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Influenza A+B Rapid Test Kit - India CDSCO Medical Device Registration

Influenza A+B Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000123_8ccaaf0d4d139c95391c449106cd5fd9_ab07aab19ee2efb843b8df967490a531. The license holder is PARAMCARE LIFE SCIENCES PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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+B Rapid Test Kit
UID: MFG/IVD/2022/000123_8ccaaf0d4d139c95391c449106cd5fd9_ab07aab19ee2efb843b8df967490a531

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Influenza A+B Rapid Test Kit is a rapid test that aid in the qualitative detection and differentiation of Influenza A virus ##PLACEHOLDER_0##, and Influenza B in in nasopharyngeal swab or nasal aspirate specimens. The test utilizes a combination of anti-influenza A +B antibodies

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