BEUDAMED
    FDA Adverse Event Summary report: N

    CENTERPULSE

    MDR report key: 512467 · Received November 18, 2003

    Report

    Report Number
    MW4003656
    Date Received
    November 18, 2003
    Report Date
    November 18, 2003
    Manufacturer
    ZIMMER DENTAL INC.
    Product Code
    DZE
    Report Source
    Voluntary report
    Reporter Location
    FL, US
    Reporter Occupation
    PATIENT

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTERPULSE DENTAL IMPLANTS DZE ZIMMER DENTAL INC. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *