Endoscopic Forceps - ANVISA Registration 81263810003

Access comprehensive regulatory information for Endoscopic Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81263810003 and manufactured by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS LTDA. The registration is held by G-FLEX AMÉRICA LATINA - INDÚSTRIA DE PRODUTOS MANUFATURADOS 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 E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, RICHARD WOLF GMBH, 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.