Syphilis Ab Rapid Test - India CDSCO Medical Device Registration
Syphilis Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000155_599b32e873699a913259abc373b9d3fd_9380ee41dd1ba5a1459d7d93b07fb20e. This device is marketed under the brand name STERGIC. The license holder is Labgene Bio-tech Pvt. Ltd., and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.
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.
Brand Name
STERGIC
License Holder
Labgene Bio-tech Pvt. Ltd.Device Class
Approving Authority
Central Drug Standards Control Organization, Ahmedabad
Product Information
Syphilis Ab Rapid test kit is a rapid immunochromatography assay for the qualitative detection of antibodies against Treponema pallidum in human whole blood, serum or plasma samples
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