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Salmonella Typhi IgG/IgM Rapid Test - India CDSCO Medical Device Registration

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.

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CDSCO Registered
Class Class B
Salmonella Typhi IgG/IgM Rapid Test
UID: MFG/IVD/2022/000088_6aae35df0a85c99b251529b85d547efc_fca4a4577803ff0e174d473baa91b508

Brand Name

HaemNest Sheath Fluid

Device Class

Class B

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

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