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HBsAg Rapid Test Device - India CDSCO Medical Device Registration

HBsAg Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000016_260cd2dad5ad5ace2d4ead4937aacc4c_95f71bedb5b1984ed1a58db94c43dfb3. This device is marketed under the brand name First View. The license holder is BIOLINE DIAGNOSTICS LLP, 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.

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CDSCO Registered
Class Class D
HBsAg Rapid Test Device
UID: MFG/IVD/2020/000016_260cd2dad5ad5ace2d4ead4937aacc4c_95f71bedb5b1984ed1a58db94c43dfb3

Brand Name

First View

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

HBsAg Rapid Test Device is rapid Chromatography Immunoassay for the qualitative detection of Hepatitis B Surface Antigen in serum and plasma

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