Semi-auto Chemistry Analyzer

Operator’s Manual
Preface
Thank you for purchasing the semi-auto chemistry analyzer of Dymind company . I would like to
thank you.
Please read this manual carefully so that you can use this product correctly.After careful reading,
please keep it properly for inquiry when necessary.
Product Name: Semi-auto chemistry analyzer
Model: DP-C16, DP-C18, DP-C19
Intended use: it is an in vitro diagnostic equipment suitable for testing human proteins, lipids, sugars,
enzymes, inorganic elements and coagulation items (PT, APTT, TT, FIB, D-Dimer) in samples under
laboratory environmental conditions, which is used for clinical diagnostic reference and scientific research.
Contraindication:None.
Management classification: the analyzer belongs to 22-02-01 clinical test equipment - biochemical
analysis equipment - biochemical analysis instrument, and the management category is class II.
Registrant / manufacturer: Shenzhen Dymind Biotechnology Co., Ltd
Domicile of the registrant: 10/F, block B, high tech innovation center, guangqiao Road, Tianliao
community, Yutang street, Guangming District, Shenzhen
Production address: 7/F, 8/F, 9/F, block B, guangqiao road high tech innovation center, Tianliao
community, Yutang street, Guangming District, Shenzhen
Production date: see the label for details
Release Date:2021-07-28

After Sales Contact Information

After sales service unit: Shenzhen Dymind Biotechnology Co., Ltd
Address: 10th floor, block B, high tech innovation center, guangqiao Road, Tianliao community,
Yutang street, Guangming District, Shenzhen
Postal Code: 518107
24Hourly Service Hotline: 400-998-7276
Tel.: (86-755) 269825
Fax: (86-755) 26746162
Email:[email protected]
Website:http://www.dymind.com
Copyright
©Shenzhen Dymind Biotechnology Co., Ltd. all rights reserved.This manual and the information
contained in it are the special confidential information of Shenzhen Dymind Biotechnology Co., Ltd.
(hereinafter referred to as Dymind company ). Without the written permission of Dymind company , no
individual or organization shall reprint, copy, modify, publish to others or disseminate it in whole or in
part.The reader of this manual is the user and authorizes them to use it as part of the purchase of Dymind
equipment.Unauthorized individuals are strictly prohibited from using this manual.

Tmax makes no warranty of any kind, including (but not limited to) the implied warranty of
commerciality and reasonableness for a specific purpose.The company has taken measures to ensure the
accuracy of this document.However, Dymind is not responsible for errors or omissions and reserves the
right to improve any product to improve product reliability, function or design.

D&M and Dymind is the registered trademark or trademark of Dymind company .

Statement
The version of this manual is 1.0.The instructions may be modified without notice.

Shenzhen Dymind Biotechnology Co., Ltd. has the final right to interpret this instruction manual.

The illustrations provided in the manual are only examples and may not be completely consistent with
the actual display on the product. The real object shall prevail and shall not be used for other purposes.

DYMIND shall be responsible for the safety, reliability and performance of products only when all
the following requirements are met, namely:

The assembly operation, re commissioning, expansion, improvement and maintenance are all carried
out by the personnel approved by tmac.

The product operation shall be carried out in accordance with this manual.

Relevant electrical equipment shall comply with national standards.

Instructions For Use

How To Use This Operating Manual

Thanks for purchasing DP-C1X series semi-auto chemistry analyzer.Scope of application of this
operation manual:
1. Users (personnel) who have received operation training from Shenzhen Dymind Biotechnology Co.,
Ltd;
2. Users (personnel) who have received operation training from authorized dealers of Shenzhen Dymind
Biotechnology Co., Ltd.
This operation manual is the use guide of DP-C1X series semi-auto chemistry analyzer (hereinafter
referred to as the analyzer) of Shenzhen Dymind Biotechnology Co., Ltd. (hereinafter referred to as the
company), mainly including analyzer installation, operation, daily maintenance and precautions.
In order to ensure the good operation of the analyzer and the accuracy and reliability of the test results,
please strictly abide by the "attention", "prompt" and "warning" items in this operation manual (shown in
BOLD).

Statement

In principle, this operation manual is correct at the time of issue.In order to continuously improve the
quality of this operation manual, the company reserves the right to revise the operation manual and
maintain the software version. Any change is subject to no notice!
No individual or organization may copy, modify or translate the contents of this operation manual
without the written consent of the company.
The company has the final right to interpret the contents of the operation manual.
The illustrations used in the operation manual are example drawings, which may be different from the
actual products. In case of any difference, the real object shall prevail.

Be Careful

Please ensure that the analyzer is used under the conditions specified in this operation manual,
otherwise the analyzer may not work normally and the test results may be unreliable.

Quality Assurance

Except the company, no other company, organization or individual has the right to test and repair the
analyzer.From the date of installation, the company promises to provide analyzer users with 12-month free
warranty service (excluding consumables), except for the following cases:
1. The analyzer is not normally used in strict accordance with the operation manual or standard
supporting consumables are not used;
2. Man made damage;
3. Disassemble the analyzer without permission of our company.
 The above quality assurance service is exclusive to the initial installation user of the analyzer, and it is
invalid to transfer or share the quality assurance service with others.

Safety Measures

In order to use the analyzer safely and effectively, please observe the following precautions:
1. Avoid Equipment Failure
The installation environment of the analyzer must meet the requirements for installation environment in
this operation manual.
2. Prevent Electric Shock
Do not open the shell of the analyzer without authorization of the company to prevent liquid splashing
into the analyzer.In order to prevent electric shock and other safety accidents, if the liquid accidentally enters
the analyzer, please contact the customer service personnel of the company before power on.
3. Pollution Prevention
When carrying out biochemical testing, you must wear protective gloves. If you don't wear protective
gloves, you will directly contact the sample to be tested, which may pose a potential risk of biological
infection.The blood samples, quality control materials, calibrators and reagents that may be carried on the
aspirator also have potential biosafety problems. Avoid direct contact with the probe by hand.In case of direct
skin contact, clean and disinfect the contact area immediately, and consult a doctor.
4. Pipeline Connection
Before connecting the pipeline, ensure that there is no foreign matter in the joint. The waste liquid pipe
cannot be bent or the tail end is immersed in the waste liquid. If it is too long, it must be cut short, otherwise it
will cause poor drainage.
5. Waste Liquid Treatment

