BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DXY·January 8, 2018

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DXY·February 8, 2018

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 23, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·January 15, 2013

    NEXGEN CR-FLEX FEMORAL COMPONENT POROUS

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·January 11, 2011

    OXF ANAT BRG LT SM SIZE 7 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 31, 2023

    OXF TWIN-PEG CMNTD FEM SM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·January 31, 2023