Pure Global

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

Chikungunya IgG & IgM Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000091_8b89126f65a810afe03dace42240bf66_66e067f53b5a87e0427f9b11237381e5. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Chikungunya IgG & IgM Antibody Rapid Test
UID: MFG/IVD/2023/000091_8b89126f65a810afe03dace42240bf66_66e067f53b5a87e0427f9b11237381e5

Brand Name

GeneBio

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

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

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing