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Semen Analysis System, X12 PRO - India CDSCO Medical Device Registration

Semen Analysis System, X12 PRO is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000153_1f39587100c7ce57ce83b7670a301b2d_a525fcc93dcf4d42e5a53b97ce3bc5cb. This device is marketed under the brand name LensHooke™. The license holder is Advy Chemical Private Limited, and it is classified as Device Class Class A. 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 A
Semen Analysis System, X12 PRO
UID: IMP/IVD/2023/000153_1f39587100c7ce57ce83b7670a301b2d_a525fcc93dcf4d42e5a53b97ce3bc5cb

Brand Name

LensHooke™

Device Class

Class A

Approving Authority

CDSCO

Product Information

For human semen analysis which provides direct and calculated quantitative measurement for Sperm DFI (LensHooke™)

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