BS-240 - Service - Manual - V4.0 - EN - Copie
BS-240 - Service - Manual - V4.0 - EN - Copie
BS-240 - Service - Manual - V4.0 - EN - Copie
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
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
WARNING
If the product is used in a manner not specified by our company, the protection provided by the product may be
impaired.
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.
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.
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.
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.
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
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.
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.
WARNING
Ethanol is flammable substance. Please exercise caution while using ethanol around the instrument in order to
prevent fire and explosion.
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.
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.
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.
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
CAUTION
To define such parameters as sample volume, reagent volume and wavelength, follow the instructions in this
manual and the instructions of reagents.
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.
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.
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.
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.
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.
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
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.
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.
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.
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
Symbol Meaning
Authorized Representative in the European
Community
Biological risks
Caution
“ON” (Power)
“OFF” (Power)
Serial interface
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.
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
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.
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
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
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
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.
Analyzing
unit
PC(Operating software)
Main unit
Printer
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)
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
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
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
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.
T1 T11
Maximum reaction time of single reagent is over 20 min
Top cover
Rear panel
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.
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
Lamp panel
Frame
Assembly
Reaction Carousel
Assembly
Sample/reagent
Left panel assembly
carousel assembly
Reagent refrigeration
Front cover assembly
board and the bracket
Dust screen
retaining screw
Optical
assembly
Reaction Carousel
Body Assembly
M4×8 cross
countersunk head
screw
Cover
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
Hexagon wrench / 1
Exploded view for installation
Reaction chamber
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:
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
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
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
Motor
M5×12 hexagon
socket head cap screw
+ spring/flat washer
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.
Sample/reagent panel
Sample/reagent
Left panel assembly
carousel assembly
11
10
9 2
3
4
5
6
8
7
Figure 3-12 Sample/Reagent carousel 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
Sample/reagent
carousel body assembly
Rubber cushion
Temperature sensor
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.
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
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.
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
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
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
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.
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
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
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
How to do
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.
Bar code
reader
Switch
Rubber
anchor plate
M3×6 cross recessed Glass cushion
M3×12 hexagon socket
pan head screw cap head screw window
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
Shielding Cover
Sample/reagent carousel cover
Wash station desk
Sample/reagent panel panel
Lamp panel
Frame Assembly
Sample/reagent
Left panel
carousel assembly Reagent refrigeration
assembly Front cover assembly
board and the bracket
10
6
3 11
7
2
8
1
12
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,
Spring guide
post
Probe
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.
When to do
When Reagent Preheating Assembly failed.
Tools
Name Code Quantity
Cross screwdriver / 1
Medical rubber gloves / 1 pair
Exploded view for installation
Reagent
Preheating
Assembly
Heat
insulation
pad
M3*6
cross pan
head
M3*8 screw
cross pan
head
screw
Hardened powder
screw(M3*6)
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
Level sense
board
Hardened
power
screws(M3X6)
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
Horizontal
rotational
synchronous belt
M3*8 hexagon
socket cap screw
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
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
Probe movement
assembly
Synchronous
belt
Fixing plate B
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
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.
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.
Lamp panel
Frame
Assembly
Reaction Carousel
Assembly
Sample/reagent
Left panel
carousel assembly Reagent refrigeration
assembly Front cover
assembly board and the bracket
9
2
1
10
Diagonal pliers / 1
Medical rubber gloves / 1 pair
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
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
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) 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
DC motor
Retaining nut
Mixer
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
Vertical
Probe movement
motor
assembly
Synchronous
belt
Motor fixing
plate B
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
Mixer arm
assembly
Mixer drive
assembly
M6×16 hexagon
socket head cap
screws and
spring/flat washer
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.
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.
Wash Station
Wash probes
optical coupler
PCBA
Wipe block
Wash probe
drive assembly
OPtical coupler
wire (S)
Wash support
plate
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
Cable anchor
plate
M2.5×4 cross
wash station recessed pan
photocoupler head screw
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
Knurled
screw
Position adjusting
plate
M4×16 hexagon
socket head cap screw
+ spring washer
Zero position
photocoupler
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 .
Damper
pad
Motor
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
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
Zero position
photocoupler
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 .
