BEUDAMED
    FDA Adverse Event Death Summary report: N

    CENTRY 2 RX

    MDR report key: 543504 · Received November 27, 2002

    Report

    Report Number
    543504
    Event Type
    Death
    Date Received
    November 27, 2002
    Date of Event
    April 5, 1994
    Report Date
    November 27, 2002
    Manufacturer
    COBE
    Product Code
    FII
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    CT, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRY 2 RX DIALYSIS MACHINE FII COBE CENTRY 2 RX *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death DIALYSIS