CENTRIFUGAL PUMP FOR CARDIOPULMONARY BYPASS SYSTEM - ANVISA Registration 80102511251

Access comprehensive regulatory information for CENTRIFUGAL PUMP FOR CARDIOPULMONARY BYPASS 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 80102511251 and manufactured by LIVANOVA DEUTSCHLAND GMBH. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until May 12, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 3 companies making the same product including BRAILE BIOMEDICA INDUSTRIA COMERCIO E REPRESENTACOES LTDA, TERUMO CARDIOVASCULAR SYSTEM CORPORATION, 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.