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FIAflex cTnI FIA Test 25T
FIAflex cTnI FIA Test 25T

FIAflex cTnI FIA Test 25T

Price 17450.0 INR/ Box

MOQ : 10 Boxes

FIAflex cTnI FIA Test 25T Specification

  • Material
  • Plastic cassette
  • Condition
  • New
  • Technology
  • Fluorescence Immunoassay (FIA)
  • Portable
  • Yes
  • Disposable
  • Yes
  • Wall Mounted
  • No
  • Measurement
  • Qualitative/Quantitative detection of cardiac Troponin I (cTnI)
  • Real-Time Operation
  • Yes
  • Operating Type
  • Manual
  • Size
  • Standard test strip size
  • Weight
  • Lightweight (single use device)
  • Color
  • White
  • Attributes
  • Single-use, fast result, easy to use, point-of-care test
  • Usage
  • Diagnostic use for detection of cTnI
  • Intended Use
  • Detection of cardiac Troponin I in whole blood, serum or plasma
  • Kit Contents
  • 25 test cassettes, buffer, instructions for use
  • Test Time
  • 10-15 minutes
  • Test Principle
  • Fluorescent immunoassay, lateral flow
  • Sensitivity
  • High clinical sensitivity for cTnI
  • Storage Condition
  • 2-30C (36-86F)
  • Sample Type
  • Whole blood/Serum/Plasma
  • Shelf Life
  • 12-24 months (refer to pack)
 
 

About FIAflex cTnI FIA Test 25T

The FIAflex cTnI FIA Test is a fluorescence immunoassay (FIA) used with an analyzer for the quantitative detection of cardiac Troponin I (cTnI) in blood samples. It is designed as an aid in diagnosing and monitoring acute myocardial infarction (AMI), also known as a heart attack.
The "25T" indicates that the kit contains 25 tests.
Key features
  • Quantitative results: The test provides a specific numerical value for the cTnI concentration in the sample, which is a significant clinical marker for cardiac injury.
  • Sample types: It can be used with human serum, plasma, or whole blood specimens.
  • Rapid testing: The test is designed to be completed quickly, often within 15 minutes, making it suitable for point-of-care settings and emergency departments.
  • High specificity: The test employs monoclonal antibodies that specifically target the cardiac troponin I antigen, leading to higher specificity compared to other cardiac markers.


Rapid and Accurate Cardiac Marker Detection

The FIAflex cTnI FIA Test leverages fluorescence immunoassay technology to deliver highly sensitive detection of cardiac Troponin I, a critical marker for cardiac events. Its quick turnaround time ensures prompt diagnostic decisions, enhancing patient care and clinical workflow efficiency in both hospital and point-of-care environments.


User-Friendly Design and Application

This portable, manual test kit contains 25 disposable cassettes and all necessary materials for immediate use. Its intuitive procedure is suitable for healthcare professionals and enables testing directly from whole blood, serum, or plasma. Clear instructions and minimal handling requirements streamline the testing process.

FAQ's of FIAflex cTnI FIA Test 25T:


Q: How does the FIAflex cTnI FIA Test detect cardiac Troponin I in blood samples?

A: The test uses a fluorescence immunoassay principle combined with lateral flow technology to accurately measure cTnI levels in whole blood, serum, or plasma. This allows rapid, sensitive, and specific detection crucial for diagnosing cardiac events.

Q: What is the recommended process for using the FIAflex cTnI FIA Test?

A: To use the test, add the specified amount of whole blood, serum, or plasma sample to the cassette, followed by the buffer. After a 10-15 minute development time, results are read using the supplied instructions, yielding either qualitative or quantitative information about cTnI levels.

Q: When should the FIAflex cTnI FIA Test be used?

A: This test should be utilized when acute myocardial infarction or cardiac injury is suspected, as rapid detection of cardiac Troponin I enables timely clinical intervention and patient management.

Q: Where can the FIAflex cTnI FIA Test be performed?

A: Due to its portability and ease of use, the test can be performed at the point of care, in clinics, emergency departments, or laboratory settings, providing flexibility for diverse clinical needs.

Q: What are the storage conditions and shelf life for this test kit?

A: The test should be stored at 2-30C (36-86F), and has a shelf life of 12 to 24 months, as indicated on the product packaging. Proper storage ensures optimal performance and reliability of results.

Q: What are the key benefits of using the FIAflex cTnI FIA Test?

A: Key benefits include rapid results within 10-15 minutes, high clinical sensitivity, ease of use, portability, and the ability to operate in real-time at the point-of-care, supporting swift diagnostic decision-making in acute settings.

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