Polypectomy Snare - ANVISA Registration 10259750034

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 10259750034 and manufactured by manufacturer not specified. The registration is held by STERIS SOLUTIONS DO BRASIL IMPORTACAO E COMERCIALIZACAO DE PRODUTOS DA SAUDE LTDA. with validity until Dec 12, 2026.

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