CORONARY ANGIOPLASTY BALLOON CATHETER - ANVISA Registration 81576620005

Access comprehensive regulatory information for CORONARY 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 81576620005 and manufactured by KANEKA CORPORATION. The registration is held by CORDIS MEDICAL BRASIL LTDA with validity until Jun 13, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including LEPU MEDICAL TECHNOLOGY (BEIJING) CO., LTD, BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH, 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.