Resin Modified Glass Ionomer - ANVISA Registration 80230400081

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 80230400081 and manufactured by VOCO GMBH. The registration is held by VOCO DO BRASIL 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 BIODINAMICA QUIMICA E FARMACEUTICA LTDA, VOCO GMBH, 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.