It is suggested that the waste liquid of the instrument should be discharged after harmless treatment, and
should not be directly poured into the sewer.Please refer to the regulations on the biosafety management of
pathogenic microorganism laboratory (Order No. 698 of the State Council of the people's Republic
of China), regulations on the management of medical waste (Order No. 588 of the State Council of the
people's Republic of China), general requirements for laboratory biosafety (GB19489-2008),
laboratory biosafety manual, etc.
 Contents
Instructions For Use.............................................................................................................................. 6
How To Use This Operating Manual .......................................................................................... 6
Statement ....................................................................................................................................... 6
Be Careful ...................................................................................................................................... 6
Quality Assurance......................................................................................................................... 6
Safety Measures ............................................................................................................................ 7
Contents ........................................................................................................................................................ 8
1 Equipment Introduction ......................................................................................................................... 10
1.1 Product Overview ......................................................................................................................... 10
1.1.1 Introduction To Analyzer ................................................................................................. 10
1.2 Technical Support ......................................................................................................................... 10
1.3 Security Information..................................................................................................................... 11
1.3.1 General Information .......................................................................................................... 11
1.3.2 Biological Hazards ............................................................................................................. 11
1.3.3 Software Use ....................................................................................................................... 11
1.3.4 Disinfect .............................................................................................................................. 12
1.3.5 Electromagnetic Compatibility (EMC) ............................................................................ 12
1.4 Symbol ............................................................................................................................................ 12
2 Installation Instructions .......................................................................................................................... 15
2.1 Injury Examination ...................................................................................................................... 15
2.2 Open Box Inspection ..................................................................................................................... 15
2.3 Analyzer Specifications And Environmental Requirements ..................................................... 15
2.4 Equipment Installation ................................................................................................................. 16
2.4.1 Place analyzer .................................................................................................................... 16
2.4.2 Connect the Power Supply ................................................................................................ 16
2.4.3 Power On ............................................................................................................................ 17
2.4.4 Main Interface.................................................................................................................... 18
2.4.5 Shut down ........................................................................................................................... 19
2.4.6 Switch Users ....................................................................................................................... 20
2.5 Installation Record Paper ............................................................................................................ 20
2.6 External Device ............................................................................................................................. 22
3 Working Principle ................................................................................................................................... 23
3.1 Principle Overview ..................................................................................................................... 23
3.2Instrument Composition And Difference..................................................................................... 23
4 Test ............................................................................................................................................................ 24
4.1 Interface Introduction .................................................................................................................. 24
4.2 Biochemical Project Test .............................................................................................................. 24
4.3 Coagulation project....................................................................................................................... 28
4.4 Button Function............................................................................................................................. 29
4.4.1 Project Parameters ............................................................................................................ 29
4.4.2 Quality Control Data ......................................................................................................... 29
4.4.3 Curve Data ......................................................................................................................... 30
4.4.4 Start..................................................................................................................................... 30
4.4.5 Printing ............................................................................................................................... 30
4.4.6 Sample Information ........................................................................................................... 31
4.5 AD Testing ..................................................................................................................................... 33
5 Review ..................................................................................................................................................... 34
5.1 Summary ........................................................................................................................................ 34
5.2 Sample Results............................................................................................................................... 34
5.2.1 Interface Content ............................................................................................................... 34
5.2.2 Detailed Information ......................................................................................................... 35
 5.2.3 Function Button ................................................................................................................. 39
5.3 Calibration Results ....................................................................................................................... 41
5.4 Quality Control Results ................................................................................................................ 43
5.4.1 Quality Control List .......................................................................................................... 43
5.4.2 Quality Control Chart ....................................................................................................... 44
5.5 Delete / Backup .............................................................................................................................. 45
6 Quality Control Settings ...................................................................................................................... 47
6.1 Overview Of Quality Control ...................................................................................................... 47
6.2 QC Settings .................................................................................................................................... 47
7 Project Settings ...................................................................................................................................... 50
7.1Test Items ........................................................................................................................................ 50
7.1.1 Coagulation Project ........................................................................................................... 50
7.1.2 Biochemical Project ........................................................................................................... 52
7.1.3 Manual Project................................................................................................................... 54
8 Setting ..................................................................................................................................................... 56
8.1General Settings ............................................................................................................................. 56
8.1.1 Printer ................................................................................................................................. 56
8.1.2 Dictionaries......................................................................................................................... 58
8.1.3 System ................................................................................................................................. 59
8.1.4 LIS ....................................................................................................................................... 62
8.2 System Time................................................................................................................................... 62
8.3 User Management ......................................................................................................................... 64
8.4 System State................................................................................................................................... 67
8.5 System Log..................................................................................................................................... 68
8.6 Touch Calibration ......................................................................................................................... 69
9 Maintain ................................................................................................................................................. 71
9.1 Clean The Pipeline ...................................................................................................................... 71
9.2 Pump Calibration And Setup ................................................................................................... 72
9.2.1Pump Calibration ............................................................................................................... 72
9.2.2Pump Setting ....................................................................................................................... 73
9.3 Optical Calibration .................................................................................................................... 73
10 Routine Maintenance .......................................................................................................................... 75
10.1 Instrument Cleaning ................................................................................................................... 75
10.2 Software Update .......................................................................................................................... 75
10.3 Analyzer return For Maintenance ............................................................................................. 76
 1 Equipment Introduction

1.1 Product Overview

1.1.1 Introduction To Analyzer

DP-C1X series semi-auto chemistry analyzer includes the following models: DP-C16,DP-C18 and DP-
C19.This series of biochemical analyzer is an in vitro diagnostic equipment suitable for testing human protein,
lipid, carbohydrate, enzymes, inorganic elements and coagulation items (PT, APTT, TT, FIB, D-Dimer) in
samples under laboratory environmental conditions. It is used for clinical diagnostic reference and scientific
research.

1.2 Technical Support

If you have any questions in the process of using the analyzer, please call our 24-hour after-sales service
hotline. Our technicians will give you professional answers.
1.3 Security Information

1.3.1 General Information

WARNING
 Before operating the instrument, be sure to check all doors / covers / plates and ensure that they
will not open or loosen during the operation of the instrument.
 Please use all safety measures provided by the instrument.Do not disable any devices or sensors
for safety purposes.
 Please be sure to respond to and handle all alarm and fault information in time.
 Do not touch moving parts.
 If any damaged parts are found, please inform tmac or its agent in time.
 Be careful when opening and closing the door / cover / plate.
 Equipment scrapping must be handled according to local regulations.

CAUTION
 Be sure to use the equipment in strict accordance with the instructions in this manual.
 Please take appropriate measures to prevent the reagent from being contaminated.

1.3.2 Biological Hazards

Biological Hazards
 All items (samples, quality control materials, reagent disks, etc.) and areas in contact with these
substances have potential biological infectious hazards.When contacting relevant articles and
areas in the laboratory, users shall abide by the laboratory safety operation regulations and wear
personal protective equipment (such as laboratory protective clothing, gloves, masks, etc.).
 If the main engine leaks, the leaked liquid has the risk of biological infectivity.

