BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TERUMO PERFUSION SYSTEM 8000

    MDR report key: 1693189 · Received May 7, 2010

    Report

    Report Number
    1828100-2010-00287
    Event Type
    Malfunction
    Date Received
    May 7, 2010
    Date of Event
    March 14, 2010
    Report Date
    May 7, 2010
    Manufacturer
    TERUMO CARDIOVASCULAR SYSTEMS CORP.
    Product Code
    JOR
    PMA / PMN Number
    K915183
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TH
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    EVALUATION IN PROGRESS BUT NOT YET CONCLUDED.

    Description of Event or Problem · 1

    DURING PRIMING OF THE DEVICE IN PREPARATION FOR A CARDIOPULMONARY BYPASS PROCEDURE, THE USER REPORTED THE ARTERIAL MONITOR UNEXPECTEDLY STOPPED WORKING. AN ALTERNATE DEVICE WAS EMPLOYED FOR THE PROCEDURE. THE USER REPORTED THE SURGICAL PROCEDURE WAS COMPLETED SUCCESSFULLY, AND THERE WAS NO ADVERSE CONSEQUENCE TO THE PT AS A RESULT OF THE EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TERUMO PERFUSION SYSTEM 8000 HEART LUNG CONSOLE ARTERIAL MONITOR JOR TERUMO CARDIOVASCULAR SYSTEMS CORP. 16413

    Patients

    Seq Age Sex Outcome Treatment
    1