BEUDAMED
    FDA Adverse Event Other Summary report: N

    UNK

    MDR report key: 265262 · Received February 24, 2000

    Report

    Report Number
    265262
    Event Type
    Other
    Date Received
    February 24, 2000
    Date of Event
    February 17, 2000
    Report Date
    February 23, 2000
    Manufacturer
    UNK
    Product Code
    HDQ
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    UTERINE PERFORATION SUSTAINED DURING HYSTEROSCOPY. BOWEL SEEN WHEN HYSTEROSCOPE INTRODUCED. SUBSEQUENT TO DILATION OF OS. PLANNED DILITATION AND CURETTAGE INTERVENTION ABORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UNK DILATOR HDQ UNK UNK *

    Patients

    Seq Age Sex Outcome Treatment
    1 50 YR Other HYSTEROSCOPE