Frame
Syringe
bracket weld
Syringe
module
Syringe left
bracket
2.5ml
syringe
assembly
Syringe lower
bracket
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.
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
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
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
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.
Filter retaining
screw
Filter retaining
washer
Filter retaining
washer
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.
NOTE:
Do not touch the optical surface of the filter with a hand during disassembling/assembling.
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
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.
Fan retaining
screws
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
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.
AD collection board
NOTE:
Wear ESD gloves when replacing the AD collection board.
Work principle
The ISE Module measures sodium, potassium, lithium and chloride in biological fluids,
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
Na
Ref
Two-points Calibration
→factor S
Calibrator Calibrator
B A
Pump Pump Pump ISE
Waste tank B A W
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
Item Features
Sample Serum,Plasma,Urine
Sample volume Serum, plasma 70uL, diluted urine 140uL
(10-fold dilution)
Method Direct method
Time 35s/cycle(Serum)
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
Peristaltic pump
–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.
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
SP3.5*8 screw
ISE module
ISE shield
M4*8 screw
Pump bracket
Pump
M2.5*6 screw
M2.5*6 screw
16 13
1-5
17 10 14 15
8 18 12
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.
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.
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.
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.
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
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.
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.
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.
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.
Power drive
board
Main Board
ISE power PCBA
Power supply
Level sense
board
Reagent
refrigeration board
AD collection
Pre-amplification Board board
Optical System
Photoelectric signal
Control signal
Temperature
control signal
Temperature control
PC RS232 Hardware System
system
Control signal
Control signal
Position signal
Reagent
Power drive
refrigeration Main Board
board
board
AD collection
board
Preamplifier
board
Main Board
Figure 4-5 Functional diagram of main board
Description
PCB
The PCB layout of the main board is as shown below.
Connectors
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.
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 Board
BA10-20-77756(before EBJ485)
050-003059-01(after EBJ485)
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.
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.
AD collection
board
Main Board
Main Board
AD
Description
PCB
The PCB layout of the AD collection board is as shown below.
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.
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..
Optical signal
AD collection
Preamplifier board
board
Optical signal
PDA
AD collection
board
Description
PCB layout
The preamplifier board layout of the main board is shown below.
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.
Vertical
collision
circuit
Description
PCB layout
The top layer of the liquid level detection board is shown below.
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.
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.
Reagent
Temperature
refrigeration Refrigeration
indication 2 Pelt iers
board control circuit
circuit
Description
PCB layout
The PCB layout of the reagent refrigeration board is shown below.
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.
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 /
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.
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.
A12V/2A Lamp
Analog Power
5V/4A AD collection Preamplifier
Main Board Supply C onversion
board board
Board
12V/5A
24V/6A
12V/11A
Reagent
refrigeration
board
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
10 Ground
12 Ground
4 screws
Top cover
AC
110/220
cable
cables
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.
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.
3) Remove the two screws that secure the switch support plate. Take the picture for the switch wiring.
