BEUDAMED
    FDA Adverse Event Other Summary report: N

    9610617-2004-00008

    MDR report key: 559606 · Received April 30, 2004

    Report

    Report Number
    9610617-2004-00008
    Event Type
    Other
    Date Received
    April 30, 2004
    Date of Event
    April 12, 2004
    Product Code
    CCW
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CCW

    Patients

    Seq Age Sex Outcome Treatment
    1