1.3.3 Software Use

CAUTION
 The upgrade and maintenance of the software shall be carried out by the personnel authorized by
tmac.Do not install or upgrade software from unknown sources to prevent computer viruses.
 Before using an external storage device (such as USB flash disk), please check the device for
anti-virus to confirm that the device is free of virus.
1.3.4 Disinfect

WARNING
 Before sterilizing the instrument, be sure to turn off and unplug the power cord to avoid the risk
of electric shock.Always wear protective gloves and clothing when cleaning the outer surface of
the instrument.
 After disinfection, please wash your hands carefully with hand sanitizer or soapy water.
 Do not open the instrument for internal disinfection.
The instrument may have potential biological pollution hazards during use.As shown in the table
below, please disinfect the instrument according to different conditions.
Scenes Requiring Disinfection Disinfection Steps

Accidents such as splashing or 1. Wipe off the contaminants on the instrument surface with
splashing of articles (samples, 75% alcohol.If the pollutants are dry, wipe repeatedly with
aspirators, etc.) on the surface 75% alcohol for 3min until the pollutants are removed,
of the instrument 2. Wipe the disinfected area with clean water to remove the
residual disinfection substances.
3. Dry the instrument surface with a dry disposable cloth.

Before moving or handling 1. Clean the instrument surface.

the instrument Wipe the surface of the instrument with 75% alcohol, then
wipe with clean water to remove the residual alcohol, and
finally dry it with a disposable rag.

1.3.5 Electromagnetic Compatibility (EMC)

WARNING
It is forbidden to use the equipment near strong radiation source (such as unshielded RF source),
otherwise it may interfere with the normal operation of the equipment.

CAUTION
 The user has the responsibility to ensure the EMC environment of the equipment, so that the
equipment can work normally.
 It is recommended to evaluate the electromagnetic environment before using the equipment.
The semi-auto chemistry analyzer meets the electromagnetic emission and immunity requirements
specified in GB / t18268.1 and GB / T 18268.26.See Appendix B for details

1.4 Symbol

This analyzer or outer package may contain the following labels or symbols.
 If the label is damaged or falls off during the use of the analyzer, please contact DYMIND
company or agent for replacement.
 All illustrations provided in this manual are only examples and should not be used for other
purposes.The graphics, settings or data in the illustration may not be completely consistent with
the actual display you see on the semi-auto chemistry analyzer.

Symbol Meaning

WARNING: please refer to the operation manual

Biological hazard: according to the standard laboratory operation

specification: considering the potential infection risk of all
human samples, all samples, quality control products, relevant
containers and used reagent discs should be treated according to
the corresponding biosafety level.

To prevent mechanical door injury

Do not lift the instrument by hand

Network interface

USB interface

Protective grounding symbol

DC symbol

Alternating current symbol

In vitro diagnostic medical devices

Batch number

Service life

Serial number

CE declaration of conformity

Date of manufacture

Manufacturer
Symbol Meaning

Temperature limit

Humidity limit

Atmospheric pressure limit

Refer to the instruction manual

Avoid the sun

Avoid rain

No rolling

No stacking

Place up

Fragile, handle with care

Recyclable

If this product is scrapped, please collect and recycle it according to

the disposal method of scrapped electronic and electrical
equipment, and do not discard it together with other domestic
wastes.
 2 Installation Instructions

2.1 Injury Examination

The analyzer shall be strictly inspected by the company's professional personnel before
transportation.
After receiving the analyzer, please carefully check the outer package for the following damage
before unpacking:
 Deformation
 There are obvious signs of immersion
 There are obvious signs of impact
 There are signs of being opened
Once the above damage is found, please do not open the box and immediately notify the after-sales
service personnel of the company or local dealers.

2.2 Open Box Inspection

After unpacking, please check the items in the box according to the packing list. If any missing or
damaged items are found, please contact our after-sales service personnel or local dealers.
After checking, take out the analyzer from the packing box and place it on a fixed horizontal table.
Please handle it with care.After installation, please cooperate with the equipment installation personnel to
fill in the after-sales warranty card and installation acceptance report, and send the scanned copies or
photos of the installation acceptance report and after-sales warranty card to the mailbox of Shenzhen
Dymind Biotechnology Co., Ltd. within 7 working days（[email protected]）In order to establish
customer files,The company will regularly send product related information and provide software upgrade
and other services after the customer file is established. The warranty period starts from the date of
analyzer installation.

2.3 Analyzer Specifications And Environmental Requirements

 Volume: 318mm (Width)×178mm( High)×313mm (Deep)

 Weight: ≤ 6.0kg
 Power supply voltage: AC 100V ~ 240V, 50 ~ 60Hz
 Input power: 80W
 Operating environment temperature: 10 ℃ ~ 35 ℃
 Storage ambient temperature: - 10 ℃ ~ 40 ℃
 Operating environment humidity: 10% ~ 85%
 Humidity of storage environment: 30% ~ 80%
  Working and storage atmospheric pressure: 70.0KPa ~ 106.0KPa

2.4 Equipment Installation

Semi-auto chemistry analyzer is only installed by tmac or its authorized agent. Users need to provide
corresponding environment and space.When the analyzer needs to be moved and transported, please
contact Dymind company or local agent.
When you receive the analyzer, please inform DYMIND company or local agent immediately.

2.4.1 Place analyzer

In order to ensure the normal use, repair and maintenance of the instrument, and to ensure the normal
flow of liquid, the installation of the instrument needs to meet the following conditions:
 The instrument is only used indoors
 The bearing platform shall be horizontal without shaking
 The installation site shall be well ventilated and away from dust
 Avoid direct sunlight
 Avoid proximity to other potential heat sources
 Keep away from corrosive and combustible gases
 The installation site shall not be disturbed by large noise or power supply
 The instrument shall not be close to the equipment with brush motor and frequent on-off
 If you can't use a mobile phone or radio near the instrument, the equipment that emits
electromagnetic waves may interfere with the operation of the instrument

2.4.2 Connect the Power Supply

Within 1m around the instrument, there is a three hole power socket with good grounding to provide the
power required by the instrument. The instrument needs to be connected to the power socket within 1m, so that
the power can be cut off in time in case of emergency.Check that the grid voltage is consistent with the
instrument voltage before use.Make sure that the power switch of the instrument is off before turning on the
power

WARNING
 The analyzer must be used under good grounding conditions.
 Before starting the analyzer, be sure to confirm that the input voltage meets the requirements of
the instrument.
 CAUTION
 The use of patch panels may introduce additional electrical interference and lead to incorrect
analysis results.Please place the analyzer close to the power socket to avoid using the patch
panel.
 Please use the supplied power cord.Using other power lines may damage the analyzer or cause
incorrect analysis results.
 When using this equipment in a dry environment, especially in the dry environment with
artificial materials (artificial fabrics, carpets, etc.), it may cause damaging electromagnetic
discharge and lead to wrong conclusions.

