BEUDAMED
    FDA Adverse Event Other Summary report: N

    TECAN FE500

    MDR report key: 5161534 · Received March 3, 2004

    Report

    Report Number
    1037985-2004-00002
    Event Type
    Other
    Date Received
    March 3, 2004
    Date of Event
    February 26, 2004
    Report Date
    March 3, 2004
    Manufacturer
    TECAN CH.
    Product Code
    LXG
    Report Source
    Distributor report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TECAN US IS INVESTIGATING THE MALFUNCTION OF THE FE500 DURING INSTRUMENT PAUSE STATUS OF ROUTINE OPERATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TECAN FE500 GENERAL PURPOSE LABORATORY INSTRUMENT LXG TECAN CH. FE500 NA

    Patients

    Seq Age Sex Outcome Treatment
    1