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.
1
Page 4
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.
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
"Periodic 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
of this manual. The device must be installed and operated according to the EMC information
provided in this manual.
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.
13. Do not operate with the glass device screen facing downward.
14. 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.
16. Note : This device has been tested
and
found to comply with the limit 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 device 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. There is no guarantee that
interference will not occur in a particular installation, which can be determined by
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 device.
• Increase the separation distance between the device.
• erent from that to which the other
device(s) are connected.
• eld service technician for help.
To satisfy FCC RF Exposure requirements for mobile and base station transmission devices,
a separation distance of 20cm or more should be maintained between the antenna of this
device and persons during operation. To ensure compliance, operation at closer than this
distance is not recommended. The antenna(s) used for this transmitter must not be
co-located or operating in conjunction with any other antenna or transmitter.
2
Page 5
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/RGB), S-video, and
C-video, and wireless RGB.
SYNK VisionPro 26” Wireless LED Display
REF: 0240-031-000
The SYNK VisionPro 26” Wireless LED Display can be used with the optional SYNK Transmitter,
which allows it to receive a high-de nition video signal over a radio-frequency link. The wireless
display supports a wireless RGB video input in addition to the video inputs supported by the
VisionPro 26” LED Display.
For details and instructions on using the SYNK Transmitter and the wireless functionality of the
SYNK VisionPro 26” Wireless LED Display, refer to the SYNK Wireless System manual (P21693)
Intended Use
The SYNK VisionPro 26” Wireless LED Display and the VisionPro 26” LED Display are intended for
video display during surgical procedures.
3
Page 6
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.
Package Contents
1
2
4
3
Package ContentsPart Number
1. VisionPro 26” LED Display or SYNK VisionPro 26”
Wireless LED Display
2. (4) M4 × 10 mm VESA screws–
4
0240-031-020 ,0240-031-000
5
Page 7
3. Hospital-grade AC power cord–
4. VisionPro 26” Series Power Supply0240-031-004
5. Cable Cover–
Optional AccessoriesPart Number
SYNK Wireless Transmitter0240-031-010
SYNK Wireless Receiver0240-031-030
SYNK Display Media Bar0240-031-003
SYNK 26” Display Cover0240-031-002
Hospital-grade AC power cord??
15-ft. (5 pin) DC extension cable??
75-ft. (5 pin) DC extension cable??
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
8
69
3
4 5
1. Display ScreenShows video image.
2. Power switch (soft)Powers the display ON and OFF.
3. Power LEDIndicates current status. Shines green if the display is
powered on or is in screen saver mode; blinks red if the
display is in standby mode; blinks amber if over voltage.
710
5
Page 8
4. Token slot (SYNK
VisionPro 26” Wireless
Token insertion site used to establish a wireless connection
with the transmitter.
LED Display only)
5. Token LED SYNK
VisionPro 26” Wireless
Provides feedback when linking the display and
transmitter.
LED Display only)
6. Audio/PIPVisionPro 26” LED Display:
Press once for the Picture in Picture adjustment menu.
SYNK VisionPro 26” Wireless LED Display:
Press once for the Audio adjustment menu (if optional
Media Bar is installed).
Press twice for Picture in Picture adjustment menu.
7. BrightAccesses the Brightness adjustment menu
8. SpecialtyAccesses the Specialty adjustment menu
9. InputAccesses the Input adjustment menu
10. Rotary controlAccesses the on-screen display and navigates through its
functions.
Rear panel
1
8
2
3
4
1. VESA mounting holes
5
Provide access points for mounting the display.
6
(100mm)
2. Power switch (hard)Powers the input DC power ON and OFF.
3. Power connectorConnects to the 24V DC power supply.
6
7
Page 9
4. HandlesAid in display positioning.
Note: The handles are not intended to bear the
entire weight of the display
5. Cable-management coverCovers cables.
Cable Cover
Installing the Cable Cover
1. Align the left and right hinges of the cable cover onto the bottom rear of the display.
2. Snap on the top section of the cable cover to the aligning clips.
3. With your ngers, turn the thumbscrews clockwise to tighten and lock the cable cover
onto the display.
