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LYSE - India CDSCO Medical Device Registration

LYSE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000031_6336504f29cd0ee4960364059a3929a7_8d1f5d05c4c19213bcbb6fdb61fd3371. The license holder is Perfexn Chem Science Mfd Private Ltd, and it is classified as Device Class Class B. The approving authority is Nashik Division.

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
LYSE
UID: MFG/IVD/2020/000031_6336504f29cd0ee4960364059a3929a7_8d1f5d05c4c19213bcbb6fdb61fd3371

Device Class

Class B

Approving Authority

Nashik Division

Product Information

Estimation of Hemogl;obin and WBC counting on blood cell counter

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