BEUDAMED
    5 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 ×

    CARDINAL HEALTH

    FDA Adverse Event
    Malfunction ·CAREFUSION 207, INC.·Product code CAI·November 19, 2009

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·May 22, 2019

    VALIANT CAPTIVIA

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·April 24, 2014

    OEM UNKNOWN

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GAM·September 26, 2012

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·July 27, 2010