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Dengue NS1 Ag Rapid Test Device - India CDSCO Medical Device Registration

Dengue NS1 Ag Rapid Test Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000099_d85ad15e9f044930c9d921fdb9225d2f_f7198081e8bd20178db23c30a9518edf. The license holder is SR Bioera 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
Dengue NS1 Ag Rapid Test Device
UID: MFG/IVD/2023/000099_d85ad15e9f044930c9d921fdb9225d2f_f7198081e8bd20178db23c30a9518edf

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Dengue NS1 Antigen Rapid Test is a lateral flow immunochromatographic test for the qualitative detection of dengue NS1 antigen in human serum/ plasma/whole blood specimen

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