lost. If it is lost, refer to Section 6.7.2 Database
Recovery.
4) Check if the LIS connection is normal. If it is abnormal, refer to LIS Setting backup content for
restoration
5) Check whether the unit parameters are consistent with the backup. If not, please refer to 6.7.4
Parameter Configuration for parameter configuration restoration.
6) If an alarm message appears: unmatched operating software version,refer to 10.2.4 Unmatched
Operating Software VersionA22039.
6.5 Software startup process and autostart settings
6.5.1 Normal Startup Procedure
The normal startup procedure of the operating software is as follows:
1) The system checks if the Bslog process has been started automatically. If not, the Bslog.exe program is
run.
2) Sql server is started, and it will exit if an error indicating database initialization failure occurs.
3) The software process is started.
4) Enter the username and password.
5) The software shakes hands with the middle-/lower-layer units. (If handshake fails, an alarm is given
prompting the unit is abnormal.)
6.5.2 Software antostart settings
Normally, with the startup of Windows, the software will start automatically. If there are special circumstances
that must prohibit the program from running automatically, you can modify the computer startup items:
How to do:
1) Switch to the desktop using the service user account, Right click the task bar and select Task Manager.

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Figure 6-34 Change Startup Item Configuration

2) Select Startup and the CL-1000i(Here is the CL-1000i as an example. The actual display is workstation)
icon. The screen is shown as follows:

Figure6-35 Task manager window


3) Deselect the checkbox to the left of "CL1000i" to disable auto startup of the operating software.
Note: To restore auto startup, repeat steps 1 to 3 and select the "CL1000i" checkbox.

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6.6 Software and SQL Database Uninstallation


6.6.1 Remove the software
1) End the BSlog process by using the KillBslog tool in the installation package.
2) Find the Workstation program on the Control Panel window and uninstall it.
6.6.2 SQL Database Uninstalling
1) Select Start menu > Control Panel > Programs > Programs and Functions on the computer
desktop, and uninstall SQL Server.
2) Then delete the "Microsoft SQL Server" folder generated during installation, run the registry, enter
regedit in Start > Run, enter the registry editor, and delete the following contents in the registry:
HKEY_CURRENT_USER\Software\Microsoft\MicrosoftSQLServeHKEY_LOCAL_MACHINE\SOFT
WARE\Microsoft\Microsoft SQL Server (note that you must delete the entire Microsoft SQL Server
folder).
3) Enter regedit in the bottom left corner of the computer Start > Run, enter the registry editor, and then
search
HKEY_LOCAL_MACHINE\SYSTEM\CurrentControlSet\Control\Session Manager,
Find the PendingFileRenameOperations value and delete all the data in it.

Figure 6-36 Delete the Database

4) After the SQL database is uninstalled, the operating software can be executed again. The software
automatically installs the SQL data during the installation process.

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6.7 Data backup and recovery


6.7.1 Data backup
To back up the data
1) First exit the operating software.
2) enter it again to refresh the database.
The database is in the Database folder under the installation directory. You can choose to back it up in the
following two ways:
1) Use the engineer account to exit the operating software, enter the installation directory, find and copy
the entire Database folder to the computer E drive. File default path:
D:\Mindray\BS240\OperationSoft\DataBase\
2) Use the engineer account to exit the operating software, enter the installation directory, copy the
BA80.bak file in the Backup folder under Database to the computer E disk. File default path:
D:\Mindray\BS240\OperationSoft\DataBase\Backup
240Pro

Figure 6-37 Database location

6.7.2 Database Recovery


To recover the database, first find the storage location of the local disk where the database to be restored is
located. It is recommended to back up the current data.
1) If you copy the entire Database folder, copy and paste directly to D:\Mindray\BS240\OperationSoft\
2) If you are copying the BA80.bak file, you need to copy and paste the file into this directory.
D:\Mindray\BS240\OperationSoft\DataBase\Backup, please delete the two files BA80_DATA, BA80_LOG,
and then restart the software.
6.7.3 Unit parameter Backup
1) Run the operating software. Select Utility -> Maintenance -> Parameter Configuration, select a unit
from the drop down list of "Unit Parameter" to inquire parameters, and then click Save. Repeat this
step for other units.

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Figure 6-38 Parameter Configuration window

2) Click Save ,the Save as dialog box is displayed. Select a partition, and create a new folder named in
the format of "Instrument SN + Unit Parameter Backup", and name the unit to be stored.
6.7.4 Parameter Configuration
Parameter configuration requires the use of R&D user name and password, user name superstar,
password, please consult TS
1) Select Utility -> Maintenance -> Parameter Configuration, select the unit of the required
configuration parameters in the “Unit Parameter” drop-down list, click Search, the following
interface appears: (to the reaction l unit For example)

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Figure 6-39 Parameter Configuration 1

2) If only one parameter needs to be configured, for example, modify the position 3 parameter shown
in the figure above, double-click the parameter value, change it to “100”, click “Configure”, and
then search the unit again to see if the modification is successful. If this is not successful, repeat
this step.

Figure 6-40 Parameter Configuration

If the instrument has an alarm message

Then the setting parameters are out of range and new setting parameters need to be replaced.
3) If you need to recover by backup parameters, take the following steps: (taking the reaction unit
as an example)Select reaction unit in the unit parameter. 1→Click Search 2→Click Load
3→Select the backup parameter path in the pop-up box→Select the reaction unit parameter
→Click to open . At this time, the parameters have been imported to the current interface,click

,complete parameter configuration.


4) Select the corresponding unit to search and check whether the parameters are configured
successfully. If not, repeat the above operation
6.8 Demo Software Setup
If you want to enter the software in Demo mode, first exit the operating software and add a command in the
start program of WorkStation.exe. To do so, create a shortcut for WorkStation.exe on the desktop, right-click on
the icon and select Properties; then modify the Target field in the pop-up window by adding three space-
separated running parameters (“-Demo”, “MCUDemo”, and “-ISEDemo”) after “WorkStation.exe”, as indicated
in the figure below. When this is done, you can launch the operating software in Demo mode.
Note: If there is no serial port on the computer, you need to install the virtual serial port software. You can run
the demo software after adding the COM1 port. Otherwise, the software will report an error and cannot enter.

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Figure 6-41 Demo Setup

6.9 upgraded to V24.00.06 instructions


The main board, together with operation software, upgraded the encryption algorithm of close reagent system.
The operation software is upgraded to V24.00.06, The main changes are as follows:
1) Closed system database encryption algorithm upgrade. The new version of the software adds the function
of self-checking whether the database is cracked or not. Please refer to " Must read_ upgrading to
V24.00.06 and above_upgrade help tool guidance" for details.
2) Added function: when the blocking reagent reaches the biochemical expiration date, the user will be alerted
in advance.
Upgrade main control board to V2.0, the main changes are as follows:
1) Order number unchanged after upgrade, but the main board is one-way compatibility and the operating
software V24.00.06 or above must be used after the upgrade.
2) Main board encryption mode optimization, improve the ability to crack.
Upgrade tools and guides are packaged with the new operating software.

The new software is uploaded to TDP.


View Files:/Bio-chemistry/Auto-Biochemistry /BS-240/Software

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7 Alignment
7.1 Basic Operation
7.1.1 Utility - Maintenance
Table 7-1 Utility - Maintenance

No Description
1 Maintenance and Diagnostics: used to maintain and diagnose the
system at user end.
2 Alignment: used to align all mechanical positions, and the
hydropneumatic, pyrology and ISE units.
3 Parameters: used to inquire and configure parameters, and to
export parameters of each unit.

Figure 7-1 Maintenance screen

7.1.2 Alignment fixtures


Fixture package code: 115-038776-00 Alignment Fixture Clamp Team (If the code cannot be requested, contact
related YS for treatment).
Note: This code contains all the alignment fixtures in the table below.
Table 7-2 Alignment fixtures

No Code Name Image/Precision Quantity


1 041-024257-00 BA24 cuvette alignment 2
fixture

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No Code Name Image/Precision Quantity


2 041-024250-00 Reagent bottle center 3
alignment fixture

3 041-016038-00 Sample position 3


alignment tool

4 041-020157-00 Pseudo probe 1

5 041-024251-00 Feeler gauge 1

6 041-024252-00 Mixer alignment lever 1

7 041-024258-00 BA24 mixer horizontal 1


position alignment
cuvette

8 041-024253-00 Mixer wash well 1


alignment fixture

9 041-024254-00 Pseudo cuvette for auto 1


wash station alignment

10 041-016047-00 probe wash well 1


alignment tool

11 / Clearance gauge 0.5mm~0.8mm 1


7.1.3 Mechanical Reset
Alignment methods and procedure:
1 Install the pseudo probe (BA60-J07), and block the collision sensor with folded thick
paper.

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2 Access the Alignment window and select Mech Reset to reset the mechanical parts of
the system.

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7.2 Alignment Procedure


Start

Download program
Installation of of upper
Preparation Powering On
Operating Software layer/lower layer
unit

Signal Collecting
Photoelectric unit Photoelectric gain
Position
adjustment adjustment
Adjustment

Bar code label Testing reagent bar


Bar Code Unit Adjusting Bar Code
printing and code scanning
(Optional) Reader Position
affixing stability

Sample/reagent Reaction Carousel


Sample/Reagent Sample/Reagent Sample Carousel
carousel unit Circumferential
Carousel Outer Ring Carousel Middle Inner Ring Radial
parameter Position
Radial Position Ring Radial Position Position
adjustment Adjustment

Adjust Horizontal Adjust Horizontal Adjust Horizontal


Setting Aligning Horizontal
Position from Probe to Position from Probe to Position from Probe to
Parameters of Position from Probe to
Sample/Reagent Carousel Sample/Reagent Carousel Sample/Reagent Carousel
Probe Unit Reaction Carousel
Outer Ring Middle Ring Inner Ring

Aligning Horizontal and Vertical Extreme Position


Sample Probe Rotary to Sample Probe Rotary to Sample Probe Cuvette
Vertical Positions from from Probe to Reagent
SIC Height (Optional) ISE (Optional) Height
Probe to Wash Well Bottle

Setting Adjust Horizontal


Cuvette Wash Station
Parameters of Position from Wash Probe
Height
Cuvette Wash Unit to Reaction Cuvette

Adjusting Horizontal Adjusting Mixing Position Adjusting Horizontal


Setting Mixer Unit
Position from Mixer from Mixer to Reaction Position from Mixer to
Parameter
to Reaction Carousel Carousel Wash Well

Preparations before Checking Floater/


Fluidics Alignment Syringe Check Fluidic Prime
Alignment Valve Status

Setting Reaction Wash Solution Reagent


Setting Pyrology Reaction carousel
Carousel Sensor Temperature refrigeration
Unit Parameter heating detection
Parameter Curve adjustment

Completing parameter
configuration table and test
record table

End

Figure 7-2 Alignment Procedure

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7.3 Photometric Unit


Select Utility—>Maintenance—>Alignment—>Photometer Unit. The window is as shown below.

Figure 7-3 The window of Photometric unit

[1 Turn On Lamp] and [2 Turn Off Lamp] are the switch light source light command.
[3 Index Setup] is set for the optical gain indicator, please do not change it at will.
7.3.1 Signal Collecting Position Adjustment
Alignment index:
The signal of No.3 cuvette of the optical cuvettes segment is within the two boundary lines.
Alignment methods and procedure:
1) Select Signal Collecting Position Adjustment to display the alignment window.
2) Make sure the lamp has been turned on for over 1 minute. If not, wait for 1 minute, and then select
Start to proceed to the next step.
3) A window pops up to prompt you to add 200 µl DI water with pipettor in the designated cuvette. Select
Next.

4) Observe the waveform in the upper part of the window and check if the photoelectric signal meets the
alignment requirement. See the figure below. If not, adjust the photocoupler.

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The green box must


be within the two
red lines.

Figure 7-4 Signal Collecting Position Adjustment

▪ If you want to adjust the position of optical coupler. The position sensor of the reaction carousel
is located on the right of the analyzer. Remove the right panel before alignment. Loosen the
three M3 hexagon screws on the optical coupler bracket. Use a wrench to knock the sensor
gently to adjust clockwise the position of the sensor and the green box moves right. If you adjust
the position counter clockwise, the green box moves left. After position adjustment, tighten
slightly the screws and click re-align. The software restarts testing.
▪ If the photocoupler is in a proper position, select Done without any adjustment.

Reaction carousel
position sensor

Figure 7-5 Reaction carousel position sensor

7.3.2 Photoelectric Gain Adjustment


Alignment index:
1) The water blank AD value of each channel is set to 50000~54000.
2) The optical gain coefficient of all channels is generally set to 40 for a new instrument, and may be set to
30 for a client-side old instrument.
3) The dark current of all channels is 1~200.

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Figure 7-6 Access the "Index Setup" screen

Alignment methods and steps:


1) Select Photoelectric Gain Adjustment.
2) Make sure the lamp has been turned on for over 3 minutes, and then select "Done". If you do not
click "Done", you need to wait for 3 minutes.
3) Add 200uL deionized water into cuvettes 1~5 in segment 1 according to step 4 on the screen.
4) The photoelectric gain is adjusted automatically. When adjustment is complete, select Done.
5) Select "Continue" to test the dark current and the water blank AD of each channel.
6) Select "Continue" to finish the alignment and exit the procedure.

Note
If you had adjust the position of optical coupler, ensure that the screws on the reaction carousel position sensor
bracket have been tightened.
Alignment parameters can be saved only after each procedure is complete. Another alignment is required if a
procedure is terminated. If the parameter is not successfully configured or out of range, the parameter range
will be displayed by the alarm message and re-perform the alignment.

7.4 Sample/Reagent carousel unit


Select Utility -> Maintenance -> Alignment -> Sample/Reagent Carousel. The window is as shown below.

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Figure 7-7 The window of Sample/Reagent Carousel Unit

7.4.1 Reaction Carousel Circumferential Position Adjustment


Alignment index:
The probe (pseudo probe BA60-J07) can pass through the through-hole on the cuvette alignment fixture (BA24-
J04).
Operation methods and steps:

Figure 7-8 Alignment procedure

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1) Select Reaction Carousel Circumferential Position Adjustment and then operate according to the
screen prompts.
2) Select Continue to reset all mechanical parts of the whole unit.
3) Place Cuvette alignment fixture BA24-J04 on the 19# and 14# cuvettes.
4) Adjust the position of probe to the reaction carousel.
a) Click the button on the software window to move the probe above the dispensing position
and the diluting position on the reaction carousel. Check if the probe can pass through the
center hole of the fixture on the two cuvettes, otherwise adjust the probe's radial position and
reaction carousel's circumferential position parameters. The left and right arrow on the
window can adjust the circumferential position of the reaction carousel.

BA60-J07

BA24-J04

Reaction carousel's orbit

The crossover point of Reaction


carousel's orbit and probe's orbit

Probe's orbit

Figure 7-9 Reaction Carousel Circumferential Position Adjustment

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b) If the software cannot be debugged successfully, there may be a deviation in the mechanical
position, so you need to adjust it as shown in the figure below.

probe's circumferential position adjustment: Loosen


the 2 screws to move the probe rocker arm.

probe's radial position adjustment : Loosen the 3


screws to move the base.

Figure 7-10 How to adjust mechanical position


c) Select Continue to proceed to the next step.
5) Click Continue. Check the position of the probe in dispensing position and diluting position.
6) Select Continue. The alignment is complete. Select Exit to close the window.

Note
• The alignment tools will be used in following alignment. Do not remove them.
• The left arrow button is equivalent to rotating clockwise and the right arrow button rotating counterclockwise.
• When selecting Large Step, you can set up the concrete steps according to the reference range.
• Once the probe arm length is determined, it must not be adjusted during alignment of probes and carousels.
• If the probe arm length is changed, the probe and carousel units should be aligned again.
• Alignment parameters can be saved only after each procedure is complete. Another alignment is required
if a procedure is terminated. If the parameter is not successfully configured or out of range, the parameter
range will be displayed by the alarm message and re-perform the alignment.
If you loosen the two fixing hex socket screws of the probe rocker arm, you need to adjust the horizontal position
of the probe to the reaction carousel, the wash well and the reagent carousel. If the debugging is out of range,
it is possible to rotate when the rocker arm is fixed. Over the rocker arm, you need to re-adjust and fix the rocker
arm.

7.4.2 Sample/Reagent Carousel Outer Ring Circumferential Position


Alignment index:
The probe (fixture: BA60-J07 pseudo probe) can pass through the center hole of the sample position alignment
fixture (BA48-J10) in sample positions 1#, 14#, and 27# of the outer ring of the sample/reagent carousel.
Alignment methods and procedure:

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Figure 7-11 Alignment procedure

1) Select "Sample/Reagent Carousel Outer Ring Circumferential Position", and then operate
according to the screen prompts.
2) Place a sample position alignment fixture BA48-J10 in sample positions 1#, 14#, and 27# of the outer
ring of the sample/reagent carousel.

The probe tip can pass


through the central hole
of the alignment tool.

BA48-J10

Figure 7-12 sample position alignment tool

3) Click to move the probe to 1# position of the sample/reagent carousel outer ring, and click the up and
down arrow buttons to stop the probe at the visually nearest position above the fixture. Check if the
probe tip is aligned with the middle of the through-hole. If it is not, click the left and right arrow buttons
to adjust the probe's circumferential position on the outer ring, so that the probe tip can pass through
the central hole of the fixture in 1# position.

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The 4 arrows are


used to control the
probe.

The 2 arrows are used to


control the carousel.

Figure 7-13 Sample/Reagent Carousel Outer Ring Circumferential Position Adjustment

4) Adjust the reagent probe in 14# and 27# positions of the sample/reagent carousel outer ring according
to step 3.
5) Select Continue. The alignment is complete.
6) Select Exit to close the window.
7.4.3 Sample/Reagent Carousel Middle Ring Circumferential Position
Alignment index:
The probe (fixture: BA60-J07 pseudo probe) can pass through the center hole of the reagent center alignment
fixture (BA10-J16) in reagent positions 1#, 14#, and 27# of the middle ring of the sample/reagent carousel.
Alignment methods and procedure:
1) Select Sample/Reagent Carousel Middle Ring Circumferential Position.
2) Place a reagent position alignment fixture BA10-J16 in positions #1, #14 and #27 of the
sample/reagent carousel, and then select "Continue".
3) Adjust the positions #1, #14 and #27 of the middle ring of the sample/reagent carousel according to
step 4 of "Sample/Reagent Carousel Outer Ring Circumferential Position".
4) Select "Continue". The alignment is complete.
5) Select Exit to close the window.
7.4.4 Sample/Reagent Carousel Inner Ring Circumferential Position
Alignment index:
The probe (fixture: BA60-J07 pseudo probe) can pass through the center hole of the reagent center alignment
fixture (BA10-J16) in reagent positions 41#, 54#, and 67# of the inner ring of the sample/reagent carousel.
Alignment methods and procedure:
1) Select "Sample/Reagent Carousel Inner Ring Radial Position".
2) Place a sample position alignment fixture BA10-J16 in positions 41#, 54#, and 67# of the sample
carousel, and then select "Continue".
3) Adjust the positions 41#, 54#, and 67# of the inner ring of the sample/reagent carousel according to
step 4 of "Sample/Reagent Carousel Outer Ring Circumferential Position".
4) Select "Continue". The alignment is complete.

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5) Select Exit to close the window.

Note
• Alignment parameters can be saved only after each procedure is complete. Another alignment is required
if a procedure is terminated. If the parameter is not successfully configured or out of range, the parameter
range will be displayed by the alarm message and re-perform the alignment.

7.5 Probe unit


Select Utility—>Maintenance—>Alignment—>Probe Unit. The window is as shown below.

Figure 7-14 The window of probe unit

7.5.1 Probe to Horizontal Position on Reaction Carousel


Alignment index:
The probe (pseudo probe BA60-J07) can pass through the through-hole on the cuvette alignment fixture (BA24-
J04).
Alignment methods and procedure:

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Figure 7-15 Alignment procedure

1) Select Probe to Horizontal Position on Reaction Carousel.


2) Place the cuvette alignment fixture (BA24-J04) in positions 19# and 14# of the reaction carousel, and
then select "Continue".
3) Select the down arrow button to lower the probe to the top of the alignment fixture in position 19# so
that it can align with the center hole..
4) Adjust the circumferential position of the probe arm and ensure that the probe can enter the central
hole on the fixture. Press the probe arm and tighten the screws on it. If error exists, click the left and
right arrow buttons to adjust the probe till it meets the requirement.

BA24-J04

Figure 7-16 The cuvette alignment fixture

5) Select Continue and verify the alignment with the up and down arrow buttons. If the index is not
satisfied, return to the previous step and try again.
6) Click "Continue". Move the probe to the top of the position 14#. Click the up and down arrows to drop
the probe to the top of the fixture. Check whether the probe tip can enter the center hole of the fixture.
If it cannot, click the left and right arrows to adjust parameters until index requirements are met.

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7) Select Continue and verify the alignment with the up and down arrow buttons. If the index is not
satisfied, return to the previous step and try again.
8) Select Continue to save parameters and exit the window.
7.5.2 Probe to Horizontal and Vertical Positions on Wash Well
Alignment index:
1) Horizontal position:The probe tip can enter the central hole on the wash well alignment tool (BA48-J12)
and the gap between the probe’s wash well and the fixture shell is even.
2) Vertical position: When reaching the bottom of the central hole on the wash well alignment fixture (BA48-
J12), the probe is lifted for 0.15mm, which means that the clearance gauge can pass with 0.15mm through
the gap between the sensor plate and the arm base and it cannot pass with 0.20mm.
Alignment methods and procedure:

Figure 7-17 Alignment procedure

1) Select Probe to Horizontal and Vertical Positions on Wash Well.


2) According to Step 2 on the screen, place a wash well alignment tool (BA48-J12) in the probe wash
well, and then select Continue.
3) Select the up/down and left/right arrow buttons to move the probe till it lowers into the center on the
alignment fixture. If the probe is greatly deviating from the alignment tool, use a big cross head
screwdriver to loosen the screws on the wash well or the bracket of the wash well, adjust the wash
well till the probe can enter to the central hole on the alignment tool, and then tighten the screws.

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Use the clearance gauge to measure


the gap here and keep it away from
BA48-J12 the slit on the photocoupler side. The
soldering lug is deformable and may
affect the measurement.
Criteria: The clearance gauge can
pass with 0.15mm and cannot pass
with 0.2mm.

Figure 7-18 Probe to Horizontal and Vertical Positions on Wash Well

4) Confirm the alignment result. If the requirements are not met, return to Step 3.
5) Adjust the probe's vertical position above the wash well by using the up and down arrow buttons.
Check that the clearance gauge can pass with 0.15mm and cannot pass with 0.20mm.
6) Check the vertical position. If the requirements are not met, return to Step 5.
7) Remove the alignment tool according to screen prompts.
8) Select Continue to save parameters and exit the window.
7.5.3 Probe to Sample/Reagent Carousel Outer Ring
Alignment index:
The probe tip can enter the center hole of the alignment fixture (BA48-J10) in positions 1#, 14#, and 27# of the
outer ring of the sample/reagent carousel.

Alignment methods and procedure:

Figure 7-19 Alignment procedure

1) Select Probe to Sample/Reagent Carousel Outer Ring.


2) Place a sample position alignment tool (BA48-J10) in position 1#, 14#, and 27# on the outer ring of
the sample/reagent carousel, and then select Continue.
3) Select the up/down and left/right arrow buttons to move the probe so that it can enter into the central
hole on the alignment tool.
4) Select Continue to save parameters and exit the window.
7.5.4 Probe to Sample/Reagent Carousel Middle Ring
Alignment index:
The probe tip can enter the central hole of the alignment fixture (BA48-J10) in 1#, 14# and 27# positions of the

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sample/reagent carousel middle ring.


Alignment methods and procedure:
1) Select Probe Rotary to Sample/Reagent Carousel Middle Ring.
2) Place a sample position alignment tool (BA10-J16) in position 1#, 14#, and 27# on the middle ring of
the sample/reagent carousel, and then select Continue.
3) Select the up/down and left/right arrow buttons to move the probe so that it can enter into the central
hole on the alignment tool.
4) Select Continue to save parameters and exit the window.
7.5.5 Probe to Sample/Reagent Carousel Inner Ring
Alignment index:
The probe tip can enter the central hole of the alignment fixture (BA48-J16) in 41#, 54#, and 67# positions of
the sample/reagent carousel inner ring.
Alignment methods and procedure:
1) Select Probe Rotary to Sample/Reagent Carousel Inner Ring.
2) Place a reagent position alignment tool (BA10-J16) in position 41#, 54#, and 67# on the inner ring of
the sample/reagent carousel, and then select Continue.
3) Select the up/down and left/right arrow buttons to move the probe so that it can enter into the central
hole on the alignment tool.
4) Select Continue to save parameters and exit the window.
7.5.6 Probe to Vertical Limit Position on Reaction Carousel
Alignment index:
When reaching the cuvette bottom, the probe is lifted for 0.15mm, which means that the clearance gauge can
pass with 0.15mm through the gap between the sensor plate and the arm base and it cannot pass with 0.20mm.
Alignment methods and procedure:

Figure 7-20 Alignment procedure

1) Select Probe to vertical limit position on reaction carousel.


2) Check that cuvettes are loaded in 1#, 14#, and 27# positions of the reaction carousel.
3) Adjust the probe over the 3 cuvette positions, and ensure that the lifting height meets the requirement.
4) Select Continue to save parameters and exit the window.
7.5.7 Probe to Vertical Limit Position in Reagent Bottle
Alignment index:
When reaching the bottom of the reagent bottle, the probe is lifted for 0.15mm, which means that the clearance
gauge can pass with 0.15mm through the gap between the sensor plate and the arm base and it cannot pass
with 0.20mm.

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Alignment methods and procedure:


1) Select Probe to Vertical Limit Position in Reagent Bottle.
2) Load the reagent bottle in 1#, 14#, and 27# position on the middle ring of the sample/reagent carousel.
3) Adjust the probe over the 3 reagent positions, and ensure that the lifting height meets the requirement.
4) Select Continue to save parameters and exit the window.
7.5.8 Probe to Horizontal Position on ISE Part (Optional)
Alignment index:
The probe has its tip above the ISE sample injection port but deviates slightly from the central hole. The probe
tip should not contact with the inwall of the sample inject port.
Alignment methods and procedure:

Figure 7-21 Alignment procedure

1) Ensure the ISE has been installed.


2) Select Probe to Horizontal Position on ISE Part.
3) According to Step 3, select the down arrow button to lower the probe to above the ISE sample injection
port. Select the left/right arrow buttons to adjust the probe radially till it is 1mm away from the center
of the sample injection port or deviating slightly from the central hole. The probe tip should not contact
with the inwall of sample inject port.

Figure 7-22 Probe to Horizontal Position on ISE Part

4) If the probe fails by adjusting parameters, loose the screws fixing the ISE module on the chassis, and
then move it till requests are met.
5) If the problem still remains, use a cross head screwdriver to loosen the screws on the ISE module and
move it till requests are met.
6) The operation in Step 3 is verified in Step 4. If requirements are not met, return to Step 3.

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7) Select Continue to save parameters and exit the window.


7.5.9 Probe to Vertical Position on ISE Part (Optional)
Alignment index:
The probe has its tip level with the third transition line in the sample injection cup.
Alignment methods and procedure:

Figure 7-23 Alignment procedure

1) Check if the Probe Rotary to ISE alignment has been completed.


2) Select Probe to Vertical Position on ISE Part.
3) According to Step 3 on the screen, select the up/down arrow buttons to make the probe tip level with
the third transition line inside the sample injection cup. (You can see three transition lines, and the
probe tip shall be level with the one at the bottom, as shown in the figure below.)
4) The operation in Step 3 is verified in Step 4. If requirements are not met, return to Step 3.
5) Select Continue to save parameters and exit the window.

Probe tip levels


with this line

Figure 7-24 Probe to Vertical Position on ISE Part

Note
Alignment of each position is verified the next step.
Alignment parameters can be saved only after each procedure is complete. Another alignment is required if a
procedure is terminated.
If the parameter is not successfully configured or out of range, the parameter range will be displayed by the
alarm message and re-perform the alignment.

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7.6 Mixer Unit


Select Utility—>Maintenance—>Alignment—>Mixer Unit. The window is as shown below.

Figure 7-25 The window of Mixer Unit

7.6.1 Mixer to Horizontal Position on Reaction Carousel


Alignment index:
The mixer (mixer alignment lever BA48-J16) can pass the through hole of the mixer horizontal position alignment
cuvette (BA24-J05) in position 31# of the reaction carousel.
Alignment methods and procedure:

Figure 7-26 Alignment procedure

1) Install the mixer alignment fixture BA48-J16, and then select Mixer to Horizontal Position on
Reaction Carousel.

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BA48-J16:
Alignment
lever
(inserted to
the end)

Figure 7-27 mixer alignment fixture

2) Place the mixer horizontal position alignment fixture (BA24-J05) in position 31# of the reaction
carousel.
3) According to Step 3 on the screen, adjust the mixer position to align with 31# cuvette.
a) Click the Up and down arrow to move the mixer to above the fixture.
b) When the mixer aligns with the center of the fixture, use M3 Hexagon wrench to
pretighten the screw to the extent that the arm cannot swing freely but the
arm can rotate when you push it with your hand.
c) Rotate the arm downward and pretighten the screw and then rotate it upward and
then tighten the radial screw.

Because the radial


screw is located at
the lower side, you
need to rotate the
BA48-J16
mixer to leave
enough space to
tighten the radial
screw.

BA24-J05

Figure 7-28 Mixer to Horizontal Position on Reaction Carousel

d) Move the mixer to above the reaction carousel fixture and tighten the
circumferential screw.
4) If the lever is not correct horizontally, select the left/right arrow buttons in Step 4 to adjust so that it can
align with the alignment tool.
5) The operation in Step 4 is verified in Step 5. If requirements are not met, return to Step 4.
6) Select Continue, remove the fixture and store it properly.
7.6.2 Mixer to Horizontal Wash Position
Alignment index:
The mixer (mixer alignment lever BA48-J16) can enter the through hole of the wash well alignment fixture
(BA40-J76) and the gap between the probe’s wash well and the fixture shell is even.
Alignment methods and procedure:

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Figure 7-29 Alignment procedure

1) Select Mixer to Horizontal Wash Position.


2) Select Continue. Place fixture BA40-J76 in the mixer wash well.
3) Click the up and down arrow to move the mixer alignment tool to above the wash well fixture. Click left
and right arrow to make the mixer alignment tool align with the center hole of the wash well fixture. If
deviation exists, loosen the screw of the wash well to adjust the position of the wash well till the
requirements are met.

BA40-J76

Figure 7-30 Mixer to Horizontal Wash Position

4) The operation in Step 2 is verified in Step 3. If requirements are not met, return to Step 2.
5) Remove the fixture. Select Continue to save parameters and exit the window. Install the real mixer.
7.6.3 Mixer to Vertical Position on Reaction Carousel
Alignment index:
The lever lowers into the cuvette, the gap between which the go gauge of the mixer alignment tool (BA80-J20-
001) can pass and the no-go gauge cannot.
Alignment methods and procedure:

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Figure 7-31 Alignment procedure

1) Select Mixer to Vertical Position on Reaction Carousel. Make sure the mixing position is holding a
cuvette instead of alignment tool.
2) Select Continue. After the system resets mechanically, the sample mixer moves into the cuvette.
3) Select the up/down arrow buttons, and insert the alignment tool (BA80-J20-001) between the mixer's
straight-knurled column and cuvette edge. Gently push the alignment tool to observe if the Go Gauge
can easily pass while the No-go Gauge cannot.

The Go Gauge (thinner


side) can easily pass while
the No-go Gauge (thicker
side) cannot.

Figure 7-32 Mixer to Vertical Position on Reaction Carousel

4) The operation in Step 2 is verified in Step 3. If requirements are not met, return to Step 2.
5) Select Continue to save parameters and exit the window.

7.7 Alignment of Cuvette Wash Unit


Select Utility -> Maintenance -> Alignment -> Wash Station. The window is as shown below.

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Figure 7-33 The window of Wash station

7.7.1 Setting Parameters of Best Alignment Position


Alignment methods and procedure:
Search the BS-240 Series Parameter Configuration Table for the best alignment cuvette segment number. Input
the best cuvette segment number of the cuvette wash unit, and the maximum deviation cuvette segment in
positive and negative directions, and then click "Configure". Select "Search" and check whether the
configuration result is correct.

7.7.2 Cuvette Wash Station Home


Alignment index:
The wash probes can pass through the hole of the wash probe fixture and no obstruction exists.

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Figure 7-34 Alignment procedure

1) Select Cuvette Wash Station Home.


2) Remove the cuvette segment of the optimal cuvette position and place the fixture. Click Continue.
3) According to Step 3 on the screen, use an M4 hexagon wrench to loosen the two screws on the wash
probe conversion board, adjust the wash probes till the wipe blocks can move vertically in the hole of
the alignment tool, and the wash probes of other phases are in the center of the cuvettes. When
requests are met, tighten the two screws gradually. Exercise caution to prevent deforming the probes.

the wash
probe
fixture two screws on the wash
probe conversion board

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Figure 7-35 Alignment of Wash Station

4) Remove the alignment tool and install the cuvette segment. Click the up and down arrow to move the
wash probes. The wash probes move smoothly and do not interfere with the interior of the cuvette. If
the requirement is not met, return to step 3 and align again.
5) The reaction carousel rotates to the forward maximum deviating cuvette position. Click the up and
down arrow buttons to move the wash station so that the wipe block and wash probes are in the center
of the cuvettes and can move smoothly.
6) The reaction carousel rotates to the reversed maximum deviating cuvette position. Click the up and
down arrow buttons to move the wash station so that the wipe block and wash probes are in the center
of the cuvettes and can move smoothly.
7) Select Continue to save parameters and exit the window.
7.7.3 Cuvette Wash Station Height
Alignment index: When the wash station lowers to the vertical washing position, the wash probes bounce for
0.7 to 0.8mm, which means that the clearance gauge can pass with 0.7mm through the gap between the anti-
collision blocks and the wash station bracket and it cannot pass with 0.8mm.
Alignment methods and procedure:

Figure 7-36 Alignment procedure

1) Select Cuvette Wash Station Height.


2) Check if the wipe blocks can insert into the center of each cuvette. Select Continue.
3) When the wash probes move vertically to the bottom of the cuvettes, make them contact the cuvette
bottom, and select Small Step or Large Step. Adjust the probes with the up/down arrow buttons while
measuring the lifting height with 0.7mm and 0.8mm clearance gauge. Make sure the smallest gap
between the anti-rotation blocks and the wash station bracket can let go a 0.7mm clearance gauge
but 0.8mm gauge cannot pass the gap.
4) Verify Step 3. If requests are not met, return to Step 3, and select the up/down arrow buttons to adjust
the mixer till requests are met.
5) Select Continue to save parameters and exit the window.
7.8 Bar Code Unit (Optional)
7.8.1 Bar Code Sticking Requirements
1) The bar code label should be clear, and not vague, dirty or scratched.
2) The sample bar code label should be stuck upright and plane and 9mm away from the tube bottom.

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Bar
Sample tube
code
area

9mm

Figure 7-37 The sample bar code Sticking Requirements

3) The reagent bar code label should be stuck in the front side below the bottle opening, and in
the middle of the vertical and horizontal directions.

Do not stick to the


corner

Do not stick to the


corner

Figure 7-38 The reagent bar code Sticking Requirements

7.8.2 Bar code Unit


Select Utility -> Maintenance -> Alignment -> Bar code unit. The window is as shown below.

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Figure 7-39 The window of Bar Code Unit

7.8.3 Bar Code reader model Adjustment


Select Utility -> Maintenance -> Alignment -> Bar code unit->Bar code reader model configuration
Note: The barcode scanner model configured for the instrument is MS-3.

Figure 7-40 Bar code reader model configuration

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7.8.4 Bar Code Reader Position Adjustment


Alignment index:
1) The light beam transmitted from the bar code reader can pass through the sample bar code slot and the
reagent bar code slot on the bar code reader alignment tool (BA24-J03).
2) The bar code in 1~5# on the outer ring and 1~5# positions on the middle ring of the sample/reagent
carousel can be identified correctly and completely and displayed on the screen.
Alignment methods and procedure:
1) Select Bar Code Reader Adjustment.

Figure 7-41 Alignment procedure

2) Use cross screw driver to remove the tube holder in 26# and 27# position on the outer ring and place
the bar code alignment tool BA24-J03(The slot facing the outside of the carousel. )Click Continue.

Insert the positioning


Reagent bar code
pin at the lower side of
scanning slot
the BA24-J03 into the
two holes after the tube
holder is removed.

Sample bar code


scanning slot

Figure 7-42 Bar Code Reader Position Adjustment 1

3) Loosen the four screws of the bar code reader and its bracket. Adjust the angle of the light beam to
make it pass through the sample bar code slot. Use the left and right arrow on the software screen to

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adjust the position until the parameters of the sample/reagent carousel meet the requirement.

Place a white paper in


front of the alignment tool.
When all the scanning
light passes through the
slot, a complete straight
Adjust the screw here (two line will fall on the paper.
more at the lower side) to
adjust the bar code reader
position.

Figure 7-43 Bar Code Reader Position Adjustment 2

4) Check again if the light goes through the slot on the fixture. If not, return to previous step to make
adjustment till requests are met.
5) Remove the alignment tool. Place the bar coded sample tube and reagent bottle respectively in 1~5#
position on the outer ring and middle ring. When the bar code is scanned, the bar code reader indicator
turns yellow-green and the software screen prompts the identification rate is ≥80%. Scan the bar codes
and check if the bar codes are correctly identified.

