SODIUM - ANVISA Registration 80615950244

Access comprehensive regulatory information for SODIUM in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80615950244 and manufactured by SPINREACT,S.A./S.A.U.. The registration is held by Diagmaster Científica ltda with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including LABTEST DIAGNOSTICA S/A, BIOTECNICA INDUSTRIA E COMERCIO 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.