PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 10341350478

Access comprehensive regulatory information for PERIPHERAL ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10341350478 and manufactured by BOSTON SCIENTIFIC CORPORATION. The registration is held by BOSTON SCIENTIFIC DO BRASIL LTDA with validity until currently active (VIGENTE).

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 BROSMED MEDICAL CO., LTD, SCITECH PRODUTOS MEDICOS SA, 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.