Removing the Cable Cover
1. With your ngers, turn the thumbscrews counterclockwise to loosen.
2. Once the thumbscrews are completely loosened, pinch the left and right clips and pull the
cable cover towards you.
3. Remove the cable cover from the left and right hinges.
7
Page 10
Display Handles
Note: The handles are intended to aid in positioning the display, not for transporting the
display. The handles should not bear the full weight of the display.
Removing or Reinstalling the Display Handles
To Remove:
1. Using a Philips screwdriver, loosen the two **(insert size)** screws and gently pull the
handle away from the display.
To Reinstall:
1. Align the handle with the screw holes on the rear of the display.
2. Using a Philips screwdriver, install the two **(insert size)** screws to attach the handle.
3. To remove the handles, loosen the screws with a Philips screwdriver and gently pull the
handle away from the display.
8
Page 11
Setup
Stryker Endoscopy considers instructional training, or inservice, an integral part
of this device. Your local Stryker Endoscopy sales representative will perform at
least one inservice at your convenience to help set up your device and instruct
on its operation and maintenance. To schedule an inservice,
contact your local Stryker Endoscopy representative after your device has arrived.
Connections
Connection Ports
Video input signals are connected to the rear of the display, as illustrated below:
VisionPro 26” LED Display
123
1. DVI
2. 3G/HD/SD
SDI-in
3. 3G/HD/SD
SDI-out
4. VGA
5. S-Video
6. C-Video/SOG
7. R/Pr
SYNK VisionPro 26” Wireless LED Display
1
456
56
8. G/Y
9. B/Pb
10. H-sync
11. V-sync
12. Option
13. RS232
66687
666966610
66611
66613
66613
66612
9
Page 12
Connecting the VisionPro 26” LED Display Power Supply
1. Connect the power supply to the 24V input on the display.
2. Connect the AC power cord to the power supply*.
3. Connect the AC power, using the supplied hospital-grade power cord.
4. (Optional, not shown) Connect an extension cord between the power supply and display.
5. Install cable cover.
* Power supply
Model Number: BPM150S24F11
Manufacturer: Bridgepower Corp.
10
Page 13
Basic Video Setup
1. Remove the cover from the cables on the rear of the display.
2. Route the video output 1 from the camera to the SDC DVI input.
3. Route the video output 1 from the SDC DVI output to the DVI input on the display.
4. Reinstall the cable cover.
11
Page 14
Operation
Operate the display using the rotary control and the four buttons located on the front panel. A list
of the display controls and their functions is provided below.
On-Screen Display (OSD)
Accessing the On-Screen Display
To use the four front-panel buttons:
3
14
2
1. Audio/PIP: Press once to activate the Audio menu (if optional Media Bar is installed),
Press twice to activate Picture Mode (Picture in Picture, Picture by Picture, Picture on
Picture)
a. Use the Rotary Control to navigate the menus once they are activated
2. Bright: Activates the Brightness adjustment menu.
3. Specialty: Activates the Specialty adjustment menu.
4. Input: Activates the Input adjustment menu.
To use the Rotary Control:
• Turn Right/Left — With the on-screen display menu activated, turning increases/
decreases the value of the selected parameter.
• Push — Accesses/selects on-screen display menu.
• Push and Hold — Exits on-screen display menu.
Operating On-Screen Display
The device OSD helps navigate through various device menus.
12
Page 15
1. Press the Rotary Control to activate the OSD menu.
2. Rotate the Rotary Control to move up or down through the menu.
The parameter will be highlighted when selected.
3. Press the Rotary Control to enter the next level OSD.
4. Rotate the Rotary Control to increase or decrease the value of the selected parameter, or
to make a selection on di erent options.
5. To exit the OSD menu screen from the second — or third — level OSD menu, select the
Exit option. To completely exit the OSD, press and hold the Rotary Control. If no keys are
pressed, the OSD will automatically exit after the factory-set predetermined time (the time
is customizable).
OSD Menus
Speciality
Menu ItemDescriptionRange
Color Temperature*Chooses between color
temperatures for Lap A, Lap B,
Standard, Arthro, PACS, NORM,
ENT, GYN.
