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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/2019/000016_d48047f9578cff055c32f1e8aca0818e_1533f58d9bebca88512e1e4e0fec09d9. The license holder is Genuine Biosystem Private Limited, 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.

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CDSCO Registered
Class Class D
HBsAg Rapid Test
UID: MFG/IVD/2019/000016_d48047f9578cff055c32f1e8aca0818e_1533f58d9bebca88512e1e4e0fec09d9

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

A HBsAg Rapid Test is a medical device, intended for the detection of HBsAg in blood/body fluids

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