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Rapid test for detection of Antigens to Malaria Plasmodium falciparum & Plasmodium Vivax in Human Whole Blood - India CDSCO Medical Device Registration

Rapid test for detection of Antigens to Malaria Plasmodium falciparum & Plasmodium Vivax in Human Whole Blood is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000085_aa5bb8f3a887ae59be44cc300357a4b7_c71d3e071aabdfb5f35cfda7aefa8e55. This device is marketed under the brand name C Reactive Protein. The license holder is Voxtur Bio Ltd, 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
Rapid test for detection of Antigens to Malaria Plasmodium falciparum & Plasmodium Vivax in Human Whole Blood
UID: MFG/IVD/2022/000085_aa5bb8f3a887ae59be44cc300357a4b7_c71d3e071aabdfb5f35cfda7aefa8e55

Brand Name

C Reactive Protein

License Holder

Voxtur Bio Ltd

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

For The Qualitative Assessment Of Plasmodium vivax And Plasmodium falciparum Antigen in Human Whole Blood sample

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