BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    10 LEAD ECG TRUNK AAMI/IEC 2M

    MDR report key: 3770505 · Received March 5, 2014

    Report

    Report Number
    9610816-2014-00050
    Event Type
    Malfunction
    Date Received
    March 5, 2014
    Report Date
    February 20, 2014
    Manufacturer
    PHILIPS MEDICAL SYSTEMS
    Product Code
    DSA
    PMA / PMN Number
    K020531
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    PARAMEDIC

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THE FAILURE OF AN M1663A ECG TRUNK CABLE. NO PT HARM WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    133343 10 LEAD ECG TRUNK AAMI/IEC 2M DSA PHILIPS MEDICAL SYSTEMS M1663A 18

    Patients

    Seq Age Sex Outcome Treatment
    1