Pure Global

HIV - 1/2 Ab Rapid Diagnostic Test Kit - India CDSCO Medical Device Registration

HIV - 1/2 Ab Rapid Diagnostic Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000164_2e2d9228c2d8542c1cbd83d40c687d9d_ff0a4bea249ecbb02d820001aa5a18fd. This device is marketed under the brand name AccuTest HBsAg Rapid Diagnostic Test Kit. The license holder is Accurex Biomedical Pvt Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West Zone.

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 - 1/2 Ab Rapid Diagnostic Test Kit
UID: MFG/IVD/2022/000164_2e2d9228c2d8542c1cbd83d40c687d9d_ff0a4bea249ecbb02d820001aa5a18fd

Brand Name

AccuTest HBsAg Rapid Diagnostic Test Kit

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

AccuTest HIV- 1/2 AB intended to be used for qualitative in vitro diagnostic detection of antibodies against HIV-1 and HIV-2 in human serum/plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing