Resin Modified Glass Ionomer - ANVISA Registration 10298559031

Access comprehensive regulatory information for Resin Modified Glass Ionomer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10298559031 and manufactured by BIODINAMICA QUIMICA E FARMACEUTICA LTDA. The registration is held by BIODINAMICA QUIMICA E FARMACEUTICA 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 VOCO GMBH, BIODINAMICA QUIMICA E FARMACEUTICA 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.