BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCUTORR PLUS MONITOR

    MDR report key: 3091536 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00296
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    August 22, 2012
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA INC.
    Product Code
    MHX
    PMA / PMN Number
    982575
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE COMPANY REP EVALUATED THE UNIT. CORRECTIONS INCLUDED REPLACEMENT OF THE PC BOARD. THE UNIT WAS TESTED TO FACTORY'S SPECS. IT FUNCTIONAL NORMALLY AND WAS RETURNED TO USE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED A FAILED PC BOARD ON THE ACCUTORR PLUS MONITOR RESULTING IN NO SPO2 READINGS. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    187346 ACCUTORR PLUS MONITOR PATIENT MONITOR MHX MINDRAY DS USA INC.

    Patients

    Seq Age Sex Outcome Treatment
    1