CDSCO UID MFG/IVD/2022/000045_35879e72979e5fa7451acfa9a5088a30_4d5c4ca019d683df2d88e3efcb1a9e31

Malaria Pan/Pf antigen rapid kit

Promea Therapeutics Private Limited·Device Class Class C·India CDSCO

Registration details

UID: MFG/IVD/2022/000045_35879e72979e5fa7451acfa9a5088a30_4d5c4ca019d683df2d88e3efcb1a9e31
Device class: Class C
License holder: Promea Therapeutics Private Limited
Approving authority: CDSCO, Zonal office, Hyderabad
Product information: Malaria Pan/Pf Ag Rapid Test is a lateral flow chromatographic immunoassay for the simultaneous detection and differentiation of Plasmodium falciparum ##PLACEHOLDER_0## antigen and P. vivax ##PLACEHOLDER_0##, P. ovale ##PLACEHOLDER_0##, or P. malaria ##PLACEHOLDER_0## antigen in human blood specimen. This device is intended to be used by professionals as a screening test and provides a preliminary test result to aid in the diagnosis of infection with plasmodium

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About this record

Malaria Pan/Pf antigen rapid kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000045_35879e72979e5fa7451acfa9a5088a30_4d5c4ca019d683df2d88e3efcb1a9e31. The license holder is Promea Therapeutics Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.

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