BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2250051-2005-00561

    MDR report key: 650088 · Received November 29, 2005

    Report

    Report Number
    2250051-2005-00561
    Event Type
    Malfunction
    Date Received
    November 29, 2005
    Date of Event
    October 31, 2005
    Product Code
    JCM
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1