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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/2022/000056_d48047f9578cff055c32f1e8aca0818e_ccb92acff6df631f76865ae5662a08a6. The license holder is Biotrol Laboratories Pvt. Ltd., 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
UID: MFG/IVD/2022/000056_d48047f9578cff055c32f1e8aca0818e_ccb92acff6df631f76865ae5662a08a6

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

HBsAg test is a rapid self-performing, qualitative determination of Hepatitis B Virus in human blood as an aid for in vitro diagnosis.

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