Pure Global

HAV IgG/IgM Rapid Test - India CDSCO Medical Device Registration

HAV IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000109_c9e9cea646184e2f01be3dcbb33480b2_3dec812f8f657c5b2d1347d964cba4e3. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is West Delhi Division.

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
HAV IgG/IgM Rapid Test
UID: MFG/IVD/2021/000109_c9e9cea646184e2f01be3dcbb33480b2_3dec812f8f657c5b2d1347d964cba4e3

Device Class

Class B

Approving Authority

West Delhi Division

Product Information

The HAV IgG/IgM Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection and differentiation of antibodies ##PLACEHOLDER_0## to hepatitis A virus ##PLACEHOLDER_0## in human serum, plasma or whole blood

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name or brand