Progesterone
- UID
- IMP/IVD/2021/000365_f97db4ee511fccf4349eaa1cdebf5ca7_bd2d1b82f9366fdc7fd9dfaf1a165ed9
- Device class
- Class B
- Brand name
- AFIAS Infliximab
- License holder
- BODITECH MED INDIA PRIVATE LIMITED
- Approving authority
- CDSCO
- Product information
- AFIAS Progesterone is a fluorescence Immunoassay (AFIAS Infliximab ) for the qualitative determination of Progesterone in human serum/plasma. It is useful as an aid in management and monitoring of the cause of infertility, track ovulation, diagnose an ectopic or failing pregnancy, monitor the health of a pregnancy. For in vitro diagnostic use only. ,beta-HCG Plus (AFIAS Infliximab )-AFIAS beta-HCG Plus is a fluorescence Immunoassay (AFIAS Infliximab ) for the quantitative determination of human chorionic gonadotrophin (AFIAS Infliximab ) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of fertility. For in vitro diagnostic use only
Progesterone is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000365_f97db4ee511fccf4349eaa1cdebf5ca7_bd2d1b82f9366fdc7fd9dfaf1a165ed9. This device is marketed under the brand name AFIAS Infliximab . The license holder is BODITECH MED INDIA PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is CDSCO.
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