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Diagnostic Kit for IgM/IgG Antibody to Coronavirus - India CDSCO Medical Device Registration

Diagnostic Kit for IgM/IgG Antibody to Coronavirus is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000351_57ce9ce0b764ee7140ef0baaad24c4e5_b22f07a9e6968eda7694be95954faa65. This device is marketed under the brand name SARS-CoV-2. The license holder is Renaissance Pharmaceuticals, 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
Diagnostic Kit for IgM/IgG Antibody to Coronavirus
UID: IMP/IVD/2020/000351_57ce9ce0b764ee7140ef0baaad24c4e5_b22f07a9e6968eda7694be95954faa65

Brand Name

SARS-CoV-2

Device Class

Class C

Approving Authority

CDSCO

Product Information

This product is used for in vitro qualitative detection of Coronavirus (SARS-CoV-2) IgM/IgG antibody in human serum, plasma and venous whole blood samples.

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