When bar code is


identified, the indicator
here turns yellow-green.
When no bar code is
scanned, it is red.

Figure 7-44 Bar Code Reader Position Adjustment 3

6) If all bar code cannot be read, check if the light direction meets the requirement and the bar code
reader works normally.
7) Select Continue to save parameters and exit the window.

Note
• If Bar Code Reader Adjustment has been performed, the bar code system will be initialized and only Code
128 will be recognized. If the client uses other code systems, you need to click Utility→System
Setup→Bar code, re-check the bar code option.

7.8.5 Bar Code Stability Test


Alignment index:
1) When the sample/reagent carousel rotates for several circles, the bar code identified in the same position
should be the same.
2) The bar code in all positions of the sample/reagent carousel can be identified correctly and completely and
displayed on the screen. Randomly choose 3 bar code on the outer ring and inner ring, and check that the
bar code displayed on the screen is same as that on the bar code label.
Note: Before doing the bar code stability test, please confirm the information of the bar code system used. If it
is not Code 128, you need to click Utility→System Setup→Bar code,and then select the corresponding bar
code.
Alignment methods and procedure:
1) Place bar-coded sample tubes in position 1-40# on the outer ring and bar coded reagent bottles in
position 1#-40# on the middle ring of the sample/reagent carousel.

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2) Select Bar Code Stability Test, set the scan circle as 10, and select Start.
3) After scanning, check if the identified bar code meets the requirement. If different bar code is read in
the same position, the position will be indicated in red.
4) If the stability test fails, find the reasons and take actions according to the following probabilities:
a) Check if the failed bar code meets the printing standard, the bar code label is not tilting, dirty or
damaged and has been applied in correct position.
b) Check if the glass scanning window is clean without contamination.
c) The scanning window is not blocked by the sponge cushion.
d) If none of the above happens, replace the bar code reader, adjust it properly and do the test again.
e) Generally, the three methods above are enough to troubleshoot the problem.

Figure 7-45 Sample Bar Code Stability Test

Note
• Check that the sponge cushion seals the bar code reader completely without blocking the scanning light.
Otherwise, adjust the bar code reader again
• After alignment, check if the screws on the bar code reader and conversion board have been tightened

7.9 Hydropneumatic Unit


Select Utility—>Maintenance—>Alignment—>Hydro Unit. The window is as shown below.

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Figure 7-46 The window of Hydro Unit

7.9.1 Preparations before Alignment


1) Check if all tubes have been connected correctly.
2) Check if the wash tubes on the 4-phase wash probes assembly have been connected properly. If not,
first connect the 4-phase aspirating tubes. Visually check that the 4-phase aspirating tubes are
inserted with the same depth and not twisted, and all tubes are smooth without crossover or protrusion.
3) Check if the solenoid valves have been connected to the correct cables.
4) The diluted wash solution tank holds sufficient diluted wash solution.
Cuvette Type Dilution ratio of diluted wash solution 1
Plastic Cuvette 10 portions of DI water:1 portion of concentrated
wash solution
5) Fill the water tank with sufficient water.
6) Connect the water supply tube to the analyzer, and connect the high-/low-concentration waste tanks.
7) Check if the inlet filter assembly has been installed.
8) Remove the pseudo probe from the probe arm, and install the real probe instead.
Installation requirements:
1) Gap between the probe plate and the arm surface is not allowed. Otherwise, check the retaining bolt
and tube, because the tube's elasticity will also affect the probe's bouncing;
2) A washer has been applied on the retaining bolt, and the nut has been tightened;
3) After fixing the probe with bolt and spring, manually lift the probe and release it, and check that the
probe can bounce back freely through the spring;
4) Adjust the liquid level detection board and the relative positions of the probe plate and photocoupler
so that the probe plate is in the middle of the photocoupler.

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7.9.2 Checking Floater and Valve Status

Figure 7-47 The window of Valve/Floater/Pump Alignment

Manually switch the floater status one by one according to the table below, and then select Query to refresh the
floater status. Check if the actual fluid level of each container is the same as the status displayed on the screen.
Tank Name Floater Status Screen
Display
Water tank, Diluted Wash Solution Floater triggered (high Not empty
Tank level)
Water tank, Diluted Wash Solution Floater not triggered (low Empty
Tank level)
High Concentration Waste Tank Floater triggered (high Full
level)
High Concentration Waste Tank Floater not triggered (low Not Full
level)

When the valve voltage is normal


1) Select Utility—>Maintenance—>Alignment—>Hydro Unit—> Valve/Floater/Pump
Alignment, see Alignment, select the corresponding valve to Turn on/Turn off, and you can hear
the crisp sound.
2) The valve is powered by DC 12V, the multimeter is adjusted to DC, the black probe is grounded,
and the red probe measures the red and black wires respectively.
Valve Red wire voltage Black wire voltage
Turn on 12V 0V
Turn off 12V 12V

When the Pump voltage is normal


1) Select Utility—>Maintenance—>Alignment—>Hydro Unit—> Valve/Floater/Pump
Alignment, see Alignment, select the corresponding Pump to Turn on, and you can feel the
vibration of the pump by hand.
2) The Pump is powered by DC 12V, the multimeter is adjusted to DC, the black probe is grounded,
and the red probe measures the red and black wires respectively.

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Pump Red wire voltage Black wire voltage


Turn on 12V 0V
Turn off 12V 12V
7.9.3 Syringe Check
1) Select Syringe Check.
2) Click DI Water Syringe and Wash Solution Syringe successively. No alarm means that the syringes
are OK.

Figure 7-48 The window of Syringe Check

7.9.4 Fluidic Prime


1) Check the Syringe, Floater and Valve Status.
2) Select Utility—>Maintenance—>Alignment—>Hydro Unit
3) Select Fluidic Prime.

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Figure 7-49 The window of Fluidic Prime

4) Check the outlet tube is connected and remove the wash probes and put it into an empty container.
5) Click Continue and Start to perform auto prime until the flow of phase 1-3 probes is continuous. Click
Stop and OK to move to the next step. If the prime is not successfully completed, set the prime cycle
again.

Figure 7-50 prime wash station

6) Install the wash station and execute auto wash according to the software prompt. Make sure no
overflow occurs.

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7) Click Continue. According to software screen, perform mixer exterior wash until the mixer wash well
can spray water continuously. Click Stop and OK to move to the next step.

Figure 7-51 Clean/Prime Mixer Exterior

8) Click Continue. According to software screen, perform probe interior/exterior wash until the probe
wash well can spray water continuously. Click Stop and OK to move to the next step.
Note: If the probe syringe has air bubbles, please remove the probe syringe and push and pull syringe
plunger repeatedly until air bubbles are removed completely from syringe. Click Stop and then re-install the
syringe. Making the V-shape slot level to scale 7.5 of the syringe. Click OK to move to the next step. Note: when
removing the syringe, do not drop the washer, refer to Replace Syringe.

Figure 7-52 Clean/Prime Probe Interior and Exterior&Probe syringe

9) Select Continue to reset the mechanical parts for 3 times. Check that the mechanical parts are moving
normally.
10) Select Continue.
11) Select Exit to finish the alignment procedure. Select Maintenance -> Parameters -> Parameter
Configuration->Wash Unit to check if the value of “is fluidic prime performed” is 1. If yes, the
prime is successful.
7.9.5 the volume of the reaction liquid during cuvette washing process
Alignment index: After the Auto Wash is done, the amount of liquid remaining in the reaction cup, the
liquid level is 5-10 mm from the reaction cup opening.
Alignment methods and procedure:
1) Select Utility -> Maintenance -> Alignment -> Pyrology Unit -> Reaction Carousel Temperature
Curve. The window is as shown below.

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Figure 7-53 The window of Reaction Carousel Temperature Curve

2) In the red box above, enter the number of Auto Wash 5 cycle, click to start.
3) Observe the action during cleaning. After the cleaning mechanism is lifted, the distance between the
liquid in the reaction cuvette and the cuvette mouth should be 5-10mm. If it is not good to watch, the
corresponding reaction cuvette can be taken out after the end to check the liquid volume of the reaction
cuvette.
4) If the cuvette has a small amount of liquid, check the infusion line and fittings.
If the cuvette contains too much liquid or overflows, check if the aspiration is normal.
7.10 Pyrology Unit
Select Utility -> Maintenance -> Alignment -> Pyrology Unit. The window is as shown below.

Figure 7-54 The window of Pyrology Unit

7.10.1 Configuration of Sensor Parameters


Alignment index: Configure the parameters correctly according to the rated values of the reaction carousel
sensors, and configure the △AD value of temperature sensors.
Alignment methods and procedure:
1) Select Sensor Configuration.

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2) According to the sequence number on the temperature sensor, contact the headquarters to find the
resistance of rated temperature points (0, 37 and 100), select sensor 1 and input the resistance for
each temperature point, and then select Calculate.
3) When a dialog box pops up indicating qualified sensor, select Configure to configure the parameters
to the relevant sensor.
4) Observe the △AD value of PCB, and input it in the edit boxes at lower-right corner of the window for
sensor 1. Select Configure, and then select Search to verify them.
5) When configuration is complete, select Exit.

Figure 7-55 The window of Sensor Parameters

7.10.2 Observe Temperature Curve


Alignment index:
The reaction carousel temperature is within 36.7~37.3 ℃ and reagent preheating temperature is within
43~47 ℃.
Alignment methods and procedure:
5) Select Reaction Carousel Temperature Curve.
6) Select Turn on heater.
7) Select Sensor temperature curve 1(reaction carousel heating curve).Select Start in the temperature
curve area. Check the reaction carousel temperature curve for 1 minute when the curve is steady and
the temperature reaches 37℃. The curve of sensor is straight and stable with value within 36.7~37.3℃.
8) Check the reagent preheating curve in the same way. Sensor temperature curve 2 is the reagent
preheating curve.
9) Select Stop. Select Exit to close the window.

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Figure 7-56 Reaction Carousel Temperature Curve

7.10.3 Wash Solution Temperature Control


Alignment index:
The temperature of cleaning fluid and wash solution is within 39℃-49℃.
Alignment methods and procedure:
1) Select Wash Station on the Parameter Configuration window, and check that the value of Fluidic Prime
Complete is 1. Select Utility -> Maintenance -> Alignment -> Pyrology Unit -> Wash Solution
Temp Curve.
2) Select Deionized Water Heater and Wash Solution Heater, and then select Turn On.
3) Select Start in the temperature curve area, and then observe if the temperature curves of cleaning
fluid and wash solution are straight and steady (for 2 minutes according to the computer time). Check
that the average temperature of cleaning fluid and wash solution is within 39℃-49℃.
4) Select Stop. Select Exit to close the window.

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Figure 7-57 Wash Solution Temp Curve

7.11 ISE Unit


Select Utility -> Maintenance -> Alignment -> ISE Unit. The window is as shown below.

Figure 7-58 ISE unit Alignment

7.11.1 Module Initialization


Handshake:
When the ISE module shakes hand with the system, click "Start". When data returns "<ISE!>", the data is
displayed on the display bar and the next line displays "Handshake successful" indicating that the module is
normally communicated with the system, as shown in the figure below.
Purger A:
a) On the Purge A interface, define the parameters as below, interval time: 5S, cycle count: 30 times.
b) Click "Start" and wait until "<ISE!>" returns on the current data display area, indicating that a calibrator
A purging cycle is completed. During this, pump A and waste liquid pump rotate clockwise and pump
liquid out. Repeat the operation above for several times and you can see that calibrator A tube is
gradually filled with liquid and drained to the dispensing port.
c) In this case, click "Stop". The software will stop purging after the current calibrator A purging cycle is
completed.
d) If no liquid flow is detected or liquid flow is slow after several executions, check whether the hose
connector is properly and reliably connected and whether the peristaltic pump works normally.
Purge B:
The operator for "Purge B" is the same as that for "Purge A".
Air Bubble Detector Calibration:
a) Click "Start" under Part Check - Pump Check.
b) After calibration, wait until the current data display area returns calibrated data (data format: <BBC A
xxx M xxx L xxx>). The next line displays "Air bubble detector calibrated", indicating the debugging is
successful.
c) If the current data display area displays calibrated data as <ERC BBC x000000>, the next line displays
"specific error" (marked with red text) according to the returned error code. For error codes, Table 7-3
ISE Error Codes..
Pump Check:
a) Place a test tube filled with deionized water in the W position of the sample carousel;

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b) Click "Start" under Part Check - Pump Check.


c) Operate as instructed on the screen. After calibration is complete, wait until the current data display
area returns data as <PMC A xxxx B xxxx W xxxx> (each value shall fall in between 1500 and 3000),
and the next line displays "Pump Check Correctly", indicating that the debugging is successful.
d) If the current data display area returns calibrated data as <ERC PMC x000000>. For x, see Appendix.
The next line displays "specific error" (marked with red text). For error codes, see Table 7-3 ISE Error
Codes.
Wash:
Prepare sufficient wash solution in the sample carousel (usage in each wash operation is 100 ul), and then input
the level of the wash solution in the cuvette in "Set liquid level in cuvette", and click "Clean". Wait until the data
area returns <ISE!> (wait for about 160 s). The next line displays "Clean completed", including the wash is
complete.
Two-point calibration:
a) Click "Start" in the "Two-point calibration" area to display the confirmation dialog for fluidic tube wash.
If it is possible to check that the last wash operation has been waited for more than 15 min, directly
click OK; otherwise, wait until the countdown time ends.
b) After the countdown time ends, automatically execute the two-point calibration testing. After the testing
is complete, the current data display area returns the calibration result "< Na xx.xx K xx.xx Cl xx.xx
xxxxxxxx>". ;
c) If an error code displays during calibration, repeat several times of two-point calibration. If the problem
persists, replace the corresponding electrode reporting error as instructed by error message. For error
codes, see Table 7-3 ISE Error Codes.

7.11.2 ISE Error Codes


Note: Error codes will be affixed to result strings. An error code is in format of 7 ASCII characters, such as
<1234567>. Each digit represents a specific meaning, as shown below:
Table 7-3 ISE Error Codes

Digit #1 Digit #2 Digit #3 Digit #4 Digit #5 Digit #6 Digit #7


Error Type (1) (2) (3) (4) (5) (6) (7)
Air bubble included S 0 0 0 0 0 0
in the sample
Air bubble included A 0 0 0 0 0 0
in the calibrator A
Air bubble included B 0 0 0 0 0 0
in the calibrator B
Air bubble included C 0 0 0 0 0 0
in the wash
solution
Air in Segment M 0 0 0 0 0 0
Pump calibration P 0 0 0 0 0 0
error
No fluid in F 0 0 0 0 0 0
electrode pipes
Air bubble D 0 0 0 0 0 0
monitoring error
Chip reading error R 0 0 0 0 0 0
Chip writing error W 0 0 0 0 0 0
Saving calibration Q 0 0 0 0 0 0
result error
Command error T 0 0 0 0 0 0
No error 0 0 0 0 0 0 0
Na+ 0 1 1 1 1 1 1
K+ 0 2 2 2 2 2 2
Na+,K+ 0 3 3 3 3 3 3

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Cl- 0 8 8 8 8 8 8
Cl-,Na+ 0 9 9 9 9 9 9
Cl-,K+ 0 A A A A A A
Cl-,K+,Na+ 0 C C C C C C
The error types in the table above are described as below:
1) - Air bubble/hardware;
2) - Electrode voltage overflowed during calibrator B calibration or blood measurement;
3) - Electrode voltage overflowed during two-point calibration or calibrator A calibration in blood
measurement mode, or calibrator B calibration in urine measurement mode;
4) - Electrode voltage noise during calibrator B calibration or blood measurement;
5) - Electrode voltage noise during two-point calibration or calibrator A calibration in blood measurement
mode, or calibrator B calibration in urine measurement mode;
6) - Voltage drift during calibrator A calibration in blood measurement mode, or slope drift
during two-point calibration;
7) - Exceeds the slope or module measurement range;

8 Installation
8.1 Installation Procedure
8.1.1 Installation Procedure
The approximate installation procedure of the analyzer is as follows: for your reference:
Table 8-1 Analyzer installation procedure

Classification Main Content Remarks


Before Check if the analyzer and reagents are arrived, check The LIS and water unit
installation whether the water unit, UPS, LIS, etc. are prepared in are not required
advance, confirm the trainees, and confirm that the arrived
reagents have been refrigerated.
Prepare tools and alignment fixtures
Download relevant information on TDP: latest software (if Please search for the
new software is released, and the version is higher than the specific file path on the
factory analyzer); download the maintenance manual for TDP
backup
Once again, confirm that the above is correct.
During Check the quantity of the goods and confirm whether the In case of any missing,
installation installed reagents are refrigerated. timely give feedback
Check Packing List
Unpacking
Transfer the analyzer to the department installation location
Remove the analyzer fixed parts and foam tape
Install accessories
Connect the pipeline
Install the PC
Software Installation
Start the analyzer
Adjust the positions
Prime the fluidic system
Set the analyzer, and initialize maintenance records
Apply for testing for performance verification
Record data, and fill in the installation report
Assist the LIS in connection (if any)
Train the customer for operations and simple troubleshooting
Print template settings (refer to the corresponding chapter of
the instruction manual)
Confirm that the analyzer works normally, and the pipeline
and wire are neat and beautiful.

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confirming the above items are correct


After Regularly visit the customer after installation, and take the The customers whose
installation initiative to care analyzers are newly
installed have more
operational problems

8.1.2 Installation Time Consumption


The estimated time spent in the installation procedure is as follows:
Table 8-2 Estimated time spent in the installation procedure

No. Work Content Time


Consumption
Step1 Confirm the installation environment, water and electricity are About 1 H
qualified, check the quantity of goods, and installed reagents,
and check the packing list
Step2 Disassemble the analyzer and accessory box About 1 H
Step3 Connect the accessories and fluidics system About 0.5 H
Step4 Install the PC About 0.5 H
Step5 Install the software (if the control software should be About 0.5 H
upgraded, about +1H will be required)
Step6 Startup About 0.5 H
Step7 Confirm and adjust the positions About 0.5 H
Step8 Prime the fluidic system About 0.5 H
Setp9 System Setup About 1 H
Step10 Verify performance and test the analyzer with running water About 2 H
Step11 Train the customer for operations and simple troubleshooting About 4 H
Step12 Reconfirm and check the analyzer and software, and perform About 1 H
5S on site
Step13 Other (such as LIS connection, signature and acceptance) About 1 H
Total About 14 H

8.2 Check before Installation


8.2.1 Installation Environment
▪ Altitude:-400~2,000m
▪ The system is for indoor use only.
▪ The bearing platform (or ground) should be level (with gradient less than 1/200).
▪ The bearing platform (or ground)should be able to support at least 100Kg weight.
▪ The installation site should be well ventilated.
▪ The installation site should be free of dust.
▪ The installation side should not be in direct sun.
▪ The installation site should be kept away from a heat or draft source.
▪ The installation site should be free of corrosive gas and flammable gas.
▪ The bearing platform (or ground) should be free of vibration.
▪ The installation site should be kept away from large noise and power supply interference.
▪ Keep the system away from brush-type motors and electrical contact device that is frequently switched on
and off.
▪ Do not use such devices as mobile phones and radio transmitter near the system.
▪ Operating temperature: 15°C-30°C with fluctuation <2°C/H.
▪ Relative humidity: 35%-85%, without condensation.
▪ Provide air conditioning equipment if the room temperature does not meet the requirements.
▪ Install the equipment near a sewer for convenient discharging of waste liquid.
▪ Dimensions before packing: 690mm(length)×580mm(depth)×595mm(height)
▪ Dimensions after packing: 825mm(length)×695mm(depth)×795mm(height)
8.2.2 Configuration Check
▪ BS-240 analyzer
▪ Packing list of accessory kit

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▪ Packing list of ISE accessory kit (for ISE module only)


8.3 Installation Requirements
8.3.1 Space and Accessibility Requirements for Installation

Wall
Minimum 500

Maximum 3000

Minimum 500

Operation Unit
708

Analyzer
Minimum 500

1180
Front

Unit: mm

Minimum 500

Figure 8-1 System Clearance

8.3.2 Power Supply and Noise


▪ Power supply: 220V: 220-240V~ 50Hz, 220/230V~ 60Hz; 110V: 110/115V~ 60Hz. Voltage fluctuation: +/-
10%. Line frequency: +/-3Hz. Three-wire power cord with good grounding performance (ground voltage ≤
5V).
▪ The instrument should be powered by a properly-grounded power supply no less than 3000VA, and the
mains socket used to connect the instrument should have its load no less than 10A.
▪ Keep the instrument at least 2.5m away from the main socket.
▪ If you are going to use a UPS to power the instrument, make sure that the UPS can provide power supply
greater than or equal to 3000VA/2100W.

WARNING
• Make sure the power socket is grounded correctly. Incorrect grounding may lead to electric shock or
equipment damage.
• Measurement of ground voltage:
• First confirm that the neutral and ground wires cannot be shorted, set the multimeter to the AC 250V scale,
connect the black probe to the earth wire and the red probe to the live wire and neutral wire. If grounding
is proper, the voltage between earth wire and neutral wire should be less than 5V, and the voltage between
earth wire and live wire should be similar to that between live wire and neutral wire.
Check if the power socket outputs voltage meets the specified requirements and has a proper fuse installed.

8.3.3 Water Supply and Drainage


▪ Water quality: resistance no less than 1 (MΩ.cm@25°C) and conductance no more than 1μS/cm.
▪ Water temperature: 5-32°C.
▪ The 15L DI water tank is provided for holding DI water.
▪ DI water tank and diluted wash solution tank are placed on the ground. The tube must not be twisted or
pulled too tight in case the tube falls off the connector.
▪ The analyzer discharges high-concentration waste and low-concentration waste separately with high-
concentration waste discharged into a waste tank and low-concentration waste to the sewer or the low
concentration waste tank. Follow the local regulations for waste discharge.
▪ When Low-concentration waste is discharged to a sewer, the diameter of the discharge outlet must be no
less than 50mm and the height of the discharge outlet must be no higher than 100mm.

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▪ The low-concentration waste tube must be shorter than 5m. The tube must be routed from high to low
smoothly without U shape or V shape twists or turns otherwise the waste liquid may flow back into the
instrument. Refer to the figure below.

Waste outlet Waste outlet Waste outlet

Waste tank Waste tank Waste tank

Waste outlet Waste outlet Waste outlet

Discharge outlet Discharge outlet Discharge outlet

Biohazards
Dispose of liquid waste according to the local regulations.

CAUTION
The supplied water must meet the requirements of water quality; otherwise, unqualified water may result in
incorrect test results.

8.3.4 Computer Requirements


Refer to 6.2.1 Computer Requirements (for International Customers).
8.4 Installing the Analyzer
8.4.1 Unpacking
1) Please check the packing list before unpacking, including: biochemical host, accessory box, deionized
water tank, diluted wash solution tank, high concentration waste tank, low concentration waste tank,
wash solution, ISE module accessory box (optional ISE).
Note: The checklist of the packing list is recorded in the BS240 Installation Acceptance Report,
see Appendix A.1 BS-240 Installation Acceptance Report.
2) The main unit of the biochemical analyzer weighs about 100 kg. You are recommended to use the
forklift to remove it from the truck. Check whether the anti-dumping indicator of the main box becomes
red (if so, the analyzer may be dumped).

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Figure 8-2 Anti-dumping indicator of main unit box

3) Use a flat-blade screwdriver to tilt the metal piece and remove the upper cover and side cover.

Figure 8-3 Remove the main unit box

4) Remove the screw with a wrench and remove the fixed angle iron so that the machine can be lifted.

Figure 8-4 Remove the fixed angle iron

The fixed angles and screws under removal are as shown below:

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Figure 8-5 the L fixing angle iron

5) Lift the main unit and place it on the bracket to ensure that the leveling feet of the main unit fit the
grooves in the bracket.

Figure 8-6 The leveling feet of the main unit fit the grooves in the bracket

8.4.2 Removing Packaging


1) Open the protective cover of the biochemical analyzer, and remove the tape and shock absorbing
foam on the face shell. Pay special attention that the shock absorbing foam behind the wash station
should be taken out, use a diagonal plier to cut off the fixing strap on the wash station.

Parameter list

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Figure 8-7 Remove tapes and foams

2) Properly save the parameter configuration table(Parameter list) attached to the reagent carousel. The
parameter configuration table contains the factory-corrected parameter information. If any parameter
is missing or changed, you can refer to this table to modify the parameter. (Recommended to take a
photo of it and save it in the hard disk of the client computer).
8.4.3 Installing Accessories
Remove the packaging and plastic from the countertop of the biochemical analyzer. Take out the probe package
box from the accessory box. Take out the white washer in the package, moisten it with water, and place it in the
metal connector of the probe.

Note: Keep the washer


carefully. If it is lost,
there is a spare washer
in the accessory box.

Figure 8-8 Install the washer of the probe

Installing the probe


1) Before installing the probe, remove the arm shell; loosen the screw that fix the probe by hand and take it
out.

If you cannot
loosen the
fixing screw
of the probe,
you can use
a flat-blade
screwdriver.

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Figure 8-9 Remove the arm shell; loosen the screw that secure the probe

2) Insert the probe through the probe hole on the arm of the probe, and align the hole on the shutter of the
probe to the column in the arm cavity.
3) Check again that the washer is inside the metal connector of the probe. If so, align the tube connector with
the connector of the probe and tighten it clockwise. If not, find it and install it in the metal connector before
connection.

Figure 8-1 Connect the metal connector of the probe

4) Make sure that the shutter of the probe is in the middle of the black sensor (on the level detection board).
If it is not in the middle position, check if the shutter is deformed, if so, correct it, and then insert the plug
connected to the end of the probe into the J1 connector socket of the level detection board.

Figure 8-10 Confirm the shutter of the probe in the middle of the sensor and connect the plug

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5) Insert the spring into the column in the arm cavity and tighten the screw compression spring.

Figure 8-11 Tighten the screw of the probe

6) Pinch the probe by the part near the probe arm. Push the probe upwards and then release it to check if the
spring works well, and if the probe can rebound in place. If it does, proceed to the next step. If not, check
if the spring is clamped or the screw fixed too tightly, and troubleshoot.

Figure 8-12 Check if the spring works well

7) After the installation is complete, turn on the main power switch and the analyzer switch, and observe that
the LED orange lamp numbered D2 on the circuit board in the probe arm flashes, indicating that the level
detection system is normal.
Note: Do not install the arm cover at this time. After waiting for the fluidic system priming, confirm that there is
no leakage at the connector of the fluidic system, and then install the arm cover, and then perform step 8.
8) Pinch the probe by the part near the probe arm. Push the probe upwards and then release it to check if the
spring works well. If it does, proceed to the next step. It not, it indicates that the arm cover is not installed
correctly. Reinstall the arm cover and check the spring until it can move freely.

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Installing the mixer


1) Take out the mixer from the accessory box and raise the mixer arm to the vertical top.
2) Screw the mixer vertically from one end of the large hole of the retaining screw until the end
surface of the mixer is flush with the end surface of the small hole of the retaining screw.
3) Install the mixer mounting hole at the uppermost end of the mixer motor shaft. Pay attention
that the close cooperation between the mounting hole and the motor shaft.
4) Tighten the mixer retaining screw clockwise and visually check that the mixer is vertical with
a straight reference, such as a ruler. If it is not vertical, reinstall it.
Note: If the retaining screw cannot be tightened by hand, you are recommended to use a
Monkey spanner and a Nipper pliers to fix it, but care must be taken not to over-force,
otherwise the motor shaft may be damaged.
5) After installing the mixer, confirm whether it is fixed firmly. Pull the mixer down by hand. If it
is not loosened, the installation is OK. If it falls off, re-fix it.

Keep the
sections flush.
Rotate the retaining screw clockwise.

Figure 8-13 Install the mixer

Check the Syringe


Check if the fixing screw of the syringe are loose, if so, loosen the screw and tighten.

Figure 8-14 Check the fixing screw of the syringe

8.4.4 Connect the pipeline


1) Fill the DI water tank with DI water.

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Note: If the client wants to connect directly to the water unit, skip this step.
2) Prepare the diluted wash solution with a ratio of 1 part of concentration solution and 10 parts of
deionized water, and fill the solution into the diluted wash solution tank.
3) Use the 2 filters configured in the accessory box to connect the connector of the deionized water tank
and that of the dilute wash solution tank, respectively. The filter is installed in the tube between the
deionized water tank (diluted wash solution tank) and the analyzer inlet, about 150 - 300 mm from the
end of the tube at the connection end of the analyzer inlet. After the filter is connected, the ends are
fastened with a clamp or a tie (for a tube with a severely deformed end, the end should be cut about
5 mm); the tube should be inserted into the root of the connector.
Note: The filter connector is not oriented.
Note: If the client is connected directly to the water unit, please connect the outlet of the water unit
directly to the water inlet of the analyzer with a tube, and install a filter in the middle of the tube.

Figure 8-15 Install the filters

4) For the filter connecting with the connector of the deionized water tank and that of the diluted wash
solution tank, place one end of the installed level sensor into the deionized water tank and into the
diluted wash solution tank, respectively, screw the screw cap, and connect the other end of the tube
respectively to the deionized water interface and to the diluted wash solution interface, and connect
them with the corresponding sensor interfaces; then for the connector of the high-concentration waste
tank, place one end of the level sensor into the high-concentration waste tank, screw the screw cap;
connect the other end to the high-concentration interface on the right side of the analyzer and install
the corresponding sensor interface; install the low-concentration waste tube.
5) If the analyzer is equipped with an ISE module, first remove the panel electrolyte plug of the ISE
sample port, remove the back plate, and put on the peristaltic pump tubes (3). The directions of the
tubes are as shown below.

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Figure 8-16 Install the peristaltic pump tubes

ISE reagent package installation

Open the small door on the left side of the instrument and remove the packaging foam and tape that
secures the ISE reagent pack reader.

Figure 8-17 Remove the packaging foam of ISE

Install the reagent package reader as shown below. When the installation is in place, you will hear the
sound, and ensure that the reader is installed in place. Otherwise, an alarm such as “ISE
communication error” will appear

Figure 8-18 Install the reagent package reader

6) After the analyzer is installed, the correct tube connections are as follows:

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Fluidic Port Panel


High
DI water Diluted wash Low conc. Low conc. Waste conc.
inlet solution inlet Waste outlet 1 Waste
outlet 2
outlet
High
Low level level
floater of floater of
Low level floater
diluted wash high
of DI water
solution conc.
waste

FL02 FL03

FL01
DI water tank Diluted wash solution Low conc. waste tank High conc. waste tank

Figure 8-19 Fluidic Port Panel

8.4.5 Connecting the Overall System


1) If a UPS is equipped, install the UPS and connect it to the UPS ground.
2) Connect the power cords and data cables of the main unit of the biochemical analyzer, the computer,
the printer, and the monitor. Be careful not to turn on the switch first.
3) Connect the serial cable of the computer and the main unit of the biochemical analyzer. Note that the
PC and the biochemical analyzer are connected by serial port, and the COM1 port on the PC is
selected.
8.4.6 Setting the PC
Please set the PC according to section 6.2 Computer Settings.
8.4.7 Software Installation
1) Install the latest version of the operating software, please refer to 6.3 Installation of Operating Software
for the specific installation steps.
2) Upgrade the control system. Please refer to 6.4.3 Upgrading Control System .
Note: If the software has not been updated after the analyzer is delivered, only the first step should be
performed when the analyzer is installed.
8.4.8 Starting up the System
1) Turn on the main power switch and the analyzer power switch.
2) Start the computer. The Workstation operating software is run automatically when the Windows is
started. You are also allowed to run the operating software by selecting the shortcut icon on the
desktop or in the Start menu. See the figure below. The system skips the initialization procedure when
detecting that the fluidic prime is not performed. Enter the username “ServiceUser” and password
“#BS8A#SEU” in the login window.

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Figure 8-20 startup screen

Figure 8-21 login screen

3) When the main screen is shown, select Utility -> System Setup -> Factory F2. Select 1 Optional
Modules, enable/disable ISE module, sample bar code and reagent bar code, probe clog detection
and then select OK. See the figure below:

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Figure 8-22 optional Modules window

8.4.9 Aligning the Analyzer


Confirm the position of the analyzer during installation of the new analyzer to avoid deviations in the position of
the analyzer during transportation or other conditions.
1) First, back up the parameters of the analyzer unit. For details, please refer to 6.7.3 Unit
parameter Backup.
2) Enter the Utility-Alignment screen.
3) Please follow the table below for alignment. For details, please refer to the index in the
reference.
Contents to be Checked and Reference
Aligned
Alignment of rotation positions of 7.4 Sample/Reagent carousel unit
reagent carousel and reaction carousel
Positions of the probe to wash well, 7.5 Probe unit
reagent carousel, and reaction carousel,
which is in the center of sample/cuvette
Positions of mixer to wash well and 7.6 Mixer Unit
reaction carousel, which is in the center
of wash well and cuvette
Position of auto wash probe 7.7 Alignment of Cuvette Wash Unit
assembly to reaction carousel, which is
in the center of cuvette
Syringe Check 7.9.3 Syringe Check
Requirements: The syringe has no
abnormal noise and no leakage, the fixing
screws are not loosened, and there is no
alarm during the test
Position of barcode scanner and 7.8 Bar Code Unit (Optional)
stability test (optional)

If there are no fixtures on site, refer to Appendix A.2 BS-240 Moving Parts Position Confirmation Guide (No
Alignment Tooling) for alignment.
8.4.10 Aligning the ISE (Optional)
If the analyzer is equipped with an ISE module, please align the ISE by referring to 14.2.3 Alignment of the ISE
module.

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8.4.11 Prime the fluidic system


Prime the fluidic system for the newly installed analyzer by referring to 7.9.4 Fluidic Prime.
8.4.12 Initial Maintenance Record
Select Utility -> Maintenance -> Maintenance to display the maintenance window. Confirm all scheduled
maintenance procedures and set up start time for them. The maintenance frequencies include Daily, Weekly,
Two-Week, Monthly, Three-Month, Six-Month, and Other. Select the Select All button on each maintenance
frequency tab page, and then select OK. The current date and time appears in the Date Performed column of
each maintenance procedure as shown in the figure below.

Figure 8-23 Scheduled Maintenance screen

8.4.13 Startup Initialization


When the fluidic prime is finished, exit the operating software and reboot the computer. The operating software
is automatically run and starts initializing. When the login window is displayed, enter the user name “Admin”
and password “#Admin”.

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Figure 8-24 Login screen

After entering the operating software, wait for the instrument to incubate for a period of time and then enter the
standby, perform the next step.
If the ISE module is selected, load ISE reagent on the Reagent/Calibration screen.
8.4.14 Importing and Configuring Chemistry Parameters of Mindray
Reagents
1) Select Utility -> Chemistries -> Config, and select Options to display the Option window.

Figure 8-25 Select Import to display the Import window

2) Select Load Default to display all Mindray reagent chemistries in the left column. Select Add All to add
all chemistries to the right column. Select Import to import the parameters and then select Exit.

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Figure 8-26 Import window

3) All Mindray reagent chemistries are displayed in the Available Chemistries column. You can delete
chemistries that will not be used in your laboratory.

Figure 8-27 Chemistry Configuration screen

4) Select OK to complete the chemistry configuration.


8.4.15 Running Water Test
Note: At present, the fully-sealed model (Close System 0 User-defined) is temporarily unable to perform the

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running water test. This step cannot be performed and skipped.


1) Select Utility →Chemistry Setup, Set a single-reagent chemistry "Water", with parameters
including: endpoint, positive reaction, primary wavelength 340nm, secondary wavelength
405nm, result unit U/L, decimal places of result 0.01, blank time (-9)-(-7), incubation time 0,
reaction time (13)-(22), sample volume 10, reagent volume R1:100.

Figure 8-28 Parameters of running water test

2) Load Wash D and Saline W.


Select Reagent →Reagent/Calibration
▪ On No. 39 position of the reagent carousel, put CD80 Conc Wash.
▪ On No. 40 position of the reagent carousel, put physiological saline.
Load Wash D and Saline W on the reagent screen, as shown in the figure below.

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Figure 8-29 Load Wash D and Saline W

3) Load the Water reagent.


In the sequence shown below, enter the Reagent/Calibration screen, select the reagent
position 1#, click Load, select the chemistry Water in the pop-up screen, and click Load.
Then click Exit, and click Load Complete. At the same time, fill the water reagent pack with
deionized water (not less than 10 ml) and place it in the 1# position of the reagent carousel.
(This manual takes 1# position as an example, and other positions can be selected in
practice)

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Figure 8-30 Load the water reagent

4) Select Reagent→ Cal Setup→ Calibration Setup


On the window, select the chemistry "Water", specify the K factor math model with K factor
10000, select Save and exit the window

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Figure 8-31 Water Calibration Setup

5) Sample preparation and application: In the sequence of the following figures, in the
Application screen, click the Water chemistry, then click Options, enter the number of
repetitions 40 in the pop-up Options dialog box, click OK to exit the current screen, and
click the OK button at the bottom right corner of the Application screen. Confirm that the
sample is placed at sample position 1 (not less than 1ml of deionized water), and then click
the Start Test button.

