BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SONICATOR PLUS 992

    MDR report key: 1210928 · Received October 23, 2008

    Report

    Report Number
    MW5008743
    Event Type
    Injury
    Date Received
    October 23, 2008
    Date of Event
    August 13, 2008
    Report Date
    October 23, 2008
    Manufacturer
    METTLER ELECTRONICS CORP.
    Product Code
    IPF
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MS, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PATIENT SUFFERED BURNS FOLLOWING TREATMENT FROM E-STIM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SONICATOR PLUS 992 E-STIM IPF METTLER ELECTRONICS CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 Other