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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/MD/2022/000072_6336504f29cd0ee4960364059a3929a7_4c95d9b61a6f1eb05ae16ef8e846994d. This device is marketed under the brand name CRP. The license holder is DELTA LAB, and it is classified as Device Class Class B. The approving authority is Kokan 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/MD/2022/000072_6336504f29cd0ee4960364059a3929a7_4c95d9b61a6f1eb05ae16ef8e846994d

Brand Name

CRP

License Holder

DELTA LAB

Device Class

Class B

Approving Authority

Kokan Division

Product Information

A Lyse reagent/kit is a IVD medical device used for lysing of cell for the estimation of complete blood count (CRP)

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