BEUDAMED
    4 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 ×

    2.0MM PARALLEL DRILL GUIDE AND DRILL SLEEVE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FZX·April 29, 2013

    UNIVERSAL DRIVER SHAFT

    FDA Adverse Event
    Malfunction ·STRYKER·Product code HXX·May 3, 2011

    ACE INSTANT COLD COMPRESS

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code IMD·July 25, 2008

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·September 27, 2018