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
1 2 3 4 5 6 7 8
BA33-21-35191
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
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
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
7 3
5 220VCTRL1 1 bl ue
AC power supply cables from
7
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
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:
1 2 3 4 5 6 7
1 2 3 4 5 6 7 8
PROBE
GND
1 black
2 red
D
D
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
7 NC
2 NC
3 NC
6 NC
22
44
1
3
Cables from m ain control board to
(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
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
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
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
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
GND
water
positi
NC 13
home
Dioni
movement motor C
zed
on
MINDRAY
A A
File: Bytes:
DWG NO. BA10 REV 1.1
Date: Time:
SHEET 3 OF 9 SIZE A2
Software & Rev: Microsoft office Visio 2003
1 2 3 4 5 6 7
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
Exterior Valve
Dispense Valve
dispense valve
Power supply board
Valve
P02:
pump
P03:
J4
D D
- +
1 white
4 orange
3 orange
1 of drive board
2 bl ack
2
1 bl ue
4 red
1
1
3 yellow
2
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
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
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
J20 23 24 24 CLK_RESERVED_MOTOR1 24
25 DIR_RESERVED_MOTOR1 25 25 26
J7
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
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
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:
DWG NO. BA23 REV 1
Date: Time:
1 2 3 4 5 6 7
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
File: Bytes:
DWG NO. BA10 REV 1.1
Date: Time:
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D Demisting
Demisting temperature
D
GND
GND
GND
12V
12V
12V
GND
protection
12V
sw itch
refrigeration/radiati
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
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
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
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
Date: Time:
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
Waste drainage
Mixer cleaning
Probe Wash
dispensing
aspiration
Inlet
SV02 T10
D06 D07
6
T103 T104 T10
7 NS MIX
SY03
T105
D05
SV03 T222
SV04
D21 W01
P01
T204
D04
D16
ZZ11
T203
D03
SY0
1
Panel
D02 T101
FL01
ZQ01
ZQ11
ZQ21
ZQ31
T613
ZQ12
SI1 SI2 SI3 SI4
T611 T612 T702
CAN02 ZZ06
ZQ15
T202 D12
SY02
SV01 T403
T402
D15 T201 D14 D13 CAN01
W03
SY01
ZZ03
Reagent Reaction
NS MIX Carouse Carouse
T602
W21 W31
W01 W11
ZQ15
T521 T511
W02 W22
T502
W03
ZZ03
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
Name Quantity
Cross screwdriver 1
Hexagon screwdriver 1
Flathead screwdriver 1
Cable tie Several
Diagonal pliers 1
Tube cutter 1
Figure 5-6 Assembly drawing of whole unit -- Probe and mixer wash module-front view
Probes exterior
Deionized water inlet T-valve Mixer Exterior Wash valve
wash valve
Figure 5-7 Assembly drawing of whole unit -- Probe wash module-rear view
Connector of wash
Connector of cleaning
solution syringe tube
fluid syringe tube
Screw
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.
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
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.
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.
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.
Heating
temperature
switch Of
cleaning fluid
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.
2) After the filter is replaced, prime it first otherwise the instrument may not work normally.
Verification steps
Refer to 7.9 Hydropneumatic Unit.
Note
• Operate carefully to prevent liquid from dropping into the reaction carousel and cuvettes.
The DI water tank and low-concentration waste tank contains one FRU.
Table 5-8 15L water tank FRU
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.
Setup folder: includes the operating software installation file setup.exe and the KillBsLog tool that can end the
Bslog service.
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.
Select None in the Turn off the display and Put the computer to sleep pull-down list boxes.
Select the Internet Time tab, and then deselect the checkbox in front of Synchronize with an Internet time server.
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:
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.
3) The following screen is displayed. Wait for the third-party program to install. Then, the PC will
automatically restart.
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:
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:
5) Choose a language that is used to display the software screens and printed reports, and then select
Next.
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
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.
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
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.
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
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
for PC communication should prevail. Select the target units to write the program. "All Units"
should be selected when the first time to upgrade.
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.
6) The control units will be download from the "Main Unit" After "Start" button clicked.
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:
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.
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)
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.
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
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.
2 Access the Alignment window and select Mech Reset to reset the mechanical parts of
the system.
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
Completing parameter
configuration table and test
record table
End
[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.
▪ 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
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.
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
Probe's orbit
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.
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.
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.
BA48-J10
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.
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.
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.
BA24-J04
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.
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:
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.
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.
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.
1) Install the mixer alignment fixture BA48-J16, and then select Mixer to Horizontal Position on
Reaction Carousel.
BA48-J16:
Alignment
lever
(inserted to
the end)
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.
BA24-J05
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:
BA40-J76
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:
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.
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.
the wash
probe
fixture two screws on the wash
probe conversion board
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:
Bar
Sample tube
code
area
9mm
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.
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.
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
adjust the position until the parameters of the sample/reagent carousel meet the requirement.
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.
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.
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.
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
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)
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.
6) Install the wash station and execute auto wash according to the software prompt. Make sure no
overflow occurs.
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.
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.
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.
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.
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.
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
Wall
Minimum 500
Maximum 3000
Minimum 500
Operation Unit
708
Analyzer
Minimum 500
1180
Front
Unit: mm
Minimum 500
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.
▪ 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.
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.
3) Use a flat-blade screwdriver to tilt the metal piece and remove the upper cover and side cover.
