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XVIVO Perfusion System (XPS
TM
) Instructions for Use
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11
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P/N: 9182
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0189 Revision Q
OPERATOR CAUTIONS
Caution:
This User
’
s Guide and the equipment it describes are for use only by qualified medical professionals trained in the
particular technique and surgical procedure to be performed.
Caution:
The safe and effective use of this medical device depends to a large degree on factors solely under the control of the
operator. It is important that all operators of this surgical system read, understand and follow the operating instructions
(User
’
s Guide) supplied with this equipment. The responsibility to adhere to the approved labeling and Instructions for Use
rests with the user.
The Instructions for Use are only provided as suggestions for procedure.
The user must, on the basis
of his or her medical training and experience, evaluate the suitability of this procedure.
Caution:
Federal (USA) law restricts this device to the order of a physician.
Caution:
This device complies with the electromagnetic compatibility standard IEC EN60601
-
1
-
2. It is possible that this device may
interfere with or be disturbed by other electrical devices.
Caution:
All disposable components of this device are designed as
single use only
and may not be reused in an ex vivo lung
procedure.
NOTE:
When administered systemically, human serum albumin and Dextran have been associated with rare allergic reactions.
However, no such reactions have been reported with either of these substances when used for ex vivo lung preservation.
NOTE:
The XPS
TM
has been tested and found to comply with the limits for a Class A device, pursuant to CISPR 11 and Part 18 of
the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a commercial
installation. However, portable and mobile RF communications equipment generates, uses and can radiate radio
frequency energy and, if not installed and used in accordance with the manufacturer
’
s instructions, may cause harmful
interference to the XPS
TM
. There is no guarantee that interference will not occur in a particular installation. If this
equipment receives harmful interference from RF communications, which can be determined by turning the RF
communications equipment off and on, the user is encouraged to try to correct the interference by one or more of the
following measures:
•
Reorient or relocate the XVIVO Perfusion Cart
•
Increase the separation between the XVIVO Perfusion Cart and the RF communications equip-
ment
•
Connect the XVIVO Perfusion Cart into an outlet on a circuit different from that to which the
RF communications equipment is connected
•
Deactivate the flow intervention. Incorrect flow values can trigger improper interventions.
•
Please note that flow values may be displayed and monitored with reduced accuracy and
alarms triggered with reduced accuracy
1.3 XPS
TM
Operator Warnings and Cautions