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CryoLife annuncia il primo impianto europeo di HeRO Graft
Date:7/31/2013

so che sono approvati dalla Society for Vascular Surgery (Società di Chirurgia Vascolare) e dalla American Medical Association (Associazione Medica Americana).  Per maggiori informazioni su HeRO Graft, visitare www.herograft.com.  Per maggiori informazioni su CryoLife, visitare il sito web della Società: www.cryolife.com.

Le dichiarazioni contenute nel presente comunicato stampa che riguardano il futuro o che esprimono opinioni, aspettative o speranze della direzione sono dichiarazioni previsionali secondo quanto previsto dal Private Securities Litigation Reform Act (Legge di riforma in materia di controversie relative a titoli privati) del 1995.  Tali dichiarazioni previsionali riflettono le opinioni della direzione al momento del loro rilascio e sono soggette a una serie di rischi, incertezze, stime e ipotesi che possono essere responsabili di differenze sostanziali rispetto ai risultati effettivi.  Queste dichiarazioni comprendono anche quelle relative alla nostra opinione che HeRO Graft sarà responsabile della crescita della Società.  L'impatto di HeRO Graft sulla nostra crescita è soggetto a una serie di rischi e incertezze, compreso il fatto che medici e pazienti potrebbero non accettare HeRO Graft quale opzione terapeutica praticabile, i legislatori potrebbero ritirare le approvazioni esistenti o imporre condizioni aggiuntive per l'uso di HeRO Graft, gli impianti futuri potrebbero non avere successo o ci potrebbero essere complicazioni a seguito di impianti, le condizioni economiche nella UE potrebbero avere dei riflessi nella decisione di utilizzare HeRO a causa del suo costo, i prodotti concorrenti potrebbero essere più efficaci o avere costi più contenuti, e la recente incapacità della Società di importare tessuti nella UE potrebbe avere dei
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SOURCE CryoLife, Inc.
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