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Figure 8-32 Apply for the running water test

For the closed models, closed water chemistry can be imported,and use the following closed reagent bar code
in the bar code input frame on the reagent/calibration window to load reagents:
序号 R1 R2
1. 9UFTB7HCRqeJe 3gqPijd9f8MNI
2. 9WaK6MV9aqmgW MEmQX2R4B9nBF
3. DEYiVIXfbyOmP SGtVQN5hUWKPn
4. QyQON8GLfm25X Tq4FYUX7SLgN3
5. E6DytdyHaghjI 0E8f078KXOKiW
6. 0fVmHCVMT2bbe XDgdeMI32t2MQ
7. yUPVjPgChtEiI qbXSGQmGXi2gd
8. n2y70YKfq5Eyq f04eUDTCSJ7YW
9. S0EPQWmLEUD9L JRTTQLgiaKRP6
10. 9qbSRLWRZS9fX nnjJSi8Y5CSRW

6) Confirm the following item during the test:


▪ The mechanical movement of each assembly is normal, without abnormal alarms
(including optical, temperature control, mechanical, communication, etc.)
▪ The probe, mixer, and cuvette wash station are washed normally, without liquid hanging.

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▪ The cuvette wash station will be jacked up after dropped to the bottom of the cuvette
each time.
▪ The reaction curves of all the samples do not show periodic fluctuations or sharp convex
jump points, and the absolute value of the test result does not exceed 10.
8.5 Verifying Basic Performance
8.5.1 Checking System Status
1) Record the temperature and humidity of the working environment of the analyzer, the grid
voltage, the zero ground voltage, and the ambient atmospheric pressure in the BS-240
_Installation Acceptance Report.
2) In the operation software, select Utility→ Status, and record the temperature, hydro and
power status in BS-240 _Installation Acceptance Report.
8.5.2 Testing Movement Positioning Performance
1) Remove the reaction carousel cover, and the reagent carousel cover, and select
Utility→Maintenance→ Biochemistry Maintenance→Home, observe the movement of
the probe, the mixer and the two carousels. There should be no alarm prompt during the
whole procedure. The probe and the mixer should be centered in the wash well (the probe
positioned in the wash well should be aligned with the wash well outlet).
2) The vertical movement of the probe syringe is normal, without abnormal sound; the position
of the auto wash station down to the cuvette should be not rubbed, and should be located
in the center of the cuvette.
3) If any of the units is positioned abnormally, select Utility→Maintenance→Alignment, and
select the corresponding unit module to align the position parameters. The alignment result
is recorded in the BS-240_Installation Acceptance Report.
8.5.3 Testing Optical Performance
1) Select Utility→Maintenance→Biochemistry Maintenance→Photometer Check. The
absorbance of each wavelength of the newly installed analyzer should be in the range of
5000 - 8000. If it exceeds 8000, please check whether the installation of the light source
lamp is in place.
2) Select Utility→Maintenance→Biochemistry Maintenance→Cuvette Check. The new
analyzer should have no red marked cuvette, if there is, please replace the red marked
cuvette.
8.5.4 Testing Bar Code Performance
Select Utility→Maintenance→Alignment→Sample/Reagent Bar Code→Bar Code
Scanning Stability Test. Put a valid barcode (the installation reagent is carried with a
barcode, which can be placed in the sample/reagent carousel for scanning). The analyzer
can accurately read the barcode. Please refer to 7)Select Continue to save parameters and
exit the window.

Note
• If Bar Code Reader Adjustment has been performed, the bar code system will be initialized and only Code
128 will be recognized. If the client uses other code systems, you need to click Utility→System
Setup→Bar code, re-check the bar code option.
Bar Code Stability Test.
8.5.5 Testing Clinical Performance
1) Select Utility→Chemistry Setup→Configuration→Options, and import the default
chemistries.
2) Put the installed reagent, select Reagent Load to load the reagent at the
corresponding position. After the reagent loading is completed, be sure to click End
Load, otherwise other operations cannot be performed;

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Select End Load after reagent


loading is completed.

Figure 8-33 Reload the reagent

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3) Select Calibration Setup to add the calibration solution and set the calibration rules,
select the reagent item to perform Calibration Request, and click Run to perform the
calibration test. After the test is finished, Succeeded is displayed in Calibration Status.
If Failed is displayed, please check the reagent placement or calibrator preparation and
re-perform Calibration Request.
4) After the calibration test is completed, prepare 2 mL of fresh serum for the chemistry
request test, and the number of repetitions is 10. If the ISE module is selected, the
repeatability tests of K, Na, and Cl are also required. The test results are recorded in
BS-240_Installation Acceptance Report.
5) After the whole installation and alignment procedures are completed, train the
operators.
8.6 LIS Connection
If the client should be connected to the LIS, please refer to 12 LIS Connection Setting and Troubleshooting.
The LIS Protocol Manual (PDF version) is available in this way:
◼ Downloaded under the LIS directory on the TDP
8.7 Backing Up Data
After the analyzer is installed, you are recommended to back up the following data:
1) Back up the tested database file BA80.bak to the computer E drive. Refer to 6.7.1 Data backup.
2) Back up the aligned analyzer parameters to the computer E drive. Refer to 6.7.3 Unit parameter
Backup.
3) Keep the paper factory parameter list safely and take a photo of it to the computer E drive. For the
paper parameter list, see Figure 8-7 Remove tapes and foams.
4) If the LIS is connected, save the screenshot of the LIS setup screen in the software to the computer
E drive. Refer to LIS Setting backup.
8.8 Handling Exceptions in Installation
◼ Logistics problems include missing accessory, package damage, and instrument damage. Generally,
this type of problems should be borne by the logistics company.
◼ Instrument allocation problems include mismatch of order with deliverables and nonconforming
accessory (for example, connection cable or shield cover) package. Generally, this type of problems
is solved by applying for new materials.
◼ Loose cable, great offset, and rack deformation problems. Generally, this type of problems is solved
by experienced engineers.
◼ If the instrument reproduces any error that is difficult to rectify or unacceptable to the customers, see
available strategies to handle the problem.
8.9 List of accessories and functions
Due to different instrument configurations, the list of accessories will vary. Please refer to the actual paper list.
Part Number Description Qty Remarks
0000-10-10916 Cleaning Tool 2 /
0040-10-32307 Washer for Probe 1 /
043-000644-00 20ml Reagent bottle (Brown) 20 /
043-002208-00 40ml Reagent bottle (Brown) 20 /
043-006855-00 20 ml reagent bottle 10 /
BA30-20-15117 Reagent bottle labeling 50 /
BA31-20-41536 Reagent bottle cap (white) 25 /
BA31-20-41640 Reagent bottle cap (red) 25 /
The standard code system supported by the
instrument is used for the sample/reagent
047-014851-00 standard bar code 1
barcode scanner scanning function test.
See Figure 8-34 Standard Bar Code.
046-008696-00 Parameter List 1 Factory default parameter configuration list
Crosshead Screwdriver Tools, remove the cover, replace the light
3001-10-07207 1
Φ4.7*100 source, etc.
DA8K-10-14454 European power cord 1 /

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BA34-20-63652 serial communication cable 1 /


115-036571-00 Reaction case(surface dispose) 2 Reaction cups, 5 cups each, semi-permanent
high-concentration waste tank and diluted
043-002159-00 10L Water Tank 2
wash solution tank
DI water tank and low-concentration waste
043-000491-00 15L Plastic Tank 2
tank
The cap assembly of external diluted wash
115-037347-00 Wash Bung module 2
solution tank and DI water tank
The cap assembly of external high-
115-037348-00 Liquid waste bung module 1
concentration waste tank
Inlet filter for deionized water and diluted wash
043-000422-00 filter 2
solution filtration
tube.Φ9.525XΦ15.875nature low-concentration waste tube
082-000384-00 2
PVC 55~ 60°
Operation Card for Whole Blood /
046-009734-00 1
HbA1c(EN)
Plug the sample hole on the reagent plate
cover to reduce condensation water, Need to
049-000398-00 Plastic Plug 3
inform the customer to take out before the
test. See Figure 8-35 Plastic Plug.
A90-000009--- 3×100mm cable tie 20 bundling of various wires and tubes
Deionized water/ diluted wash solution inlet
082-002374-00 Tube3.2*6.4mm TPU 2
tube, high-concentration waste tube
046-008985-00 BS-240 Operator's Manual (EN) 1 /
046-008987-00 BS-240 Operation Card (EN) 1 /
BS-240 Maintenance Card /
046-008989-00 1
(EN)

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Figure 8-34 Standard Bar Code

Figure 8-35 Plastic Plug

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9 Preventive maintenance
9.1 Overview
9.1.1 Preventive maintenance
Preventive maintenance is a preventive measure taken by service personnel of Mindray or authorized by
Mindray with the aim of eliminating hidden troubles to ensure system reliability and achieve best performance
during operation. The Preventive maintenance cycle for the chemistry analyzer is one year and for ISE module,
half a year. The maintenance includes changing, cleaning or checking the parts as shown in the table below.
Table 9-1 Maintenance items to be performed by service personnel

Category Procedure When to do


Replacement Item Replacing Lamp 2000 hours, or more than 6
months
Replacing cuvettes More than 3 months
Replace probe washer More than 1 year.
Replace Water Inlet Filter More than 1 year
Replace Diluted Wash Solution More than 1 year
Filter
Replace Syringe over 100,000 times
Replace Calibrator Tube(ISE More than 1 year
configured)
Replace Pump Tube(ISE More than half year
configured)
Replace the ISE electrode(ISE More than 6 months or
configured) over 10,000 tests
Clean Item Clean Dust Screens When needed
Clean the dust of the heatsink When needed
fan
Clean Wash Well When needed
Clean Cuvette Wash Station When needed
and Tubes
Clean ISE Injection Port (ISE When needed
Configured)
Clean DI Water Tank When needed
Clean Diluted Wash Solution When needed
Tank
Clean Sample/Reagent When needed
Compartment
Clean Analyzer Panels When needed
Special Wash When needed
Clean Probe Exterior When needed
Clean Mixers When needed
Check Item Pump Calibration (ISE When needed
Configured)
Air Bubble Detector When needed
Calibration(ISE configured)
Cuvette Check When needed
Photometer Check When needed
Check Waste Pump When needed
Replace Cleaning Fluid Syringe When needed
Replace Wash Solution Syringe When needed
9.1.2 Biochemistry maintenance commands

Table 9-2 Biochemistry maintenance commands

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Biochemistry Usage Execution time


maintenance
command
Home Reset the probe, mixer and wash station, and clean · Check probe/mixer/wash well
the probe and mixer. · Clean probe interior
· Replace probe
· Replace mixer
· Clean wash wells
· Special wash probe
Clean Reset the probe and mixer mechanically to return Check probe/mixer/wash well
probes/mixers/wash them to the wash position.
wells
Clean probes Remove air bubbles possibly existing in the tubes, After maintenance of probe and
interior and clean the probe and wash well. wash wells
Special wash Use concentrated wash solution to clean the probe, Special wash
mixer, cuvettes, and wash station.
Special wash Use concentrated wash solution to clean the probe Special wash probe
probes in order to eliminate cross contamination.
Circulate Wash This command is used to wash reaction cuvettes in Circulate Wash Cuvettes
Cuvettes circulating mode to judge if the aspiration,
dispensing, liquid residue, waste discharging are
normal.
Clean Remove air bubbles possibly existing in the tubes, After maintenance of probe and
probes/mixers and clean the probe and wash well. wash wells
exterior
Prime wash station Prime the wash station and tubes to remove air Clean wash station
bubbles.
Replace cuvettes Replace cuvettes. Replace cuvette
Cuvette check Check for dirty cuvettes by running water blank. · Cuvette check
· Special wash
Photometer check Check the light intensity by measuring the average · Photometer check
absorbance of 5 cuvettes at 340 nm. · Replace lamp
Replace lamp Replace the lamp. Replace lamp

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Figure 9-1 Biochemistry maintenance commands

9.1.3 ISE maintenance commands


Table 9-3 ISE maintenance commands

ISE maintenance command Usage Execution time


Two-point calibration Calibrate the ISE module with calibrators When needed
A and B.
Clean electrode tubes Clean the electrode tubes with ISE wash Clean electrode tubes
solution to remove the materials on the
electrode surface.
Pump calibration Calibrate the peristaltic pump to ensure Pump calibration
accurate test result.
Maintenance Discharge the calibrator from the When needed Or automatically
electrode inside before electrode executed during "Clean sample
replacement. injection port" and "Replace
electrode"
Air bubble detector calibration Calibrate the air bubble detector to Air bubble detector calibration
ensure good sensitivity.
Purge A Dispense 100 μL calibrator A to the When needed Or automatically
inside of the electrodes through the executed during " Clean sample
sample injection port. injection port", "Replace electrode"
and "Unload reagent pack"
Purge B Dispense 100 μL calibrator B to the When needed Or automatically
inside of the electrodes through the executed during " Clean sample
sample injection port. injection port", "Replace electrode"
and "Unload reagent pack"
Replace electrode Replace the ISE electrodes. Replace electrode

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ISE maintenance command Usage Execution time


Replace tubes of pump and Replace the aging tubes of the peristaltic Used by service engineers to
calibrator pump and calibrator. replace the tubes of pump and
calibrator
Unload reagent pack Remove the reagent pack and empty the Remove reagent pack
tubes.
Program check View the software version of the ISE When needed
module.
Air bubble detector calibration View the result of air bubble detector After performance of "Air bubble
result calibration. detector calibration"
Pump calibration result View the result of pump calibration. After performance of "Pump
calibration"
Write dallas chip Write information on the Dallas chip. When needed
Read dallas chip Read the information on the Dallas chip. When needed
Store Electrodes Remove the electrodes and store them When needed
Clean Sample Injection Port Clean the sample injection port When needed

Figure 9-2 ISE maintenance commands

9.2 Maintenance Tools


Table 9-4 Maintenance Tools

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Name Applicable Maintenance


Philips-head screwdriver φ3.3×100 Removing the system enclosure
and the cooling fans
Philips-head screwdriver φ4.7×100 Installing and removing the
probes and lamp
Slot-head screwdriver φ4.7×100 Removing probe and pipe hoop
Round-head cleaning tool, 0.25+/- Unclogging the probes
0.01mm*125mm round tip
Hair brush Cleaning filter core and dust
screens
Gauze clean probe/mixer exterior and
sample/reagent compartment
Cotton swabs Clean Wash Well
Suction cleaner Cleaning fans and dust screens
Tweezers Removing/Installing probes and
syringe washers
Beaker Maintaining wash station
Pipette clean ISE sample injection port
Ethanol Cleaning probes, mixers and
wash station
CD 80 Clean Wash Well

9.3 Maintenance Procedure


9.3.1 Procedure
Among the Preventive maintenance items, some of them are performed with the main power switched off, while
the other are performed through the maintenance window on the operating software, where maintenance logs
are recorded. To improve the efficiency and shorten the field maintenance time, you are recommended to follow
the procedure below:
Table 9-5 Execution order of maintenance items

No Procedure Maintenance Tools Operations


1 Clean Analyzer Panels Ethanol and gauze Wipe
2 Clean Dust Screens Hair brush, suction cleaner Remove dust
3 Clean the dust of the Hair brush, suction cleaner Remove dust
heatsink fan
4 Replace Water Inlet Filter Filter 043-000422-00 Replace
5 Replace Diluted Wash Filter 043-000422-00 Replace
Solution Filter
6 Clean DI Water Tank / Washing
7 Clean Diluted Wash / Washing
Solution Tank
8 Replace Syringe Syringe801-BA23-00025-00 Replace
9 Replace Probe Washer Washer0040-10-32307 Replace
10 Replace Pump Tube(ISE Pump Tube801-BA34-00105-00 Replace
configured)
11 Replace Calibrator Calibrator Tube801-BA34-00106-00 Replace
Tube(ISE configured)
12 Clean Probe Exterior Ethanol and gauze Wipe
13 Clean Mixers Ethanol and gauze Wipe
14 Clean Wash Well NaClO solution and cotton swabs Wipe
15 Clean Wash Station Ethanol and cotton swab Wipe
16 Clean Sample/Reagent Ethanol, gauze, cotton swab Disassemble and wipe
Compartment
17 Clean ISE Injection Port Ethanol and cotton swab Wipe
(ISE Configured)

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No Procedure Maintenance Tools Operations


18 Pump Calibration (ISE / Execute
Configured)
19 Air Bubble Detector / Execute
Calibration(ISE configured)
20 Special Wash Concentrated wash solution Execute
21 Cuvette Check / Execute
22 Photometer Check / Execute
23 Check Waste Pump / Execute
24 Replace Cleaning Fluid / Execute
Syringe
25 Replace Wash Solution / Execute
Syringe
9.3.2 Steps
Clean Analyzer Panels
1) Open the upper protective shield of the analyzer, see Figure 3-1 Shells assembly .
2) Use clean gauze moistened with ethanol to clean the analyzer panels and carousel covers.
3) Use wash solution to clean the monitor screen and keyboard.
4) Restore the upper protective shield.
5) After maintenance, open the logs and record related information.

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Figure 9-3 maintenance list and logs

Clean Dust Screens


1) Switch off the analyzer power.
2) Pull the handle of the dust screen to remove it.See Figure 3-3 Frame assembly.
3) Tidy and clean the dust screens.
4) Dry the dust screens in air.
5) Restore the dust screens in place.
6) After maintenance, open the logs and record related information.

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Clean the dust of the heatsink fan


1) Refer to 3.1.8 Remove the dust from the fans for cleaning dust of the fans.
2) After maintenance, open the logs and record related information.

Replace Water Inlet Filter


1) Check the maintenance log and when the inlet filter maintenance interval is more than 1
year, change it.
2) Refer to Removing/Reinstalling Filter for the removing and installing steps.
3) After maintenance, open the logs and record related information.

Replace Diluted Wash Solution Filter


1) Check the maintenance log and when the diluted wash solution filter maintenance interval
is more than 1 year, change it.
2) Refer to Removing/Reinstalling Filter for the removing and installing steps.
3) After maintenance, open the logs and record related information.

Clean DI Water Tank


1) Remove the tank connector, clean the tank with deionized water, and connect the water
outlet of the tank.
2) After maintenance, open the logs and record related information.

Clean Diluted Wash Solution Tank


1) Remove the tank connector, clean the tank with deionized water, and connect the water
outlet of the tank.
2) After maintenance, open the logs and record related information.

Replace Syringe
1) Check the using count of the syringe on the status screen. When the syringe has been used
for 100,000times, change it.
2) Prepare a new syringe and washer, put the syringe in the deionized water beaker to remove
air from the syringe, and then moisten the washer in the deionized water.
3) Place the analyzing unit power to the OFF position.
4) Loosen the screw on the shield of the syringe.
5) Loosen counterclockwise the retaining screw at the bottom of the syringe and then remove
it.
6) Loosen counterclockwise the four retaining screws on top of the syringe, and then remove
the screws and the fixing blocks
7) Hold the T piece with one hand and the syringe connector with the other hand. Loosen the
syringe counterclockwise. And then remove the washer.
8) Soak the new syringe connector in the deionized water beak, pull gently the plunger head
to aspirate half syringe of deionized water, and then push the plunger head to remove the
air.
9) If no washer is found in the T piece, put the new washer in the T piece. Hold the T piece
with one hand and the syringe connector with the other hand, and then screw the T piece
clockwise.
10) Install the syringe on the bracket.
11) Install the fixing blocks and 4 retaining screws while having the retaining screws not
tightened.
12) Pinch the plunger guide cap to adjust the syringe height. Make the syringe head over the
upper fixing block for 7.5 scales.
13) Tighten the four retaining screws on the fixing blocks.
14) Align the plunger head to the retaining screw at the bottom of the syringe, and then tighten
clockwise the retaining screw.
15) After finishing replacement, switch on the analyzer power.
16) Perform the Home maintenance procedure. Check the new syringe for leak and bubbles.
If leak occurs, check the syringe and the connector.

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17) Tighten the syringe shield.


18) The procedure is completed. Write the maintenance log and input the maintenance
information and clear the using count of the syringe.

Cleaning probe interior


When to do
Perform this procedure when you find that the probe is clogged and cannot aspirate or dispense
sample and reagent, or when the probe is detected with abnormal liquid flow during the "Checking
probe/mixer/wash well" maintenance.
Materials required
Unclogging device (or needle), small slot-head screwdriver, small Philips-head screwdriver, beaker,
tweezers, deionized water, and thread syringe
How to do
1) To remove the probe, refer to 3.5.4 Replacing probe assembly , Anti-collision spring and powder
screws.
2) To clean the probe
a) Connect the unclogging device to the probe.
b) Fill the syringe with deionized water and then connect it to the unclogging device.
c) Put the probe inside the beaker while keeping the probe tip not contacting the
beaker.
d) Push the syringe to rinse the interior of the probe. Repeat this step for 10 times.
e) If the syringe plunger leaks and the probe cannot be unclogged due to serious
blockage, replace the probe.
f) Check if continuous water flow comes out of the probe in the same direction with
the probe. If it does, it indicates the cleaning procedure is finished successfully.
g) If water flow is still abnormal after unclogging, replace the probe with a new one.
h) Remove the unclogging device.
3) To install the probe, refer to3.5.4 Replacing probe assembly,Anti-collision spring and powder screws.
4) To check the probe, refer to3.5.4 Replacing probe assembly,Anti-collision spring and powder screws.

Replace Probe Washer


1) Check the maintenance log. When the probe washer has been used for 1 year and change
it.
2) Remove the probe and its washer.
3) Install the washer and install back the probe.
4) Run the operating software, and select Utility-Maintenance-Maintenance- Biochemistry
Maintenance and then select Probe interior clean and prime.
5) After maintenance, open the logs and record related information.

Replace Pump Tube (ISE configured)


1) Check the maintenance log. When Pump Tube has been used for half year, change it.
2) Refer to 3.10.4 Replacing Pump Tube for replacing Pump Tube.
3) After maintenance, open the logs and record related information.

Replace Calibrator Tube (ISE configured)


1) View the maintenance log. When the Calibrator Tube has been used for more than 1 year,
change it.
2) Refer to3.10.5 Replacing Calibrator Tube for Replace Calibrator Tube.
3) After maintenance, open the logs and record related information.

Replace ISE electrode(ISE configured)


1) View the maintenance log. When the Ref electrode has been used for more than 6 moths,
and K,Na,Cl electrodes are used for 6 months or 10,000 tests, change it.
2) Refer to 3.10.6 Replacing ISE electrode for replacing ISE electrode.

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3) After maintenance, open the logs and record related information.

Clean Probe Exterior


1) Place the analyzing unit power to the OFF position.
2) Lift gently the probe to the utmost height and move it to the position convenient for
maintenance.
3) Use gauze soaked with ethanol to gently wipe the probe exterior. Clean the probe tip until it
becomes clear without stain. Use gauze moistened with deionized water to clear the ethanol
on the probe. Do not pull the probe vertically to prevent probe damage.
4) After the procedure, restore the upper protective shield of the analyzer. Power on the
analyzing unit and select Home.
5) After maintenance, open the logs and record related information.

Clean Mixers
1) Place the analyzing unit power to the OFF position.
2) Lift gently the mixer to the utmost height and move it to the position convenient for
maintenance.
3) Use gauze soaked with ethanol to gently wipe the mixer exterior. Clean it until it becomes
clear without stain. Use gauze moistened with deionized water to clear the ethanol on the
mixer. Do not pull the mixer vertically to prevent probe damage.
4) After the procedure, restore the upper protective shield of the analyzer. Power on the
analyzing unit and select Home.
5) After maintenance, open the logs and record related information.

Clean Wash Well


1) Place the analyzing unit power to the OFF position.
2) Move the probe and mixer away from the wash well for the convenience of maintenance.
3) Use clean cotton swabs moistened with CD80 to clean the wash wells.
4) After the procedure, switch on the analyzer power.
5) Execute Home command or Check Probes/Mixers/Wash Wells maintenance command.
Check if the wash wells have a normal water flow.
6) After maintenance, open the logs and record related information.

Clean Wash Station


1) The analyzing unit should be powered off, or in failure mode or in standby or incubation
status.
2) Open the upper protective shield of the analyzer. Remove the wash station, and use gauze
moistened with ethanol to clean the nozzles and wipe blocks.
3) Use the gauze soaked with DI water to clear the ethanol left on the nozzles.
4) Install back the wash station and close the upper shielding cover of the analyzer.
5) Execute the Prime Wash Station maintenance command.
6) After maintenance, open the logs and record related information.

Clean Sample/Reagent Compartment


1) The analyzing unit should be powered off, or in failure mode or in standby or incubation
status.
2) Remove the carousel cover and carousel, and then store them properly.
3) Use clean gauze soaked with deionized water or ethanol to clean the interior of the
compartment. If necessary, you can use gauze moistened with neutral wash solution.
4) Use clean gauze soaked with deionized water or ethanol to clean the carousel body and
bar code scanning window, and then use cotton swabs dipped with ethanol to clean the
sample or reagent positions.
5) Install the carousel and the carousel cover.
6) After maintenance, open the logs and record related information.

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Clean ISE Injection Port (ISE Configured)


1) Make sure that the system status is Incubation or Standby.
2) Enter ISE maintenance screen and select Clean ISE injection port.
3) Open the upper protective shield of the analyzer.
4) Open the cover of the ISE module on the analyzer’s front panel.
5) Use clean cotton swab soaked with ethanol to wipe the sample injection port (interior of the
sample injection cup of the ISE module ) until it is clean; then use a clean cotton swab
soaked with DI water to wipe the interior and periphery of the sample injection port.
6) Enter the ISE Maintenance window and execute purge A and purge B each for three times.
7) Restore the cover of the ISE module on the analyzer’s front panel. Restore the upper
protective shield of the analyzer.
8) After maintenance, open the logs and record related information.

Pump Calibration (ISE Configured)


1) Make sure that the system status is Incubation or Standby.
2) Enter ISE maintenance screen and click Pump Calibration.
3) Fill a sample cup with at least 500μL DI water, and place it in No.40 position of the sample
carousel.
4) Continue the procedure until it is completed.
5) After the procedure is completed, the calibration results are displayed. If calibration is
successful, the procedure is completed. If not, ISE enters error status.
6) After maintenance, open the logs and record related information.

Air Bubble Detector Calibration (ISE configured)


1) Ensure ISE is standby.
2) Enter ISE maintenance screen, and select Air Bubble Detector Calibration. The procedure
is performed automatically.
3) After the procedure is completed, the calibration results are displayed. If calibration is
successful, the procedure is completed. If not, ISE enters error status.
4) After maintenance, open the logs and record related information.

Special Wash
1) Open the upper protective shield of the analyzer.
2) Place 40ml concentrated wash solution on the No.49 position of the reagent carousel.
3) Select Utility-Maintenance-Maintenance- Biochemistry Maintenance and select special
wash.
4) Confirm if cuvette check is needed after the concentrated wash. If it is, mark the checkbox
in front of Check Cuvettes.
5) Select Continue. The system starts cleaning the probe, mixer, cuvettes and wash station.
When special wash is finished, the system performs cuvette check automatically.
6) Select Done.
7) Restore the upper protective shield of the analyzer.
8) After maintenance, open the logs and record related information.

Cuvette Check
1) Select Utility-Maintenance-Maintenance- Biochemistry Maintenance and then select
Cuvette check.
2) After check, check the cuvette check results for yellow indication. Record the cuvettes
highlighted in yellow and perform the Clean Cuvettes or Replace Cuvettes procedure.
3) After maintenance, open the logs and record related information.

Photometer Check
1) Select Utility-Maintenance-Maintenance- Biochemistry Maintenance and then select
Photometer Check.
2) If the result is Normal, the system will give no alarms, otherwise the following alarm will be
given.

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a) If the alarm is “Lamp is not turned on”, refer to 10.2.10 Lamp Is Not Turned On C07005
b) If the alarm is “Light intensity is too strong”, refer to 8)If it still cannot be solved, consider
the optical signal transmission problem, check the optical signal wiring, replace the AD
collection board, refer to 3.9.9 Replacing AD collection board. If it is still not resolved,
you need to consider the main board and replace it, refer to Installation Methods and
Precautions.
c) Light Intensity Is Too Strong C07006.
d) If the alarm is “Light intensity is too weak”, refer to10.2.8 Light Intensity Is Too Weak
C07003 .

Check Waste Pump


1) Power off the analyzer. Remove the desk panels and reaction carousel cover. Run the
operating software and home the system. The analyzer enters standby status. Use a plate
to shield the photometer to complete the dark current check.
2) Select Utility-Maintenance-Maintenance- Biochemistry Maintenance and then select
Circulate Wash Cuvettes.
3) Check the volume of the reaction liquid during cuvette washing process, refer to 7.9.5
process. If the reaction liquid reaches the top of the cuvette or overflows, remove the rear
panel and check and replace the waste pump. The pump P02 is for phase 1 wash probe
and P03 for phase 2 and 3 wash probes. If phase 4 wipe block cannot aspirate clean the
cuvette, check and replace pump P04.
4) If the reaction liquid volume is small, execute the Prime Wash Station maintenance
command.
5) If no abnormality occurs, restore the panels.
6) After maintenance, open the logs and record related information.

Replace Cleaning Fluid Syringe


1) Power off the analyzing unit and remove the rear panel. Run the operating software and
home the system. The analyzer enters standby status.
2) Select Utility-Maintenance-Maintenance-Biochemistry Maintenance and then select
Circulate Wash Cuvettes.
3) Check if the 10ml wash syringe leaks. If so, replace it. For the removing steps, refer to
Aassembly. After maintenance, open the logs and record related information.
4) If no abnormality occurs, restore the rear panel.

Replace Wash Solution Syringe


1) Power off the analyzing unit and remove the rear panel. Run the operating software and
home the system. The analyzer enters standby status.
2) Select Utility-Maintenance-Maintenance- Biochemistry Maintenance and then select
Circulate Wash Cuvettes.
3) Check if the 2.5ml wash syringe leaks. If so, replace it. For the removing steps, refer to
Assembly, After maintenance, open the logs and record related information.
4) If no abnormality occurs, restore the panels.

Check Probes/Mixers Exterior Wash Flow


1) Open the upper cover of the analyzer and home the system.
2) Select Utility -> Maintenance -> Maintenance, then select Biochemistry Maintenance.
3) Select Probes/Mixers Exterior, and then select Continue.
4) Liquid flows out of the probe and mixer wash well automatically. Observe the liquid flow of the wash
wells. Spillage, overflow or no liquid flow should not occur. The probe wash height should be no less
than 5mm. The liquid in the mixer wash well should flow out of its center and form a convex with a
height of 1-2mm.

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Figure 9-4 Check Probes/Mixers Exterior Wash Flow

5) Repeat the above steps for more than 3 times to check if the probe/mixer flow is normal. If not, check
the exterior wash tubes. (First check if the restrictive tube at the exterior wash valve's outlet is clogged.)
Check the flow again after solving the problem.
6) Select Done.
7) Close the maintenance window.
9.4 Post-maintenance Check
Check after maintenance according to the contents of the A.5 BS-240 Series Recovery Checklist.

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10 Troubleshooting
This chapter describes how to locate failure and determine relevant corrective actions.
10.1 Overview
10.1.1 Classification of logs
The fault log records all types of faults that occur with various parts of the instrument. All faults are classified by
part as shown in the following table.

Table 10-1 fault classification


No. Item. No. Item.
1 Operating system 11 Reaction carousel unit
2 Instrument connection 12 Sample/reagent carousel
unit
3 Database 13 Wash station
4 Result calculation 14 Temperature unit
5 Sample bar code 15 Probe Interior Wash Unit
6 Reagent bar code 16 ISE unit
7 Host communication 17 Light source
8 Instrument instruction 18 Other error of operation
unit
9 Sample probe unit 19 Home Process
10 Mixer unit

Error logs
Each error has a unit code used for identification and locating probable causes and solutions. An error code
consists of 6 letters and numbers, such as "C01001", in which "C" indicates that the error occurs on the operation
unit, "01" is the error description of instrument connection, and "001" is the serial number of the error. Therefore,
"C01001" is described as "the first error of instrument connection on the operation unit".
The following tables provide a summary of error codes for the operation unit and analyzing unit.
Table 10-2 Error code of the operation unit

Error Code Description


C Indicates that the error occurs on the operation unit.
00~99 Indicates the specific component on which the error occurs.
00-Operating system
01- System communication
02-Database
03-Result calculation
04-Sample bar code
05-Reagent bar code
06-LIS host communication
07-Other
000~999 Serial number of the error.

Table 10-3 Error code of the analyzing unit

Error Code Description


A Indicates that the error occurs on the analyzing unit.
00~99 Indicates the specific component on which the error occurs.
00-Command execution
01/02-Probe unit
05-Mixer
06-Reaction carousel unit

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07-Sample /reagent carousel unit


11-Wash unit
12-Temperature unit
21-Probe interior wash unit
22-Home process or ISE unit
000~999 Serial number of the error

10.1.2 Viewing and handling logs

Description of Error Log screen


Select Alarm in the function buttons area of the main screen. The Error Log screen is displayed by default and
shows all errors occurring on the current day.

Figure 10-1 Error Log screen

Every error log contains the event ID, date/time, error description (by processing method), event class (by
subsystem) and symptom.
Choose the following buttons as needed:
▪ Search F1: to search for error logs by date, event ID, symptom, or event class.
▪ Refresh F2: to refresh the error logs based on the current search conditions.
▪ Delete F3: to remove specified error logs on the screen.
▪ Print F7: to print all error logs currently displayed on the screen.

Recalling logs
Error logs can be recalled by all users in any system status. Error logs can be recalled by date, event ID,
symptom and event class.
Perform the following steps to recall desired event logs:
1) Select Alarm > Error Log .
2) Select Search F1.
3) Enter one or more of the following conditions:
▪ Date
▪ Event ID (available for error logs only)

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▪ Symptom (available for error logs only)


▪ Event class (available for error logs only)
4) Select OK. The event logs satisfying the conditions are displayed on the screen.
5) Choose the following buttons as needed:
▪ Refresh F2: to refresh the logs based on the current search conditions.
▪ Delete F3: to remove specified logs on the screen.
▪ Print F7: to print all logs currently displayed on the screen.
10.1.3 Error Troubleshooting
When an error occurs, it will be indicated in many ways. The following pages describe how to troubleshoot errors
and help you determine solutions to such errors.
Generally, troubleshooting is divided into the following steps:
▪ An error occurs and is indicated in various ways.
▪ Check the error logs and component status.
▪ Identify the error and determine relevant solutions.
▪ Implement the solutions.
▪ Check and evaluate the implementation of the solutions.

Error indications

Errors may occur on hardware, software and the entire system. When an error occurs, it will be indicated in
many ways to help identify it and determine the possible causes and solutions. Errors can be indicated by
alarm tone, alarm message, color, alarm message box, result flag and error log, through which you will obtain
detailed information about errors and find the relevant solutions.

Alarm tone
When an error occurs, the buzzer gives alarm tone reminding you to notice the error and take corrective actions.
Alarm tone can be adjusted manually or silenced.
Perform the following steps to adjust the alarm tone:
1) Select Utility > System Setup.
2) Adjust the alarm tone in the Alarm Volume field.
3) Test the alarm tone until it is satisfied.
4) To silence the alarm tone, drag the slider to the leftmost position of the scale.
5) Select Save F8 to save the adjustment.
Alarm message
When an error occurs, the system gives an alarm and displays the alarm message in the second line of the
prompt message area.
Color highlight
An error will be indicated by highlighting relevant buttons and screen texts with different colors. Yellow indicates
a warning, and red indicates a serious warning or error.
▪ Reagent button
▪ Utility button
▪ Alarm button
Select a button to access relevant function page, check for abnormities and take corrective actions. When the
problem is solved, the alarm indication disappears.
Alarm message box
An error can also be shown in an alarm message box, which contains the date/time, event ID, time(s) and help
icon.
Errors that are indicated through an alarm message box are divided into the following types:
▪ Common error: including those that are indicated by warning the user, and by invalidating tests,
reagents and samples. When such error occurs, the alarm message box shows with the title bar
highlighted in yellow.
▪ Serious error: including those except for the common error. When such error occurs, the alarm
message box shows with the title bar highlighted in red, and you are only allowed to reboot or exit the
system.
When an alarm message box appears, select the Alarm button to view the new error logs, analyze the possible
causes and determine relevant corrective actions.
Flag
Flag is also called data alarm. When calibration error or failure, or sample result error occurs due to the sample,
reagent or system failure, a flag will appear near the corresponding calibration result or sample results.

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Error log
All alarms are recorded in the error logs. By recalling the error logs you are enabled to master the current status
of the system and troubleshoot errors.

Identifying errors
To identify errors, understand the error indication thoroughly, check the error logs and system status, and then
determine relevant solutions.
The table below shows the error types that may occur on the system. Find relevant corrective actions according
to the description.
Table 10-4 Error types

Error Type Description


Instrument failure and Instrument failure and error may be detected on all
error subsystems and processed in different ways. Such errors
are shown in the Error messages and corrective actions
table, and can be identified through the event ID.
Data alarm Data alarm is a flag indicating biochemistry or ISE chemistry
result error. The flags are included in the Result flags table,
and can be identified through the flag symbol.

10.2 Common Troubleshooting


10.2.1 Database initializing failed
Symptom: Analyzer alarm database initializing failed
Fault Mechanism: this alarm is generated if the database cannot be initialized when the analyzer is turned on.
Fault Scenario: this alarm is generated when the software is turned on.

Figure 10-2 Database initializing failed alarm

Procedure:
1)Confirm that the current account of the system is the administrator account by referring to 6.2.8
Confirmation of Administrator Permission and UAC.

