BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 621286 · Received July 12, 2005

    Report

    Report Number
    8030665-2005-00025
    Event Type
    Death
    Date Received
    July 12, 2005
    Date of Event
    March 31, 2005
    Report Date
    July 11, 2005
    Manufacturer
    REYNOSA MANUFACTURING, C D
    Product Code
    FOZ
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * FOZ REYNOSA MANUFACTURING, C D NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *