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H. pylori Antibody Rapid Test - India CDSCO Medical Device Registration

H. pylori Antibody Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000091_7caa6965d917ec52151d2f8b3d9ad5d5_ecf44203a71e0fd23a47ea2191dec92f. This device is marketed under the brand name GeneBio. The license holder is GeneBio Healthare Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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
H. pylori Antibody Rapid Test
UID: MFG/IVD/2023/000091_7caa6965d917ec52151d2f8b3d9ad5d5_ecf44203a71e0fd23a47ea2191dec92f

Brand Name

GeneBio

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

H. Pylori Antibody Rapid Test is a sandwich lateral flow chromatographic immunoassay for the qualitative detection of antibodies (GeneBio) against Helicobacter pylori (GeneBio) in human serum, plasma or whole blood

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