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2)Select the software startup program, right-click Properties→Compatibility, and confirm that
Open in Compatibility View is not ticked.
3)Back up the database file Database. Please refer to 6.7.1 Data backup.
4)Enter the Database folder in the software installation directory. The default path:
D:\Mindray\BS240\OperationSoft\DataBase. Only keep the Backup folder. After the rest of the files are
deleted, start the software. If the operating software can be entered normally, the current database file
is wrong, if not, proceed to the next step.
5)Uninstall the SQL Database. Please refer to 6.6.2 SQL Database Uninstalling .
6)Reinstall the software. The software will automatically install the database during the installation
procedure. Refer to 6.3 Installation of Operating Software.
7)Reinstall the operating system. For domestic customers, please use the backup GHOST file in
the E drive for recovery.
8)Repeat step 6.
10.2.2 Database backup failed
Symptom: Analyzer alarm database backup failed
Fault Mechanism: this alarm is generated if the database cannot be backed up when the analyzer is
turned on.
Fault Scenario: this alarm is generated when the software is turned on.

Figure 10-3 Database backup failed alarm

Procedure:
1) Exit to the desktop with the engineer username and password
2) Go to the software installation directory, enter the Databasebase folder, enter the Backup folder and
find the BA80.bak file. The default path is D:\Mindray\BS240\OperationSoft\DataBase\Backup.
3) Delete the BA80.bak file. See Figure 6-36 Delete the Database.
4) Restart the software.
10.2.3 Database Version Is Higher Than the Current Software Version
Symptom: Database version is higher than the software version when the analyzer software is turned on.

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Figure 10-4 Database version is higher than the software version

Alarm Mechanism: this alarm is caused by a mismatch between the SQL database software version and
the database file version of the operating software.
Fault Scenario: this fault may occur when the software is repeatedly installed or upgraded.
Procedure:
1) In the software installation directory, find the Databaseconfig file, open it with Notepad, and find the
last character.<Property name="DBVer">210</Property> </SessionFactory></DBConfigure>
Note: Due to different software versions, the 210 number here may be 215 or 213, etc.
2) Modify the "210" number, which is higher than the current version value. If you add 100 to this, modify
it to 310. If there are still problems, please continue to add this number.
3) Restart the software.

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Figure 10-5 Database version is higher than the software version

10.2.4 Unmatched Operating Software VersionA22039


Error Code: A22039
Fault Information: unmatched operating software version.
Fault Scenario: this is generated when the software is turned on.
Fault Mechanism: this alarm is caused by a mismatch between the operating software version and the
control software version.
Procedure:
1) Upgrade the software. Refer to 6.4.2 Upgrading of Operating Software.
2) Upgrade the control system. Refer to 6.4.3 Upgrading Control System.
3) Confirm the version after upgrading. Refer to 6.4.4 Confirmation after Upgrading.
10.2.5 Water Residues Exist in the Cuvette A02027
Error Code: A02027
Fault Information: water residues exist in the cuvette or Probe level detection failed
Fault Scenario: this alarm occurs during the analyzer test.
Fault Mechanism: the residual water is detected in the cuvette when the probe adds the R1 reagent to
the reaction carousel.
Possible Cause:
▪ Horizontal and vertical positions of the probe to the reaction carousel not correct
▪ Damaged probe
▪ Fluidics leakage of the probe
▪ Overflow of the reaction carousel
▪ Ground interference
▪ Level detection signal processing problem
Procedure:
1) Open the reaction carousel cover and check if there is any residual water in the cuvette corresponding
to the alarm. If there is, proceed to step 5, if not, proceed to the next step.
2) Check if the horizontal and vertical positions of the probe to the reaction carousel are correct. If they
are not correct, please refer to 7.5.1 Probe to Horizontal Position on Reaction Carousel and 7.5.6
Probe to Vertical Limit Position on Reaction Carousel in the alignment guide, if the positions are correct,

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please proceed to the next step.


3) Check the verticality of the probe, visually measure it, or use a vertical reference for comparison. If
the probe is not straight, please replace the probe.
Refer to A.2 BS-240 Moving Parts Position Confirmation Guide (No Alignment Tooling)Judging and
Calibrating Verticality of Probe.
4) Check if the analyzer is falsely alarmed due to interference:
a) Confirm that the analyzer has a grounding wire and the zero ground voltage is <5V. The
measuring method is: set the multimeter to AC 250V voltage, and connect the black test lead to
the ground wire jack, and the red test lead to the live wire/zero wire jack, respectively. When the
grounding is good, the voltage between the ground wire and the zero wire is less than 5V, and
the voltage between the ground wire and the live wire is similar to the voltage between the live
wire and the zero wire.
b) Check whether the connection line of the level detection board is damaged, or is tied too tightly
by the cable tie. Check if the board connector is loose. The specific operation method is
Power off the whole analyzer, open the protective cover, remove 2 hardened dusting screws
(M3X6), remove the arm cover of the probe (DS193), refer to A.2 BS-240 Moving Parts Position
Confirmation Guide (No Alignment Tooling)Judging and Calibrating Verticality of Probe:
disconnect the J1 and J2 connectors of the level detection board, and re-connect them. If the
connection wire of the J2 connector to the J11 connector of the Main Board is damaged, wind it
with an electrical tape. If the cable tie is too tight, loosen the cable tie and re-plug the J11 connector.
c) If other level detection alarms appear at the same time, the level detection board is suspected
and should be replaced. Refer to 3.5.6 Replacing liquid level detection board.
5) Check the residual water source of the cuvette. There are two general conditions for the overflow of
the wash station: one is that the liquid absorption is not smooth, and the other is excessive liquid
dispensing. The first case is more common, please refer to steps3) in section 10.2.9.
10.2.6 Bar Code Scanning Faults
The barcode scanning problems are generally divided into two types:
1) Software alarm, with specific alarm information.
For example: A09011, the reagent barcode device is not working properly;
C04001, the sample barcode is repeated. Sample ID/bar code: %s Repeated position 1: %s Repeated
position 2: %s.
For such alarms, please refer to Table 10-6 Error messages and corrective actions for the cause
description and procedure to process them.
2) There is no alarm in the software, but the reagent or sample barcode placed in the sample/reagent
carousel is not recognized.
The procedure below is for the second case.
Procedure:
Scanning reagent bar code failed.
1) Confirm the client environment and usage habits:
If the client environment is under high humidity condition, with too much condensed water, it will affect the
scanning of the reagent barcode. The fault is that some reagent barcodes cannot be scanned occasionally.
Customers are advised to install air conditioners to ensure air humidity.
The client usually puts the reagent carousel in the refrigerator and then shuts down the analyzer. This operation
may cause the reagent barcode to be unscanned. There are two ways to improve it:
Method 1: the customer is recommended not to take the reagent carousel out. Leave it in the analyzer, keep
the power of the analyzer on at night, and plug the reagent carousel cover.
Method 2: Remove the reagent carousel at night and put it in the refrigerator. The analyzer can be powered
off. The next morning, power on the analyzer first to start the Reagent Refrigeration Unit, and after the Reagent
Refrigeration Unit is stable (about 5° under normal temperature conditions), take the reagent carousel out from
the refrigerator, and place it in the reagent compartment as quickly as possible to reduce the contact time with
the outside air.
2) Check if there is too much condensed water in the sample/reagent carousel, if the barcode window is
dirty or if there is condensed water, please clean it.
3) View the reagent scanning situations, which are divided into the following types:
a) All reagents cannot be scanned:
Check whether the barcode scanner has red light. If not, check whether the J5 connection line
form the reagent barcode scanner to the Main board is normal, re-plug and check if the connection
line is damaged or is tied too tightly by the cable tie. To replace the barcode scanner, please refer
to 3.4.10 Replacing Bar Code Reader. If the replacement of the Main board is invalid, replace the
barcode scanner (this is rare).

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Note: If all reagents cannot be scanned, the Item parameter may not be imported, or the Item
parameter are wrong.
b) The reagent cannot be scanned.
Try to manually load the reagent position. Operation method: enter the software, Reagent
→Reagent Calibration, select the position where the reagent is placed, click Reagent Load,
input the barcode on the reagent pack at the barcode field in the pop-up screen. Note: Please
keep in mind that the barcode is case sensitive.
If the reagent can be loaded successfully, the barcode may have water mist or scratches or poor
adhesion.
If the reagent cannot be loaded successfully, it may be due to a item parameter problem. Re-
import the Item parameter.
c) The barcode occasionally cannot be scanned; the position is not fixed.
Enter the software, align the barcode scanning position by referring to 7.8 Bar Code Unit
(Optional).
If it still cannot be solved after alignment, please replace the barcode scanner.
10.2.7 Cuvette Blank Out of Range C07004
Error Code: C07004
Fault Information: cuvette blank out of range. Cuvette No.: XX
Fault Mechanism: the phase-6 water blank is less than the lower limit of the allowable light intensity alarm
Note: the phase-6 here is actually the 2nd phase of the wash station (facing the analyzer, from right to left), and
the 240 wash station has only four phases. See below figure

Figure 10-6 Wash Station

Possible Cause:
▪ The cuvette is polluted.
▪ The lamp is aging.
▪ The lamp is not installed correctly.
▪ The wash station dispenses liquid incorrectly.
▪ The wash station is overflowed.
▪ The optical lens is dirty.
▪ The light splitter lens assembly is abnormal.
Procedure:
1) Check the alarm information and determine the alarm cuvette No. If the interior of the cuvette is dirty,
please perform the cuvette detection and special wash by referring to Cuvette Check and Special
Wash. If the interior of the cuvette cannot be cleaned or the exterior is dirty, follow the steps in 3.3.7
Replacing Reaction Cuvette to replace the abnormal cuvette.

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IVD Global Technical Support Dept

2) If the lamp is used for more than 2000 hours or 6 months, replace it. Refer to3.9.3 Replacing Lamp.
3) Check if the wash station overflows. If overflow occurs, refer to 3) in section 10.2.9.
4) Check the liquid dispensing volume in the 6th phase of the wash station and check the liquid volume
left in the cuvette according to7.9.5 the volume of the reaction liquid during cuvette washing process.
If the volume of liquid stored in the 6th phase is too small or there are bubbles, focus on the tubes and
connectors between SY01 and the wash probe. There may be leakage or blockage, please refer to
A.7 Fluidic Diagram.
10.2.8 Light Intensity Is Too Weak C07003
Error Code: C07003
Fault Information: light intensity is too weak
Fault Mechanism: this alarm is triggered after Cuvette blank out of range occurs successively
Possible Cause: refer to 10.2.7 .
Procedure: refer to 10.2.7 .
10.2.9 Water Blank Out of Range (10X) C07009
Error Code: C07009
Fault Information: water blank out of range (10X)
Fault Mechanism: when the lamp fluctuates or the wash station overflows, the 340 nm water blank (light
intensity) of the phase-6 in the same cuvette will change significantly compared with the previous water blank.
If the changes in the 340 nm water blank (light intensity) of the phase-6 in 10 consecutive cuvettes exceed the
alarm threshold compared with the previous water blank, the alarm Water blank out of range (10X) is generated.
Note: the phase-6 here is actually the 2nd phase of the wash station (facing the analyzer, from right to left), and
the 240 wash station has only four phases. See Figure 10-6 Wash .
Possible Cause:
▪ Fluctuation of the lamp
▪ The wash station is overflowed.
▪ Insufficient dispensing volume of the 6th phase
▪ Bubbles in the 6th phase washing
▪ Dirty DI water
▪ The cuvette is contaminated and not cleaned thoroughly.
▪ Human factors:
a) The lamp is not replaced according to the maintenance software procedure. If the lamp is
replaced according to the procedure, the water blank reference value will be automatically
cleared.
b) The cuvette is not replaced according to the maintenance software procedure. If the cuvette is
replaced according to the procedure, the water blank reference value will be automatically
cleared.
c) Change the brightness value of the lamp in the parameter configuration. Direct change will also
cause a difference from the previous brightness. The alarm will then be generated.
d) To change the photoelectric gain value in the parameter configuration, align the photoelectric
gain according to the alignment procedure. The number cannot be directly changed.
e) After resetting the photoelectric collection bit, the water blank reference value is not cleared.
Replace the lamp again, and so the water blank reference value can be cleared.
Procedure:
1) First, eliminate the human factors, please check the human factors in the possible causes, if any,
replace the lamp (actually, only perform the flow but do not change the lamp). Refer to 3.9.3 Replacing
Lamp.
2) If the lamp is used for more than 2000 hours or 6 months, replace it. Refer to 3.9.3 Replacing Lamp.
Note: If the lamp fluctuates greatly, replace it. Inspection method: View the reaction curve of the
sample result with "L!". If the reaction curve has significant fluctuations, and the fluctuations of adjacent
tests have similar curves, it can be judged that the lamp fluctuates greatly, and the problem generally
occurs at the end of the life of the lamp.
3) Check if the wash station is overflowed
Inspection method: Take out the cuvette and observe whether there is liquid on the exterior of the

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cuvette. First, check if the waste tube is drained smoothly, such as the tube is bent, too long, etc.
The tube must be routed from high to low smoothly without U shape or V shape twists or turns
otherwise the waste liquid may flow back into the instrument. Refer to the figure below.

Waste outlet Waste outlet Waste outlet

Waste tank Waste tank Waste tank

Waste outlet Waste outlet Waste outlet

Discharge outlet Discharge outlet Discharge outlet

If there is overflow, please confirm which phase of overflow occurs and perform corresponding
processing according to fluidic diagram.
a) If there is overflow in the 1st, 2nd, and 3rd phases, (the 4th phase overflow is unlikely with dry
cuvette). According to the following hydropneumatic map, consider whether the external waste
discharge tube of the analyzer is folded or crystallized, resulting in poor discharging of waste
liquid. Secondly, check the corresponding ZQ01, ZQ02, and ZQ03 tubes, the W09, W10, W12,
W14, W16, and W17 tubes, and whether the wash probe of the wash station is blocked or
loosened, and whether the pumps P02 and P03 (082-002426-00) are damaged. To replace the
tube, please refer to A.7 Fluidic Diagram.
b) If only the 1st-phase overflow occurs, check whether the 1st-phase probe of the wash station is
blocked, and then check whether the corresponding ZQ01, ZQ02, and ZQ03 tubes are blocked
or loosened. Check whether the high-concentration waste discharge tube outside the analyzer is
folded or blocked, and check the P02 pump.
Note: You can use the replacement method to exclude the causes.
If the P02 problem is suspected, P03 and P02 can be replaced. If the fault is transferred, the
pump is faulty.
The ZQ01 and ZQ11 tubes on the aspirate probe of the wash station can be exchanged. If the
fault is transferred, the 1st-phase related fluidic system is faulty.
c) If only the 2nd-phase overflow occurs, because the 2nd and 3rd phases adopt P03 as the power,
consider that the 2nd-phase wash probe is blocked, or the ZQ11 tube is blocked or loosened.
d) If only the 3rd-phase overflow occurs, consider that the 3rd-phase wash probe is blocked, or the
ZQ21 tube is blocked or loosened.
e) If the 2nd and 3rd-phase overflows occur, focus on whether the external low-concentration waste
tube is blocked, check whether the ZQ12,ZQ13,ZQ14,ZQ15 and ZQ16 tubes are loosened or
blocked, and then use the replacement method to check whether the P03 is damaged. The ZQ11
and ZQ21 tubes are seldom blocked at the same time as and the 2nd and 3rd phase wash probe,
but investigation is required.

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IVD Global Technical Support Dept

ZQ01
ZQ11
ZQ21
ZQ31

T613

ZQ12
SI1 SI2 SI3 SI4
T611 T612 T702

ZQ32 ZQ13 ZQ02

P04 P03 P02


T312
ZZ33 ZZ34
ZZ24
SV05 ZZ23 T305
SV07 ZZ08
ZZ32 ZQ33 ZQ14 ZQ03
ZZ22
T311
T304
ZZ21 T404 T405
ZZ31
1 2 3
T303
ZZ05
ZZ07 T602
SV06
ZZ12
ZZ04

CAN02 ZZ06
ZQ15

T203 T301 T302

T202 D12
SY02
SV01 T403
T402
D15 T201 D14 D13 CAN01

W03

SY01
ZZ03

4) Check the liquid dispensing volume in the 6th phase of the wash station and check the liquid volume
left in the cuvette according to 7.9.5 the volume of the reaction liquid during cuvette washing process..
If the volume of liquid stored in the 6th order is too small or there are bubbles, focus on the tubes and
connectors between SY01 and the wash probe. There may be leakage or blockage, please refer to
A.7 Fluidic Diagram.
10.2.10 Lamp Is Not Turned On C07005
Error Code: C07005
Fault Information: lamp is not turned on
Fault Mechanism: after the lamp is tuned on, the detected light intensity is less than the lower alarm limit.
Fault Scenario: the error is reported when the analyzer is running, or is turned on.
Possible Cause(s)
▪ The lamp is damaged.
▪ The lamp post is not tightened.
▪ The power board of the lamp is not connected properly.
▪ The power supply of the analyzing unit is disconnected.
▪ The wash station overflows.
▪ The light splitter lens assembly is faulty.
Procedure:
1) Open the reaction carousel cover and check if the lamp is turned on. If it is not, rerun the operating
software.
2) At the same time, check if the wash station overflows. If overflow occurs, refer to 3) in section 10.2.9.
3) Open the upper panel of the lamp to confirm that the post nut is tightened. Refer to 3.9.3 Replacing
Lamp.
4) Replace the lamp.
5) Re-plug the J4 connector of the power board and check the wire of the J4 connector to the lamp for
damage.
6) Enter the Utility —> Maintenance—>Alignment —>Photometric Unit. Click Turn On Lamp, turn
the multimeter to the DC gear, and measure the J4 connector on the power board. If it is not in the
range of 11.4 -12.6 V, replace the board, refer to Installation Methods and Precautions.
7) Replace the optical assembly, refer to 3.9.4 Disassembling/Assembling Optical Assembly.
8) If it still cannot be solved, consider the optical signal transmission problem, check the optical signal
wiring, replace the AD collection board, refer to 3.9.9 Replacing AD collection board. If it is still not

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resolved, you need to consider the main board and replace it, refer to Installation Methods and
Precautions.
10.2.11 Light Intensity Is Too Strong C07006
Error Code: C07006
Fault Information: light intensity is too strong
Fault Mechanism: After the lamp is tuned on, the detected light intensity is greater than the upper alarm
limit
Fault Scenario: The error is reported when the analyzer is running or is turned on
Possible Cause:
▪ Fluctuation of light source or lamp problem
▪ Cuvette uninstalled
▪ The wash station is overflowed.
▪ Photoelectric gain adjustment too high
▪ Incorrect fiber splice position
▪ Faulty light splitter lens assembly
Procedure:
1) For lamp problems, if the lamp is used for more than 2000 hours or 6 months or a non-original bulb is
used, replace it. Refer to 3.9.3 Replacing Lamp.
2) Check if the cuvette is installed, or if the wash station overflows. Refer to 3) in section 10.2.9.
3) Enter the Utility->Maintenance->Parameter Search and Configuration screen of the operating
software, select Reaction Carousel Unit, and view the photoelectric gain value of each wavelength,
which is normally 30 to 255. The larger the value, the smaller the measured AD value and the higher
the absorbance.
There are two ways to adjust the value. Method a) is recommended.
a) Refer to 7.3.2 Photoelectric Gain Adjustment for auto adjustment of photoelectric gain. The value
will change automatically after adjustment.
b) Re-configure the gain value by referring to 6.7.4 Parameter Configuration.
4) Enter the Utility screen —> Maintenance—>Alignment —>Photometric Unit. Click Turn On Lamp,
turn the multimeter to the DC gear, and measure the J4 connector on the power board. If it is not in
the range of 11.4 -12.6 V, replace the board, refer to Installation Methods and Precautions.
5) If it still cannot be solved, replace the optical assembly, refer to 3.9.4 Disassembling/Assembling
Optical Assembly.
6) If it still cannot be solved, consider the optical signal transmission problem, check the optical signal
wiring, replace the AD collection board, refer to 3.9.9 Replacing AD collection board. If it is still not
resolved, you need to consider the main board and replace it, refer to Installation Methods and
Precautions.
10.2.12 Analyzer cannot be connected
There are several types of faults when the analyzer cannot be connected:
▪ Software alarm: Fault code: C01001 Fault Information: the analyzer cannot be connected
▪ An error occurred while you enter the software. The prompt: Inquiring instrument configuration failed.
The following information is displayed on the screen:

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Figure 10-7 Inquiring instrument configuration failed

▪ An error occurred while you enter the software. The following information is displayed on the screen:
Note: It is generally not found in the COM port information.

Figure 10-8 Operating software starting up failed

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Note: When upgrading V24.00.06 software, configuration may not be performed using auxiliary tools, which
may cause the instrument to query the configuration failure. Please refer to the upgrade instructions in 6.9
upgraded to V24.00.06 instructions.
Procedure:
1) Check that the main switch of the analyzer and the switch of the analyzing unit are turned on. Normally,
the power switch indicator should be always on. If the switch is not on, please check and reconnect
the power cord of the analyzer. If it is confirmed that there is no problem with the power supply, replace
the switch. Refer to 4.5.4 Replacing Power switch.
2) Check that the analyzer is connected to the computer, re-plug the serial cable, and check whether the
serial cable is normal.
Serial cable inspection mode: The serial cable is the RS232 direct connection, connect to 2, 3, 4, 5,
and 7 directly. Use the multimeter to adjust to the buzzer gear and measure whether the 2, 3, 4, 5,
and 7 at both ends of the serial cable are connected. If not, replace the serial cable.
3) View the serial port status of the computer, exit to the desktop of the computer, right click on the
computer, select the device manager, and view the port. Confirm that there is a COM port on the
computer, and the status is not ! or ?. If it is abnormal, please reinstall the serial port driver or replace
the serial port card.
4) Check the configuration file information and view if the COM port is set the same as the actual COM
port. If it is different, please change it. Please refer to 6.3.3 Confirm the configuration file.
5) Download the latest version of the software and upgrade it. Refer to 6.4 Software Upgrading.
6) If the above cannot be solved, please check the wiring of the serial port of the analyzer to the main
board, and apply for the main board to replace it. Refer to of the main board Installation Methods and
Precautions.
10.2.13 Sample Probe Fails to Detect the Level of the Wash Well A01028
Error Code: A01028
Fault Information: the probe fails to detect the level of the wash well
Fault Mechanism: When the probe is cleaned in the wash well, the upper computer does not receive the
level detection signal or the level detection signal does not last for a long time.
Procedure:
Confirm the current software version. If the version is lower than V24.00.04(See Figure 6-25
Operating Software Version for software version), please upgrade the software to the latest version
first, refer to 6.4 Software Upgrading.
1)Confirm that whether there is water in the wash well, and whether the water quantity meets the
requirements when the analyzer generates the alarm. Please follow the Check Probes/Mixers Exterior
Wash Flow method for inspection.
2)If the wash well is dry, check the hydropneumatic system. First check the water in the mixer
wash well.
a)If there is water in the mixer, focus on the exterior cleaning tube of the probe, especially
whether the restricting capillary of the SV03 valve outlet is blocked, and then check whether the
tubes and connectors of D31, D32, D33 and D34 are blocked.
▪ Check if SY01 is blocked or loosened. If you need to replace it, please refer to
Removing/Reinstalling Cuvette Wash Preheating Assembly.
▪ Check the SV01 valve. Refer to 7.9.2 Checking Floater and Valve Status.
▪ Then consider the SV03 valve failure, you can open the valve with reference to the
content of 7.9.2 Checking Floater and Valve Status and check if there is a crisp sound.
If not, the valve may be damaged, replace it. In addition, the replacement method can
be used, SV03 and SV04 are interchanged. If the fault is transferred, the SV03 is faulty.
If it is not transferred, check whether the J6 connector from SV03 to the power drive
board is damaged or loosened. If not, apply for the power drive board for replacement.
Refer to Installation Methods and Precautions.
b)If the mixer is also waterless, check the shared tube and check it in the following order:
▪ If the tank does not have enough deionized water, add the deionized water.
▪ If the inlet filter is blocked or damaged, try to replace it. Please refer to
Removing/Reinstalling Filter
▪ If the tubes (D01 - D03) ,D11 and D12related to the exterior cleaning are blocked, try to
dredge the tubes.
3)If there is little water in the wash well, focus on the exterior cleaning tube of the probe, especially
whether the restricting capillary of the SV03 valve outlet is blocked.
4)If there is water in the wash well and the flow rate is normal, check if the probe is bent. Check
the verticality of the probe, visually measure it, or use a vertical reference for comparison. If the probe

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is not straight, please replace the probe. Refer to A.2 BS-240 Moving Parts Position Confirmation Guide
(No Alignment Tooling)Judging and Calibrating Verticality of Probe.
5)If the wash well is not well drained, causing the DI water retained, check whether the waste
tube of the wash well is blocked. If so, dredge the tube and check it according to the fluidics diagram
of the whole machine.
6)Check if the horizontal and vertical positions of the probe to the wash well are correct. Refer to
7.5.2 Probe to Horizontal and Vertical Positions on Wash Well for alignment.
7)Check if the analyzer is falsely alarmed due to interference:
a) Confirm that the analyzer has a grounding wire and the zero ground voltage is <5V. The
measuring method is: set the multimeter to AC 250V voltage, and connect the black test lead to
the ground wire jack, and the red test lead to the live wire/zero wire jack, respectively. When the
grounding is good, the voltage between the ground wire and the zero wire is less than 5V, and
the voltage between the ground wire and the live wire is similar to the voltage between the live
wire and the zero wire.
b)Check whether the connection cable of the level detection board is damaged, or the cable
is bound too tightly by the cable tie, or the board connector is loose. The specific operation method
is: power off the whole analyzer, open the protective cover, remove 2 hardened dusting screws
(M3X6), remove the arm cover of the probe (DS193), refer to Figure 3-27 Removing liquid level
detection board, disconnect the J1 and J2 connectors of the level detection board, and re-connect
them. If the connection wire of the J2 connector to the J11 connector of the Main Board is
damaged, wind it with an electrical tape. If the cable tie is too tight, loosen the cable tie and re-
plug the J11 connector.
8)If the level detection board 051-002479-00 is faulty replace it by referring to3.5.6 Replacing
liquid level detection board.
9)If the Main Board is faulty, replace it refer to Installation Methods and Precautions.

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IVD Global Technical Support Dept

SV02 T10
D06 D07
6
T103 T104 T10
7 NS MIX
SY03
T105

D05
SV03 T222

T221 D32 D33 D34

SV04

T211 D22 D23 T212 D24


D31

D21 W01

P01

T204
D04

D16

ZZ11
T203

D11 T202 D12


T10
SV01
2
D15 T201 D14 D13

D03

SY0
1

Panel
D02 T101
FL01

,
10.2.14 Sample Probe Fails to Detect the Level on the Reaction Carousel
when Dispensing A01033
Error Code: A01033
Fault Information: the sample probe fails to detect the liquid level on the reaction carousel when
dispensing
Alarm Mechanism: When the probe is dispensing in the reaction carousel, firstly, detect the R1 volume
added before, and determine the number of steps of the vertical movement of the probe adding the sample
according to the R1 volume (volume tracking technology). This alarm is triggered if no level is detected within
the specified number of steps.
Troubleshoot as follows:
When analyzing the problem, follow this sequence: level signal generation (probe) → signal analysis (level
detection board) → transmission (connection line) → signal processing (Main Board).
Procedure:
Confirm the current software version. If the version is lower than V24.00.04(See Figure 6-25 Operating
Software Version for software version), please upgrade the software to the latest version first, refer to 6.4
Software Upgrading.
1)First check the alarm log of the analyzer and check if the analyzer still has an alarm that the
probe does not detect the liquid level in the sample carousel or during cleaning. If there is a similar
alarm, judge that the level detection function is faulty. At this time, check if the probe, the level detection
board, and the power supply and wire of the level detection board are normal.
2)If there is only this alarm, according to the alarm mechanism, first check whether the reagent

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IVD Global Technical Support Dept

in the reagent pack is sufficient, if not, add the reagent in time.


Note: There should be no air bubbles in the reagent pack; if it is an open reagent, do not pour too
much reagent.
3)Observe the probe. If the reagent probe lowers into the reagent pack during the whole
procedure of aspirating the reagent, focus on whether the probe is blocked, and whether the reagent
volume added to the cuvette is insufficient due to the leakage of the sample syringe and the pipeline.
If the probe is blocked, please dredge the probe by referring to Cleaning probe interior.
If the syringe leaks, please replace it by referring to Replace Syringe.
Check the Teflon tubing between the probe and the syringe. There should be no wear and tear, if
any, please replace it directly.
4)If the probe does not lower to aspirate the reagent but return directly during the test, judge that
the function of the level detection board may be damaged or interfered. At this time, check the power
supply and wire of the level detection board. Replace the level detection board.
5)Check the vertical reagent dispense position from the probe to the reaction carousel, and align
it according to 7.5.6 Probe to Vertical Limit Position on Reaction Carousel.
10.2.15 Dark current is too high C07007
Error Code: C07007
Fault Information: Dark current is too high
Fault Mechanism: The dark current value of any wavelength exceeds the alarm limit. Under normal
conditions, the dark current value should be less than 200
Fault Analysis:

1.zero ground voltage needs less than 5VWhether


Dark current is Is it power the power supply is shared with other high-power
Y equipment, such as centrifuges, refrigerators, etc. If
too high interference
so, separate power

N
In the vicinity of the
telecommunication base
Is it base station signal
Y station, interference is likely to
interference
occur. Such as signal towers,
etc.
N

Whether the optical gain is Adjust the photoelectric gain to


Y
adjusted too low the normal range

Is the AD collection board


Y Replace AD collection board
abnormal

Replace the main board

Figure 10-9 Troubleshooting flowchart for Dark current is too high

Procedure:
1) Confirm that the analyzer has a grounding wire and the zero ground voltage is <5V. The measuring method
is: set the multimeter to AC 250V voltage, and connect the black test lead to the ground wire jack, and the
red test lead to the live wire/zero wire jack, respectively. When the grounding is good, the voltage between
the ground wire and the zero wire is less than 5V, and the voltage between the ground wire and the live
wire is similar to the voltage between the live wire and the zero wire.

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2) Confirm whether the power supply of the instrument is powered separately and avoid sharing with high-
power equipment such as refrigerators, centrifuges, etc.
3) The instrument installation environment needs to be confirmed and cannot be placed near the base station.
4) Enter the Utility->Maintenance->Parameter Search and Configuration screen of the operating software,
select Reaction Carousel Unit, and view the photoelectric gain value of each wavelength, which is
normally 30 to 255. The larger the value, the smaller the measured AD value and the higher the absorbance.
There are two ways to adjust the value. Method a) is recommended.
a) Refer to 7.3.2 Photoelectric Gain Adjustment for auto adjustment of photoelectric gain. The value will
change automatically after adjustment.
b) Re-configure the gain value by referring to 6.7.4 Parameter Configuration.
5) Check the wiring of the AD collection board, and connect to the main control board to re-plug. Refer to 4.6
Wiring Diagram of Analyzer.
6) Check the optical signal wiring, replace the AD collection board, refer to 3.9.9 Replacing AD collection
board.
7) Replace the optical assembly, refer to 3.9.4 Disassembling/Assembling Optical Assembly.
8) If it is still not resolved, you need to consider the main board and replace it, refer to Installation Methods
and Precautions.
10.2.16 Clinical Result Problems
Troubleshoot as follows:

Result inaccurate

Result of individual Results of multiple


chemistry inaccurate chemistries inaccurate

Good Different Same


Poor repeatability repeatability wavelengths wavelength

Confirm Fluctuated
Check the start Check the Normal
Reage that the reaction curve
position of the use time of reaction
nt parameters
photoelectric the curve
invalid are set Check the start
acquisition and reagent, correctly, Check the position of
replace the and and probe, photoelectric
optical replace the perform syringe, acquisition,
assembly if reagent for cross- cuvette, and cuvette, lamp,
necessary recalibratio contaminat optics and mechanical
n. ion check. position

Figure 10-10 Troubleshooting clinical result problem

Client FAQ:
1) Common errors in parameters
▪ The parameter is set incorrectly, or the increment and decrement are set to the parameter.
▪ The 2nd generation reagents are used, but the parameters input are the 1st generation ones.
2) Calibration setup error
▪ The concentration value of the calibrator is set incorrectly, or a wrong calibrator is taken.
▪ The calibration rule is set incorrectly, and the wrong calibration rule is selected.
▪ The number of calibration repetitions is set incorrectly or may be set to only once, which usually
should be 2 to 4 times by default.
▪ The calibrator displayed by the software expired and was not modified in time, and could not be
calibrated.

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▪ In the calibration rule, the calibrator is incorrectly selected, and there may be multiple calibrators
for one chemistry.
3) QC setup error
▪ The control target value and SD value are set incorrectly, or the wrong control is taken.
▪ The QC rule is set incorrectly, and the correct control is not selected.
▪ The control displayed by the software expired and was not modified in time, and the QC could
not be applied.
4) Redissolution error
▪ Dry powder calibrator and QC solution should be redissolved before use. An error occurs when
redissolution with water, for example, only 3 ml of water is required, but 5 ml is added.
▪ The redissolved water is used incorrectly, for example, use the distilled water placed for a long
time, or directly use the mineral water for redissolution. For redissolution, the distilled water for
injection is recommended.
▪ Pipettes are recommended for redissolution when syringe or an uncalibrated sample gun is used.
▪ After redissolution, the storage is incorrect. After normal redissolution, the solution should be split
charged and stored frozen, and the freezing and thawing cannot be repeated. The storage is
recommended not to exceed 1 month.
5) Reagent problem
▪ Reagent is expired
▪ Reagent is not placed in the refrigerator
▪ Air bubbles in the reagent pack.
▪ Rgt load error
▪ Reagent tilt
6) Calibrator and control problem
▪ Matching calibrator and control are not used
▪ Calibrator and control used is not assigned
7) Analyzer problem
▪ Micro-blocking of the probe may result in an assignment or a low result
▪ The sample syringe leaks, which may result in poor repeatability
▪ The Teflon tubing from the probe to the sample syringe is folded or damaged, which may lead to
poor repeatability of the results.
▪ If the lamp life exceeds 2000 hours or 6 months, the stability of the results may be poor, and the
reaction curve may fluctuate. In particular, the enzymatic chemistry will frequently send an alarm
of linearity limit out of range.
▪ If the photoelectric acquisition position is wrong, all the results will be unstable.
▪ If the cuvette is contaminated, the result will be unstable.
▪ If the mixer is dirty, the result will be unstable.
▪ Position shift will affect loading and mixing, resulting in unstable results.
8) Water quality problem
▪ Poor water quality will affect the results of chemistries such as ions.
▪ The TBA chemistry is affected by the pH value of water
▪ The water quality will affect the cleaning effect. There will be cleaning residue, affecting the results
9) Sample problem
▪ Sample centrifugation problem. The sample containing fibrinogen may block the probe.
▪ Sample trait problems, hemolysis, jaundice, chyle blood, etc.
▪ Blood collection tube problems. Separation of glue, etc. may be easy to result in probe blockage.
▪ Some patients have taken certain drugs and caused abnormal detection in some chemistries.

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10.3 Data alarms


Data alarm is a result flag indicating that an error or abnormity occurs to a result. By identifying results flags can evaluate if the results are reliable and acceptable. Data
alarm is not necessarily an error but will definitely influence the result and should be considered carefully.
The system provides monitoring of biochemistry results and ISE chemistry results. When calibration error or failure, or sample result error occurs due to the sample,
reagent or system failure, a flag will appear near the corresponding calibration result or sample results. The following pages summary the result flags of the system.
Table 10-5 Data alarms and corrective actions

Flag Alarm Type Description Probable Causes Corrective Actions


Exceeds linearity range The result exceeds the low limit of the linearity
< Result related Take no actions, or rerun the test for confirmation.
low range.
Exceeds measurement Sample or control result exceeds the low limit of the
< ISE result related Take no actions, or rerun the test for confirmation.
range low measurement range.
Exceeds linearity range The result exceeds the high limit of the linearity
> Result related Rerun the test with sample diluted or decreased.
high range.
Exceeds measurement Sample or control result exceeds the high limit of the
> ISE result related Rerun the test with sample diluted or decreased.
range high measurement range.
Sample volume is
▲ Result related Sample volume is Increased one No actions are required.
Increased one
Sample volume is
▼ Result related Sample volume is decreased one No actions are required.
decreased one
Exceeds reference range The result exceeds the high limit of the reference
^ Result related No actions are required.
high range.
Exceeds critical range The result exceeds the high limit of the critical
^! Result related No actions are required.
high range.
Exceeds reference range The result exceeds the low limit of the reference
v Result related No actions are required.
low range.
Exceeds critical range
v! Result related The result exceeds the low limit of the critical range. No actions are required.
low
Results of five runs (10 results), or 10 continuous Check if the reagent is qualified, control sample is
10-x Result related 10-x
results of a control are on the same side. normal, and the instrument is working correctly.
The current QC result is between ±2 and ±3
1-2s Result related 1-2s standard deviations from the assigned mean No actions are required.
concentration.
The current QC result is greater than ±3 standard Check if the reagent is qualified, control sample is
1-3s Result related 1-3s
deviations from the assigned mean concentration. normal, and the instrument is working correctly.

