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SCoV-2 IgM ELISA Kit - India CDSCO Medical Device Registration

SCoV-2 IgM ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000145_6ae80dabdee145375fd0b2348f78405b_480c25512abe1e82765eb0b53715b13c. This device is marketed under the brand name SCoV-2 DetectTM IgM ELISA. The license holder is SIRUS BIOCARE 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
SCoV-2 IgM ELISA Kit
UID: IMP/IVD/2019/000145_6ae80dabdee145375fd0b2348f78405b_480c25512abe1e82765eb0b53715b13c

Brand Name

SCoV-2 DetectTM IgM ELISA

Device Class

Class C

Approving Authority

CDSCO

Product Information

The SCoV-2 Detect™ IgM ELISA is an in vitro diagnostic test for the qualitative detection of IgM antibodies to SARS-CoV-2 in human serum

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