9 Using the QC Program The sample probe automatically aspirates the control. 6. When you hear the beep, remove the control. When analysis finishes, the QC results will be displayed in the current screen and be saved in the QC file automatically. NOTE: Up to 372 QC results can be saved in each QC file. 7. Do the above procedures to continue running QC analysis if necessary.
9 Using the QC Program 9.2.3 Reviewing QC Results After QC analysis, you can review the QC results in the “QC Table” review or “QC Graph” review. QC graph review Reviewing QC Graph: 1. Tap “Menu > QC > Setup” to enter the QC file setup screen. 2. Select the desired QC file to review. The “*” mark displays next to the “File No.” of the selected QC file. 3. Tap “QC Graph” to enter the QC graph review screen of the selected QC file. 1 2 7 3 5 6 4 1.
9 Using the QC Program If necessary, follow below instruction to enter the reasons for the outliers. 1. Tap “Menu > QC > Setup” to enter the QC setup screen. 2. Select the desired QC file to review. The “*” mark displays next to the “File No.” of the selected QC file. 3. Tap “QC Graph” to enter the QC graph screen of the selected QC file. 4. Moving the green line to the desired QC point, and tap the “Outliers” button. A dialog box displays the QC results, targets and limits of all the parameters.
9 Using the QC Program 1 1 2 1. The sequence number of the QC results saved in the QC file (earliest to the latest from top to down). 2. QC result. 3. QC parameters (displayed in the same order as those on the QC graph screen). Deleting QC records (administrators) Administrators may deleted selected or all QC record in the QC file. Delete selected QC record(s): 1. Tap “Menu > QC > Setup” to enter the QC file setup screen. 2. Select the desired QC file. The “*” mark displays next to the “File No.
9 Using the QC Program 1. Tap “Menu > QC > Setup”. 2. Tap the “QC Table” button to enter the QC table screen of the corresponding QC file. 3. Tap “Delete”. The following dialog box displays. 4. Tap to select “All records” and then tap “OK” to delete all records. Communication You can transmit QC data to the external data management software or LIS/HIS. Before transmitting QC data, make sure the network is properly connected. 1. Tap “Menu > QC > Setup” to enter the QC file setup screen. 2.
9 Using the QC Program 3. Tap the “QC Table” button to enter the QC table screen of the corresponding QC file. 4. Select the QC record(s) you want to export. The selected QC records are highlighted. 5. Tap “Export”. The following dialog box displays. 6. Tap to select “Selected records” and then tap “OK” to export the selected records. Export all QC records: 1. Tap “Menu > QC > Setup” to enter the QC file setup screen. 2.
9 Using the QC Program 9.3.2 Analyzing the Causes Retest the samples with outliers. If the retest result still contains outliers and the trend is the same as that of the previous result with outliers, see “Figure 9-5 Analyze the cause of QC outliers” to find out the cause of outliers.
10 10.1 Calibrating Your Analyzer Overview 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 two calibration programs available on this analyzer: manual calibration, calibration using calibrators.
10 Calibrating Your Analyzer 10.4 Running the Calibration Programs The analyzer supports the following calibration programs: • Manual • Calibrator (administrators) 10.4.1 Notes before Calibration Before calibration, check and make sure the analyzer works properly and enough reagents have been prepared for the calibration. You need to start over the calibration if the reagents run out during the process. It is recommended that you create a log table for your analyzer.
Calibrating Your Analyzer /FX DBMJCSBUJPO GBDUPS $VSSFOU DBMJCSBUJPO GBDUPS ¨ 3FGFSFODF WBMVF .FBO For example: Suppose the WBC reference value of a calibrator is 8.40, and the current calibration factor of the whole blood mode is 98.90%. Run the sample under whole blood mode and take the WBC results of the 10 runs to calculate: 8.10, 8.00, 8.10, 8.10, 8.30, 8.30, 8.20, 8.00, 8.10, 8.30. The obtained CV is 1.5% and Mean is 8.16, which meet the requirements. Therefore: /FX $BMJCSBUJPO 'BDUPS 6.