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Flag Alarm Type Description Probable Causes Corrective Actions


Results of two controls in the same run or two
continuous results of a control are on the same side Check if the reagent is qualified, control sample is
2-2s Result related 2-2s
and greater than ±2 standard deviations from the normal, and the instrument is working correctly.
assigned mean concentration.
Results of two runs (4 results), or 4 continuous
results of a control are on the same side and greater Check if the reagent is qualified, control sample is
4-1s Result related 4-1s
than ±1 standard deviation from the assigned mean normal, and the instrument is working correctly.
concentration.
Check if the reagent is qualified and control is normal. If
Multiple QC data and threshold values or cumulative
2.7s Result related 2.7s the error remains, contact our customer service
sum exceed ±2.7SD.
department or your local distributor.
Check if the reagent is qualified and control is normal. If
Multiple QC data and threshold values or cumulative
3.0s Result related 3.0s the error remains, contact our customer service
sum exceed ±3.0SD.
department or your local distributor.
Check if the reagent is qualified and control is normal. If
Multiple QC data and threshold values or cumulative
5.1s Result related 5.1s the error remains, contact our customer service
sum exceed ±5.1SD.
department or your local distributor.
Check the sample for foreign matters or interferents;
The absorbance of primary or secondary
check if the reagent is qualified and placed in the
ABS Result related Absorbance out of range wavelength used for calculating results is greater
correct position; check the cuvette is clean; check if the
than 3.4A.
photometric system is working normally.
Check if the cuvette is not overflowed, the reagent is
The reagent goes wrong; insufficient reagent is
Blank response out of sufficient without air bubbles, the light does not drift and
BLK Calibration related dispensed; the cuvette contains air bubbles; the light
range the chemistry parameters are reasonable. If yes,
drifts; or the cuvette is overflowed.
replace the reagent and then rerun the test.
The sample concentration is too high, and substrate Check the reaction curve and the substrate depletion
BOE Result related Substrate depletion
depletion occurs during fixed-time measurements. limit. Rerun the test with diluted sample.
The results of constituent
The test results of constituent chemistries of the
CalcE Result related chemistries of a No actions are required.
calculation are out of linearity range.
calculation out of range
CALE Result related Edited calibration factor The calibration factors are edited. No actions are required.
Calibration failed.(for
CALF Result related The calibration fails. Recalibrate.
biochemistries)
1. Waste pump tube is aging, blocked, or broken; 1. Replace the reagent pack with a new one
CALF Result related No fluid in tubing 2. Sample injection port and fluidic path are blocked 2. Perform purge B to remove bubbles
or leaking. 3. /4. Replace the pump tube

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Flag Alarm Type Description Probable Causes Corrective Actions


3. Air bubble detector failed. 5. Clean the sample injection port and reinstall
electrodes.
6. Replace the bubble detector.

1. Place sufficient ISE wash solution.


2. Replace the pump tube
3. Clean the sample injection port and reinstall
electrodes.
4. Replace the bubble detector.
1. Replace the reagent pack with a new one
2. Perform purge B to remove bubbles
3. /4. Replace the pump tube
5. Clean the sample injection port and reinstall
1. Waste pump tube is aging, blocked, or broken; electrodes.
2. Sample injection port and fluidic path are blocked 6. Replace the bubble detector.
CALF Calibration related No fluid in tubing
or leaking.
3. Air bubble detector failed. 1. Place sufficient ISE wash solution.
2. Replace the pump tube
3. Clean the sample injection port and reinstall
electrodes.
4. Replace the bubble detector.
Rejected calibration
CALJ Calibration related The calibration factors are rejected. No actions are required.
factor
1. Waste pump tube is aging, blocked, or broken; 1. Replace the pump tube
2. Sample injection port and fluidic path are blocked 2. Clean the sample injection port and reinstall
CALM Result related Air in segment
or leaking. electrodes.
3. Air bubble detector failed. 3. Replace the bubble detector.
1. Waste pump tube is aging, blocked, or broken; 1. Replace the pump tube
2. Sample injection port and fluidic path are blocked 2. Clean the sample injection port and reinstall
CALM Calibration related Air in segment
or leaking. electrodes.
3. Air bubble detector failed. 3. Replace the bubble detector.
Recalculated calibration
CALR Result related The calibration factors are recalculated. No actions are required.
factor
Check that the reagent and calibrator are normal, and
Calibration curve not For nonlinear calibration, a satisfying base cannot
COV Calibration related then recalibrate. If the error remains, contact our
convergent be calculated and no calibration curve is drawn.
customer service department.

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Flag Alarm Type Description Probable Causes Corrective Actions


Calibration curve
The calculated standard deviation of the calibration Check if the acceptance limit is reasonable and the
CSD Calibration related standard deviation out of
curve exceeds the specified limit. reagent and calibrator are normal, and then recalibrate.
range
DEL Calibration related Deleted QC result The QC result has been deleted. No actions are required.
Calibration determination The calculated determination coefficient of the Check if the acceptance limit is reasonable and the
DET Calibration related
coefficient out of range calibration curve exceeds the specified limit. reagent and calibrator are normal, and then recalibrate.
1. ISE communication cable failure. 1. Replace the ISE communication cable.
Saving calibration result 2. Communication interface or pins failure 2. Replace the interface or pins.
DEP Calibration related
error 3. Main board of the ISE module goes wrong. 3. Replace the Main board of the ISE module.
4. Software error. 4. Upgrade the operating software or reinstall it.
Insufficient probe wash The probe wash solution is insufficient during
DTGL Result related Fill more probe wash solution.
solution measurement.
The difference between the maximum and minimum
Calibration repeatability Check if the acceptance limit is reasonable,
DUP Calibration related response of the calibrator exceeds the specified
error troubleshoot the error, and then recalibrate.
limit.
EDT Result related Edited result The result has been edited. No actions are required.
EDT Calibration related Edited calibration factor The calibration factors have been edited. No actions are required.
The sample concentration is too high, and substrate
Check the reaction curve and the substrate depletion
ENC Result related No calculation interval depletion occurs within the lag time of rate check
limit. Rerun the test with diluted sample.
measurements.
The high-concentration sample leads to substrate
Enzyme linearity range depletion during the reaction time, and the result is
EXP Result related Rerun the test with diluted sample.
extension calculated by using measuring points within the lag
time.
Extended calibration The result is obtained by extending the calibration
EXT Result related Take no actions, or recalibrate.
factor time.
The slope difference is applicable to linear
Calibration slope calibration only and refers to the K factor (slope) Check if the acceptance limit is reasonable and the
FAC Calibration related
difference out of range difference between two adjacent calibrations. It reagent and calibrator are normal, and then recalibrate.
exceeds the specified limit.
The response is normal,
ICA Result related but results cannot be The chemistry has not been calibrated. Rerun it after calibration.
calculated.
Water blank fluctuation is 1. The cuvette is overflowing. 1. Check if the cuvette is overflowing.
L! Result related
out of range. 2. The lamp has been replaced incorrectly. 2. Check if the Replace Lamp command is executed

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Flag Alarm Type Description Probable Causes Corrective Actions


3. Cuvette check is not performed after maintenance. during lamp replacement.
4. The cable connectors are not tightened. 3. Check if the cable connectors and retaining screw of
5. The retaining screw is not tightened. the lamp have been tightened.
6. Cleaning liquid inside the cuvette is little. 4. Check if the cleaning liquid inside the cuvette is no
7. The lamp is aged. less than half of the cuvette.
8. The photometer goes wrong. 5. Check if the reaction curve fluctuates irregularly. If
yes, replace the lamp.
6. If the error remains, contact our customer service
department.
The measuring points for result calculation are Check the reaction curve and the substrate depletion
nonlinear, because the sample concentration is too limit. Rerun the test with diluted sample. If the alarm
LIN Result related Non-linear
high, or the substrate depletion limit is not specified occurs for more than one chemistry, and the reaction
or unreasonable. The lamp is aged. curve fluctuates irregularly, replace the lamp.
The sample concentration is lower than the
Response less than that For ascending calibration curve, rerun the test with
sensitivity indicated on the reagent pack, making
LOW Result related of the minimum- standard or increased sample volume; for descending
response less than that of the lowest-concentration
concentration calibrator calibration curve, rerun the test with diluted sample.
calibrator.
Check if the cuvette is clear and not overflowed, the
The reagent goes wrong; the cuvette is not clear;
Mixed blank absorbance reagent is sufficient without air bubbles, and the
MBK Calibration related the reaction cuvette is overflowed; or insufficient
out of range chemistry parameters are reasonable. If yes, replace
reagent is dispensed.
the reagent and then rerun the test.
Calibration curve not The calibration data and calibration curve are not Check if the calibrator is defined and placed correctly,
MON Calibration related
monotonic monotonic. and then recalibrate.
The high-concentration sample leads to less than 3
NLN Result related No linear interval valid measuring points within the reaction time of Rerun the test with diluted sample.
rate check measurements.
1. Electrode failure.
1. Replace the electrode.
2. Environment interference.
2. Relocate the instrument.
NOIS Result related Electrode voltage noise 3. ISE Main board failure.
3. Replace the Main board of the ISE module.
4. Salt buildup around electrodes or tubes due to
4. Clean the tubes and electrodes.
fluidic leaks.
1. Electrode failure.
1. Replace the electrode.
2. Environment interference.
2. Relocate the instrument.
NOIS Calibration related Electrode voltage noise 3. ISE Main board failure.
3. Replace the Main board of the ISE module.
4. Salt buildup around electrodes or tubes due to
4. Clean the tubes and electrodes.
fluidic leaks.

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Flag Alarm Type Description Probable Causes Corrective Actions


Overridden calibration The result is obtained by overriding a failed
OVE Result related Take no actions, or recalibrate.
factor calibration.
1. Calibrator A is exhausted.
1. Replace the reagent pack with a new one
2. Bubbles exist in calibrator tube A
3. Pump tube A is aging, blocked, or broken. 2. Perform purge B to remove bubbles
3. /4. Replace the pump tube
PUGA Result related Air in calibrator A 4. Waste pump tube is aging, blocked, or broken;
5. Clean the sample injection port and reinstall
5. Sample injection port and fluidic path are blocked
electrodes.
or leaking.
6. Replace the bubble detector.
6. Air bubble detector failed.
1. Calibrator A is exhausted.
1. Replace the reagent pack with a new one
2. Bubbles exist in calibrator tube A
2. Perform purge B to remove bubbles
3. Pump tube A is aging, blocked, or broken.
3. /4. Replace the pump tube
PUGA Calibration related Air in calibrator A 4. Waste pump tube is aging, blocked, or broken;
5. Clean the sample injection port and reinstall
5. Sample injection port and fluidic path are blocked
electrodes.
or leaking. 6. Replace the bubble detector.
6. Air bubble detector failed.
1. Calibrator B is exhausted.
1. Replace the reagent pack with a new one
2. Bubbles exist in calibrator tube B
3. Pump tube A is aging, blocked, or broken. 2. Perform purge B to remove bubbles
3. /4. Replace the pump tube
PUGB Result related Air in calibrator B 4. Waste pump tube is aging, blocked, or broken;
5. Clean the sample injection port and reinstall
5. Sample injection port and fluidic path are blocked
electrodes.
or leaking.
6. Replace the bubble detector.
6. Air bubble detector failed.
1. Calibrator B is exhausted.
1. Replace the reagent pack with a new one
2. Bubbles exist in calibrator tube B
2. Perform purge B to remove bubbles
3. Pump tube A is aging, blocked, or broken.
3. /4. Replace the pump tube
PUGB Calibration related Air in calibrator B 4. Waste pump tube is aging, blocked, or broken;
5. Clean the sample injection port and reinstall
5. Sample injection port and fluidic path are blocked
electrodes.
or leaking. 6. Replace the bubble detector.
6. Air bubble detector failed.
Antibody excess occurs due to too high sample Check the reaction curve and the prozone check
PRO Result related Prozone check error
concentration. parameters. Rerun the test with diluted sample.
R Result related Rerun result The result is obtained by rerunning the test. No actions are required.
One result of a run is greater than +2 standard
Check if the reagent is qualified, control sample is
R4S Result related R4S deviations from the assigned mean and the other
normal, and the instrument is working correctly.
greater than -2SDs.

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Flag Alarm Type Description Probable Causes Corrective Actions


Check if the cuvette is clear and not overflowed, the
The reagent goes wrong; the cuvette is not clear;
R1 blank absorbance out reagent is sufficient without air bubbles, and the
RBK Result related the reaction cuvette is overflowed; or insufficient
of range chemistry parameters are reasonable. If yes, replace
reagent is dispensed.
the reagent and then rerun the test.
Response calculation Absorbance data for calculation is incomplete, or the Rerun the test. If the error remains, contact our
RCE Result related
error dividend is 0. customer service department.
The sample result is recalculated manually with the
REC Result related Recalculated result /
latest calibration factors.
ISE response check code 1. ISE communication cable failure. 1. Replace the ISE communication cable
error 2. Communication interface or pins failure 2. Replace the interface or pins.
RESP Result related
Command format or 3. Main board of the ISE module goes wrong. 3. Replace the Main board of the ISE module.
execution error 4. Software error. 4. Upgrade the operating software or reinstall it.
ISE response check code 1. ISE communication cable failure. 1. Replace the ISE communication cable.
error 2. Communication interface or pins failure 2. Replace the interface or pins.
RESP Calibration related
Command format or 3. Main board of the ISE module goes wrong. 3. Replace the Main board of the ISE module.
execution error 4. Software error. 4. Upgrade the operating software or reinstall it
RGTE Result related Expired reagent The result is based on an expired reagent. Replace the reagent.
RGTL Result related Insufficient reagent The result is based on insufficient reagent. Replace the reagent.
The calibration result is based on insufficient
RGTL Calibration related Insufficient reagent Replace the reagent.
reagent.
Response greater than
The sample concentration exceeds the high limit of
RRN Result related that of the maximum- Rerun the test with diluted sample.
the calibrator concentration.
concentration calibrator
The difference of final response of the maximum
Calibration sensitivity Check if the acceptance limit is reasonable and the
SEN Calibration related and minimum concentration calibrators exceeds the
error reagent and calibrator are normal, and then recalibrate.
specified limit.
Probe clogging is detected during sampling or the
SJAM Result related probe is clogged Sample treatment.
probe is clogged during sampling.
1. Replace the problematic electrode and reagent pack.
1. Electrode or reagent pack fails.
2. New electrode will become steady after 15 minutes
2. Electrode is unsteady.
since installed.
3. New reagent pack is unsteady.
3. Run a couple of calibrations after installing new
SLDR Calibration related Electrode slope drift 4. Reference electrode has been used for over 66
reagent pack.
months.
4. Replace the reference electrode.
5. ISE Main board failure.
5. Replace the ISE Main board.
6. Ambient temperature fluctuates drastically
6. Control the ambient temperature to make the

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Flag Alarm Type Description Probable Causes Corrective Actions


fluctuation within +/-4℃.
1. Reinstall the electrode
1. Electrode is not installed correctly. 2. Replace the calibrator.
2. Calibrator expired. 3. Replace the problematic electrode and rerun.
3. Electrode degenerated 4. Remove the electrode and clap on it to eliminate
SLEX Calibration related Slope out of range 4. Bubbles in reference electrode bubbles. Reinstall the electrode and run calibration.
5. Reference electrode has been used for a long time 5. Replace reference electrode and rerun.
6. Electrodes interfered. 6. Troubleshoot the electrodes by replacing them in
7. Module or tubing temperature above 32℃. different groups.
7. Monitor temperature, if too high, relocate equipment.
SLP Result related Corrected result The result is adjusted with calculation factors. No actions are required.
The results are produced
when the calibration
factors instead of the Calibration factors instead of the default ones are
SLP Result related No actions are required.
default ones are configured for the second time calibration.
configured for the
second time calibration.
1. Sample is insufficient or contains many bubbles
after dispensing.
1. Increase the sample volume. At least 90μl sample
2. No or insufficient sample has been dispensed into
should be prepared.
SMPA Result related Air in sample the sample injection port.
2. Electrode is not installed correctly. Reinstall it.
3. The electrodes are not properly installed, causing
3. Check the waste tube, and if necessary, replace it.
leakage.
4. The waste pump tube is aging or broken.
SMPE Result related Expired sample The sample is expired. Replace the sample.
SMPL Result related Insufficient sample The sample is insufficient during analysis. Refill the sample.
SMPL Calibration related Insufficient sample The sample is insufficient during analysis. Refill the sample.
1. Replace the problematic electrode and reagent pack.
1. Electrode or reagent pack fails.
2. New electrode will become steady after 15 minutes
2. Electrode is unsteady.
since installed.
3. New reagent pack is unsteady.
3. Run a couple of calibrations after installing new
VDRF Result related Electrode voltage drift 4. Reference electrode has been used for over 66
reagent pack.
months.
4. Replace the reference electrode.
5. ISE Main board failure.
5. Replace the ISE Main board.
6. Ambient temperature fluctuates drastically.
6. Control the ambient temperature to make the

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Flag Alarm Type Description Probable Causes Corrective Actions


fluctuation within +/-4℃
1. Replace the problematic electrode and reagent pack.
1. Electrode or reagent pack fails.
2. New electrode will become steady after 15 minutes
2. Electrode is unsteady.
since installed.
Electrode Voltage 3. New reagent pack is unsteady.
VOUT Result related 3. Run a couple of calibrations after installing new
Overflow 4. Reference electrode has been used for over 66
reagent pack.
months.
4. Replace the reference electrode.
5. ISE Main board failure.
5. Replace the ISE Main board.
1. Replace the problematic electrode and reagent pack.
1. Electrode or reagent pack fails.
2. New electrode will become steady after 15 minutes
2. Electrode is unsteady.
since installed.
Electrode Voltage 3. New reagent pack is unsteady.
VOUT Calibration related 3. Run a couple of calibrations after installing new
Overflow 4. Reference electrode has been used for over 66
reagent pack.
months.
4. Replace the reference electrode.
5. ISE Main board failure.
5. Replace the ISE Main board.
1. The ambient temperature is out of range.
2. The temperature sensor goes wrong. (component
error and cable error)
3. The temperature protection switch goes wrong.
Reaction disk (component error and cable error) 1. Check if the error is accidental.
T1 Result related
temperature error 4. The heater goes wrong. (component error and 2. If not, contact our customer service department.
cable error)
5. PCB error
6. Parameters are lost.
7. Electromagnetic interference exists.
Photoelectric
measurement period is 1. Rerun the operating software.
out of rangePhotoelectric 2. Reboot the operation unit.
TD Result related 1. Software error
measurement period is 3. If the error remains, contact our customer service
out of range department or your local distributor.

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10.4 Error messages and corrective actions


Table 10-6 Error messages and corrective actions

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
Equipment 1. Switch off the analyzing unit power and switch
Middle layer configuration cannot it on again. Recover the failure by performing the
A00006 Error / E2PROM read/write error.
unit be read or saved Home maintenance procedure.
Error: 2. Refer to 6.7.4 for processing
1. Switch off the analyzing unit power and switch
it on again. Recover the failure by performing the
Middle layer Instruction execution Instrument instructions cannot be
A00007 Error / Home maintenance procedure.
unit error executed.
2. If this message appears for 3 times, contact our
R&D department.
Probe vertical movement error Probe vertical movement error
Sample probe vertical 1. Sensor status error.2.Motor belt or belt 1. Sensor status error:
movement error pulley is loose. 2. Failed to find the zero Check if belt or belt wheel is loose, tighten them
Position: position: if so.
Error: 1) The assembly is jammed; 2) Driving 2. Failed to find the zero position:
circuit error; 3) Vertical motor error; 4)
1) Remove obstacle or replace with a new
Or Vertical sensor error; 5) Belt pulley is
assembly.
loose; 3. Collision occurs during operation
Sample probe other than aspirating: 1) Collision sensor 2) Replace PCB.
horizontal movement or circuit or cable failure; 2) Collision 3) Replace motor.
Sample
A01006 Error error / sensor is not blocked when assembling the 4) Replace sensor.
probe unit
Position: probe; 3) Incorrect probe positioning; 4) 5) Tighten properly.
Error: Incorrect sample/reagent carousel 3. Collision occurs during operation other than
positioning; 4. Collision error remains: aspirating:
Or 1) Collision sensor or circuit or cable
1) Replace sensor or PCB or cable.
failure; 2) Collision sensor is not blocked
Sample syringe 2) Reassemble.
when assembling the probe; 3)
movement error. 3) Rotate positioning sensor to remove dust or
Collision sensor is not blocked due to
Position: adjust probe to be vertical; if problem remains,
deformation of blocking plate’s driving
Error: adjust positioning parameters.
spring; 5. Vertical movement is not
allowed in current horizontal position: 4) Adjust reagent carousel positioning

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Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
Software error. parameters.
4. Collision error remains:
Probe horizontal movement error 1) Replace sensor or PCB or cable.
1. Sensor status error.2.Motor belt or belt 2) Reassemble.
pulley is loose. 2. Failed to find the zero 3) Mount the spring of blocking plate again.
position: 1) Driving circuit error; 2) 5. Vertical movement is not allowed in current
Motor error; 3) Home position sensor horizontal position:
error; 4) Belt pulley is loose; 3. Collision
Home instrument or probe unit.
occurs during horizontal movement: 1)
Driving circuit error; 2) Motor error; 3) Reagent probe horizontal movement error
Home position sensor error; 4) Belt 1. Sensor status error:
pulley is loose;4. Horizontal movement is Check if belt or belt wheel is loose, tighten them
not allowed in current vertical position: if so.
Software error 2. Failed to find the zero position:
1) Replace PCB.
Probe syringe movement error 2) Replace motor.
1. Sensor status error.2.Motor belt or belt 3) Replace sensor.
pulley is loose. 2. Failed to find the zero 4) Tighten properly.
position: 1) The assembly is jammed;
3. Collision occurs during horizontal movement:
2) Driving circuit error; 3) Motor error;
1) Replace PCB.
4) Sensor error; 5) Belt pulley is loose.
2) Replace motor.
3) Replace sensor.
4) Tighten properly.
4. Horizontal movement is not allowed in current
vertical position: Home instrument or reagent
probe unit.
Probe horizontal movement error
1. Sensor status error:
Check if belt or belt wheel is loose, tighten them
if so.
2. Failed to find the zero position:
1) Remove obstacle or replace with a new

No.HSH-19021-BS-240 Version:4.0 10-31


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
assembly.
2) Replace PCB.
3) Replace motor.
4) Replace sensor.
5) Tighten properly.
3. Horizontal Collision occurs during operation:
1) Replace PCB.
2) Replace motor or sensor.
3) Tighten.
4. Horizontal movement is not allowed in current
vertical position: Home instrument or probe unit.
Probe syringe movement error
1. Sensor status error:
Check if belt or belt wheel is loose, tighten them
if so.
2. Failed to find the zero position:
1) Remove obstacle or replace with a new
assembly.
2) Replace PCB.
3) Replace motor.
4) Replace sensor.
5) Tighten properly.
Sample probe 1) Collision sensor or circuit or cable 1) Replace sensor or PCB or cable.
collides with an failure; 2) Reassemble.
obstacle when 2) Collision sensor is not blocked when 3) Rotate the positioning sensor to remove dust or
Sample
A01007 Warning aspirating / assembling the probe; adjust the probe to be vertical; if problem
probe unit
Sample position: 3) Incorrect probe positioning; remains, adjust the positioning parameters.
Sample ID/bar code:
4) Incorrect Sample/reagent carousel 4) Adjust sample/reagent carousel positioning
Specific position:
positioning. parameters.
Sample Insufficient sample 1. No sample is loaded on the designated 1. Check if there is sufficient sample, and run the
A01024 Warning /
probe unit or position. test again.

No.HSH-19021-BS-240 Version:4.0 10-32


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Event Event Error Message and


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ID class Event Log
Sample probe level 2. Insufficient sample. 2. If there are level detection error, check the
detection failed. 3. Probe level detection error. probe, level detection board and connecting
cable; replace if any abnormality is identified.
Sample probe fails to
Sample 1. No DI water or hydro error;
A01028 Error detect liquid level / Refer to 10.2.13 .
probe unit 2. Probe level detection error.
during cleaning
Sample probe fails to
detect liquid level on
reaction carousel
when dispensing. 1. There is no reagent or insufficient
Cuvette No.: reagent in the cuvette;
Sample ID/bar code:
Sample 2. Incorrect vertical extreme position
A01033 Warning Chemistry: / Refer to 10.2.14 .
probe unit parameter for the probe on reaction
or
Sample probe level carousel;
detection failed. 3. Probe level detection error.
Cuvette No.:
Sample ID/bar code:
Chemistry:
1. Switch off analyzing unit power and switch on
again; Home the system.
Instruction execution Instrument instructions cannot be
A01039 Probe unit Error / 2. If this message appears for 3 times, contact our
error executed.
customer service department or your local
distributor.
1) Collision sensor or circuit or cable 1) Replace sensor or PCB or cable.
Probe R2 collides failure; 2) Reassemble.
with an obstacle 2) Collision sensor is not blocked when 3) Rotate positioning sensor to remove dust or
A02007 Probe unit Warning when aspirating / assembling the probe; adjust probe to be vertical; if problem remains,
Reagent position: 3) Incorrect probe positioning; adjust positioning parameters.
Specific position:
4) Incorrect Sample/reagent carousel 4) Adjust sample/reagent carousel positioning
positioning. parameters.
Insufficient reagent 1. Check if there is sufficient sample, and run the
1.There is no reagent or insufficient
Or test again.
A02023 Probe unit Warning / reagent on the designated position;
Probe R2 level 2. If there are level detection error, check the
detection failed. 2. Probe level detection error.
probe, level detection board and connecting

No.HSH-19021-BS-240 Version:4.0 10-33


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
cable; replace if any abnormality is identified.
1. Check if the reagent meets the requirement
Probe dispenses 1. Sample probe aspirates nothing; and is sufficient in volume, and then try again.
A02025 Probe unit Warning /
insufficient reagent Syringe assembly error. 2. Check if there is any abnormity of syringe
assembly.
Water residues exist
in the cuvette or
A02027 Probe unit Warning / Refer to 10.2.5 . Refer to 10.2.5 .
Probe level detection
failed
1. Check if the reagent meets the requirements,
1. The reagent probe aspirates nothing. and is sufficient in volume and free of air bubbles.
Reagent is Then try again.
insufficient or 2. The probe syringe assembly goes
A02032 Probe unit Warning contains air bubbles / wrong. 2. Check if the probe syringe assembly works
Chemistry: 3. There is an error with the vertical properly.
Position: extreme position of the sample probe 3. Check if the vertical extreme position of the
above the reagent carousel. sample probe above the reagent carousel is
correct.
Mixer vertical movement error Mixer vertical movement error
1. Sensor status error 1. Sensor status error: Check if belt or belt wheel
Belt or belt pulley is loose. is loose, tighten them if so.
2. Failed to find the zero position. 2. Failed to find the zero position: 1) Remove
1) Assembly is jammed; obstacle or replace with a new assembly. 2)
Replace PCB; 3) Replace motor. 4) Replace sensor.
2) Driving circuit error;
Mixer vertical 5) Tighten properly.
3) Vertical motor error;
movement error 3. Vertical movement is not allowed in current
A05006 Mixer unit Error / 4) Vertical sensor error;
Mixer horizontal horizontal position: Home instrument or unit.
movement error 5) Belt pulley is loose;
3. Vertical movement is not allowed in Mixer horizontal movement error
current horizontal position.
1. Sensor status error: Check if belt or belt wheel
Software error is loose, tighten them if so.
2. Failed to find the zero position: 1) Replace
Mixer horizontal movement error PCB. 2) Replace motor. 3) Replace sensor. 4)
1. Sensor status error Tighten properly.

No.HSH-19021-BS-240 Version:4.0 10-34


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
Belt or belt pulley is loose. 3. Horizontal movement is not allowed in current
2. Failed to find the zero position. vertical position: Home instrument or unit.
1) Driving circuit error;
2) Motor error;
3) Home position sensor error;
4) Belt pulley is loose;
3. Horizontal movement is not allowed in
current vertical position.
Software error
1. Switch off the analyzer power and switch on it
again. Recover failure by performing the Home
Instruction execution Instrument instructions cannot be
A05007 Mixer unit Error / maintenance procedure.
error executed.
2. If this message appears for 3 times, contact our
R&D department.
Reaction carousel movement error 1. Failed to find the home position.
1. Failed to find the zero position. Replace sensor or cable
Home position sensor error 2. The coded disk missed steps
2. The coded disk missed steps 1) Remove obstacle or replace with a new
1) Assembly is jammed; assembly;
Reaction carousel
Reaction 2) Driving circuit error; 2) Replace PCB;
A06006 Error movement error /
carousel unit 3) Motor error; 3) Replace motor;
Error:
4) Sensor error; 4) Replace sensor or cable;
5) Belt pulley is loose; 5) Replace belt pulley and motor assembly;
3. The reagent carousel inner ring missed 3. The reagent carousel inner ring missed steps
steps when moving to the home position. when moving to the home position.
Home position sensor error Replace sensor or cable
1. Switch off the analyzer power and switch on it
1. Software instruction execute error
Reaction again. Recover failure by performing the Home
Filter wheel 2. The filter wheel motor goes wrong. maintenance procedure.
A06007 Carousel Error /
movement error 3. The home position sensor of the filter
Unit 2. Check if the cable of the filter wheel motor and
wheel goes wrong. the sensor are normal.

No.HSH-19021-BS-240 Version:4.0 10-35


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
3. Check if the filter wheel motor and the sensor
are faulty.
1. Switch off analyzing unit power and switch on
again; Home the system.
Reaction Instruction execution Instrument instructions cannot be
A06008 Error / 2. If this message appears for 3 times, contact our
carousel unit error executed.
customer service department or your local
distributor.
Sample/Reagent carousel movement
error.
Sample/reagent carousel outer ring movement
1. Failed to find the zero position.
error
Home position sensor error
1. Failed to find the zero position Replace sensor
2. The coded disk missed steps or cable.
Sample 1) Assembly is jammed;
Sample/reag 2. The coder missed steps: 1) Remove obstacle or
carousel movement
A07006 ent carousel Error / 2) Driving circuit error; replace with a new assembly. 2) Replace PCB. 3)
error
unit 3) Motor error; Replace motor. 4) Replace sensor or cable. 5)
Error:
4) Sensor error; Replace belt pulley and motor assembly.
5) Belt pulley is loose; 3. The reaction carousel missed steps when
moving to the home position Replace sensor or
3. The reagent carousel inner ring missed
cable
steps when moving to the home position.
Home position sensor error
Due to the system error, the sample bar
code reader cannot work normally. If the
Recover the failure. If the error remains, initialize
error repeats and cannot be removed,
the sample bar code reader. If initialization cannot
Sample/reag then the bar code reader has not
Sample bar code be performed, check if bar code reader is
A07009 ent carousel Error / performed the initialization normally or
reader error connected properly. If the error remains, then
unit the communication cables are replace the bar code reader or the control drive
disconnected. board.
If bar code reader is not available, please
try again.
Scan the bar code again. If the problem still
Sample/reag Sample bar code
Sample bar code reader does not work remains, check the cable of the bar code reader
A07010 ent carousel Warning error /
normally due to communication error. or replace the bar code reader or the control drive
unit Position:
board.

No.HSH-19021-BS-240 Version:4.0 10-36


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
Sample/reag
Sample bar code Sample bar code sending buffer is full due
A07011 ent carousel Error / Recover the failure or reboot the analyzing unit.
sending buffer is full to communication error.
unit
Reagent bar code reader connection error
due to system failure. If the error Recover the failure. If the error remains, initialize
repeats and cannot be removed, then the the sample bar code reader. If initialization cannot
Sample/reag Reagent bar code
bar code reader has not performed the be performed, check if bar code reader is
A09011 ent carouse Error reader does not work /
initialization normally or the connected properly. If the error remains, then
unit normally
communication cables are disconnected. replace the bar code reader or the control drive
If bar code reader is not available, please board.
try again.
Scan the bar code again. If the problem still
Sample/reag Reagent bar code
Communication error. Reagent bar code remains, check the cable of the bar code reader
A09012 ent carousel Warning error /
instruction buffer is full. or replace the bar code reader or the control drive
unit Position:
board.
Sample/reag Reagent bar code
Reagent bar code reader does not work
A09014 ent carousel Error sending buffer is full / Recover the failure or reboot the analyzing unit.
normally due to communication error.
unit Position:
1. Sensor status error
Belt pulley is loose;
2. Home position is not found.
1. Sensor status error: Check if belt or belt wheel
1) Driving circuit error; is loose, tighten them if so.
2) Motor error; 2. Failed to find the home position: 1) Replace
Wash station 3) Home position sensor error; PCB. 2) Replace motor. 3) Replace sensor. 4)
A11005 Wash station Error movement error / 4) Belt pulley is loose; Tighten properly.
Error: 3. The wash station collides with an 3. The wash station collides with an obstacle
obstacle when moving. when moving: 1) Align wash probes. 2) Align
1) Wash probes are not vertical; reaction carousel positioning. 3) Replace sensor,
cable or PCB.
2) Reaction carousel positioning is
deviated;
3) Collision sensor or circuit error
1. Check if the water level of the water tank is at a
A11013 Wash station Error Water tank is empty / 1. Water tank is empty.
low level and add it;

No.HSH-19021-BS-240 Version:4.0 10-37


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
2. The low-level floater of the water tank 2. Check if the low float of the water tank is
goes wrong. normal. Refer to 7.9.2 for the float check. If the
float is faulty, replace it.
3. Check if the wiring of the float sensor to the
main board is broken or the contact is poor.
4. Replace the main board.
1.Add diluted wash solution.
1. Diluted wash solution tank is empty. 2.Check if the low-level float signal of the diluted
wash solution tank is correct. Refer to 7.9.2 for the
Insufficient diluted 2. The low-level floater of the diluted
A11015 Wash station Error / float check. If the float is faulty, replace it.
wash solution wash solution tank goes wrong. 3. Check if the wiring of the float sensor to the
main board is broken or the contact is poor.
4. Replace the main board.
1.Check the high-concentration waste tank. If the
tank is full, replace it. Cover the full tank and
The high concentration waste tank is full dispose of the waste properly.
2.Check if high-concentration waste goes wrong.
High concentration The floater of the high concentration
A11020 Wash station Error / Refer to 7.9.2 for the float check. If the float is
waste tank is full waste tank goes wrong. faulty, replace it.
3. Check if the wiring of the float sensor to the
main board is broken or the contact is poor.
4. Replace the main board.
1. Sensor status error.
2. The syringe assembly is probably forced 1. Replace sensor cable.
to move.
2. Remove obstacle or replace with a new
Cuvette wash 3. Failed to find the zero position.
A11034 Wash station Error syringe movement / assembly.
1) Assembly is jammed; 3. Change the drive board.
error.
2) Driving circuit error; 4. Change the motor.
3) Motor error;
4) Sensor error;
1. Switch off analyzing unit power and switch on
Instruction execution Instrument instructions cannot be again; Home the system.
A11038 Wash station Error /
error executed. 2. If this message appears for 3 times, contact our
customer service department or your local

No.HSH-19021-BS-240 Version:4.0 10-38


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
distributor.
1. Reproduce failure.
2. Observe ambient temperature through the
1. The ambient temperature is out of Status screen, to check if temperature is out of
range. range.
2. The temperature sensor goes wrong. 3. Temperature sensor error: check for any signs
(component error, cable error) of short circuit or broken circuit; check if
3. The temperature protection switch connections are secure.
goes wrong. (component error, cable 4. Temperature protection switch error: check if
Reaction carousel error) protection switch is shut and connections are
Temperature
A12005 Warning temperature is out of T1 secure.
unit 4. The heater goes wrong. (component
range
error, cable error) 5. Heater error: check if resistance under normal
5. The fan goes wrong. (component error, temperature is correct, and connections are
cable error) secure.
6. Fan error: check if fan is working normally, and
6. PCB error
connections are secure.
7. Parameters are lost.
7. PCB failure.
8. Electromagnetic interference exists. 8. Parameters are lost. Check if the temperature
control parameters are correct.
9. Electromagnetic interference exists.
1. Reproduce failure.
1. The ambient temperature is out of
range. 2. Observe ambient temperature to check if
2. The temperature sensor goes wrong. temperature is out of range.
(component error, cable error) 3. Temperature sensor error: check for any signs
Temperature of wash of short circuit or broken circuit; check if
3. The temperature protection switch
solution for cleaning connections are secure.
Temperature goes wrong. (component error, cable
A12006 Warning cuvettes is out of / error) 4. Temperature protection switch error: check if
unit
range protection switch is shut and connections are
Temperature: 4. The heater goes wrong. (component
secure.
error, cable error)
5. PCB error 5. Heater error: check if resistance under normal
temperature is correct, and connections are
6. Parameters are lost.
secure.
7. Electromagnetic interference exists. 6. PCB error

No.HSH-19021-BS-240 Version:4.0 10-39


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
7. Parameters are lost: check if temperature
control parameters are correct.
8. Electromagnetic interference exists.
1. Reproduce failure.
2. Observe ambient temperature to check if
1. The ambient temperature is out of temperature is out of range.
range.
3. Temperature sensor error: check for any signs
2. The temperature sensor goes wrong. of short circuit or broken circuit; check if
(component error, cable error) connections are secure.
Temperature of 3. The temperature protection switch 4. Temperature protection switch error: check if
Temperature deionized water for goes wrong. (component error, cable protection switch is shut and connections are
A12007 Warning /
unit cleaning cuvettes is error) secure.
out of range 4. The heater goes wrong. (component 5. Heater error: check if resistance under normal
error, cable error) temperature is correct, and connections are
5. PCB error secure.
6. Parameters are lost. 6. PCB failure.
7. Electromagnetic interference exists. 7. Parameters are lost. Check if the temperature
control parameters are correct.
8. Electromagnetic interference exists.
1. The ambient temperature is out of 1. Reproduce failure.
range. 2. Measure ambient temperature to check if
temperature is out of range.
2. The temperature sensor goes wrong.
(component error, cable error) 3. Temperature sensor error: check for any signs
of short circuit or broken circuit; check if
3. The temperature protection switch
Reagent preheating connections are secure.
Temperature goes wrong. (component error, cable
A12010 Warning temperature is out of / 4. Temperature protection switch error: check if
unit error)
range. protection switch is shut and connections are
4. The heater goes wrong. (component
error, cable error) secure.
5. Heater error: check if resistance under normal
5. PCB error
temperature is correct, and connections are
6. Parameters are lost. secure.
7. Electromagnetic interference exists.
6. PCB failure.

