Typhoid IgM/IgG Antibody Rapid Test Kit - India CDSCO Medical Device Registration
Typhoid IgM/IgG Antibody Rapid Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000091_a17e8bb6bdd290a8d3ef98e6c1502e1a_a462807e8327d464f3b5240185a3a7f0. 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.
Brand Name
GeneBio
License Holder
GeneBio Healthare Pvt LtdDevice Class
Approving Authority
Uttar Pradesh
Product Information
GeneBio Typhoid IgM/IgG Antibody Rapid Test Kit is indirect lateral flow chromatographic immunoassay for the qualitative detection of antibodies (GeneBio) against S. typhi) in human serum, plasma, or whole blood
SARS-CoV-2 Antigen Rapid Test Kit
Brand: GeneBio
GeneBio Healthare Pvt Ltd
Chikungunya IgG & IgM Antibody Rapid Test
Brand: GeneBio
GeneBio Healthare Pvt Ltd
Dengue IgG & IgM Antibody Rapid Test Kit
Brand: GeneBio
GeneBio Healthare Pvt Ltd
GeneBio HCG Pregnancy Rapid
Brand: GeneBio
GeneBio Healthare Pvt Ltd
H. pylori Antibody Rapid Test
Brand: GeneBio
GeneBio Healthare Pvt Ltd
Viral Transport Media
Brand: GeneBio
GeneBio Healthcare Private Limited

