BEUDAMED
    FDA Adverse Event Summary report: N

    8031673-2005-00015

    MDR report key: 580274 · Received March 2, 2005

    Report

    Report Number
    8031673-2005-00015
    Date Received
    March 2, 2005
    Date of Event
    November 29, 2004
    Product Code
    JJE
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1