BC-5150 Operator's Manual V10.0 en

BC-5150 Auto Hematology Analyzer
Operator’s Manual
© 2013-2016 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights Reserved.
For this Operator’s Manual, the issue date is 2016-06.
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.
Mindray intends to maintain the contents of this manual as confidential information.

Disclosure of the information in this manual in any manner whatsoever without the written
permission of Mindray is strictly forbidden.
Release, amendment, reproduction, distribution, rental, adaptation, translation or any other
derivative work of this manual in any manner whatsoever without the written permission of
Mindray is strictly forbidden.
, , 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.
Responsibility on the Manufacturer Party

Contents of this manual are subject to change without prior notice.
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;
 the electrical installation of the relevant room complies with the applicable national and
local requirements; and the product is used in accordance with the instructions for use.
I
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.
 Be sure to operate the analyzer under the situation specified in this manual;
otherwise, the analyzer will not work normally and the analysis results will be
unreliable, which would damage the analyzer components and cause personal
injury.
NOTE
 This equipment must be operated by skilled/trained clinical professionals.
II
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.
Company Contact
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: Shanghai International Holding Corp. GmbH(Europe)
Address: Eiffestraβe 80, 20537 Hamburg, Germany
Tel: 0049-40-2513175
Fax: 0049-40-255726
III
Table of Contents
1 Using This Manual ............................................................................................... 1-1

1.1. Introduction ............................................................................................................ 1-1
1.2. Who Should Read This Manual ............................................................................. 1-2
1.3. How to Find Information ........................................................................................ 1-3
1.4. Conventions Used in This Manual ......................................................................... 1-4
1.5. Safety Information ................................................................................................. 1-5
1.6. When you see… .................................................................................................... 1-7
2 Understanding the Analyzer ............................................................................... 2-1

2.1. Introduction ............................................................................................................ 2-1
2.2. Parameters ............................................................................................................ 2-2
2.3. Product Description ............................................................................................... 2-4
2.4. Status Indicator ...................................................................................................... 2-9
2.5. Buzzer.................................................................................................................. 2-10
2.6. System Menu ....................................................................................................... 2-11
2.7. Reagents, Controls and Calibrators .................................................................... 2-12
2.7.1. Reagents ................................................................................................ 2-12
2.7.2. Controls and Calibrators ........................................................................ 2-12
3 Understanding the System Principles ............................................................... 3-1

3.1. Introduction ............................................................................................................ 3-1
3.2. Aspiration ............................................................................................................... 3-2
3.3. Dilution ................................................................................................................... 3-3
3.4. WBC Measurement ............................................................................................... 3-5
3.5. HGB Measurement ................................................................................................ 3-6
3.6. RBC/PLT Measurement ......................................................................................... 3-7
4 Installing Your Analyzer ...................................................................................... 4-1

4.1. Introduction ............................................................................................................ 4-1
4.2. Installation Requirements ...................................................................................... 4-2
4.2.1. Space Requirements ................................................................................ 4-2
4.2.2. Power Requirements ................................................................................ 4-2
4.2.3. General Environment ............................................................................... 4-3
4.2.4. Moving and Installing the Analyzer........................................................... 4-3
4.3. Connecting the Analyzer System .......................................................................... 4-4
4.4. Notes ..................................................................................................................... 4-8
5 Operating Your Analyzer ..................................................................................... 5-1

5.1. Introduction ............................................................................................................ 5-1
5.2. Initial Checks ......................................................................................................... 5-3
1
Table of Contents
5.3. Startup and Login .................................................................................................. 5-4

5.4. Daily Quality Control .............................................................................................. 5-8
5.5. Sample Collection and Handling ........................................................................... 5-9
5.5.1. Sample Preparation ............................................................................... 5-11
5.5.2. Sample Analysis ..................................................................................... 5-13
5.5.3. Processing Analysis Results .................................................................. 5-18
5.6. Auto-Standby ....................................................................................................... 5-22
5.7. Shutdown ............................................................................................................. 5-24
6 Reviewing Sample Results ................................................................................. 6-1

6.1. Introduction ............................................................................................................ 6-1
6.2. Browsing in the "Table Review" mode ................................................................... 6-2
6.2.1. Table ......................................................................................................... 6-2
6.2.2. Graph Review........................................................................................... 6-3
6.2.3. validate/Cancel validate (for administrators only) .................................... 6-4
6.2.4. Delete (for administrators only) ................................................................ 6-5
6.2.5. Edit info. ................................................................................................... 6-6
6.2.6. Edit results ................................................................................................ 6-7
6.2.7. Search ...................................................................................................... 6-7
6.2.8. Print .......................................................................................................... 6-8
6.2.9. Transmission ............................................................................................ 6-9
6.2.10. Export ............................................................................................. 6-10
7 Using the QC Programs ...................................................................................... 7-1

7.1. Introduction ............................................................................................................ 7-1
7.2. L-J QC ................................................................................................................... 7-3
7.2.1. Editing L-J settings (for administrators only) ............................................ 7-3
7.2.2 L-J QC Run ................................................................................................... 7-6
7.2.3 Reviewing L-J Results ................................................................................ 7-10
7.3. X-B QC Program ................................................................................................. 7-14
7.3.1 Introduction ................................................................................................. 7-14
7.3.2 Editing X-B settings (for administrators only) ............................................. 7-14
7.3.3 X-B QC Run ................................................................................................ 7-18
7.3.4 Reviewing X-B Results ............................................................................... 7-18
8 Calibrating Your Analyzer ................................................................................... 8-1

8.1. Introduction ............................................................................................................ 8-1
8.2. When to Calibrate .................................................................................................. 8-3
8.3. How to Calibrate .................................................................................................... 8-4
8.3.1 Preparing Your Analyzer ............................................................................... 8-4
8.3.2 Manual Calibration........................................................................................ 8-5
8.3.3 Calibration with Calibrator ............................................................................ 8-6
8.3.4 Calibration with Fresh Blood ...................................................................... 8-11
2
Table of Contents
9 Customizing the Analyzer Software .................................................................. 9-1

9.1. Introduction ............................................................................................................ 9-1
9.2. Setting Up the Analyzer ......................................................................................... 9-2
9.2.1 System Setup ............................................................................................... 9-2
9.2.2 Access Setup .............................................................................................. 9-10
9.2.3 Auxiliary Setup ............................................................................................ 9-13
9.2.4 Parameter Setup ........................................................................................ 9-15
9.2.5 Maintenance Setup (for administrators only) ............................................. 9-20
9.2.6 Reagent Setup ............................................................................................ 9-21
9.2.7 Gain Setup (for administrators only) ........................................................... 9-24
9.3. Save the settings ................................................................................................. 9-26
10 Servicing Your Analyzer .................................................................................... 10-1

10.1. Introduction .......................................................................................................... 10-1
10.2. Maintaining Your Analyzer ................................................................................... 10-2
10.2.1 Maintenance ............................................................................................. 10-2
10.2.2 Cleaning ................................................................................................... 10-4
10.2.3 Servicing the Fluidics ............................................................................... 10-5
10.3. Touch Screen Calibration .................................................................................. 10-10
10.4. Viewing Logs ..................................................................................................... 10-11
10.5. Checking the Analyzer Status ........................................................................... 10-13
10.5.1 Counter ................................................................................................... 10-13
10.5.2 Temp. & Pressure ................................................................................... 10-14
10.5.3 Voltage and Current................................................................................ 10-15
10.5.4 Sensor .................................................................................................... 10-16
10.5.5 Version Info. ............................................................................................ 10-17
11 Troubleshooting Your Analyzer ........................................................................ 11-1

11.1. Introduction .......................................................................................................... 11-1
11.2. Error Information and Handling ........................................................................... 11-2
12 Appendices ..........................................................................................................A-1
A. Index .....................................................................................................................A-1
B. Specifications ......................................................................................................B-1
B.1. Classification ......................................................................................................... B-1
B.2. Reagents ............................................................................................................... B-1
B.3. Applicable Tubes ................................................................................................... B-1
B.4. Parameters ............................................................................................................ B-1
B.5. Sampling Features ................................................................................................ B-2
B.5.1. Sample Volumes Required for Each Analysis .................................. B-2
B.5.2. Throughput ....................................................................................... B-2
B.6. Performance Specifications ................................................................................... B-2
3
Table of Contents
B.6.1. Display Range .................................................................................. B-2

B.6.2. Background/Blank Count .................................................................. B-3
B.6.3. Linearity Range................................................................................. B-3
B.6.4. Deviation of Reading ........................................................................ B-3
B.6.5. Compatibility ..................................................................................... B-3
B.6.6. Reproducibility .................................................................................. B-4
B.6.7. Carryover .......................................................................................... B-4
B.7. Input/Output Device ............................................................................................... B-4
B.7.1. External Computer (optional) ............................................................ B-5
B.7.2. Keyboard (Optional) ......................................................................... B-5
B.7.3. Mouse (Optional) .............................................................................. B-5
B.7.4. External Barcode Scanner (Optional) ............................................... B-5
B.7.5. Printer (Optional) .............................................................................. B-5
B.8. Interfaces ............................................................................................................... B-5
B.9. Power Supply ........................................................................................................ B-5
B.10. FUSE ..................................................................................................................... B-5
B.11. EMC Description .................................................................................................... B-6
B.12. Sound .................................................................................................................... B-6
B.13. Operating Environment.......................................................................................... B-6
B.14. Storage Environment ............................................................................................. B-6
B.15. Running Environment ............................................................................................ B-7
B.16. Dimensions and Weight ......................................................................................... B-7
B.17. Contraindications ................................................................................................... B-7
B.18. Safety Classification .............................................................................................. B-7
4
1 Using This Manual
1.1. Introduction
This chapter explains how to use your BC-5150 operator’s manual, which is shipped with
your BC-5150 AUTO HEMATOLOGY ANALYZER and contains reference information about
the analyzer and procedures for operating, troubleshooting and maintaining the analyzer.
Read this manual carefully before operating your BC-5150 analyzer and operate your
BC-5150 analyzer strictly as instructed in this manual.
1-1
Using This Manual
1.2. Who Should Read This Manual

This manual is intended to be read by clinical laboratory professionals. This equipment must
only be operated by skilled/trained clinical professionals. This information contains
information for clinical laboratory professionals to:
 learn about the BC-5150 hardware and software.
 customize system settings.
 perform daily operating tasks.
 perform system maintenance and troubleshooting.
1-2
Using This Manual
1.3. How to Find Information

This operator’s manual comprises 11 chapters and 3 appendices. Refer to the table below to
find the information you need.
If you want to … See …

learn about the intended use and parameters of the Chapter 2 Understanding
BC-5150 Your Analyzer
learn about the hardware, interface and software of the Chapter 2 Understanding
BC-5150 Your Analyzer
learn about how the BC-5150 works Chapter 3 Understanding
the System Principles
learn about the installation requirements of the BC-5150 Chapter 4 Installing Your
Analyzer
learn about the process of sample collection and analysis Chapter 5 Operating Your
Analyzer
learn about how to use the BC-5150 to perform your daily Chapter 5 Operating Your
operating tasks Analyzer
review sample results Chapter 6 Reviewing
Sample Results
learn about how to use the quality control programs of the Chapter 7 Using the QC
BC-5150 Programs
learn about how to calibrate the BC-5150 Chapter 8 Using the
Calibration Programs
learn about how to define/adjust system settings Chapter 9 Customizing the
Analyzer Software
learn about how to maintain/service the BC-5150 Chapter 10 Maintaining
Your Analyzer
learn about how to solve the problems of the BC-5150 Chapter 11
Troubleshooting Your
Analyzer
learn about the technical specifications of the BC-5150 Appendix B Specifications
1-3
Using This Manual
1.4. Conventions Used in This Manual

This manual uses certain typographical conventions to clarify meaning in the text:
Format Indication
[××] all capital letters enclosed in [ ] indicate a key name on the
analyzer or external keyboard, such as [ENTER]
"××" bold letters included in " " indicate text you may find on the
screen of BC-5150, such as “Clear”
×× bold letters indicate chapter titles, such as Chapter 1 Using
This Manual.
All illustrations in this manual are provided as examples only. They may not necessarily
reflect setup of the BC-5150 or data displayed.
1-4
Using This Manual
1.5. Safety Information

The following symbols are used to indicate danger and alert information in this manual.
When you see… Meaning

read the statement below the symbol. The statement is alerting
you to a potentially biohazardous condition.

WARNING you to an operating hazard that can cause personnel injury.

CAUTION you to a possibility of analyzer damage or unreliable analysis
results.
NOTE you to information that requires your attention.
 All the samples, controls, calibrators, reagents, wastes and areas contacted
them are potentially biohazardous. Wear proper personal protective equipment
(e.g. gloves, lab coat, etc.) and follow safe laboratory procedures when handling
them and the contacted areas in the laboratory.
 If leak happens to the analyzer, the leak liquid is potentially biohazardous.
WARNING
 Please check the firmness of all the doors and covers before running the
analyzer.
 Make sure all the safety measurements are adopted. Disable any safety device or
sensor is prohibited.
 Please take action to any alarm and problem indication immediately.
 Do not touch the moving parts.
 Contact Mindray or Mindray-authorized distributors in time if any damaged part

is found.
 Be careful when opening/closing and removing/installing the doors, covers and
1-5
Using This Manual
boards of the analyzer.
 Discard the analyzer according to government regulations.
 Do not contact the patients’ sample blood directly.
 Be sure to dispose of reagents, waste, samples, consumables, etc. according to

government regulations.
 The reagents are irritating to eyes, skin and airway. Wear proper personal
protective equipment (e.g. gloves, lab coat, etc.) and follow safe laboratory
procedures when handling them and the contacted areas in the laboratory.
 If reagents accidentally spill on your skin or in your eyes, rinse the area with
ample amount of clean water; seek medical attention immediately.
 Keep your clothes, hairs and hands away from the moving parts to avoid injury.
 The sample probe tip is sharp and may contain biohazardous materials. Exercise
caution to avoid contact with the probe when working around it.
 Before maintaining or servicing the analyzer, its surface or the sample probe and
other parts concerned must be cleaned and sterilized (it is recommend that the
parts be wiped with alcohol of which the concentration is 75%) to avoid
biohazards or other damages.
CAUTION
 Please use the analyzer strictly according to this manual.
 Please adopt proper measurements to prevent the reagents from being polluted.
NOTE
 Use the reagents specified by the manufacturer only. Store and use the reagents
as instructed by instructions for use of the reagents.
 Check if the reagent tubes are properly connected before using the analyzer.
1-6
Using This Manual
1.6. When you see…

You will find the following symbols in this manual:

read the statement below the symbol. The statement is
alerting you to a potentially biohazardous condition.

