NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL) - ANVISA Registration 81040530050

Access comprehensive regulatory information for NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81040530050 and manufactured by TAEWOONG MEDICAL CO., LTD. The registration is held by PROSURGERY- IMPORTAÇÃO E COMÉRCIO DE MATERIAL CIRÚRGICO LTDA ME with validity until Nov 18, 2029.

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 M.I. TECH CO., LTD, MI TECH 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.