BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CM ALVIM IMPLANT 3.5X11.5

    MDR report key: 7013043 · Received November 9, 2017

    Report

    Report Number
    3008261720-2017-00707
    Event Type
    Injury
    Date Received
    November 9, 2017
    Date of Event
    July 10, 2015
    Report Date
    October 27, 2015
    Manufacturer
    NEODENT - JJGC S.A.
    Product Code
    DZE
    UDI-DI
    07898237569062
    PMA / PMN Number
    K101945
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    DENTIST

    Narratives

    Additional Manufacturer Narrative · 0

    EXEMPTION NUMBER: E2015015. INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF NEODENT - JJGC.

    Description of Event or Problem · 0

    RP.000251 - THE DENTIST REPORTED THAT 1 MONTH AFTER THE DENTAL IMPLANT WAS INSTALLED IN INTRAORAL REGION #8 IT WAS VERIFIED ITS NON- OSSEOINTEGRATION. FORTY-FIVE NCM OF PRIMARY STABILITY WAS ACHIEVED AND IMMEDIATE LOAD WAS NOT PERFORMED. PATIENT PRESENTED BONE TYPE III.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    792859 CM ALVIM IMPLANT 3.5X11.5 ENDOSSEOUS DENTAL IMPLANT DZE NEODENT - JJGC S.A. 07898237569062

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention