BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNK

    MDR report key: 360042 · Received November 1, 2001

    Report

    Report Number
    360042
    Event Type
    Malfunction
    Date Received
    November 1, 2001
    Date of Event
    October 18, 2001
    Report Date
    October 31, 2001
    Manufacturer
    UNK
    Product Code
    HTY
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    TX, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    REMOVAL OF K-WIRE NOSE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    49045 UNK K-WIRE HTY UNK UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Other