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Rapid Test for detection of IgM and IgG Antibodies to S.Typhi Device - India CDSCO Medical Device Registration

Rapid Test for detection of IgM and IgG Antibodies to S.Typhi Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000091_41c3aaff3ba05727bb9768a8296e6475_c29f3b6d68227a41ce604b5b60d8e095. This device is marketed under the brand name DENGUCHECK WB Device. The license holder is VIOLA DIAGNOSTIC SYSTEMS - A DIVISION OF TULIP DIAGNOSTICS PRIVATE LIMITED,, and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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CDSCO Registered
Class Class B
Rapid Test for detection of IgM and IgG Antibodies to S.Typhi Device
UID: MFG/IVD/2021/000091_41c3aaff3ba05727bb9768a8296e6475_c29f3b6d68227a41ce604b5b60d8e095

Brand Name

DENGUCHECK WB Device

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

Rapid Qualitative Sandwich Immunoassay for the detection of IgM and IgG Antibodies to S.typhi in human serum, plasma or whole blood specimen

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