BEUDAMED
    5 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SAVINA 300

    FDA Adverse Event
    Malfunction ·DRAGER MEDICAL GMBH·Product code CBK·June 9, 2015

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·January 25, 2013

    7900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·December 2, 2010

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 11, 2014

    BD SERO-FUGE¿ 2001 CENTRIFUGE, 1 SPEED, 115V

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code LXG·October 10, 2019