BEUDAMED
    FDA Adverse Event Other Summary report: N

    NO-SCALPEL VAS GRASPING FCP

    MDR report key: 380343 · Received March 4, 2002

    Report

    Report Number
    1038548-2002-00001
    Event Type
    Other
    Date Received
    March 4, 2002
    Date of Event
    January 27, 2002
    Report Date
    March 4, 2002
    Manufacturer
    SNOWDEN PENCER, INC.
    Product Code
    GEN
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    IT BROKE DURING A SURGERY. A PIECE OF THE ITEM FELL INTO THE PATIENT. DR RECOVERED THE PIECE AND THE PATIENT WAS NOT HARMED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 NO-SCALPEL VAS GRASPING FCP * GEN SNOWDEN PENCER, INC. 88-0427 *

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN