PERIPHERAL ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 81576620011

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 III medical device is registered under ANVISA number 81576620011 and manufactured by CORDIS US CORP.. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Jan 14, 2028.

This page provides complete technical specifications for 3 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.