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Malaria Pf/Pv Antigen Rapid Test Device - India CDSCO Medical Device Registration

Malaria Pf/Pv Antigen Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000016_5bde4e9e30372a4820fffc2b09385753_c3c7e12a57738df88692d7cb3f03b450. This device is marketed under the brand name CRP. The license holder is BIOLINE DIAGNOSTICS LLP, and it is classified as Device Class Class C. The approving authority is CDSCO -North Zone, Ghaziabad.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
Malaria Pf/Pv Antigen Rapid Test Device
UID: MFG/IVD/2020/000016_5bde4e9e30372a4820fffc2b09385753_c3c7e12a57738df88692d7cb3f03b450

Brand Name

CRP

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

FirstView Malaria Pf/Pv Antigen test is a rapid self-performing, qualitative determination of malaria antigen in human blood as an aid for in vitro diagnosis of malaria infection

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