Sensit Salmonella Typhi /Paratyphi Test - India CDSCO Medical Device Registration

Sensit Salmonella Typhi /Paratyphi Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000095_9caba38a7e819edbdacc9c11f6f36e76_020c30ec87628d12805a0562be4191fe. This device is marketed under the brand name Sensit Rapid. The license holder is Ubio Biotechnology Systems Private Limited, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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CDSCO Registered

Class Class C

Sensit Salmonella Typhi /Paratyphi Test

UID: MFG/IVD/2020/000095_9caba38a7e819edbdacc9c11f6f36e76_020c30ec87628d12805a0562be4191fe

Brand Name

Sensit Rapid

License Holder

Ubio Biotechnology Systems Private Limited

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

Sensit Salmonella Typhi/Paratyphi Test is a rapid and convenient immunochromatographic assay for the qualitative detection of S.typhi and Paratyphi antigens in human fecal, whole blood, serum or plasma samples(Sensit Rapid). It is intended for professional use as an aid in the diagnosis of Salmonella Typhi and Paratyphi bacterial infection. This assay provides only a preliminary result. Clinical expertise and professional judgment should be sought to further evaluate the result of the test