User Name EntryEnters custom user name display for boot-up display
Serial NumberDisplays device serial number
RuntimeDisplays current device total run time
Input FormatDisplays current input format
Note: Actual on-screen display values may vary with updated versions of the rmware
and user settings.
Receiver
Transmitter
Troubleshooting
Before returning your display for service, consult the troubleshooting list below:
15
Page 18
ProblemCurrent StatusRemedy
No picturePower LED onUsing the OSD Menu, adjust the
brightness and contrast to maximum, or
reset them to their default settings.
Power LED o Ensure the power switch at the front and
rear of the display are set to ON.
Check if the AC power cord is properly
connected to the AC adapter and outlet.
Power LED blinkingCheck if the video signal cable isproperly
connected at the back ofthe display.
Check if power of the video signal source
system is ON.
Abnormal pictureOversized,
undersized,
ormissing display;
or center shift.
OSD error message“Out of Range”Ensure that an acceptable video source
Using the Screen Control Menu, adjust
the Phase, Frequency, Horizontal, and
Vertical settings in order to correct the
display image.
Wait a few seconds after initial sync of
video signals, or power cycle the display.
is connected. Refer to the “Technical
Speci cations” section of this manual for
a list ofacceptable video formats.
16
Page 19
Cleaning and Maintenance
Warning
• To avoid electric shock and potentially fatal injury, unplug the display from the
electrical outlet before cleaning.
Caution
• Do not spray cleaning liquid directly onto the display as product damage may result.
Spray on the cloth before wiping the unit.
• Do not immerse the display in any liquid as product damage will result.
• Do not use corrosive cleaning solutions to clean the display as product damage may
result.
• Do not sterilize the display as product damage may result.
Cleaning
Should the unit need cleaning:
1. Spray cleaning liquid onto a dry, sterile cloth. Avoid excess liquid or drips.
2. Wipe the unit.
3. Take extra care when cleaning the screen. Excess liquid or drips that enter the bottom of the
screen may result in product damage.
Disposal
This product contains electrical waste or electronic equipment. It must not be
disposed of as unsorted municipal waste and must be collected separately in
accordance with applicable national or institutional related policies relating to
obsolete electronic equipment.
Dispose of any system accessories according to normal institutional practice relating to
potentially contaminated items.
Power AdapterInput: 100 – 240 VAC; 50 – 60 Hz; 2.5 A
Power Consumption150W(max)
CurrentDirect
Current/Voltage Rating
Please ensure the respective power cord complies with applicable local regulations and
standards.
110V +/- 10V power
outlets
220V +/- 20V power
outlets
(a-Si TFT active matrix LCD)
1Component (Y/G, Pb/B, Pr/R, H, VS), 1Wireless
Output: 24V; 6.25 A
Model Number: BPM150S24F11
Select a power supply cord that is UL Listed and C.S.A
Certi ed, type SJT or SVT, 3 – conductor, 18AWG,
terminated in a molded on hospital grade plug cap rated
110V+/-10V, 15A, with a minimum length of six feet.
Select a power supply cord that is internationally
harmonized and marked “<HAR>”, 3 – conductor, 0.75
mm^2 minimum wire, rated 220V+/-20V, 10A with a PVC
insulated jacket. The cord must have a molded on plug
cap rated 220V+/-20V,10A. The cord and plug cap must
be suitable for medical use.
Dimensions
Dimensions (W × H
× D)
Weight (approximate)8.6kg;19lbs.
VESA Mounting
Interface
Operating Conditions
18
660.4×442×86.4mm
26×17.4×3.4in
VESA100×100mm
Page 21
Operating
Temperature
Relative Humidity
Electrical Input Rating
Transport & Storage Conditions
Storage
Relative Humidity
Range
cation and Approvals
Class I Equipment
IP23 Water Ingress Protection
Continuous Operation
Compliance
FCC Regulations
41 – 104°F (5 – 40°C)
30 – 95%
24V DC 6.92A
-0.4 – 140°F (-18 – 60°C)
15 – 90%
re, and mechanical hazards only in
SYNK VisionPro 26” Wireless LED Display
FCC Part 15 Class B
FCC Part 15 Class C
VisionPro 26” LED Display
FCC Part 15 Class B
IC RegulationsIC: 4919C-0240031000 (SYNK VisionPro 26” Wireless LED
Note: Please contact your local Stryker Endoscopy sales representative for information on
changes and new products.
