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ADI Lyse - India CDSCO Medical Device Registration

ADI Lyse is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000034_e99f9483f6c67459a09849ff4ae635de_08fba828f932a91fd981c2b6f526b5f0. This device is marketed under the brand name GPO-PAP. The license holder is ADI Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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
ADI Lyse
UID: MFG/IVD/2019/000034_e99f9483f6c67459a09849ff4ae635de_08fba828f932a91fd981c2b6f526b5f0

Brand Name

GPO-PAP

Device Class

Class B

Approving Authority

Telangana

Product Information

quantitative detection of white blood cells number in whole blood and hemoglobin concentration

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