WARNING alerting you to an operating hazard that can cause
personnel injury.
CAUTION alerting you to a possibility of analyzer damage or
unreliable analysis results.
NOTE alerting you to information that requires your attention.
You may find the following symbols of the analyzer system:
CAUTION
 Make sure the symbols are in good condition during daily use and maintenance.
CAUTION,
CONSULT ACCOMPANYING
DOCUMENTS.
BIOLOGICAL RISK
WARNING, LASER BEAM
PROTECTIVE EARTH (GROUND)
USB PORT
NETWORK PORT
1-7
Using This Manual
ALTERNATING CURRENT
FOR IN VITRO DIAGNOSTIC USE
BATCH CODE
USE BY
SERIAL NUMBER
DATE OF MANUFACTURE
EXERCISE CAUTION WHEN WORKING

AROUND TO AVIOD PRICKING
MANUFACTURER
TEMPERATURE LIMITATION
CONSULT THE OPERATOR'S MANUAL
THE DEVICE IS FULLY CONFORMANCE

WITH THE COUNCIL DIRECTIVE
CONCERNING IN VITRO DIAGNOSTIC
MEDICAL DEVICES 98/79/EC.
1-8
Using This Manual
Figure 1-1 Back of the analyzer
(1)
Connect only to a properly earth grounded outlet.
To avoid electric shock, disconnect power cord prior to removing or replacing fuse.
Replace fuse only with the type and rating specified.
(2)
Warning, potential biological risk.
1-9
Using This Manual
Figure 1-2 Front of the analyzer
(1)
Warning, potential biohazardous risk.
(2)
The sample probe is sharp and potentially biohazardous. Exercise caution to avoid contact
with the probe when working around it.
1-10
Using This Manual
Figure 1-3 Front of the analyzer (front cover open)
(1)
Do not put hands under the syringe or in the guide slot when the analyzer is running.
1-11
Using This Manual
Figure 1-4 Right of the analyzer
(1)
Do not put hands under the syringe or in the guide slot when the analyzer is running.
1-12
Using This Manual
Figure 1-5 Left of the analyzer
(1)
Caution: Class 3B Laser radiation when open and interlocks defeated avoid exposure to the
beam
1-13
2 Understanding the Analyzer
2.1. Introduction
This chapter introduces the parameters, major components, interfaces, buttons, menus,
software help system, operation information and reagent system of the BC-5150 AUTO
HEMATOLOGY ANALYZER.
2-1
Understanding the Analyzer
2.2. Parameters
NOTE
 The purpose of this analyzer is to identify the normal patient, with all normal
system-generated parameters, and to flag or identify patient results that require
additional studies.
The analyzer determines 25 parameters, 4RUO parameters, histograms and 1 scattergram

of blood samples. The parameters under CBC and CBC+DIFF mode are listed as follows:
Table 2-1 Parameters
Parameter
Name Abbreviation CBC CBC + DIFF
Group
White Blood Cell count WBC √ √
Basophils number Bas# / √
Basophils percentage Bas% / √
Neutrophils number Neu# / √
Neutrophils percentage Neu% / √
WBC group (15), including 4 RUO parameters
Eosinophils number Eos# / √

Eosinophils percentage Eos% / √
Lymphocytes number Lym# / √
Lymphocytes Lym% / √
percentage
Monocytes number Mon# / √
Monocytes percentage Mon% / √
Abnormal Lymphocytes ALY# / √
number
Abnormal Lymphocytes ALY% / √
percentage
Large Immature Cells LIC# / √
number
Large Immature Cells LIC% / √
percentage
Red Blood Cell count RBC √ √
Hemoglobin HGB √ √
RBC group (8)
Concentration
Mean Corpuscular MCV √ √
Volume
Mean Corpuscular MCH √ √
Hemoglobin
2-2
Mean Corpuscular MCHC √ √

Hemoglobin
Concentration
Red Blood Cell RDW-CV √ √
Distribution Width -
Coefficient of Variation
Red Blood Cell RDW-SD √ √
Distribution Width -
Standard Deviation
Hematocrit HCT √ √
Platelet count PLT √ √
Mean Platelet Volume MPV √ √
Platelet Distribution PDW √ √
PLT group (6)
Width
Plateletcrit PCT √ √
Platelet larger cell ratio P-LCR √ √
Platelet larger cell count P-LCC √ √
 Histograms
Table 2-2 Histograms
Name Abbreviation CBC CBC + DIFF

White Blood Cell Histogram WBC Histogram √ √
Red Blood Cell Histogram RBC Histogram √ √
Platelet Histogram PLT Histogram √ √
 Scattergram
Table 2-3 Scattergram
Abbreviation CBC CBC + DIFF

Diff Scattergram / √
NOTE
 "√"means "available under the mode","/"means "not available under the mode".
 ALY%, LIC%, ALY# and LIC# are for research use only. For more information
about RUO parameters, see 9.2.4 Parameter Setup-RUO parameters.
2-3
2.3. Product Description

BC-5150 AUTO HEMATOLOGY ANALYZER includes the Sample Processing Unit (SPU),
Data Managing Unit (DMU), Result Output Unit (ROP) and accessories. The appearance of
the product is as follows:
WARNING
 Please check the firmness of all the doors and covers before running the
analyzer, and make sure they do not get loose when the analyzer is running.
2-4
Figure 2-1 Front of the analyzer
1 ---- [Aspirate] key 2 ---- Sample probe

3 ----Probe wipe block 4 ----Power/status indicator
5 ----Display
2-5
Figure 2-2 Back of the analyzer
1 --- M-52D diluent inlet 2 ---Waste outlet

3 --- Waste sensor 4 ---AC input
5 --- Power switch
2-6
Figure 2-3 Left of the analyzer (left door open)
1 --- Left door 2 --- DIFF reagent bottle

3 --- LH reagent bottle 4 --- Front cover assembly
 --- Network port, USB port
2-7
 Power switch
Power switch is located on the back of the analyzer.
CAUTION
 Do not turn on/off the switch repeatedly in a short time to avoid damaging the
analyzer.
 [Aspirate] key
The aspirate key is on the front of the analyzer, press it to start analysis, dispense diluent or
exit from standby mode.
 USB/network port
The USB port and network port are on the left of the analyzer. They can be used to connect
the printer, barcode scanner, etc., and to transmit data.
The supported printer models are: EPSON LQ-590K, HP Laser Jet P1505n, HP OfficeJet Pro
K5300 and HP LaserJet P1606dn.
2-8
2.4. Status Indicator

The status indicator is on the front of the analyzer; it indicates the ready, running, error and
standby status of the analyzer.
The indicator illuminates in 3 colors to indicate the current status of the analyzer; its flickering
interval is 2 seconds. See the following table:
Table 2-4 the indicator and analyzer status
Status Indicator Note

Ready Solid green Ready to sequence actions
Running Flickering green sequence actions in

progressing
Running with error Flickering red The analyzer is running

with error
Error Solid red An error has occurred, and
the analyzer is not running
No error, but fluidic Solid yellow Initializing (not involving

actions are not sequence actions) in
allowed. startup process, standby
status
Entering/exiting Flickering yellow Entering/exiting standby

standby status status
2-9
2.5. Buzzer
The buzzer indicates errors of the analyzer. When you click the touch screen or the error is
cleared, the alarming sound of the buzzer can be cleared.
Table 2-5 the buzzer and analyzer status
When... How... Note

The startup process completes 1 short beep The startup process
completes and the analyzer
ready to run analysis.
Open vial sample aspiration 2 short beeps

finishes
Press the aspirate key at the 1 long beep When dialog box message is
analysis screens (including given, the buzzer may not
sample analysis, QC, calibration, beep.
Reproducibility, carryover,
background, aging, optical gain
calibration screens) when
analysis cannot be started.
Error Long beeps at intervals Tap the touch screen to turn

off the buzzer.
The analyzer enters ready status 1 short beep The analyzer enters ready
status from another status.
When the analyzer screen turns Turn off the buzzer. If error occurs during the
black and the message "Please shutdown process, please
power off the analyzer" appears turn off the buzzer when the
screen turns black.
2-10
2.6. System Menu
2-11
2.7. Reagents, Controls and Calibrators

As the analyzer, reagents (diluent, lyses, and probe cleanser), controls, and calibrators are
components of a system. Performance of the system depends on the combined integrity of all
components. Only Mindray-specified reagents (see Appendix B Specifications), which are
formulated specifically for the fluidic system of your analyzer in order to provide optimal
system performance, could be used. Do not use the analyzer with reagents from multiple
suppliers. Otherwise, the analyzer may not meet the performance specified in this manual
and may provide unreliable results. All references related to reagents in this manual refer to
the reagents specifically formulated for this analyzer.
Each reagent package must be examined before use. Product integrity may be compromised
in packages that have been damaged. Inspect the package for signs of leakage or moisture.
If there is evidence of leakage or improper handling, do not use the reagent.
NOTE
 Store and use the reagents as instructed by instructions for use of the reagents.
 When you have changed the diluents or lyse, implement a background test to
see if the results meet the requirement.
 Pay attention to the expiration dates and open-container stability days of all the
reagents. Be sure not to use expired reagents.
2.7.1.Reagents
 M-52 D Diluent
It is used to dilute blood samples and provide a stable environment for counting and sizing
blood cells.
 M-52 DIFF Lyse
It is used to lyse red blood cells and differentiate WBCs.
 M-52 LH Lyse
It is used to lyse red blood cells, count and differentiate WBCs, and determine the HGB.
 Probe Cleanser
Probe cleanser is used to clean the analyzer regularly.
2.7.2.Controls and Calibrators

The controls and calibrators are used to verify accurate operation of and calibrate the
2-12
analyzer.
The controls are commercially prepared whole-blood products used to verify that the
analyzer is functioning properly. They are available in low, normal, and high levels. Daily use
of all levels verifies the operation of the analyzer and ensures reliable results are obtained.
The calibrators are commercially prepared whole-blood products used to calibrate the
analyzer. Store and use the controls and calibrators as instructed by their instructions for use.
All references related to controls and calibrators in this manual refer to the controls and
calibrators specifically formulated for this analyzer by Mindray. You must buy those controls
and calibrators from Mindray or Mindray-authorized distributors.
2-13
3 Understanding the System
Principles
3.1. Introduction
The measurement methods used in this analyzer are: the Electrical Impedance method for
determining the RBC and PLT data; the colorimetric method for determining the HGB; flow
cytometry by laser for determining the WBC data. Other parameter results are obtained via
calculation.
3-1
Understanding the System Principles
3.2. Aspiration
If you are to analyze a whole blood sample in the open vial sampling mode, the analyzer will
aspirate 15μL (CBC+DIFF mode) or 11.7μL (CBC mode) of the sample.
If you are to analyze a capillary blood sample in the open vial sampling mode, you should first
manually dilute the sample (20μL of capillary sample needs to be diluted by 480μL of diluent,
dilution ratio: 1:25) and then present the pre-diluted sample to the analyzer, which will
aspirate 200μL of the sample.
3-2
3.3. Dilution
The aspirated sample will quickly and precisely be diluted in RBC bath and then segmented
into two portions. One of these two portions will then be diluted again and processed by
different reagents. After this, they are ready for analysis.
This analyzer can process two types of blood samples – whole blood samples and
pre-diluted sample.
 Whole Blood Mode
Aspirate
sample 15ul
Diluent
550ul
Dilution ratio Aspirate 12ul of

1:37.67 sample
Aspirate 380ul of DIFF lyse 1ml

the compound
LH lyse 200ul Diluent 2.4ml
WBC DIFF sample WBC BASO sample RBC sample

Dilution ratio Dilution ratio Dilution ratio
1:105.8 1:123.8 1:7533.3
Figure 3-1 Dilution procedure of whole blood CBC+DIFF mode
3-3
 Pre-diluted Mode
Capillary blood
sample 20ul
Diluent 480ul
Dilution ratio
1:25
Aspirate
200ul of
Diluent sample
358ul
Aspirate 21.6ul of
Dilution ratio sample
1:69.75
DIFF lyse 1ml

Aspirate 380ul of
the compound
LH lyse 200ul Diluent 2.4ml
WBC DIFF sample WBC BASO sample RBC sample

Dilution ratio Dilution ratio Dilution ratio
1:199.8 1:234.3 1:7750
Figure 3-2 Dilution procedure of pre-diluted CBC+DIFF mode
3-4
3.4. WBC Measurement

 Flow Cytometry by Laser
Figure 3-3 WBC Measurement
After a predetermined volume of blood is aspirated and diluted by a certain amount of

reagent, it is injected into the flow cell. Surrounded with sheath fluid (diluent), the blood cells
pass through the center of the flow cell in a single column at a faster speed. When the blood
cells suspended in the diluent pass through the flow cell, they are exposed to a laser beam.
The intensity of scatter light reflects the blood cell size and intracellular density. The
low-angle scattered light reflects cell size, and the high-angle scattered light reflects
intracellular density (nucleus size and density). The optical detector receives this scatter light
and converts it into electrical pulses. Pulse data collected can be used to draw a
3-dimensional distribution (scattergram).
3-5
3.5. HGB Measurement
 Colorimetric Method
The WBC/HGB dilution is delivered to the HGB bath where it is bubble mixed with a certain
amount of lyse, which converts hemoglobin to a hemoglobin complex that is measurable at
530 nm. An LED is mounted on one side of the bath and emits a beam of monochromatic
light, whose central wavelength is 530nm. The light passes through the sample and is then
measured by an optical sensor that is mounted on the opposite side. The signal is then
amplified and the voltage is measured and compared to the blank reference reading
(readings taken when there is only diluent in the bath), and the HGB is measured and
calculated in the analyzer automatically.
 HGB
The HGB is calculated per the following equation and expressed in g/L.
HGB(g/L) = Constant×Log 10 (Blank Photocurrent/Sample Photocurrent)
3-6
3.6. RBC/PLT Measurement

 Electrical Impedance Method
RBCs/PLTs are counted and sized by the Electrical Impedance method. This method is
based on the measurement of changes in electrical resistance produced by a particle, which
in this case is a blood cell, suspended in a conductive diluent as it passes through an
aperture of known dimensions. A pair of electrodes is submerged in the liquid on both sides
of the aperture to create an electrical pathway. As each particle passes through the aperture,
a transitory change in the resistance between the electrodes is produced. This change
produces a measurable electrical pulse. The number of pulses generated represents the
number of particles that passed through the aperture. The amplitude of each pulse is
proportional to the volume of each particle.
Figure 3-4 Electrical Impedance method
Each pulse is amplified and compared to the internal reference voltage channel, which only
accepts the pulses of certain amplitude. If the pulse generated is above the RBC/PLT lower
threshold, it is counted as a RBC/PLT. The analyzer presents the RBC/PLT histogram, whose
x-coordinate represents the cell volume (fL) and y-coordinate represents the number of the
cells.
 Derivation of RBC-Related Parameters

 RBC
12
RBC (10 /L) is the number of erythrocytes measured directly by counting the erythrocytes
passing through the aperture.
 MCV
3-7
Based on the RBC histogram, this analyzer calculates the mean cell volume (MCV) and
expresses the result in fL.
 HCT, MCH, and MCHC
This analyzer calculates the HCT(%), MCH (pg) and MCHC (g/L) as follows:
RBC  MCV
HCT 
10
HGB
MCH 
RBC
HGB
MCHC   100
HCT
12
Where the RBC is expressed in 10 /L, MCV in fL and HGB in g/L.
 RDW-CV
Based on the RBC histogram, this analyzer calculates the CV (Coefficient of Variation) of the
erythrocyte distribution width, it is expressed in %.
 RDW-SD
Based on the standard deviation of erythrocyte size distribution, this analyzer calculates the
RDW-SD, its unit is fL.
 Derivation of PLT-Related Parameters

 PLT
9
PLT (10 /L) is measured directly by counting the platelets passing through the aperture.
 MPV
Based on the PLT histogram, this analyzer calculates the mean platelet volume (MPV, fL).
 PDW
Platelet distribution width (PDW) is the geometric standard deviation (GSD) of the platelet
size distribution. Each PDW result is derived from the platelet histogram data and is reported
as 10(GSD).
 PCT
This analyzer calculates the PCT as follows and expresses it in ％.

