Resin Modified Glass Ionomer - ANVISA Registration 82124109015

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 82124109015 and manufactured by DENTELINE INDÚSTRIA DE PRODUTOS ODONTOLÓGICOS LTDA. The registration is held by DENTELINE INDÚSTRIA DE PRODUTOS ODONTOLÓGICOS 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.