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Newport e360 - Responsibility for Patient Safety

Newport e360
150 pages
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OPR360U A0509
5-1
5
OPR360U A0509
5-1
5
OPR360U A0509
5-1
5
OPR360U A0509
5-1
5
OPR360US H0711
1-10
1
Introduction
• Thiswarrantyisapplicabletotheoriginalpurchaser/facilityandis
non-transferable.
• Repairs,maintenanceorservicingoftheNewporte360Ventilator
by personnel other than Newport Factory Trained Technicians or
authorized representatives will void this warranty.
In order to assure complete protection under this warranty the
customer must register the product within ten (10) days of receipt of
the equipment by visiting the Newport Medical website and filling out
the product registration form at www.ventilators.com.
The above is the sole warranty provided by Newport Medical. No
other warranty expressed or implied is intended. Representatives
of Newport Medical are not authorized to modify the terms of this
warranty.
Responsibility for Patient Safety
To use this product correctly and effectively and to avoid hazards,
carefully read and observe all sections of this manual prior to use.
Because the operating manual and labeling of the e360 Ventilator
System assume that its sale and use are restricted to qualified,
trained professionals under the direction of a physician who
understand the general operating characteristics of ventilators, this
manual includes instructions, warnings, and cautions that are specific
to the design of this ventilator. This manual excludes references to
hazards that are obvious to medical professionals, the consequences
of product misuse, or to potentially adverse effects in patients with
abnormal conditions.
Product modification or misuse can be dangerous. Newport Medical
disclaims all liability for the consequences of product alterations
or modifications, as well as for the consequences that might result
from the combination of this ventilator with other products, whether
supplied by Newport Medical or by other manufacturers, if such a
combination is not endorsed by Newport Medical.
It is the responsibility of the ventilator operator to choose appropriate
monitoring of equipment performance and patient condition.
Electronic surveillance of equipment performance and patient
condition cannot take the place of directly observing clinical signs.
The ventilator operator is solely responsible for selecting the optimum
level of patient monitoring.
Federal Law and Regulations in the United States and Canada
restrict this device to sale by or on the order of a physician.

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