9
Where the PLT is expressed in 10 /L and the MPV in fL.
3-8
PLT  MPV
PCT 
10000
 P-LCR
Platelet larger cell ratio (P-LCR) is the ratio of the larger platelet (volume larger than 12fL)
count to the total PLT count. This analyzer calculates the P-LCR based on the PLT histogram
and expresses the result in %. In the following figure, S2 represents the number of larger
platelet cells, and S1+S2 represents the total PLT count.
 P-LCC
This analyzer calculates the platelet large cell count (P-LCC) and expresses the result in
9
10 /L.
P- 3-9
4 Installing Your Analyzer
4.1. Introduction
WARNING
 Installation by personnel not authorized or trained by Mindray may cause
personal injury or damage your analyzer. Do not install your analyzer without the
presence of Mindray-authorized personnel.
 The installation, authorization, upgrade and modification of the analyzer

software must be performed by Mindray-authorized personnel.
Your analyzer is tested before it is shipped from the factory. International symbols and special
handling instructions tell the carrier how to treat this electronic instrument. When you receive
your analyzer, carefully inspect the carton. If you see any signs of mishandling or damage,
contact Mindray customer service department or your local distributor immediately.
4-1
Installing Your Analyzer
4.2. Installation Requirements

4.2.1.Space Requirements
Check the site for proper space allocation. In addition to the space required for the analyzer
itself, arrange for:
 proper height to place the analyzer;
 at least 50 cm on each side, which is the preferred access to perform service procedures;
 at least 10 cm behind the analyzer for cabling and ventilation;
 enough room on and below the countertop to accommodate the reagents and waste
containers;
 diluent container shall be put within 1.0m under the analyzer, lyse containers are placed
inside the analyzer.
 The countertop (or the floor) where the analyzer is placed shall be able to withstand at
least 40kg of weight.
4.2.2.Power Requirements
WARNING
 Make sure the analyzer is properly grounded.
 Before turning on the analyzer, make sure the input voltage meets the
requirements.
CAUTION
 Using pinboard may bring the electrical interference and the analysis results
may be unreliable. Please place the analyzer near the electrical outlet to avoid
using the pinboard.
 Please use the original power cable shipped with the analyzer. Using other power
cable may damage the analyzer or cause unreliable analysis results.
Table 4-1 Power specification
Voltage Input power Frequency
Analyzer (100V-240V～)±10% 300VA （50Hz/60Hz）±1Hz
4-2
4.2.3.General Environment
 Optimal operating temperature: 10 ℃～30 ℃
 Optimal operating humidity: 20 %～85 %
 Atmospheric pressure: 70 kPa～106 kPa
 The environment shall be as free as possible from dust, mechanical vibrations, loud
noises, and electrical interference.
 It is advisable to evaluate the electromagnetic environment prior to operation of this

analyzer.
 Do not use this analyzer in close proximity to sources of strong electromagnetic radiation
(e.g. unshielded intentional RF sources), as these may interfere with the proper operation.
 Do not place the analyzer near brush-type motors, flickering fluorescent lights, and
electrical contacts that regularly open and close.
 Do not place the analyzer in direct sunlight or in front of a source of heat or drafts.
 The environment shall be ventilated.
 Do not place the analyzer on a slope.
 Connect only to a properly earth grounded outlet.
 Only use this analyzer indoors.
4.2.4.Moving and Installing the Analyzer
WARNING
 Installation by personnel not authorized or trained by Mindray may cause
personal injury or damage your analyzer. Do not install your analyzer without the
presence of Mindray-authorized personnel.
NOTE
 Before the analyzer is shipped out, the sample probe is fixed by a plastic cable
tie to avoid damaging the sample probe during transportation. Remove the cable
tie before using the analyzer.
Moving and installation of the analyzer shall be conducted by Mindray-authorized personnel.

Do not move or install your analyzer without the presence of Mindray-authorized personnel.
4-3
4.3. Connecting the Analyzer System

Connect the analyzer and the reagents as shown in the following figures. Make sure the
connections are correct and firm.
Figure 4-1 Connecting the analyzer to power outlet
4-4
Figure 4-2 Connecting the network cable
WARNING
4-5
Figure 4-3 Connecting reagents placed outside the analyzer
4-6
Figure 4-4 Connecting reagents placed inside the analyzer
CAUTION
 Make sure the diluent pipe and waste pipe are no longer than 1500mm.
 The waste and diluent containers must be placed lower than the countertop that
accommodates the analyzer.
4-7
4.4. Notes
 The analyzer performance may be undermined if it has been placed in environment of
high dustiness.
 The surface of the analyzer shall be cleaned and sterilized regularly with alcohol (75%).
 The probe wipe block of the analyzer (see Figure 4-5 Front of the analyzer) shall be wiped
with alcohol (75%) regularly.
 Sample collection and preparation must be done following standard procedures.
 If any of the pipes or fluidic components is worn out, stop using the analyzer and contact
Mindray customer service department immediately for inspection or replacement.
 Check and make sure the reagents, lyse and waste pipes are not pressed or bent.
 You must only use the Mindray-specified reagents, otherwise the analyzer may be
damaged or provide unreliable results.
 Pay attention to the expiration dates and open-container stability days of all the reagents.
Be sure not to use expired reagents.
4-8
5 Operating Your Analyzer
5.1. Introduction
This chapter provides step-by-step procedures for operating your analyzer on a daily basis.
A flow chart indicating the common daily operating process is presented below.
WARNING
 Do not contact the patients' sample blood directly.
5-1
Operating Your Analyzer
 The sample probe tip is sharp and may contain biohazardous materials. Exercise
caution to avoid contact with the probe when working around it.
CAUTION
 Do not reuse disposable products such as collection tubes, test tubes, capillary
tubes and so on.
NOTE
 Use the reagents specified by the manufacturer only. Store and use the reagents
as instructed by instructions for use of the reagents.
 Check if the reagent tubes are properly connected before using the analyzer.
 Be sure to use clean EDTAK2 or EDTAK3 anticoagulant collection tubes, fused

silica glass/plastic test tubes, centrifugal tubes and borosilicate glass capillary
tubes.
 Be sure to use the evacuated collection tubes recommended in the Appendix.
 Be sure to use the Mindray-specified disposable products including evacuated

blood collection tube, anticoagulant collection tubes and capillary tubes etc.
5-2
5.2. Initial Checks

Perform the following checks before turning on the analyzer.
 Checking the waste container
Check and make sure the waste container is not full.
 Checking reagents
Check to see if the reagents are expired or frozen. Reagents must be equilibrated for 24 hours
before use.
 Checking tubing and power connections
Check and make sure the reagents, waste and pneumatic unit tubes are properly connected
and not bent.
Check and make sure the power cord of the analyzer is properly plugged into the power
outlet.
 Checking the printer
Check and make sure enough printer paper is installed. Check and make sure the power
cord of the printer is properly plugged into power outlet, and the printer is properly connected
to the analyzer.
5-3
5.3. Startup and Login

Start up the analyzer:
1. Change the power switch at the backside to ON position ('I') will power on the instrument.
2. The indicator light turns on.
3. The analyzer will perform self-test and initialization.
NOTE
 Time needed for initializing the fluidic systems depends on how the analyzer was
previously shut down.
 Background check is the measurement of particle and electric interference by

the analyzer.
 If the results of the first background check do not meet requirement, the analyzer
will perform background check again.
 The sample ID of background check results is "background".
 The error message "Background abnormal" will be given when the background
results are out of range.
5-4
4. Enter the current user name and the password respectively into the "User ID" box and the
"Password" box.
5-5
NOTE
 If the software cannot be started successfully after being launched for several
times, contact Mindray Customer Service Department or the authorized
distributors.
 After starting up the analyzer, check if the date/time is correct.
 The default user name and password for administrator are both "Admin".
 The user name and password may be consisted of 1-12 letters, and the password
cannot be null.
5. Tap "Login" to enter the system.
NOTE
 If error occurs during the initialization process (e.g., background check fails), the
analyzer will report the error. See Chapter 11 Troubleshooting Your Analyzer for
the solution.
5-6
 See Appendix B Specifications for the background range of each parameter.
 The system opens different function for the user according to the user level. The
user level depends on the user name and the password when the user logs in.
 If user switching is necessary, click the "Logout" icon on the system menu.
Enter the desired user name and the password into the pop-up dialog box and
Click the "OK" button to log in.
 Running sample with the background abnormal error present will lead to
unreliable results.
5-7
5.4. Daily Quality Control

Perform daily quality control before running any samples. See Chapter 7 Using the QC
Programs for details.
5-8
5.5. Sample Collection and Handling
WARNING
 The sample probe is sharp and potentially biohazardous. Do not contact the
sample probe during operations.
CAUTION
tubes and so on.
NOTE
 Make sure the probe tip does not contact the sample tube to avoid potential
spillage.
5-9
1）Whole blood
sample
5.5.1 Sample 2）Capillary whole

preparation blood sample
3）Predilute sample
1）Enter sample
info.
2）Select “Whole
Blood” or
“Predilute” mode
3）Press Aspirate
5.5.2 Sample analysis key
4）Remove the
sample when hear
the beep sound
5）Run sample
analysis and report
results
1）Save the results
2）Print or transmit to
LIS
5.5.3 Processing
analysis results 3）Parameter flags
4）Flag info.
5-10
5.5.1.Sample Preparation
The analyzer can run 3 types of samples: whole blood samples, capillary whole blood
samples and pre-diluted samples.
CAUTION
 Prepare samples following the recommend procedure of the manufacturer.
 All samples shall be mixed as shown in the following figure.
1) Whole blood samples
1. Use clean EDTAK2 or EDTAK3 anticoagulant collection tubes to collect venous blood
samples.
2. Mix the sample according to your laboratory's protocol.
CAUTION
 Be sure to collect at least 0.5 mL of blood to ensure the accuracy of the results.
2) Capillary whole blood samples
1. Use tubes to collect capillary whole blood samples.
5-11
CAUTION
 Be sure to collect at least 120uL of capillary whole blood to ensure the accuracy
of the results.
NOTE
 Be sure to run the capillary whole blood samples within 3 minutes to 2 hours
after being collected.
3) Pre-diluted samples
1. Click the diluent dispensing icon, the following dialog box pops up.
2. Present a clean tube to the sample probe, press the aspirate key to dispense diluents
(480μL). The dispensing progress bar will be displayed on the screen.
3. To continue with diluent dispensing, repeat the step 1-2.
4. Add 20μL of venous blood or capillary blood to the diluent, close the tube cap and mix it
properly according to your laboratory's protocol.
5-12
5. Click “Cancel” after preparing all the samples, the analyzer will clean the sample probe
automatically.
NOTE
 You can also use pipette to aspirate 480μL of diluent.
 Be sure to keep dust from the prepared diluent.
 After mixing the capillary sample with the diluent, be sure to wait 3 minutes and
then remix before running the sample.
 Be sure to run the pre-diluted samples within 30 minutes after the mixing.
 Be sure to mix any sample that has been prepared for a while before running it.
Do not mix the samples with massive force using swirl mixer.
 Be sure to evaluate pre-diluted stability based on your laboratory’s sample

population and sample collection techniques or methods.
5.5.2.Sample Analysis
Tap "Sample Analysis" to enter the sample analysis screen. Tap "Mode" button to select
"Whole blood-CBC+DIFF", "Whole blood-CBC", "Capillary whole blood-CBC+DIFF",
"Capillary whole blood-CBC", "Pre-diluted-CBC+DIFF" or "Pre-diluted-CBC" mode.
1) Enter sample information

The analyzer provides two ways for you to enter sample information: entering sample ID only
and entering all sample information.
If you want to enter sample information after analysis, you may skip this chapter, and enter
sample information at the result review screen (see Chapter 6 Reviewing Sample Results).
You may first set up the way to enter sample information at the "Setup→Auxiliary" screen as
instructed in Chapter 9 Customizing the Analyzer Software, then you may enter sample
information at the “Analysis” screen.
 Entering Patient Demographics

When the way to enter patient demographic information is set to "Enter all information", click
"Next Sample" at the sample analysis screen, the following dialog box will display.
When the analyzer is connected to LIS, you may click the “LIS Fetch” button to get the
complete information of the next sample.
You may enter complete information of the next sample into the dialog box. The “Ref. group”
will be selected by the system.
5-13
 Entering the sample ID
Enter the sample ID in the "Sample ID" box.
NOTE
 Letters, numerics and all characters (including special characters) supported by
the keyboard are allowed for sample ID entering.
 The allowed length of sample ID is [1, 20], and the ID cannot be null.
 Entering the medical record number
Enter the medical record number in the "Patient ID" box.
 Entering the patient name
Enter the patient name into the “Name” box.
 Selecting patient gender
Select patient gender from the "Gender" pull-down list. There are two options: "Male" and
"Female".
5-14
 Entering the date of birth
Enter the patient's date of birth into the "Date of Birth" box. Its format must be the same with
the system date format.
 Entering the patient’s age
The analyzer provides four ways for you to enter the patient’s age – in years, in months, in
days and in hours. The first way is designed for the adult or pediatric patients no younger
than one year; the second for the infant patients one month to two years; the third for the
neonatal no older than one month, and the fourth for the neonatal no older than 48 hours.
You may choose one of the four ways to enter the patient age.
NOTE
 If the patient's date of birth is entered, his/her age will be calculated
automatically, and the age field will gray out and cannot be edited.
 If the entered date of birth is later than the current system, then it is considered
invalid.
 Entering the patient type
Select patient type from the "Patient Type" pull-down list.
 Entering the department name
Enter the name of the department into the “Department” box or select it from the
"Department" pull-down list (when there are previously saved records in the list). The saved
contents will be added in the pull-down list automatically.
 Entering the bed number
Enter the number of the patient’s bed into the “Bed No.” box.
 Entering the draw time
Enter the time when the sample is collected into the “Draw Time” box.
 Entering the delivery time
Enter the delivery time of analysis into the "Delivery Time" box.
5-15
 Entering the Clinician
To enter the name of the person who sent the sample for analysis, enter the name into the
“Clinician” box or SELECT the desired name from the “Clinician” pull-down list (if there are
previously saved names in the list). The saved contents will be added in the pull-down list
automatically.
 Entering comments
Enter comments in the “Comments” box.
 OK
When you have finished entering the work list information, click the "OK" button to save the
changes and return to the "Sample Analysis" screen.
 Cancel
If you do not want to save the entered work list information, click the "Cancel" button to return
to the "Analysis" screen without saving the changes.
 Entering sample ID only

