BEUDAMED
    4 results · 27ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code CEC·April 23, 2012

    HEARTSTART XL+ DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 13, 2014

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code LWP·February 9, 2013

    LIVIAN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 7, 2011