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Novel Coronavirus IgM/IgG Antibody Test Kit - India CDSCO Medical Device Registration

Novel Coronavirus IgM/IgG Antibody Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000406_48a1f476756e87698df2cb361efebd60_8569b3c61e204f7a8387e410787b9210. This device is marketed under the brand name 2019-nCoV. The license holder is S A Diagnostics 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
Novel Coronavirus IgM/IgG Antibody Test Kit
UID: IMP/IVD/2020/000406_48a1f476756e87698df2cb361efebd60_8569b3c61e204f7a8387e410787b9210

Brand Name

2019-nCoV

Device Class

Class C

Approving Authority

CDSCO

Product Information

For in vitro qualitatively detecting novel coronavirus (2019-nCoV) IgM and IgG antibodies in human serum, plasma or whole blood.

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