BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1020407 · Received March 6, 2008

    Report

    Report Number
    8010042-2008-00033
    Event Type
    Malfunction
    Date Received
    March 6, 2008
    Manufacturer
    MAQUET CRITICAL CARE AB
    Product Code
    CBK
    PMA / PMN Number
    k041223
    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