BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PADGETT ELECTRO-DERMATOME MODEL B 110 V

    MDR report key: 468031 · Received June 23, 2003

    Report

    Report Number
    1910735-2003-00013
    Event Type
    Malfunction
    Date Received
    June 23, 2003
    Report Date
    June 23, 2003
    Manufacturer
    PADGETT INSTRUMENTS
    Product Code
    GFD
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VT, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE CUSTOMER CLAIMS THAT THE THICKNESS OF THE GRAFT IS NOT CORRECT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PADGETT ELECTRO-DERMATOME MODEL B 110 V ELECTRIC DERMATOME GFD PADGETT INSTRUMENTS 3539-250 1-4735

    Patients

    Seq Age Sex Outcome Treatment
    1 *