BEUDAMED
    FDA Adverse Event Other Summary report: N

    LINA LOOP

    MDR report key: 1672787 · Received April 27, 2010

    Report

    Report Number
    MW5015755
    Event Type
    Other
    Date Received
    April 27, 2010
    Date of Event
    January 25, 2010
    Report Date
    April 27, 2010
    Manufacturer
    LINA MEDICAL APS
    Product Code
    KNF
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    THE PT UNDERWENT A SEEMINGLY UNEVENTFUL LAPAROSCOPIC SUPRACERVICAL HYSTERECTOMY USING A LINA LOOP -MONOPOLAR ENDOSCOPIC LOOP-. SHE WAS READMITTED 5 DAYS POSTOPERATIVELY AND FOUND TO HAVE A DISTAL URETER TRANSECTION WHICH WAS REPAIRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LINA LOOP MONOPOLAR ENDOSCOPIC LOOP KNF LINA MEDICAL APS UNAVAILABLE UNAVAILABLE

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR Other