BEUDAMED
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    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·October 25, 2016

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·December 2, 2016

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·May 26, 2014

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·October 17, 2017

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·August 14, 2015

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·December 8, 2017

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·December 1, 2017

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·December 5, 2014

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·October 28, 2014

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·September 14, 2015

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIP·July 29, 2015

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC PLC·Product code NIP·October 26, 2018

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC PLC·Product code NIP·October 26, 2018

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIP·November 2, 2018

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·COVIDIEN·Product code NIP·November 2, 2018

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC PLC·Product code NIP·October 26, 2018

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code FGE·October 1, 2009

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code NIP·March 12, 2014

    COMPLETE SE SFA

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR SANTA ROSA·Product code NIP·March 12, 2014

    COMPLETE SE SFA

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR·Product code FGE·May 1, 2009