BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TIBIAL NAIL, STANDARD T2 TIBIA Ø9X270 MM

    MDR report key: 3203685 · Received February 12, 2013

    Report

    Report Number
    0009610622-2013-00040
    Event Type
    Malfunction
    Date Received
    February 12, 2013
    Date of Event
    January 11, 2013
    Report Date
    January 21, 2013
    Manufacturer
    STRYKER OSTEOSYNTHESIS-KIEL
    Product Code
    HSB
    PMA / PMN Number
    K003018
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    62719 TIBIAL NAIL, STANDARD T2 TIBIA Ø9X270 MM IMPLANT HSB STRYKER OSTEOSYNTHESIS-KIEL UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Other