10 Calibrating Your Analyzer 10.4.3 Calibrating with Calibrators (administrators) BIOLOGICAL RISK All the samples, controls, calibrators, wastes and areas contacting them are potentially biohazardous. Wear proper personal protective equipment (e.g., gloves, lab coat, glasses) and follow safe laboratory procedures when handling them and the contacted areas in the laboratory. Sample requirements for calibrators You must use Mindray Animal Medical-specified calibrators for calibration.
10 Calibrating Your Analyzer 6. (Optional) You may select to use which calibration results to calculate the calibration factors. Check the “Select” cells of the calibration results that are to be involved in the calculation of calibration factors. Select at least 3 groups of calibration results. The calibration results are invalid under the following circumstances.
11 Printing You can set up the print templates for sample results report, graphs, QC results, QC graphs, manual calibration factors etc., and print them using the print templates. 11.1 Setting up Print Template For information about print setup, see “6.3.1 System Setup”. 11.2 Printing Sample Result Report NOTE: The analyzer prints at most 700 records at one time. Before printing a sample test report, confirm the following items: • The printer has been set and connected correctly.
11 Printing 4. Set up the print methods. See below for setting descriptions. Item Description Print pattern Print record 5. Table print Select “Table print”, only to print sample results, but not to print graphs (histograms and scattergrams). Graph print Select “Graph print”, print sample results as well as the graphs (histograms and scattergrams). Selected records Check “Selected records” to print the selected sample records. All records Check “All records” to print all the sample records.
11 Printing 1. Tap “Menu > Table Review” or tap “Table Review” button to enter the “Table Review” screen. 2. Select one or more sample records of which you want to review the microscopic parameters. The selected sample record is highlighted. 3. Tap “Graph” to enter the “Graph” screen. 4. Tap “Other Para. > Microscopic Para.” to enter the “Microscopic Para.” screen. Tap “Print” button to print the microscopic parameter results. 11.
11 Printing Follow below instructions: 1. Tap “Menu > Calibration > Manual” in turn to enter the “Manual” screen. 2. Tap “Print” in the utility button area. The analyzer prints the manual calibration factors.
12 12.1 Service Overview Preventive and corrective maintenance procedures are required to keep the analyzer in good operating conditions. This analyzer provides multiple maintenance functions for this purpose. This chapter introduces how to use the provided functions to maintain and troubleshoot your analyzer. CAUTION • • Improper maintenance may damage the analyzer. Operators must follow the instruction of this Operator's Manual to perform maintenance operations.
12 Service Table 12-1 Replacing and priming with reagent Prime Reagent (Service > Maintenance > Reagent) DS Diluent Prime HGB lyse when reagents are contaminated or expired Replace the residue reagent in the pipelines Prime DIFF lyse Prime RET diluent Prime DIFF dye Prime RET dye SR Solution Reagent 12.2.2 12.2.3 Replacing the Parts and Components CAUTION Only parts supplied by Mindary Animal Medical can be used for maintenance. For any question, contact Customer Service Department. 12.
12 Service BIOLOGICAL RISK After replacing the reagent container/bag, check the tubing connected to the cap assembly and make sure it is not bent over. WARNING While installing or replacing the fluorescent dye bag, hold the upper corners of the bag or the part under the bag mouth (where the interior tube is located), in order not to extrude the reagent out. Read reagent information by swiping RFID card Follow below instructions: 1. Enter the “Setup” dialog box.
12 Service Identification rules: – A beep sound occurs if the reagent information is successfully identified. – Three beep sounds occur if there is a mismatch between the RFID card and the reagent. NOTE: • The current system date is set as the open date of the reagent if the reagent information is successfully identified for the first time. • A RFID card can only be used for once. • When you are entering an expired reagent, the analyzer will prompt you to check whether the reagent is expired.
12 Service 3. Insert the pickup tube of the cap assembly into the new container, and then turn the cap clockwise until it is secured. 4. Cap the old container with the cap of the new container and dispose of the container properly. Tap “Replace” button After swiping RFID card and installing new reagents, tap “Replace” button in the “Setup” dialog box. The analyzer will automatically prime reagent and replace the old reagent. 12.3.
