NON-VASCULAR STENT (NOT CLASSIFIED AS BILIARY, BRONCHIAL, ESOPHAGEAL, PANCREATIC, URINARY AND VAGINAL) - ANVISA Registration 10306840187

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 10306840187 and manufactured by manufacturer not specified. The registration is held by PROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA with validity until Oct 26, 2030.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 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.