BEUDAMED
    FDA Adverse Event Other Summary report: N

    CT9000 ADV

    MDR report key: 310754 · Received December 27, 2000

    Report

    Report Number
    1518293-2000-00021
    Event Type
    Other
    Date Received
    December 27, 2000
    Date of Event
    November 17, 2000
    Report Date
    December 22, 2000
    Manufacturer
    LIEBEL-FLARSHEIM CO.
    Product Code
    DXT
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CT9000 ADV * DXT LIEBEL-FLARSHEIM CO. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other