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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/2023/000046_c18246e2ad673151f2cd1eaa7c99fb84_9103eee4f60b4ca86ed6406676a51a09. This device is marketed under the brand name DSA. The license holder is M/s Avantor Performance Materials India Private Limited, and it is classified as Device Class Class B. The approving authority is Uttarakhand.

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/2023/000046_c18246e2ad673151f2cd1eaa7c99fb84_9103eee4f60b4ca86ed6406676a51a09

Brand Name

DSA

Device Class

Class B

Approving Authority

Uttarakhand

Product Information

For accurate count of WBCs, estimation of Hb and trimodal differential of WBCs

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