BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2021283-1996-00003

    MDR report key: 50523 · Received November 13, 1996

    Report

    Report Number
    2021283-1996-00003
    Event Type
    Malfunction
    Date Received
    November 13, 1996
    Date of Event
    September 26, 1996
    Product Code
    FRN
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1