Oestradiol ELISA - India CDSCO Medical Device Registration
Oestradiol ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000005_d8d08e748ca45123a9098e2b475f89ee_9105aa30f2e70ea428ee8a06db44ddde. This device is marketed under the brand name Pathozyme® Ultrasensitive TSH. The license holder is Omega DX (Asia) Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.
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Brand Name
Pathozyme® Ultrasensitive TSH
License Holder
Omega DX (Asia) Private LimitedDevice Class
Approving Authority
CDSCO
Product Information
Pathozyme® Oestradiol is an in-vitro diagnostic kit used for the quantitative determination of total Oestradiol (Pathozyme® Ultrasensitive TSH) in human serum or plasma
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