When the way to enter patient demographic information is set to "Enter sample ID only", click
"Next Sample" at the sample analysis screen, the following dialog box will display.
Enter the sample ID in the "Sample ID" box. Click "OK" to save the ID and close the dialog
box, the ID will be displayed on the screen as the next sample ID.
2) Selecting mode
Make sure the analyzer indicator is green. Select whole blood (CBC+DIFF or CBC), capillary
whole blood (CBC+DIFF or CBC), or pre-diluted (CBC+DIFF or CBC) mode based on your
needs on the mode selection screen. The selected mode will be displayed at the bottom of
the screen.
5-16
3) Aspirate sample
Present the sample to the sample probe. Press the aspirate key to start the analysis.
4) Remove the sample

The sample probe will automatically aspirate sample. When you hear the beep sound, you
may remove the sample.
5) Auto analysis and result reporting

The analyzer will automatically run the sample. When the analysis is finished, the results will
be displayed on the screen.
5-17
NOTE
 During the analysis process, if errors like clog or bubble occur, the analyzer will
automatically display the results of related parameters as invalid, and alarm
information will show on the error information area. See Chapter 11
Troubleshooting Your Analyzer for the way to remove errors.
 If the ambient temperature is outside the specified operating range, thus causing
the analyzer temperature (the temperature tested by the sensor inside the
analyzer) goes out its specified range, the analyzer will alarm you for abnormal
ambient temperature and the analysis results may be unreliable. See Chapter
11 Troubleshooting Your Analyzer for solutions.
5.5.3.Processing Analysis Results
1) Automatic saving of analysis results

This analyzer automatically saves sample results. When the maximum number of results that
can be saved has been reached (40,000 records), the newest result will overwrite the oldest.
5-18
2) Printing and Transmission to LIS

If "Auto print after sample analysis" function is enabled, the analyzer will print reports
automatically; and if "Auto Communicate" function is enabled, the analysis results, sample
and patient information will be auto transmitted to LIS.
3) Parameter flags
See the following section for details about parameter flags.
 If the parameter is followed by a “H” or “L”, it means the analysis result has exceeded the
upper or lower limit of the reference range (See Section 9.2.4 Ref. range).
 If the parameter is followed by an “R”, it means the analysis result is questionable.
 If you see “*****”, as opposed to the result, it means the result is invalid; if you see
“+++++” as opposed to the result, it means the result is out of the display range (See
Table 6-1 Display Range for details).
Table 5-1 Display Range
Parameter Display Range

9
WBC, Bas#, Neu#, Eos#, Mon#, Lym#, ALY#, LIC # 0.00 ～ 999.99×10 /L
Bas%, Neu%, Eos%, Mon%, Lym%, ALY%, LIC % 0.0 ～ 99.9 %
12
RBC 0.00 ～ 18.00 ×10 /L
HGB 0 ～ 300 g/L
HCT 0.0 ～ 80.0 %
MCV 0.0 ～ 250.0 fL
MCH 0.0 ～ 999.9 pg
MCHC 0 ～ 9999 g/L
RDW-SD 0.0 ～ 999.9 fL
RDW-CV 0.0 ～ 99.9 %
9
PLT 0 ～ 9999×10 /L
PDW 0.0 ～ 99.9
MPV 0.0 ～ 99.9 fL
PCT 0.0 ～ 0.999 %
9
P-LCC 0 ～ 9999×10 /L
P-LCR 0.0 ～ 99.9 %
4) Flags of Abnormal Blood Cell Differential or Morphology

The following table lists all flags and their indications.
5-19
Table 5-2 Flags of Abnormal Blood Cell Differential or Morphology
Flag
Flag Meaning Judgment criterion
Type
Interference of PLT clump or
The DIFF and BASO channels are
WBC Abnormal NRBC to WBC count and
unproportionate.
differential may exist:
Immature cells or blasts may Many scatter-points in the immature
Immature Cell?
exist cell area of the scattergram
Abnormal lymphocytes or Many scatter-points in the abnormal/
Abn./Atypical Lym? atypical lymphocytes may atypical lymphocytes area of the
exist. scattergram
9
Leucopenia Low WBC analysis results WBC < 2.50×10 /L
9
Leucocytosis High WBC analysis results WBC > 18.00×10 /L
Low neutrophils analysis 9
Neutropenia NEUT# < 1.00×10 /L
results
WBC High neutrophils analysis 9
Flag Neutrophilia NEUT# > 11.00×10 /L
results
Low lymphocytes analysis 9
Lymphopenia LYMPH# < 0.80×10 /L
results
High lymphocytes analysis 9
Lymphocytosis LYMPH# > 4.00×10 /L
results
High monocytes analysis 9
Monocytosis MONO# > 1.50×10 /L
results
High eosinophils analysis 9
Eosinophilia EO# > 0.70×10 /L
results
9
Basophilia High basophils analysis results BASO# > 0.20×10 /L
9
WBC < 4.0×10 /L and RBC <
Pancytopenia WBC, RBC and PLT low 12 9
3.5×10 /L and PLT < 100×10 /L
Possible presence of
microcytes, macrocytes,
The distribution of RBC histogram is
RBC Histogram Abn. anisocytosis, RBC
abnormal
agglutination and dimorphic
histogram
HGB abnormal or RBC
RBC MCHC > 380 g/L
HGB Abn./Interfere? agglutination, or interference
Flag or HGB interference
may exist (e.g., WBC high)
Microcytosis MCV low MCV < 70fL
Macrocytosis MCV high MCV > 110fL
Anemia Anemia HGB < 90g/L

12
Erythrocytosis RBC high RBC > 6.5×10 /L
5-20
Possible presence of
PLT Scattergram The distribution of PLT scattergram
microcytes, red blood cell
PLT Abn. is abnormal
debris, giant PLT or PLT clump
Flag 9
Thrombopenia PLT low PLT < 60×10 /L
9
Thrombocytosis PLT high PLT > 600×10 /L
5-21
5.6. Auto-Standby
When the time for which the analyzer is free from fluidic operations reaches that you have set
at the "Setup" screen of the analyzer (default setting is 15 minutes), a dialog box will pop up,
prompting "Entering standby status…".
And the analyzer will prompt you to backup data.
After entering standby status, the message "Standby. Press the aspirate key to exit. " will be
displayed at the bottom left of the screen.
NOTE
 The analyzer will not enter standby status from the Status screen.
 If it is time for auto-Standby and the analyzer is reporting error, then the error
must be resolved first.
 During this condition, you can still perform any other operations (e.g., printing
and transmission) other than fluidic operations.
5-22
 Refer to Section 9.2.5 Maintenance Setup for how to edit waiting time before
entering standby mode.
 Under stand-by mode, if there are unfinished printing or communication tasks,

the analyzer will go on processing them.
 Aspirate key
Press the aspirate key to exit the standby status.
After the auto-Standby is canceled, the dialog box above will close automatically.
NOTE
 When exiting from the standby status, the analyzer will perform different
maintenance operations based on the time consumed entering standby status.
 If error occurs when the analyzer is exiting from the standby status, see Chapter
11 Troubleshooting Your Analyzer for solutions.
 After exiting the standby status, the analyzer will resume its original status. The
Analysis icon will turn into solid green. And the analyzer indicator will also turn
into solid green.
5-23
5.7. Shutdown
CAUTION
 Do not start up the analyzer immediately after it is shut down. Wait for at least 10
seconds.
NOTE
 To ensure stable analyzer performance and accurate analysis results, be sure to
perform the "Shutdown" procedure to shut down the analyzer after it has been
running continuously for 24 hours.
Perform the shutdown procedure to shut down the analyzer daily.
1. Click the shutdown button on the menu and the following shutdown dialog box will display.
2. Click "OK".
3. When dialog box prompting probe cleanser maintenance displays, present probe cleanser
to the sample probe, press aspirate key. The probe will aspirate probe cleanser automatically.
4. After shutting down finishes, the message "Please turn off the power of the analyzer!" will
be displayed. Press the Power switch on back of the instrument to power off.
WARNING
5-24
NOTE
 Do not disconnect power during the shutdown process.
 If error that will affect shutdown occurs during the showdown process, the
analyzer will resume to its original status and report the error. See Chapter 11
Troubleshooting Your Analyzer for solutions.
5-25
6 Reviewing Sample Results
6.1. Introduction
The analyzer automatically saves analysis results. The BC-5150 can store up to 40,000
analysis results.
You can review all the analysis results, scattergrams and histograms either in table or graph
mode.
6-1
Reviewing Sample Results
6.2. Browsing in the "Table Review" mode

Operators can review, validate, search, edit and export saved results at the "Table Review"
screen.
Tap "Table Review" to enter the following screen.
6.2.1.Table
The table lists all analyzed samples, including basic sample information like sample ID,
sample state and so on.
6-2
NOTE
 The table displays the latest sample results at the top.
6.2.2.Graph Review
Tap "Graph Review" button at the table review screen, or tap the "Previous" button at the
analysis screen to view the analysis results of samples.
6-3
6.2.3.validate/Cancel validate (for administrators only)

 validate sample data
Select one or more sample records, tap "validate", the sample state of the record will be
marked with "validated".
6-4
 Cancel validate
Select one or more validated sample records, tap "Cancel validate", the "validated" will
disappear.
6.2.4.Delete (for administrators only)

1. Select the sample record to be deleted.
2. Tap "Delete", the following dialog box will display.
6-5
3. Tap "OK" to delete the record, and the dialog box will be closed.
6.2.5.Edit info.
Click the desired sample result and it will be highlighted. Click the "Edit Info." button and the
following dialog box will display.
You may edit the sample and patient information, and tap "OK" to save the change. The
6-6
information on the table review screen will be refreshed.
6.2.6.Edit results
Click the desired sample result and it will be highlighted. Click the "Edit Result" button and the
following dialog box will display.
Modify the results and tap "OK" to save the changes. The information on the graph review
screen will be refreshed.
6.2.7.Search
1. Tap "Search", the following dialog box will display.
6-7
2. Enter search conditions into the edit boxes or select them from the pull-down lists.
3. Tap "OK" to start search, the results will displayed in the table.
6.2.8.Print
 Print reports as per the default report template
Select sample records to be printed, and then tap "Print" to print them. In the table
review interface, a 'printed' sign will be applied to each printed sample in the sample
state sector.
6-8
NOTE
 In sample state sector, ‘Validated’ sign is prior to ‘Printed’ sign.
6.2.9.Transmission
Transmit selected data
1. Select samples to be transmitted at the table review screen.
2. Tap "Comm.", the following dialog box will display.
6-9
3. Tap the "Selected" radio button.
4. Tap "OK" to start transmitting specified results to the data management software.
Transmit all data
2. Tap the "All" radio button.
4. Tap "OK" to start transmitting all results to the data management software.
6.2.10. Export
1 Tap "Export", the following dialog box will display.
6-10
2 Select "Selected" or "All" in the "Export range" area.
3 Check the type of information to be exported in the "Export data" area.
6-11
7 Using the QC Programs
7.1. Introduction
Quality Control (QC) consists of strategies and procedures that measure the precision and
stability of the analyzer. The results imply the reliability of the sample results.
QC involves measuring materials with known, stable characteristics at frequent intervals.
Analysis of the results with statistical methods allows the inference that sample results are
reliable. Mindray recommends you run the QC program daily with normal level controls.
A new lot of controls should be analyzed in parallel with the current lot prior to their expiration
dates.
This may be accomplished by running the new lot of controls twice a day for five days using
any empty QC files. The QC files calculate the mean, standard deviation and coefficient of
variation for each selected parameter. The instrument-calculated means of these ten runs
should be within the expected ranges published by the manufacturer.，
This analyzer provides 2 QC programs: L-J QC and X-B QC.
WARNING
 The sample may spill from the uncapped collection tubes and cause biohazard.
Exercise caution to the uncapped collection tubes.
7-1
Using the QC Programs
CAUTION
 Running QC sample with error present will lead to unreliable results. If errors are
reported during QC analysis, remove the errors first and then continue with the
analysis.
tubes and so on.
 Sample agglutination may result in inaccurate analysis results. Check the

control samples to see if there is any agglutination, if yes, process the samples
according to your laboratory's protocols.
NOTE
 Use the controls and reagents specified by the manufacturer only. Store and use
the controls and reagents as instructed by their instructions for use. Store and
use the controls and reagents as instructed by instructions for use of the
controls and reagents.
 Refer to the instructions for use of the control for its use and storage.
 Be sure to mix any control sample that has been prepared for a while before
running it.

7-2
7.2. L-J QC
7.2.1.Editing L-J settings (for administrators only)
Before running a new lot of controls, you must set up a QC file for each lot of controls.
1 Tap the menu option "QC" > "L-J QC" > "Setup".
2 Enter the L-J QC setup screen.
You may set up QC information by any of the following two ways.
 Reading the information provided by the manufacturer
 Manual Entry
Reading the information provided by the manufacturer
1. Enter the L-J QC setup screen.
2. Tap "New", or select a QC file without QC results, and then tap "Edit".
3. Tap "Import File".
7-3
4. Select the QC file to be imported.
5. Tap "OK" to close the dialog box and return to the L-J QC setup screen.
6. Tap "OK" to read the selected QC information to the current QC file.
NOTE
 The "Import target/limits" check box is selected by default. If it is
deselected, the operator must enter the target and limits of QC
parameters manually.
8. Select "Control type" from the pull-down list.
9. Select the QC mode.
10 Set QC sample ID: if you are used to analyze control together with blood samples, you
can set a unique ID for the control. The analyzer will recognize the sample as control
when it reads the unique ID. After the analysis completes, the results will be saved into
the QC file of the QC sample ID.
11 Tap other icons to switch screen and save the QC information.
Manual Entry
1. Enter the L-J QC setup screen.