Display)
Electromagnetic Compatibility
Like other electrical medical equipment, the VisionPro 26” LED Display requires special
precautions to ensure electromagnetic compatibility with other electrical medical
operated according to the EMC information provided in this manual. The display has been
designed and tested to comply with IEC 60601-1-2:2001 requirements for EMC with other
devices.
When this device is connected with other electrical
equipment, leakage currents may be additive. To
Warning
Caution
minimize total leakage current per patient, ensure that all
systems are installed according to the requirements of IEC
60601-1-1.
Portable and mobile RF communications equipment may
ect the normal function of the display.
Do not use cables or accessories other than those
provided with the display, as this may result in increased
electromagnetic emissions or decreased immunity to
such emissions.
If the display is used adjacent to or stacked with other
equipment, observe and verify normal operation of the
guration in which it will be used prior
to using it in a surgical procedure. Consult the tables
below for guidance in placing the display.
19
Page 22
Guidance and Manufacturer’s Declaration: Electromagnetic Emissions
The VisionPro 26” LED Display is intended for use inthe electromagnetic environment speci ed below. The customer
or the user of the display should ensure it is used in such an environment.
RF emissions CISPR 11Group 1The VisionPro 26” LED Display uses RF energy only for its
RF emissions CISPR 11Class BThe VisionPro 26” LED Display is suitable for use in all
Harmonic emissions IEC61000-3-2Class D
Voltage Fluctuations/ icker
emissions IEC61000-3-3
Guidance and Manufacturer’s Declaration — Electromagnetic Immunity
The VisionPro 26” LED Display is intended for use in the electromagnetic environment speci ed below. The customer
or the user of the display should ensure that it is used in such an environment.
Immunity TestIEC 60601 Test LevelCompliance Level
Electrostatic
Discharge (ESD)
IEC61000-4-2
Electrical fast
transient/burst
IEC61000-4-4
Surge
IEC61000-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC61000-4-11
Power frequency
(50/60Hz) magnetic
eld
IEC 61000-4-8
Note: Ut is the AC mains voltage prior to application of the test level.
6kV contact
8kV air
2kV for power supply lines
1kV for input/output lines
1kV di erential mode
2kV common mode
• <5% Ut (>95% dip in Ut)
• 40% Ut (60% dip in Ut) for
• 70% Ut (30% dip in Ut) for
• <5% Ut (>95% dip in Ut)
3.0 A/m3.0 A/mPower-frequency
Complies
for 0.5 cycle
5 cycles
25 cycles
for 5 sec.
internal function; therefore, its RF emissions are very low and
are not likely to cause any interference in nearby electronic
equipment.
establishments other than domestic establishments and
those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic
purposes, provided the following warning is heeded:
Warning: This system is intended for use by health care
professionals only. This system may cause radio interference
or may disrupt the operation of nearby equipment. It may be
necessary to take mitigation measures, such as reorienting or
relocating the system or shielding the location.
Electromagnetic
Environment-Guidance
6kV contact
8kV air
2kV line to ground
1kV line to line
1kV di erential mode
2kV common mode
• <5% Ut (>95% dip in Ut)
for 0.5 cycle
• 40% Ut (60% dip in Ut) for
5 cycles
• 70% Ut (30% dip in Ut) for
25 cycles
• <5% Ut (>95% dip in Ut)
for 5 sec
Floors should be wood,
concrete, or ceramic tile.
If oors are covered with
synthetic material, the
relative humidity should
be at least 30%.
Mains power quality
should be that of a typical
commercial or hospital
environment.
Mains power quality
should be that of a typical
commercial or hospital
environment
Mains power quality
should be that of a typical
commercial or hospital
environment. If the
user of the transmitter
requires continued
operation during power
mains interruptions, it
is recommended that
the Wireless Transmitter
be powered from an
uninterruptible power
supply or a battery.
magnetic elds should be
at levels characteristic of a
typical location in a typical
commercial or hospital
environment.
