PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 80202910112

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 80202910112 and manufactured by manufacturer not specified. The registration is held by TECMEDIC COMÉRCIO DE PRODUTOS MÉDICOS LTDA with validity until Jul 07, 2035.

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