Chemiluminescence Assay for the Detection of Antibodies to Hepatitis C Virus in Human Serum or Plasma.
- UID
- MFG/IVD/2021/000113_3adc8d1953a9b92bb5e8f805dd77f111_3188e4e355e1b6e7e0f7b76e1d7dc4cd
- Device class
- Class D
- Brand name
- Device
- Approving authority
- Sub Zonal Goa
- Product information
- ELECTRA HCV Ab CLIA is intended to be used for the detection of antibodies to Hepatitis C Virus in Human Serum or Plasma
Chemiluminescence Assay for the Detection of Antibodies to Hepatitis C Virus in Human Serum or Plasma. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000113_3adc8d1953a9b92bb5e8f805dd77f111_3188e4e355e1b6e7e0f7b76e1d7dc4cd. This device is marketed under the brand name Device. The license holder is QUALPRO DIAGNOSTICS A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class D. The approving authority is Sub Zonal Goa.
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.