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Typhoid Antibody Test reagent for the detection of antibodies to Widal S.Paratyphi CO - India CDSCO Medical Device Registration

Typhoid Antibody Test reagent for the detection of antibodies to Widal S.Paratyphi CO is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000044_d6a781cefa10e7c3febaa2f59d098c76_aa37fe8150ef48bff4db8f420461589f. 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 the detection of antibodies to Widal S.Paratyphi CO
UID: MFG/IVD/2019/000044_d6a781cefa10e7c3febaa2f59d098c76_aa37fe8150ef48bff4db8f420461589f

Brand Name

TULIP'S FEBRILE ANTIGEN SET

Device Class

Class B

Approving Authority

Goa

Product Information

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

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