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Estradiol Fast Test Kit (E2 Fast Test Kit ) - India CDSCO Medical Device Registration

Estradiol Fast Test Kit (E2 Fast Test Kit ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001031_9d7a06b35fc9f6c12d239d2a848f2908_3ac8781f719ad47107bc18f96875bac3. This device is marketed under the brand name Getein. The license holder is M/s. Peerless Biotech Pvt. 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
Estradiol Fast Test Kit (E2 Fast Test Kit )
UID: IMP/IVD/2020/001031_9d7a06b35fc9f6c12d239d2a848f2908_3ac8781f719ad47107bc18f96875bac3

Brand Name

Getein

Device Class

Class B

Approving Authority

CDSCO

Product Information

Estradiol Fast Test Kit (Getein) is intended for in vitro quantitative determination of Estradiol in human serum, plasma samples. Estradiol tests are used to measure ovarian function. For professional and laboratory use

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