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MAGNESIUM liquicolor - India CDSCO Medical Device Registration

MAGNESIUM liquicolor is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000206_d5965c3af04db7d6019e1317afbeee9a_85fe08910dbadb9ffa315a78bdb6c5f6. The license holder is Stedman Pharmaceuticals 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
MAGNESIUM liquicolor
UID: IMP/IVD/2019/000206_d5965c3af04db7d6019e1317afbeee9a_85fe08910dbadb9ffa315a78bdb6c5f6

Device Class

Class B

Approving Authority

CDSCO

Product Information

Photometric Colorimetric Test for Magnesium with Lipid Clearing Factor ##PLACEHOLDER_0##

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