2. Tap "New", or select a QC file without QC results, and then tap "Edit".
7-4
3. Enter the lot No. of the controls in the edit box manually.
NOTE
 The lot No. shall not be empty and up to 16 digits can be entered. You
can enter characters, numbers, letters and special characters.
4. Select the control level.
5. Enter the expiration date of the lot
6. Select the control type.
7. Select the QC mode.
8. Set QC sample ID: if you are used to analyze control together with blood samples, you
can set a unique ID for the control. The analyzer will recognize the sample as control
when it reads the unique ID. After the analysis completes, the results will be saved into
the QC file of the QC sample ID.
9. Enter the target and limits in the edit boxes according to the package insert of the lot of
controls.
10 Tap other icons to switch screen and save the QC information.
7-5
Setting limits
You can adjust the format of limits as per the following procedure:
1. Tap "Set Limits".
2. Click “By SD” to display the limits in the form of absolute value;
Or click “By CV” to display the limits in the form of percentage.
3. Click the “OK” button to save the settings.
7.2.2 L-J QC Run

You can select one of the two ways below to run controls:
 Run controls under the "QC" screen.
 Put controls together with normal samples, and run the controls under the sample
analysis screen.
7.2.3 Run controls under the "QC" screen
After editing the QC information, you can start QC analysis by one of the following ways
according to the selected QC mode.
 Whole blood
 Pre-diluted
7-6
CAUTION
 Running QC sample with error present will lead to unreliable results. If errors are
reported during QC analysis, remove the errors first and then continue with the
analysis.
 Sample agglutination may result in inaccurate analysis results. Check the

control samples to see if there is any agglutination, if yes, process the samples
according to your laboratory's protocols.
NOTE
 When switching mode from "Pre-diluted" to "Whole Blood", a progress bar will
be displayed while the analyzer runs mode switching sequence.
1. Tap "QC" > "L-J QC" > "Count" to enter the QC count screen.
2.
NOTE
 Be sure that the level of the control to be run is the same with the current
QC file, and the control is not expired.
 The expiration date of expired controls is displayed in red.
7-7
3.
4. Prepare the control as instructed by instructions for use of the controls.
5. Run QC analysis:
1) Make sure the analysis mode is "Whole Blood" or "Pre-diluted" and the indicator of
the analyzer is green.
2) Shake the vial of sample as instructed by instructions for use of the control to mix
the sample thoroughly.
3) Present the control sample to the sample probe. Press the aspirate key to start QC
run.
4) When you hear the beep, remove the control.
6. When analysis finishes, the QC results will be displayed in the current screen and be
saved in the QC file automatically.
NOTE
 Up to 100 QC results can be saved in each QC file.
7. Do the above procedures to continue running QC analysis if necessary.
7-8
Put controls together with normal samples, and run the
controls under the sample analysis screen.
After setting special "QC Sample ID" for a control under the QC setup screen, you can put the
control together with normal samples, and run it under the “Count” screen.
When editing worklist or entering next sample information in the "Next Sample" dialog box
before daily analysis, enter the special "QC Sample ID" as "Sample ID".
Based on the QC mode selected, you can choose to run QC analysis from one of the
following ways:
 Whole blood
 Pre-diluted
1. Prepare the control as instructed by instructions for use of the controls.
2. Refer to section 5.5.1 Sample Collection and Handling for sample preparation under
whole blood and pre-diluted modes.
3. When it is ready to run a sample (i.e. the status icon and the analyzer indicator is
green), present the sample to the sample probe.
4. When you hear the beep, remove the control.
5. When analysis finishes, the QC results will be displayed in the current screen and be
saved in the QC file automatically.
NOTE
 Up to 100 QC results can be saved in each QC file.
6. Do the above procedures to continue running QC analysis if necessary.
NOTE
 When switching mode from "Pre-diluted" to "Whole Blood", a progress bar will
be displayed while the analyzer runs mode switching sequence.
Editing and saving results (for administrators only)
Tap "Edit Result" on the QC screen to edit results and tap "OK" to save the edited results.
The edited results will be marked with an "E".
7-9
Restore results (for administrators only)
Operators of administrator access level can restore the edited results to the original
measurement results.
1. Tap "Restore" on the edit result screen.
2. Tap "OK" to restore the measurement values.
3. Tap "OK" to close the dialog box.
7.2.3 Reviewing L-J Results

After QC analysis, you can review the QC results in the following ways:
QC Graph
 QC Table
L-J QC graph review
1. Tap "Graph" button on the "L-J QC" screen to enter the L-J QC graph screen.
2. You can tap the arrow buttons on the right of the graph to browse graphs of the
parameters. You can tap the arrow buttons under the graph horizontally to browse all
the QC results.
7-10
NOTE
 If a parameter target/limits of the QC files with QC results are modified and
saved, and the targets/limits of other parameters changes accordingly, those
changed data will be highlighted in yellow.
Print
Tap the "Print" icon in the status bar to print information of the current QC file and the QC
graph of all parameters.
NOTE
 The green vertical line and values of the corresponding QC points will not be
printed.
L-J QC table review
1. Tap "Table" button on the "L-J QC" screen to enter the L-J QC table screen.
7-11
2. You can tap the arrow buttons on the right of the graph to browse all QC records. You
can tap the arrow buttons under the graph horizontally to browse all the parameter
results.
NOTE
 If a parameter target/limits of the QC files with QC results are modified and
saved, and the targets/limits of other parameters changes accordingly, those
changed data will be highlighted in yellow.
Delete (for administrators only)
1. Tap "Delete", the following dialog box will display.
2. Tap "Yes" to delete the selected records.
NOTE
 The operation will be recorded in the system log.
Print
You can tap the "Print" icon in the status bar to print the QC table.
Transmission
To transmit QC data to external data management software or HIS/LIS/HIS, do as follows:
7-12
2. Select to transmit "Selected" or "All" records.
3. Tap "OK" to start transmitting specified results to the data management software.
NOTE
 If auto-communication is enabled and a sample is run during the transmission of
the QC data, then only when the QC data transmission finished will the
auto-communication of the sample result start.
 The QC data saved in the process of transmission will not be transmitted.
Export
To Export QC information and results of the current QC file, do as follows:

1. Insert an USB and then tap "Export".
2 The system will detect the USB and export data automatically.
3 The prompt "Export succeeded!" will display.
7-13
7.3. X-B QC Program

7.3.1 Introduction
The X-B analysis is a weighted moving average analysis that uses values obtained from
patient samples. It uses the 3 red cell indices, MCV, MCH and MCHC to indicate the
hematology instrument performance.
It is recommended the X-B analysis be activated when the sample volume of your laboratory
is greater than 100 samples per day. Effective use of X-B requires randomization of samples
and a normal cross section of patients to prevent skewing of indices. It observes the trend of
QC results in the reference range formed by the specified target and limits.
The analyzer implement X-B QC on the 3 parameters: MCV, MCH and MCHC, each group of
samples for X-B analysis consists of 20-200 sample results obtained from normal analysis of
both WB and PD modes. The analyzer can save up to 500 X-B QC results. When the saved
QC results have reached the maximum number, the newest result will overwrite the oldest.
7.3.2 Editing X-B settings (for administrators only)
1. Click the menu option "QC" - "X-B QC" - "Setup", the following screen will display.
At the X-B QC setting screen, you may activate/deactivate X-B QC, set target/limits, and
configure the sample validity setup.
7-14
Editing X-B settings
1. In the “Sample number/group” edit box, you may enter the amount of samples [within
the range 20(default) to 200] to be included in calculating for an X-B QC point.
2. Activate/deactivate X-B QC If X-B QC is activated, the samples meeting validity

requirements will be included in X-B QC.
Set target/limits
Before the X-B QC analysis, you shall set up the target and limit for each parameter at the
X-B QC setup screen.
NOTE
 The units of target/limits of all parameters are the same as those in the parameter
unit setup screen.
1. In the “Target/Limit” area of the X-B QC setup screen, specify the targets and limits in
the “Target/Limit” table by entering manually.
NOTE
 Do not leave any of the targets and limits for the QC parameters blank.
 When first use, the default setting will provide the initial values for the
targets and limits of all QC parameters.
2. Tap other icons to switch screen and save the settings.
Setting sample validity
In X-B QC, sample results conforming to any of the following conditions will be considered as
invalid and cannot be used in the QC calculation.
 Sample results exceeding the linearity range;
 Background results;
 Sample results not conforming to the "Sample Validity Setup";
7-15
 QC data for QC programs other than X-B;
 Calibration data;
 Results generated while there are errors which could affect the accuracy of the results
(insufficient aspiration volume or clogging for example).
"Sample Validity Setup" is to set up the ranges of valid RBC, MCV, MCH and MCHC results.
Only when the results of all these four parameters are within the specified ranges, the sample
results can be used for X-B QC calculation. Do as follows to set the sample validity:
1. Select "On" to activate X-B QC.
In the "Sample Validity Setup" of the X-B QC setup screen, set the upper and lower
limits of the 4 parameters in the sample validity setup area.
The default validity range of each parameter is shown in the following figure.
7-16
2. Tap "Save" to save the setup.
NOTE
 In the sample validity setup, the upper limit shall be no smaller than the lower
limit. Otherwise, there will be prompted message asking you to revise.
 The valid ranges of the RBC parameters are their linearity ranges; the valid
ranges of other parameters are their display ranges.
 All the entries shall be numbers with only one decimal point. The length of the
number entered cannot be longer than the length of the text box.
 Once the validity range is changed, the previous results will not be used in the
QC calculation as valid results. For example, if 20 valid samples are needed for
the X-B QC calculation, when you change the validity range after 10 groups of
valid sample results have been acquired, these 10 groups of results will be
discarded, and only valid sample results generated afterwards will be used in the
QC calculation.
 The units of lower and upper limits of all parameters are the same as those in the
parameter unit setup screen. See section 9.2.4 Setup - Parameter Unit Setup.
Setting limits
You can adjust the format of limits as per the following procedure:
1. Tap "Set Limits".
7-17
2. Click “By SD” to display the limits in the form of absolute value;
Or click “By CV” to display the limits in the form of percentage.
3 Click the “OK” button to save the settings.
Restore defaults
If you want to restore the default targets and limits of the parameter, tap "Restore Defaults".
The default values of the target and limits of each parameter are as follows:
Parameter Target Limits (#)

MCV 89.5 2.7
MCH 30.5 0.9
MCHC 340 10
7.3.3 X-B QC Run

After editing X-B setup, the system will start X-B run automatically.
After every 20~200 results (determined by the setting) are obtained, the system will perform
the X-B calculation once automatically. You can review the result in X-B QC graph or X-B QC
table.
7.3.4 Reviewing X-B Results

After QC analysis, you can review the QC results in the following ways:
 QC Graph
7-18
 QC Table
X-B QC graph review
1. Click the menu option "QC" > "X-B QC" > "Graph", the following screen will display.
2. Select QC file No., the information of the file and the QC graph will be displayed on the
screen.
3. You can tap the arrow buttons under the graph horizontally to browse all the QC results.
X-B QC table review
1. Enter the X-B QC graph screen.
2. Tap "Table" button to enter the X-B QC table screen.
7-19
3. You can tap the arrow buttons on the right of the graph to browse all QC records.
The delete, print and export operations can all be performed same as stated in the L-J QC
table review section.
7-20
8 Calibrating Your Analyzer
8.1. Introduction
Calibration is a procedure to standardize the analyzer by determining its deviation under
certain specified conditions. In order to get accurate sample analysis results, you should
calibrate the analyzer per the procedure below when necessary.
There are three calibration programs available on this analyzer: manual calibration, auto
calibration using calibrators and auto calibration using fresh blood samples.
All the parameters or part of the parameters of WBC, RBC, HGB, MCV and PLT can be
calibrated by the calibration programs.
them and they contacted areas in the laboratory.
WARNING
procedures when handling them and they contacted areas in the laboratory.

CAUTION
tubes and so on.
8-1
Calibrating Your Analyzer
NOTE
 Calibration procedures can only be performed by users of the

administrator-level.
 Use the calibrators and reagents specified by the manufacturer only. Store and
use the calibrators and reagents as instructed by their instructions for use.
 The analyzer identifies a sample as a calibration sample only if the analysis is

started from the "Calibration" screen.
 Calculation of reproducibility is included in the calibration procedure.
8-2
8.2. When to Calibrate

This analyzer is calibrated at the factory just before shipment. It is electronically stable and
does not require frequent recalibration if you operate and maintain it as instructed by this
manual. You only need to recalibrate this analyzer if:
 you are going to use this analyzer for the first time (usually done by a Mindray-authorized
representative when installing the analyzer).
 an analytical component has been changed.
 you are going to re-use the analyzer after a long-term storage.
 the quality control results indicate there may be a problem.
 use environment changes significantly.
NOTE
 All of the measured parameters must be calibrated before readings of this
analyzer can be used as valid analysis results.
8-3
8.3. How to Calibrate

8.3.1 Preparing Your Analyzer
Do the following pre-calibration procedures before calibration. If problems are detected during
these checks, do not attempt to calibrate the analyzer. If necessary, call Mindray Customer
Service Department or your local distributor for assistance.
1. Check and make sure enough reagents have been prepared for the calibration. You need to
start over the calibration if the reagents run out during the process.
2. Check the background (for calibration right after startup) or blank count results .If the
analyzer alarms for abnormal background results, see Chapter 11 Troubleshooting for
solutions. ( see Appendix B Specifications for the background range).
Run a vial of normal control consecutively for 10 times under Whole Blood -CBC+DIFF mode.
Enter the "Table" review screen to check the reproducibility of the 10th runs and make sure
they meet the following requirements.
Parameter Range Whole Blood Pre-diluted

Reproducibility Reproducibility
(CV) (CV)
9 9
WBC 4.00×10 /L～15.00 10 / L ≤ 2.0% ≤ 4.0%
3.50  10 / L ~ 6.00  10 / L
12 12
RBC ≤ 1.5% ≤3.0%
HGB 110 g/L ~ 180 g/L ≤ 1.5% ≤3.0%
MCV 70 fL～120 fL ≤ 1.0% ≤2.0%
100  10 / L ~ 149  10 / L
9 9
PLT ≤ 6.0% ≤ 10.0%
150  10 / L ~ 500  10 / L ≤4.0% ≤8.0%
9 9
4. It is recommended that you create a log table for your analyzer. This log table should
contain all necessary information that is pertinent to your analyzer. Suggested items that you
may want to include in the log table are: calibration date, supplier of calibrator, lot number,
expected results and limits, and result of background check.
NOTE
 Be sure to use the evacuated collection tubes recommended in the Appendix.
 If fresh blood samples are used for reproducibility test, make sure the sample
volume is enough to support the test.
8-4
8.3.2 Manual Calibration

Tap "Calibration" > "Manual" in the menu to enter the following screen.
NOTE
 If you log in at the operator access level, you can only view the calibration
factors. To perform calibration, please log out and then log in at the
administrator access level.
Do as follows to calibrate the analyzer.
1. At the "Manual” calibration screen, check the calibration factors and calculate the new
factors per the following equation:
old factor  reference value

new factor 
calculated mean
For example: Suppose the WBC reference value of a calibrator is 8.4, and the current
calibration factor of the whole blood mode is 98.90％.
Run the calibrator under the whole blood mode for 11 consecutive times and take the WBC
results of the 2nd to 11th runs to calculate: 8.1, 8.0, 8.1, 8.1, 8.3, 8.3, 8.2, 8.0, 8.1, 8.3. The
obtained CV is 1.5% and Mean is 8.16, which meet the requirements.
The new calibration factor is obtained:
8-5
98.90%  8.4
New factor＝＝101.81%
8.16
The calculated calibration factors shall be between 75.00％～125.00％. In case of an invalid
calibration factor, try to find out the reason (e.g. calibration material not thoroughly mixed,
misoperation, etc.). Then recalibrate the analyzer and recalculate the calibration factors.
2. Enter the new calibration factors into the factor cell of the parameter that requires
calibration.
3. When you switch screen after entering the new calibration factor, a prompt will display.
If the entered calibration factors are valid, a dialog box will pop up asking you to save the new
factor when you are exiting the screen. And the calibration date of the corresponding
parameter changes to current system date.
If the entered calibration factors are invalid, a dialog box will pop up prompting "Invalid entry"
when you are switching to another screen. The new calibration factor will not be saved, and
the calibration date will not be refreshed.
Other Operations
Print
Tap "Print" to print the current calibration factor.

