BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VIKING M

    MDR report key: 3854195 · Received June 3, 2014

    Report

    Report Number
    8030916-2014-00037
    Event Type
    Malfunction
    Date Received
    June 3, 2014
    Manufacturer
    LIKO AB
    Product Code
    FSA
    Report Source
    Manufacturer report

    Narratives

    Description of Event or Problem · 1

    (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    323237 VIKING M NON-AC POWERED PATIENT LIFT FSA LIKO AB

    Patients

    Seq Age Sex Outcome Treatment
    1