Pure Global

HBsAg Rapid Test - India CDSCO Medical Device Registration

HBsAg Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000055_d48047f9578cff055c32f1e8aca0818e_6178d5c870263eb51996850d0c309124. This device is marketed under the brand name LIFELINE. The license holder is Rapha Diagnostics Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South 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
HBsAg Rapid Test
UID: MFG/IVD/2021/000055_d48047f9578cff055c32f1e8aca0818e_6178d5c870263eb51996850d0c309124

Brand Name

LIFELINE

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

LIFELINE The HBsAg Rapid Test is a colloidal gold enhanced, rapid immunochromatographic assay for the qualitative detection of of hepatitis B surface antigen (LIFELINE) in serum or plasma

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from Rapha Diagnostics Pvt. Ltd.
Products from the same license holder (2 products)