12 Service 12.4 Probe Cleanser Maintenance 12.4.1 Daily Probe Cleanser Maintenance After you set the probe cleanser maintenance time in “Setup > Maintenance”, the analyzer prompts you to maintain the probe cleanser at the set time every day. Follow below instructions: 1. When the “Time for maintenance. Perform Probe Cleanser maintenance now?” dialog box displays, tap “Yes”. – The analyzer prepares for Probe Cleanser maintenance.
12 Service 4. Press the [Aspirate] key to start probe cleanser maintenance. The analyzer aspirates probe cleanser. 5. Remove the probe cleanser. The analyzer automatically completes probe cleanser maintenance. 12.5 Auto-cleaning of the Parts and Components You should clean the following parts or components when: Follow below instructions: 1. Tap “Menu > Service > Maintenance > Cleaning” to enter the “Cleaning” screen. 2. Tap the corresponding cleaning program.
12 Service 2. Clean the probe wipe and blood barrier bracket a. 12 - 8 Push the sample probe assembly forward slightly to reserve sufficient operation and maintenance space.
12 Service Item Name 1. sample probe assembly 2. Probe wipe 3. Blood barrier bracket 3. b. Use a sterilized cotton swab dipped with probe cleanser to wipe the surface of the probe wipe. Then, use a sterilized cotton swab dipped with clean water to wipe the surface until no blood residue or other residues are visible. c. Use a sterilized cotton swab dipped with alcohol to wipe the surface of the blood barrier bracket until no blood residue or other residues are visible.
12 Service 12.6 Preparing to Pack-up If the analyzer is not to be used for a long time (over 10 days), you should perform this procedure. Follow below instructions: 12.7 1. Tap “Menu > Service > Maintenance > Fluidics” to enter the “Fluidics” screen. 2. Tap “Pack-up”, and follow the software instruction to complete the pack-up procedure. Screen Calibration If the touch screen does not correctly respond to the positions you touched, perform the procedure to calibrate the touch screen.
12 Service Table 12-2 Log Types Item Administrator's level Common user’s level Error View error information and Cannot review Information troubleshooting information of the analyzer. 12.8.1 Viewing Logs Follow below instructions: 1. Tap “Menu > Service > Log” in turn to enter the “Log” screen. 2. Tap a type of logs to be viewed. 3. (Optional) Review the logs at specified date range. a. Tap “Go to“. A confirm dialog box displays. b.
12 Service 2. Tap “Export“. A confirm dialog box displays. 3. In the “Start date:” and “End date:” edit boxes, specify the time range in which logs need to be exported. 4. Tap “OK“. The analyzer automatically exports the logs in specified time range to the USB device. After export ends, the screen displays the “Export succeeded.” dialog box. NOTE: Analyzer upgrade may only be performed under the instruction from a Mindary Animal Medicalauthorized service personnel.
13 13.1 Troubleshooting Overview 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. 13.
13 Troubleshooting Temp.&Pressure Displays the current temperature and pressure as well as the acceptable range for various items. Menu > Status > Temp.&Pressure Administrator's level Out-of-range values are highlighted in red background. Floater Status Displays the full or empty Menu > Status > Floater status of the bathes and Status waste cistern. Administrator's level Sensor Displays the status of Menu > Status > Sensor fluorescent reagent detect sensor and motherboard sensor.
13 Troubleshooting Tap the “Remove Error” button to clear all the errors that can be removed automatically. For the errors that cannot removed automatically, follow the troubleshooting method to solve them. • To mute the alarm sound Tap the touch screen to eliminate the alarm sound of the main unit. • Close the “Error Information” dialog box Tap “Off” to close the dialog box, but the errors will still be displayed in the error info. area on the screen. Tap the error info.
13 Troubleshooting Error ID Error Message Description Solution 0x10002 No DR Diluent. No DR Diluent. Follow below instructions: Replace the reagent Replace the reagent 1. Touch “Remove Error” button and register new reagent information into the reagent setup dialog box displayed. 2. Touch “Replace” to prime reagent after replacing the reagent container. 3. If error persists, contact Technical Support Services. 0x10005 No FD Dye. No FD Dye.
