Pure Global

HBsAg Test - India CDSCO Medical Device Registration

HBsAg Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000020_a268f09f892fb022038662fc97f389c8_49c7bf79b27088b787630c9b0a660354. The license holder is Koshbio Private Limited, and it is classified as Device Class Class D. The approving authority is Sub Zonal Baddi.

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
HBsAg Test
UID: MFG/IVD/2023/000020_a268f09f892fb022038662fc97f389c8_49c7bf79b27088b787630c9b0a660354

Device Class

Class D

Approving Authority

Sub Zonal Baddi

Product Information

HBsAg TEST is a rapid card test based upon immuno-chromatography principle for the qualitative detection of HBsAg (NA) in human specimen to an aid in the diagnosis of infection with Hepatitis B virus. For professional and in-vitro diagnostic use only

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