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URIT Medical Electronic PFS-30 - User Manual

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URIT
PFS-30/PFS-30A
Blood Lipid Analyzer
OPERATION MANUAL
URIT Medical Electronic Co., Ltd.

Questions and Answers

  • A
    Antonio DiazAug 14, 2025
    What to do if the URIT Medical Electronic Measuring Instruments shows a low battery?
    • G
      Gary GriffinAug 14, 2025
      If the screen displays a low battery warning in the right lower corner, replace the batteries.
  • L
    leroyroyAug 17, 2025
    What to do if the URIT Medical Electronic PFS-30 Measuring Instruments displays an overdue test strip error?
    • W
      wgayAug 17, 2025
      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.
  • D
    Darlene HarperAug 20, 2025
    What to do if the URIT Medical Electronic Measuring Instruments requires more blood?
    • G
      gilbert57Aug 20, 2025
      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.
  • S
    Suzanne MathisAug 23, 2025
    What to do if the URIT Medical Electronic Measuring Instruments gives a mismatched code card error?
    • J
      Jane MurphyAug 25, 2025
      If a mismatched code card is inserted, use the correct, matched code card for your URIT Medical Electronic Measuring Instruments.
  • A
    alexanderleeAug 27, 2025
    What to do if the URIT Medical Electronic Measuring Instruments shows that the code card is not properly inserted?
    • G
      Gabrielle DavisAug 27, 2025
      If the code card is not properly inserted, remove it and re-insert the code card correctly into the URIT Medical Electronic Measuring Instruments.
  • E
    Elizabeth GarrettAug 30, 2025
    What to do if I apply blood before the sampling indicator flashes on the URIT Medical Electronic PFS-30 Measuring Instruments?
    • B
      Beth ParkAug 30, 2025
      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.
  • J
    John BaldwinSep 3, 2025
    What to do if the test strip is moved during automatic detection process of URIT Medical Electronic PFS-30 Measuring Instruments?
    • R
      Ronald KingSep 3, 2025
      If the test strip is moved during the automatic detection process, ensure you do not move the test strip during this process.
  • A
    Andrew Hayes Jr.Sep 6, 2025
    What to do if the test hole is blocked by foreign substances before turning on the URIT Medical Electronic PFS-30 Measuring Instruments?
    • D
      dale79Sep 6, 2025
      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.
  • S
    Sharon EvansSep 9, 2025
    How to clean the mirror surface of URIT Medical Electronic PFS-30?
    • D
      Dylan JohnsonSep 9, 2025
      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.

Summary

Warnings and Safety Precautions

General Safety Precautions

Essential safety instructions and warnings for operating the blood lipid analyzer.

Brief Introduction to the Analyzer

Product Name and Specifications

Identifies the analyzer's name and lists its technical specifications and models.

Test Strip and Sample Requirements

Details compatible test strips and blood sample handling requirements.

Intended Use and Contraindications

Defines the analyzer's purpose, applications, and situations where it should not be used.

Packaging and Components

Lists the items included in the product package and optional accessories.

Operation Principles

Explains the technical basis and working mechanism of the blood lipid analyzer.

Operating Instructions

Battery Installation and Replacement

Provides step-by-step guide for installing and replacing the analyzer's batteries.

Analyzer Button Functions

Explains the functions of the analyzer's buttons and their operation modes.

Display Screen Information

Details the meaning of symbols and numbers displayed on the analyzer screen.

System Configuration Settings

Guides users through configuring analyzer settings like date, time, and units.

Date and Time Configuration

Instructs on how to set the current date and time on the analyzer.

CHD Risk Evaluation Setup

Explains how to enable and configure the CHD risk assessment feature.

Measurement Unit Selection

Details how to select measurement units (mg/dL or mmol/L) for test results.

Test Strip Code Entry

Guides on inserting the code card to match test strips for accurate readings.

Blood Lipid Testing Procedure

Covers preparation, sample collection, and test strip insertion for blood lipid testing.

Viewing Test Results and Printing

Details how to view test results and print them when connected to a printer.

Important Operational Safety

Highlights important safety precautions to follow during analyzer operation and sample handling.

Data Transfer and Management

Explains data communication, saving, review, and deletion procedures.

Erasing Stored Data

Provides instructions on how to erase all stored test results from the analyzer.

CHD Risk Evaluation

Evaluation Method Selection

Explains the two methods (FRA, PRO) for assessing CHD risk.

Configuring FRA Risk Assessment

Guides on setting FRA parameters like gender, age, smoking history, and blood pressure.

Configuring PRO Risk Assessment

Details PRO settings for age, smoking history, diabetes, heart conditions, and blood pressure.

Interpreting CHD Risk Display

Shows how the final CHD risk percentage is displayed after data input.

CHD Risk Classification and Validity

Defines CHD risk levels and explains the validity conditions for risk evaluation methods.

Systemic Performance Data

Accuracy and Linearity Performance

Presents the accuracy, bias, and linearity correlation coefficients of the analyzer.

Repeatability and Precision Metrics

Details the precision and repeatability evaluation results of the analyzer.

Errors & Troubleshooting Guide

Analyzer Error Codes and Meanings

Lists common error symbols and their descriptions encountered during operation.

Troubleshooting Common Issues

Provides solutions and corrective actions for specific analyzer errors and issues.

Maintenance & Care of Analyzer

Analyzer Cleaning Procedures

Instructions for cleaning the analyzer's parts after contamination or regular use.

Analyzer Storage and Handling

Guidance on storing the analyzer when not in use and general handling precautions.

Technical Specifications

Test Parameters and Sample Requirements

Defines the tested parameters, sample types, volumes, and compatible reagents.

Detection Ranges and Display Features

Specifies detection duration, ranges for measured parameters, and display type.

Physical and Power Characteristics

Details the analyzer's memory capacity, weight, power consumption, dimensions, and battery life.

Environmental and Connectivity

Covers environmental requirements, transport/storage, connectivity options, and Bluetooth.

Additional Analyzer Features

Highlights additional features like temperature detection, error detection, and risk evaluation.

Symbols Guide

Diagnostic and Safety Symbols

Explains symbols related to in vitro diagnostics, warnings, and biological risks.

Operational and Handling Icons

Details symbols for environmental use, instructions, power, disposal, and storage.

Identification and Compliance Marks

Defines symbols for manufacturing date, manufacturer, serial number, temperature, and compliance.

Basic Information and Contacts

Manufacturer Contact and Location

Provides the address, phone, fax, website, and email for URIT Medical Electronic Co., Ltd.

European Representative and Certifications

Lists the EC REP details and CE marking with notified body ID.

Product Version and Date Info

Indicates where to find production date and the current version number of the manual.

RED Declaration of Conformity

Product Conformity Statement

Contains the DoC identifying the product and its compliance with RE Directive.

Applicable Standards and Documents

Lists the specific standards and documents ensuring product conformity.

Technical File and Issuance Details

Specifies the technical file holder, place, date of issue, and authorizing signature.

URIT Medical Electronic PFS-30 Specifications

General IconGeneral
CategoryMeasuring Instruments
ModelPFS-30
ManufacturerURIT Medical Electronic
Battery2 x AAA batteries
Measurement TimeLess than 10 seconds
Memory1000 test results
Operating ConditionsTemperature: 10°C to 40°C; Humidity: ≤85% RH

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