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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.

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CDSCO Registered
Class Class B
Progesterone ELISA
UID: IMP/IVD/2019/000380_0d1c1807257e19e8cbbf5b8d2999a226_8bae93f3d845d7ddf0017fb43c699542

Brand Name

ERBALisa IgE

Device Class

Class B

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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