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LIPASE - India CDSCO Medical Device Registration

LIPASE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000040_da420ad455b311de7240696d109fe287_80ce07861005a216b4a48a5843dbf32a. This device is marketed under the brand name COULTER LH Series Pak Reagent Kit. The license holder is Beckman Coulter India Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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
LIPASE
UID: IMP/IVD/2019/000040_da420ad455b311de7240696d109fe287_80ce07861005a216b4a48a5843dbf32a

Brand Name

COULTER LH Series Pak Reagent Kit

Device Class

Class B

Approving Authority

CDSCO

Product Information

Kinetic colour test for the quantitative determination of lipase in human serum and plasma on AU Beckman Coulter analysers

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