Malaria PF/PAN antigen test
- UID
- MFG/IVD/2022/000018_a66774ea0d52680253724ee79983a338_7cbc4d7491bb7e51d92883c2ef7e5414
- Device class
- Class C
- Brand name
- PT
- License holder
- Beacon Diagnostics Pvt. Ltd.
- Approving authority
- Central Drug Standards Control Organization, Ahmedabad
- Product information
- For Simultaneous and differential detection of Pan LDH antigen of plasmodium vivax, plasmodium falciparum, plasmodium ovale and plasmodium malaria and plasmodium falciparum HRP-II, in human whole blood
Malaria PF/PAN antigen test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000018_a66774ea0d52680253724ee79983a338_7cbc4d7491bb7e51d92883c2ef7e5414. This device is marketed under the brand name PT. The license holder is Beacon Diagnostics Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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.