BEUDAMED
    3 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code JDI·February 6, 2013

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·July 21, 2014

    FLEXTEND II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 4, 2011