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Troponin I Rapid Test Device - India CDSCO Medical Device Registration

Troponin I Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000016_cd54ab87db1a14e5868436b08aa83c31_ace0b3dffedd1479a28acc0d9d89609f. This device is marketed under the brand name CRP. The license holder is BIOLINE DIAGNOSTICS LLP, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

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.

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CDSCO Registered
Class Class C
Troponin I Rapid Test Device
UID: MFG/IVD/2020/000016_cd54ab87db1a14e5868436b08aa83c31_ace0b3dffedd1479a28acc0d9d89609f

Brand Name

CRP

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Troponin I Rapid Test Device is a rapid one-step chromatographic immunoassay for the qualitative detection of human cardiac Troponin I in whole blood, serum or plasma as an aid in the determination of myocardial infarction (CRP)

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