cTnT Rapid Quantitative Test - India CDSCO Medical Device Registration

cTnT Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000074_6a0a97dd28a872a95fe3d51438fab72b_1f4aa661eabc6248774925e0ed2c8d5c. This device is marketed under the brand name Cardiac Troponin T. The license holder is FINOVA HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free Database

CDSCO Registered

Class Class C

cTnT Rapid Quantitative Test

UID: IMP/IVD/2022/000074_6a0a97dd28a872a95fe3d51438fab72b_1f4aa661eabc6248774925e0ed2c8d5c

Brand Name

Cardiac Troponin T

License Holder

FINOVA HEALTHCARE PRIVATE LIMITED

Device Class

Class C

Approving Authority

CDSCO

Product Information

The cTnT (Cardiac Troponin T) Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer (Cardiac Troponin T) is intended for vitro quantitative determination of Cardiac troponin T(Cardiac Troponin T) in human whole blood, serum or plasma. It is mainly used for auxiliary diagnosis of myocardial infarction