BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 4112550 · Received September 24, 2014

    Report

    Report Number
    1525712-2014-06163
    Event Type
    Malfunction
    Date Received
    September 24, 2014
    Report Date
    September 2, 2014
    Manufacturer
    UNKNOWN
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    THE STRAPS ON A R101 SLING, FOR AN UNKNOWN LIFT, ARE FRAYED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    593193 NON AC-POWERED PATIENT LIFT 880.5510 FSA UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other