BEUDAMED
    FDA Adverse Event Injury Summary report: N

    9681900-1997-00036

    MDR report key: 120731 · Received September 17, 1997

    Report

    Report Number
    9681900-1997-00036
    Event Type
    Injury
    Date Received
    September 17, 1997
    Date of Event
    August 21, 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