BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNK

    MDR report key: 2945633 · Received December 31, 2012

    Report

    Report Number
    2945633
    Event Type
    Malfunction
    Date Received
    December 31, 2012
    Date of Event
    December 4, 2012
    Report Date
    December 31, 2012
    Manufacturer
    UNK
    Product Code
    GES
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IL, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK BLADE, SCALPEL GES UNK UNK *

    Patients

    Seq Age Sex Outcome Treatment
    1 23 YR