BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NEUROMONITOR BASIC KIT

    MDR report key: 2120236 · Received June 7, 2011

    Report

    Report Number
    1226348-2011-00210
    Event Type
    Injury
    Date Received
    June 7, 2011
    Manufacturer
    CODMAN & SHURTLEFF, INC, MEDOS S.A.
    Product Code
    GWM
    PMA / PMN Number
    K914479
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    UPON COMPLETION OF THE INVESTIGATION, A F/U REPORT WILL BE FILED.

    Description of Event or Problem · 1

    AFFILIATE REPORTED A FEW HOURS AFTER IMPLANTATION THE SENSOR PRESSURE ROSE, HOWEVER, THE CLINICAL SYMPTOMS OF THE PT DID NOT CHANGE. AS A RESULT THE SENSOR WAS REVISED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NEUROMONITOR BASIC KIT DEVICE, INTRACRANIAL PRESSURE MONITORING GWM CODMAN & SHURTLEFF, INC, MEDOS S.A. NA 513295

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Required Intervention