Stryker 1688 Series, Руководство пользователя, Страница: 6 / 68

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6. The camera head and coupler are shipped non-sterile. You must sterilize
these devices before the first use and after each use. To prevent device
damage and infection risk to the patient or user, follow all cleaning and
sterilization instructions in this manual.
7. To minimize electromagnetic interference that may impact functionality
of the 1688 Video Camera, position any active electrosurgical generator
and its cables at least 12 inches (30 cm) away from the camera console.
When the electrosurgical generator is placed on a boom with the camera
console, it is advised to position the generator on the lowest shelf.
8. Do not position the console so that it is difficult to disconnect the power
cord from the supply mains.
9. To avoid the risk of electric shock, this equipment must only be
connected to a supply mains with protective earth ground.
10. Portable multiple socket-outlets shall not be placed on the floor.
Additional portable multiple socket-outlets or extension cords shall not
be used with the equipment.
11. Use of third-party HDMI cables with the camera console is not
recommended due to potential problems with secure connections or
electromagnetic compatibility. Use the provided HDMI high speed cable
(or other Stryker-approved HDMI cable) with the camera console.
12. Never use the camera system in the presence of flammable or explosive
gases or in an oxygen-rich environment.
13. To prevent tampering, physically secure the device when not in use.
14. Disconnect the console from the electrical outlet when inspecting fuses.
15. Do not remove covers on the console, as doing so may cause damage to
electronics and/or electric shock.
16. Do not disassemble any part of the camera head; doing so may break the
seals, causing leakage and/or electric shock.
17. Attempt no internal repairs or adjustments not specifically detailed in this
operating manual.
18. Do not repair or adjust the device through a third-party service
organization. Devices repaired by or purchased from third-party service
organizations could expose patients to significant risk. These devices
are no longer validated by Stryker for cleanliness, disinfection, and
sterilization, or for safety and efficacy.