BEUDAMED
    183 results · 69ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC.·Product code MKJ·December 4, 2007

    LUCAS¿ CPR CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·JOLIFE AB - 3005445717·Product code DRM·June 2, 2022

    LUCAS¿ CPR CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC. - 3015876·Product code DRM·July 12, 2021

    LUCAS¿ 2 CPR CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·JOLIFE AB·Product code DRM·October 24, 2016

    LUCAS¿ 2 CPR CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·JOLIFE AB - 3005445717·Product code DRM·December 7, 2018

    LUCAS (T) CPR CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·JOLIFE AB·Product code DRM·July 1, 2014

    LIFEPAK 20 DEFIBRILLATOR

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC / PHYSIO-CONTROL MANUFACTURING, INC.·Product code MKJ·November 13, 2018

    LIFEPAK 15

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC./PHYSIO-CONTROL MANUFACTURING, INC.·Product code MKJ·October 2, 2018

    EDGE SYSTEM ELECTRODES WITH QUIK-COMBO CONNECTOR

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL INC., PHYSIO-CONTROL MANUFACTURING, INC.·Product code MKJ·March 9, 2016

    LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC·Product code MKJ·February 24, 2012

    3015876-2012-00100

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC.·March 20, 2012

    QUIK-COMBO RTS DEFIBRILLATION/ECG ELECTRODES

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC.·Product code MLN·March 17, 2009

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC.·Product code MKJ·May 20, 2010

    QUIK COMBO

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL INC.·Product code MKJ·June 22, 2010

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC.·Product code MKJ·May 7, 2010

    LIFEPAK(R) 15 MONITOR/DEFIBRILLATOR

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC·Product code MKJ·December 12, 2017

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC·Product code LDD·December 30, 2014

    LIFEPACK 20

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC.·Product code LDD·October 8, 2014

    DEFIBRILLATOR PADS

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC.·Product code MKJ·May 27, 2022

    LIFEPAK 12

    FDA Adverse Event
    Injury ·PHYSIO-CONTROL, INC·Product code MKJ·May 19, 2012