Progesterone ELISA - India CDSCO Medical Device Registration
Progesterone ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000380_0d1c1807257e19e8cbbf5b8d2999a226_8bae93f3d845d7ddf0017fb43c699542. This device is marketed under the brand name ERBALisa IgE. The license holder is M/s.Transasia Bio-Medicals Ltd., 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
ERBALisa IgE
License Holder
M/s.Transasia Bio-Medicals Ltd.Device Class
Approving Authority
CDSCO
Product Information
The Progesterone ELISA Kit is intended for the quantitative measurement of Progesterone in human serum or plasma
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