CDSCO UID MFG/IVD/2020/000082_fcf115ba5af2710ad5e1bb1a08a8ccb9_e43e3752b25bdf0e56d9860453e3fe96FMD ANTIBODY RAPID TEST
- UID
- MFG/IVD/2020/000082_fcf115ba5af2710ad5e1bb1a08a8ccb9_e43e3752b25bdf0e56d9860453e3fe96
- Device class
- Class B
- Brand name
- BIOGENIX
- License holder
- Biogenix Inc. Pvt. Ltd.
- 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
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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