BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    D 903 AVANT ADULT HOLLOW FIBER OXYGENATOR

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·February 27, 2014

    D903 DIDECO AVANT 2 VAVD PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·February 19, 2014

    IT PADOVA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·August 8, 2013

    D903 DIDECO AVANT VAVD PHISIO

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DTZ·August 16, 2013

    ARTICULEZE M HEAD 36MM+5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·April 3, 2013

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·February 28, 2011

    GE OEC 6800

    FDA Adverse Event
    Injury ·GE OEC MEDICAL SYSTEMS, INC·Product code JAA·April 23, 2008

    C20441 IL HAIFA

    FDA Adverse Event
    Other ·SORIN GROUP ITALIA·Product code DWF·March 28, 2012