BEUDAMED
    FDA Adverse Event Summary report: N

    MECHANICAL (MANUAL) WHEELCHAIR

    MDR report key: 4240389 · Received November 10, 2014

    Report

    Report Number
    9616091-2014-02409
    Date Received
    November 10, 2014
    Date of Event
    October 23, 2014
    Report Date
    November 7, 2014
    Manufacturer
    INVAMEX
    Product Code
    IOR
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

    Narratives

    Description of Event or Problem · 1

    DEALER STATED THAT FACILITY, (B)(6), REPORTED THAT A PATIENT ALLEGEDLY GOT THEIR HANDS STUCK ON THE SIDE OF THE SEAT FRAME WHILE TRYING TO PUT THE PATIENT IN THE (B)(4) WHEELCHAIR. UNSPECIFIED INJURY. NO MALFUNCTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    722503 MECHANICAL (MANUAL) WHEELCHAIR 890.3850 IOR INVAMEX T424RFA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other