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Abiomed Europe GmbH Neuenhofer Weg 3 52074 Aachen, Germany http://www.abiomed.com
Contact Ms Aimee Genzler +1 978-646-1553
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Abiomed Europe GmbH

Abiomed Impella®-Therapie erhält FDA-Genehmigung für den Einsatz bei kardiogenem Schock nach einem Herzinfarkt oder einer Herzoperation

Gesamte Familie der linksseitigen Impella-Herzpumpen erhalten FDA-Genehmigung bei der Behandlung von Herzerkrankungen

(PresseBox) (Danvers, Massachusetts, USA, )
Abiomed, Inc. (NASDAQ:ABMD), ein führender Anbieter bahnbrechender Herzunterstützungstechnologien, gab heute bekannt, dass er für die Herzpumpen Impella 2.5(TM), Impella CP®, Impella 5.0(TM) und Impella LD(TM) von der U.S. Food and Drug Administration (FDA) die Zulassung vor dem Inverkehrbringen (PMA) zur Behandlung kardiogener Schocks erhalten hat. In diesem Kontext stabilisieren die Herzpumpen von Impella die Hämodynamik des Patienten, entlasten den linken Ventrikel, sorgen für ein Durchströmen der Endorgane und ermöglichen die Wiederherstellung der normalen Herzfunktion. Diese neue Genehmigung ergänzt die vorherige FDA-Indikation für Impella 2.5 bei hochriskanten perkutanen Koronarinterventionen (PCI) oder Protected PCI(TM) vom März 2015.

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