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Typhoid Rapid Test Ki - India CDSCO Medical Device Registration

Typhoid Rapid Test Ki is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000001_ee2bb694944499268457c5188a043ad7_d14bef988816d252e5645832587c8404. The license holder is M/S. MEDSOURCE OZONE BIOMEDICALS PVT LTD, and it is classified as Device Class Class B. The approving authority is Haryana.

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 B
Typhoid Rapid Test Ki
UID: MFG/IVD/2020/000001_ee2bb694944499268457c5188a043ad7_d14bef988816d252e5645832587c8404

Device Class

Class B

Approving Authority

Haryana

Product Information

Rapid immunochromatographic assay for qualitative detection and differentiation of IgG & IgM antibodies of Salmonella typhi and paratyphi in human serum/ plasma

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