Malaria Pf/Pv Rapid test kit - India CDSCO Medical Device Registration

Malaria Pf/Pv Rapid test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_714d9608306a9caf2d833ef78bfd6b0f_5b6b674939b4929f3d897bc3a50796a5. This device is marketed under the brand name Immunoreactive Tripsinogen. The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class C

Malaria Pf/Pv Rapid test kit

UID: MFG/IVD/2020/000053_714d9608306a9caf2d833ef78bfd6b0f_5b6b674939b4929f3d897bc3a50796a5

Brand Name

Immunoreactive Tripsinogen

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Biocard® Malaria Pf/Pv Rapid test is an immunochromatographic assay for the qualitative detection of Plasmodium falciparum (Immunoreactive Tripsinogen) and Plasmodium vivax (Immunoreactive Tripsinogen) antigen in the human whole Blood specimen

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Neoscreen IRT EIA Kit

Brand: Immunoreactive Tripsinogen

Trivitron Healthcare Pvt. Ltd

Malaria Pf/Pv Rapid test kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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