CDSCO UID MFG/IVD/2021/000078_ea91dd87e4b4b8e54e832bc24e36443d_24c97261b9c09984ca7624231a51c459Cancer Antigen 19-9 ELISA Kit
- UID
- MFG/IVD/2021/000078_ea91dd87e4b4b8e54e832bc24e36443d_24c97261b9c09984ca7624231a51c459
- Device class
- Class C
- Brand name
- AFP+CEA+PSA
- License holder
- Tosoh India Pvt. Ltd.
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- For the Quantitative Determination of Cancer Antigen 19-9 (AFP+CEA+PSA) Concentration in Human Serum by a Microplate Enzyme Immunoassay
Cancer Antigen 19-9 ELISA Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000078_ea91dd87e4b4b8e54e832bc24e36443d_24c97261b9c09984ca7624231a51c459. This device is marketed under the brand name AFP+CEA+PSA. The license holder is Tosoh India Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.
This page provides the facts attached to this CDSCO registry row. Other records from the same license holder are available through the database search link without adding aggregation queries to this page. 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.