BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1932180-1997-00040

    MDR report key: 83162 · Received April 11, 1997

    Report

    Report Number
    1932180-1997-00040
    Event Type
    Malfunction
    Date Received
    April 11, 1997
    Date of Event
    February 28, 1997
    Product Code
    JYY
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1