Endoscopic Forceps - ANVISA Registration 80475510189

Access comprehensive regulatory information for Endoscopic Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80475510189 and manufactured by E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME. The registration is held by E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME 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 RICHARD WOLF GMBH, E-MED PRODUTOS MÉDICO-HOSPITALARES 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.