BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DPM 6/7 MONITOR

    MDR report key: 3091121 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00909
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    March 11, 2013
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    MHX
    PMA / PMN Number
    092449
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    SERVICE REPRESENTATIVES REPAIRED THE SOLDER ON THE FRONT PANEL CONNECTORS. CALIBRATED AND SAFETY TESTED UNIT TO FACTORY SPECIFICATIONS.

    Description of Event or Problem · 1

    CUSTOMER REPORTED A DPM 6/7 MONITOR DID NOT DISPLAY SPO2 WHICH MAY HAVE RESULTED IN A LOSS OF SPO2 MONITORING. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    187100 DPM 6/7 MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1