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

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    Filters FDA Adverse Event ×

    AUTOPULSE NIMH BATTERY

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION INC·Product code DRM·January 2, 2013

    FUSION OMNI-TOME PRE-LOADED SPHINCTEROTOME

    FDA Adverse Event
    Malfunction ·COOK ENDOSCOPY·Product code KNS·December 3, 2010

    HEARTWARE® VENTRICULAR ASSIST SYSTEM

    FDA Adverse Event
    Death ·HEARTWARE, INC·Product code DSQ·July 15, 2014