BEUDAMED
    4 results · 23ms · 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 ×

    UNKNOWN SCREW

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PAO·February 4, 2015

    NEXGEN LPS-FLEX OPTION FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER·Product code NJL·June 11, 2014

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code LGS·December 2, 2010

    ULTRAFLEX

    FDA Adverse Event
    Malfunction ·KING SYSTEMS·Product code CAI·December 17, 2012