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Hepatitis C virus – Rapid kit - India CDSCO Medical Device Registration

Hepatitis C virus – Rapid kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000009_9ecf374fd2e11d5188b164c246fdac5a_3626d7bd62e34f5655f4aceec1ee64cf. This device is marketed under the brand name RAPID. The license holder is Vimek Bioconcept Pvt 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
Hepatitis C virus – Rapid kit
UID: MFG/IVD/2022/000009_9ecf374fd2e11d5188b164c246fdac5a_3626d7bd62e34f5655f4aceec1ee64cf

Brand Name

RAPID

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

A Hepatitis C virus – (RAPID) test reagent/kit is medical device intended for the detection of Hepatitis C virus – (RAPID) in Blood/serum/Plasma/body fluids.

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