Pure Global

HIV Rapid Kit - India CDSCO Medical Device Registration

HIV Rapid Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000045_4be19d46d7bc299b9620efa5a43769e2_6263f070e298b809a0849241970a5113. This device is marketed under the brand name IgG and IgM. The license holder is Promea Therapeutics Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO, Zonal office, Hyderabad.

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 D
HIV Rapid Kit
UID: MFG/IVD/2022/000045_4be19d46d7bc299b9620efa5a43769e2_6263f070e298b809a0849241970a5113

Brand Name

IgG and IgM

Device Class

Class D

Approving Authority

CDSCO, Zonal office, Hyderabad

Product Information

HIV1/2 rapid test PROFLOW is immuno- chromatography test used for the detection of HIV antibody from human plasma/serum

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing