BEUDAMED
    FDA Adverse Event Other Summary report: N

    STRAIGHT CATHETER

    MDR report key: 4170761 · Received October 10, 2014

    Report

    Report Number
    MW5038556
    Event Type
    Other
    Date Received
    October 10, 2014
    Date of Event
    August 29, 2014
    Report Date
    October 10, 2014
    Manufacturer
    CURE MEDICAL LLC
    Product Code
    EZD
    Report Source
    Voluntary report
    Reporter Location
    WI, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PATIENT COMPLAINED OF BLADDER SPASMS SINCE (B)(6) 2014, WHEN A CATHETER WAS USED ON HIM IN THE ER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    640143 STRAIGHT CATHETER STRAIGHT CATHETER EZD CURE MEDICAL LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 48 YR