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LIAISON® Analyzer - India CDSCO Medical Device Registration

LIAISON® Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000368_54c1975ca9f5de396972c7f4dd71bcad_946ad4f26ecbeddf737fd83947c36459. This device is marketed under the brand name LIAISON® Analyzer. The license holder is Diasorin Healthcare India Pvt. Ltd., 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
LIAISON® Analyzer
UID: IMP/IVD/2023/000368_54c1975ca9f5de396972c7f4dd71bcad_946ad4f26ecbeddf737fd83947c36459

Brand Name

LIAISON® Analyzer

Device Class

Class B

Approving Authority

CDSCO

Product Information

The LIAISON® Diagnostic System measures chemiluminescence. It is intended strictly for professional In-vitro-Diagnostic use. It is to be used only with Chemiluminescence Immunoassays, authorized by DiaSorin Italia S.p.A. for the LIAISON® Analyzer.

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