If the calibration factors are invalid, you will not be able to print them and the dialog box "New
calibration factor is invalid." will display.
If the calibration factors are valid but not saved, a dialog box will display asking you to save the
factors.
Click "Yes" to save and print the factors. Or click "No" to cancel the operation without saving or
printing them.
8.3.3 Calibration with Calibrator

Tap "Calibration" > "Calibrator" in the menu to enter the following screen.
8-6
NOTE
 The calibrator calibration can be performed under Whole Blood -CBC+DIFF,
Whole Blood -CBC, pre-diluted -CBC+DIFF and pre-diluted -CBC mode.
 Only Mindray-specified calibrators shall be used. Mindray will not be responsible

for any erroneous result caused by using other calibrators.
 See the instruction for use of the calibrators for the lot No., expiration date and
the target.
 The out-of-range CV% does not influence the display of calibration factors.
Do as follows to calibrate the analyzer with calibrators.
1. Check the mode on the analyzer screen.
2. Enter the lot No. of the calibrator into the "Lot No." box.
3. Enter the “Exp. date”. The entered expiration date should be either the expiration date
printed on the labeling or the open-container expiration date, whichever is earlier. The
open-container expiration date is calculated as follows: the date that container is opened + the
open-container stability days.
4. Enter the targets into the "Target" cells.
8-7
5. Prepare the calibrator as instructed by instructions for use of the calibrators.
6. Press the aspirate key to start calibration.
After the analysis, the analyzer will have different responses to different analysis results.
When the current running is done, if there is a parameter whose calibration data is out of its
linearity range but still within the display range, then the calibration data will be displayed in the
list and a message box will also pop up.
Tap “OK” to close the message box, and the data will be deleted from the table without saving
automatically.
When the running is done, if there is a parameter whose calibration data is out of the display
range, then the non-numeric parameter values "***" will be displayed in the list and a message
box will pop up.
Tap “OK” to close the message box, and the data will be deleted from the table without saving
automatically.
The valid results within the linearity range will be displayed directly. Valid calibration results will
be marked with "√” per the default setting, and will be taken to calculate calibration factors.
8. If the calibration factors have not been calculated but you switch to another screen, then a
message box will pop up.
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Tap "Yes" to switch to another screen while discarding the calibration data and closing the
message box. The original calibration factors remain.
9. When calibration count has been performed to a sample for n times (n≥5), the analyzer will
calculate the Mean, CV% and calibration factors of all the calibration data marked with "√"
(calibration data of the first run is not marked with "√", so it is not included in the calculation).
You can select several data to calculate the calibration factors, but only after at least 5 groups
of the data are marked with "√" can you get the calibration factors. The calibration factors will
be refreshed whenever you select “√” or deselect “√”.
When the amount of valid calibration data in the list reaches 10, a message box "Calibration is
completed!" will pop up. Then, if you press the aspirate key again, the analyzer will beep
without starting analysis.
10. There may be two cases when you are switching to another screen:
If the calibration factors of any parameter is out of the range [75%-125%] or the CV% of any
parameter exceeds the reproducibility range, then the calculated calibration factors of all
parameters will not be saved and a message box will also pop up.
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Tap "Yes" to close the dialog box and switch to another screen. The calibration factors and
dates of all parameters will not be changed.
If the calculated calibration factors of all parameter are within the range [75%-125%] and the
CV% of all parameter are also within the reproducibility range, then a message box will pop up.
Tap "Yes" to save the new calibration factors while closing the message box and switching to
another screen.
Other Operations
Print
If the calibration factors are invalid, tap print, the dialog box "New calibration factor is invalid."
will display.
If the calibration factors are valid but not saved, tap "Print", a dialog box will display asking you
to save the factors.
Click "Yes" to close the dialog box, save and print the calibration results. Or click "No" to
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cancel the operation without saving or printing them.
8.3.4 Calibration with Fresh Blood

Tap "Calibration" > "Fresh Blood" in the menu to enter the following screen.
Do as follows to calibrate the analyzer with fresh blood.
1. Prepare 3 to 5 normal fresh blood samples as instructed by 5.5.1 Preparing Samples.
2. Run each of the prepared samples on the reference instrument (or by the reference method)
five times at least. Calculate the mean values and use them as the targets. Or perform
measurement and calculation as per the reference method and take the calculated data as the
targets.
3. Select mode for fresh blood calibration, which can be Whole Blood-CBC+DIFF, Whole
Blood-CBC, Pre-diluted-CBC+DIFF and Pre-diluted-CBC.
4. Select the ID of current sample from the pull-down box "Current Sample ID".
5. Enter the targets into the "Target" cells.
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6. Prepare fresh blood sample.
7. Press the aspirate key to start calibration.
After the analysis, the analyzer will have different responses to different analysis results.
If the results are out of the linearity range but still within the display range, a dialog box will pop
up when the results are displayed in the table.
Tap “Yes” to close the message box, and the data will be deleted from the table without saving
automatically.
If the results are out of the display rage, the non-numeric parameter values "***" are obtained
and a dialog box will pop up.
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Tap “Yes” to close the message box, and the data will be deleted from the table without saving
automatically.
The valid results within the linearity range will be displayed directly.
Valid calibration results will be marked with "√” per the default setting, and will be taken to
calculate calibration factors.
9. When calibration count has been performed to a sample for n times (n≥5), the analyzer will
calculate the Mean, CV% and calibration factors of all the calibration data marked with "√"
automatically.
You can select several data to calculate the calibration factors, but only after at least 5 groups
of the data are marked with "√" can you get the calibration factors. The calibration factors will
be refreshed whenever you select “√” or deselect “√”.
When the amount of valid calibration data in the list reaches 10, a message box "Calibration
with the current blood sample is completed." will pop up when you start calibration again.
10. Select other calibration sample ID from the "Current Sample ID" pull-down box, analyze
other samples according to Step 7-9 above to obtain the calibration factors of all samples.
11. There may be several cases when switching to another blood sample:
If the calibration factors of the blood sample are invalid or the CV% of any parameter exceeds
the reproducibility range, a dialog box will pop up when switching to another blood sample.
Tap "Yes" to empty the entered target of the current sample, all the calibration data obtained
and each calculated value including calibration factors, then close the dialog box and switch to
another blood sample.
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If the calibration factors have not been calculated, a dialog box will pop up.
Tap “Yes” to empty the entered target of the current sample and all the calibration data
obtained, then close the dialog box and switch to another blood sample.
If the calibration factors of the sample are valid and the CV% of all the parameters do not
exceed the reproducibility range, you can switch to another blood sample directly.
12. After calibration factors of at least 3 fresh blood samples are obtained, tap the "Calculate"
button to enter the screen of calibration calculation.
Select or deselect the calibration factors of a blood sample for the calculation of the Mean
calibration factors by tapping the check boxes before the calibration factors.
When 3 or more groups of calibration factors are checked, CV% will be re-calculated
automatically base on the checked calibration factors.
When 3 or more groups of calibration factors are checked, the mean calibration factor will be
re-calculated automatically base on the checked calibration factors. The mean calibration
factors are regarded as invalid if the deviation of absolute value between the calibration factors
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included in calculating the mean and the original calibration factors reaches or exceeds 5%; a
dialog box will pop up when you exit the current fresh blood calibration screen.
Tap "Yes" to close the dialog box and exit with the current calibration data emptied, and then
switch to another screen.
Tap "No" to return to the current screen. Invalid mean calibration factors are followed with a "?",
and displayed in red.
13. If the mean calibration factors have not been calculated, when you exit the fresh blood
screen or switch to another calibration mode, a dialog box will pop up.
Tap "Yes" to discard the calibration data, close the dialog box, and switch to another screen or
calibration mode. The original calibration factors and date remain the same.
14. If the calculated mean calibration factors are valid, when exiting the fresh blood calibration
screen or switching to another calibration mode, a dialog box will pop up.
Tap "Yes" to save the current mean calibration factors. Then, you can switch to another screen
or calibration mode. Tap "No" to close the dialog box and switch to another screen or
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calibration mode without saving the mean calibration factors and all the calibration data.
Other Operations
Print
If the mean calibration factors are invalid, tap print, the dialog box "Calibration factor is invalid."
will display.
If the mean calibration factors are valid, you can tap "Print" to print the calibration factors of a
group (or more) of blood samples in table form, no matter whether they are selected ("√") or
not. The results obtained in the calibration process and the mean calibration factors can also
be printed.
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9 Customizing the Analyzer Software
9.1. Introduction
The BC-5150 is a flexible laboratory instrument that can be tailed to your working
environment. You can use the “Setup” program to customize the software options as
introduced in this chapter.
For the security of the settings and data, two access levels are provided to the operator of the
analyzer. The administrator access level provides the operator with access to more functions
or settings, some of which can be configured to be accessible to operators.
See the following figure for the setup menu.
9-1
Customizing the Analyzer Software
9.2. Setting Up the Analyzer

9.2.1 System Setup
 Date/Time
Tap the menu option "Setup" > "System Setup" > "Date/Time" to enter the "Date/Time" screen
as shown below. You can set up the date, time and date format of the analyzer at the screen.
 Print
Tap the menu option "Setup" > "System Setup" > "Date/Time" to enter the "Print setup"
screen as shown below. You can set up the following contents:
 Print setup
 Printing content
 Auto print
9-2
 Print setup
Print device
There are 2 types of printing device available: printer and recorder. You can select either of
them from the pull-down list.
Printer driver
Tap the pull-down list to select printer driver of the analyzer.
Paper
Tap the pull-down list to select the paper type of the reports to be printed.
Parameter language
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Tap the pull-down list to select the parameter language of the reports.
Copies
Enter the number of copies to be printed for each report into the edit box "Copies".
Report title
Report template
Applicable report templates for printer are shown as below：
Applicable report templates for recorder are shown as below.
 Printing content
You can choose to select the functions based on your needs by tapping on the check boxes.
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 Auto print
You can choose to disable auto print or set up printing conditions.
 Communication setup
Tap the menu option "Setup" > "System Setup" > "Communication" to enter the
communication setup screen as shown below. You can set up the following contents:
 Protocol Setup
 Transmission Mode
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 Protocol Setup
Tap the "IP Address", "Subnet Mask" and "Default Gateway" edit boxes to enter the contents.
Communication Protocol
Tap the "Comm. Protocol" pull-down list to select the communication protocol.
ACK synchronous transmission
Tap on the "ACK synchronous transmission" check box to activate the function.
When the function is activated, ACK overtime is 10 seconds by default. You can re-enter the
ACK overtime is the edit box.
 Transmission Mode
You can choose to select the functions based on your needs by tapping on the check boxes.
 Auto retransmit
 Auto Communicate
 Auto Fetch Info from LIS
 Transmit as Print Bitmap Data
Transmission mode of histogram and scattergram

Tap the pull-down lists to select the transmission modes of histogram and scattergram.
 Not to be transmitted
 Bitmap
 Data
 Flag alarm sensitivity

Tap the menu option "Setup" > "System Setup" > "Flag alarm sensitivity" to enter the screen
as shown below. This function allows you to set up flag alarm sensitivity based on your own
needs.
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This screen shows the values that may trigger flag alarm. Operators of administrator access
level can modify the reference values of the flags, which indicated the possibility of triggering
flags. The lower the values are, the higher the possibility can be.
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 Shortcut code setup

Tap the menu option "Setup" > "System Setup" > "Shortcut Code Setup" to enter the screen
as shown below. This function allows you to set up shortcut codes for the contents in sample
information setup screens.
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 Add shortcut codes
1. Select "Department" or "Clinician" tab.
2. Tap "Add", a line will be added in the table.
3. Enter the "Name", "Shortcut Code" and "Digital Code" based on your needs.
 Edit shortcut codes
1. Select "Department" or "Clinician" tab.
2. Select the line of the shortcut code to be edited.
3. Modify it directly in the table.
 Delete shortcut codes
1. Tap the shortcut code to be deleted.
2. Select the line of the shortcut code to be deleted.
3. Tap "Delete" to delete it.
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 Lab info. setup

Tap the menu option "Setup" > "System Setup" > "Lab Info. Setup" to enter the screen as
shown below. Operators may enter, save and view lab information. Tap on the edit boxes to
enter the information.
NOTE
 The analyzer SN cannot be edited.
 The date of installation is the date the analyzer is installed by default. It can be
edited, but cannot be later than the current system date.
9.2.2 Access Setup

Tap "Setup" > "Access Setup" in the menu to enter the following screen.
9-10
 Modify password
You can modify your own password.
1. Select the current user, and then tap "Modify password", the following dialog box will
display.
2. Enter the required information in the edit boxes.
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3. Tap "OK" to save the change and close the dialog box.
NOTE
 The password cannot be null, and 12 characters can be entered at most.
 Create new user
1. Tap "New", the following dialog box displays.
2. Enter the "User ID", "Name" and "Password" information.
3. Select access level of the user:
 Operator
 Administrator
4. Tap "OK" to save the change and close the dialog box.
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NOTE
 The user ID cannot be null, and 12 characters can be entered at most.
 The password cannot be null, and 12 characters can be entered at most.
 The name cannot be null, and 20 characters can be entered at most.
 Delete user
Select a user and then tap "Delete" to delete it.
NOTE
 The current login user cannot be deleted.
9.2.3 Auxiliary Setup

Tap "Setup" > "Auxiliary Setup" in the menu to enter the following screen. You can set up the
following contents:
 Setting of the next sample
 Setting of the first sample after startup
 Other settings
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 Setting of the next sample
Entry of the next sample ID

Tap the pull-down list to select the way to enter the next sample ID.
 Auto Increase
 Manual Entry
Not counted as an auto increase character

Operators can set up the number of characters in the sample ID that will not be auto
increased.
When "Auto Increase" is selected as the way to enter the next sample ID, this edit box will be
activated.
Enter a number n into the edit box. The first n characters in the sample ID will not be auto
increased.
 Setting of the first sample after startup
Operators may:
Customize the first sample ID after startup by entering it into the edit box. Or select to
continue with the sample ID before last shutdown.
 Other settings
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On/Off radio buttons
Select "On" or "Off" to activate or deactivate the functions.
Flags
Operators may set up the suspect flag by entering a character into the edit box, or selecting a
letter from the pull-down list (the default character is "R").
Operators may set up the high/low flag by entering two characters into the edit boxes, or
selecting two letters from the pull-down lists (the default character of high flag is "H", and that
of low flag is "L").
9.2.4 Parameter Setup

