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ELECTROLYTE ANALYZER - India CDSCO Medical Device Registration

ELECTROLYTE ANALYZER is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000371_20984c662d5a0bf9dc12c8f56c2d33e2_93ffe7e355ae529795e7c61bcf2c7976. This device is marketed under the brand name BIOLYTE. The license holder is M/S. MEDSOURCE OZONE BIOMEDICALS PVT LTD, and it is classified as Device Class Class A. 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 A
ELECTROLYTE ANALYZER
UID: IMP/IVD/2019/000371_20984c662d5a0bf9dc12c8f56c2d33e2_93ffe7e355ae529795e7c61bcf2c7976

Brand Name

BIOLYTE

Device Class

Class A

Approving Authority

CDSCO

Product Information

The Biolyte 2000 is intended for in vitro diagnostic use by healthcare professionals in the quantitative determination of sodium, potassium, chloride, or lithium (BIOLYTE) in whole blood, serum, and plasma; sodium, potassium, and chloride in whole blood, serum, plasma, urine and CSF.

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