2.4.3 Power On

After the power is turned on, press the switch button of the analyzer, the display will light up, the
analyzer will start, and the startup login interface will be displayed on the screen:

After entering the login user and password, the analyzer will enter the startup process, and the system
will initialize. After completion, the system will automatically enter the main menu interface, and the
screen is shown as follows:
 Tips: The analyzer display screen is a touch screen, and all buttons can be directly clicked on the
screen for operation.

2.4.4 Main Interface

After the startup process, the user logs in to enter the main menu interface.Click the "test" button to
enter the sample test interface, the analyzer is ready for the first test, and the screen will display:

1 3 4

5 6 7 8
This Interface Can be Divided Into The Following Areas by Function:
1- Menu Navigation Area
The top area of the interface is the menu navigation area.When clicking a menu button, the system will
immediately enter the corresponding interface.
2- Menu Content Display Area
According to the item button selected by the user in the menu navigation, the test interface of the currently
selected item is displayed.
3- Test Status And Step Display Area
When the system is conducting sample test, the operation steps and the remaining time of the current test
are displayed.
4- Status Display Area
It is located at the top right of the interface. From left to right, it is the connection status of the analyzer and
LIS system, and the status of the printing equipment
The corresponding icon changes as the state changes, as shown in Table 5-1.
Table 5 - 1 Status Icon Display Description

Status Item Icon Remarks

The analyzer is not connected to

Grey
Connection status between LIS system.
analyzer and LIS system
The analyzer is connected to LIS
White
system.

The analyzer is not connected to

Grey
the external printing equipment.
Print device status
The analyzer is connected to the
White
external printing equipment.

5-Number Of Test Items

Displays the number of test items on the current page
6- Fault Display Area
In case of system fault, the corresponding fault information will be displayed in this area.When there is
more than one fault, the latest fault information will be displayed in this area.
Click this area to handle the fault in the pop-up fault help dialog box.
7- The Current Operating User Of The Analyzer
8- The Current Date And Time Of The Analyzer

2.4.5 Shut down

Click on the current interface“ ”Icon to enter the main interface, click“ ”The button screen is
displayed as follows:
Click "OK" to turn off the analyzer, and then turn off the power switch. The power off is successful.
Click "Cancel" to return to the main interface.
2.4.6 Switch Users

Click the "" icon on the current interface to enter the main interface, click the "" button on the main
interface, and the screen is as follows:
Click "OK" to return to the login interface to switch users without restarting the software;
Click "Cancel" to return to the main interface.

2.5 Installation Record Paper

CAUTION
 The thermal recording paper meeting the requirements must be used, otherwise the thermal
printer may be unable to record, the recording quality may be poor, or the thermal print head
may be damaged.
 During the printing process of the thermal printer, do not pull the recording paper outward,
otherwise the thermal printer may be damaged.
 Do not keep the thermal printer door open until you change the paper or correct the problem.
 Incorrect installation of recording paper may cause paper jam or no print results.

 Before installing the recording paper for the first time, remove the protective paper from the
thermal printer.
 The non printing surface of the printing recording paper contacts the rubber roller. If the
installation direction of the thermal paper is incorrect, the analyzer will not be able to print the
test results normally.
 Please refer to the following steps to install the recording paper.
1. Pull the open key of the thermal printer door outward to open the thermal printer door.

2. Put the recording paper into the paper cavity, and the paper head is located outside the paper
outlet.The non printing surface of the printing recording paper contacts the rubber roller.

3. Close the thermal printer compartment door.

4. Check the position of the recording paper to ensure that the recording paper is aligned with the
paper outlet.

5. Press the paper feed key to make the thermal printer send a small piece of paper to the paper outlet,
and then press the paper feed key again to stop paper output, so as to ensure that the recording paper can be
used normally.
2.6 External Device

The instrument can be connected to the external USB keyboard and USB mouse of the traditional
computer. Just connect the USB mouse or USB keyboard to the USB port of the instrument and it can be
used normally
Built in thermal printer and external USB printer are used to print various types of test reports.
Installation steps of external USB printer:
Connect the printer cable to the USB port of the instrument;
Enter "Settings" - > "general settings" in the main interface of the instrument, and the name of the
external printer can be viewed and selected in the "printer" interface.

Please do not use the right button of the USB mouse, it does not have this function.
 3 Working Principle

3.1 Principle Overview

The test principle of the analyzer mainly uses Lambert Beer law , mix the reagent with the sample of the
patient to be tested according to a certain proportion, incubate the mixed solution in the colorimetric cell at a
certain temperature, continuously measure its absorption of specific wavelength light, and finally automatically
calculate the concentration or time of the measured substance according to the absorbance value (change).

3.2Instrument Composition And Difference

DP-C16, DP-C18 and DP-C19 were classified according to the sample storage.
 4 Test

4.1 Interface Introduction

How to operate the analyzer for detection will be described in detail below.The analyzer starts, the
system initializes, and then enters the main menu interface. After clicking test, the screen displays as
follows:

The display screen of the analyzer is a touch screen, and all items in the screen can be operated directly
by clicking the screen.

Click the item button on the screen to enter the item test interface. You can select a page from page 1-
6 and click the button of the test item to test the item.

The system defaults to 6 test pages, including 180 test items. If the total number of test items exceeds
180, the page number will be automatically increased.

4.2 Biochemical Project Test

The test interface is shown in the figure below:

 The user can perform biochemical project test as follows:
1. First of allClick "test" in the main interface to enter the test item interface, select the biochemical
item on the current interface, and click to enter the corresponding item test interface.
2.By default, in the "blank voltage test" interface, the blank voltage test should be done before each
sample test. After clicking the "start" button, the operation steps will be prompted in the upper right
corner to operate according to the operation steps.
3.Display ad value, response curve and other parameters after completing blank voltage test

When blank voltage is selected in project setting, reagent blank test cannot be selected. Only when
reagent blank is selected can reagent blank and blank voltage be tested.

The reagent blank test interface is as follows:

4.When the calibration type is 1-point linear in project settings, the standard test cannot be selected.
 The standard test interface is as follows:

5.Quality control test can only be operated after the quality control information of the new item is
created in the quality control settings, otherwise it cannot be tested.
The QC test interface is as follows:

6.Click the "sample test" button to the sample test interface, click the "start" button, and carry out the
sample test according to the steps.
The sample test interface is as follows:
 Standard test and quality control test shall be conducted before the test of each new project.

