BEUDAMED
    4 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BD PEN NEEDLE 29 G X1 2.7 MM

    FDA Adverse Event
    Injury ·BECTON DICKINSON AND CO.·Product code FMI·January 6, 2016

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·March 13, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·March 28, 2011

    INSIGNIA ENTRA

    FDA Adverse Event
    Injury ·CARDIAC PACEMAKERS, INC·Product code DXY·May 8, 2008