HCV ELISA kit
- UID
- MFG/IVD/2020/000053_8cce71abc9b9dd5a6571726fac1895a2_89a7788aa80ce17b195c17a7f4bf89e4
- Device class
- Class D
- Brand name
- HBsAg ELISA Kit, Labsystems Diagnostics
- License holder
- Trivitron Healthcare Pvt. Ltd
- 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
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.