BEUDAMED
    3 results · 19ms · 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 ×

    ATLAS II PLUS DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·June 6, 2014

    ULTRAFLEX ESOPHAGEAL STENT SYSTEM, ULTRAFLEX DIAMONDBILIARY STENT SYSTEM, ULTRAF

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code JCT·October 5, 2010

    SCREW LOCKING

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·December 3, 2012