BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 1081678 · Received July 9, 2008

    Report

    Report Number
    3003768277-2008-00019
    Event Type
    Other
    Date Received
    July 9, 2008
    Manufacturer
    PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
    Product Code
    LNH
    PMA / PMN Number
    K031815
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * LNH PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. * *

    Patients

    Seq Age Sex Outcome Treatment
    1