13 Troubleshooting Error ID Error Message Description Solution 0x10201 LD Lyse expires. LD Lyse expires. Follow below instructions: Replace the reagent Replace the reagent 1. Touch “Remove Error” button and register new reagent information into the reagent setup dialog box displayed. 2. Touch “Replace” to prime reagent after replacing the reagent container. 3. If error persists, contact Technical Support Services. 0x10202 LH Lyse expires. LH Lyse expires.
13 Troubleshooting Error ID Error Message Description Solution 0x10205 FR Dye expires. FR Dye expires. Follow below instructions: Replace the reagent Replace the reagent 1. Touch “Remove Error” button and register new reagent information into the reagent setup dialog box displayed. 2. Touch “Replace” to prime reagent after replacing the reagent container. 3. If error persists, contact Technical Support Services. 0x10400 DS Diluent low DS Diluent low Follow below instructions: volume.
13 Troubleshooting Error ID Error Message Description Solution 0x10403 DR Diluent low DR Diluent low Follow below instructions: volume. Replace the volume. Replace the 1. Touch “Remove Error” button and reagent reagent register new reagent information into the reagent setup dialog box displayed. 2. Touch “Replace” to prime reagent after replacing the reagent container. 3. If error persists, contact Technical Support Services. 0x10404 FD Dye low FD Dye low Follow below instructions: volume.
13 Troubleshooting Error ID Error Message Description Solution 0x10101 Cistern floater status abnormal SCI cistern floater status abnormal Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 0x30105 FS baseline abnormal FS baseline abnormal Follow below instructions: 1. Tap the “Remove Error” button to remove the error; 2. Switch off and then switch on the instrument power; 3.
13 Troubleshooting Error ID Error Message Description Solution 0x00301 DIL syringe action abnormal Conflicting DIL syringe actions Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 0x00303 DIL syringe action abnormal Error occurs when DIL syringe leaves sensor area Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2.
13 Troubleshooting Error ID Error Message Description Solution 0x00310 DIL syringe action abnormal DIL syringe action time out Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 0x00309 DIL syringe action abnormal DIL syringe dispensed volume too high Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2.
13 Troubleshooting Error ID Error Message Description Solution 0x00206 SP syringe action abnormal SP syringe aspiration/ dispensation action not allowed 1 Follow below instructions: SP syringe aspiration/ dispensation action not allowed 2 Follow below instructions: 0x00207 0x00208 SP syringe action abnormal SP syringe action abnormal 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 1.
13 Troubleshooting Error ID Error Message Description Solution 0x10107 SCI priming out of time SCI priming out of time Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 0x99805 Background abnormal Background abnormal Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department.
13 Troubleshooting Error ID Error Message Description Solution 0x20008 Closed-reagent RFID board communication timeout Closed-reagent RFID board communication timeout Follow below instructions: 0x30109 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. Optical signal board Optical signal board Follow below instructions: communication communication 1. Tap the “Remove Error” button to timeout timeout remove this error; 2.
13 Troubleshooting Error ID Error Message Description Solution 0x10303 SCI bath pressure release abnormal SCI bath pressure release abnormal Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 0x10305 WC2 bath pressure release abnormal WC2 bath pressure release abnormal Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2.
13 Troubleshooting Error ID Error Message 0x30004 Preheating bath Preheating bath temperature control temperature out of abnormal the lower limit for counting Follow below instructions: Ambient temperature low Follow below instructions: 0x30006 Description Ambient temperature low Solution 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 1. Make sure the ambient temperature is within acceptable range. 2.
13 Troubleshooting Error ID Error Message Description Solution 0x30100 Optical system working voltage abnormal PMT voltage abnormal Follow below instructions: 1. Tap the “Remove Error” button to remove the error; 2. Switch off and then switch on the instrument power; 3. If the error still exists after the restart, contact our customer service department. 0x30201 HGB blank voltage HGB blank voltage Follow below instructions: abnormal abnormal 1.
