BEUDAMED
    FDA Adverse Event Other Summary report: N

    POWER TRIALYSIS TRAY

    MDR report key: 19659824 · Received July 1, 2024

    Report

    Report Number
    MW5156933
    Event Type
    Other
    Date Received
    July 1, 2024
    Date of Event
    June 27, 2024
    Report Date
    June 27, 2024
    Manufacturer
    BD / BARD ACCESS SYSTEMS, INC.
    Product Code
    NIE
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    BD# 5605200 GUIDEWIRE BENT WHEN DR ATTEMPTED INSERTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    551163 POWER TRIALYSIS TRAY CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED NIE BD / BARD ACCESS SYSTEMS, INC. 5605200

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown