BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2.3 MM DRILL BIT FOR BIORAPTOR

    MDR report key: 1000302 · Received February 14, 2008

    Report

    Report Number
    1219602-2008-00037
    Event Type
    Malfunction
    Date Received
    February 14, 2008
    Date of Event
    January 15, 2008
    Report Date
    January 17, 2008
    Manufacturer
    SMITH & NEPHEW INC., ENDOSCOPY DIV.
    Product Code
    HTW
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 2.3 MM DRILL BIT FOR BIORAPTOR DRILL HTW SMITH & NEPHEW INC., ENDOSCOPY DIV. 72201108 50227297

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK