Polypectomy Snare - ANVISA Registration 80022069037

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 80022069037 and manufactured by FUJIFILM MEDWORK GMBH. The registration is held by FUJIFILM DO BRASIL 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), 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.