Integra Ti6 Gebrauchsanweisung Seite 8

EN – ENGLISH
Sterility – Ti6
The Ti6 Internal Fixation System components are provided non-sterile and must be cleaned and sterilized prior
to use. The Ti6 Internal Fixation System (instruments and screws) must be wrapped in FDA cleared wraps, pouches
or containers for steam sterilization. Do not re-use implants, as they are single use only. Detailed reprocessing
instructions are provided in LC-04-0000-0004.
Device Set System
Ti6 Internal Fixation System Low Profile Screw Set
Ti6 Internal Fixation System Solid Screw Tray
Ti6 Internal Fixation System Base Instrument Set
Ti6 Internal Fixation System Headless/Quicksnap Screws
Ti6 Internal Fixation System Digital Fusion Screws
1. EU representation is located in France.
2. This system does not have a registered CE mark.
PRODUCT INFORMATION DISCLOSURE
INTEGRA LIFESCIENCES CORPORATION ("INTEGRA") HAS EXERCISED REASONABLE CARE IN THE SELECTION OF MATERIALS AND
THE MANUFACTURE OF THESE PRODUCTS. INTEGRA EXCLUDES ALL WARRANTIES, WHETHER EXPRESSED OR IMPLIED, INCLUDING
BUT NOT LIMITED TO, ANY IMPLIED WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. INTEGRA
SHALL NOT BE LIABLE FOR ANY INCIDENTAL OR CONSEQUENTIAL LOSS, DAMAGE, OR EXPENSE, DIRECTLY OR INDIRECTLY ARISING
FROM USE OF THESE PRODUCTS. INTEGRA NEITHER ASSUMES NOR AUTHORIZES ANY PERSON TO ASSUME FOR IT ANY OTHER OR
ADDITIONAL LIABILITY OR RESPONSIBILITY IN CONNECTION WITH THESE PRODUCTS.
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