BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9681900-1997-00025

    MDR report key: 109220 · Received July 25, 1997

    Report

    Report Number
    9681900-1997-00025
    Event Type
    Malfunction
    Date Received
    July 25, 1997
    Date of Event
    July 1, 1997
    Product Code
    CAE
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1