BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 1182321 · Received July 14, 2008

    Report

    Report Number
    9680515-2008-00007
    Event Type
    Other
    Date Received
    July 14, 2008
    Manufacturer
    TONTARRA MEDIZINTECHNIK GMBH
    Product Code
    HTX
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL DEVICES INVOLVED AND RESPECTIVE MANUFACTURE DATES: 1 EA. OF 280-062DT - 10/2004; 1 EA. OF 280-062DT - 10/2004; 1 EA. OF 280-060DT - 02/2005; 1 EA. OF 281-060DT - 09/2005.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * HTX TONTARRA MEDIZINTECHNIK GMBH * *

    Patients

    Seq Age Sex Outcome Treatment
    1