Malaria Antigen Rapid Test Device(BioSci true-detect Malaria Antigen Test) - India CDSCO Medical Device Registration

Malaria Antigen Rapid Test Device(BioSci true-detect Malaria Antigen Test) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000041_3f791d795474200814618ea3db29be1a_acb3d99064b8911eefbce140a9a94e23. 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.

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CDSCO Registered

Class Class C

Malaria Antigen Rapid Test Device(BioSci true-detect Malaria Antigen Test)

UID: MFG/IVD/2021/000041_3f791d795474200814618ea3db29be1a_acb3d99064b8911eefbce140a9a94e23

Brand Name

Pv/Pf

License Holder

BIOSCI HEALTH CARE

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Malaria Antigen (Pv/Pf) Rapid Test Device is a rapid lateral flow through immunochromatographic test for the qualitative detection of two kinds of circulating antigens of plasmodium. vivax (Pv/Pf) and plasmodium falciparum (Pv/Pf) & in human whole blood