BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PASSPORT 2 MONITOR

    MDR report key: 3091136 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00869
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    February 21, 2013
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    DSI
    PMA / PMN Number
    020550
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SVC REP COULD NOT CONFIRM THE REPORTED FUNCTION. CABLES WERE RESEATED AND THE UNITS WERE CALIBRATED AND SAFETY TESTED TO FACTORY SPECIFICATIONS.

    Description of Event or Problem · 1

    CUSTOMER REPORTED NO ECG WAVEFORM OR GAS READINGS ON A PASSPORT 2 MONITOR WHICH MAY HAVE RESULTED IN A LOSS OF ECG AND GAS MONITORING. NO INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    187134 PASSPORT 2 MONITOR PATIENT MONITOR DSI MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1