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Uric acid kit - India CDSCO Medical Device Registration

Uric acid kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000018_677a581e12bf14ef7c9db797d7178d6d_7306707b23ee081f8b83c80fa268056b. This device is marketed under the brand name M-52 D diluent. The license holder is M/s Avantor Performance Materials India 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
Uric acid kit
UID: IMP/IVD/2018/000018_677a581e12bf14ef7c9db797d7178d6d_7306707b23ee081f8b83c80fa268056b

Brand Name

M-52 D diluent

Device Class

Class B

Approving Authority

CDSCO

Product Information

In vitro test for the quantitative determination of UA concentration in serum, plasma or urine on photometric systems

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