No.HSH-19021-BS-240 Version:4.0 10-40


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
7. Parameters are lost. Check if the temperature
control parameters are correct.
8. Electromagnetic interference exists.
1. Sensor status error.
2. The syringe assembly is probably forced 1. Replace sensor cable.
Probe interior wash to move. 2. Remove obstacle or replace with a new
Probe 3. Failed to find the zero position.
syringe movement assembly.
A21001 Interior Wash Error /
error. 1) Assembly is jammed; 3. Change the drive board.
Unit
Error: 2) Driving circuit error; 4. Change the motor.
3) Motor error;
4) Sensor error;
1. Remove and reinstall the electrode.
2. Replace the calibrator.
3. Replace the failed electrode and run tests
1. Electrode is not installed correctly.
again.
2. Calibrator expired.
4. Remove the electrode and clap on it to
3. Electrode degenerated eliminate bubbles. Reinstall the electrode and run
4. Bubbles in reference electrode calibration.
Slope out of range,
A22001 ISE unit Error SLEX 5. Reference electrode has been used for 5. Replace the reference electrode and run tests
electrode:
a long time. again.
6. Electrodes interfere with each other. 6. Replace electrode by different combinations to
7. Module or fluidic temperature exceeds troubleshoot the failed one.
32℃. 7. Monitor temperature, if too high, relocate
equipment.
8. Contact our customer service department or
your local distributor.
1. Sample is insufficient, or contains 1. Increase the sample volume. At least 90μl
bubbles after being dispensed. sample should be prepared.
Air in sample.
A22002 ISE unit Error SMPA 2. No or insufficient sample has been 2. Electrode is not installed correctly. Reinstall it.
Position:
dispensed into the sample injection port. 3. Check the waste tube, and if necessary,
3. The electrodes are not properly replace it.

No.HSH-19021-BS-240 Version:4.0 10-41


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
installed, causing leakage.
4. The waste pump tube is aging or
broken.
1. Power supply of ISE module goes wrong.
2. Communication cable between ISE 1. Replace the 24V power supply board.
ISE unit cannot be module and middle-layer unit goes wrong. 2. Replace the ISE communication cable.
A22004 ISE unit Error /
connected. 3. Communication interface or pins failure 3. Replace the interface or pins.
4. Replace the ISE Main board.
4. Main board of the ISE module goes
wrong.
1.Communication cable between ISE
module and middle-layer unit goes wrong. 1. Replace the ISE communication cable.
ISE unit response 2. Communication interface or pins failure 2. Replace the interface or pins.
A22005 ISE unit Error /
error 3. Main board of the ISE module goes 3. Replace the ISE Main board.
wrong. 4. Upgrade the operating software or reinstall it.
4. Software error
1. Leaks exist due to improper installation
of electrode or O ring's missing. 1. Reinstall the electrode and check for the O
2. Sample injection port of electrode ring.
inside is blocked. 2. Use warm water to rinse the sample injection
3. Calibrator in the reagent pack is port, and unclog the electrode tube. Check the
A22006 ISE unit Error Purge A and B failed. / exhausted. inside of the reference electrode for salt buildup.
4. Purge cycle is not enough. 3. Replace the reagent pack.
5. Peristaltic pump tube is aging, blocked 4. Increase the prime cycle.
or broken. 5. Replace the pump tube.
6. Calibrator cannot be output due to the 6. Use warm water to unclog the wand tube.
blocked wand tube.
ISE reagent is going
A22007 ISE unit Warning / Calibrator is exhausted. Replace the reagent pack with a new one.
to be exhausted.
1. Electrode or reagent pack is invalid. 1. Replace the problematic electrode and reagent
Voltage overflow, 2. Electrode is unsteady. pack.
A22008 ISE unit Error VOUT
electrode: 3. New reagent pack is unstable. 2. New electrode will become steady after 15
4. Reference electrode has been used for minutes since installed.

No.HSH-19021-BS-240 Version:4.0 10-42


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
over 6 months. 3. Run a couple of calibrations after installing new
5. ISE Main board failure. reagent pack.
4. Replace the reference electrode.
5. Replace the ISE Main board.
1. Replace the failed electrode or reagent pack.
1. Electrode or reagent pack is invalid.
2. New electrode will become steady after 15
Electrode slope drift. 2. Electrode is unsteady. minutes since installed.
(during calibration)
3. New reagent pack is unstable. 3. Run a couple of calibrations after installing new
Or
VDRF/ 4. Reference electrode has been used for reagent pack.
A22009 ISE unit Error Electrode voltage
SLDR over 6 months.
drift. (during sample 4. Replace the reference electrode.
analysis) 5. ISE Main board failure. 5. Replace the ISE Main board.
Electrode: 6. The ambient temperature is fluctuating 6. Control the ambient temperature to make the
greatly.
fluctuation within +/-4℃.
1. Electrode is invalid.
1. Replace the electrode.
2. Environment interference.
Voltage noise, 2. Relocate the instrument.
A22010 ISE unit Error NOIS 3. ISE Main board failure.
electrode: 3. Replace the ISE Main board.
4. Salt buildup around electrodes or tubes 4. Clean the tubes and electrodes.
due to fluidic leaks.
1. Calibrator B is exhausted.
2. Bubbles exist in calibrator tube B
1. Replace the reagent pack with a new one.
3. Peristaltic pump B tube is aging,
2. Perform purge B to remove bubbles.
clogged and broken.
3. &4. Replace the pump tube.
A22011 ISE unit Error Air in calibrator B PUGB 4. Waste pump tube is aging, blocked, or 5. Clean the sample injection port and reinstall
broken: electrodes.
5. Sample injection port and fluidic path 6. Replace the air bubble detector.
are blocked or leaking.
6. Air bubble detector failed
1. Calibrator A is exhausted. 1. Replace the reagent pack with a new one
2. Calibrator A tube contains many air 2. Perform purge A to remove air bubbles.
A22012 ISE unit Error Air in calibrator A PUGA
bubbles. 3. and 4. Replace the peristaltic pump tube.
3. Peristaltic pump A tube is aging, 5. Clean the sample injection port and reinstall

No.HSH-19021-BS-240 Version:4.0 10-43


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
clogged and broken. electrodes.
4. Waste pump tube is aging, blocked, or 6. Replace the bubble detector.
broken:
5. Sample injection port and fluidic path
are blocked or leaking.
6. Air bubble detector failed
1. Peristaltic pump tube is aging.
ISE pump calibrating 1. Replace the pump tube.
A22013 ISE unit Error / 2. Aspiration and dispensing of sample
failed! 2. Replace the sample probe.
probe goes wrong.
1. Air bubble detector board is eroded due
Air bubble detector to the leaks at the joint of sample
A22014 ISE unit Error / Replace the air bubble detector.
failure injection port and bubble detector.
2. Air bubble detector failed
Reading reagent 1. Reagent pack is not installed. 1. Install reagent pack.
A22015 ISE unit Error /
pack chip error 2. Reagent pack wand is failed. 2. Replace the wand.
Reagent pack chip
writing error. Unload 1. Reagent pack is not installed. 1. Install reagent pack.
A22016 ISE unit Error /
the reagent pack and 2. Reagent pack wand is failed. 2. Replace the wand.
load it again.
1. ISE wash solution is insufficient.
1, Place sufficient ISE wash solution.
2. Waste pump tube is aging, blocked, or
2. Replace the pump tube
Air in ISE wash broken:
A22017 ISE unit Error / 3. Clean the sample injection port and reinstall
solution 3. Sample injection port and fluidic path
electrodes.
are blocked or leaking.
4. Replace the bubble detector.
4. Air bubble detector failed
1. ISE wash solution is insufficient.
1, Place sufficient ISE wash solution.
2. Waste pump tube is aging, blocked, or
2. Replace the pump tube.
broken:
A22018 ISE unit Error No fluid in tubing CALF 3. Clean the sample injection port and reinstall
3. Sample injection port and fluidic path electrodes.
are blocked or leaking. 4. Replace the air bubble detector.
4. Air bubble detector failed
A22019 ISE unit Error Saving calibration DEP 1. Communication cable is disconnected. 1. Replace the ISE communication cable.

No.HSH-19021-BS-240 Version:4.0 10-44


IVD Global Technical Support Dept

Event Event Error Message and


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ID class Event Log
result error 2. The interface or pin goes wrong. 2. Replace the interface or pins.
3. ISE Main board failure. 3. Replace the ISE Main board.
4. Upgrade the operating software or reinstall it.
4. Wrong Software Version.
1. Communication cable is disconnected. 1. Replace the ISE communication cable.
Command format or 2. The interface or pin goes wrong. 2. Replace the interface or pins.
A22021 ISE unit Error RESP
execution error 3. ISE Main board failure. 3. Replace the ISE Main board.
4. Wrong Software Version. 4. Upgrade the operating software or reinstall it.
1. ISE wash solution is insufficient.
1, Place sufficient ISE wash solution.
2. Waste pump tube is aging, blocked, or
2. Replace the pump tube.
broken:
A22022 ISE unit Error No fluid in tubing / 3. Clean the sample injection port and reinstall
3. Sample injection port and fluidic path electrodes.
are blocked or leaking. 4. Replace the air bubble detector.
4. Air bubble detector failed
No reagent module 1. Reagent pack is not installed. 1. Install the reagent pack.
A22023 ISE unit Error /
has been loaded. 2. Wand error. 2. Install the reagent pack wand.
1. Communication cable is disconnected. 1. Replace the communication cable.
ISE response check 2. The interface or pin goes wrong. 2. Replace the interface or pins.
A22024 ISE unit Error RESP
code error 3. ISE Main board failure. 3. Replace the Main board of the ISE module.
4. Wrong Software Version. 4. Upgrade the operating software or reinstall it.
1.If fluidic prime is not performed, refer to 7.9.4
for fluidic prime.
2. Enter the Parameter Configuration screen,
select Wash Unit, find the Is Fluidic Prime
A22027 / Error Fluidic prime failed. / Fluidic prime is not performed.
Performed parameter, check whether the value of
this parameter is 1.Refer to Figure 13-9
Parameter Configuration -Change the Is Fluidic
Prime Performed parameter
Due to the system error, the sample bar
Initializing sample code reader cannot work normally. If the
A22036 / Error bar code reader / error repeats and cannot be removed, Refer to 10.2.6 .
failed. then the bar code reader has not
performed the initialization normally or the

No.HSH-19021-BS-240 Version:4.0 10-45


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
communication cables are disconnected.
Scanning reagent
A22038 / Error / Scanning reagent bar code failed. Refer to 10.2.6 .
bar code failed.
1. Executing version query instruction
failed.
Unmatched software
A22039 / Error / 2. Returned control software version and Refer to 10.2.4 .
version.
that stored in the operating software does
not match.
1. Reproduce failure.
2. Measure ambient temperature to check if
temperature is out of range.
3. Temperature sensor error: check for any signs
Warning No. 1:Sensor shortcut or of short circuit or broken circuit; check if
temperature above 75℃. connections are secure.
Temperature of 4. Temperature protection switch error: check if
Warning No. 2:Sensor disconnected or
Temperature cuvette cleaning fluid protection switch is shut and connections are
A22042 Warning / temperature below 0℃.
control unit is out of range: %s\r\n secure.
Temperature: %s Warning No.3:Heater is heating for a long
5. Heater error: check if resistance under normal
time
temperature is correct, and connections are
Warning No.4: Heater control is locked.
secure.
6. PCB failure.
7. Parameters are lost. Check if the temperature
control parameters are correct.
8. Electromagnetic interference exists.
1. Reproduce failure.
Warning No. 1:Sensor shortcut or 2. Measure ambient temperature to check if
temperature above 75℃. temperature is out of range.
Temperature of
Warning No. 2:Sensor disconnected or 3. Temperature sensor error: check for any signs
Temperature cuvette wash solution
A22043 Warning / temperature below 0℃. of short circuit or broken circuit; check if
control unit is out of range: %s\r\n
Temperature: %s Warning No.3:Heater is heating for a long connections are secure.
time 4. Temperature protection switch error: check if
Warning No.4: Heater control is locked. protection switch is shut and connections are
secure.

No.HSH-19021-BS-240 Version:4.0 10-46


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
5. Heater error: check if resistance under normal
temperature is correct, and connections are
secure.
6. PCB failure.
7. Parameters are lost. Check if the temperature
control parameters are correct.
8. Electromagnetic interference exists.
Reboot the computer and operating software. If
Operating CPU performance
C00007 Error / The CPU is too busy. this message appears for 3 times, contact our
system low
R&D department.
The last abnormal
exit may cause
carryover not
handled. Execute the
Operating Special Wash The operating software is abnormal or the After rebooting the software, perform the special
C00011 Error /
system maintenance analyzer is powered off accidentally. wash procedure.
command before
starting analysis to
ensure accurate
results.
Operating No sound card is installed; Sound card
C00012 Warning Sound card failure / Reinstall sound card or sound card driver
system failure; Incorrect sound card driver
Database software is not installed;
Instrument Equipment cannot be database is not established; database
C01001 Error / Refer to 10.2.12 for processing.
connection connected system or database file is damaged or
lost; database is opened exclusively
Database initialing
C02001 Database Error / Database upgrade failed Refer to 10.2.1 for processing.
failed
Database upgrade Database record is under use; database
C02002 Database Error / Refer to 10.2.1 for processing.
failed is locked
Database backup Cannot read or write necessary
C02004 Database Warning / Refer to10.2.2 for processing.
failed information from or into database
Database software is not installed;
Reading/Writing
C02005 Database Warning / database is not established; database Refer to 10.2.1 for processing.
database failed
system or database file is damaged or

No.HSH-19021-BS-240 Version:4.0 10-47


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
lost; database is opened exclusively
Result cannot be
calculated
Result Absorbance data for calculation is Investigate the cause of photoelectric data loss;
C03001 Warning Sample ID/bar code: RCE
calculation incomplete, or the dividend is 0. contact our R&D department
Position:
Chemistry:
Check the reaction curve. If the absorbance of R1
Absorbance out of is too high, check if reagent has air bubbles or
range The absorbance measured at the primary syringe leak.
Result
C03002 Warning Sample ID/bar code: ABS and secondary wavelength is greater than 2. Check if the reagent is placed in the correct
calculation
Position: 3.3A. position.
Chemistry: 3. Rerun the test after dilution.
4. Contact our R&D department.
Check if cuvette is clean or overflowed; check if
The reagent goes wrong; the cuvette is
reagent is sufficient, without air bubbles; check if
not clear; the reaction cuvette is
Result R1 blank absorbance chemistry parameters are reasonable; if previous
C03003 Warning RBK overflowed; or insufficient reagent is
calculation out of range problems do not exist, replace reagent and rerun
dispensed.
the test.

Substrate depletion
The sample concentration is too high, and
Result Sample ID/bar code: Check the reaction curve and the substrate
C03004 Warning BOE substrate depletion occurs during fixed-
calculation Position: depletion limit. Rerun the test with diluted sample.
time measurements.
Chemistry:
Result cannot be
calculated The sample concentration is too high, and
Result Check the reaction curve and the substrate
C03005 Warning Sample ID/bar code: ENC substrate depletion occurs within the lag
calculation depletion limit. Rerun the test with diluted sample.
Position: time of rate check measurements.
Chemistry:
Linearity limit out of The measuring points for result
range calculation are nonlinear, because the
Result Check the reaction curve and the substrate
C03006 Warning Sample ID/bar code: LIN sample concentration is too high, or the
calculation depletion limit. Rerun the test with diluted sample.
Position: substrate depletion limit is not specified or
Chemistry: unreasonable.
C03007 Result Warning Prozone check error PRO Antigen excess occurs due to too high Check the reaction curve and the prozone check

No.HSH-19021-BS-240 Version:4.0 10-48


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
calculation Sample ID/bar code: sample concentration. parameters. Rerun the test with diluted sample.
Position:
Chemistry:
Sample
concentration is
higher than that of the
Result highest-level The sample concentration exceeds the
C03008 Warning RRN Dilute and Rerun
calculation calibrator high limit of the calibrator concentration.
Sample ID/bar code:
Position:
Chemistry:
Mixed blank The reagent goes wrong; the cuvette is Check if the cuvette is clear and not overflowed,
Result absorbance out of not clear; the reaction cuvette is the reagent is sufficient without air bubbles, and
C03009 Warning MBK
calculation range overflowed; or insufficient reagent is the chemistry parameters are reasonable. If yes,
Chemistry: dispensed. replace the reagent and then rerun the test.
Check if the cuvette is not overflowed, the
The reagent goes wrong; insufficient
Blank response out of reagent is sufficient without air bubbles, the light
Result reagent is dispensed; the cuvette contains
C03010 Warning range BLK does not drift and the chemistry parameters are
calculation air bubbles; the light drifts; or the cuvette
Chemistry: reasonable. If yes, replace the reagent and then
is overflowed.
rerun the test.
Calibration The difference between the maximum and
Result Check if the acceptance limit is reasonable,
C03011 Warning repeatability exceeds DUP minimum response of the calibrator
calculation troubleshoot the error, and then recalibrate.
limit. Chem: exceeds the specified limit.
The difference of final response of the Check if the acceptance limit is reasonable and
Result Calibration sensitivity
C03012 Warning SEN maximum and minimum concentration the reagent and calibrator are normal, and then
calculation exceeds limit. Chem:
calibrators exceeds the specified limit. recalibrate.
The calculated standard deviation of the Check if the acceptance limit is reasonable and
Result Calibration curve SD
C03013 Warning CSD calibration curve exceeds the specified the reagent and calibrator are normal, and then
calculation exceeds limit, Chem:
limit. recalibrate.
Calibration
Check if the acceptance limit is reasonable and
Result determination The calculated fit of the calibration curve
C03014 Warning DET the reagent and calibrator are normal, and then
calculation coefficient exceeds exceeds the specified limit.
recalibrate.
limit, Chem:
Result Calibration slope The slope difference is applicable to linear Check if the acceptance limit is reasonable and
C03015 Warning FAC
calculation difference out of calibration only and refers to the K factor the reagent and calibrator are normal, and then

No.HSH-19021-BS-240 Version:4.0 10-49


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
range. Chem: (slope) difference between two adjacent recalibrate.
calibrations. It exceeds the specified
limit.
Calibration curve is
Result The calibration data and calibration curve Check if the calibrator is defined and placed
C03016 Warning not monotonic, MON
calculation are not monotonic. correctly, and then recalibrate.
Chem:
Calibration curve is For nonlinear calibration, a satisfying base Check that the reagent and calibrator are normal,
Result
C03017 Warning not convergent, COV cannot be calculated and no calibration and then recalibrate. If troubleshooting fails,
calculation
Chem: curve is drawn. choose other calibration rules and recalibrate.
The QC result is between ±2 and ±3
Result Chemistry:
C03018 Warning 1-2s standard deviations from the assigned No actions are required.
calculation Control: 1-2s warning
mean concentration.
Chemistry: The current QC result is greater than ±3
Result Check if the reagent is qualified, control sample is
C03019 Warning Control: 1-3s out of 1-3s standard deviations from the assigned
calculation normal, and the instrument is working correctly.
control mean concentration.
Results of two controls or two results of
Chemistry: one control within a run are
Result Check if the reagent is qualified, control sample is
C03020 Warning Control: 2-2s out of 2-2s simultaneously greater than +2 or -2
calculation normal, and the instrument is working correctly.
control standard deviations from the assigned
mean.
Chemistry: One result of a run is greater than +2
Result Check if the reagent is qualified, control sample is
C03021 Warning Control: R-4s out of R-4s standard deviations from the assigned
calculation normal, and the instrument is working correctly.
control mean and the other greater than -2SDs.
Results of two runs (4 results), or 4
Chemistry: continuous results of a control are on the
Result Check if the reagent is qualified, control sample is
C03022 Warning Control: 4-1s out of 4-1s same side and greater than ±1 standard
calculation normal, and the instrument is working correctly.
control deviation from the assigned mean
concentration.
Chemistry: Results of five runs (10 results), or 10
Result Check if the reagent is qualified, control sample is
C03023 Warning Control: 10-x out of 10-x continuous results of a control are on the
calculation normal, and the instrument is working correctly.
control same side.
Rerun the test, or reboot the operating software
Biochemistry test
Result Software error and analyzing unit. If the error remains, contact
C03024 Error period time out. /
calculation Operating system error our customer service department or your local
Cannot continue
distributor.
C03026 Result Warning Photoelectric data is / Communication error. If the error persists, contact our R&D department.

No.HSH-19021-BS-240 Version:4.0 10-50


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
calculation lost
Chemistry:
Result Multiple QC data and threshold values or Check if the reagent is qualified and control is
C03027 Warning Control: 1.0-2.7 out 2.7s
calculation cumulative sum exceed ±2.7SD. normal. Refer to 10.2.16 for processing.
of control
Chemistry:
Result Multiple QC data and threshold values or Check if the reagent is qualified and control is
C03028 Warning Control: 1.0-3.0 out 3.0s
calculation cumulative sum exceed ±3.0SD. normal. Refer to 10.2.16 for processing.
of control
Chemistry:
Result Multiple QC data and threshold values or Check if the reagent is qualified and control is
C03029 Warning Control: 0.5-5.1 out 5.1s
calculation cumulative sum exceed ±5.1SD. normal. Refer to 10.2.16 for processing.
of control
1. Rerun the operating software.
2. Reboot the operation unit.
Photoelectric
3. Check if the ground voltage is normal
measurement period
4. Check for interference, poor contact between
Result is out of range
C03030 Error TD Software error the splitter assembly and the Main board, or
calculation Sample ID/bar code:
damage to the cable.
Position:
5. Check the serial port connection, computer
Chemistry:
serial port
6. Replace the main board
1. Rerun the operating software.
Multiple consecutive 2. Reboot the operation unit.
photoelectric 3. Check if the ground voltage is normal
measurements are 4. Check for interference, poor contact between
Result
C03031 Error time out / Software error the splitter assembly and the Main board, or
calculation
Sample ID/bar code: damage to the cable.
Position: 5. Check the serial port connection, computer
Chemistry: serial port
6. Replace the main board
Duplicate sample bar
code.
Sample bar
C04001 Warning Sample ID/bar code: / Duplicate bar code is used. Replace the duplicate sample bar code label.
code
Position 1:
Position 2:
Bar code has no
Sample bar The sample of the bar code has not been
C04002 Warning corresponding / Program the sample of the bar code.
code programmed.
programming.

No.HSH-19021-BS-240 Version:4.0 10-51


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
Sample ID/bar code:
Position:
The sample is expired. Replace the sample and
Sample is expired
Sample bar The sample is loaded after its shelf life is program it again. Reject the expired sample. If
C04006 Warning Sample ID/bar code: /
code exceeded. the sample shelf life is too short, change it to a
Position:
reasonable one.
Sample bar Sample bar code too The bar code length is greater than the Redefine the bar code with no more than 27
C04008 Warning /
code long. Position: maximum value of 27 digits. digits.
Sample bar code is
Sample bar The bar code length is less than the
C04009 Warning less than 3 digits. / Redefine the bar code with no less than 3 digits.
code minimum value of 3 digits.
position:
Sample bar code
Sample bar analysis error Bar code data does not accord with the Reset the bar code format, or reprint and scan the
C04012 Warning /
code Sample bar code: defined format. bar code.
Position:
Incorrect reagent or reagent bar code is
Duplicate reagent bar being used, or an invalid reagent bar code
code is being used in a closed-reagent system.
Reagent bar Reprint the reagent bar code, or replace the
C05001 Warning Reagent: / Closed-reagent bar code is aligned with
code reagent bottle with an invalid bar code.
Position 1: closed reagents, and cannot be used
Position 2: again for new reagent when a reagent is
exhausted.
Incorrect reagent bar code is being used,
Print the new reagent bar code with correct
or reagent bar code is not configured
Reagent bar code settings and check the bar code against the
Reagent bar reasonably. The reagent bar code
C05002 Warning data error. / settings. In the case of a closed-reagent system,
code contains incomplete or incorrect reagent
Position: replace the reagent bottle, or contact the reagent
information, such as expiration date,
supplier.
reagent volume, etc.
Incorrect reagent bar code is being used,
or reagent bar code settings are incorrect. Check the reagent bar code settings, or reprint the
Reagent bar code
Reagent bar Non-closed reagent bar code is being reagent bar code against the settings. In the
C05003 Warning analysis error /
code used in a closed-reagent system. The case of a closed-reagent system, contact the
Position:
system fails to extract reagent information reagent supplier.
from the bar code.
Reagent bar Wash solution Reagent rather than wash solution is Reposition the reagent, or remove it from the
C05006 Error /
code position on reagent placed in the fixed wash solution position sample diluent position.

No.HSH-19021-BS-240 Version:4.0 10-52


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
carousel is occupied on reagent carousel.
by another reagent
Position:
Physiological saline
position on reagent Reagent rather than physiological saline
Reagent bar Reposition the reagent, or remove it from the
C05008 Error carousel is occupied / is placed in the fixed physiological saline
code sample diluent position.
by another reagent position on reagent carousel.
Position:
The pretreatment
The pretreatment reagent position is
Reagent bar reagent position is
C05010 Error / occupied by other reagent. Place the pretreatment reagent in correct position.
code occupied by other
reagent. Position:
The ISE wash
Reagent bar solution position is The ISE wash solution position is
C05011 Error / Place the pretreatment reagent in correct position.
code occupied by another occupied by another reagent.
reagent.
Host
C06001 communicati Error LIS initialization error / Host file is damaged or does not exist. Reboot operating software; initialize LIS module
on
Host
LIS communication Check system configuration parameters; re-
C06002 communicati Error / Host parameters error
parameter error connect LIS
on
If the error occurs accidentally, send or receive
Host
LIS communication the instruction again. If the error occurs for several
C06003 communicati Error / Communication failure
error times, contact LIS vendor. If problem remain,
on
contact our R&D department.
Host
LIS host cannot be Abnormal network connection, or the LIS Check if LIS host and LIS station is started
C06004 communicati Error /
connected host is not started. normally.
on
Sending sample If the error occurs accidentally, send or receive
Host
results failed. the instruction again. If the error occurs for several
C06005 communicati Warning / Communication failure
Sample ID/bar code: times, contact LIS vendor. If problem remain,
on
Position: contact our R&D department.
Host Sending sample If the error occurs accidentally, send or receive
C06006 communicati Warning information failed. / Communication failure the instruction again. If the error occurs for several
on Sample ID/bar code: times, contact LIS vendor. If problem remain,

No.HSH-19021-BS-240 Version:4.0 10-53


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
Position: contact our R&D department.
Inquiring sample If the error occurs accidentally, neglect it. Neglect
Host
information failed. the error. If the error occurs for several times,
C06007 communicati Warning / LIS host failure.
Sample ID/bar code: contact LIS vendor. If the problem remains,
on
Position: contact our R&D department.
Downloading sample
Host
failed. Incorrect channel settings; or insufficient Check and re-set the chemistry correspondence
C06008 communicati Warning /
Sample ID/bar code: or redundant chemistries on the LIS host. between the operating software and the LIS host.
on
Position:
1. The lamp is not installed correctly.
2. The cuvette is contaminated.
Light intensity is too
C07003 Light source Error / 3. The lamp is aging. Refer to 10.2.8 for processing.
weak
4. The wash station dispenses liquid
incorrectly.
1. The cuvette is contaminated.
2. The lamp is aging.
3. The lamp is not installed correctly.
Cuvette blank out of
C07004 Light source Warning range / 4. The wash station dispenses liquid Refer to 10.2.7 for processing.
Cuvette No.: incorrectly.
5. The photoelectric collection board goes
wrong.

1. The lamp is damaged.


2. The lamp cable is not connected
properly.
Lamp is not turned 3. The power board of the lamp is not
C07005 Light source Error / connected properly. Refer to 10.2.10 for processing.
on
4. The power supply of the analyzing unit
is disconnected.
5. The photoelectric collection board goes
wrong.
Light intensity is too
C07006 Light source Error / 1. A cuvette position has no cuvette Refer to 8) for processing.
strong

No.HSH-19021-BS-240 Version:4.0 10-54


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
installed.
2. The circuit gain is too high and beyond
the measurement range.
1. Perform dark current fluctuation test to identify
failure.
2. Check if the abnormal channel has something
to do with the channel gain. If it does, adjust the
1. The circuit gain is too high and beyond channel gain.
the measurement range. 3. Check if the cables on the AD collection board
Dark current is too
are installed correctly.
high 2. The power board of the lamp is not
C07007 Light source Error / 4. Unplug the cables from the AD collection board
Channel: connected properly. and pre-amplification board and perform the dark
AD: 3. The photoelectric collection board goes current fluctuation test again. Check if the failure
wrong. is related to the pre-amplification board. If yes,
replace the optical measurement assembly.
5. Replace the AD collection board.
6. If problem remains, contact our R&D
department.
1.Overflow
2. The lamp has been replaced
incorrectly.
3. Cuvette Check is not performed after
cuvette maintenance.
Water blank out of
C07009 Light source Error L! 4. Wash solution inside the cuvette is Refer to 10.2.9 for processing.
range (10X)
little.
5. The cable connector or retaining screw
of the lamp are not tightened.
6. The lamp is aging.
7. The photometer goes wrong.
No floppy disk or U disk is inserted. No file
Other error of
Storage device error. is found in the floppy disk or U disk, or file Check if U disk or floppy disk is inserted or full;
C07012 operation Warning /
Cannot import data error, or file is damaged. The floppy disk Check if storage device is damaged
unit
or U disk is locked or damaged.
C07013 Other error of Warning Storage device error. / No floppy disk or U disk is inserted. Check if U disk or floppy disk is inserted or full;

No.HSH-19021-BS-240 Version:4.0 10-55


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
operation Cannot export data Insufficient disk space. The floppy disk or Check if storage device is damaged
unit U disk is locked or damaged.
Other error of Reagent exhausted All reagents in this kind of bottles do not
C07014 operation Warning Chemistry: / reach minimum limit; All reagents of this Refill or replace the reagent.
unit Position: kind cannot be detected
Other error of Insufficient wash
Insufficient wash solution on the Refill the wash solution on the sample/reagent
C07016 operation Warning solution /
sample/reagent carousel. carousel.
unit Position:
Other error of Wash solution is
Wash solution is exhausted on the Refill the wash solution on the sample/reagent
C07017 operation Warning exhausted /
sample/reagent carousel. carousel.
unit Position:
Other error of Less than X tests are All reagents in this kind of bottles do not
C07022 operation Warning left in biochemistry / reach minimum limit; All reagents of this Refill or replace the reagent.
unit reagent. Chemistry: kind cannot be detected
Other error of Chemistry: %s, 30
The calibration factors are about to be
C07023 operation Warning minutes left for next / Recalibrate the chemistry.
expired.
unit calibration.
Other error of
Calibrator %s has
C07027 operation Warning / The calibrator is expired. Replace the calibrator.
been expired
unit
Chemistry: %s, lot
Other error of
No.: %s,
C07028 operation Warning / Expired Replace the reagent.
position: %s, has
unit
been expired
Chemistry: %s, lot
Other error of No.: %s,
The uncapping time of the reagent pack is
C07029 operation Warning position: %s, has / Replace the reagent.
too long.
unit exceeded the on-
board stability time
Other error of Insufficient
Insufficient physiological saline on Refill the physiological saline on the
C07034 operation Warning physiological saline /
sample/reagent carousel sample/reagent carousel.
unit Position:
Other error of Physiological saline
Physiological saline is exhausted on Refill the physiological saline on the
C07035 operation Warning is exhausted /
sample/reagent carousel. sample/reagent carousel.
unit Position:
C07036 Other Warning Chemistry: %s. / The calibration factors have been expired. Recalibrate the chemistry.

No.HSH-19021-BS-240 Version:4.0 10-56


IVD Global Technical Support Dept

Event Event Error Message and


Component Flag Probable Causes Corrective Actions
ID class Event Log
Calibration factors
are expired
Reagent bottle
number of %s
Reagent serial number of the chemistry is
C07037 Other Warning chemistry is / Serial number of the reagent is changed.
changed. Please recalibrate
changed. Please
recalibrate
Reagent lot number
of %s chemistry is Reagent lot number of the chemistry is changed.
C07038 Other Warning / Lot number of the reagent is changed.
changed. Please Please recalibrate
recalibrate
Calibration factors
C07039 Other Warning of %s chemistry are / The calibration factors are expired. The calibration factors are expired.
expired. Recalibrate
Reagent exhausted Reagent exhausted
C07040 Other Warning / Refill or replace the reagent.
Chemistry: Reagent probe does not detect liquid level
ISE reagent is less Inventory of the ISE reagent is lower than Check the inventory, and refill ISE reagent if
C07041 Other Error /
than %s the alarm limit. necessary.
%s, lot number: %s,
One or more special reagents have
C07042 Other Warning position: %s, has / Replace the reagent.
expired.
been expired
Pretreatment reagent
The test for whole blood needs pretreatment
C07043 Other Warning is exhausted. / Pretreatment reagent is used up.
reagent. Fill the pretreatment reagent.
Position:
Pretreatment reagent
The test for whole blood needs pretreatment
C07044 Other Warning is insufficient. / Pretreatment reagent is insufficient.
reagent. Fill the pretreatment reagent.
Position:
ISE wash solution is
C07045 Other Warning / ISE Wash solution is exhausted. Add the ISE wash solution.
exhausted.
ISE wash solution is
C07046 Other Warning / ISE wash solution is insufficient. Add the ISE wash solution.
insufficient.

No.HSH-19021-BS-240 Version:4.0 10-57


IVD Global Technical Support Dept

11 Assembly Explosive Views


11.1 Overview
This section shows the diagram and Order Number for each assembly. Such information can help engineer
order and change the parts.
NOTE
⚫ All the Order Numbers in the tables below are intended for engineer to query the order number.
⚫ When you order spare parts, please use the order number in the spare parts list from Mindray.
⚫ If the Order Number is shown as /, that means the part cannot be ordered as a spare part. It is intended to
help reader understand the machine. Tubes or connectors are not mention in this section.
⚫ Please refer to the liquid system section.

