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HCV Rapid Test - India CDSCO Medical Device Registration

HCV Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000056_20d6715f0cee5a1c5ccd80e1b50d178b_aca534745680d346d9f87f206dd7ce71. 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
HCV Rapid Test
UID: MFG/IVD/2022/000056_20d6715f0cee5a1c5ccd80e1b50d178b_aca534745680d346d9f87f206dd7ce71

Device Class

Class D

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The HCV Rapid Device Kit is a rapid and convenient immune chromatographic in vitro assay for detection of HCV Antibody in human serum, plasma. The test provides a visual, qualitative result, and all positive specimens are advised to be confirmed with other qualified assays

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