BEUDAMED
    FDA Adverse Event Other Summary report: N

    ARTHROSCOPY BLADE, 5.0 MM

    MDR report key: 11733 · Received February 24, 1994

    Report

    Report Number
    MW1000875
    Event Type
    Other
    Date Received
    February 24, 1994
    Manufacturer
    STRYKER ENDOSCOPY
    Product Code
    HRX
    Report Source
    Voluntary report
    Reporter Location
    NY, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    DURING A CASE THE TIP BROKE OFF IN THE PT. TIP RETRIEVED AND RPTR NOTIFIED SALES REP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ARTHROSCOPY BLADE, 5.0 MM HRX STRYKER ENDOSCOPY

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other