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Scrub Typhus Ab Rapid Test - India CDSCO Medical Device Registration

Scrub Typhus Ab Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000088_bdf5de7195099aedc506733495ea5668_097b612351c12b954fe3ffae21e6a2cb. 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.

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CDSCO Registered
Class Class B
Scrub Typhus Ab Rapid Test
UID: MFG/IVD/2022/000088_bdf5de7195099aedc506733495ea5668_097b612351c12b954fe3ffae21e6a2cb

Brand Name

HaemNest Sheath Fluid

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

The Scrub Typhus Ab Rapid Test (HaemNest Sheath Fluid) is a rapidchromatographic immunoassay for thequalitative detection of Ab antibody to ScrubTyphus in human's whole blood, serum orplasma specimen

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