Symbols and De nitions ....................................................................................... 22
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
and/or damage to this device.
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 and/or damage to this device, 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 eld.
5. Do not place the device or any other heavy object on the power cord. Damage to the cable
can cause re 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
con guration in which it will be used.
8. Test this device prior to a surgical procedure. This device was fully tested at the factory
before shipment.
9. Do not attempt internal repairs or adjustments not speci cally detailed in this manual.
Ensure that readjustments, modi cations, and/or repairs are carried out by persons
authorized by Stryker Endoscopy.
10. Do not put any liquid or solid object into the panel. If this occurs, unplug the device and
have it checked by quali ed personnel before operating it any further.
11. Use appropriate caution to prevent contact with uids if the device is being used with a
power supply in patient environments.
12. The use of cables and/or other accessories with this device, other than those speci ed, may
result in increased emissions or decreased immunity of this device.
Cautions
1. Connect the device to an AC adapter connected to a hospital grade power cord ensuring the
power cord is plugged into a grounded power outlet to achieve grounding reliability.
2. Do not sterilize the device, as the delicate electronics cannot withstand this procedure.
3. Use only the proprietary surgical display power supply for the display. Completely secure the
connection between the DC power cord and the extension cord.
1
4. Never operate the device immediately after transportation from a cold location to a warm
location.
5. To connect to an international power supply, use an attachment plug appropriate for the
cations" section of this manual.
6. Unplug the device if it is not to be used for an extended period of time. To disconnect the
rst, then pull the cord out by the plug. Never pull the cord itself.
7. Do not expose the device to moisture or apply liquid cleaners directly to the screen. Spray
the cleaning solution into a soft cloth and clean gently. For further detail, refer to the
"Cleaning and Maintenance" section of this manual.
8. Allow adequate air circulation to prevent internal heat buildup. Do not place the device
on surfaces (rugs, blankets, etc.) or near materials (curtains, draperies) that may block the
ventilation slots. The device is cooled by natural convection and has no fan.
9. Do not touch the patient with signal input or output connectors. Equipment with SIP/
national standards or the combination should be evaluated for safety.
10. To ensure electromagnetic compatibility, refer to the “Electromagnetic Compatibility” section
11. Pay close attention to the cleaning instructions in this manual. A deviation may cause
damage.
12. Do not install the device near sunlight, excessive dust, mechanical vibration, or shock.
cult to disconnect the power cord from the supply
mains.
14. Do not operate with the glass device screen facing downward.
15. Handle the device with care. Do not strike or scratch the screen.
cations not expressly approved by the party responsible for compliance
could void the user’s authority to operate the device.
The warranty is void if any of these warnings or cautions are disregarded.
This product contains electrical waste or electronic equipment. It must not be disposed of as
unsorted municipal waste and must be collected separately.
For a Class B digital device or peripheral, the instructions furnished the user shall include the
following or similar statement, placed in a prominent location in the text of the manual:
NOTE: This equipment has been tested and found to comply with the limits for a Class B digital
device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable
protection against harmful interference in a residential installation. This equipment generates,
uses and can radiate radio frequency energy and, if not installed and used in accordance with
the instructions, may cause harmful interference to radio communications. However, there is no
guarantee that interference will not occur in a particular installation. If this equipment does cause
harmful interference to radio or television reception, which can be determined by turning the
equipment o and on, the user is encouraged to try to correct the interference by one or more of
the following measures:
—Reorient or relocate the receiving antenna.
—Increase the separation between the equipment and receiver.
—Connect the equipment into an outlet on a circuit dierent from that to which the receiver
is connected.
—Consult the dealer or an experienced radio/TV technician for help.
(c) The provisions of paragraphs (a) and (b) of this section do not apply to digital devices exempted
from the technical standards under the provisions of § 15.103.
(d) For systems incorporating several digital devices, the statement shown in paragraph (a) or (b) of
this section needs to be contained only in the instruction manual for the main control unit.
(e) In cases where the manual is provided only in a form other than paper, such as on a computer
disk or over the Internet, the information required by this section may be included in the manual in
that alternative form, provided the user can reasonably be expected to have the capability to access
information in that form.
2
About Your Device
VisionPro 26” LED Display
REF: 0240-031-020
The VisionPro 26” LED Display is a wide screen LED surgical display that can support a maximum
resolution of WUXGA (1920x1200). The display supports various video inputs, including digital
RGB, analog RGB, serial digital interface (SDI), component video (YPbPr/RGBS), S-video, and
C-video.
Intended Use
The VisionPro 26” LED Display is intended for video display during surgical procedures.
Indications
This device is indicated for the following surgical procedures:
• Arthroscopy (orthopedic surgery)
• Laparoscopy (general and gynecological surgery)
• Thorascopy
• Endoscopy (general, gastroenterological and ENT)
• ENT
• Gynecology
• General surgery
The display is a non-sterile, reusable device not intended for use in the sterile eld. The display
is intended for use by quali ed physicians having complete knowledge of these surgical
procedures.
Contraindications
There are no known contraindications for this device.
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Package Contents
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2
4
3
Reference Part NumberPackage Contents
10240-031-020 VisionPro 26” LED Display
5
2–(4) M4 × 16 mm VESA screws
3–Hospital-grade AC power cord
40240-031-004Medical Power Supply
5–Cable Cover
Part NumberOptional Accessories
0240-031-002VisionPro 26” Display Cover
0240-030-95115-ft. (5 pin) DC extension cable
0240-030-95275-ft. (5 pin) DC extension cable
4
Device Features
Front panel
Operate the display using the rotary control located on the front panel. A list of the display
controls and their functions is provided below.
1
2
3
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4
1. Auxilliary device status
indicator
2. Display ScreenShows video image.
3. Power switch (soft)Powers the display ON and OFF.
4. Power LEDIndicates current status. Shines green if the display is
5. PIPAccesses the Picture in Picture adjustment menu.
6. BrightAccesses the Brightness adjustment menu
7. SpecialtyAccesses the Specialty adjustment menu
8. InputAccesses the Input selection menu
9. Rotary controlAccesses the on-screen display and navigates through
LED shines red to indicate an active connection to a
connected device.
powered on or is in screen saver mode; blinks red if the
display is in sleep mode; blinks amber if over or under
voltage.
its functions.
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5
Rear panel
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12
2
3
4
5
6
7
11
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1. Accessory mountProvides an access point for mounting optional
accessories.
2. VESA mounting holes Provide access points for mounting the display.
3. Power switch (hard)Powers the input DC power ON and OFF.
4. Power connectorConnects to the 24V DC power supply.
5. HandlesAid in display positioning.
Caution: The handles are not intended to bear the
entire weight of the display
6. Cable cover hingesAttach the bottom of the cable cover to the display.
7. Velcro strapsStraps aid in cable management.
8. Cable cover thumbscrewsAttach the cable cover to the display, and are
tightened or loosened using ngers.
9. Cable coverCovers and conceals cables.
10. Cable cover clipsAttach the top of the cable cover to the display.
11. Cable wrapProvides a location for wrapping cables.
12. Locking featureA locking mechanism or cable may be routed here
for security purposes.
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