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S.typhi IgG/IgM Ab Test - India CDSCO Medical Device Registration

S.typhi IgG/IgM Ab Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000145_2777372b75d6f5343ddb55a0a8d047ba_2b1c1baf486cf14ab7cfa8c58c5b2503. This device is marketed under the brand name SickleCatchโ„ข. The license holder is Mylab Discovery Solutions Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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CDSCO Registered
Class Class B
S.typhi IgG/IgM Ab Test
UID: MFG/IVD/2023/000145_2777372b75d6f5343ddb55a0a8d047ba_2b1c1baf486cf14ab7cfa8c58c5b2503

Brand Name

SickleCatchโ„ข

Device Class

Class B

Approving Authority

Kokan Division

Product Information

The of S.typhi IgG/IgM Ab test card is used as rapid visual test for simultaneous and differential detection of IgG & IgM antibodies to specific S. typhi antigens in whole blood /serum of humans in human specimens

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