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Dengue IgG & IgM Antibody Rapid Test Kit - India CDSCO Medical Device Registration

Dengue IgG & IgM Antibody Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000091_85a8fa5c66f899fc25b588b30176d8a1_eff84f35c0ecd81832a251cbc5f6b9a0. This device is marketed under the brand name GeneBio. The license holder is GeneBio Healthare Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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 B
Dengue IgG & IgM Antibody Rapid Test Kit
UID: MFG/IVD/2023/000091_85a8fa5c66f899fc25b588b30176d8a1_eff84f35c0ecd81832a251cbc5f6b9a0

Brand Name

GeneBio

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

GeneBio Dengue IgG & IgM Antibody Rapid Test Kit is indirect lateral flow chromatographic immunoassay for the qualitative detection of antibodies (GeneBio) against Dengue Virus infection in human serum, plasma, or whole blood.

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