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H. Pylori antibody test - India CDSCO Medical Device Registration

H. Pylori antibody test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000107_eab9b89ba2a93e8e7f0e82ade20161b4_4c5dd3b62cc69378d1da0246b0156f82. This device is marketed under the brand name human Chorionic Gonadotropin. The license holder is M/s ASTAM DIAGNOSTICS PVT. LTD., and it is classified as Device Class Class B. The approving authority is Rajasthan.

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 test
UID: MFG/IVD/2020/000107_eab9b89ba2a93e8e7f0e82ade20161b4_4c5dd3b62cc69378d1da0246b0156f82

Brand Name

human Chorionic Gonadotropin

Device Class

Class B

Approving Authority

Rajasthan

Product Information

H.pylori test is a rapid, qualitative, sandwich immunoassay for simultaneous detection of total antibodies (human Chorionic Gonadotropin) to H. pylori in human serum / plasma / WB. For professional use only.

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