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INFLUENZA-A ANTIGEN - India CDSCO Medical Device Registration

INFLUENZA-A ANTIGEN is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000075_f73ac9d121865c090caacef9626497d0_8aac5024f6c52137bdc3cbddcb1520e5. This device is marketed under the brand name RECOMBIGEN. The license holder is RECOMBIGEN LABORATORIES PVT. LTD, 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
INFLUENZA-A ANTIGEN
UID: MFG/MD/2020/000075_f73ac9d121865c090caacef9626497d0_8aac5024f6c52137bdc3cbddcb1520e5

Brand Name

RECOMBIGEN

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The Influenza A Antigen Test is a rapid chromatographic immunoassay for the qualitative detection of Influenza A antigens in nasal swab specimens. It is intended to aid in the rapid diagnosis of influenza A viral infections

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