7.After the test is completed, it will prompt that the test is completed. At this time, click the
cleaning button to clean the flow cell and pipeline.
8.The analyzer saves the test results to the database, and click the next sample number to search the
test results of the item with different sample numbers.

 001It is the default value of the first sample of the day. The sample number can be edited by clicking
"+" and "-"
 Click the "clean" button to suck distilled water to clean the flow cell
 If the current sample results are abnormal, it is necessary to flush the colorimetric cell before testing
the next sample to prevent cross contamination

Biological Hazards
All items (samples, test discs, etc.) and areas in contact with these substances have potential
biological infectious hazards.When contacting relevant articles and areas in the laboratory, users shall
abide by the laboratory safety operation regulations and wear personal protective equipment (such as
laboratory protective clothing, gloves, masks, etc.).

WARNING
Users are obliged to abide by the relevant regional and national regulations on the discharge and
treatment of waste liquid, waste samples and consumables.

9.Click "Test" again to start the next test.

4.3 Coagulation project

The test interface is shown in the figure below:

The user can perform coagulation test as follows:

1. First, click "test" in the main interface to enter the test item interface, select the coagulation item
on the current interface, and click to enter the corresponding item test interface.
2. by default, in the "QC test" interface, QC test shall be performed for items without QC before
sample test. Click the "start" button, and then the operation steps will be prompted in the upper right
corner. Operate according to the operation steps.
3After completing the quality control test, click sample test to enter the sample test interface and
perform the operation according to the operation steps.
The sample test interface is as follows:
4.4 Button Function

4.4.1 Project Parameters

Click the "project parameters" button to view the project parameters of the project.

4.4.2 Quality Control Data

After setting the quality control information for the project, select the batch number of the quality control
file to view the information, and click the quality control data pop-up window to display the quality control
data of the project.

When there are no quality control parameters of the item in the quality control settings, the
quality control data button cannot be clicked.
4.4.3 Curve Data

When you click the curve data, a dialog box will pop up, and the user can view the parameters of the test
response curve

 When the item is not tested, the curve data button is grayed out.
 When the interface is switched, the curve data will be refreshed.

4.4.4 Start

Biochemical project
1.For biochemical project test, first place the sampling tube in the sample, click the "Start" button to start
the test, and the start button becomes the Cancel button;
2.After the sample is sucked by the pump, it enters the incubation, and the test is carried out according to
the steps, and the user can observe the reaction curve.
Coagulation project
1.Coagulation test is to inject the sample into the disposable colorimetric cup, place it in the light path
room, and click "start" to react;
2. incubate according to the set incubation time, wait for the setting time, and observe the reaction curve.

4.4.5 Printing

1.Click the "print" button to pop up the dialog box. The analyzer will print the test data and sample
information of the current test sample by default, and the wrong results are not allowed to be printed;You
can also set to automatically print the test results, and automatically print the results after the test is
completed.The screen is as follows:
 2. After clicking OK, a prompt box will pop up indicating that the printing data is being processed

3.After printing successfully, a prompt box will pop up to prompt printing successfully

4. The print template is printed according to the print template selected in the setting (see Chapter
8.1.1 printer for details).

4.4.6 Sample Information

In the "Sample Information" interface, you can view and edit the patient information of the current
sample.

1.Click "Sample Information" to enter the interface shown in the figure below:
2.According to the parameter description in table 4-1, enter the patient information.
Table 4-1 parameter description
Parameter Meaning Operation
The system displays it automatically and needs to be
Sample The number of the
modified in the test interface. It cannot be modified
number selected sample.
in the sample information.

Full Name Name of the patient. Enter directly in the edit box.

The gender of the

patient.include:
Gender  Unknown Select from the drop-down list. It is blank by default.
 Male
 Female

 Automatically calculated according to the

difference between "current system date" and
"date of birth", and updated in the age field
Age Patient's age
 You can also fill in the age directly without
selecting the date of birth
 The default units are year, month and day

Department to which the

Department Select from the drop-down list.
patient belongs.

Doctor Diagnostic testing doctor. Select from the drop-down list or enter directly.

The number of the patient

Patient ID It can be entered manually or by scanning code.
sample.
Click "save" to save the information.

 Sample information can be edited before or after the test.

 The sample number needs to be modified in the test interface before sample testing.
4.5 AD Testing

Click "ad detection" in the upper right corner of the test interface to enter the ad detection interface, and the user
can view the ad information, as shown in the following figure:

1. users need to select the wavelength by themselves.

2. elect the corresponding wavelength and click the "start" button to test the gain after optical calibration.
3. The curve data shows the parameter results of the test, and the curve of the test is displayed below.
4. Click clear to clear the calculated ad value and re display the newly obtained ad value.
5. After the test is completed, click clean to carry out the cleaning process.
 5 Review

5.1 Summary

The analyzer test results are stored in the analyzer database, and the results can be searched and
printed on the "Review" page.When the analyzer is connected to an external computer or USB storage
device, the test result data can also be transferred to the storage path set by the above device.
Users can browse, query, edit, print and export the previous results in the review interface.
Click "Review" to enter the review interface.As shown in the figure.

The review interface includes four parts: sample results, calibration results, quality control results and
delete / backup. Users can view the results of different tests accordingly.

5.2 Sample Results

5.2.1 Interface Content

Click sample results to view sample test results and sample information
The sample result interface is as follows:
1. after entering the interface, you can see the sample results of all sample numbers and tests
2. elect one of the sample numbers and click the sample information to display the patient information of the
number.

5.2.2 Detailed Information

1. Select one of the sample numbers and click Details to display the patient information of the patient with the
number and all the items and historical results of the test.

2. you can modify the result and click save.

3. Click the delete button to delete the sample information, a pop-up window will prompt to delete the
information, and click "OK" to delete the selected item.
4. Click the curve button to pop up a dialog box to display the response curve and information parameters of the
selected item of the sample test. Click "export" to export the sample number, item name, results, points and data
of the corresponding curve;Biochemical items are exported as absorbance and coagulation items are exported as
ad value.

5. Click the transfer button to transfer the item result information parameters in the sample number, pop up the
selection, and press Select to transfer the sample information.

6. Click the print button and select the sample to be printed in the pop-up window to print the item result
information parameters in the sample number.
7. you can add, delete, and modify manual items. Click manual items to open a dialog box to edit manual items.

5.2.2.1Manual Items

1. Click new to create a new manual item, select the manual item set in item setting, enter the result, and click
OK to successfully create a new manual item.
2. Select a manual item and click Edit to open a dialog box where you can edit the result.

