BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GH3 PATIENT LIFT

    MDR report key: 9391739 · Received November 29, 2019

    Report

    Report Number
    9391739
    Event Type
    Malfunction
    Date Received
    November 29, 2019
    Date of Event
    November 22, 2019
    Report Date
    November 26, 2019
    Manufacturer
    V. GULDMANN A/S
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    AS A PATIENT WAS BEING LIFTED WITH THE CEILING LIFT, ONE OF THE SLINGS POPPED OFF THE CROSSBAR.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1185339 GH3 PATIENT LIFT LIFT, PATIENT, AC-POWERED FSA V. GULDMANN A/S

    Patients

    Seq Age Sex Outcome Treatment
    1