BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TERUMO ADVANCED PERFUSION SYSTEM I

    MDR report key: 1842293 · Received August 27, 2010

    Report

    Report Number
    1828100-2010-01180
    Event Type
    Malfunction
    Date Received
    August 27, 2010
    Date of Event
    August 2, 2010
    Report Date
    August 27, 2010
    Manufacturer
    TERUMO CARDIOVASCULAR SYSTEMS CORP.
    Product Code
    DTQ
    PMA / PMN Number
    K022947
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING PREVENTATIVE MAINTENANCE OF THE DEVICE, THE FIELD SERVICE TECHNICIAN REPORTED THE SYSTEM DID NOT POWER UP ON BATTERY MODE AND DID NOT SWITCH TO BATTERY MODE UPON THE LOSS OF A/C POWER. NO OTHER DETAILS REGARDING THE NATURE OF THE EVENT WERE PROVIDED. SINCE THE EVENT OCCURRED DURING PREVENTATIVE MAINTENANCE OF THE DEVICE, THERE WAS NO PT INVOLVEMENT DURING THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TERUMO ADVANCED PERFUSION SYSTEM I POWER MANAGER BOARD DTQ TERUMO CARDIOVASCULAR SYSTEMS CORP. 802095

    Patients

    Seq Age Sex Outcome Treatment
    1