BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 1240441 · Received August 14, 2008

    Report

    Report Number
    9710641-2008-00119
    Event Type
    Other
    Date Received
    August 14, 2008
    Manufacturer
    *
    Product Code
    BTG
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    CONMED CORP REC'D USER FACILITY UF/IMPORTER REPORT. AFTER A REVIEW OF THE EVENT DESCRIPTION AS REPORTED, CONMED HAS DETERMINED THIS EVENT NOT TO BE CONSIDERED REPORTABLE. HOWEVER, CONMED IS FILING THIS REPORT IN RESPONSE TO THE INITIAL REPORT SUBMITTED BY FACILITY. THIS COMPLAINT IS BEING PROCESSED THROUGH THE CONMED CORP QUALITY SYSTEM OF COMPLAINT HANDLING FOR NON REPORTABLE EVENTS. NO SUPPLEMENTAL WILL BE FILED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * BTG * NA *

    Patients

    Seq Age Sex Outcome Treatment
    1