BEUDAMED
    3 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    2520274-2013-10067

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code MNI·February 11, 2013

    LIFEPAK 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code LDD·December 16, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 28, 2014