BEUDAMED
    FDA Adverse Event Other Summary report: N

    FOGARTY ARTERIAL EMBOLECTOMY CATHETER

    MDR report key: 508357 · Received January 21, 2004

    Report

    Report Number
    6000002-2004-00012
    Event Type
    Other
    Date Received
    January 21, 2004
    Date of Event
    October 22, 2003
    Report Date
    January 5, 2004
    Manufacturer
    EDWARDS LIFESCIENCES
    Product Code
    DXE
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FOGARTY ARTERIAL EMBOLECTOMY CATHETER EMBOLECTOMY CATHETER DXE EDWARDS LIFESCIENCES UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 *