H. Pylori antibody test
- UID
- MFG/IVD/2020/000107_eab9b89ba2a93e8e7f0e82ade20161b4_4c5dd3b62cc69378d1da0246b0156f82
- Device class
- Class B
- Brand name
- human Chorionic Gonadotropin
- License holder
- M/s ASTAM DIAGNOSTICS PVT. LTD.
- 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.
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.