BEUDAMED
    FDA Adverse Event Other Summary report: N

    VIRIDIA 26/24 COMPONENT MONITORING SYSTEM

    MDR report key: 317635 · Received February 22, 2001

    Report

    Report Number
    1218950-2001-00064
    Event Type
    Other
    Date Received
    February 22, 2001
    Report Date
    January 23, 2001
    Manufacturer
    AGILENT TECHNOLOGIES, INC.
    Product Code
    DRT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE PT HAD CYANOSIS DUE TO DEFICIENT OXYGENATION OF THE BLOOD. PH SAMPLES WERE TAKEN. THEY WERE JUST OUTSIDE OF NORMAL RANGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    7029 VIRIDIA 26/24 COMPONENT MONITORING SYSTEM OMNICARE CMS DRT AGILENT TECHNOLOGIES, INC. M1205A NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA