Intra-aortic Balloon - ANVISA Registration 80120820024

Access comprehensive regulatory information for Intra-aortic Balloon in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80120820024 and manufactured by BALTON SP. ZO.O.. The registration is held by BIOLINE COMERCIAL LTDA with validity until May 31, 2035.

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