Salmonella Typhi IgG/IgM Rapid Test
- UID
- MFG/IVD/2022/000088_6aae35df0a85c99b251529b85d547efc_fca4a4577803ff0e174d473baa91b508
- Device class
- Class B
- Brand name
- HaemNest Sheath Fluid
- License holder
- Genenest Biotech Pvt. Ltd.
- Approving authority
- Uttar Pradesh
- Product information
- The Typhoid Rapid Test Cassette is a rapidchromatographic immunoassay for thesimultaneous detection and differentiation ofIgG and IgM types of antibodies againstSalmonella typhi (HaemNest Sheath Fluid) in human serum orplasma. It is intended to be used as ascreening test as an aid in the diagnosis ofinfection with S. typhi. Any reactive specimenwith the Typhoid rapid lest cassette needs tobe confirmed with alternative testing method
Salmonella Typhi IgG/IgM Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_6aae35df0a85c99b251529b85d547efc_fca4a4577803ff0e174d473baa91b508. This device is marketed under the brand name HaemNest Sheath Fluid. The license holder is Genenest Biotech 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.