Dengue virus NS1 Antigen Rapid Test Device
- UID
- MFG/IVD/2021/000041_4ab6d95df090043d35d8c2157bb7edca_d9831b9a66bc9a8fe6d57770bcdcfd3a
- Device class
- Class C
- Brand name
- Pv/Pf
- License holder
- BIOSCI HEALTH CARE
- Approving authority
- Central Drug Standards Control Organization, West Zone
- Product information
- Dengue virus NS1 Antigen Rapid Test Device is a rapid lateral flow through immunochromatographic test for the qualitative detection of dengue NS1 antigen in human serum/ plasma/ whole blood
Dengue virus NS1 Antigen Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000041_4ab6d95df090043d35d8c2157bb7edca_d9831b9a66bc9a8fe6d57770bcdcfd3a. This device is marketed under the brand name Pv/Pf. The license holder is BIOSCI HEALTH CARE, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West 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.