PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 10341350987

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 IV medical device is registered under ANVISA number 10341350987 and manufactured by HEMOTEQ AG. The registration is held by BOSTON SCIENTIFIC DO BRASIL LTDA with validity until Mar 01, 2031.

This page provides complete technical specifications for 3 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION, BROSMED MEDICAL 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.