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HBsAg ELISA Kit - India CDSCO Medical Device Registration

HBsAg ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_f3f23a888627c4d3ca02f0f5e0c95fd8_1e1c8959992c2677a50038f61928a1b0. This device is marketed under the brand name Rapid Plasma Reagin. The license holder is Voxtur Bio Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, West 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 ELISA Kit
UID: MFG/IVD/2022/000085_f3f23a888627c4d3ca02f0f5e0c95fd8_1e1c8959992c2677a50038f61928a1b0

Brand Name

Rapid Plasma Reagin

License Holder

Voxtur Bio Ltd

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

ELISA- Enzyme Linked Immunosorbent Assay kit for the detection of Antigens to HBsAg in Human Serum/Plasma

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