SILICONE GEL IN TUBE - ANVISA Registration 82130519022

Access comprehensive regulatory information for SILICONE GEL IN TUBE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 82130519022 and manufactured by ITS DO BRASIL INDUSTRIA E COMÉRCIO DE PRODUTOS MÉDICOS LTDA. The registration is held by ITS DO BRASIL INDUSTRIA E COMÉRCIO DE PRODUTOS MÉDICOS 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 FRESCO INTERNATIONAL 2005, SA, EUROFARMA LABORATÓRIOS S.A, 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.