 Parameter unit setup
Tap the menu option "Setup" > "System Setup" > "Reference Unit Setup" to enter the screen
as shown below. You can set up parameter unit at this screen.
9-15
 Select unit system
Tap the "Unit system" pull-down list to select unit system.
 Customizing parameter units
Under each unit system, you can tap the "Unit" cell to customize the parameter unit.
Tap the "Default" button to restore the default units.
NOTE
 The units displayed will be different when different unit system is selected.
 Reference range setup

Tap the menu option "Setup" > "System Setup" > "Reference Range Setup" to enter the
screen as shown below. 5 factory reference group and 10 customized reference groups are
provided for your choice. Each laboratory shall select a proper reference range of its own
based on its patient demographics. The reference range differs among races, genders, ages
and geographic locations.
9-16
 Customizing reference groups
Select a reference group and tap "New" or "Edit" to enter the reference group setup screen.
You can set up the name, lower and upper limits of age and parameter range.
9-17
Tap the "Set to Default" button, the reference ranges of the selected factory reference group
can be restored to the default settings.
NOTE
 The name of the reference group cannot be null.
 The names of the customized reference groups shall not repeat the names of the
5 default groups, and they shall not repeat each other either.
 Setting as default reference group
Select a reference group and then tap "Set to Default" to set it as default reference group.
NOTE
 The name, lower and upper limits of age and gender of the factory reference
groups cannot be modified.
 The input range of age is [0,999].
 Modify reference range(s)
To modify the reference range of a reference group,

Select the group from the reference group list on the left, and then click the cells of upper and
lower limits in the table and re-enter the values.
To restore the reference ranges to default, click the “Default” button on top right of the screen.
Select "Match customized ref. group first ", when the age ranges of the customized reference
group and the default reference group contradicts with each other, the customized reference
group will be matched first on the sample analysis and review screens.
 RUO parameter setup

Tap the menu option "Setup" > "System Setup" > "RUO Para". Setup to enter the screen as
shown below. You may modify RUO parameter related settings.
9-18
Select "Enable RUO parameters". The 4 RUO parameter results will be given for the samples
analyzed thereafter.
 Microscopic parameter setup

Tap the menu option "Setup" > "System Setup" > "Microscopic Para. Setup" to enter the
screen as shown below. You may modify microscopic parameter related settings.
9-19
 Add new parameter
Tap the “New” button to add a new row in the table, and then you can enter the name of the
parameter in the row.
 Delete
Select a row in the table, click the “Delete” button to delete the parameter.
 Editing parameter name
Tap a parameter name in the table to edit the name.
NOTE
 You can add up to 40 microscopic parameters.
 The reconfigured setup will not be applied to sample records which already have
microscopic results saved, but only applied to sample records with unsaved
microscopic results and records attained after the new setup is applied.
9.2.5 Maintenance Setup (for administrators only)

Tap "Setup" > "Maintenance" in the menu to enter the following screen. You can set up the
9-20
following contents:
 Standby
Tap the text box "Wait" and enter the waiting time before entering the standby status. The
range allowed is 10 -30 minutes, and the default setting is 15 minutes.
 Probe cleanser maintenance

Tap the first text box in the "Probe Cleanser Maintenance" area to enter the time to start
time-based probe cleanser maintenance. Tap the second text box to enter a time in the text
box. Then when the operator cancels the time-based maintenance, a reminder dialog box will
pop up after the defined minutes.
9.2.6 Reagent Setup

Tap "Setup" > "Reagent Setup" in the menu to enter the following screen.
9-21
It is recommended that you replace the reagents when their residue volume icons turn from
BLUE to RED.
This function may also be used to refill reagent inside the fluidic system when a new
container of reagent is loaded.
NOTE
 The reagents must be kept still for at least a day after long-term transportation.
 When you have changed the diluents or lyse, run a background test to see if the
results meet the requirement.
You should replace reagents when:
 the reagent ran out and a new container of reagent is installed.
 the reagent in the tubing is contaminated.
 there are bubbles in the tubing.
You can replace the following reagents in the fluidics:
 Diluent
 DIFF lyse
9-22
 LH lyse
Do as follows to replace the reagents.
1. Tap the reagent you want to replace, and then tap "Setup".
2 Enter reagent information at the screen.
3 Or scan in the barcode. If the barcode is valid, the corresponding reagent information
will automatically display.
4 Tap "Replace" to save the exp. date and start to replace the reagent. A progress bar
will be displayed in the process.
5 Replace other reagents as per the above procedures if needed.
NOTE
 Please keep the diluent container from severe shock or crashing against other
object. Otherwise, the alarming would be unreliable.
 When replacing diluent container, do as follows: 1) Install the supporting board

under the cap of the diluent container as instructed below. 2) Insert the diluent
cap assembly into the container as shown in the figure below, and tighten the
cap. Otherwise the alarming may be unreliable.
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9.2.7 Gain Setup (for administrators only)

Tap "Setup" > "Gain Setup" in the menu to enter the following screen. Gain setup function
allows you to adjust the digital potentiometers. The operation shall not be performed
frequently.
 Setup
9-24
 RBC gain
Tap the MCV-G "Set Value" cell, and enter the new value of RBC gain.
 HGB gain
The purpose of adjusting HGB gain is to change HGB background voltage.

Tap the "Auto Cal. to 4.2V" button, and the HGB blank voltage will be set to 4.2V
automatically.
NOTE
 The gains of LAS, MAS and WAS cannot be modified.
9-25
9.3. Save the settings

To save the modified settings, you may switch to another screen, the following dialog box will
display.
Click "Yes" to save the settings and switch to the corresponding screen. Click "No" to switch
to the corresponding screen without saving the settings.
9-26
10 Servicing Your Analyzer
10.1. Introduction
Preventive and corrective maintenance procedures are required to keep the analyzer in a
good operating condition. This analyzer provides multiple maintenance functions for this
purpose.
This chapter introduces how to use the provided functions to maintain and troubleshoot your
analyzer.
 All the analyzer components and surfaces are potentially infectious, take proper
protective measures for operation or maintenance.
WARNING
CAUTION
 Improper maintenance may damage the analyzer. Operators must follow the
instruction of this Operator's Manual to perform maintenance operations.
 For any questions, contact Mindray customer service department.
 Only Mindray-supplied parts can be used for maintenance. For any questions,
contact Mindray customer service department.
 Exercise caution to avoid contact with the sharp sample probe when performing
maintenance.
The following table lists the tools that may be used in maintenance.
No. Tools
1. Cross-headed screwdriver
2. Slotted head screwdriver
3. Medical gloves
4. Alcohol
10-1
Servicing Your Analyzer
10.2. Maintaining Your Analyzer

Maintenance options of the analyzer includes: maintenance, cleaning and fluidics
maintenance.
10.2.1 Maintenance
Tap "Service" > "Maintenance", and select the "Maintenance" tab to enter the following
screen.
Unclog aperture
Unclogging includes zapping and flushing the aperture. When clog error us reported, you
should unclog the aperture.
The unclogging procedures are:
1. Tap the "Unclog" button to start unclogging.
2. When the progress ends, a message will display indicating "Maintaining finished!".
3. Do the above procedures to continue unclogging aperture if necessary. If the error

persists, perform probe cleanser maintenance of the related channels.
10-2
Probe cleanser maintenance
You should perform the probe cleanser soaking procedure when:
 background results are out of range, QC results abnormal or scattergram abnormal due
to long term idleness of the analyzer; or when other maintenance operations fail to solve
the clog error.
 the analyzer shuts down due to abnormal power break-off; probe cleanser maintenance
must be performed after it is started up again.
The probe cleanser maintenance procedures are:
1. Tap "Overall Soak" button, the following dialog box will display.
2. Tap "Yes", the analyzer starts to prepare for the maintenance.
3. When the preparation is done, the following dialog box will display.
4. After aspirating probe cleanser, the analyzer performs probe cleanser soak
automatically, and a progress bar will display indicating the progress.
10-3
5. When the progress ends, the following dialog box will display, click “OK” to close the
dialog box.
10.2.2 Cleaning
You should clean the following components when:
 WBC and (or) HGB background results exceed their limits, perform WBC bath cleaning.
If WBC bath cleaning does not solve the problem, perform WBC probe cleanser
maintenance.
 RBC and (or) PLT background results exceed their limits, perform RBC bath cleaning. If
RBC bath cleaning does not solve the problem, perform RBC probe cleanser
maintenance.
 there are too many particles in the scattergram of background results, perform WBC
bath cleaning. If WBC bath cleaning does not solve the problem, perform WBC probe
cleanser maintenance.
 sample probe gets dirty, perform sample probe cleaning.
Tap "Service" > "Maintenance", and select the "Cleaning" tab to enter the following screen.
10-4
You may perform cleaning operation to the following components:
 Fluidics
 Flow cell
 Sample probe
 Unclog flow cell
 WBC bath
 RBC bath
The cleaning procedures are:
1. Tap the button of the component you want to clean. The message "Cleaning in
process. Please wait..." will display.
2. When the progress ends, a message will display indicating "Cleaning finished!".
3. Clean other components as per the above procedures if needed.
10.2.3 Servicing the Fluidics
Tap "Maintenance", and select the "Fluidics" tab to enter the following screen.
10-5
Pack-up
If the analyzer is not to be used for over 2 weeks, you should perform this procedure.
Do as follows to pack up:
1. Tap "Pack-up", the dialog box "Start pack-up?" will pop up.
2. Tap "Yes" to perform the pack-up procedure. The following dialog box will be displayed.
3. Take out the tubes as instructed and then tap "OK" to drain the fluidics.
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4. The following dialog box will be displayed after draining the fluidics.
5. Put the tubes into distilled water as instructed, and tap "OK" to start priming.
6. When the priming progress ends, the following dialog box will be displayed.
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7. Take out the tubes as instructed and then tap "OK" to drain the fluidics again.
8. The following dialog box will be displayed after draining the fluidics.
9. When the pack-up is finished, shut down the analyzer as prompted.
NOTE
 This software can still be used after the pack-up.
Reset
When major components of the analyzer have been replaced, or the fluidic system has been
serviced, you must reset the fluidics.
Do as instructed below:
1. Tap "Reset Fluidics", a dialog box will pop up asking you to confirm the operation.
2. Tap "OK" to start initialization, the message "Resetting fluidics. Please wait..." will be
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displayed.
3. When the progress ends, a dialog box will display indicating “Resetting fluidics
finished!”.
4. Do the above procedures to continue resetting fluidics if necessary.
10-9
10.3. Touch Screen Calibration

Tap "Maintenance" > "Calibrate Touchscreen" in the menu to enter the following screen.
10-10
10.4. Viewing Logs

Tap "Maintenance" > "Log" in the menu to enter the following screen.
You may view the error info., parameter modification info. And records of daily operation in
the log.
The “Log” screen records all activities of the analyzer. It contributes significantly to searching
for operation history and troubleshooting the analyzer.
NOTE
 The oldest record will be overwritten automatically when number of log records
reaches the utmost.
 Records of two years can be stored at most.
 Exporting logs
1. Tap "Export", the following dialog box will display.
10-11
2. Select the range of the logs that you want to export.
3. Tap "OK" to close the dialog box and export the logs.
10-12
10.5. Checking the Analyzer Status
NOTE
 If the status is outside normal range, it will be highlighted with red background.
10.5.1 Counter
The counter counts the running times of the analyzer and the occurrence times of some
major parameters.
 Viewing details
You may tap the "Detail..." buttons following "Runs", "QC Runs" or "Calibration Runs" to view
the related details.
 Print
Tap the "Print" icon to print all information on the screen.
10-13
10.5.2 Temp. & Pressure

Tap "Status" > "Temp. & Pressure" in the menu to enter the following screen. You may check,
export or print the temperature and pressure values of different components of the analyzer.
10-14
10.5.3 Voltage and Current

Tap "Status" > "Voltage & Current" in the menu to enter the following screen.
You may check the Voltage and Current values of different components of the analyzer.
10-15
10.5.4 Sensor
Tap "Status" > "Sensor" in the menu to enter the following screen.
You may check the sensor status of the analyzer.
10-16
10.5.5 Version Info.

Tap "Status" > "Version Info." in the menu to enter the following screen. You may view the
current version information of the analyzer.
10-17
11 Troubleshooting Your Analyzer
11.1. Introduction
This chapter contains information that is helpful in locating and correcting problems that may
occur during operation of your analyzer.
NOTE
 This chapter is not a complete service manual and is limited to problems that are
readily diagnosed and/or corrected by the user of the analyzer.
11-1
Troubleshooting Your Analyzer
11.2. Error Information and Handling

During the operation, if error(s) is detected, the analyzer will beep and display the
corresponding error message in the error information area at the bottom right of the screen.
Meanwhile, the indicator will turn red.
According to the severity of the errors, the colors of error messages are red, orange, blue and
green.
 Red: fatal error. When this kind of error occurs, the analyzer will stop running
immediately, and any further operation is prohibited.
 Orange: error that stops operation. When this kind of error occurs, the analyzer will stop
running immediately.
 Blue: error that restricts certain operations. When this kind of error occurs, the analyzer
can still continue with the current operation, but any other operations related to the error
will be restricted.
The following Figure is the error info. dialog box.
The name and troubleshooting method of the errors are displayed. Names of the errors are
displayed by the order of their occurrence.
You may tap to select the error, and view its troubleshooting information in the
troubleshooting box. The troubleshooting information of the first error is displayed by default.
Please follow the troubleshooting to resolve the error by sequence.
11-2
The following functions are provided:
 Remove error
Tap the "Remove Error" button to clear all the errors that can be removed automatically. For
the errors that cannot be removed automatically, follow the troubleshooting method to solve
them.
 Close the error info. dialog box
Tap "Close" to close the dialog box, but the errors will still be displayed in the error info. area
on the screen. Tap the error info. area again, the dialog box will be displayed.
The possible error(s) and the corresponding troubleshooting information are listed below:
Error Name Actions

1. Tap “Remove Error” to see if the error can be removed.
Communication error 2. If the error still exists, contact our customer service
department.
1. Power off the analyzer directly, and then contact our

Digital board error
customer service department.

System clock error
1. please modify the IP address in the interface of

IP address collision
communication settings
1. Tap "Remove Error", and enter the new barcode of the
diluent into the reagent setup dialog box.
2. After replacing the diluent container, tap "Apply" to prime
Diluent ran out
diluent.
3. If the error still exists after replacing the diluent, contact
our customer service department.

LH lyse into the reagent setup dialog box.
2. After replacing the lyse container, tap "Apply" to prime
LH lyse ran out
the lyse.
3. If the error still exists after replacing the lyse, contact our

DIFF lyse ran out DIFF lyse into the reagent setup dialog box.
11-3
the lyse.

Diluent expired
the lyse.

