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

TYPHOID ANTIBODY TEST REAGENT FOR DETECTION OF ANTIBODIES TO WIDAL S.PARATYPHI BO is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000044_d5a86807aaf4e32ca5a83b87ae889bdc_34343d96f01af6f19dc31e8521b42e14. 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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Class Class B
TYPHOID ANTIBODY TEST REAGENT FOR DETECTION OF ANTIBODIES TO WIDAL S.PARATYPHI BO
UID: MFG/IVD/2019/000044_d5a86807aaf4e32ca5a83b87ae889bdc_34343d96f01af6f19dc31e8521b42e14

Brand Name

TULIP'S FEBRILE ANTIGEN SET

Device Class

Class B

Approving Authority

Goa

Product Information

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

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