Intra-Aortic Balloon Pump System - ANVISA Registration 80259110220

Access comprehensive regulatory information for Intra-Aortic Balloon Pump System in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80259110220 and manufactured by DATASCOPE CORP.. The registration is held by GETINGE DO BRASIL EQUIPAMENTOS MEDICOS LTDA. with validity until Dec 07, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search. 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.