HCV ELISA kit - India CDSCO Medical Device Registration

HCV ELISA kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_8cce71abc9b9dd5a6571726fac1895a2_89a7788aa80ce17b195c17a7f4bf89e4. 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.

Free Database

CDSCO Registered

Class Class D

HCV ELISA kit

UID: MFG/IVD/2020/000053_8cce71abc9b9dd5a6571726fac1895a2_89a7788aa80ce17b195c17a7f4bf89e4

Brand Name

HBsAg ELISA Kit, Labsystems Diagnostics

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

HCV ELISA Kit for in vitro diagnostics qualitative immunoassay for the detection of antibodies against HCV (HBsAg ELISA Kit, Labsystems Diagnostics ) in human serum or plasma. The kit is basically intended to screen blood donation samples to identify and eliminate the infected units of blood and for clinical diagnostic testing