BEUDAMED
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    Filters FDA Adverse Event ×

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    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 2, 2014

    2010 RACK ELECSYS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code MMI·November 1, 2007

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·October 4, 2012