Pure Global

Hepatitis-B Rapid Card Test - India CDSCO Medical Device Registration

Hepatitis-B Rapid Card Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000133_6856fba37c88630db9bfbf1d6c203a40_3325fd589d5fa6885775c455f97e9327. This device is marketed under the brand name Lateral Flow. The license holder is M/s Avantor Performance Materials India Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO -North Zone, Ghaziabad.

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
Hepatitis-B Rapid Card Test
UID: MFG/IVD/2023/000133_6856fba37c88630db9bfbf1d6c203a40_3325fd589d5fa6885775c455f97e9327

Brand Name

Lateral Flow

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

Rapid card test for detection of hepatitis-B surface antigen in human serum and plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing