BEUDAMED
    FDA Adverse Event Other Summary report: N

    ICON P SYSTEM G3 BLUE

    MDR report key: 282976 · Received June 22, 2000

    Report

    Report Number
    1423253-2000-00020
    Event Type
    Other
    Date Received
    June 22, 2000
    Date of Event
    May 25, 2000
    Report Date
    June 22, 2000
    Manufacturer
    SIEMENS MEDICAL SYSTEMS, INC., NGM GROUP
    Product Code
    JWM
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    LOADED 3 REVIEW FILES INTO CARDIAC REVIEW-1 STRESS/REST, 1 GATED REST ONLY & 1 STRESS/REST IF USER SELECTS THE 1 STUDY TO DISPLAY-OK, SELECT THE SECOND (GREST FILE)-OK. SELECT THE THIRD STRESS/REST STUDY AND THE PREVIOUS GREST IS DISPLAY FROM THE PREVIOUS PT IT DOES NOT UPDATE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ICON P SYSTEM G3 BLUE COMPUTER JWM SIEMENS MEDICAL SYSTEMS, INC., NGM GROUP 5963744 *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other