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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/2020/000053_9dd8df493249956bc5b51d16e5cb0969_f58cf2db92f4d9e915b3268be5d7eb5b. This device is marketed under the brand name HBsAg ELISA Kit, Labsystems Diagnostics . The license holder is Trivitron Healthcare Pvt. Ltd, 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/2020/000053_9dd8df493249956bc5b51d16e5cb0969_f58cf2db92f4d9e915b3268be5d7eb5b

Brand Name

HBsAg ELISA Kit, Labsystems Diagnostics

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Biocard HCV Rapid test is an immunochromatographic immunoassay for the qualitative detection of anti-Hepatitis C Virus antibodies (HBsAg ELISA Kit, Labsystems Diagnostics ) in human serum, plasma and Whole Blood.

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