SILICONE GEL IN TUBE - ANVISA Registration 80164799011

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 80164799011 and manufactured by EUROFARMA LABORATÓRIOS S.A. The registration is held by EUROFARMA LABORATORIOS S.A. 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, STRATPHARMA AG, 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.