Stryker 0240-031-050, Руководство пользователя

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EN-3
Warnings and Cautions
Please read this manual and follow its instructions carefully. The words warning, caution,
and note carry special meanings and should be carefully reviewed:
Warning
: Indicates measures to avoid potential serious injury to the user and the patient.
Caution
: Indicates risks to the equipment. Failure to follow cautions may result in product
damage.
Note
: Provides special information to clarify instructions or present additional useful information.
Warnings
To avoid potential serious injury to the user and the patient, please note the following warnings:
1. Read this manual thoroughly and be familiar with its contents prior to using this device.
2. Federal law (United States of America) restricts this device to sale by, or on the order of, a
physician.
3. Carefully unpack the device and check if any damage occurred during shipment.
4. This device is non-sterile and therefore should not be placed in the sterile field.
5. Do not place the device or any other heavy object on the power cord. Damage to the cable
can cause fire or electric shock.
6. To avoid electric shock, avoid removing the bezel.
7. This device should not be used adjacent to or stacked with other devices. If adjacent or
stacked use is necessary, the device should be observed to verify normal operation in the
configuration in which it will be used.
8. Ensure weight compatibility with mounting apparatus. Do not mount the display on a cart
arm unless it is labeled with a maximum load ≥ 11.9 kg/26.3 lb.
9. Test this device prior to a surgical procedure. This device was fully tested at the factory
before shipment.
10. Do not attempt internal repairs or adjustments not specifically detailed in this manual.
Ensure that readjustments, modifications, and/or repairs are carried out by persons
authorized by Stryker Endoscopy.
11. Do not put any object into the panel. If this occurs, unplug the device and have it checked by
qualified personnel before operating it any further.
12. Use appropriate caution to prevent contact with fluids if the device is being used with a
power supply in patient environments.
13. The use of cables and/or other accessories with this device, other than those specified, may
result in increased emissions or decreased immunity of this device.
14. This device has no means to be incorporated in an IT-network in the clinical environment.
15. The protective screen is made of tested high-resistance PMMA (polymethyl methacrylate).
Nonetheless there is the possibility that it may crack if subject to strong impacts. Evaluate
and prevent the risk of possible breakages of the protective screen by correctly handling and
positioning the monitor in the operating room.