Returned Goods Policy; Repairs And Maintenance - Integra LifeSciences Jarit Instrucciones De Uso

Any kind of corrosion will lead to rust on steel. Rust particles can
be transferred from one instrument to another, therefore, remove
corroding instruments from service to prevent formation of rust on other
instruments.
Protect sharp cutting edges and fine working ends of inserts during all
maintenance procedures. Avoid loading heavy items on top of delicate
and hollow instruments.
Diagnosing Spots and Stains: It is common for instruments to become
stained or spotted. Adhering to proper technique during cleaning and
sterilizing procedures will prevent most staining occurrences. The
following identifies some of the various instrument-related problems
hospitals may encounter.
• Brown Stains: Detergents containing polyphosphates may dissolve
copper elements in the sterilizer resulting in brown stains. A dull blue
or brown stain is the result of oxidation on the surface.
• Black Stains: Black stain may be the result of contact with ammonia.
• Light or Dark Spots: Spots are often the result of the mineral content
in the water used for rinsing, use of non-neutral instruments or an
unclean sterilizer chamber.
• Rust Deposits: It is very unlikely for surgical grade steel to rust. Rust
colored spots usually appear in localities where water has high iron
content.

RETURNED GOODS POLICY

Products must be returned in unopened packages with manufacturer's
seals intact to be accepted for replacement or credit unless returned
due to a complaint of product defect. Determination of a product defect
will be made by Integra. Products will not be accepted for replacement
if they have been in the possession of the customer for more than 90
days.

REPAIRS AND MAINTENANCE

Should your instruments require repair or maintenance, contact Integra
for return authorization and address. Instruments returned to Integra for
repair must have a statement testifying that each instrument has been
thoroughly cleaned and sterilized. Failure to supply evidence of cleaning
and disinfection will result in a cleaning charge and delayed processing
of your instrument repair.
PRODUCT INFORMATION DISCLOSURE
INTEGRA AND ITS SUBSIDIARIES ("INTEGRA") AND MANUFACTURER
EXCLUDE ALL WARRANTIES, EXCEPT INTEGRA'S APPLICABLE
STANDARD WARRANTY WHETHER EXPRESSED OR IMPLIED, INCLUDING
BUT NOT LIMITED TO, ANY IMPLIED WARRANTIES OF MERCHANTABILITY
OR FITNESS FOR A PARTICULAR PURPOSE. NEITHER INTEGRA
NOR MANUFACTURER SHALL BE LIABLE FOR ANY INCIDENTAL
OR CONSEQUENTIAL LOSS, DAMAGE, OR EXPENSE, DIRECTLY OR
INDIRECTLY ARISING FROM USE OF THIS PRODUCT. NEITHER INTEGRA
NOR MANUFACTURER ASSUME NOR AUTHORIZE ANY PERSON TO
ASSUME FOR THEM ANY OTHER OR ADDITIONAL LIABILITY OR
RESPONSIBILITY IN CONNECTION WITH THESE PRODUCTS.
SYMBOLS USED ON LABELING
Manufacturer
European Authorized Representative
EC REP
Catalog Number
REF
LOT
Lot Number
Caution! See Warnings and Precautions
Consult instructions for use
CAUTION: Federal (USA) law restricts this device to sale by or
on order of a physician.
Product complies with requirements of directive 93/42/EEC
for medical devices
Integra York PA, Inc.
589 Davies Drive
York, PA 17402 USA
www.integralife.com/Jarit
EC REP
Integra LifeSciences Services (France) SAS Immeuble Sequoia 2
97 allée Alexandre Borodine
Parc Technologique de la Porte des Alpes
69800 Saint Priest–France
Telephone: 33 (0) 4 37 47 59 10
Fax: 33 (0) 4 37 47 59 29
Integra, the Integra logo and Jarit are registered trademarks of Integra
LifeSciences Corporation or its subsidiaries in the United States and/or other
countries. ©2015 Integra LifeSciences Corporation. All Rights Reserved.
JL-00102 Rev 3 1/21/2015