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Dengue NS1 ELISA - India CDSCO Medical Device Registration

Dengue NS1 ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000145_e90d4578a82ec4f40c8f2612a026df64_e70479e7085a607a5a81623db14d7079. 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
Dengue NS1 ELISA
UID: IMP/IVD/2019/000145_e90d4578a82ec4f40c8f2612a026df64_e70479e7085a607a5a81623db14d7079

Brand Name

SCoV-2 DetectTM IgM ELISA

Device Class

Class C

Approving Authority

CDSCO

Product Information

The DENV Detect NS1 ELISA is for the early detection of Dengue virus (SCoV-2 DetectTM IgM ELISA) NS1 antigen in human serum

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