BEUDAMED
    FDA Adverse Event Death Summary report: N

    *

    MDR report key: 513109 · Received February 25, 2004

    Report

    Report Number
    1713683-2004-00001
    Event Type
    Death
    Date Received
    February 25, 2004
    Date of Event
    January 15, 2004
    Manufacturer
    GAMBRO RENAL PRODUCTS, INC.
    Product Code
    FII
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * FII GAMBRO RENAL PRODUCTS, INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *