Resin Modified Glass Ionomer - ANVISA Registration 80432419025

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 80432419025 and manufactured by AAF DO BRASIL PRODUTOS ODONTOLOGICOS LTDA. The registration is held by AAF DO BRASIL PRODUTOS ODONTOLOGICOS 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 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.