Acon FIAflex cTnI FIA Test

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Product Details:

Accuracy >97% (as per product claims)
Usage Type Diagnostic, professional use
Instruments Type Fluorescence Immunoassay Test Cassette
Features Rapid, sensitive, and quantitative detection; for use with FIA analyzer
Storage Instructions Store at 2-30C, keep away from direct sunlight
Measurement Range 0.150 ng/mL (quantitative range for cTnI detection)
Function Cardiac marker detection assay
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Acon FIAflex cTnI FIA Test Price And Quantity

Acon FIAflex cTnI FIA Test Product Specifications

Technology Fluorescence Immunoassay (FIA)
Measurement Range 0.150 ng/mL (quantitative range for cTnI detection)
Equipment Type In-Vitro Diagnostic Test Kit
Function Cardiac marker detection assay
Portable Yes
Usage Type Diagnostic, professional use
Display Type Requires external FIA analyzer (Results displayed on instrument)
Material Plastic, reagents, membrane strip
Shelf Life 18 months from date of manufacture
Color White, with color-coded labeling
Wall Mounted No
Condition New
Operating Type Automatic
Accuracy >97% (as per product claims)
Power Source Not Applicable (for test kit only)
Dimension (L*W*H) Test cassette ~75 mm x 25 mm (Approx.)
Instruments Type Fluorescence Immunoassay Test Cassette
Features Rapid, sensitive, and quantitative detection; for use with FIA analyzer
Real-Time Operation Yes
Use For quantitative detection of cardiac Troponin I (cTnI) in human whole blood, serum or plasma
Storage Instructions Store at 2-30C, keep away from direct sunlight
Weight Test cassette ~10g (Approx.)

Product Description

Brand Acon

Sample Type Serum/ Plasma/ WB

Pack Size 25T

CAT No F131-40111

Biomarker Cardiac

The cTnI FIA Test is a fluorescence immunoassay that is used with theFIAflex Fluorescent Immunoassay Analyzer for the quantitative detection ofcTnI in human serum, plasma and venous whole blood. It is useful as an aidin management and monitoring of acute myocardial infarction (AMI).

Rapid Detection for Cardiac Events

Designed for quick response situations, the Acon FIAflex cTnI FIA Test can quantitatively detect cardiac Troponin I from whole blood, serum, or plasma samples in just 15 minutes. This rapid turnaround is essential for acute cardiac care, enabling healthcare professionals to make timely treatment decisions and improve patient outcomes with confidence.

Simple Operation and Reliable Performance

Utilizing advanced fluorescence immunoassay technology, this test delivers highly sensitive results (>97% accuracy) without the need for extensive sample preparation. Each test cassette is individually packaged for easy handling and features built-in procedural controls to ensure reliability and consistency, supporting routine use in laboratories, clinics, or emergency settings.

Flexible Use and Storage Advantages

The FIAflex cTnI FIA Test is portable and operates in real time, requiring no external power source for the cassette. It remains stable for up to 18 months when stored at 2-30C and protected from direct sunlight, making it suitable for diverse storage and operational environments across healthcare facilities.

FAQ's of Acon FIAflex cTnI FIA Test:

Q: How is the Acon FIAflex cTnI FIA Test performed?

A: To perform the test, collect 80 L of whole blood, serum, or plasma, and apply it to the test cassette. Insert the cassette into the FIAflex Analyzer or a compatible fluorescence analyzer. The result will be displayed in approximately 15 minutes, providing a quantitative measurement of cTnI.

Q: What samples are compatible with this cardiac marker test?

A: This test can be used with human whole blood, serum, or plasma. The flexibility in sample type allows for use in various clinical settings, such as emergency rooms, laboratories, or outpatient clinics.

Q: When should I use the Acon FIAflex cTnI FIA Test?

A: It is recommended for use when rapid, reliable detection of cardiac Troponin I is required-such as when evaluating potential myocardial infarction or other acute cardiac events-in both emergency and routine diagnostic scenarios.

Q: Where can the FIAflex cTnI Test be used?

A: The test is intended for professional use in medical laboratories, emergency departments, clinics, and other healthcare facilities equipped with compatible fluorescence analyzers.

Q: What is the process for interpreting results?

A: Results from the test are read by the connected fluorescence analyzer, which displays the quantitative cTnI value. Interpretation is instrument-based for accuracy and standardization, minimizing subjective assessment.

Q: What are the benefits of using this FIA cTnI test kit?

A: Key benefits include rapid (15-minute) results, high sensitivity (0.1 ng/mL), ease of use with minimal sample volume, and excellent accuracy (>97%). The integrated controls and robust packaging ensure reliability and convenience for consistent cardiac marker assessment.

Q: How should the test kits be stored, and what is their shelf life?

A: Store the test kits at 2-30C away from direct sunlight. Each kit has a shelf life of 18 months from the date of manufacture, supporting effective inventory management in professional healthcare environments.

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