BEUDAMED
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    Filters FDA Adverse Event ×

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·June 19, 2014

    TRI-LOCK BPS SZ 2 HI OFFSET

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·October 22, 2010

    RADIUS VITALLIUM ROD 5.5 X 600 MM

    FDA Adverse Event
    Injury ·STRYKER SPINE BORDEAUX·Product code NKB·December 19, 2012