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H. Pylori Ag Rapid Test - India CDSCO Medical Device Registration

H. Pylori Ag Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000056_e02bed17e7e95f1ace29df0c91c0ec47_33c41d3baf5e41ceb0f9ccdf29c40519. The license holder is Biotrol 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
H. Pylori Ag Rapid Test
UID: MFG/IVD/2022/000056_e02bed17e7e95f1ace29df0c91c0ec47_33c41d3baf5e41ceb0f9ccdf29c40519

Device Class

Class C

Approving Authority

CDSCO -North Zone, Ghaziabad

Product Information

The H. pylori Ag Rapid Test is a lateral flow chromatographic immunoassay for the qualitative detection of H. pylori antigen in human fecal specimen

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