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TYPHOID ANTIBODY TEST REAGENT FOR DETECTION OF ANTIBODIES TO WIDAL S.PARATYPHI AO - India CDSCO Medical Device Registration

TYPHOID ANTIBODY TEST REAGENT FOR DETECTION OF ANTIBODIES TO WIDAL S.PARATYPHI AO is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000044_ebc3caa3c139f84690708bc3578c523d_0746fb54eaa5edbcd49c7e1245694ecc. This device is marketed under the brand name TULIP'S FEBRILE ANTIGEN SET. The license holder is TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is Goa.

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CDSCO Registered
Class Class B
TYPHOID ANTIBODY TEST REAGENT FOR DETECTION OF ANTIBODIES TO WIDAL S.PARATYPHI AO
UID: MFG/IVD/2019/000044_ebc3caa3c139f84690708bc3578c523d_0746fb54eaa5edbcd49c7e1245694ecc

Brand Name

TULIP'S FEBRILE ANTIGEN SET

Device Class

Class B

Approving Authority

Goa

Product Information

Widal S.paratyphi โ€˜AOโ€™ is a slide and tube agglutination test for the detection of antibodies to S. paratyphi โ€˜AO' in the patientโ€™s serum, with paratyphoid fever

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