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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/2022/000121_6336504f29cd0ee4960364059a3929a7_48274f14e7ceab724aaa27d84f714ce6. This device is marketed under the brand name MyBio. The license holder is Beacon Diagnostics Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Gujarat.

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/2022/000121_6336504f29cd0ee4960364059a3929a7_48274f14e7ceab724aaa27d84f714ce6

Brand Name

MyBio

Device Class

Class B

Approving Authority

Gujarat

Product Information

Lyse (MyBio)

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