13 Troubleshooting Error ID Error Message Description 0x99804 Front cover is open Front cover is open Solution Follow below instructions: 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 0x30108 Optical system shielding box is open Optical system shielding box is open Follow below instructions: 1. Close the Optical system shielding box;\r\n2.Tap the “Remove Error” button to remove this error; 2.
13 Troubleshooting Error ID Error Message Description Solution 0x30303 Clog RBC sample preparation abnormal Follow below instructions: 1. RBC sample preparation abnormal. 2. Tap the “Remove Error” button to remove this error. 3. If the error still exists, contact our customer service department. 0x20200 Power fan error Power fan blocked Follow below instructions: 1. Check whether the power fan is stuck. 2. If the error persists, contact our Customer Service Department.
13 Troubleshooting Error ID Error Message Description Solution 0x20003 Air pressure detection board error Air pressure detection board calibration parameter error Follow below instructions: 1. Tap the “Remove Error” button to remove the error; 2. Switch off and then switch on the instrument power; 3. If the error still exists after the restart, contact our customer service department. 0x30202 Waste channel abnormal HGB waste channel Follow below instructions: clogged 1.
13 Troubleshooting Error ID Error Message Description Solution 0x30603 Waste channel abnormal RET waste channel Follow below instructions: clogged 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department. 0x30604 Waste channel abnormal RET waste channel Follow below instructions: clogged 1. Tap the “Remove Error” button to remove this error; 2. If the error still exists, contact our customer service department.
13 Troubleshooting Error ID Error Message Description Solution 0x30306 Waste channel abnormal Cleaning channel of Follow below instructions: RBC sample 1. Tap the “Remove Error” button to preparation clogged remove this error; 2. If the error still exists, contact our customer service department.
A Index A O Analyzer shutdown 7-9 Operating Your Analyzer 7-1 B P Blood type 8-5 Parameters 3-1 Blood Sample Test Histograms 3-3 Blood Sample Test Report Parameters 3-2 Blood Sample Test Scattergrams 3-3 HGB 4-5 Microscopic Parameters Define Microscopic Parameters 6-10 Print Microscopic Parameter Results C Calibrate Calibrate with Calibrators 10-4 Calibration History 10-5 Calibration Programs 10-2 Manual calibration 10-2 Notes before Calibration 10-2 Verify calibration factors 10-5 When to Calibrat
A Index Auto Standby 7-9 Date/Time 6-5 Flag Alarm Sensitivity 6-5 HGB Gains 6-11 Permissions 6-1 Save Changes 6-2 System Principles SF CUBE Cell Analysis Technology 4-5 Sheath Flow Impedance Method 4-5 T Troubleshooting Check Analyzer Status 13-1 W WBC Measurement 4-1 Working Principles RBC/PLT Measurement 4-5 A-2 Operator’s Manual
B B.1 Specification Reagent The analyzer can be used with the following reagents, controls, and calibrators. NOTE: For any questions related to reagents, controls, and calibrators, please consult your local distributor. .
B Specification B.
B Specification B.3 Sampling Features B.3.1 Sample Mode and Test Panel Table B-4 Sample mode, test panel Sample Modes Test Panel Whole blood mode CD CDR B.3.2 Sample Volumes Required for Each Analysis Table B-5 Sample Volumes Required for Each Analysis B.3.3 Sample Mode Test Panel Sample Volume Required for Each Analysis (μl) Whole blood CD ≤ 28 CDR ≤ 34 Throughput Table B-6 Throughput Sample Mode Test Panel Throughput (test/hour) Whole blood CD 60 CDR 40 B.
B Specification B.4.2 Repeatability Table B-8 Repeatability requirements for blood samples B.4.3 Parameter Range Whole Blood (CV/Absolute Deviation d*/SD) WBC (3.50 ~ 4.50)×109/L ≤ 3.0% ≥4.50×109/L ≤ 2.5% RBC ≥3.50×1012/L ≤ 1.5% HGB (110 ~ 180) g/L ≤ 1.0% MCV (80.0 ~ 100.0) fL ≤ 1.0% PLT ≥100×109/L ≤ 4.0% Carryover Table B-9 Carryover requirements for blood samples Parameters Carryover WBC ≤1.0% RBC ≤1.0% HGB ≤1.0% HCT ≤1.0% PLT ≤1.0% B.5 Input/Output Devices. B.5.
