BEUDAMED
    FDA Adverse Event Death Summary report: N

    FRESENIUS A2008H

    MDR report key: 508650 · Received December 17, 2003

    Report

    Report Number
    508650
    Event Type
    Death
    Date Received
    December 17, 2003
    Date of Event
    December 17, 2003
    Manufacturer
    FRESENIUS USA
    Product Code
    FII
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MS, US
    Reporter Occupation
    NURSE

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FRESENIUS A2008H HEMODIALYSIS MACHINE FII FRESENIUS USA A2008H *

    Patients

    Seq Age Sex Outcome Treatment
    1 64 YR Death| H