BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DAMON COPPER NITI WIRE

    MDR report key: 680767 · Received February 27, 2006

    Report

    Report Number
    2016150-2006-00006
    Event Type
    Malfunction
    Date Received
    February 27, 2006
    Date of Event
    January 1, 2006
    Report Date
    February 3, 2006
    Manufacturer
    ORMCO CORPORATION
    Product Code
    DZC
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    IN 2006 A DOCTOR INFORMED ORMCO CORPORATION THAT HE HAD DAMON CUNITI WIRE BREKAGES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DAMON COPPER NITI WIRE WIRE ORTHONDONTIC DZC ORMCO CORPORATION NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other