BEUDAMED
    FDA Adverse Event Other Summary report: N

    MAQUET

    MDR report key: 692916 · Received March 24, 2006

    Report

    Report Number
    8010652-2006-00002
    Event Type
    Other
    Date Received
    March 24, 2006
    Date of Event
    January 11, 2006
    Report Date
    February 24, 2006
    Manufacturer
    MAQUET GMBH & CO. KG
    Product Code
    FSE
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MAQUET OPERATING TABLE FSE MAQUET GMBH & CO. KG 1132.11B2

    Patients

    Seq Age Sex Outcome Treatment
    1