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Test for Cardiac Troponin-I - India CDSCO Medical Device Registration

Test for Cardiac Troponin-I is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000203_53c8adc48de56f85f8476cafb86a4af9_d30b3ad63217835aa676d56231f1e219. This device is marketed under the brand name QDx Instacheck™ AFP. The license holder is DiaSys Diagnostics India 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.

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CDSCO Registered
Class Class C
Test for Cardiac Troponin-I
UID: IMP/MD/2018/000203_53c8adc48de56f85f8476cafb86a4af9_d30b3ad63217835aa676d56231f1e219

Brand Name

QDx Instacheck™ AFP

Device Class

Class C

Approving Authority

CDSCO

Product Information

QDx Instacheck™ Tn-I along with QDx Instacheck™ Reader is a fluorescence immunoassay that measures cardiac Troponin-I (QDx Instacheck™ AFP) concentration in human serum/plasma

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