BEUDAMED
    FDA Adverse Event Other Summary report: N

    BRACCO DIAGNOSTIC INC 017345

    MDR report key: 20894528 · Received December 6, 2024

    Report

    Report Number
    MW5163441
    Event Type
    Other
    Date Received
    December 6, 2024
    Report Date
    December 4, 2024
    Manufacturer
    BRACCO INJENEERING S.A.
    Product Code
    DXT
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    BRACCO SYRINGE EXPLODED OFF THE INJECTOR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2569934 BRACCO DIAGNOSTIC INC 017345 INJECTOR AND SYRINGE, ANGIOGRAPHIC DXT BRACCO INJENEERING S.A.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown