HIV 1/2 RAPID TEST KIT - India CDSCO Medical Device Registration

HIV 1/2 RAPID TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000053_cf6591e51af721614d16a033d73b4c39_a997d70af7a4f6af8e4a40adee886644. This device is marketed under the brand name HBsAg ELISA Kit, Labsystems Diagnostics . The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class D

HIV 1/2 RAPID TEST KIT

UID: MFG/IVD/2020/000053_cf6591e51af721614d16a033d73b4c39_a997d70af7a4f6af8e4a40adee886644

Brand Name

HBsAg ELISA Kit, Labsystems Diagnostics

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class D

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Biocard HIV 1/2 Rapid test is an immunochromatographic immunoassay for the qualitative simultaneous detection and differentiation of HIV-1 and HIV-2 antibodies (HBsAg ELISA Kit, Labsystems Diagnostics ) in human serum, plasma and whole blood