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Typhoid Antigen Rapid Test Device - India CDSCO Medical Device Registration

Typhoid Antigen Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000016_e0b9d8c7866d261ad66700e5c23272da_4da6b184147eb428378a13f1fbb9d2df. 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
Typhoid Antigen Rapid Test Device
UID: MFG/IVD/2020/000016_e0b9d8c7866d261ad66700e5c23272da_4da6b184147eb428378a13f1fbb9d2df

Brand Name

CRP

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

First View Typhoid Antigen Rapid test is a rapid self-performing, qualitative determination of Typhoid Antigen in human Serum as an aid for in vitro diagnosis of malaria infection.

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