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HCV RAPID TEST KIT - India CDSCO Medical Device Registration

HCV RAPID TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000082_9dd8df493249956bc5b51d16e5cb0969_3b4f41dbe829a41d34d1da719fc25209. The license holder is PEERLESS BIOTECH 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
HCV RAPID TEST KIT
UID: MFG/IVD/2022/000082_9dd8df493249956bc5b51d16e5cb0969_3b4f41dbe829a41d34d1da719fc25209

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

The HCV Rapid Test Kit is a rapid chromatographic immunoassay for the qualitative detection of antibody to Hepatitis C Virus in whole blood, serum or plasma.

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