BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 547982 · Received September 9, 2004

    Report

    Report Number
    9616240-2004-00014
    Event Type
    Other
    Date Received
    September 9, 2004
    Date of Event
    August 11, 2004
    Report Date
    August 12, 2004
    Manufacturer
    GAMBRO DASCO
    Product Code
    FII
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * HEMODIALYSIS EQUIPMENT FII GAMBRO DASCO PHOENIX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 *