BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TI TITAMAX IMPLANT (41)4.0X13 MM

    MDR report key: 4972213 · Received July 14, 2015

    Report

    Report Number
    3010593814-2015-00718
    Event Type
    Malfunction
    Date Received
    July 14, 2015
    Date of Event
    January 1, 2014
    Report Date
    January 30, 2015
    Product Code
    DZE
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    (OS 16.762). THE DENTIST REPORTED THAT AFTER THE DENTAL IMPLANT WAS INSTALLED IN INTRAORAL REGION #3 IT WAS VERIFIED ITS NON OSSEOINTEGRATION. PATIENT PRESENTED LOW BONE QUALITY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    457971 TI TITAMAX IMPLANT (41)4.0X13 MM ENDOSSEOUS DENTAL IMPLANT DZE NA 800072926

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Required Intervention