20
Page 23
Guidance and Manufacturer’s Declaration: Electromagnetic Immunity
The VisionPro 26” LED Display is intended for use in the electromagnetic environment speci ed below.
The customer or the user of the display should ensure that it is used in such an environment.
Immunity TestIEC 60601 Test levelCompliance Level Electromagnetic Environment - Guidance
Portable and mobile RF communications
equipment should be used no closer to any part
of theVisionPro 26” LED Display, including its
cables, than the recommended separation distance
calculated from the equation applicable to the
frequency of the transmitter.
Recommended Separation Distance:
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is a ected by absorption and
re ection from structures, objects, and people.
(a) Field strengths from xed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast, cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to xed RF transmitters, an electromagnetic site survey
should be considered. If the measured eld strength in the location in which the VisionPro 26” LED Display is used
exceeds the applicable RF compliance level above, the display and transmitter should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or
relocating the VisionPro 26” LED Display.
(b) Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3 V/m.
3 Vrms
150 kHz to 80 MHz
3 V/m
80MHz to 2.5 GHz
3 Vd = 1.17√P
3 V/md = 1.17√P 80 MHz to 800 MHz
d = 2.33√P 800 MHz to 2.5 GHz
where P is the maximum output power rating
of the transmitter in watts (W) according to
the transmitter manufacturer and d is the
recommended separation distance in meters (m).
Field strengths from xed RF transmitters, as
determined by an electromagnetic site survey (a),
should be less than the compliance level in each
frequency range(b).
Interference may occur in the vicinity of equipment
marked with the following symbol:
Recommended Separation Distances Between Portable and Mobile RF Communications Equipment
and the VisionPro 26” LED Display
The VisionPro 26” LED Display is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The user of the VisionPro 26” LED Display can help prevent electromagnetic interference
by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters)
and the VisionPro 26” LED Display as recommended below, according to the maximum output power of the
communications equipment.
Separation distance (m) according to frequency of transmitter
Rated maximum output power (W)
of transmitter
0.010.120.120.23
0.10.370.370.74
11.171.172.33
103.703.707.37
10011.7011.7023.30
150 kHz to 80 MHz
d = 1.17√P
80 kHz to 800 MHz
d = 1.17√P
800 kHz to 2.5
GHz
d = 1.17√P
21
Page 24
For transmitters rated at a maximum output power not listed above, the recommended separation distance (d)
in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is a ected by absorption and
re ection from structures, objects, and people.
22
Page 25
Symbols
The following symbols appear on the product, its labeling, or the product packaging. Each
ned below:
Direct CurrentFor Indoor Use Only
Do Not Get Device WetDC Power Control Switch
Maximum StackingThis Side Up
Wireless TransmissionFragile
Tested to comply with FCC
Class B standards
Operating Humidity RatingsOperating Temperature Ratings
Medical Equipment is in
accordance with UL 60601-1
and CAN/CSA C22.2 No. 601.1
in regards to electric shock,
re hazards, and mechanical
hazards.
ICIndustrial Canada
No Serviceable Parts
Consult instructions for useCatalog number
Date of ManufactureLegal manufacturer
Japan PSE Mark Denan
ciency Level
IP23
MADE IN KOREA
Degrees of protection against the
ingress of water
This symbol indicates that this
product is compliant to applicable
standards and is suitable for the
Australian market.
Made in Korea
Warning/Caution: See Instructions
for Use
UL Functional Safety Recognized
Component
This product contains waste
electrical or electronic equipment.
It must not be disposed of as
unsorted municipal waste and
must be collected separately.
Federal law restricts this device to sale by or on the order of a physician
23
Page 26
Stryker Endoscopy
5900 Optical Court
San Jose, CA 95138 USA
1-408-754-2000, 1-800-624-4422
www.stryker.com
European Representative:
Regulatory Manager, Stryker France
ZAC Satolas Green Pusignan
Av. De Satolas Green
69881 MEYZIEU Cedex, France
P22286A
2012/11
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