4) Remove the screw with a wrench and remove the fixed angle iron so that the machine can be lifted.
The fixed angles and screws under removal are as shown below:
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
Parameter list
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.
If you cannot
loosen the
fixing screw
of the probe,
you can use
a flat-blade
screwdriver.
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.
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
5) Insert the spring into the column in the arm cavity and tighten the screw compression spring.
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.
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.
Keep the
sections flush.
Rotate the retaining screw clockwise.
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.
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.
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.
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
6) After the analyzer is installed, the correct tube connections are as follows:
FL02 FL03
FL01
DI water tank Diluted wash solution Low conc. waste tank High conc. waste tank
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:
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.
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.
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.
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 8-29 Load Wash D and Saline W
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.
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
▪ 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;
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 /
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
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.
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.
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.
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 .
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.
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.
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
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)
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.
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
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.
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.
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.
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.
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
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.
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
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.
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.
ZQ01
ZQ11
ZQ21
ZQ31
T613
ZQ12
SI1 SI2 SI3 SI4
T611 T612 T702
CAN02 ZZ06
ZQ15
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
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:
▪ 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.
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
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.
SV02 T10
D06 D07
6
T103 T104 T10
7 NS MIX
SY03
T105
D05
SV03 T222
SV04
D21 W01
P01
T204
D04
D16
ZZ11
T203
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
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
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.
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
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
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.
▪ 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.
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
2
1
Part Name
1 115-036337-00 1 /
2 115-036570-00 1 /
1 2
3
4
3
2
4
5
1
3
2
4
7
5
6
1 2
2
8
7
1 5
3 4
1
5
2 6
3
7
2 2
5 6
1
2
5 8
6 9
1
2
Figure 11-19 Heater cables above and under Reaction Carousel Explosive View
1
2
1 2
1 8
7
4 5 6
4
2
5
6
3
2
4
5
1 5
7
3
3
5
2
1 8
3
2
3
2
3
2
1
1
2
5 6
7 8 9
1
2 3 4
1 2 3
1 3
3 / Connector.1/4-28UNF,1/8"ID,PP 4 /
6 5
1 2 3
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
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.
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:
5) Input ping + IP of the LIS computer. If you are actually returned with bytes, the network is connected.
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.
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.
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].
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.
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.
The configuration file is mainly intended for maintaining item information and patient information sent to the
machine during bidirectional LIS communication testing.
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.
The EnableUA value is normally 0: from the Registry, change the EnableUA value to 0
HKEY_LOCAL_MACHINE\SOFTWARE\Microsoft\Windows\CurrentVersion\Policies\System
If there is a problem with message ACK, then an error will occur when item information is transmitted to the
machine later.
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>
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>
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>
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
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
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.
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
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.
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.
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.
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.
8 This procedure is complete. Select Continue to save it and exit the screen. Select Continue to exit the alignment.
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.
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".
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
13.4 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:
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.
2) After attaching the serial number label on the box, bind the box with four straps as shown.
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.
Shielding box
Four screws for fixing
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.
Check the
connector of the
ISE waste tube.
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.
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.
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:
8) Connect the power cord of the ISE module to the corresponding 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.
Wire harness
retainer (small)
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.
base when you install the last electrode, to make sure the electrode is fixed well.
▪ Double check if the electrodes are fixed well.
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.
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.
3) Install the reagent carousel anti-fog heating unit onto the reagent chamber with four M3X8 Phillips pan
head screws.
4) Attach the dust cover with the sponge adjustment pad to the fixing plate with four M3X6 Phillips pan
head screws.
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.
Scanner bracket
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
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.
Appendices
A.1 BS-240 Installation Acceptance Report
BS-240_Installatio
n Acceptance Report_V1.0_EN.doc
BS-240_Moving
Parts Position Confirmation Guide (No Alignment Tooling)_V1.0_EN.doc
Tool list.xlsx
BS-230&240_Erro
r Information Feedback Form_V1.0_EN.doc
BS-240_Series
Recovery Checklist_V1.0_EN.docx
BS-240_Maintena
nce log sheet_V1.0_EN.xlsx
Tube label
SV02 T10
Deionized water
D05 T61
SV03 T222 3
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
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.
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
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)