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Creatinine Enzymatic - India CDSCO Medical Device Registration

Creatinine Enzymatic is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000348_8b1e65a1fc0b23fbb8dbc628391f4bd6_80145bdc4488d84a58084dba479f766a. This device is marketed under the brand name QuantILab. The license holder is Instrumentation Laboratory 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
Creatinine Enzymatic
UID: IMP/IVD/2019/000348_8b1e65a1fc0b23fbb8dbc628391f4bd6_80145bdc4488d84a58084dba479f766a

Brand Name

QuantILab

Device Class

Class B

Approving Authority

CDSCO

Product Information

Creatinine Enzymatic is intended for the quantitative in vitro diagnostic determination of creatinine in human serum, plasma and urine using the ILab Chemistry System

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