BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BLT Ø4.8MM RC, SLA® 10MM, TIZR, LOXIM

    MDR report key: 18554803 · Received January 22, 2024

    Report

    Report Number
    0001222315-2024-001861
    Event Type
    Injury
    Date Received
    January 22, 2024
    Date of Event
    October 23, 2023
    Report Date
    January 22, 2024
    Manufacturer
    INSTITUT STRAUMANN AG
    Product Code
    DZE
    UDI-DI
    07630031707543
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    OH, US
    Reporter Occupation
    DENTIST
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE CLINICIAN REPORTS THE IMPLANT WAS INSERTED (B)(6) 2023 IN ADA 14. ON 2023-10-23, NON-OSSEOINTEGRATION WAS VERIFIED. THE DEVICE WAS FORWARDED TO THE MANUFACTURER. THERE WERE NO REPORTED PATIENT INJURIES OR COMPLICATIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1717942 BLT Ø4.8MM RC, SLA® 10MM, TIZR, LOXIM ENDOSSEOUS DENTAL IMPLANT DZE INSTITUT STRAUMANN AG NRV42 07630031707543

    Patients

    Seq Age Sex Outcome Treatment
    1 Female Required Intervention