BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCUTORR V MONITOR

    MDR report key: 3091754 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00612
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    January 7, 2013
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    DXN
    PMA / PMN Number
    983575
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    SERVICE REP DISCONNECTED AND RECONNECTED THE SPO2 BOARD, CALIBRATED AND SAFETY TESTED UNIT TO FACTORY SPECIFICATIONS.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE ACCUTORR V MONITOR HAD NO SPO2 FUNCTION RESULTING IN A POSSIBLE LOSS OF SPO2 MONITORING. NO PATIENT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    187240 ACCUTORR V MONITOR NONE DXN MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1