Hs-CRP/CRP Rapid Quantitative Test - India CDSCO Medical Device Registration

Hs-CRP/CRP Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000074_44aac9670745b5beb3b7375099c443ac_3076858f56404c897bee826a77460d63. 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.

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CDSCO Registered

Class Class C

Hs-CRP/CRP Rapid Quantitative Test

UID: IMP/IVD/2022/000074_44aac9670745b5beb3b7375099c443ac_3076858f56404c897bee826a77460d63

Brand Name

Cardiac Troponin T

License Holder

FINOVA HEALTHCARE PRIVATE LIMITED

Device Class

Class C

Approving Authority

CDSCO

Product Information

The CRP (Cardiac Troponin T) Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer (Cardiac Troponin T) is intended for vitro quantitative determination of C- reactive protein (Cardiac Troponin T) in human whole blood, serum or plasma