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Antonio DiazAug 14, 2025
What to do if the URIT Medical Electronic Measuring Instruments shows a low battery?
- GGary GriffinAug 14, 2025
If the screen displays a low battery warning in the right lower corner, replace the batteries.
What to do if the URIT Medical Electronic Measuring Instruments shows a low battery?
If the screen displays a low battery warning in the right lower corner, replace the batteries.
What to do if the URIT Medical Electronic PFS-30 Measuring Instruments displays an overdue test strip error?
If the test strip is overdue, first, check and correct the analyzer's current date and time, ensuring it is accurate. Second, ensure you are using the test strip within its valid date range.
What to do if the URIT Medical Electronic Measuring Instruments requires more blood?
If the blood volume is insufficient, ensure the volume of blood sample applied complies with the recommended volume in the test strip's instructions for use.
What to do if the URIT Medical Electronic Measuring Instruments gives a mismatched code card error?
If a mismatched code card is inserted, use the correct, matched code card for your URIT Medical Electronic Measuring Instruments.
What to do if the URIT Medical Electronic Measuring Instruments shows that the code card is not properly inserted?
If the code card is not properly inserted, remove it and re-insert the code card correctly into the URIT Medical Electronic Measuring Instruments.
What to do if I apply blood before the sampling indicator flashes on the URIT Medical Electronic PFS-30 Measuring Instruments?
If you apply the blood sample before the Sampling Indicator is flashing on the display, do not apply the blood sample on to the test strip until the Sampling Indicator is flashing.
What to do if the test strip is moved during automatic detection process of URIT Medical Electronic PFS-30 Measuring Instruments?
If the test strip is moved during the automatic detection process, ensure you do not move the test strip during this process.
What to do if the test hole is blocked by foreign substances before turning on the URIT Medical Electronic PFS-30 Measuring Instruments?
If the test hole is blocked by foreign substances, such as a test strip or fingers, before turning on the analyzer, move the foreign substances away and then turn on the analyzer.
How to clean the mirror surface of URIT Medical Electronic PFS-30?
To clean the mirror surface, turn off the analyzer. Wipe the mirror surface clean using a dry and soft cloth or paper. Then, turn the analyzer back on.
General| Category | Measuring Instruments |
|---|---|
| Model | PFS-30 |
| Manufacturer | URIT Medical Electronic |
| Battery | 2 x AAA batteries |
| Measurement Time | Less than 10 seconds |
| Memory | 1000 test results |
| Operating Conditions | Temperature: 10°C to 40°C; Humidity: ≤85% RH |
Essential safety instructions and warnings for operating the blood lipid analyzer.
Identifies the analyzer's name and lists its technical specifications and models.
Details compatible test strips and blood sample handling requirements.
Defines the analyzer's purpose, applications, and situations where it should not be used.
Lists the items included in the product package and optional accessories.
Explains the technical basis and working mechanism of the blood lipid analyzer.
Provides step-by-step guide for installing and replacing the analyzer's batteries.
Explains the functions of the analyzer's buttons and their operation modes.
Details the meaning of symbols and numbers displayed on the analyzer screen.
Guides users through configuring analyzer settings like date, time, and units.
Instructs on how to set the current date and time on the analyzer.
Explains how to enable and configure the CHD risk assessment feature.
Details how to select measurement units (mg/dL or mmol/L) for test results.
Guides on inserting the code card to match test strips for accurate readings.
Covers preparation, sample collection, and test strip insertion for blood lipid testing.
Details how to view test results and print them when connected to a printer.
Highlights important safety precautions to follow during analyzer operation and sample handling.
Explains data communication, saving, review, and deletion procedures.
Provides instructions on how to erase all stored test results from the analyzer.
Explains the two methods (FRA, PRO) for assessing CHD risk.
Guides on setting FRA parameters like gender, age, smoking history, and blood pressure.
Details PRO settings for age, smoking history, diabetes, heart conditions, and blood pressure.
Shows how the final CHD risk percentage is displayed after data input.
Defines CHD risk levels and explains the validity conditions for risk evaluation methods.
Presents the accuracy, bias, and linearity correlation coefficients of the analyzer.
Details the precision and repeatability evaluation results of the analyzer.
Lists common error symbols and their descriptions encountered during operation.
Provides solutions and corrective actions for specific analyzer errors and issues.
Instructions for cleaning the analyzer's parts after contamination or regular use.
Guidance on storing the analyzer when not in use and general handling precautions.
Defines the tested parameters, sample types, volumes, and compatible reagents.
Specifies detection duration, ranges for measured parameters, and display type.
Details the analyzer's memory capacity, weight, power consumption, dimensions, and battery life.
Covers environmental requirements, transport/storage, connectivity options, and Bluetooth.
Highlights additional features like temperature detection, error detection, and risk evaluation.
Explains symbols related to in vitro diagnostics, warnings, and biological risks.
Details symbols for environmental use, instructions, power, disposal, and storage.
Defines symbols for manufacturing date, manufacturer, serial number, temperature, and compliance.
Provides the address, phone, fax, website, and email for URIT Medical Electronic Co., Ltd.
Lists the EC REP details and CE marking with notified body ID.
Indicates where to find production date and the current version number of the manual.
Contains the DoC identifying the product and its compliance with RE Directive.
Lists the specific standards and documents ensuring product conformity.
Specifies the technical file holder, place, date of issue, and authorizing signature.
