BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1043572-1997-00012

    MDR report key: 92297 · Received May 16, 1997

    Report

    Report Number
    1043572-1997-00012
    Event Type
    Malfunction
    Date Received
    May 16, 1997
    Date of Event
    April 18, 1997
    Product Code
    JEB
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1