BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    JOIMAX

    MDR report key: 9180131 · Received October 11, 2019

    Report

    Report Number
    9180131
    Event Type
    Malfunction
    Date Received
    October 11, 2019
    Date of Event
    August 7, 2019
    Report Date
    August 20, 2019
    Manufacturer
    JOIMAX GMBH
    Product Code
    LXH
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    SPINE GRASPER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    976950 JOIMAX ORTHOPEDIC MANUAL SURGICAL INSTRUMENT LXH JOIMAX GMBH 29/18

    Patients

    Seq Age Sex Outcome Treatment
    1 23360 DA