SILICONE GEL IN TUBE - ANVISA Registration 82320590004

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 I medical device is registered under ANVISA number 82320590004 and manufactured by BIODERMIS CORPORATION. The registration is held by MEDISET IMPORTAÇÃO E COMÉRCIO DE MATERIAL HOSPITALAR 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 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.