BEUDAMED
    11 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PASSPORT 2 MONITOR

    FDA Adverse Event
    Malfunction ·MINDRAY DS USA, INC.·Product code MHX·March 7, 2014

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·November 14, 2012

    ACCURUS 800CS

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 3, 2010

    NI

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·November 21, 2018

    NI

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·November 21, 2018

    IN.PACT ADMIRAL PACLITAXEL-ELUTING PTA BALLOON CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code ONU·May 22, 2019

    ZOLL QUATTRO EU CATHETER

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code NCX·September 12, 2018

    NI

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·February 27, 2019

    NI

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·February 27, 2019

    PIPELINE

    FDA Adverse Event
    Death ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 29, 2020

    PIPELINE

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code OUT·May 29, 2020