Mouth Gag - ANVISA Registration 10334780052

Access comprehensive regulatory information for Mouth Gag in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 10334780052 and manufactured by G-FLEX EUROPE SPRL. The registration is held by G.F.E. DO BRASIL 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 MAQUIRA INDÚSTRIA DE PRODUTOS ODONTOLÓGICOS S.A., PRISMA INSTRUMENTOS ODONTOLÓGICOS LTDA - ME, 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.