BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TI TITAMAX IMPLANT (5.0) 5.0X9

    MDR report key: 7380767 · Received March 29, 2018

    Report

    Report Number
    3008261720-2018-01459
    Event Type
    Injury
    Date Received
    March 29, 2018
    Date of Event
    January 1, 2018
    Report Date
    March 29, 2018
    Manufacturer
    NEODENT - JJGC S.A.
    Product Code
    DZE
    UDI-DI
    07898237566955
    PMA / PMN Number
    K101207
    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. EXEMPTION NUMBER: E2015015. INSTRADENT USA, INC IS SUBMITTING THE REPORT ON BEHALF OF NEODENT - JJGC S.

    Description of Event or Problem · 0

    (B)(4) - ¿ THE DENTIST REPORTED THAT AFTER DENTAL IMPLANT WAS INSTALLED IN PATIENT¿S MOUTH, ITS NON-OSSEOINTEGRATION WAS OBSERVED. NO FURTHER INFORMATION WAS PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    223972 TI TITAMAX IMPLANT (5.0) 5.0X9 ENDOSSEOUS DENTAL IMPLANT DZE NEODENT - JJGC S.A. 800239084 07898237566955

    Patients

    Seq Age Sex Outcome Treatment
    1 59 YR Required Intervention