Resin Modified Glass Ionomer - ANVISA Registration 10068879064

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 10068879064 and manufactured by VIGODENT INDUSTRIA E COMERCIO LTDA.. The registration is held by VIGODENT INDUSTRIA E COMERCIO 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.