BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ACCUTORR V

    MDR report key: 3172848 · Received May 21, 2013

    Report

    Report Number
    2221819-2013-00126
    Event Type
    Malfunction
    Date Received
    May 21, 2013
    Date of Event
    August 16, 2011
    Report Date
    February 28, 2013
    Manufacturer
    MINDRAY DS USA, INC
    Product Code
    DXN
    PMA / PMN Number
    091068
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE ACCUTORR V MONITOR FAILED, WHICH MAY HAVE RESULTED IN A LOSS OF PRIMARY MONITORING. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    225618 ACCUTORR V PATIENT MONITOR DXN MINDRAY DS USA, INC

    Patients

    Seq Age Sex Outcome Treatment
    1