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CryoLife kündigt erste Implantation des HeRO Transplantats in Europa an
Date:7/31/2013

auert. Das Produkt verfügt in den USA über eingeführte Erstattungssätze und Erstattungscodes, die von der Society for Vascular Surgery [Gesellschaft für Gefäßchirurgie] und der American Medical Association [Amerikanische Ärztevereinigung] anerkannt werden. Weitere Informationen über das HeRO Transplantat erhalten Sie bei einem Besuch von www.herograft.com. Weitere Informationen über CryoLife finden Sie auf der Website des Unternehmens: www.cryolife.com.

Aussagen in dieser Pressemitteilung, die sich auf künftige Ereignisse oder Überzeugungen, Erwartungen oder Hoffnungen des Managements beziehen, sind zukunftsbezogene Aussagen im Sinne des Private Securities Litigation Reform Act von 1995. Derartige zukunftsbezogene Aussagen geben die Ansichten des Managements zu dem Zeitpunkt wieder, zu dem sie getätigt werden, und sie unterliegen einer Reihe von Risiken, Unabwägbarkeiten, Prognosen und Annahmen, die dazu führen können, dass die tatsächlichen Ergebnisse nennenswert von den derzeitigen Erwartungen abweichen. Diese Aussagen schließen unter anderem unsere Überzeugung ein, dass das HeRO Transplantat ein Wachstumstreiber unseres Unternehmens sein wird. Die Auswirkungen des HeRO Transplantats auf unser Wachstum unterliegen einer Reihe von Risiken und Unabwägbarkeiten, darunter die Möglichkeit, dass Ärzte und Patienten das HeRO Transplantat nicht als brauchbare Behandlungsalternative annehmen, Behörden bestehende Zulassungen zurückziehen oder zusätzliche Bedingungen für die Verwendung des HeRO Transplantats stellen, künftige Transplantate nicht erfolgreich sind oder Komplikationen nach dem Einsetzen auftreten, sich das wirtschaftliche Umfeld in der EU aus Kostengründen auf die Entscheidung zur Verwendung des HeRO
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SOURCE CryoLife, Inc.
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