BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCUTORR PLUS II MONITOR

    MDR report key: 3091107 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00934
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    March 19, 2013
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC.
    Product Code
    MHX
    PMA / PMN Number
    983575
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    SERVICE REPRESENTATIVES REPAIRED THE UNITS SPO2 MODULE, CALIBRATED, SAFETY TESTED AND RAN DIAGNOSTIC TESTING TO FACTORY SPECIFICATIONS.

    Description of Event or Problem · 1

    CUSTOMER REPORTED AN ISSUE WITH THE ACCUTORR PLUS II MONITOR, 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
    187712 ACCUTORR PLUS II MONITOR PATIENT MONITOR MHX MINDRAY DS USA, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1