BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HEART START XL

    MDR report key: 1873475 · Received October 14, 2010

    Report

    Report Number
    1218950-2010-01959
    Event Type
    Malfunction
    Date Received
    October 14, 2010
    Report Date
    September 20, 2010
    Manufacturer
    AGILENTTECHNOLOGIES, INC
    Product Code
    MKJ
    PMA / PMN Number
    K001725
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4): THE CUSTOMER REPORTED THAT THIS UNIT POWERS UP IN CONFIGURATION MODE. 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 THAT THIS UNIT POWERS UP IN CONFIGURATION MODE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HEART START XL MKJ AGILENTTECHNOLOGIES, INC M4735A

    Patients

    Seq Age Sex Outcome Treatment
    1