FSH - India CDSCO Medical Device Registration
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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Brand Name
HUBI TSH
License Holder
MPRS Biological Private LimitedDevice Class
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
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