BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CODEMASTER XL+

    MDR report key: 2489391 · Received March 7, 2012

    Report

    Report Number
    1218950-2012-00841
    Event Type
    Malfunction
    Date Received
    March 7, 2012
    Report Date
    February 20, 2012
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    LDD
    PMA / PMN Number
    K954957
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). THE CUSTOMER REPORTED A POWER SUPPLY FAILURE, WHICH COULD INDICATE A FAILURE TO POWER UP. THERE WAS NO REPORT OF PT INVOLVEMENT. THIS COMPLAINT IS STILL BEING INVESTIGATED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED A POWER SUPPLY FAILURE, WHICH COULD INDICATE A FAILURE TO POWER UP. THERE WAS NO REPORT OF PT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CODEMASTER XL+ LDD, MKJ, DQA LDD AGILENT TECHNOLOGIES, INC. M1722B

    Patients

    Seq Age Sex Outcome Treatment
    1