BEUDAMED
    3 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    TRIDENT ACET WINDOW TRIAL 64MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·June 16, 2014

    VKS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC. BROOKS MANUFACTURING SITE·Product code NJL·October 19, 2010

    ARTICULEZE M HEAD 36MM +5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·December 17, 2012