BEUDAMED
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    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, INC.·Product code DRM·October 20, 2001

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, INC.·Product code DRM·October 20, 2001

    THUMPER

    FDA Adverse Event
    Other ·MICHIGAN INSTRUMENTS, INC.·Product code DRM·October 20, 2001

    THUMPER

    FDA Adverse Event
    Malfunction ·MICHIGAN INSTRUMENTS, INC.·Product code DRM·October 20, 2001

    AUTOPULSE® LIFEBAND

    FDA Adverse Event
    Death ·ZOLL CIRCULATION·Product code DRM·March 1, 2023

    AUTOPULSE® RESUSCITATION MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION INC·Product code DRM·January 13, 2023

    LUCAS ® CPR CHEST COMPRESSION SYSTEM

    FDA Adverse Event
    Injury ·JOLIFE AB - 3005445717·Product code DRM·January 13, 2023

    LUCAS 2, 2.2, IN SHIPPING BOX,EN,DA,SV,FI,NO

    FDA Adverse Event
    Injury ·JOLIFE AB - 3005445717·Product code DRM·January 25, 2023

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 31, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 21, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·November 29, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 31, 2012

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·October 18, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 14, 2012

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·October 26, 2012

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·October 11, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·November 30, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 14, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·December 26, 2012

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·December 14, 2012