BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9681900-1997-00021

    MDR report key: 106274 · Received July 7, 1997

    Report

    Report Number
    9681900-1997-00021
    Event Type
    Malfunction
    Date Received
    July 7, 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