BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·March 13, 2019

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 3, 2014

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 16, 2011

    FORCE FX

    FDA Adverse Event
    Malfunction ·COVIDIEN FORMERLY VALLEY LAB·Product code GEI·July 9, 2013

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·April 10, 2019

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code OLO·February 22, 2019

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code OLO·March 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·April 3, 2019