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HCV Rapid Test Device - India CDSCO Medical Device Registration

HCV Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000016_065521ea0892e33de8f29e4821ebdcb9_aca534745680d346d9f87f206dd7ce71. This device is marketed under the brand name First View. The license holder is BIOLINE DIAGNOSTICS LLP, 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 Device
UID: MFG/IVD/2020/000016_065521ea0892e33de8f29e4821ebdcb9_aca534745680d346d9f87f206dd7ce71

Brand Name

First View

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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