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Alinity i LH Reagent kit - India CDSCO Medical Device Registration

Alinity i LH Reagent kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000223_eeec7adac5a42c3051e7ac386b7c4bf5_a51c1f4bfff94027db79a5788b3e616e. The license holder is Abbott Healthcare 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
Alinity i LH Reagent kit
UID: IMP/MD/2018/000223_eeec7adac5a42c3051e7ac386b7c4bf5_a51c1f4bfff94027db79a5788b3e616e

Device Class

Class B

Approving Authority

CDSCO

Product Information

Used for the quantitative determination of human luteinizing hormone ##PLACEHOLDER_0## in human serum and plasma on the Alinity i analyzer

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