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MR Serum Standard - India CDSCO Medical Device Registration

MR Serum Standard is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000357_eefd83294a679ab091739d792fd47da5_0402ae0b72d68728e9ed90b30141f6d0. This device is marketed under the brand name VOX Method. The license holder is M/s. Golden Harvest Industries, 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
MR Serum Standard
UID: IMP/IVD/2019/000357_eefd83294a679ab091739d792fd47da5_0402ae0b72d68728e9ed90b30141f6d0

Brand Name

VOX Method

Device Class

Class B

Approving Authority

CDSCO

Product Information

MR Serum Standard is intended for use as calibrator for in vitro testing for the quantitative determination of sodium, potassium, and chloride concentration in serum and plasma sample on ion-selective electrode on ISE Modules on BS series automatic chemistry analyzers). Before carrying out clinical practice, parameters of the chemistry analyzer need to be calibrated as instructed in instrument manual

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