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HCV ELISA kit - India CDSCO Medical Device Registration

HCV ELISA kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_8cce71abc9b9dd5a6571726fac1895a2_0dfa915414669ed3749dd965d77b8208. 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
HCV ELISA kit
UID: MFG/IVD/2022/000085_8cce71abc9b9dd5a6571726fac1895a2_0dfa915414669ed3749dd965d77b8208

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 Antibodies to HCV(Rapid Plasma Reagin) in Human Serum/Plasma

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