Polypectomy Snare - ANVISA Registration 80050039012

Access comprehensive regulatory information for Polypectomy Snare in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80050039012 and manufactured by JIANGSU VEDKANG MEDICAL SCIENCE & TECHNOLOGY CO., LTD.. The registration is held by GASTRO COMÉRCIO E REPRESENTAÇÕES COMERCIAIS DE EQUIPAMENTOS MEDICO HOSPITALARES 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 United States Endoscopy Group, Inc. (US Endoscopy), FUJIFILM MEDWORK 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.