BEUDAMED
    FDA Adverse Event Other Summary report: N

    8010047-1999-00037

    MDR report key: 242888 · Received September 30, 1999

    Report

    Report Number
    8010047-1999-00037
    Event Type
    Other
    Date Received
    September 30, 1999
    Date of Event
    August 16, 1999
    Product Code
    JJE
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1