BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2132280-2002-00003

    MDR report key: 423677 · Received October 22, 2002

    Report

    Report Number
    2132280-2002-00003
    Event Type
    Malfunction
    Date Received
    October 22, 2002
    Date of Event
    October 8, 2002
    Product Code
    ---
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1