Acon FIAflex CK-MB FIA Test

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Product Details:

Storage Instructions Store at 2-30C, avoid light and moisture
Display Type Requires compatible fluorescence reader (Not included)
Shelf Life 18 months from manufacturing
Instruments Type Fluorescence Immunoassay System
Function Cardiac Marker Detection
Accuracy 99% (when used as directed)
Usage Type Single Use
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Acon FIAflex CK-MB FIA Test Price And Quantity

Acon FIAflex CK-MB FIA Test Product Specifications

Voltage 100-240V (if used with instrument)
Equipment Type FIAflex CK-MB FIA Test
Instruments Type Fluorescence Immunoassay System
Shelf Life 18 months from manufacturing
Display Type Requires compatible fluorescence reader (Not included)
Power Consumption Minimal, depends on instrument
Material Diagnostic-grade materials, plastic housing
Use CK-MB quantification in human serum or plasma
Storage Instructions Store at 2-30C, avoid light and moisture
Color White
Technology Fluorescent Immunoassay (FIA)
Features Rapid, sensitive, specific, easy to use
Operating Type Automatic
Real-Time Operation Yes
Power Source Battery or Adapter (depending on reader)
Accuracy 99% (when used as directed)
Portable Yes
Wall Mounted No
Weight Test Cassette: ~15 g
Function Cardiac Marker Detection
Dimension (L*W*H) Test Cassette: Approx. 90 x 20 x 6 mm
Condition New
Measurement Range 0.5 80 ng/mL
Usage Type Single Use
Noise Level Silent Operation

Pack Size 25 tests/kit
Reading Device Compatibility FIAflex Instrument or compatible FIA analyzers
Storage Temperature 2-30°C
Application Clinical diagnosis of acute myocardial infarction
Catalog Number CKMB-501
Principle Sandwich immunodetection
Packaging Individual foil pouches with desiccant
Test Time Approx. 15 minutes
Result Interpretation Quantitative via analyzer
Internal Control Integrated in cassette
Quality Control Included in kit
Sample Type Human serum/plasma
Limit of Detection (LOD) 0.5 ng/mL
CE Marked Yes

Product Description

Brand Acon

Sample Type Serum/ Plasma/ WB

Pack Size 25T

CAT No F131-40211

Biomarker Cardiac

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

Rapid and Quantitative Cardiac Marker Detection

The FIAflex CK-MB FIA Test offers swift and precise quantification of CK-MB, a critical cardiac marker for myocardial infarction. Results are available in about 15 minutes, supporting timely clinical decisions during emergencies. The test's quantitative output enhances diagnostic accuracy, aiding healthcare professionals in patient management.

Advanced Fluorescent Immunoassay Technology

Employing sensitive fluorescent immunoassay technology, this test ensures reliable and specific detection of CK-MB in human serum or plasma. Its sandwich immunodetection method increases specificity, while compatibility with FIAflex and compatible analyzers ensures seamless integration into existing diagnostic workflows.

Convenient and User-Friendly Design

Each test cassette is individually packed with desiccant, designed for single use, and includes integrated internal and quality controls for added assurance. The portable and silent-operating format, along with simple storage at 2-30C, make it ideal for both laboratory and field settings, supporting fast and efficient cardiac marker testing.

FAQ's of Acon FIAflex CK-MB FIA Test:

Q: How is the FIAflex CK-MB FIA Test performed?

A: To perform the FIAflex CK-MB FIA Test, collect human serum or plasma and dispense the sample onto the test cassette. Insert the cassette into a compatible FIAflex reader or similar fluorescence immunoassay analyzer. The instrument will automatically quantify CK-MB levels, providing results in approximately 15 minutes.

Q: What sample types are accepted for this test?

A: The FIAflex CK-MB FIA Test is validated for use with human serum or plasma samples only. It is not compatible with whole blood or other biological fluids.

Q: When should I use the FIAflex CK-MB FIA Test?

A: This test should be used when there is a clinical suspicion of acute myocardial infarction, such as new or worsening chest pain, or to monitor cardiac injury in hospital or emergency care settings.

Q: Where can I use the FIAflex CK-MB FIA Test kit?

A: The test is suitable for hospitals, clinics, emergency departments, and diagnostic laboratories equipped with a compatible fluorescence immunoassay analyzer, such as the FIAflex Instrument.

Q: What is the process for storing the FIAflex CK-MB FIA Test?

A: Store the sealed test cassettes at temperatures between 2C and 30C, protected from light and moisture. Proper storage ensures the kit's integrity throughout its 18-month shelf life.

Q: How do I interpret the test results?

A: Insert the used cassette into the compatible reader. The analyzer will display a quantitative CK-MB value. Results are interpreted according to clinical guidelines for CK-MB, aiding in the diagnosis of myocardial infarction.

Q: What are the benefits of using this CK-MB FIA Test?

A: The test offers rapid and highly accurate quantification of CK-MB, has a wide measuring range (0.5-80 ng/mL), integrates quality control, and is user-friendly. Its rapid turnaround facilitates timely clinical decisions in critical cardiac care.

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