UREA - ANVISA Registration 80812770024

Access comprehensive regulatory information for UREA in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80812770024 and manufactured by ARKRAY FACTORY, INC.. The registration is held by MEX GLOBAL EQUIPAMENTOS PARA DIAGNÓSTICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including BIOSYSTEMS S.A., QUIBASA QUÍMICA BÁSICA LTDA, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.