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URIC ACID Reagent Test Kit - India CDSCO Medical Device Registration

URIC ACID Reagent Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000036_c412d1a5e38f1b33653d2aeca43c9d66_227e871316826a350f47064debbc871e. This device is marketed under the brand name SEDONA. The license holder is M/s STEDMAN PHARMACEUTICALS PVT. LTD., and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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 Reagent Test Kit
UID: MFG/IVD/2019/000036_c412d1a5e38f1b33653d2aeca43c9d66_227e871316826a350f47064debbc871e

Brand Name

SEDONA

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

Diagnostic reagent is intended for in vitro quantitative determination of Uric acid in human serum, plasma and Urine

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