BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STERI-OSS DENTAL IMPLANT

    MDR report key: 59040 · Received December 13, 1996

    Report

    Report Number
    2027763-1996-05044
    Event Type
    Malfunction
    Date Received
    December 13, 1996
    Date of Event
    July 24, 1996
    Report Date
    December 13, 1996
    Manufacturer
    STERI-0SS, INC.
    Product Code
    DZE
    Removal / Correction Number
    NA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    DENTIST

    Narratives

    Description of Event or Problem · 1

    RECEIVED REPORT OF A FAILURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 STERI-OSS DENTAL IMPLANT Implant ENDOSSEOUS DENTAL IMPLANT DZE STERI-0SS, INC. 2416 88343

    Patients

    Seq Age Sex Outcome Treatment
    1 61 YR Required Intervention