BEUDAMED
    3 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·January 18, 2013

    VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY USE

    FDA Adverse Event
    Other ·RESPIRONICS, INC.·Product code MNT·January 14, 2011

    PENUMBRA SYSTEM REPERFUSION CATHETER 041

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 31, 2014