non-occlusive peristaltic pumps. The use of other types of
pump must be agreed with SORIN GROUP ITALIA.
J. RETURN OF USED PRODUCT
Should the user be dissatisfied with anything related to the
quality of the product, the product distributor or the authorized
local SORIN GROUP ITALIA representative should be
notified.
All parameters considered critical by the user must be
reported with particular care and urgency. The following is the
minimum information that should be provided:
Detailed description of the event and, if pertinent, the
conditions of the patient;
Identification of the product involved;
Lot number of the product involved;
Availability of the product involved;
All the indications the user considers useful in order to
understand the origin of the elements of dissatisfaction.
SORIN GROUP ITALIA reserves the right to authorize, if
necessary, recall of the product involved in the notification for
assessment. If the product to be returned is contaminated, it
must be treated, packed and handled in conformity with the
provisions of the legislation in force in the country where the
product was used.
It is the responsibility of the health care institution to
adequately prepare and identify the product for return
shipment. Do not return products that have been exposed
to blood borne infectious diseases.
ONLY for US customers
If for any reason the product must be returned to the
manufacturer, a returned good authorisation (RGA) number is
required from Sorin Group USA Inc. prior to shipping .
If the product has been in contact with blood or blood fluids, it
must be thoroughly cleaned and disinfected before packing. It
should be shipped in either the original carton or an equivalent
carton to prevent damage during shipment, and it should be
properly labelled with an RGA number and an indication of the
biohazardous nature of the content in the shipment.
It is the responsibility of the health care institution to
adequately prepare and identify the product for return
shipment. Do not return products that have been exposed
to blood borne infectious diseases
The shipping address for returned goods in the US is:
Sorin Group USA, Inc.
Returned CV Products
14401 West 65th Way
Arvada, CO 80004-3599
FAX (800) 323 4031.
K. LIMITED WARRANTY
This Limited Warranty is in addition to any statutory rights of
the Purchaser pursuant to applicable law.
SORIN GROUP ITALIA warrants that all reasonable care has
been taken in the manufacture of this medical device, as
required by the nature of the device and the use for which the
device is intended.
SORIN GROUP ITALIA warrants that the medical device is
capable of functioning as indicated in the current instructions
for use when used in accordance with them by a qualified user
and before any expiry date indicated on the packaging.
However, SORIN GROUP ITALIA cannot guarantee that the
user will use the device correctly, nor that the incorrect
diagnosis or therapy and/or that the particular physical and
biological characteristics of an individual patient, do not affect
the performance and effectiveness of the device with
damaging consequences for the patient, even though the
specified instructions for use have been respected.
SORIN GROUP ITALIA, whilst emphasizing the need to
adhere strictly to the instructions for use and to adopt all the
precautions necessary for the correct use of the device,
cannot assume any responsibility for any loss, damage,
expense, incidents or consequences arising directly or
indirectly from the improper use of this device.
SORIN GROUP ITALIA undertakes to replace the medical
device in the event that it is defective at the time of placing on
the market or whilst being shipped by SORIN GROUP ITALIA
up to the time of delivery to the final user unless such defect
has been caused by mishandling by the purchaser.
The above replaces all other warranties explicit or implicit,
written or verbal, including warranties of merchantability and
fitness for purpose. No person, including any representative,
agent, dealer, distributor or intermediary of SORIN GROUP
ITALIA or any other industrial or commercial organization is
authorized to make any representation or warranty concerning
this medical device except as expressedly stated herein.
SORIN
GROUP
merchantability and any warranty of fitness for purpose with
regard to this product other than what is expressedly stated
herein. The purchaser undertakes to comply with the terms of
this Limited Warranty and in particular agrees, in the event of
a dispute or litigation with SORIN GROUP ITALIA, not to
make claims based on alleged or proven changes or
alterations
made
representative, agent, dealer, distributor or other intermediary.
The existing relations between the parties to the contract (also
in the case that it is not drawn up in writing) to whom this
Warranty is given as well as every dispute related to it or in
any way connected to it as well as anything related to it or any
dispute concerning this Warranty, its interpretation and
execution, nothing excluded and/or reserved, are regulated
exclusively by the Italian law and jurisdiction.
chosen is the Court of Modena (Italy).
GB – ENGLISH
ITALIA
disclaims
any
to
this
Limited
Warranty
warranty
of
by
any
The court
7