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

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    Filters FDA Adverse Event ×

    LCS COMPLETE LO PRO POLPAT LG+

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code NJL·January 3, 2013

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·November 5, 2010

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 21, 2014