Dengue virus NS1 Antigen Rapid Test Device - India CDSCO Medical Device Registration

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.

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CDSCO Registered

Class Class C

Dengue virus NS1 Antigen Rapid Test Device

UID: MFG/IVD/2021/000041_4ab6d95df090043d35d8c2157bb7edca_d9831b9a66bc9a8fe6d57770bcdcfd3a

Brand Name

Pv/Pf

License Holder

BIOSCI HEALTH CARE

Device Class

Class C

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