BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GAS MODULE III

    MDR report key: 3091065 · Received April 30, 2013

    Report

    Report Number
    2221819-2013-00821
    Event Type
    Malfunction
    Date Received
    April 30, 2013
    Date of Event
    March 23, 2013
    Report Date
    April 30, 2013
    Manufacturer
    MINDRAY DS USA, INC
    Product Code
    BZK
    PMA / PMN Number
    062754
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE UNIT WAS RETURNED TO MINDRAY'S REPAIR CTR FOR REPAIR.

    Description of Event or Problem · 1

    CUSTOMER REPORTED AN ISSUE WITH THE GAS MODULE III WHICH MAY HAVE RESULTED IN A LOSS OF GAS MONITORING. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    186817 GAS MODULE III GAS MODULE BZK MINDRAY DS USA, INC

    Patients

    Seq Age Sex Outcome Treatment
    1