BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    REPLACEMENT HEART VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 19, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·PURITAN BENNETT CORP.·Product code CBK·October 20, 2010

    ACRYSOF RESTOR

    FDA Adverse Event
    Injury ·ALCON RESERCH, LTD. / HUNTINGTON·Product code HQL·December 19, 2012