User manual

WARRANTY/REPAIR INFORMATION
 2001 Xantrex Technology, Inc.
5916 - 195th Street N. E.
Arlington, WA 98223
Telephone: [phone]
Fax: [phone]
www.traceengineering.com
SW Series Inverter/Charger
Part No. 2031-5
Rev. C: February 2001
Page
135
WARRANTY/REPAIR INFORMATION
LIMITED WARRANTY
Xantrex Technology Inc. warrants its power products against defects in materials and workmanship for a
period of two (2) years from the date of purchase and extends this warranty to all purchasers or owners of the
product during the warranty period. This warranty is void under the following circumstances:
(1) improper and/or unauthorized repair not provided by Xantrex Technology Inc., or its Authorized
Service Centers;
(2) when the product is installed or exposed or exposed to an unsuitable environment as evidenced
by generalized corrosion or biological infestation;
(3) abnormal use of the product or use in violation of the instructions;
(4) when used as a component parts of a product expressly warranted by another manufacturer.
Xantrex Technology Inc., agrees to supply all parts and labor or repair or replace defects covered by this
warranty with parts or products of original or improved design, at the company’s option. Xantrex
Technology Inc., also reserves the right to improve the design of its products without obligation to modify
or upgrade those previously manufactured. Defective products must be returned to Xantrex Technology
Inc., or its Authorized Service Center in the original packaging. The cost of transportation and insurance
on items returned for service is the responsibility of the customer.
All remedies and the measure of damages are limited to the above. Xantrex Technology Inc., shall in no
event be liable for consequential, incidental, contingent, or special damages, even if Xantrex Technology Inc.,
has been advised of the possibility of such damages. Any and all other warranties, expressed or implied,
arising by law, course of dealing, course of performance, usage of trade or otherwise, including, but not
limited to, implied warranties of merchantability and fitness for a particular purpose, are limited in duration for
a period of two (2) years from the original date of purchase.
Some countries or states do not allow limitations on the term of an implied warranty, or the exclusion or
limitation of incidental or consequential damage, which means the limitations and exclusions of this
warranty, may not apply to you. Even though this warranty gives you specific legal rights, you may also
have other rights that vary from state to state.
WARRANTY REGISTRATION
Complete the warranty card and mail it to Xantrex Technology Inc., within 10 days from the date of
purchase. keep your bill of sale as proof of purchase, should any difficulties arise concerning the
registration of the warranty card.
Warranty Registration is tracked by model and serial numbers only, not by owner’s name. Therefore, any
correspondence or inquiries made to Xantrex Technology Inc., must include the model and serial number
of the product in question.
LIFE SUPPORT POLICY
As a general policy, Xantrex Technology Inc., does not recommend the use of any of its products in life
support applications where failure or malfunction of the Trace Engineering product can be reasonably
expected to cause failure of the life support device or to significantly affect its safety or effectiveness.
Xantrex Technology Inc., does not recommend the use of any of its products in direct patient care.
Xantrex Technology Inc., will not knowingly sell its products for use in such applications unless it receives
in writing assurances satisfactory to Xantrex Technology Inc., that (a) the risks of injury or damage have
been minimized, (b) the customer assumes all such risks, and the liability of Xantrex Technology Inc., is
adequately protected under the circumstances
Examples of devices considered to be life support devices are neonatal oxygen analyzers, nerve
stimulators (whether used for anesthesia, pain relief, or other purposes), autotransfusion devices, blood
pumps, defibrillators, arrhythmia detectors and alarms, pacemakers, hemodialysis systems, peritoneal
dialysis systems, neonatal ventilator incubators, ventilators for both adults and infants, anesthesia
ventilators, and infusion pumps as well as any other devices designated as “critical” by the U.S. FDA.