3. Select the item and click delete. A dialog box will pop up to prompt the user. Click OK to delete the manual
item.
4. Click "return" to return to the details pop-up window.

5.2.3 Function Button

1. Query
(1) Click query to pop up a dialog box. Users can search by name, doctor, department and date range

(2) Click "Cancel" to cancel the query;Click "OK" to query the content;Click all samples to display all sample
result data
(3) If the date range selection does not meet the requirements, the pop-up window will prompt the user that the
end date must not be earlier than the start date
2. Sample Information
Click sample information to pop up the patient details dialog box, where you can modify the transmitted sample
information.

3. Delete
Click Delete to delete the test information of all items under the sample number
4. See the above for details. Select a sample number and click Details to display all test item result parameters
under the number.
5. Transmission
(1) Select an item and click upload to open the dialog box

(2) Users can select more than one content to upload and click OK to upload the sample results to LIS
(3) Click OK to display the progress bar

(4) After uploading, you will be prompted that the transmission is successful / failed.

You need to open lis to transfer. This function cannot be performed when LIS is not connected.
5.3 Calibration Results

Click the calibration result to enter the interface and display the calibration information of each item

1. Select an item and click the calibration data to pop up a dialog box to display the calibration curve and
parameters of the item.

2. Click parameters to display specific parameters.

 When the calibration type is linear, there are R0 and K values

3. Observable points and concentration reactivity.

4. Click the calibration history button to enter the calibration history interface to view the historical calibration
data.

5. To delete, select the blank test or standard test results to be deleted, click "delete", a pop-up window will
prompt whether to delete the data, and click "OK" to delete the calibration data.

Click once to select, and click again to deselect

5.4 Quality Control Results

After the quality control test is completed, click the quality control result to query the quality control
result

5.4.1 Quality Control List

1. Select the quality control information column in the left column, and the detailed historical quality control
results of the selected quality control will be displayed in the right column.
2. The scroll bar can slide to view the complete QC information.
3. Click query to pop up the dialog box. You can query according to the batch number, test items and date
range of the QC file, and click all samples to return to the QC list.
 4. Transmission
Click transfer to transfer the quality control results to LIS
5. Delete
Select one or more QC results and click Delete to delete QC data

5.4.2 Quality Control Chart

1. Click the QC chart to enter the interface and display the QC chart. The latest QC chart is displayed by
default

2. Select L-J QC chart or Westgard QC chart from the drop-down list to view the corresponding QC
information
3. Click query to query according to the batch number, test items and date range of quality control documents.

4. Click Print to print the quality control chart according to the print template.

5.5 Delete / Backup

Click "Delete / Backup" in the review interface to enter the interface and display the deletion results, backup
database and other information
1. Select the date range, check the result type and click the delete button to delete the result data.
2. Click backup to back up the current machine data to the USB disk. After success, a pop-up window will
prompt that the backup is successful / failed.
3. Click restore to restore the data in the USB disk to the machine. After successful recovery, the pop-up
window will prompt success / failure.

When the machine detects that no removable disk is inserted, a pop-up window will prompt the
user
 6 Quality Control Settings

6.1 Overview Of Quality Control

The performance of the analyzer can be verified by quality control test.The sample prepared for
quality control is called quality control material, and the reference material of quality control material is
the same as the test sample.
The company suggests that the customer should do quality control at least once a month, and when
the laboratory conditions of the analyzer change or the test results are inconsistent with the clinical
manifestations of the patient, quality control should also be done to verify.
The test results of quality control products and samples are stored in two different databases of the
analyzer. When querying the quality control results, you can also print the quality control report.

 It is necessary to store and use the quality control materials and reagents in strict accordance
with the instructions.Quality control materials must be used before their effective date.
 Ordinary users only have the permission to browse and execute QC settings, but do not have the
permission to edit.

6.2 QC Settings

Click the "QC Setting" button in the main interface of the system, and the screen is shown as follows:
1. You can create, edit and delete QC files in the QC list

2. Select the established QC file to create, edit and delete the item parameters under the QC file in the item list
on the right.
3. After the setting is successful, the quality control test can be performed in the test.
4. After deleting the item QC test setting, QC test cannot be performed during the test
 7 Project Settings

This chapter mainly introduces how to set the analyzer items, which are mainly divided into test items
and manual items.The test items include coagulation items and biochemical items.

Click "project setting" in the main interface to enter the project setting interface, as shown in the
following figure:

7.1Test Items

7.1.1 Coagulation Project

1. Select a test item in item setting to enter the test item parameter interface. The short name of the item is
displayed in the left column. The first item is selected by default.

The default coagulation items are TT, APTT, Pt, FIB and D-dimer, which cannot be deleted.
 2. Select the coagulation item, and the default is the analysis setting. In the analysis setting, you can set the
parameters of the coagulation item
3. Select coagulation test, and set the calibration method and item inspection parameters of coagulation

4. After modifying the settings, click Save to save the parameters to the coagulation project
 If the project information is complete, the pop-up window will prompt "project settings saved
successfully"
 If the test item is set to be blank or the required item is not filled in, it is not allowed to save, then a
window will pop up and prompt "test item cannot be blank" and "required item cannot be blank"
 5. Click Print to prompt whether to print, and click OK to print the project parameters.

7.1.2 Biochemical Project

1. Select the biochemical item in the left column to enter the biochemical item interface. You can
enter the biochemical item parameters and set the calibration settings of the item
2. Click the new button to add a new biochemical project in the left column.
3. Click Delete to pop up a dialog box prompt, and click OK to delete the currently selected item

4. After modifying the project information, click Save to save the current modification
(1) If the project information is completely filled in, you will be prompted with "project settings saved
successfully"
 (2) If the test item is set to be blank or the required items are not filled in, it is not allowed to save, and
the pop-up prompt "test item cannot be blank" and "required items cannot be blank" will pop up

(3) Click "OK" and navigate to the item filled in incorrectly until it is saved successfully
5. Click Print to pop up a prompt box, and click "OK" to print parameters

7.1.3 Manual Project

1. Click manual item in the item setting interface to enter the manual item setting interface
 2. Click new to create a blank manual item information interface, where you can enter manual item
information.
3. Click delete, and a pop-up window will prompt "delete the currently selected item", and click "OK" to
delete the manual item.

