BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2110898-1997-00028

    MDR report key: 146485 · Received November 4, 1997

    Report

    Report Number
    2110898-1997-00028
    Event Type
    Malfunction
    Date Received
    November 4, 1997
    Date of Event
    September 18, 1997
    Product Code
    IWJ
    Removal / Correction Number
    N-007/009-6
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1