BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LID F/BATT-HANDPIECE NO. 05.001.201 F/TR

    MDR report key: 4141034 · Received October 3, 2014

    Report

    Report Number
    8030965-2014-01116
    Event Type
    Malfunction
    Date Received
    October 3, 2014
    Report Date
    May 27, 2013
    Manufacturer
    SYNTHES GMBH
    Product Code
    MOQ
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO (B)(4) AND REPAIR FILES LEGACY REVIEW/REMEDIATION PROTOCOL-COMPLAINT HANDLING AND MDR REPORTING. BLANK FIELDS ON THIS FORM INDICATE THE INFORMATION IS UNKNOWN, UNAVAILABLE OR UNCHANGED. DEVICE LISTED IN THIS REPORT IS USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR. DURING PRE-REPAIR ASSESSMENT PERFORMED BY A TECHNICIAN, FUNCTIONAL TESTING WAS PERFORMED AND NO FAILURE OR DEFECT WAS FOUND. INVESTIGATION WAS PERFORMED AND THE DEVICE WAS RETURNED TO THE CUSTOMER ON 06/10/2013. PLACEHOLDER.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THAT WHEN YOU GET TO THE BONE, THE SAW STOPS OSCILLATING. THIS IS REPORT 1 OF 1 FOR COMPLAINT #(B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    618786 LID F/BATT-HANDPIECE NO. 05.001.201 F/TR MOQ SYNTHES GMBH 3718

    Patients

    Seq Age Sex Outcome Treatment
    1