4. After modifying the manual project settings, click save, the pop-up window will prompt "manual project
settings saved successfully", and click OK to save the current interface modification.
 8 Setting

This chapter mainly introduces how to set up the analyzer to optimize the performance of the
analyzer.In order to ensure the security of product settings and data, the analyzer divides users into two
permission levels: ordinary users and administrators (administrators have all the permissions of ordinary
users).This chapter describes the setting functions after logging in to the software as an administrator.
Click the "setting" button in the main interface to enter the system setting interface, and the screen is
shown as follows:

In the setting interface, the administrator can set the following functions:
 General settings
 System time
 User management
 System state
 System log
 Touch calibration

8.1General Settings

8.1.1 Printer

1. Click "general setting" in the main setting interface to enter the main general setting interface, and
select the printer column to set the printer.
 2. When an external printer is connected, select the name of the connected printer in the printer name drop-
down selection, and select the corresponding printer name to select the printer.
3. Users can set the number of copies to print according to their needs, and check the built-in or external
printer. The built-in printer uses the thermal printer by default, and the external printer can be selected according
to the printer name
4. You can select the report form template, click template to open the dialog box, where you can select the
built-in report type and print template, or import, export and delete the report template

The default print template cannot be deleted. When you click delete, a window will pop up
indicating "default template cannot be deleted"!
 5. When biochemical item or coagulation item is selected, you can enter the title of the report, and if Auto
print is checked, it will be printed according to the set print content. If manual item is checked, each report will
be printed with manual item.

8.1.2 Dictionaries

Select the dictionary column to set the information of gender, Department, doctor and unit. The interface is
shown as follows:

1. Click the left column to select one of the categories, click new to pop up a dialog box, enter the new
dictionary information, and click OK to save the settings

2. Click Edit to open the dialog box where you can edit and modify the information. Click OK to save the
settings
 3. Click Delete to pop up a prompt box to prompt whether to delete

Built in dictionary option content cannot be deleted.

Refer to the dictionary for other operations.

8.1.3 System

After selecting the system column, enter the interface to set standby time, system parameters and software
upgrade. The interface is as follows:
 1. Users can set system parameters, and use software disk is checked by default.
2. Display the local IP, users can modify the local IP as needed.
3. Standby time can be set, the default is 40 minutes. When it reaches 40 minutes, the machine will go to
sleep.
4. Flow cell and colorimetric cup can be selected for colorimetric mode, and flow cell is selected by default.
5. Click "save" to save the interface modification.
6. Click "upgrade" to pop up a dialog box to select the upgrade method. Users can choose local upgrade or
network online upgrade

(1) Insert the USB flash disk, click upgrade, select local upgrade, pop up a window to confirm whether to
perform local upgrade, and click "OK" to enter the local upgrade process
 (2) When the USB flash disk is read, the upgrade package in the USB flash disk will be displayed in the
pop-up window. Select the upgrade package and click "upgrade" to update the software

(3) After the software update is completed, the instrument needs to be restarted manually.
7. Click the "upgrade" button to pop up a dialog box to select the upgrade method and select network
online upgrade
(1) Network online upgrade is to upgrade the server through WiFi network connection. A dialog box will
pop up after opening the data transmission button

(2) After checking auto upgrade, check and download the upgrade file. The upgrade package list displays
the upgrade package information. The user selects the upgrade package and clicks upgrade to proceed with the
upgrade process.
8.1.4 LIS

Click LIS page to set communication and protocol, as shown in the interface below:

1. Open lis, enter the IP address and port number of LIS, and click Save to connect lis, and the LIS status
icon in the upper right corner is highlighted.
2. After automatic transmission is checked, the test data will be automatically uploaded to LIS terminal
after being obtained.
3. After "LIS / HIS Bidirectional Transmission" is checked, the "Automatic Transmission" is
automatically checked and cannot be edited.
4. The protocol type can be selected from the drop-down list. When ack synchronous communication is
checked, ACK timeout is available.
5. The "Ack Timeout" time can be an integer greater than 0, the default is 30 seconds.
6. After setting LIS information, click "save" to save LIS settings.

8.2 System Time

1. Click "Setting" and select "System Time" in the main interface to display the following interface, where
you can set the date time and date format.
 2. Click the calendar icon after the date and time to pop up the setting box to set the current date and time

3. You can click the up and down arrows of the setting item (month, day, hour, minute and second) to set it,
or click the digital part to edit it.
4. Click year +, click year -.
5. The broom icon in the upper left corner is the empty button. Click to empty all dates and times.
6. Set the date format. Select the drop-down box to set the date format:
 yyyy-MM-dd
 yyyy/MM/dd
 MM-dd-yyyy
 MM/dd/yyyy
 dd-MM-yyyy
 dd/MM/yyyy
The date format of yyyy / mm / DD is selected by default.
7. Click "confirm" to set successfully.
8. Click the "save" button to save the date setting of the current interface.
8.3 User Management

Click the "user management" button in the setting interface, as shown in the figure. Users can add
users, set user permissions, set user passwords, etc.

1. Click "new" to pop up the following dialog box, where you can set new user information, such as
user name, password, user group, etc.

User groups include ordinary users and administrators.The system assigns different permissions
to users according to the user group they belong to.

2. after selecting the user to edit, click Edit to pop up the following dialog box, where you can modify
the information as needed.
  If the current login administrator changes his level to "normal user", the login setting will
not take effect until he logs off again
 Administrators can modify the information of ordinary users and other administrators. They can
only modify their names and notes.

3. Select a user in the user list and click the "Reset Password" button to reset the password of the
selected user to 123456.
4. After the password is reset successfully, a pop-up window will prompt that the password is reset
successfully, and the new password will be displayed.

The administrator can reset the passwords of all administrators and ordinary users;Ordinary
users do not have permission to reset their passwords.

5. Click "Modify Password", enter the user's old password, new password and confirmation
password in the pop-up dialog box, and then click OK.
 Other users can only change their own passwords.

6. If the new password is consistent with the original password or the new password is inconsistent
with the confirmed password, a window will pop up to prompt the user.

7. After the modification is successful, a pop-up window will prompt that the password is modified
successfully.
 8. Select the user, and then click "set default user" to set the user as the default user directly. A dialog
box will pop up to prompt that the setting is successful, and the default user column of the user is checked.

9. When the user logs in the system next time, the default user name will be displayed in the login box.
The user only needs to enter the corresponding password.

10. Select the user to delete, click delete, and click Yes in the pop-up dialog box to delete the selected
user.

 The factory default administrator user name and password are not allowed to be deleted,
and other information except the user name is allowed to be modified.
 Administrators can delete the information of ordinary users and other administrators, but
they are not allowed to delete their own information.