LH lyse expired
the lyse.

DIFF lyse into the reagent setup dialog box.
DIFF lyse expired
the lyse.
Empty the waste container or use a new waste container.

Waste container full
3. If the error still exists, contact our customer service
department.
Power source error

Temperature sensor error

Preheat assembly error

Laser error
Syringe module error
11-4
department.
Aspiration module lift
mechanism error
department.
Aspiration module rotary
mechanism error
department.
Background abnormal 2. If the error still exists, contact our customer service
department.
Exiting standby mode failed 2. If the error still exists, contact our customer service
department.
Replacing diluent failed 2. If the error still exists, contact our customer service
department.
Replacing DIFF lyse failed 2. If the error still exists, contact our customer service
department.
Replacing LH lyse failed 2. If the error still exists, contact our customer service
department.
1. Check if there is diluent reagent in the container. If not,
replace the container with a new one.
HGB blank voltage abnormal 2. Tap "Remove Error" to remove the error.
3. If the error persists, contact our customer service
department.
1.Please do "Probe Cleanser Maintenance".
2.Please do "Clear Flow Cell".
3. Power off the analyzer directly, and restart it after a
Liquid pressure overloaded
while.
department.
Vacuum pressure abnormal 2. If the error still exists, contact our customer service
department.
Preheat bath temperature
error
department.
11-5
1. The ambient temperature shall be within [10℃, 30℃]

Machine temperature too high 2. Diluent temperature shall be within [10℃, 30℃].
Diluent temperature is too 1. Diluent temperature shall be within [10℃, 30℃].

high
Diluent temperature is too low 1. Diluent temperature shall be within [10℃, 30℃].
Clogging 2. If the error still exists, contact our customer service
department.
Aperture voltage abnormal 2. If the error still exists, contact our customer service
department.
Impedance channel signal 1. Please eliminate sources of interference.

abnormal
1. Tap "Remove Error" button to remove the error.
2. If the error persists, power off the analyzer and power on
Analysis is abnormal later.
department.
1. Please check the analysis mode.
3. If the error persists, power off the analyzer and power on
RBC channel is abnormal
later.
department.
1. Please check the DIFF lyse residue and the analysis
mode.
DIFF channel is abnormal 3. If the error persists, power off the analyzer and power on
later.
department.
1. Please check the LH lyse residue and the analysis
mode.
BASO channel is abnormal 3. If the error persists, power off the analyzer and power on
later.
department.
Abnormal liquid pressure fluctuation. Check if the diluent
Abnormal liquid pressure
has run out
11-6
Abnormal HGB blank voltage. Check if the diluent has run

Abnormal HGB blank voltage
out
Abnormal mean liquid pressure. Check if the diluent has
run out. Perform “Valve Self-test” to check the status of all
Abnormal liquid pressure
valves. Check if the if the liquid pressure sensor work
normally
11-7
12 Appendices
A. Index
Analysis, 5-12 maintenance, 10-1
Aspiration, 3-2 Manual Calibration, 8-5
Auto-Sleep, 5-21 Parameter flags, 5-18
buzzer, 2-10 Parameters, 2-2
Calibration, 8-1 Prediluted samples, 5-10
calibrators, 2-13 Quality Control, 7-1
Capillary whole blood samples, 5-10 Reagents, 2-12
Colorimetric Method, 3-6 Self-Test, 10-10
controls, 2-13 Setup, 9-1
Dilution, 3-3 Shutdown, 5-23
Electrical Impedance Method, 3-7 software, 1-2
Flow Cytometry by Laser, 3-5 Startup, 5-4
Graph Review, 6-3 Table Review, 6-2
hardware, 1-2 Touch Screen Calibration, 10-13
Initial Checks, 5-3 Transmission, 6-8
Installation, 4-2 troubleshooting, 11-2
Logon, 5-4 Whole blood samples, 5-10
Logs, 10-14
A-1
B. Specifications
B.1. Classification
According to the CE classification, the BC-5150 belongs to In vitro diagnostic medical devices
other than those covered by Annex II and devices for performance evaluation.
B.2. Reagents
Diluent M-52 D diluent
Lyse M-52 DIFF lyse

M-52 LH lyse
/ Probe cleanser
B.3. Applicable Tubes

The following tubes can be used:
Ф12～15×75mm evacuated collection tube (without cap) for whole blood mode
Ф11×40mm (1.5ml centrifugal tube) and 0.5ml centrifugal tube for pre-dilute and capillary
whole blood mode.
Ф10.7×42mm small closed anticoagulated tube (without cap), 0.5ml, can be used with cap
opened, for capillary whole blood mode. Recommended tube: No. 365974 closed
anticoagulated tube (0.5ml) manufactured by BD.
B.4. Parameters
Parameter Abbreviation Default Unit
9
White Blood Cell count WBC 10 /L
9
Basophils number Bas# 10 /L
Basophils percentage Bas% %
9
Neutrophils number Neu# 10 /L
Neutrophils percentage Neu% %
9
Eosinophils number Eos# 10 /L
Eosinophils percentage Eos% %
9
Lymphocytes number Lym# 10 /L
Lymphocytes percentage Lym% %
9
Monocytes number Mon# 10 /L
Monocytes percentage Mon# %
9
Abnormal Lymphocyte number ALY# (RUO parameter) 10 /L
Abnormal Lymphocytes ALY% (RUO parameter) %
percentage 9
Large Immature Cell number LIC# (RUO parameter) 10 /L
Large Immature Cell percentage LIC% (RUO parameter) %
B-1
Specifications
12
Red Blood Cell count RBC 10 /L
Hemoglobin Concentration HGB g/L
Mean Corpuscular Volume MCV fL
Mean Corpuscular Hemoglobin MCH pg
Mean Corpuscular Hemoglobin MCHC g/L
Red BloodConcentration
Cell Distribution Width RDW-CV %
Coefficient
Red Blood of VariationWidth
Cell Distribution RDW-SD fL
Standard Deviation
Hematocrit HCT %
9
Platelet count PLT 10 /L
Mean Platelet Volume MPV fL
Platelet Distribution Width PDW None
Plateletcrit PCT %
Platelet-Large Cell Ratio P-LCR %
9
Platelet Larger Cell Count P-LCC 10 /L
White blood Cell Histogram WBC Histogram None
Red blood Cell Histogram RBC Histogram None
Platelet Histogram PLT Histogram None
Differential Scattergram Diff Scattergram None
B.5. Sampling Features
B.5.1. Sample Volumes Required for Each Analysis

Whole blood and capillary
≤15ul under both CBC and CBC+DIFF modes
whole blood mode
Pre-diluted mode ≤20ul under both CBC and CBC+DIFF modes
B.5.2. Throughput
Open vial-whole blood, open vial-pre-diluted and open vial-capillary whole blood modes: no
less than 60 samples per hour
B.6. Performance Specifications

B.6.1. Display Range
Parameter Display range
9 9
WBC 0.00×10 /L～999.99×10 /L
12 12
RBC 0.00×10 /L～18.00×10 /L
HGB 0 g/L～300g/L
9 9
PLT 0×10 /L～9999×10 /L
HCT 0%~80%
B-2
Specifications
B.6.2. Background/Blank Count

Parameter Background/blank count requirements
9
WBC ≤ 0.2010 / L
12
RBC ≤ 0.02 10 / L
HGB ≤1g/L
HCT ≤ 0.5 %
≤ 10  10 / L
9
PLT
B.6.3. Linearity Range

Parameter Linearity Range Deviation Range Deviation Range
(Whole Blood) (Pre-diluted)
9 9 9
WBC 0.00×10 /L ～ ±0.30×10 /L or ±5％ ±0.60×10 /L or ±6%
9
100.00×10 /L
9
100.01×10 /L ～ ±10% ±12%
9
500.00×10 /L
12 12 12
RBC 0.00×10 /L ～ ±0.05×10 /L or ±5% ±0.10×10 /L or ±10%
12
8.00×10 /L
HGB 0 g/L～250g/L ±2g/L or±2％ ±4g/L or±4%

9 9 9 9
PLT 0×10 /L～1000×10 /L ±10×10 /L or ±8% ±20×10 /L or ±16%
9
1001×10 /L ～ ±12% ±20%
9
5000×10 /L
B.6.4. Deviation of Reading

Parameter Deviation of Reading
WBC ≤±10％
RBC ≤±6%
HGB ≤±7%
PLT ≤±15%
B.6.5. Compatibility
Deviation ranges: WBC ≤± 5%, RBC ≤±2%, HGB ≤±2%, PLT ≤±8%, HCT/MCV ≤±3%.
B-3
Specifications
B.6.6. Reproducibility
Parameter Condition Whole Blood Pre-diluted

Reproducibility Reproducibility
(CV/absolute (CV/absolute
deviation d) deviation d)
9 9
WBC 4.00×10 /L～15.00 10 / L ≤2.5％ ≤4.0%
Neu% 50.0％～70.0％ ±4.0(d) ±8.0(d)
Lym% 20.0%～40.0% ±3.0(d) ±6.0(d)
Mon% 5.0%～10.0% ±2.0(d) ±4.0(d)
Eos% 2.0%～5.0% ±1.5(d) ±2.5(d)
Bas% 0.5%～1.5% ±0.8(d) ±1.2(d)
3.50  10 / L ~ 6.00  10 / L
12 12
RBC ≤1.5% ≤3.0%
HGB 110 g/L ~ 180 g/L ≤1.5% ≤3.0%
MCV 70 fL～120 fL ≤1.0% ≤2.0%
100  10 / L ~ 149  10 / L
9 9
≤6.0% ≤10.0%
PLT
150  10 / L ~ 500  10 / L
9 9
≤4.0% ≤8.0%
MPV / ≤4.0% ≤8.0%
B.6.7. Carryover
Parameter Carryover
WBC ≤0.5%
RBC ≤0.5%
HGB ≤0.6%
HCT ≤0.5%
PLT ≤1.0%
B.7. Input/Output Device
WARNING
 Be sure to use the specified devices only.
B-4
Specifications
NOTE
 If the analyzer is to be connected with LIS, the PC must be configured with dual
network cards.
B.7.1. External Computer (optional)

Recommended PC configurations: CPU Intel® 1.6GHz and above
RAM: 1G or above
Hard disk: 160GB or above
Recommended resolution of the display1280*1024(standard), 1680*1050 (wide screen)
Operating system: Microsoft Windows 7 or above, with DVD-ROM.
B.7.2. Keyboard (Optional)

101-Key alpha-numeric keyboard
B.7.3. Mouse (Optional)
B.7.4. External Barcode Scanner (Optional)
B.7.5. Printer (Optional)
B.8. Interfaces
4 USB ports
B.9. Power Supply

Voltage Input power Frequency
Analyzer (100V-240V～)±10% 300 VA (50Hz/60Hz)±1Hz
B.10. FUSE
WARNING
 Use specified fuse only.
Fuse specification: 250V T3.15AH
B-5
Specifications
B.11. EMC Description

 Do not use this device in close proximity to sources of strong electromagnetic radiation
(e.g. unshielded intentional RF sources), as these may interfere with the proper operation.
 This equipment complies with the emission and immunity requirements of the EN
61326-1:2013 and EN 61326-2-6:2013.
 This equipment has been designed and tested to CISPR 11 Class A. In a domestic
environment it 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 the device will
perform as intended.
B.12. Sound
Maximal sound: 65 dBA
NOTE
 Be sure to use and store the analyzer in the specified environment.
B.13. Operating Environment

 Optimal operating temperature: 10 ℃～30 ℃
 Optimal operating humidity: 20 %～85 %
B.14. Storage Environment

 Ambient temperature: -10 ℃～40 ℃
B-6
Specifications
 Relative humidity: 10 %～90 %
B.15. Running Environment

 Ambient temperature: 10 ℃～40 ℃
 Relative humidity: 10 %～90 %
B.16. Dimensions and Weight
Height
Depth
Width
BC-5150 Analyzer
Width(mm) ≤ 325
Dimensions Height (mm)≤ 435 (with foot)
Depth (mm) ≤ 410
Weight ≤25Kg
B.17. Contraindications
None
B.18. Safety Classification

Level of transient overvoltage: Category II.
Rated pollution degree: 2.
B-7
P/N: 046-005389-00(10.0)

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BC-5150 Auto Hematology Analyzer

Intellectual Property Statement

Mindray intends to maintain the contents of this manual as confidential information.

Release, amendment, reproduction, distribution, rental, adaptation, translation or any other

Mindray is strictly forbidden.

, , are the trademarks, registered or otherwise, of Mindray in

Responsibility on the Manufacturer Party

THIS WARRANTY IS EXCLUSIVE AND IS IN LIEU OF ALL OTHER WARRANTIES,

This warranty shall not extend to:

Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Fax: +86 755 26582680

EC-Representative: Shanghai International Holding Corp. GmbH(Europe)

Address: Eiffestraβe 80, 20537 Hamburg, Germany

1 Using This Manual ............................................................................................... 1-1

2 Understanding the Analyzer ............................................................................... 2-1

3 Understanding the System Principles ............................................................... 3-1

4 Installing Your Analyzer ...................................................................................... 4-1

5 Operating Your Analyzer ..................................................................................... 5-1

5.3. Startup and Login .................................................................................................. 5-4

6 Reviewing Sample Results ................................................................................. 6-1

7 Using the QC Programs ...................................................................................... 7-1

8 Calibrating Your Analyzer ................................................................................... 8-1

9 Customizing the Analyzer Software .................................................................. 9-1

10 Servicing Your Analyzer .................................................................................... 10-1

11 Troubleshooting Your Analyzer ........................................................................ 11-1

B.6.1. Display Range .................................................................................. B-2

1.2. Who Should Read This Manual

 learn about the BC-5150 hardware and software.

 customize system settings.

 perform daily operating tasks.

 perform system maintenance and troubleshooting.

1.3. How to Find Information

If you want to … See …

1.4. Conventions Used in This Manual

1.5. Safety Information

When you see… Meaning

read the statement below the symbol. The statement is alerting

read the statement below the symbol. The statement is alerting

 If leak happens to the analyzer, the leak liquid is potentially biohazardous.

 Please take action to any alarm and problem indication immediately.

 Do not touch the moving parts.

 Contact Mindray or Mindray-authorized distributors in time if any damaged part

 Be careful when opening/closing and removing/installing the doors, covers and

boards of the analyzer.

 Discard the analyzer according to government regulations.

 Do not contact the patients’ sample blood directly.

 Be sure to dispose of reagents, waste, samples, consumables, etc. according to

1.6. When you see…

When you see… Meaning

read the statement below the symbol. The statement is

You may find the following symbols of the analyzer system:

When you see… Meaning

WARNING, LASER BEAM

PROTECTIVE EARTH (GROUND)

FOR IN VITRO DIAGNOSTIC USE

EXERCISE CAUTION WHEN WORKING

CONSULT THE OPERATOR'S MANUAL

THE DEVICE IS FULLY CONFORMANCE

Figure 1-1 Back of the analyzer