BEUDAMED
    57 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    ADAPTA D

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2015

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·March 27, 2015

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·May 1, 2018

    MEDTRONIC LEAD

    FDA Adverse Event
    Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DSI·August 9, 2016

    ENRHYTHM

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code NVZ·December 23, 2014

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVZ·December 22, 2016

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·February 16, 2016

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·February 23, 2016

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWS·February 10, 2015

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2016

    ALINITY I ANTI-HBS REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·May 6, 2026

    ALINITY I ANTI-HBS REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·March 16, 2026

    ALINITY I ANTI-HBS REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code LOM·May 15, 2026

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KXA·June 4, 2014

    HIRES 90K IMPLANT

    FDA Adverse Event
    Injury ·ADVANCED BIONICS, LLC·Product code MCM·November 26, 2012