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/2019/000191_15df4cccba92a9228178a9d9a83282cb_76178ff470f6d0ebbaa65f2c9084d81e. This device is marketed under the brand name Testosterone Rapid Quantitative Test. The license holder is Matrix Labs, and it is classified as Device Class Class B. The approving authority is CDSCO.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Brand Name
Testosterone Rapid Quantitative Test
License Holder
Matrix LabsDevice Class
Approving Authority
CDSCO
Product Information
Intended for quantitative measurement of follicle-stimulating hormone (Testosterone Rapid Quantitative Test) in humanwhole blood, serum or plasma. This test used as an aid to evaluate the ovarian functions in clinical
FSH
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FSH
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FSH
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TSH
Brand: Testosterone Rapid Quantitative Test
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HbA1c
Brand: Testosterone Rapid Quantitative Test
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PRL
Brand: Testosterone Rapid Quantitative Test
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CK-MB
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Sample Target Plate (Autobio )
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