Progesterone Test - India CDSCO Medical Device Registration
Progesterone Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000103_943d0ff03a9779731dea9beb14c62011_222393448865551414fa579015270b01. The license holder is Genovik Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Rajasthan.
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License Holder
Genovik Biotech Pvt. Ltd.Device Class
Approving Authority
Rajasthan
Product Information
Progesterone is applicable to the quantitative detection of the concentration of Progesterone in human serum or plasma
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