Pure Global

Typhoid antibody test (Typhoid antibody test ) - India CDSCO Medical Device Registration

Typhoid antibody test (Typhoid antibody test ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000079_45bbff930dca9130dbf912044cf61557_2f72708b5d3afbeabc2f820ced00184e. This device is marketed under the brand name IgM/IgG. The license holder is Oscar Medicare Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Typhoid antibody test (Typhoid antibody test )
UID: MFG/IVD/2021/000079_45bbff930dca9130dbf912044cf61557_2f72708b5d3afbeabc2f820ced00184e

Brand Name

IgM/IgG

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

TYPHOID IgM / IgG TEST DEVICE is an in vitro diagnostic rapid test based on the principle of immunochromatography on a membrane for differential detection of IgM and IgG antibodies to Salmonella typhi (IgM/IgG) in human serum or plasma. For professional use only

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing