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

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    Filters FDA Adverse Event ×

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON MANUFACTURING, LTD./ HUNTINGTON·Product code HQL·January 22, 2013

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·November 24, 2010

    HEARTMATE II LVAS

    FDA Adverse Event
    Injury ·THORATEC CORPORATION·Product code DSQ·July 11, 2014

    EMBRYO RPLCMNT CATHETER

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code MQF·September 24, 2019