BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TERUMO PERFUSION SYSTEM 8000

    MDR report key: 2090176 · Received April 11, 2011

    Report

    Report Number
    1828100-2011-00900
    Event Type
    Malfunction
    Date Received
    April 11, 2011
    Date of Event
    March 13, 2011
    Report Date
    April 11, 2011
    Manufacturer
    TERUMO CARDIOVASCULAR SYSTEMS CORP.
    Product Code
    DRY
    PMA / PMN Number
    K915183
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KS
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    DURING PREVENTATIVE MAINTENANCE OF THE DEVICE, THE USER REPORTED THAT THE MONITOR WAS BLACK AND FAILED TO BOOT UP WHEN POWERED ON. SINCE THE EVENT OCCURRED DURING PREVENTATIVE MAINTENANCE, THERE WAS NO PATIENT INVOLVEMENT DURING THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TERUMO PERFUSION SYSTEM 8000 HEART LUNG MACHINE DRY TERUMO CARDIOVASCULAR SYSTEMS CORP. 152346

    Patients

    Seq Age Sex Outcome Treatment
    1