Polypectomy Snare - ANVISA Registration 10334780042

Access comprehensive regulatory information for Polypectomy Snare in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10334780042 and manufactured by G-FLEX EUROPE SPRL. The registration is held by G.F.E. DO BRASIL LTDA. with validity until Jul 11, 2026.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including United States Endoscopy Group, Inc. (US Endoscopy), JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD., 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.