BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1140279 · Received June 19, 2008

    Report

    Report Number
    8010042-2008-00081
    Event Type
    Malfunction
    Date Received
    June 19, 2008
    Manufacturer
    MAQUET CRITICAL CARE AB
    Product Code
    CBK
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * CBK MAQUET CRITICAL CARE AB * *

    Patients

    Seq Age Sex Outcome Treatment
    1