BEUDAMED
    FDA Adverse Event Other Summary report: N

    CODEMASTER XL

    MDR report key: 317542 · Received February 21, 2001

    Report

    Report Number
    1218950-2001-00060
    Event Type
    Other
    Date Received
    February 21, 2001
    Report Date
    January 22, 2001
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    LDD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THERE WAS NO SIGNAL COMING FROM THE CABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    7040 CODEMASTER XL DEFIB/MON/REC LDD AGILENT TECHNOLOGIES, INC. M1722A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA