Related Manuals for URIT Medical Electronic PFS-30
Summary of Contents for URIT Medical Electronic PFS-30
- Page 1 URIT PFS-30/PFS-30A Blood Lipid Analyzer OPERATION MANUAL URIT Medical Electronic Co., Ltd.
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Page 2: Table Of Contents
Contents 1. Warnings............................1 2. Brief Introduction..........................3 2.1 Product Name........................3 2.2 Specifications and Models....................3 2.3 Assorted Test Strip......................3 2.4 Sample requirements......................3 2.5 Intended Use........................3 2.6 Contraindications....................... 3 2.7 Packaging & Components....................3 2.8 Operation Principles......................5 3. Operating Instructions........................6 3.1 Installation and Change of Batteries................ -
Page 3: Warnings
1. Warnings (1) Before using the analyzer, please be sure to read the product Operation Manual, please be sure to as stipulated in the manufacturer of ways to use analyzer, otherwise it may cause the analyzer's protective destroyed, at the same time, please pay special attention to the instrument identification there is symbol, please refer to the attached documents in time, in order to know the potential risk nature and any measures must... - Page 4 (23) If this equipment is used in a medical institution, it is recommended to evaluate the electromagnetic environment before operating the equipment. (24) Use of this instrument in a dry environment, especially if synthetic materials are present (synthetic clothing, carpets etc.) may cause damaging electrostatic discharges that may cause erroneous results.
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Page 5: Brief Introduction
2. Brief Introduction 2.1 Product Name Blood Lipid Analyzer (hereinafter referred to as analyzer) 2.2 Specifications and Models PFS-30 (with Bluetooth); PFS-30A 2.3 Assorted Test Strip PFS 30 Blood Lipid Test Strip (produced by URIT) 2.4 Sample requirements Sample type：whole blood (venous blood or capillary blood) Sample collection and storage：... - Page 6 Figure 1 analyzer Front Figure 2. analyzer Back The PFS-30 or PFS-30A Blood Lipid analyzer (hereinafter as referred to as analyzer) is used to detect the content of total cholesterol (TC), high-density lipoprotein cholesterol (HDL), triglyceride (TG) in human whole blood (venous blood and capillary blood) sample, as well as their ratios such as TC/HDL and low-density lipoprotein cholesterol (LDL) based on the above measurements.
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Page 7: Operation Principles
easily detect blood lipid related measurements. In order to maintain the accuracy of test results, make sure that you have followed the standard operating instructions and maintenance guidance of this analyzer. Please read instructions for use carefully before using this machine. Otherwise, inaccurate operating methods may lead to inaccurate test results or even unnecessary harm to the operators as well as patients. -
Page 8: Operating Instructions
3. Operating Instructions 3.1 Installation and Change of Batteries 3 AAA batteries are used to make the analyzer working. In order to save the power of batteries, the analyzer will be automatically powered off when there have be no operations for 5 minutes. -
Page 9: Display Information
3.3 Display Information Figure 5. Display Information Meanings of displayed numbers or symbols: 1. Current date and time. 2. Test No.: An sequencing number of test item, which can be used for test result inquiry. 3. Test result :Test result after one detection and code when the analyzer is just turned on. 4. - Page 10 Note: The detection time of every blood sample will be automatically recorded by the analyzer for subsequent inquiry and statistical analysis. Thus in order to maintain the accuracy of recorded time, when you have inserted an new code card or replaced the batteries, always remember to check the date and time and make sure they are right.
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Page 11: Code
Figure 8. Setting of Date and Time When you have finished the settings of date and time, press Button to save the changes and move along to the next page for CHD Risk Evaluation Function. 3.4.3 CHD Risk Evaluation Function Press M Button or S Button to turn on or off the “CHD Risk Evaluation Function”. -
Page 12: Detection Of Blood Lipid
Figure 13 Insert the Code Card Figure 14. Display Information of No.159 Code Card Note: Check the displayed number with the code number printed on the package of test strips and make sure they are the same. When the above settings are finished, take the code card out, press and hold button to turn off the analyzer or the analyzer can automatically be power off when there have been no operations for 5 minutes. - Page 13 Figure 15. Code is “159” Figure 16. Indicator to insert the test strip Figure 17. Indicator to apply the blood sample Note: Before inserting the test strip, check the code displayed on the screen and make sure it is the same as the code on the package of test strip which you have picked. If not, please stop this detection and reset the code following steps listed in Section 3.5.
- Page 14 Figure 19. Press M or S Button to see more results When “Lo” is displayed on the screen for one of the paraanalyzers, the measurement of this paraanalyzer in the blood sample is lower than the lower limit of detection range for this analyzer. On the other hand, when “Hi”...
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Page 15: Data Communication
Besides, the PFS-30 type Blood Lipid analyzer is also equipped with Bluetooth function, making it possible to directly transfer the data of current test immediately to equipment which has been connected with the analyzer through Bluetooth, including cellphones and tablets. - Page 16 generated after the memory capacity is full, the result record of earliest test will be automatically deleted so that the new one can be saved. Beside, the sequence number of the new test result will be named from 1 again after 300 have been reached. 3.8.1 Inquiry When the analyzer is turned off, press M Button to initiate the analyzer for inquiry.
- Page 17 In the page of “Review Test Result”, press and hold M button can print the result using connected printer, as showed in Figure 25 Figure 25. The printer is printing the result. When the above settings are finished, take the code card out, press and hold “ ”...
