FMD ANTIBODY RAPID TEST - India CDSCO Medical Device Registration

FMD ANTIBODY RAPID TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000082_fcf115ba5af2710ad5e1bb1a08a8ccb9_e43e3752b25bdf0e56d9860453e3fe96. This device is marketed under the brand name BIOGENIX. The license holder is Biogenix Inc. Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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CDSCO Registered

Class Class B

FMD ANTIBODY RAPID TEST

UID: MFG/IVD/2020/000082_fcf115ba5af2710ad5e1bb1a08a8ccb9_e43e3752b25bdf0e56d9860453e3fe96

Brand Name

BIOGENIX

License Holder

Biogenix Inc. Pvt. Ltd.

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

FMD Antibody Rapid Detection Test is a lateral flow Immuno chromatographic assay for the qualitative detection of FMD Specific antigen n Whole blood/Serum or plasma. It is intended to be used as a screening test and as an aid in the diagnosis of infection with FMD virus. Any reactive specimen with the FMD Ab Rapid Detection Test must be confirmed with alternative testing method(BIOGENIX) and clinical findings

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FT3 CLIA Test Reagent Kit

Brand: BIOGENIX

Biogenix Inc. Pvt. Ltd.

FMD ANTIBODY RAPID TEST - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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