SILICONE GEL IN TUBE - ANVISA Registration 81039450006

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 81039450006 and manufactured by FRESCO INTERNATIONAL 2005, SA. The registration is held by Ortolab Órtese e Prótese 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.