BEUDAMED
    FDA Adverse Event Other Summary report: N

    MULTILINK AUTOMIX

    MDR report key: 2016277 · Received February 15, 2011

    Report

    Report Number
    9612352-2011-00001
    Event Type
    Other
    Date Received
    February 15, 2011
    Date of Event
    February 1, 2011
    Report Date
    February 15, 2011
    Manufacturer
    IVOCLAR VIVADENT, AG
    Product Code
    EMA
    PMA / PMN Number
    K032470
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    SENSITIVITY REPORTED AFTER USE OF DEVICE WHICH RESULTED IN ENDODONTIC TREATMENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MULTILINK AUTOMIX DENTAL CEMENT EMA IVOCLAR VIVADENT, AG UNK

    Patients

    Seq Age Sex Outcome Treatment
    1