Verathon AORTASCAN AMI 9700, Operation & Maintenance Manual

Page: 75 / 88

67
Operations & Maintenance Manual: Warranty
WARRANTY
Verathon
®
warrants the AortaScan AMI 9700 against defects in material and workmanship as long as it is
covered by the Premium Warranty.
Verathon’s policy is to honor product warranties and to perform services only on products purchased from
an authorized Verathon entity. If you purchase a Verathon product or system components from unauthorized
entities or if the original factory serial number has been removed, defaced, altered, or if the product is
past its expiration date, your Verathon warranty will be invalidated. Purchasing Verathon products from
unauthorized entities could result in receipt of products or system components that are counterfeit, used,
expired, defective, or not intended for use in your region.
Pursuant to this warranty, a service center authorized by Verathon will repair or replace units that prove to be
defective during the warranty period.
This warranty does not apply if the unit was misused or modified by anyone other than an authorized
service center.
The unit must be used in accordance with the instructions contained in this manual. Consumable items are
not covered in this warranty and should be used in conformance with Verathon product specifications, as
provided in the
Product Specifications chapter.
For further details, consult your Premium Warranty. Warranty conditions may differ in some countries outside
the United States. Contact your local distributor for warranty terms.
DISCLAIMER OF ADDITIONAL WARRANTIES
There are no understandings, agreements, representations of warranties expressed or implied (including
warranties of merchantability or fitness for a particular purpose) other than those set forth in the preceding
Warranty section. The contents of this manual do not constitute a warranty.
Some states disallow certain limitations on applied warranties. The purchaser, user, and patient
should consult state law if there is a question regarding this disclaimer. This information, descriptions,
recommendations, and safety notations in this manual are based upon Verathon experience and judgment
with the AortaScan AMI 9700 as of December 2013. The contents of this manual should not be considered
to be all‑inclusive, or to cover all contingencies.
The physician who directs the use of the AortaScan AMI 9700 at the institution where it is in use is
responsible for keeping current with clinical research in aortic diameter measurements.
Please direct any questions or problems concerning aortic diameter measurement, using the instrument, or
the interpretation of data to the responsible physician.