BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HENRY SCHEIN

    MDR report key: 19020124 · Received April 2, 2024

    Report

    Report Number
    3007007357-2024-00010
    Event Type
    Injury
    Date Received
    April 2, 2024
    Date of Event
    March 5, 2024
    Report Date
    April 1, 2024
    Manufacturer
    TTBIO CORP
    Product Code
    EFB
    UDI-DI
    00304040133682
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    AZ, US
    Reporter Occupation
    003

    Narratives

    Description of Event or Problem · 0

    BUR USED IN HANDPIECE BENT WHILE IN USE AND INJURED PATIENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1362675 HENRY SCHEIN HANDPIECE EFB TTBIO CORP MAXIMA PRO 2L AR 00304040133682

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female Other