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Page 18: Chd Risk Evaluation
operations for 5 minutes. 3.9 CHD Risk Evaluation When the CHD risk evaluation function of the analyzer has been successfully initiated, CHD symbol in setting page will be turned on. First, go to “Review Test Result” screen, press and hold S Button can move to the screen of CHD risk evaluation, in which the test result of the number which you have selected will be analyzed for risk of CHD. - Page 19 Figure 29. FRA Settings After selecting PRO, press and hold S Button to confirm your selection, and the analyzer will automatically display the screen of “Age Selection”, in which you can select the right gender for the test subject. Press and hold S Button can determine the age, smoking history, history of diabetes mellitus, history of myocardial infarction and systolic blood pressure in turns.
- Page 20 Figure 30. PRO Settings When all paraanalyzers have been determined, the CHD risk for this test subject will be evaluated and displayed as Figure 31. Figure31. Display of CHD Risk Note: It’s allowed to press button at anytime during this evaluation procedure to go back to “Data Inquiry”...
- Page 21 Infos: 1. According to National Cholesterol Education Program (NCEP) ATP III，2001, the risk of CHD in 10 years can be classified as 3 levels: CHD Risk≤10%: Low Risk; 20%≥CHD Risk>10%: Intermediate Risk; CHD Risk>20%: High Risk. 2. The RPO method for CHD risk evaluation is only valid when the TC/HDL result is valid for the test subject, which means that both TC and HDL test results have to been within the detection range of this analyzer, as discussed before.
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Page 22: Systemic Performance Data
4. Systemic Performance Data 4.1 Accuracy The accuracy of this analyzer is generated using comparison to automatic biochemical analyzer in a parallel test. For this analyzer, the allowable deviation of test results for different paraanalyzers are listed in the table below: Inspection Item Detection Range (mmol/L) Bias... -
Page 23: Errors & Troubleshooting
Errors & Troubleshooting Errors or hints for instructions may occur during the operation of this analyzer. The following table has listed possible errors and corresponding solutions which you need to follow. If these solutions are unable to solve your problem, please do not tear the analyzer apart. -
Page 24: Maintenance & Care Of Analyzer
6. Maintenance & Care of analyzer ▲ If the analyzer is accidentally contaminated by blood sample, immediately clean the analyzer. Use wet cotton swab or soft flannelet to carefully wipe the contaminated part. ▲ The connector of test strip on the analyzer needs to be immediately cleaned when too much blood has been applied during sampling process. -
Page 25: Technical Paraanalyzers
Connection: Standard USB port, which can be connected to the computer for data transmission. The analyzer can be connected with portable printer to print test results. PFS-30 type analyzer support Bluetooth communication while PFS-30A type analyzer does not support Bluetooth. -
Page 26: Symbols
Symbols In vitro diagnostic medical device Caution Biological risks Environment-friendly use period Batch code Continuous current Consult instructions for use AAA * 3 This analyzer requires 3 AAA batteries as power supply Waste recycle Protect from heat and radioactive sources Keep dry Date of manufacture Manufacturer... -
Page 27: Basic Information
9. Basic Information URIT Medical Electronic Co., Ltd. Add: No.D-07 Information Industry District, High-Tech Zone, Guilin, Guangxi 541004, P.R.China. Tel: +86 (773) 2288586 Fax: +86 (773) 2288586 Website: www.urit.com E-mail: service@uritest.com Enterprise Hub, NW Business Complex,1 Beraghmore Rd. Derry, BT48 8SE, N. Ireland, UK Production Date: See labels. -
Page 28: Red Doc
10.RED DoC...
Need help?
Do you have a question about the PFS-30 and is the answer not in the manual?
Questions and answers
What are good readings for HDL and LDL and Triglycerides.
For the URIT Medical Electronic PFS-30 analyzer:
- HDL (High-Density Lipoprotein): Normal is greater than 1.0 mmol/L.
- LDL (Low-Density Lipoprotein): Normal is less than or equal to 0.20 mmol/L.
- Triglycerides: Normal is less than or equal to 1.0 mmol/L.
This answer is automatically generated
Can’t seem to change unit of measurement from metric to American
To change the unit of measurement on the URIT Medical Electronic PFS-30:
1. Press the M Button or S Button to switch between “mg/dL” (American unit) and “mmol/L” (metric unit).
2. Press the Button to confirm the current setting.
This will change the unit used for test results.
This answer is automatically generated
Hola, compre el Analizador PFS-30/PFS. Pongo la tira reactiva. Cuando agrego la gota de sangre no response. Cual es el problema. Agrego que El numero de la tira corresoonde a el numero que figura en el Analizador. Cual es la solution.
If the URIT Medical Electronic PFS-30 analyzer does not respond after adding a drop of blood to the test strip, possible issues include:
1. Insufficient Blood Sample – The analyzer requires 35–40 µL of blood. If the sample is too small, the device may not start the test.
2. Incorrect Test Strip Insertion – The test strip must be properly inserted into the analyzer before applying the sample.
3. Expired or Contaminated Test Strip – Ensure the test strip is not expired or exposed to air for too long after opening the container.
4. Code Mismatch – The code displayed on the screen must match the code on the test strip packaging. If not, reset the code.
5. Electrostatic Discharge (ESD) Interference – If used in a dry environment with synthetic materials, electrostatic discharge may interfere with operation.
6. Battery Issue – The analyzer requires three AAA batteries. If the battery capacity is low, the device may not function properly.
7. Hemolytic or Improperly Stored Blood Sample – Blood samples should not be hemolyzed and must be stored as per guidelines to avoid inaccurate results.
Check these factors to resolve the issue.
This answer is automatically generated
what does Lo signify on my Urit?
"Lo" on the URIT Medical Electronic PFS-30 signifies that the measurement of the parameter in the blood sample is lower than the lower limit of the detection range for the analyzer.
This answer is automatically generated