Acon FIAflex CRP FIA Test

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Product Details:

Function CRP Quantification
Usage Type Diagnostic Laboratory & Point-Of-Care Testing
Features Rapid Results, High Sensitivity, User Friendly, CE Certified
Frequency Single Use Test Kit
Display Type Digital Display (on Analyzer)
Accuracy High (as per manufacturers validation)
Storage Instructions 2-30C, Keep Away from Sunlight
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Acon FIAflex CRP FIA Test Price And Quantity

Acon FIAflex CRP FIA Test Product Specifications

Weight Lightweight (Device Specific)
Power Consumption Low
Equipment Type In Vitro Diagnostic Test Kit
Shelf Life 18 Months
Voltage 220V AC
Material Plastic, Paper, Electronic Components
Storage Instructions 2-30C, Keep Away from Sunlight
Instruments Type FIA Analyzer Compatible
Measurement Range 0.5 320 mg/L
Condition New
Portable Yes
Accuracy High (as per manufacturers validation)
Operating Type Automated
Features Rapid Results, High Sensitivity, User Friendly, CE Certified
Dimension (L*W*H) Based on Analyzer: Typically Compact Design
Display Type Digital Display (on Analyzer)
Frequency Single Use Test Kit
Technology Fluorescence Immunoassay (FIA)
Use Quantitative Detection of C-Reactive Protein (CRP) in Serum, Plasma or Whole Blood
Wall Mounted No
Power Source Electric
Noise Level Silent Operation
Function CRP Quantification
Usage Type Diagnostic Laboratory & Point-Of-Care Testing
Color Multi-Color (as per Kit)
Real-Time Operation Yes

Batch Number Available on Kit
User Manual Included with Kit
Test Time ~3 minutes per test
Sample Types Serum, Plasma, Whole Blood
Intended Use Professional In Vitro Diagnostic Use Only
Compatible Devices FIAflex Analyzer Series
Readout Method Fluorescent Signal Detection
Packaging Details 25 Tests/Kit or customized
Expiry Date Printed on Each Box
Sample Volume 10 L

Product Description

Brand Acon

Sample Type Serum/ Plasma/ WB

Pack Size 25T

CAT No F131-50111

Biomarker Infection

The CRP FIA Test is a fluorescence immunoassay that is used with the FIAflex Fluorescent Immunoassay Analyzer for the quantitative detection of C-reactive protein (CRP) in human serum, plasma, venous whole blood or fingertip blood.

Rapid and Accurate CRP Quantification

Designed for immediate use in clinical environments, the Acon FIAflex CRP FIA Test offers real-time, quantitative results within 3 minutes. Its high sensitivity fluorescence immunoassay technology allows healthcare professionals to obtain crucial diagnostic data promptly, optimizing patient management and care.

Flexible Sample and Easy Handling

This test kit is compatible with serum, plasma, and whole blood samples, requiring just a minimal 10 L volume. All materials are user-friendly, enabling straightforward preparation and analysis. The included manual provides step-by-step instructions for seamless test execution.

Comprehensive Packaging and Safe Storage

Each kit, containing 25 tests (or customized quantity), features clearly marked batch numbers and expiry dates. Designed with convenient and safe storage in mind, tests should be kept at 2-30C and away from sunlight to ensure their 18-month shelf life is maintained.

FAQ's of Acon FIAflex CRP FIA Test:

Q: How do I use the Acon FIAflex CRP FIA Test kit?

A: Begin by collecting a 10 L sample of serum, plasma, or whole blood. Follow the instructions in the included user manual to prepare the sample and apply it to the test device. Insert the cartridge into a compatible FIAflex Analyzer to obtain quantitative CRP results in about 3 minutes.

Q: What types of samples can be tested with this kit?

A: The kit is validated for use with serum, plasma, or whole blood, providing flexibility for various clinical and point-of-care settings.

Q: When should the CRP test be performed?

A: The test is suitable when rapid CRP quantification is needed for diagnostic assessments, particularly in acute infection, inflammation, or to monitor treatment effectiveness.

Q: Where can this test be used?

A: This kit is designed for use in diagnostic laboratories and point-of-care environments. Its portability and ease of use make it suitable for clinical settings, urgent care, and physician offices.

Q: What is the process for obtaining results with this kit?

A: After sample application to the test cartridge, the device is run in the automated FIAflex Analyzer. Results, measured via fluorescence detection, are digitally displayed in about 3 minutes, ensuring rapid decision-making.

Q: What are the benefits of using the Acon FIAflex CRP FIA Test?

A: Key benefits include rapid turnaround, high sensitivity and accuracy, low sample requirement, and user-friendly handling. The kit's portability and compatibility with automated analyzers streamline workflow for healthcare professionals.

Q: How should the kit be stored for maximum shelf life?

A: Store the kit at temperatures between 2-30C, ensuring it is kept away from direct sunlight. Proper storage maintains the kit's quality and extends its shelf life up to 18 months.

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