8.4 System State

1. Select "System Status" in the setting interface to enter the sensor interface by default.
 2. By clicking the "Refresh" button, the user can view the real-time motor optocoupler and the
temperature of flow tank and incubation tank.
3. Click the "Version" page to view the version information. The factory software version is default.
If it is updated, it will be modified automatically

8.5 System Log

1. Select "System Log" in the setting interface to enter the system log interface
 2. Click the "▲" arrow and "▼" arrow to slide up and down and turn pages, and users can view the
log information (visible to users at the current level).
3. Select a date in the date edit box to view all log records within the date range, including time,
operator, event type and description.
4. Select event type and operator from the drop-down list to view all log records of the selected
content.
5. Click the "Export" button to export relevant log records, and a dialog box will pop up to select the
export path and export name

6. If the inspection is passed, the export starts, and the export process is displayed as a progress bar.

8.6 Touch Calibration

The touch screen of the analyzer has been calibrated before leaving the factory. Please do not set it by
yourself.However, when the sensing position of the touch screen slightly deviates, the operator can
calibrate by himself through the "touch calibration" interface.
1. Select "Settings" in the main interface and click the "Touch Calibration" button to enter the
service interface.

2. Click "Start Calibration", the system enters the calibration interface, and click the five points
gradually according to the system instructions to complete the calibration operation.

3. After touching the calibration, the pop-up window will prompt "calibration is completed, please
restart the instrument"

4. Manually restart the analyzer and enter the main interface, and the calibration is completed.

If you click the interface incorrectly in the calibration process, the sensing point on the analyzer
touch screen will deviate from the position. Please interrupt the calibration process immediately and
recalibrate after it returns to normal.
 9 Maintain

Click the main interface and select maintenance to enter the instrument maintenance interface. The
interface is as follows

9.1 Clean The Pipeline

1. In the maintenance interface, click the "pipeline cleaning" button to enter the pipeline cleaning interface

2. Cleaning times can be adjusted by -, + or input directly.

 3. when the interface is modified, click save before clicking other buttons.
4. after saving the setting of cleaning times, click "cleaning", and the cleaning operation will be carried out
according to the setting.
5. Click "empty" to empty the liquid in the pipe

Please click "empty" after cleaning the flow tank and pipeline to prevent residues in the water
from remaining in the pipeline system.

9.2 Pump Calibration And Setup

Click "Pump Calibration And Setting" on the maintenance page to set the calibration of peristaltic
pump. The interface is shown as follows:

9.2.1Pump Calibration

1. Pull down to select the sample suction volume for pump calibration. The selection contents are 500,
1000, 1500, 2000 and 5000, and the unit is μ L.
2. The sampling time is automatically obtained by the instrument according to the sampling key or key,
and can also be changed according to the specific needs of the user, with the unit of milliseconds.
3. Duty cycle can be entered directly. The input range is 1-100, not 0, and the default is 70.

4. Click calibration, and the pop-up window will display the set sample suction volume, sample suction
time and pump calibration steps.
 5. The sample suction volume is automatically displayed, and the sample suction time is read and
displayed according to the start and end time of sample suction.
6. Click the sample suction button or the external sample suction button to start sample suction.

9.2.2Pump Setting

1. Pull down to set the delayed sample absorption amount, and you can select 50, 100 and 150 μ L.
2. Pull down the delay sample interval time, the selection range is 1-10, unit millisecond, the pump will
stop according to the delay interval time, and then continue to pump, the sample volume is according to the
delay sample volume.
3. It will be drained automatically after the test is completed. Yes is checked by default. After the test is
checked, the liquid remaining in the colorimetric cell will be drained automatically.
4. Cleaning volume can be used to set the volume of cleaning fluid for cleaning pipeline system.
5. Click the "save" button to save the current interface settings.

9.3 Optical Calibration

Click the "Optical Calibration" button in the maintenance interface to display the interface shown in
the figure below, where the user can calibrate the optical signals of all filters
1. The normal range of, ad value and offset is displayed in the interface, and the colorimetric mode is flow
cell.
2. The left column displays the parameters of the last optical calibration, and the right column displays the
latest optical calibration parameters.
3. The parameters are only read and displayed and cannot be modified. Red indicates that the optical
parameters are outside the normal range.
4. The ad value range of each filter is [55050,62914], and the offset value range is [0-2000].
5. Click "Calibrate" to pop up a dialog box

(1) Click the sample aspirating or external sample aspirating button to start / stop the sample aspirating
operation.
(2) When the optical calibration starts after sample suction, the sample suction button will change to cancel
button to cancel the optical calibration.
(3) Click OK only after the calibration is completed. Click "OK" to complete the calibration and display
the current data in the right column.
8. Click "Clean" to clean the colorimetric cell and pipeline
9. Click Save to save the calibrated optical parameters, and the last optical calibration parameters will be
overwritten.

If the value of optical calibration is out of range, please contact technical support.
 10 Routine Maintenance

10.1 Instrument Cleaning

In order to maintain the long-term stability of the analyzer, regular maintenance is required
 Once a week: wipe the external surface of the analyzer with soft cleaning agent and soft cloth;
 Once a month: clean the touch screen with soft detergent and soft cloth;
 Once a month or according to the tips: once a month or according to the tips of the analyzer to
clean the ventilation hole.
 Accurate temperature control is very important for the normal operation of the analyzer. Please
clean the ventilation hole of the instrument regularly.
 Please unplug the power cord behind the analyzer before cleaning;

Biological Hazards
The surface of all components of the analyzer has potential infectivity, so safety protection
measures should be taken during operation and maintenance.

CAUTION
 Improper maintenance may damage the analyzer.The user must carry out maintenance according
to the instructions in the operation manual.
 If there are no clear problems in the manual, please contact the after-sales service department of
Dymind company , and the professional designated by Dymind company will give maintenance
suggestions.
 The analyzer must be maintained using the parts provided by Dymind.If you have any questions,
please contact the after sales department.Shenzhen Dymind Biotechnology Co., Ltd

10.2 Software Update

According to the demand feedback of the market and customers and the continuous upgrading of
technology, the company will irregularly optimize the analyzer software to ensure that users get the
experience of "faster detection, better performance and more convenient operation".When the version
needs to be updated, the after-sales service personnel of the company will contact the user in time and
upgrade it through USB flash disk.

You can contact the after-sales service personnel to send a special upgrade USB flash disk.Insert the
U disk into the USB interface at the back of the device, and then click the "Settings" button to enter the
 "general settings" interface, and click the "upgrade" button in the "system" interface to realize the software
upgrade.

WARNING
Do not cut off the power supply or disconnect the network during the software update to avoid
the failure of the update.

10.3 Analyzer return For Maintenance

When it is confirmed that the analyzer needs to be returned to the factory for maintenance, please
transport the equipment through the express company designated by the company.Before transportation,
please call the after-sales service hotline 400-998-7276 for consultation