BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CODEMASTER XL

    MDR report key: 4231790 · Received October 14, 2014

    Report

    Report Number
    1218950-2014-06143
    Event Type
    Malfunction
    Date Received
    October 14, 2014
    Report Date
    September 23, 2014
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    LDD
    PMA / PMN Number
    K954957
    Report Source
    Manufacturer report
    Reporter Location
    TW
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE DEVICE CAN'T CHANGE ON AC POWER. THERE WAS NO REPORT OF PT INVOLVEMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    649985 CODEMASTER XL LDD, MKJ, DQA LDD PHILIPS MEDICAL SYSTEMS M1723B

    Patients

    Seq Age Sex Outcome Treatment
    1