BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DPM 5 MONITOR

    MDR report key: 3091441 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00985
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    August 23, 2012
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    MHX
    PMA / PMN Number
    070791
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE COMPANY REP EVALUATED THE UNIT. CORRECTIONS INCLUDE REPLACEMENT OF UNIT'S CABLES.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED FAILED CABLES ON THE DPM 5 MONITOR RESULTING IN NO SPO2 READINGS. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    186615 DPM 5 MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1