BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MAQUET GMBH & CO. KG

    MDR report key: 1299084 · Received January 21, 2009

    Report

    Report Number
    1225700-2008-00258
    Event Type
    Injury
    Date Received
    January 21, 2009
    Date of Event
    August 7, 2008
    Report Date
    August 19, 2008
    Manufacturer
    MAQUET GMBH AND CO. KG
    Product Code
    FQO
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    GM
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAQUET GMBH & CO. KG TABLE, OPERATING ROOM, AC POWERED, FQO FQO MAQUET GMBH AND CO. KG 1120.000R0 *

    Patients

    Seq Age Sex Outcome Treatment
    1 *