11.2 Instrument Panels Exploded


11.2.1 Front Right Panels

2
1

Figure 11-1 Front Right Panels View

No.HSH-19021-BS-240 Version: 4.0 11-1


IVD Global Technical Support Dept

Part Name

No. Order Number Quantity Remark

Front panel assembly(BA24)

1 115-036337-00 1 /

Right cover assembly

2 115-036570-00 1 /

11.2.2 Back Left Panels

1 2
3
4

Figure 11-2 Back Left Panels View

No. Order Number Part Name Quantity Remark


1 / Rear Cover 1 /
2 BA10-20-77801 Top Cover 1 /
3 115-036338-00 Left cover assembly 1 Contain ④
4 BA40-20-61392 ISE Cover 1 /

No.HSH-19021-BS-240 Version: 4.0 11-2


IVD Global Technical Support Dept

11.2.3 Top Panels

3
2
4
5

Figure 11-3 Top Cover Explosive View

No. Order Number Part Name Quantity Remark


1 115-036339-00 Sample Reagent plate cover assembly 1 /
2 043-006892-00 Sample Reagent table-board 1 /
3 043-006896-00 Automatic wash table-board 1 /
4 115-036340-00 Reaction plate table-board assembly(BA24) 1 /
5 043-006894-00 Lamp table-board 1 /

No.HSH-19021-BS-240 Version: 4.0 11-3


IVD Global Technical Support Dept

11.2.4 Front Left Panels

1
3

2
4
7
5
6

Figure 11-4 Front Left Panels Explosive View

No. Order Number Part Name Quantity Remark


1 115-036337-00 Front panel assembly(BA24) 1 /
2 115-037736-00 Protective Cover Hinge Assembly 2 /
3 M6T-010005--- Air Spring 2 /
4 / Upright Support Plate 2 /
5 / Mid baffle plate(BA24) 1 /
6 / Syringe Cover Assembly 1 /
7 / Spring Screw 1 /

No.HSH-19021-BS-240 Version: 4.0 11-4


IVD Global Technical Support Dept

11.3 ISE Unit


11.3.1 ISE Unit Position

1 2
2

Figure 11-5 ISE Unit Position View

No. Order Number Part Name Quantity Remark


1 BA34-10-63812 ISE Reagent Connector 1 /
2 / ISE Unit

No.HSH-19021-BS-240 Version: 4.0 11-5


IVD Global Technical Support Dept

11.3.2 ISE Unit Exploded

8
7

1 5

3 4

Figure 11-6 ISE Unit Explosive View

No. Order Number Part Name Quantity Remark


1 / ISE Shield Cover 1 /
2 / 4 Channel ISE Module 1 /
3 / ISE Shield Box 1 /
4 082-000684-00 Peristaltic Pump 3 /
5 BA34-10-63664 ISE Pump Tube Kit 3 /
6 BA34-10-63659 4 Channel PCB Preamp Board Kit 1 /
7 BA34-10-63657 4 channel PCB Main Board I/O kit 1 /
8 BA34-10-63661 ISE Sample Cup 1 /

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11.4 S/R Probe Unit


11.4.1 S/R Probe Unit Position

Figure 11-7 S/R Probe Unit Position View

No. Order Number Part Name Quantity Remark


1 S/R Probe Unit 1 /

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11.4.2 S/R Probe Unit Exploded

1
5

2 6

3
7

Figure 11-8 S/R Probe Unit Explosive View

No. Order Number Part Name Quantity Remark


1 043-002344-00 130mm rocker cover 1 /
2 115-037552-00 Reagent Preheater Assembly 1 /
3 / 130mm Rocker 1 /
4 115-036662-00 S/R Probe Drive Assembly 1 /
5 115-016462-00 Probe Pole & Spring 1 /
6 051-002479-00 Integration Liquid Detecting Board PCBA 1 /
7 / Support Boss 1 /
8 115-037085-00 Sugar sample probe assembly 1 /

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11.4.3 S/R Probe Drive Assembly Exploded

2 2

Figure 11-9 S/R Probe Drive Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 / Timing belt,B123MXL6. 2 /
2 009-002204-00 Optical Assembly(BA24) / /
3 / Belt (B175MXL6.4) 2 /
4 115-038797-00 Vertical motor assembly(BA24) 2 /
5 115-038796-00 Horizontal motor assembly(BA24) 2 /

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11.5 Reagent/sample Disk


11.5.1 Reagent/sample Disk Position

Figure 11-10 Reagent/sample Disk Position View

No. Order Number Part Name Quantity Remark


1 Reagent/sample Disk 1 /

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11.5.2 Reagent/sample Disk Exploded

5 6

Figure 11-11 Reagent/sample Disk Explosive View

No. Order Number Part Name Quantity Remark


1 115-036341-00 Sample Reagent Disk assembly 1 /
2 / Reagent/sample refrigeration assembly 1 /
3 / Reagent/sample Disk drive Assembly 1 /
4 / Belt.180XL037 Rubber 1 /
5 009-002204-00 Optical Assembly(BA24) / /
6 115-036317-00 Reagent/sample Disk Motor Assembly 1 /

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11.5.3 Reagent Refrigeration Unit Exploded

Figure 11-12 Reagent Refrigeration Unit Explosive View

No. Order Number Part Name Quantity Remark


Reagent Refrigeration Reagent Temp
1 024-000110-00 1
Temperature Sensor Sensor
Peltier Cooler 53W 40*4.03mm
2 / 2 Replace two together
510mm
Fan For Reagent
3 BA10-20-78146 Fan 1.1A 2
Refrigeration

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11.6 Barcode Scanner Unit


11.6.1 Barcode Scanner Unit Position

Figure 11-13 Barcode Scanner Unit Position View

No. Order Number Part Name Quantity Remark


1 / Barcode Scanner Unit 1 /

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11.6.2 Barcode Scanner Unit Exploded

Figure 11-14 Barcode Scanner Unit Explosive View

No. Order Number Part Name Quantity Remark


1 023-000738-00 MS-3 Laser scanner 1 Barcode Scanner
2 115-036320-00 Reagent Disk Antifogging Assembly 1 /

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11.6.3 Reagent Disk Antifogging Assembly Exploded


1 2 3 4
5

Figure 11-15 Reagent Disk Antifogging Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 / Anti-fog Fixed Block 1 /
2 / Antifogging Heater 1 /
3 / Thermal Protector 70C 1 /
4 / Dustproof Cover Plate 1 /
5 / Sponge Adjust Pillow 1 /

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11.7 Reaction Disk Unit


11.7.1 Reaction Disk Unit Position

Figure 11-16 Reaction Disk Position View

No. Order Number Part Name Quantity Remark


1 Reaction Disk Unit 1 /

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11.7.2 Reaction Disk Unit Exploded

1
2

5 8

6 9

Figure 11-17 Reaction Disk Unit Explosive View

No. Order Number Part Name Quantity Remark


1 115-036362-00 Cover Component 1 /
2 042-011592-00 Press Board Assembly 8 /
3 115-036356-00 Reaction disk assembly 1 /
4 115-036357-00 Reaction disk heat preservation assembly 1 /
5 115-038798-00 Reaction Plate Motor assembly 1 Contain ⑥
6 BA40-10-62044 Shock Relief Pad 1 /
7 115-036355-00 Reactor Axletree Assembly 1 /

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No. Order Number Part Name Quantity Remark


8 / Belt .18L037 Rubber 1 /
9 009-002204-00 Optical Assembly(BA24) / /

11.7.3 Heat Insulation Chamber of Reaction Carousel Exploded

1
2

Figure 11-18 Heat Insulation Chamber of Reaction Carousel Explosive View

No. Order Number Part Name Quantity Remark


Reaction carousel temperature
1 BA10-20-78144 Fan 0.05A 4
control 60 fan cable
Temperature Sensor Wire
2 009-006306-00 1 Reaction Disk Temperature Sensor
of Reaction Disk

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11.7.4 Heater cables above and under Reaction Carousel Exploded

Figure 11-19 Heater cables above and under Reaction Carousel Explosive View

No. Order Number Part Name Quantity Remark


1 BA10-21-78142 Reaction Top Heater 1 /
Reaction Disk Thermal
2 BA10-21-78147 1 Thermal Protector (70°C)
Protector
3 / 3/8"connecter 1 /
Reaction Disk Bottom
4 BA10-21-78143 1 Reactor lower Heater connector
Heater

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11.8 Wash Well


11.8.1 Wash Well Positions

1
2

1 2

Figure 11-20 Wash Well Position Views

No. Order Number Part Name Quantity Remark


1 043-000556-00 Washing Panel 1 Wash well
2 BA10-20-77752 Washing Well 1 Wash Well

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11.9 Photometer Unit Exploded


11.9.1 Optical Assembly Position

Figure 11-21 Optical Assembly Position View

No. Order Number Part Name Quantity Remark


1 115-035724-00 Optical Assembly(BA24) 1 /

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11.9.2 Optical Assembly(BA24) Exploded

1 8
7

4 5 6

Figure 11-22 Optical Assembly (BA24) Explosive View

No. Order Number Part Name Quantity Remark


1 BA10-30-77760 Pre-amplification Board 1 Pre-amplifier Board
2 / Filter Wheel Assembly 1 /
3 115-038466-00 20W Lamp Module (FRU) 1 Lamp
4 041-001143-00 Lamp base retaining screw 1 /
5 / Terminal 2 /
6 009-002204-00 Optical Assembly(BA24) / wire of Optical Switch(s)
7 024-000793-00 Optical Assembly(BA24) 1 stepping motor
8 BA10-20-78211 FAN(FRU) 1 Fan for Lamp

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11.10 Mixer Assembly


11.10.1 Mixer Assembly Position

Figure 11-23 Mixer Assembly Position View

No. Order Number Part Name Quantity Remark


1 Mixer Assembly 1 /

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11.10.2 Mixer Assembly Exploded

4
2
5
6

Figure 11-24 Mixer Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 043-003064-00 Cover for Mixing Bar(65mm) 1 Cover for Mixer Arm
2 044-000333-00 Base of the Mix Probe Arm(65mm) 1 /
3 115-036665-00 Mixer Drive Assembly 1 drive of mixer
4 BA30-10-15052 DC Motor(6V) 1 /
⑤ and ⑥ , Order Number:
5 BA30-20-06774 Retaining Nut 1
801-BX50-00012-00, Mixer
6 BA31-20-41651 Mixer 1 Paddle with Nut.

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11.10.3 Mixer Drive Assembly Exploded

3
2

4
5

Figure 11-25 Mixer Drive Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 BA30-10-06619 Timing belt,B123MXL6.4 1 /
2 115-038796-00 Horizontal motor Assembly(BA24) 1 Horizontal Motor
3 009-002204-00 Optical Assembly(BA24) / wire of Optical Switch(s)
4 / Belt (B175MXL6.4) 1 /
5 115-038797-00 Vertical Motor Assembly(BA24) 1 /

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11.11 Wash Station Assembly


11.11.1 Wash Station Assembly Position

Figure 11-26 Wash Station Assembly Position View

No. Order Number Part Name Quantity Remark


1 Wash Station Assembly Position 1 Front right view

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11.11.2 Wash Station Assembly Exploded

1 5

7
3

Figure 11-27 Wash Station Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 BA40-20-61570 Knurled Screw 1 /
2 009-002204-00 Optical Assembly(BA24) / wire of Optical Switch(s)
3 115-036352-00 Wash Station Drive Assembly Contain①②④
4 024-000793-00 Stepping motor 1 /

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No. Order Number Part Name Quantity Remark


BA48 Wash Photo Connector Anti-collision Sensor for Wash
5 051-001147-00 1
PCBA Station
6 041-001845-00 Cleaner of Wash Probe 1 White Wash Blocker
Contain ⑤ and ⑥ , Wash
7 115-036353-00 Washing Probe Assembly 1
Probe Assembly

11.12 Rear Frame Part


11.12.1 Rear Frame Part Exploded

3
5
2

1 8

Figure 11-28 Rear Frame Part Explosive View

No. Order Number Part Name Quantity Remark


1 / PCB Bracket 1 /
2 115-011901-00 10ml Syringe Module 1 /
3 / 2.5ml Syringe Module 1 /
4 / Valve Assembly 1 /
5 / PCB Fan Assembly 1 /
6 / Power Supply Assembly 1 /

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No. Order Number Part Name Quantity Remark


Communication and Power Power Grounding, Serial
7 / 1
Joint Communication cable, Switch
8 Analyzer Switch Analyzer Switch 1 Rocker Switch
9 082-002720-00 2-way Solenoid Valve SV07, WIRE FOR Solenoid Valve

11.12.2 Power Supply Assembly Exploded

Figure 11-29 Power Supply Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 051-002404-00 BA24 Power Board PCBA 1 Power Board
2 BA10-20-78145 Fan 0.17A 2 Fan 0.17A

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11.12.3 10ml Syringe Module Exploded

3
2

Figure 11-30 10ml Syringe Module Explosive View

No. Order Number Part Name Quantity Remark


1 0033-30-74615 Syringe (10mL) 1 /
2 / Special Bolt 3 2 /
3 009-002204-00 Wire of Optical Switch(s) / Optical Assembly(BA24)
4 115-035628-00 2.5ml Syringe Drive Assembly 1 2.5ml drive assembly

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11.12.4 2.5ml Syringe Drive Assembly Exploded

Figure 11-31 2.5ml Syringe Drive Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 024-000366-00 Stepping motor 1 /

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11.12.5 PCB Bracket Exploded

Figure 11-32 PCB Bracket Explosive View

No. Order Number Part Name Quantity Remark


1 051-002413-00 BA24 Power Driver Board 1 BS-240 Drive Board
Depend on
2 115-038795-00 Main board ( Opened System ) 1
Configuration
Main board ( Close System 3 User- Depend on
115-038787-00 1
defined ) Configuration
Main board ( Close System 5 User- Depend on
115-038788-00 1
defined ) Configuration
Main board ( Close System 0 User- Depend on
115-038789-00 1
defined ) Configuration

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11.12.6 Communication and Power Joint Exploded

3
2

Figure 11-33 Communication and Power Joint Explosive View

No. Order Number Part Name Quantity Remark


1 / Power Outlet and Cable 1 /
2 M07-00061S--- Main Power Switch 1 Main Power Switch
Computer Communication Cable from main board to serial
3 BA10-20-78212 1
Patch Cord cable port

11.12.7 Valve Assembly Exploded

3
2
1

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Figure 11-34 Valve Assembly Explosive View

No. Order Number Part Name Quantity Remark


082-002273-00/082- EM valve LVMK21-6J wire/2-way Solenoid
1 1 SV03
002720-00 Valve
082-002273-00/082- EM valve LVMK21-6J wire/2-way Solenoid
2 1 SV04
002720-00 Valve
082-002273-00/082- EM valve LVMK21-6J wire/2-way Solenoid
3 1 SV05
002720-00 Valve
4 082-002435-00 wire of 0127 solenoid valve 1 SV02
082-002373-00/801- Three-way valve of LVMK/WTB-3R-N4E 3-
5 1 SV06
BA38-00011-00 way solenoid valve wire
082-002373-00/801- Three-way valve of LVMK/WTB-3R-N4E 3-
6 1 SV01
BA38-00011-00 way solenoid valve wire

11.13 Front Right Frame Part


11.13.1 S/R Syringe Assembly Position

Figure 11-35 S/R Syringe Assembly Position View

No.HSH-19021-BS-240 Version: 4.0 11-34


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No. Order Number Part Name Quantity Remark


1 / S/R Syringe Assembly / /

11.13.2 S/R Syringe Assembly Exploded

1
2

Figure 11-36 S/R Syringe Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 115-038595-00 Drive Assembly of syringe 1 /
2 / 3-way connector of syringe 1 /
3 082-000430-00 Reagent Syringe.500ul(ZDV)(FRU) 1 Reagent Syringe

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11.13.3 Drive Assembly of Syringe Exploded

Figure 11-37 Drive Assembly of Syringe Explosive View

No. Order Number Part Name Quantity Remark


1 / Synchronous belt B63MXL6.4 1 /
2 115-038630-00 S/R syringe drive assembly 1 Motor module of syringe
3 041-024153-00 Screw of piston fixed 1 /
4 BA31-30-41501 Initial Position Sensor of Syringe 1 Home sensor of syringe
5 BA31-20-41404 Fixing Screw 4 /

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11.13.4 Front Right Frame Part Exploded

5 6
7 8 9

1
2 3 4

Figure 11-38 Front Right Frame Part Explosive View

No. Order Number Part Name Quantity Remark


1 BA20-30-75227 Reagent Refrigeration Board 1 /
2 048-006112-00 The Back Net 1 /
3 048-006111-00 The Front Net 1 /
4 / Fluidic Joint 1 /
5 BA10-30-77759 A/D Conversion Board 1 /
6 115-036601-00 Wash Station Preheater Assembly 1 /
7 BA30-21-15311 Probe Interior-washing Pump 1 /
8 2000-21-06116 P02&P03 Waste Pumps 2 P02&P03 Wash Pump
diaphragm pump of
9 082-002426-00 Diaphragm Pump 1
NMP830

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11.13.5 Wash Station Preheater Assembly Exploded

1 2 3

Figure 11-39 Wash Station Preheater Assembly Explosive View

No. Order Number Part Name Quantity Remark


1 009-000485-00 AC heater 100W cable 2 /
2 024-000111-00 Sensor Temperature 5Kohm B3470K Column 2 /
3 / Switch of Temperature 2 /

11.13.6 Fluidic Joint Bracket Exploded

1 3

Figure 11-40 Fluidic Joint Bracket Explosive View

No. Order Number Part Name Quantity Remark


1 / Waste connector 1 /
2 / Waste connector nut 1 /

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3 / Connector.1/4-28UNF,1/8"ID,PP 4 /

11.14 Optional Module


11.14.1 Drainage Unit (BA40-30-61346)

6 5

1 2 3

Figure 11-41 Drainage Unit Exploded View

No. Order Number Part Name Quantity Remark

1 010-000310-00 Power Switch 3 /


2 BA40-21-61666 Water inlet module power socket wiring 3 /
3 BA40-30-72955 Power Supply Board of WIM 2 /
4 BA40-30-61498 Mainboard of Drain Module 1 /
5 082-001263-00 Water Pump of WIM 1 /
6 BA40-30-61690 Waste Liquid Buffer Tank Assembly of DM 1 /
7 BA40-20-61307 Waste buffer bottle holder 1 /

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12 LIS Connection Setting and


Troubleshooting
12.1 Overview of LIS
The LIS system is abbreviated from Laboratory Information System (Laboratory) and an important part of the
hospital information management. The LIS system has the main features including but not limited to specimen
check and acceptance, report processing, report review and specimen transfer. The stability of the LIS system
will significantly affect the normal operation of the laboratory department and even the diagnosis of clinicians.
The LIS system is also an important part for 15189 review process of the laboratory department. Medical
organizations pay more and more attention to medical information technology, including establishment of the
LIS system. The LIS system is also closely related to other systems in a hospital, including HIS system and
electronic medical records system. When an operator reviews a report in the LIS system, the self-service report
printer, out-patient medical workstation, in-patient medical workstation, including WeChat official account and
Alipay can receive the test result from the LIS system in real time. The LIS system has more and more data
interactions with other HIS subsystems.
For a equipment manufacturer, the equipment is normally connected to the LIS system which will print the lab
report. This is one of the most important sign indicating whether the equipment is enabled. To allow an engineer
to effectively coordinate the debugging operation of the LIS interface, the following sections focus on basic
knowledge and common problems concerning LIS connection.
12.2 LIS Networking
The communication between a computer (hereinafter referred to as workstation) and the LIS system is based
on TCP/IP protocol and data is transmitted via serial port or Ethernet port (cable transmission). The stability of
the network is very critical to the communication of the LIS system. The workstation configured for the
equipment shall have 2 or more network cards, and the workstation resides in the same network as that of the
equipment and LIS computer.

Figure 12-1 LIS connection diagram

12.2.1 Querying State of RS232 Serial Port Card and Network Card
Identifying the installation state of RS232 serial port and network card driver is an important part for detecting
the network state. If the driver is not installed, or any exception occurs to the installed driver, even if the
hardware including serial cable or network cable works normally, the network communication may be faulty.
Select [Computer] - [Property] - [Device Manager] - [Port] to check the installation of serial port card driver to
check the state of the serial port.
Select [Computer] - [Property] - [Device Manager] - [Network Adapter] to check the installation of network card

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driver to check the state of the network card. Open Network and Sharing Center -> Control Panel\Network &
Internet\Network Connection to check network connection.
12.2.2 Checking Network Status
One of the network cards configured to the workstation is used to communicate with the LIS computer. Use a
network cable to connect the workstation to the LIS computer and use the "ping" command to check the
connectivity of the network.
ping is also a communication protocol as a part of TCP/IP protocol. The "ping" command can be used to check
the connectivity of the network and helpful in analyzing and identifying network failure. It is applied in the
following format: ping (a space) IP address.
Use the following steps to set the IP address of one of network works in the workstation computer to the same
network segment as that of the LIS system:
1) Click the "Network Connections" icon on the computer, open "Network and Sharing Center" and then
click "Local Connection".
2) Click "Details" to check IP address, subnet mask, default gateway and DNS server.
3) Open Network and Sharing Center -> check Active Network -> click and select Network Connections
- Connection - Properties (select Internet protocol version 4).
Set IP address and other information on this interface. The network between workstation computer and LIS
system is set according to the network architecture of a hospital.

Figure 12-2 Input IP address

IP setting of workstation computer in a hospital

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Figure 12-3 IP setting of workstation computer in a hospital

The IP address of the workstation computer shall be in the same network segment as that of LIS computer.
4) On the workstation, use the Win + R combination key and input CMD into the Run input box to enter
the command console:

Figure 12-4 Run screen

5) Input ping + IP of the LIS computer. If you are actually returned with bytes, the network is connected.

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Figure 12-5 Network connected

Request timeout, data lost.

Figure 12-6 Network disconnected

6) Perform step 5 on the LIS computer to check if the network is connected


12.3 LIS Parameter Setup
12.3.1 Introduction to Protocols
Mindray devices strictly follow HL7 protocol and ASTM protocol. LIS manufacturers, at their discretion, decide
to use what protocol to implement LIS interface connection, i.e. via Ethernet port or serial port.
There are detailed descriptions about field and domain for message headers and separator domains defined
in HL7 protocol and ASTM protocol. LIS interface engineers shall strictly follow the examples given in the

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communication protocol to develop LIS interfaces. This User Manual further explains the communication
protocol so that LIS engineers can be directed more effectively to develop interfaces.
The ASTM protocol is not specific to serial port. It is also applicable to Ethernet port. ASTM and HL7 protocols
define the message transfer format while serial port and Ethernet port are means for transferring data.
Note:
Serial port or Ethernet port is only a means for transferring data. The cross serial port cable used in data
transfer shall meet RS232C specifications.
12.3.2 Parameter Setup on a Workstation Computer
[Apply] - [System Setup] - [LIS Setup]
If Auto Connect to LIS is checked, the machine will be automatically connected to the LIS interface. A port is
set by the LIS system. The port on the workstation shall be set the same as that of the LIS system. Do not set
the port number to 80/8080.
After Retry after Disconnect is checked, the machine will automatically connect to the LIS system if LIS
disconnection is detected.

Figure 12-7 Transport setup

BS-240 allows interaction with the LIS system via serial port or Ethernet port. ASTM and HL7 standards are
only protocols and not related to transport medium. Both HL7 protocol and ASTM protocol allow transfer of
test data via serial port or Ethernet port.
12.3.3 Basic Concept of Unidirectional/Bidirectional LIS
Communication
Unidirectional LIS communication:
The machine only sends the test result to the LIS system and receives no any instruction from the LIS system.
The machine, after test, will automatically send related data to the LIS system which will then analyze the
received test result.
Bidirectional LIS communication:
The machine not only sends the test data to the LIS system but also receives an instruction from the LIS
system.
After recognizing the barcode containing sample information, the machine will send the "Inquiring sample
information" instruction to the LIS system which will then retrieve the matching information about test items
therefrom according to received sample information. If the information about test items are retrieved, the LIS
system shall return messages in a fixed format to the machine within the specified period of time.
The uniqueness of a sample is identified by a bar code. Once a barcode for a sample is generated, it is unique
and cannot be changed.

Note: Regardless of bidirectional LIS communication or unidirectional LIS communication, the LIS shall always
make response to the information sent from the machine.

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The unidirectional and bidirectional LIS communications have the basically same settings on LIS Setup ->
Transport Setup, with the only difference in
Bidirectional LIS setup:
1) From [Apply] - [System Setup] - [LIS Setup], select Bidirectional for the communication mode.
2) From [Apply] - [System Setup] - [Barcode Setup], select [Auto Number Scanned Samples].

Figure 12-8 Sample Bar Code

12.3.4 Channel ID Setup


Purpose of channel ID (item code): A channel ID plays an important role in LIS communication. In unidirectional
LIS communication, if there is a test item without setting a channel ID (item code), the result will not be sent to
the LIS system. Missing of test results is often resulted from failure to set a channel ID.
When a sample shall be diluted before testing, a channel ID is divided into a general channel ID and a dilution
channel ID which have the same setting method. However, a general channel ID shall not be the same as a
dilution channel ID, and do not carry out the original content test and dilution test for the same specimen at the
same time. The LIS system can process the general testing and dilution testing separately, but only one
channel ID is active when the machine is communicating with the LIS system.
The role of a channel ID is more important in bidirectional LIS communication. Without setting a channel ID,
or when the channel ID (item code) of the machine does not match that of the LIS system, when the machine
identifies the sample barcode and then sends the "Inquiring sample information" instruction to the LIS system,
the LIS system will not match correct information about sample items from the background according to the
barcode. To correctly transfer information about sample items, use the channel ID set in the LIS system. If the
LIS system sends a channel ID not set in the machine or a wrong channel ID, the machine will receive the
information with an alarm and reject to process it.
Steps to set a channel ID:
1) Disconnect the LIS system before maintaining a channel ID
2) Double click the blank area after an item and input the pre-defined channel ID (it is determined by
the LIS engineer).

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Figure 12-9 Channel ID setup

Note: In general, only the LIS system administrator has permission to set a channel ID in the LIS system. Any
other persons are not authorized to edit a channel ID.
The channel ID maintained on the workstation computer shall be the same as that on the LIS system.
For example, the channel ID setup interface of the LIS system.
12.4 Operation Guidance of Test Tool
Please download the LIS test tool from the TDP platform
TDP/Bio-chemistry/LIS/LIS tool
Role of test tool: The tool is mainly intended for testing the LIS communication function of the machine (the
capability of sending the test result after specimen testing)
The LIS communication function is one of the most basic functions of the software. Methods to process raw
data may be different, depending on LIS manufacturers. When a test result is missed or part of results goes
wrong during transfer, you can use a data reception tool to check the cause. If it is checked that data sent from
the machine is completely consistent with that displayed in the workstation log, you can simply locate the LIS
interface to address the problem with raw data. Therefore, you can simply use the test tool to find out the
reason for an LIS problem. This tool mainly helps an engineer to check raw data sent from the machine.
The machine and LIS system cannot be used as the client or server side at the same time. Instead, there can
be the case where one is the client and the other is the server side. Note that port numbers are consistent. If
the 2 conditions above are met, the basic communication conditions are established. As a client, the machine
has the function to automatically connect to the LIS system.
12.4.1 Operation Procedure of Test Tool
1) Double click the "Mindray.exe" app
Note: The bi-direction test checkbox is checked by default. The server side mode is used by default.
Copy the Mindray.exe test tool to the workstation computer. Open Mindray.exe and exit the LIS system. Set
the port number and IP address in LIS setup on the workstation computer the same as that on the test tool,
and use the test tool as the client.

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Figure 12-10 LIS tool

2) Setting port number and IP address


Setting port number and IP address is the most important link for implementing simulation of bidirectional LIS
communication.
Note: Click the "Log" button to generate a log which can be accessed from the path :LisDebug\Lislog.txt.
Click the "Clear" button to clear raw data.

Figure 12-11 LIS tool

Setting port number: The port number shall be identical to that set in the test tool.
IP is set to point to LIS IP. If the LIS system is installed on the computer connected to the machine, IP can be
set to Local IP (127.0.0.1). If the LIS system is not installed on the computer connected to the machine, IP is
set to Distance IP.

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Figure 12-12 LIS tool

3) Simulating bidirectional LIS communication


When simulating bidirectional LIS communication, this tool can visualize the communication between the test
tool and the machine and generate a communication log which can be used to describe how to implement
bidirectional LIS communication to be used for simulation by an engineer. This can be an important guidance
for LIS engineers to develop bidirectional LIS interfaces.
The communication protocol and principle used by this test tool is identical to LIS system. However, it has only
part of LIS features and cannot completely be used as an alternative for LIS.
This test tool completely gives the data flow of bidirectional LIS communication and reduces the difficulty in
understanding bidirectional LIS communication and interface development on the engineer side.

Figure 12-13 LIS tool

The configuration file is mainly intended for maintaining item information and patient information sent to the
machine during bidirectional LIS communication testing.

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Figure 12-14 LIS channel ID

Note: By default, the Mindray.exe tool assigns default values to basic patient information during programming.
A channel ID shall be manually entered in MRsettings.ini.
LIS Engineer's Need-to-Know
▪ Start character: char(11) Ox0B
▪ Carriage return character: char(13) Ox0B
▪ Stop character: char(13)+char(28) Ox0D+Ox1C
▪ ASCII (American Standard Code for Information Interchange) is a computer encoding system based
on Latin alphabet and mainly used for displaying Modern English and other Western-European
languages. It is now the most common single-byte coding system https://baike.baidu.com/item/编码
/80092. In interactions of LIS communication information, part of codes in the ASCII chart are used
as control characters. Therefore, LIS engineers shall identify the start character and stop character
when developing LIS interfaces. If all conditions are met, data is valid, with the start character being
single-byte char(11) Ox0B and stop character being multi-byte char(13)+char(28) Ox0D+Ox1C.
08,00:46:09:140,LinkLayer
Log: =><SB>MSH|^~\&|||||20180708004609||QRY^Q02|2487|P|2.3.1||||||ASCII|||<CR>
QRD|20180708004609|R|D|1169|||RD|120000116538|OTH|||T|<CR>
QRF||||||RCT|COR|ALL||<CR>
<EB><CR>
,

Messages in LIS communication use fixed format. Each sample message contains control characters which
are invisible to the naked eye but they have to exist. The machine will convert the start character to <SB> and
stop character to <EB><CR> in order to completely express received messages.
Regardless of receiving the sample application information or response message from the LIS system, the
machine will always detect both the start and stop characters in the message frame. An LIS engineer shall not
treat the start character and stop character as a character in the LIS interface, nor add or delete control
characters.
12.5 Common Problems and Corrective Measures
12.5.1 LIS cannot be connected
First, check whether the port number set on the workstation computer matches that of the LIS interface. Do
not use port number 80/8080. Next, check whether the IP address of the workstation matches that of the LIS
host and check that the workstation is properly connected to the LIS host.
The machine is used as the client and the LIS is used as the server side by default. The machine can be
automatically connected to the LIS.

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12.5.2 LIS communication interrupted suddenly


▪ LIS sudden interruption: The "Transmission (TX)" button of the LIS is grayed out. The button is black
in normal state.
▪ The HOST status bar flashes always. It is blue in normal state. (In the condition that the LIS interface
is active)
▪ The machine software displays that the LIS is connected, but the "TX" button is grayed out (in the
condition that the LIS interface is active)
▪ The machine software displays that the LIS is not connected, and the "TX" button is grayed out (in
the condition that the LIS interface is active)
▪ The Connect icon is on and then grayed out (In the condition that the LIS interface is active)
For Mindray machines, the administrator permission is required for LIS communication to normally transmit
test results and implement information interaction. Change administrator permissions as below:

Figure 12-15 Run regedit

Figure 12-16 Registry

The EnableUA value is normally 0: from the Registry, change the EnableUA value to 0
HKEY_LOCAL_MACHINE\SOFTWARE\Microsoft\Windows\CurrentVersion\Policies\System

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Figure 12-17 LIS state

12.5.3 Issues with firewall


Firewall settings will also affect the LIS communication. Check the firewall settings in both the machine and
LIS system sides.
Firewall policy: For the sake of security, some labs will customize some policies to allow only the port number
specified by the LIS system for communication. This is wrong. Although the port number used for LIS
communication is fixed, data communication inside the machine is randomly assigned with a port number.
Therefore, a port number shall not be fixed or limited to a certain range.
Windows system is a copy: Some computer systems are not an authorized edition, especially for non-
authorized edition with the desktop displayed as black ground that will affect the LIS communication. In this
case, please install an authorized edition and then deploy the LIS environment again.
12.5.4 Invalid LIS response
During LIS communication, especially when transmitting test results, the workstation can continue
communication only when a correct response message is received from the LIS system; otherwise, the
communication is blocked.
Error C06005 Sending sample results failed
Main cause: After sending the sample results, the machine does not receive the valid ACK message from the
LIS system.
The machine will identify this as sending failure.
Error C06007 Inquiring sample information failed
Main cause: The machine issues the "Inquiring sample information" instruction to the LIS system. That is, the
machine scans the barcode and then sends the barcode information to the LIS system. However the LIS
system fails to return the information about what is test item on the barcode in the specified period of time or
correct format, and an alarm is generated. For an example of this, see below.
22,10:28:59:523,LinkLayer
Log: =><SB>MSH|^~\&|||||20190222102859||QRY^Q02|10|P|2.3.1||||||ASCII|||<CR>
QRD|20190222102859|R|D|9|||RD|1902224828|OTH|||T|<CR>
QRF||||||RCT|COR|ALL||<CR>
<EB><CR>
22,10:28:59:668,LinkLayer
Log: <=<SB>MSH|^~\&|||||20190222102859||QCK^Q02|10|P|2.3.1||||||ASCII||<CR>
MSA|AA|10|Message accepted|||0|<CR>
ERR|0|<CR>
QAK|SR|OK|<CR>
<EB><CR>

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22,10:28:59:669,MSH segment field count < 19 error[Count = 18].,


22,10:28:59:669, Parse segment[1] of message error[Ret = -2147090430]. ,
22,10:28:59:669,LinkLayer Log: CLinkLayer::DealFrame create FetchRcvFrm(),

Figure 12-18 LIS code

If there is a problem with message ACK, then an error will occur when item information is transmitted to the
machine later.

Figure 12-19 LIS item information

12.5.5 ISE response time out


27,11:33:07:185,LinkLayer
Log: =><SB>MSH|^~\&|||||20180727113307||ORU^R01|3583|P|2.3.1||||0||ASCII|||
27,11:33:37:194,AppLayer Log: Application Layer Timeout !!!,
:
:
:
27,11:33:37:198, sending sample results failed. Sample ID/bar code: 3032, position: N0016-2,

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Figure 12-20 LIS sample result

When the "Sending sample results failed" error occurs, check whether a response message is developed for
the LIS interface.
The response time can be set to 10 s, 20 s or 30 s in LIS setup.
When the workstation sends sample results, the LIS system shall make response. If the response is given for
more than 10 s, the machine will alert response timeout. An alarm will be also generated when the response
format is wrong. An LIS engineer shall pay special attention to start character, stop character and message ID
when processing response messages. Message ID is a variable. Not all message IDs sent each time are 1.
<SB>MSH|^~\&|LIS-Server|NanShan
Hospital|Mindray|BS-400|20090216201111||ACK^R01|64|P|2.3.1||||0||ASCII|||<CR>
MSA|AA|64|Message accepted|||0|<CR>
<EB><CR>,
Problems with bidirectional LIS communication due to problems with channel ID
12.5.6 LIS communication result slowly transmitted
The machine has a mechanism to check response. That is, the machine will continue communication only
when it receives a valid response from the LIS system after a sample result is sent out. Otherwise, it will wait
for a valid response. Sending the test result from the machine to the LIS system may take a very short time. If
an engineer finds that transmitting a test result takes several minutes or longer, there is a high probability that
the LIS system has no response or gives wrong response.
In this case, an LIS engineer is recommended to check the response format of the LIS interface.
Note:
Message ID in a response message is a variable but not a constant. Message ID uses that given in the sample
result.
Response message:
<SB>MSH|^~\&|LIS-Server|NanShan
Hospital|Mindray|BS-400|20090216201111||ACK^R01|64|P|2.3.1||||0||ASCII|||<CR>
MSA|AA|64|Message accepted|||0|<CR>
<EB><CR>,
12.5.7 Part of item results missed during LIS communication
If part of item results are missed when transmission to the LIS system, check the channel ID, especially
checking whether this is a calculation item.
12.6 Bidirectional LIS communication interaction log

11,09:57:56:467,LinkLayer Log:=>
<SB>MSH|^~\&|||||20180811095756||QRY^Q02|1|P|2.3.1||||||ASCII|||<CR>
QRD|20180811095756|R|D|1|||RD|002100418080230050|OTH|||T|<CR>
QRF||||||RCT|COR|ALL||<CR>
<EB><CR>

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11,09:57:56:558,LinkLayerLog: <=<SB>MSH|^~\&|||||20180811095756||QCK^Q02|1|P|2.3.1||||||ASCII|||<CR>
MSA|AA|1|Message accepted|||0|<CR>
ERR|0|<CR>
QAK|SR|OK|<CR>
<EB><CR>

MSH|^~\&|||||20180811095756||DSR^Q03|1|P|2.3.1||||||ASCII|||<CR>
MSA|AA|1|Message accepted|||0|<CR>
ERR|0|<CR>
QAK|SR|OK|<CR>
QRD|20180811095756|R|D|2|||RD||OTH|||T|<CR>
QRF||||||RCT|COR|ALL||<CR>
DSP|1|||||<CR>
DSP|2|||||<CR>
DSP|3|||||<CR>
DSP|4|||||<CR>
DSP|5|||||<CR>
DSP|6|||||<CR>
DSP|7|||||<CR>
DSP|8|||||<CR>
DSP|9|||||<CR>
DSP|10|||||<CR>
DSP|11|||||<CR>
DSP|12|||||<CR>
DSP|13|||||<CR>
DSP|14|||||<CR>
DSP|15|||||<CR>
DSP|16|||||<CR>
DSP|17|||||<CR>
DSP|18|||||<CR>
DSP|19|||||<CR>
DSP|20|||||<CR>
DSP|21|002100418080230050||||<CR>
DSP|22|||||<CR>
DSP|23||20180811095756|||<CR>
DSP|24||N|||<CR>
DSP|25|||||<CR>
DSP|26||serum|||<CR>
DSP|27|||||<CR>
DSP|28|||||<CR>
DSP|29||2^^^|||<CR>
DSP|30||13^^^|||<CR>
DSP|31||6^^^|||<CR>
DSP|32||7^^^|||<CR>
DSP|33||8^^^|||<CR>
DSP|34||9^^^|||<CR>
DSP|35||10^^^|||<CR>
DSP|36||11^^^|||<CR>
DSP|37||12^^^|||<CR>
DSP|38||1^^^|||<CR>
DSC||<CR>
<EB><CR>

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11,09:57:56:732,LinkLayer
Log: =><SB>MSH|^~\&|||||20180811095756||ACK^Q03|1|P|2.3.1||||||ASCII|||<CR>
MSA|AA|1|Message accepted|||0|<CR>
ERR|0|<CR>
<EB><CR>
Role of Analysis Tool
A data analysis tool allows copy and paste of raw data of the machine for analysis.

