BEUDAMED
    FDA Adverse Event Other Summary report: N

    MAQUET

    MDR report key: 575449 · Received February 2, 2005

    Report

    Report Number
    8010652-2005-00001
    Event Type
    Other
    Date Received
    February 2, 2005
    Date of Event
    December 26, 2004
    Report Date
    December 21, 2004
    Manufacturer
    MAQUET GMBH AND CO. KG
    Product Code
    FQO
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAQUET OR TABLE FQO MAQUET GMBH AND CO. KG 1420.02B *

    Patients

    Seq Age Sex Outcome Treatment
    1 *