BEUDAMED
    FDA Adverse Event Summary report: N

    NON AC-POWERED PATIENT LIFT

    MDR report key: 2914705 · Received January 14, 2013

    Report

    Report Number
    1531186-2013-00207
    Date Received
    January 14, 2013
    Report Date
    January 14, 2013
    Manufacturer
    SAGITTARIUS-XIAMEN FEIPENG
    Product Code
    FSA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    MDR DECISION DATE: (B)(6). NO SERIOUS INJURY ALLEGED. MALFUNCTION ALLEGED. DEALER STATES THAT ALLEGEDLY THE HANDLE WILL NOT HOLD WEIGHT. MDR FILED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    20957 NON AC-POWERED PATIENT LIFT 880.5510 FSA SAGITTARIUS-XIAMEN FEIPENG 9805

    Patients

    Seq Age Sex Outcome Treatment
    1 Other