BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PASSPORT 2 MONITOR

    MDR report key: 3091894 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00521
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    September 21, 2012
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    DSI
    PMA / PMN Number
    993531
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NM, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    MINDRAY SERVICE REP EXCHANGED THE SPO2 ASSEMBLY.

    Description of Event or Problem · 1

    CUSTOMER REPORTED A PASSPORT 2 MONITOR DISPLAYED INACCURATE SPO2 AND P-WAVE DATA. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    187207 PASSPORT 2 MONITOR PASSPORT 2 MONITOR DSI MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1