BEUDAMED
    22 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    AUTOPULSE® RESUSCITATION MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·March 18, 2015

    2124215-2012-11397

    FDA Adverse Event
    Injury ·GUIDANT PUERTO RICO BV·Product code DTB·October 9, 2012

    AUTOPULSE® RESUSCITATION MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·March 23, 2015

    AUTOPULSE® RESUSCITATION MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·February 13, 2015

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·March 7, 2022

    UNK DISTRIBUTED DIALYZER

    FDA Adverse Event
    Injury ·*·Product code FJI·April 24, 1996

    MEDFUSION 2001H SYRINGE INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDEX·Product code FRN·January 5, 2001

    ACRYSOF

    FDA Adverse Event
    Malfunction ·ALCON LABORATORIES, INC·Product code HQL·February 19, 1999

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·January 20, 2015

    EDWARDS INSPIRIS RESILIA AORTIC VALVE

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·June 26, 2024

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVN·June 14, 2019

    SELECTSECURE MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code NVN·June 14, 2019

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·October 9, 2014

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·November 11, 2014

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·September 15, 2014

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·September 10, 2014

    REVEAL XT

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DSI·April 21, 2023

    AUTOPULSE® RESUSCITATION MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·January 29, 2015

    AUTOPULSE® RESUSCITATION MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·February 24, 2015

    AUTOPULSE® RESUSCITATION MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION·Product code DRM·March 5, 2015