BEUDAMED
    11 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SERVO-I

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·April 29, 2014

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCO·Product code CBK·February 1, 2013

    KINAIR MEDSURG PULSE

    FDA Adverse Event
    Death ·KCI-USA, INC·Product code IOQ·January 14, 2011

    AIA-900

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·February 24, 2016

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·July 25, 2025

    TOSOH AIA-900

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·December 13, 2016

    A1A-600II

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·October 28, 2016

    TOSOH AIA-1800

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·November 11, 2016

    AIA-360

    FDA Adverse Event
    Injury ·TOSOH CORPORATION·Product code KHO·March 3, 2016

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024

    PLEURX DRAINAGE KIT 500ML 10/CS

    FDA Adverse Event
    Malfunction ·CAREFUSION, INC·Product code DWM·December 24, 2024