BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    FR3

    MDR report key: 3952727 · Received May 19, 2014

    Report

    Report Number
    3030677-2014-01257
    Event Type
    Malfunction
    Date Received
    May 19, 2014
    Report Date
    May 15, 2014
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    MKJ
    PMA / PMN Number
    K111693
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). PRODUCT EVALUATION PENDING. ISSUE IS BEING REPORTED AS ALERT COULD NOT BE CLEARED BY OPERATOR. 501(K): K111693.

    Description of Event or Problem · 1

    IT HAS BEEN REPORTED THAT THE AED IS NOT FUNCTIONING CORRECTLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    296305 FR3 MKJ PHILIPS MEDICAL SYSTEMS

    Patients

    Seq Age Sex Outcome Treatment
    1