B Specification B.5.5 USB Drive Supporting the protocol of USB2.0 and above. B.6 Interfaces NOTE: The USB interfaces on the back of the analyzer shall only be used to connect the peripheral devices specified in this manual. For details about supported devices and models, see “B.5 Input/Output Devices.”. B.7 • One network port (compatible with 10/100/1000M Ethernet and complying with the 802.3u/ 802.3ab standard) • Four USB ports including three supporting USB2.0 and one supporting USB3.
B Specification • This equipment complies with the emission and immunity requirements described in IEC 61326-1:2012 / EN 61326-1:2013. • The intended use environments of this equipment includes typical healthcare environments (hospitals, clinics, doctor’s offices), 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.
B Specification • l'utilisateur de l'appareil doit accepter tout brouillage radioélectrique subi, même si lebrouillage est susceptible d'en compromettre le fonctionnement. La distance entre l'utilisateur et de produits ne devrait pas être inférieure à 20cm Industry Canada ICES-003 Compliance:CAN ICES-3(B)/NMB-3(B) B.11 Noise Level Maximal noise level: 80 dBA NOTE: Be sure to use and store the analyzer under the specified environment conditions. B.
B Specification B.15 Dimensions and Weight Figure B-1 Main Unit Dimensions H D D W Main Unit Dimensions and Weight Value Width (W) ≤325 mm Height (H) ≤450 mm Depth (D) ≤500 mm Weight ≤35 kg B.16 Contraindication None B.17 Safety Classification Level of transient overvoltage: Category II. Rated pollution degree: 2.
C C.1 Accessories and Packing List Accessories of the Analyzer • Reagent cap assembly • Waste tube assembly • Main power cords NOTE: The accessories actually attached to the product depend on your product configuration. For details about the configured/optional accessories, consult your sales representative. C.2 C.
D Communication The LIS/HIS function of this analyzer enables the communication between the analyzer and the PC in laboratory through Ethernet, including sending analysis results to and receiving worklist from PC. In the LIS/HIS communication process of the analyzer involves the HL7 communication protocol. For details about the connection control, and the introduction, message definition and examples, please contact Customer Service Department or your local distributor.
E Operator’s Manual Declaration of Conformity E-1
F References 1. CLSI. Interference Testing in Clinical Chemistry; Approved Guideline; Second Edition. CLSI document EP7-A2. Clinical and Laboratory Standards Institute; 2005. 2. Levey S, Jennings ER. The use of control charts in the clinical laboratory. Am J Clin Pathol. 1950;20” 1059-1066 3. Westgard, J.O., P.L. Barry, and M.R. Hunt (1981). “A Multi-rule Shewhart Chart for Quality Control in Clinical Chemistry,”Clinical Chemistry, vol. 27, pp. 493-501. 4. Westgard, J.O., P.L. Barry (1986).
G Maintenance Logs NOTE: • You are advised to prepare a maintenance checklist suitable for the operating environment of the analyzer. • For more information about the maintenance procedure, see “12 Service”.
20 21 22 23 24 25 26 27 28 29 30 31 4 5 6 7 8 9 10 11 12 13 14 15 16 19 3 Date 18 Probe wipe cleaning 2 Cleaning the Analyzer Front Cover 17 Probe Cleanser Maintenance 1 Date Probe Cleanser Maintenance Routine Maintenance Items Cleaning the Analyzer Front Cover Probe wipe cleaning
Maintenance Items Signature, MM/ DD/YYYY Signature, MM/ DD/YYYY Maintenance Items When Necessary Maintenance Items Signature, MM/ DD/YYYY Signature, MM/ DD/YYYY Replacing Reagents and Parts
P/N: 046-024913-00 (2.