BEUDAMED
    FDA Adverse Event Other Summary report: N

    CODEMASTER XL

    MDR report key: 314940 · Received February 1, 2001

    Report

    Report Number
    1218950-2001-00039
    Event Type
    Other
    Date Received
    February 1, 2001
    Report Date
    January 4, 2001
    Manufacturer
    AGILENT TECHNOLOGIES, INC
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED AN OPEN LEAD IN THE ACCESSORY ECG CABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    4031 CODEMASTER XL DEFIB/MON/REC LDD AGILENT TECHNOLOGIES, INC M1722B NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA