BEUDAMED
    FDA Adverse Event Other Summary report: N

    THERATRON

    MDR report key: 194599 · Received October 26, 1998

    Report

    Report Number
    9610077-1998-00015
    Event Type
    Other
    Date Received
    October 26, 1998
    Report Date
    September 22, 1998
    Manufacturer
    THERATRONICS
    Product Code
    IWH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    WV, US
    Reporter Occupation
    SERVICE PERSONNEL

    Narratives

    Description of Event or Problem · 1

    A PT REC'D A CUT FINGER WHILE HOLDING ONTO THE TREATMENT TABLE STRETCHER TOP WHEN THE OPERATOR MOVED THE TOP LONGITUDINALLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THERATRON COBALT TELETHERAPY DEVICE IWH THERATRONICS T1000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Required Intervention