BEUDAMED
    FDA Adverse Event Other Summary report: N

    CT9000 INJECTOR

    MDR report key: 371713 · Received January 11, 2002

    Report

    Report Number
    1518293-2002-00002
    Event Type
    Other
    Date Received
    January 11, 2002
    Date of Event
    December 21, 2001
    Report Date
    December 24, 2001
    Manufacturer
    LIEBEL-FLARSHEIM
    Product Code
    DXT
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    SUSPENSION ARM BROKE. NO INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CT9000 INJECTOR ANGIOGRAPHIC INJECTOR & SYRINGE DXT LIEBEL-FLARSHEIM CT 9000 *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other