Diagnostic Kit for Cardiac Troponin I (cTnI) (Time-resolved Fluorescence Immunochromatographic Assay)
Basic Information
- Primary DI
- 06974521000501
- Basic UDI-DI Code
- B-06974521000501
- Reference
- SUPF013025
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Shenzhen Superbio Technology Co.,Ltd.
Additional Description
This kit is suitable for in vitro quantitative detection of the concentration of Troponin I (cTnI) in human serum, plasma and whole blood. This product is used for testing in medical and health institutions for the auxiliary diagnosis of myocardial injury caused by acute myocardial infarction and other diseases. Troponin is composed of three subunits of troponin I, T and C, which, together with tropomyosin, regulate the interaction between actin and myosin by regulating the activity of Ca^2+ on rhabdomyactin ATPase. When myocardial injury, the cardiac troponin complex is released into the blood, and the increase can be detected in the blood after 4~6 hours. The elevated troponin I can remain in the blood for 6 to 10 days, providing a longe detection period. Cardiac calcitonin I (cTnI) has high specificity and sensitivity, so it has become an ideal marker of myocardial infarction (AMI).
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102160703 | TROPONIN I/T - RT & POC |
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