Light-Cured Composite Resin - ANVISA Registration 10346410114

Access comprehensive regulatory information for Light-Cured Composite Resin in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10346410114 and manufactured by DMG – CHEMISCH-PHARMAZEUTISCHE FABRIK GMBH. The registration is held by STERNGOLD 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 VIGODENT INDUSTRIA E COMERCIO 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.