FSH
- UID
- IMP/IVD/2019/000091_15df4cccba92a9228178a9d9a83282cb_209b201983407350ef65e01090f7663b
- Device class
- Class B
- Brand name
- HUBI TSH
- License holder
- MPRS Biological Private Limited
- Approving authority
- CDSCO
- Product information
- HUBI FSH is an in-vitro diagnostic test based on immunochromatography. Te test is required to be applied to HUBI QUAN pro, an analyzer designed for quantitative determination of Follicle Stimulating Hormone (HUBI TSH) in human blood specimens
FSH is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000091_15df4cccba92a9228178a9d9a83282cb_209b201983407350ef65e01090f7663b. This device is marketed under the brand name HUBI TSH. The license holder is MPRS Biological Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.
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