08,23:03:18:947,LinkLayer
Log: =><SB>MSH|^~\&|||||20180708230318||ORU^R01|2800|P|2.3.1||||0||ASCII|||<CR>
PID|1472|||||||O|||||||||||||||||||||||<CR>
OBR|1472||9015|^|N|20180708224731|20180708224703|20180708224703||1^1||||20180708224703|serum|||
|||||||5|||||||||||||||||||||||<CR>
OBX|1|NM|4|calcium|2.252133|mmol/L|-|N|||F||2.252133|20180708225609|||0|<CR>
OBX|2|NM|5|magnesium|0.569389|mmol/L|-|N|||F||0.569389|20180708225829|||0|<CR>
OBX|3|NM|6|inorganic phosphorus|1.578690|mmol/L|-|N|||F||1.578690|20180708230304|||0|<CR>
OBX|4|NM|10|total bilirubin (vanadate oxidation method)|8.779144|μmol/L|-
|N|||F||8.779144|20180708230315|||0|<CR>
OBX|5|NM|11|direct bilirubin (vanadate oxidation method)|3.441980|μmol/L|-
|N|||F||3.441980|20180708230318|||0|<CR>
OBX|6|NM|16|adenosine deaminase|7.739112|U/L|-|N|||F||7.739112|20180708230311|||0|<CR>
OBX|7|NM|17|prealbumin|230.296762|mg/L|-|N|||F||230.296762|20180708230300|||0|<CR>
OBX|8|NM|18|total bile acid|1.787443|μmol/L|-|N|||F||1.787443|20180708230130|||0|<CR>
OBX|9|NM|19|alanine aminotransferase|19.820950|U/L|-|N|||F||19.820950|20180708230134|||0|<CR>
OBX|10|NM|20|aspartate amino transferase |39.088345|U/L|-|N|||F||39.088345|20180708230137|||0|<CR>
OBX|11|NM|21|alkaline phosphatase|130.115058|U/L|-|N|||F||130.115058|20180708230130|||0|<CR>
OBX|12|NM|22|γ-glutamyltransferase|67.893341|U/L|-|N|||F||67.893341|20180708230134|||0|<CR>
OBX|13|NM|23|lipoprotein (a)|71.263917|mg/L|-|N|||F||71.263917|20180708230217|||0|<CR>
OBX|14|NM|24|total protein|48.843538|g/L|-|N|||F||48.843538|20180708230224|||0|<CR>
OBX|15|NM|25|cholinesterase|4114.479156|U/L|-|N|||F||4114.479156|20180708225949|||0|<CR>
OBX|16|NM|26|albumin|29.379028|g/L|-|N|||F||29.379028|20180708225721|||0|<CR>
OBX|17|NM|27|lipase|10.279494|U/L|-|N|||F||10.279494|20180708230130|||0|<CR>
OBX|18|NM|28|α-amylase|63.568402|U/L|-|N|||F||63.568402|20180708230039|||0|<CR>

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OBX|19|NM|29|apolipoprotein A1|1.740667|g/L|-|N|||F||1.740667|20180708230217|||0|<CR>
OBX|20|NM|30|apolipoprotein B|1.241503|g/L|-|N|||F||1.241503|20180708230231|||0|<CR>
OBX|21|NM|31|triglyceride|5.302102|mmol/L|-|N|||F||5.302102|20180708230235|||0|<CR>
OBX|22|NM|33|low density lipoprotein cholesterin|2.838998|mmol/L|-
|N|||F||2.838998|20180708230231|||0|<CR>
OBX|23|NM|34|high density lipoprotein cholesterin|1.156541|mmol/L|-
|N|||F||1.156541|20180708230235|||0|<CR>
OBX|24|NM|35|total cholesterol|5.675223|mmol/L|-|N|||F||5.675223|20180708225732|||0|<CR>
OBX|25|NM|36|creatinine (sarcosine oxidase method)|61.837352|μmol/L|-
|N|||F||61.837352|20180708230239|||0|<CR>
OBX|26|NM|38|uric acid|436.774956|μmol/L|-|N|||F||436.774956|20180708230242|||0|<CR>
OBX|27|NM|40|cystatin C|1.232627|mg/L|-|N|||F||1.232627|20180708230246|||0|<CR>
OBX|28|NM|41|urea|3.750785|mmol/L|-|N|||F||3.750785|20180708230116|||0|<CR>
BX|29|NM|43|creatine kinase MB isoenzyme|32.245208|U/L|-|N|||F||32.245208|20180708230242|||0|<CR>
OBX|30|NM|44|creatine kinase|62.994467|U/L|-|N|||F||62.994467|20180708230249|||0|<CR>
OBX|31|NM|45|lactic dehydrogenase |324.101538|U/L|-|N|||F||324.101538|20180708230217|||0|<CR>
OBX|32|NM|46|α-hydroxybutyrate dehydrogenase|243.997631|U/L|-
|N|||F||243.997631|20180708230213|||0|<CR>
OBX|33|NM|58|C reactive protein|36.545503|mg/L|-|N|||F||36.545503|20180708230257|||0|<CR>
OBX|34|NM|61|β2-microglobulin|2.708314|mg/L|-|N|||F||2.708314|20180708230300|||0|<CR>
OBX|35|NM|62|α-L-fucosidase |53.824504|U/L|-|N|||F||53.824504|20180708230123|||0|<CR>
OBX|36|NM|63|Fe|10.033768|μmol/L|-|N|||F||10.033768|20180708230257|||0|<CR>
OBX|37|NM|65|homocysteine (enzymatic cycling methods)|13.780098|μmol/L|-
|N|||F||13.780098|20180708230304|||0|<CR>
OBX|38|NM|1|Na|136.355000|mmol/L|-|N|||F||136.355000|20180708225006|||0|<CR>
OBX|39|NM|2|K|4.220000|mmol/L|-|N|||F||4.220000|20180708225006|||0|<CR>
OBX|40|NM|3|Cl|101.729000|mmol/L|-|N|||F||101.729000|20180708225006|||0|<CR>
OBX|41|NM|135|Glo|19.400000|g/L|-|N|||F||19.400000|||||<CR>
OBX|42|NM|136|A/G|1.515464||-|N|||F||1.515464|||||<CR>
OBX|43|NM|137|AST/ALT|1.972250||-|N|||F||1.972250|||||<CR>
OBX|44|NM|138|IBIL-V|5.340000|μmol/L|-|N|||F||5.340000|||||<CR>
<EB><CR>

This tool can display how the LIS interface process raw data from the machine and how the raw data from the
machine is analyzed and extracted, and generates a log in a specified format

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Sample ID 9015
Channel ID -------------4--------|| item name --------calcium:--------:result 2.252133
Channel ID -------------5--------|| item name --------magnesium:--------:result 0.569389
Channel ID -------------6--------|| item name --------inorganic phosphorus:--------:result 1.578690
Channel ID-------------10--------||item name--------total bilirubin (vanadate oxidation method):--------:result
8.779144
Channel ID-------------11--------||item name--------direct bilirubin (vanadate oxidation method):--------:result
3.441980
Channel ID -------------16--------|| item name --------adenosine deaminase:--------:result 7.739112
Channel ID -------------17--------|| item name --------prealbumin:--------:result 230.296762
Channel ID -------------18--------|| item name --------total bile acid:--------:result 1.787443
Channel ID -------------19--------|| item name --------alanine aminotransferase:--------:result 19.820950
Channel ID -------------20--------|| item name --------aspartate amino transferase:--------:result 39.088345
Channel ID -------------21--------|| item name --------alkaline phosphatase:--------:result 130.115058
Channel ID -------------22--------|| item name --------γ-glutamyltransferase:--------:result 67.893341
Channel ID -------------23--------|| item name --------lipoprotein (a):--------:result 71.263917
Channel ID -------------24--------|| item name --------total protein:--------:result 48.843538
Channel ID -------------25--------|| item name --------cholinesterase:--------:result 4114.479156
Channel ID -------------26--------|| item name --------albumin:--------:result 29.379028
Channel ID -------------27--------|| item name --------lipase:--------:result 10.279494
Channel ID -------------28--------|| item name --------α-amylase:--------:result 63.568402
Channel ID -------------29--------|| item name --------apolipoprotein A1:--------:result 1.740667
Channel ID -------------30--------|| item name --------apolipoprotein B:--------:result 1.241503
Channel ID -------------31--------|| item name --------triglyceride:--------:result 5.302102
Channel ID -------------33--------|| item name --------low density lipoprotein cholesterin:--------:result 2.838998
Channel ID -------------34--------|| item name --------high density lipoprotein cholesterin:--------:result 1.156541
Channel ID -------------35--------|| item name --------total cholesterol:--------:result 5.675223
Channel ID -------------36--------|| item name --------creatinine (sarcosine oxidase method):--------:result
61.837352

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Channel ID -------------38--------|| item name --------uric acid:--------:result 436.774956


Channel ID -------------40--------|| item name --------cystatin C:--------:result 1.232627
Channel ID -------------41--------|| item name --------urea:--------:result 3.750785
Channel ID -------------43--------|| item name --------creatine kinase MB isoenzyme:--------:result 32.245208
Channel ID -------------44--------|| item name --------creatine kinase:--------:result 62.994467
Channel ID -------------45--------|| item name --------lactic dehydrogenase:--------:result 324.101538
Channel ID -------------46--------|| item name --------α-hydroxybutyrate dehydrogenase:--------:result 243.997631
Channel ID -------------58--------|| item name --------C-reactive protein:--------:result 36.545503
Channel ID -------------61--------|| item name --------β2-microglobulin:--------:result 2.708314
Channel ID -------------62--------|| item name --------α-L-fucosidase:--------:result 53.824504
Channel ID -------------63--------|| item name --------Fe:--------:result 10.033768
Channel ID------------65--------||item name--------homocysteine (enzymatic cycling methods):--------:result
13.780098
Channel ID -------------1--------|| item name --------Na:--------:result 136.355000
Channel ID -------------2--------|| item name --------K:--------:result 4.220000
Channel ID -------------3--------|| item name --------Cl:--------:result 101.729000
Channel ID -------------135--------|| item name --------Glo:--------:result 19.400000
Channel ID -------------136--------|| item name --------A/G:--------:result 1.515464
Channel ID -------------137--------|| item name --------AST/ALT:--------:result 1.972250
Channel ID -------------138--------|| item name --------IBIL-V:--------:result 5.340000

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13 Instrument Relocation and Emptying


13.1 Overview
When the analyzer is deactivated or should be moved to another working environment, process as follows.

13.1.1 Short-Term Suspension


If the analyzer is deactivated for a short term (within 3 days), the following operations are required on the
analyzer:
1) Enter the software, select Empty Fluidic Tubes. Refer to13.2 .
2) Remove all reagents and cleansers from the analyzer.
3) Exit the operating software, shut down the computer, and close the analyzing unit.
4) If the analyzer should be removed for storage, disconnect the main unit of the biochemical
analyzer from the computer, printer, display, and data cable, and follow the reverse steps of
8.4.4 Connect the pipeline to disconnect the tubing from the back end of the analyzing unit.

13.1.2 Long-Term Suspension


If the analyzer is deactivated for a long term (more than 3 days or several years), the following operations are
required on the analyzer:
1) Enter the software, select Empty Fluidic Tubes. Refer to13.2 .
2) Remove all reagents and cleansers from the analyzer.
3) Exit the operating software, shut down the computer, and close the analyzing unit.
4) Pack the analyzer according to section 13.4 Packing.

13.1.3 Analyzer Relocation


In the daily business of the laboratory, you may encounter the following situations that require the analyzer to
be relocated:
Out-Hospital Relocation
◼The laboratory will be relocated with the hospital or the analyzer will be transferred to another
branch for use.
◼The analyzer was donated to a lower-level hospital.
In-Hospital Relocation
◼The laboratory is refurbished and the analyzer must first be moved to a temporary department.
◼The laboratory is moved to a new room or a new building.
Relocation target: The movement of the analyzer may affect its normal use and have a certain impact on its
performance. The goal of the relocation is to ensure that its performance meets the business requirements
through subsequent alignment and verification as it moves.
Relocation steps:
1) Enter the software, select Empty Fluidic Tubes. Refer to13.2 .
2) Remove all reagents and cleansers from the analyzer.
3) Exit the operating software, shut down the computer, and close the analyzing unit.
4) Pack the analyzer according to section 13.4 Packing.
5) Transport to the target location
6) Install the analyzer according to 8 Installation..

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13.2 Emptying Fluidic Tubes


Click Utility →Maintenance→Alignment →Empty Fluidic Tubes to enter the screen.

Figure 13-1 Utility →Maintenance→Alignment →Empty Fluidic Tubes screen

13.2.1 Empty ISE Tube (optional)


Empty Index
1) After the ISE tube is emptied, no water flows out from the tube connecting the ISE reagent pack.
2) All electrodes have been removed and the peristaltic pump tubing has been removed.
Empty method and steps:
1) Prepare the pipette, as shown below, and enter the Empty ISE Tube screen.
2) Use the pipette to aspirate 200 μl calibrator A from the sample loading port.
3) Place enough ISE wash solution at the required location on the sample\reagent carousel screen.
Execute the cleaning command and wait for the cleaning completed before proceeding to the
next step;

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Figure 13-2 Empty ISE Tube screen

4) Remove all electrodes except the reference electrode. Dispense the aspirated calibrator A into
electrodes K+, Cl- and Na+, and use adhesive tape to seal both ends of the electrodes.
5) Install 4 spacers, use an emptying device to connect the A/B ports on the wand to deionized water,
and then execute Purge A/B periodically for 40 times.
6) Disconnect deionized water from A/B ports and continue with the purging.
Remarks: The number of purging operations can be set according to the emptying condition until the residual
deionized water in the A and B tubes is completely drained, and no liquid flows out from the waste outlet.

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Figure 13-3 Empty ISE Tube -Set purging times

7) Remove all electrodes and the emptying device, place the wand in the reagent pack, remove the

peristaltic pump tube, install the shielding box door, and tighten the screws on the shielding box.

Figure 13-4 Remove the pump tube from the peristaltic pump

13.2.2 Emptying Wash Tube


Empty Index
1) After emptying, no water flows out from the inlet of the auto DI water and the wash solution.
2) No water drops are sprayed out from the tip of the probe, and no water is sprayed out from the
outlet of the exterior wash well.
3) No water is sprayed out from the outlet of the exterior wash well of the mixer.
4) Check the waste outlet and there should be no colored waste liquid flowing out.
Empty method and steps:

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Figure 13-5 Empty Wash Tubes screen

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Note Prompt on the software screen Manual operation

Manually remove the diluted wash solution tank, empty and clean it, fill it 1) Make sure the waste tubes are connected.
with deionized water for half, and then install it 2) Click Continue. A dialog box will pop up. Confirm that the prompt
content is consistent with the real object, and click OK.

Clean the wash solution tube: 1) Operate according to the prompts on the screen. There is no
visible wash solution foam in the pack after cleaning. Click
Continue. A prompt dialog box will pop up. Confirm that the
prompt content is consistent with the real object, and click OK.
2 2) Set the number of emptying to 60, click Start to perform Prime
Wash Station.
3) If there is still colored liquid out from the waste tube at the end of
the cleaning procedure, click Start again and execute cleaning
again.

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Remove the wash prove and put it in an opening container. Operate according to the prompts on the screen. Select Continue to
proceed to the next step.

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1) Click Continue to set the number 20, and click Start.


2) Empty the wash tubes till no water is sprayed from phases 1~3
wash probes, otherwise the number of perfusion times is
increased.

Reinstall the wash probe onto the wash station. Click Continue. A dialog box will pop up. Confirm that the prompt
content is consistent with the real object, and click OK.

Empty the water in the exterior and interior wash tubing of the probe. 1) Click Continue, set the number of emptying, and click Start to
6
Observe if no water is sprayed out from the probe tip and the wash well. perform Empty Probe Interior and Exterior Wash Tubes.

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Otherwise, increase the priming times. 2) If there is still water out from the probe tip or from the outlet of the
probe exterior wash well at the end of the procedure, click Start,
and execute emptying again.

Empty the water in the exterior wash tubing of the mixer. Observe if no 1) Click Continue, set the number of emptying, and click Start to
water is sprayed out from the wash well of the mixer. Otherwise, increase perform Empty Mixer Exterior Wash Tube.
7 the priming times. 3) If there is still water from the outlet of the mixer exterior wash well
at the end of the procedure, click Start, and execute emptying
again.

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8 This procedure is complete. Select Continue to save it and exit the screen. Select Continue to exit the alignment.

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13.2.3 Emptying Waste Tubes


Empty Index
1) No water flows out from the low-concentration waste connector of the fluidics outlet assembly.
2) Wipe the water in the reagent\sample carousel.
Empty method and steps:

Figure 13-6 Empty Waste Tubes

1) Enter the Wash Waste Pump screen. Click Continue and a dialog box will pop up. Confirm that
the prompt content is consistent with the real object, and click OK.

Figure 13-7 Empty Vacuum and Waste Tube-Wash Waste Pump

2) Click Start to perform Empty Waste Pump Tubes, and observe that no water flows out from the
outlet of the waste tube. Click Stop to end the process. Tap "OK".

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Figure 13-8 Empty Waste Pump Tubes

3) Click Continue until the process on the software screen ends.


4) Wipe the water on the fluidics inlet and outlet assemblies with a clean cloth and seal the inlet of
the DI water and wash solution with high temperature adhesive tape.
5) Remove the sample/reagent carousel, wipe the liquid in the chamber and in the carousel with a
clean cloth, and then reinstall it.

13.2.4 Use Count of Emptying Pump and Syringe

13.2.5 Confirmation after emptying


1) Refer to the table below to confirm that the emptying has been completed.

Table 13-1 Confirmation list after emptying fluidic tubes

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No. Chemistry Inspection Standard/Requirement

No water flows out from the tube connecting the ISE


Empty ISE Tube reagent pack.
1
(optional) All electrodes have been removed and the peristaltic
pump tubing has been removed.
Empty Cuvette Wash No liquid flows out from the aspirate port of DI water and
2
Tube wash solution.
No water is sprayed out from the outlet of the exterior
wash wells of the probe and the mixer.
3 Empty exterior tubing
There should be no colored waste liquid flowing out the
waste outlet.
4 Empty Interior Tube No water drops are sprayed out from the tip of the probe.
No water flows out from the waste connector of the fluidics
5 Emptying Waste Tubes outlet assembly.
Wipe the water drops in the sample reagent chamber.

2) Enter the Parameter Configuration screen, select Wash Unit, find the Is Fluidic Prime Performed
parameter, check whether the value of this parameter is 0. If yes, click Done to exit the screen;
otherwise confirm whether emptying has been performed as required, and change the parameter to
0, and then click Configure to configure the parameter.

Figure 13-9 Parameter Configuration -Change the Is Fluidic Prime Performed parameter

13.3 Clearing Data


Note: This step is only performed when needed. By default, this step is skipped. This will erase all data on the

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computer and cannot be recovered. Please be cautious!


If you need to delete historical data, please operate as follows:
1)Exit the BS-240 system software, return to the WINDOWS operation screen, open the control
panel from the Start menu, and uninstall the BS-240 system software.
2)Delete all system-independent files under the operating software installation path.
3)Delete all desktop shortcuts and files related to the BS-240 system, then perform Empty
Recycle Bin.

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13.4 Packing
◼If the analyzer should be packed, please confirm whether the contents in the table below are
completed and whether the relevant materials have been prepared.
No. Check Item
1 The sample/reagent carousel has been emptied and cleaned
2 The reagents, cleansers, etc. in the analyzer have been taken out
3 The fluidic tubes have been emptied. Refer to 13.2 .
4 The materials list is as below:
◼ Tape. TESA4298 tape ivory white, 18 mmX50 (material ID: 095-000039-00)
◼ Stretch film width 450 mmX thickness 0.02 mm (material ID: A90-000095---)
◼ Roll foam. 53 M*1 M*8 mm (Material ID: 0000-10-10765)
◼ Bubble film Width 1 m Double flat Bubble Diameter 10 mm (material ID: A90-000077---)
◼ Heat shrinkable sleeve. Φ2.0 mm 105 Celsius degrees 600 V transparent (material ID: A20-
000018---), 1 for protecting the probe
◼ Cable tie (common tools, self-provided)
◼ Transparent sealed bag (self-provided)
◼ Sealing transparent tape (self-provided)
◼ Computer box (package left when installed)
◼ Accessory box (package left when installed)
◼ Main box and fixing screws (retained items when installed)
After confirming that the above items are correct, follow the installation guide in reverse. The specific steps are
as follows:

13.4.1 Removing the Tubes


Remove all tubes and tanks in reverse order of section8.4.4 Connect the pipeline, clean all tubes and tanks and
put them into the accessory box.

13.4.2 Removing the Accessories


1) According to the reverse order of 8.4.3 , respectively remove the probe and the mixer. Wrap the probe
tip with a heat shrinkable sleeve, place it into a sealed bag, and place it into the accessory box.
Note: Be careful not to lose the washer of the probe.
2) Remove the computer and the display, the serial cable and the power cable of the main unit.

13.4.3 Securing the Assemblies by Tape and Foam


As shown in the figure below, place the foam under the probe arm, the mixer arm, and the wash station, and
then fix them with tape. Fix each loading hole, sample/reagent carousel cover, and reaction carousel cover with
tape. Refer to Figure 8-7 Remove tapes and foams.

13.4.4 Securing and Packing the Main Unit


1) Separate the main unit from the cabinet and wrap them with stretch film separately, first from the lower
side to the upper side, and then wrap the protective cover diagonally (the whole machine is wrapped
around tightly with 3-4 layers), and expose the carrying handle.

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2) Pack the main unit and the cabinet according to the reverse order of section 8.4.1 Unpacking.

Among them, the four fixed brackets are shown as shown, and should not be misplaced. “F” is the front
of the instrument.

Figure 13-10 Pack the main unit

13.4.5 Packing the Accessories


Check that the accessories are complete (probe, mixer, tubing, tanks, instructions, operating cards, etc.) and
then wrap them in clear tape.

13.4.6 Packing the Main Unit and Display of the PC


1) Attach warning labels to the hand holes on both sides of the box of the computer main unit, and seal the
hand holes.

2) After attaching the serial number label on the box, bind the box with four straps as shown.

3) Bind the display box with two straps.

Figure 13-11 Pack the Main Unit and Display of the PC

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14 Optional Modules
14.1 Overview
The optional modules include the ISE module, clog detection module and barcode scanning module.
When the client wants to add the above functions, you should perform the upgrade installation and alignment
work as follows to ensure that the modules function properly.

14.2 ISE Module


14.2.1 Overview of ISE Module
Please refer to 3.10 ISE Unit (Optional).
The ISE module upgrade requires ISE upgrade package (BS-240) 115-038791-00 and ISE accessory box (with
packaging) 115-003320-00

14.2.2 Installing the ISE Module


1) Power off the whole machine, and remove the sample/reagent face plate, left side plate and back plate
of the analyzer. Refer to Figure 3-1 Shells assembly .
2) Remove the ISE module packaging and the accessories in the list.
3) Install the electrolyte module on the shielding box with four US screws #6-32X5/16 UNC-2A.

Shielding box
Four screws for fixing

Figure 14-1 Install the electrolyte module on the shielding box

4) Insert the connector of the waste tube into the ISE module, which should be tightly fit. Pay
attention to the installation direction, and the red seal should not fall off.

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Check the
connector of the
ISE waste tube.

Figure 14-2 ISE waste tube connection

5)Install the adapter cable of the ISE module onto the ISE module, and install the ISE module on the
mainframe bottom plate with four M4X8 pan head combination screws. The screws are not tightened
at the moment, and then tighten them after confirming the position of the ISE module. Be careful not
to press on the wire.

Figure 14-3 Adapter cable of the ISE module

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Figure 14-4 Secure the ISE module to the mainframe

6) Remove the six M3X6 screws from the three peristaltic pumps, add one M3 spring washer to each
screen, and then re-tighten the screws. Use twelve M2.5X6 Phillips pan head screws with flat
washers and spring washers to fix the three peristaltic pumps onto the lower bracket hole of the
syringe. Note that the wiring directions are upwards as shown in the figure.

Figure 14-5 Secure the peristaltic pumps of the ISE module

7) Use four M3X6 pan head screws with washers to mount the ISE power board onto the board
bracket: The position of the ISE power board, is shown as below:

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Figure 14-6 The position of ISE Power board

8) Connect the power cord of the ISE module to the corresponding ISE power board.

ISE power board ISE module power cord

Figure 14-7 Connect the cable of the ISE power board

9) Connect the cables between the ISE module and the three peristaltic pumps.
Note: Bundle the cables at the peristaltic pumps during the assembly procedure, and prevent the cables from
coming into contact with the shafts of the three peristaltic pumps.
10) Connect the ISE tubes as shown in the following figure. Use the small cable ties on the ISE module
interface to attach the A and B tubes to the shielding box. Install a retaining ring SB-1316 in the
outlet hole of the shielding box of the ISE waste tube.

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Figure 14-8 Connection diagram of ISE tubes

Figure 14-9 Physical map of ISE peristaltic pumps

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Wire harness
retainer (small)

Figure 14-10 Cable tie of ISE module

11) After the installation is complete, follow the above steps to check again.
12) Open the operating software with the engineer user name and password and click Utility→System
Setup→Factory Setup.

Figure 14-11 Utility-System Setup-Factory Setup

13) Click Optional Modules.

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Figure 14-12 Factory Setup-Optional Modules

14) Tick the Enable/Disable ISE checkbox, and click OK.

Figure 14-13 Optional Modules-Enable/Disable ISE

15) Align the ISE module

14.2.3 Alignment of the ISE module


1) Select Utility—>Maintenance—>Alignment—>ISE Unit. See Figure 7-58 ISE unit Alignment.
2) Install the reference, Cl-, K+, Na+ and the spacer into the ISE module from the bottom to the top.
Caution:
▪ Please be careful not to lose the O-ring seals;
▪ It is recommended to install the electrodes from the bottom to the top. You need to press down the

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base when you install the last electrode, to make sure the electrode is fixed well.
▪ Double check if the electrodes are fixed well.

Figure 14-14 Installation of ISE module electrodes

3) Connect the reagent pack to the reagent pack wand: as shown in the figure below, install the reagent
pack wand in place until you hear a "click" sound. Therefore, the "ISE communication error" appears.

Figure 14-15 Install the reagent pack wand

4) Align the probe position. (Refer to7.5.8 Probe to Horizontal Position on ISE Part (Optional) and 7.5.9
Probe to Vertical Position on ISE Part (Optional))
5) Module Intialization,refer to 7.11.1 Module .
6) Put away the panels including the ISE shielding shell.

Note: After the ISE module is installed, do not cut off the mains power (the power switch for
the analyzing unit can be cut off). If the mains power must be cut off and the downtime is more than 2
hours, empty the ISE and remove the electrodes. For details, refer to rob in 13.2.1 Empty ISE Tube
(optional). To remove electrodes, the ISE module shall be cleaned and emptied as well.

14.2.4 Precautions for ISE


▪ Don’t turn off the main switch if the machine has ISE module. Because the machine primes every half an

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hour automatically. Long time no priming can lead to damage of electrode


▪ After the upgrade of ISE module. We suggest standing and auto-prime for 24 hours before calibration and
normal test.
▪ After the ISE cleaning, please wait at least 15 minutes before calibration because the electrode is unstable
right after the cleaning.
▪ When execute calibration, we suggest calibrating 3-4 times, waiting the calibration data to be stable before
control or sample test.
▪ After electrodes are installed, the reagent pack shall be installed as well and at the same time, the mains
power for the analyzer shall be turned on to ensure that the ISE is continuously powered on.
▪ Carry out the calibration before ISE testing and the calibration result is normal. Otherwise, the accuracy of
the test result cannot be ensured.
▪ Clean it with MEDICA-specific wash solution at the end of daily operation (for details, refer to user manual);
▪ If testing for samples is carried out continuously for more than 8 hours or more than 50 consecutive samples
are tested, clean it and carry out calibration again.
▪ To remove electrodes, execute maintenance instructions and remove electrodes, along with the reagent
pack. Then, execute the ISE emptying procedure. For details, refer to 13.2.1 Empty ISE Tube (optional).

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14.3 Bar Code Scanning Module


14.3.1 Overview of Bar Code Scanning Module
Auto entry of reagent/sample information: automatically enter the reagent/sample information using barcode
scanning module
For sample barcode indicators, please refer to Table 2-3 Sample bar code.
For reagent barcode indicators, please refer to Table 2-4 Reagent bar code.
To upgrade the barcode scanning module, a barcode module upgrade package is required (BA36) 115-047663-
00

14.3.2 Installing the Barcode Scanner


1) Power off the whole machine, and remove the front face plate of the analyzer, sample/reagent face
plate, left side plate and back plate. Refer to Figure 3-1 Shells assembly.
2) Remove the four M3X12 screws on the barcode scanning window cover on the sample/reagent
carousel and remove the cover.

Figure 14-16 Remove the scanning window cover

3) Install the reagent carousel anti-fog heating unit onto the reagent chamber with four M3X8 Phillips pan
head screws.

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Figure 14-17 Install the reagent carousel anti-fog heating unit

4) Attach the dust cover with the sponge adjustment pad to the fixing plate with four M3X6 Phillips pan
head screws.

Figure 14-18 Install the dust cover

5) Use two M3X8 hex socket head caps with spring washers and large flat pads to secure the scanner
bracket to the barcode mounting plate. Use two M3X10 hex socket screws with spring washers and
large flat pads to mount the barcode scanner onto the scanner bracket. In this step, do not tighten the
two sets of screws. Align the position of the scanner first and then tighten the screws. Use two M3X8
hexagon socket screws with spring washers and large flat pads to secure the barcode mounting plate
to the underside of the frame beam and tighten the screws.

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Barcode mounting plate

Scanner bracket

Barcode scanner

Figure 14-19 Secure and install the barcode scanner

6) Connect the cables between the anti-fog heater and the protection switch and between the Main board
and the barcode module to the corresponding connectors as shown in the figure.

The bar code scanner is connected to the main control board, and the wire is routed to the right
along the side of the bottom plate

Figure 14-20 Barcode wiring

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Use a cable tie to


tie the bar code
scanner wire to the
rack, and the long
wire loops are
bundled behind the
bar code meter

Figure 14-21 Connection precautions

7) For barcode alignment, please refer to 7.8 Bar Code Unit (Optional).
8) After alignment, open the operating software with the engineer user name and password and click
Utility→System Setup→Factory Setup. See Figure 14-11 Utility-System Setup-Factory Setup
9) Click Optional Modules. See Figure 14-12 Factory Setup-Optional Modules.
10) Tick the Enable/Disable Sample Carousel Bar Code and Enable/Disable Reagent Bar Code
checkboxes, and click Save.
Note: Please tick the checkboxes according to the actual conditions of the client. For example, if the
client only scans with the reagent barcode, but does not use the sample barcode scanning, you can
tick only Enable/Disable Reagent Bar Code.

Figure 14-22 Optional Modules-Enable/Disable Bar Code

11) Complete the installation of the barcode scanning module.

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Appendices
A.1 BS-240 Installation Acceptance Report

BS-240_Installatio
n Acceptance Report_V1.0_EN.doc

A.2 BS-240 Moving Parts Position Confirmation Guide (No


Alignment Tooling)

BS-240_Moving
Parts Position Confirmation Guide (No Alignment Tooling)_V1.0_EN.doc

A.3 Tool list

Tool list.xlsx

A.4 BS-240_Error Information Feedback Form_V1.0_EN

BS-230&240_Erro
r Information Feedback Form_V1.0_EN.doc

A.5 BS-240 Series Recovery Checklist

BS-240_Series
Recovery Checklist_V1.0_EN.docx

A.6 Maintenance log sheet

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BS-240_Maintena
nce log sheet_V1.0_EN.xlsx

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A.7 Fluidic Diagram

Tube label
SV02 T10
Deionized water

D06 D07 Low-concentration waste


6 Reagent Reaction High-concentration waste Optional

T103 T104 T10


7 NS MIX Carouse Carouse
SY03 ZQ01
T105 ZQ11
ZQ21
ZQ31

D05 T61
SV03 T222 3

T221 D32 D33 D34


ZQ12
SI1 SI2 SI3 SI4
SV04 T61 T70
T612
1 2

T211 D22 D23 T212 D24 ZQ32 ZQ13 ZQ02


D31

T312
P04 P03 P02
W21 W31
D21 W01 W11
ZZ33 ZZ34
T30 ZZ24
SV05 ZZ23 5
SV07 ZZ08
ZZ32 ZQ33 ZQ14 ZQ03
ZZ22
T52 T311 T30
1 T511
P01 W02 W22
4
ZZ21 T404 T405
ZZ31
1 2 3
T303
ZZ05
T204 T502 ZZ07 T602
D04 SV06
ZZ12
D16 ZZ04

CAN02 ZZ06
ZQ15
ZZ11
T203 T301 T302

D11
SY02
T202 D12
T40
T10
SV01 T40
2 3
2 CAN01
D15 T201 D14 D13

D03
W03

SY01
ZZ03

Panel
D02 T101 ZZ02 T401 T60 T701
T501
1
FL01 W04 ZQ16 ZQ04
FL02
D01 ZZ01 FS03
FS01
FS02
V01 V02 V03 (optional) V04

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Fluidic Port Panel


High
DI water Diluted wash Low conc. Low conc. Waste conc.
inlet solution inlet Waste outlet 1 Waste
outlet 2
outlet
High
Low level level
floater of floater of
Low level floater
diluted wash high
of DI water
solution conc.
waste

FL02 FL03

FL01
DI water tank Diluted wash solution Low conc. waste tank High conc. waste tank

Analyzing Unit

Sensor
Tube
DI water tank

waste
concentration
Low-
solution tank
Wash

waste
concentration
High-

The tube length tolerance of the tube is not specified: when the tube length ≤ 100mm, the tolerance is ±5mm; when the tube length > 100mm, the tolerance is ±10mm.

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Tube label Rubber hose Type Part No. Actual length Number of Labels Tube Label type Remark
D03 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 220 1 PVC hose 8mm Assembling fluidic outlet assembly
D04 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 200 1 PVC hose 8mm Assembling fluidic outlet assembly
D05 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 350 1 PVC hose 8mm
D06 Rubber hose .PTFEID1.5mmXOD2.5mm×100M M6G-020049--- 320 / /
D07 Rubber hose .PTFE,0.040"IDX0.066"OD 0040-10-32301 2300 / / Assembling reagent preheating assembly
D11 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 400 1 PVC hose 8mm Assembling fluidic outlet assembly
D12 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Assembling fluidic outlet assembly
D13 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 500 1 PVC hose 7mm
D14 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Exterior wash tubing
D15 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 40 1 PVC hose 8mm Exterior wash tubing
D16 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 30 1 PVC hose 8mm Exterior wash tubing
D21 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 60 1 PVC hose 8mm Exterior wash tubing
D22 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Exterior wash tubing
D23 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Assembling instrument body assembly
D24 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 900 2 PVC hose 8mm Assembling instrument body assembly
D31 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 60 1 PVC hose 8mm Exterior wash tubing
D32 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Exterior wash tubing
D33 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Assembling instrument body assembly
D34 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 800 2 PVC hose 8mm Assembling instrument body assembly
ZZ03 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 560 2 PVC hose 8mm Assembling fluidic outlet assembly
ZZ04 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 360 1 PVC hose 8mm
ZZ05 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm
ZZ06 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 200 1 PVC hose 7mm
ZZ07 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 90 1 PVC hose 7mm Assembling wash tube
ZZ08 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 220 1 PVC hose 1.5mm Assembling wash tube
ZZ11 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 160 1 PVC hose 8mm Exterior wash tubing
ZZ12 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 200 1 PVC hose 8mm Deionized waster preheater tubing
ZZ21 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 50 1 PVC hose 8mm Deionized waster preheater tubing
ZZ22 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Deionized waster preheater tubing
ZZ23 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 120 1 PVC hose 7mm Assembling wash tube
ZZ24 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 260 1 PVC hose 1.5mm Assembling wash tube
ZZ31 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 200 1 PVC hose 8mm Deionized waster preheater tubing
ZZ32 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 50 1 PVC hose 7mm Deionized waster preheater tubing
ZZ33 Rubber hose .3/32"X5/32",ND-100-65,Tygon M90-100071--- 120 1 PVC hose 7mm Assembling wash tube
ZZ34 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 260 1 PVC hose 1.5mm Assembling wash tube
ZQ01 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 350 1 PVC hose 1.5mm Assembling wash tube
ZQ02 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 400 1 PVC hose 8mm Assembling wash tube
ZQ03 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 400 1 PVC hose 8mm Assembling fluidic outlet assembly
ZQ11 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 280 1 PVC hose 1.5mm Assembling wash tube
ZQ12 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 100 1 PVC hose 1.5mm Assembling wash tube

No.HSH-19021-BS-240 Version: 4.0 V


IVD Global Technical Support Dept.

ZQ13 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 400 1 PVC hose 8mm Assembling wash tube
ZQ14 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 100 1 PVC hose 8mm Assembling fluidic outlet assembly
ZQ15 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 300 1 PVC hose 8mm Assembling fluidic outlet assembly
ZQ21 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 280 1 PVC hose 1.5mm Assembling wash tube
ZQ31 Rubber hose .1.6*3.2mm TPU polyether 082-002375-00 420 1 PVC hose 1.5mm Assembling wash tube
ZQ32 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 400 1 PVC hose 8mm Assembling wash tube
ZQ33 Rubber hose .3.2*6.4mm TPU polyether 082-002374-00 140 1 PVC hose 8mm Assembling fluidic outlet assembly
W01 Rubber hose .Φ9.525XΦ15.875 natural color PVC 55~60° 082-000384-00 240 / / Assembling instrument body assembly
W02 Rubber hose .Φ9.525XΦ15.875 natural color PVC 55~60° 082-000384-00 180 / / Assembling instrument body assembly
W03 Rubber hose .Φ9.525XΦ15.875 natural color PVC 55~60° 082-000384-00 150 / / Assembling fluidic outlet assembly
W11 Rubber hose .Φ9.525XΦ15.875 natural color PVC 55~60° 082-000384-00 200 / / Assembling instrument body assembly
W21 Rubber hose .Φ9.525XΦ15.875 natural color PVC 55~60° 082-000384-00 110 / / Assembling instrument body assembly
W22 Rubber hose .Φ9.525XΦ15.875 natural color PVC 55~60° 082-000384-00 140 / / Assembling instrument body assembly
W31 Rubber hose .Φ9.525XΦ15.875 natural color PVC 55~60° 082-000384-00 150 / / Assembling instrument body assembly

P/N:046-009169-00(4.0)

No.HSH-19021-BS-240 Version: 4.0 VI

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