BARCO AMM213TDS3 Users Manual

Test Report No.: GETEC-E3-06-043
FCC Class B Certification

APPENDIX G

: USER’S MANUAL

EUT Type: 21” FLAT PANEL MONITOR

FCC ID: QVXAMM213TDS3

VISIONELECT

21'' High-Definition

LCD Monitor

REF 240-030-930

User Guide

2006/05 www.stryker.com 1000-400-895 A

16.42

(417.20 mm)

19.21

(488 mm)

3.94

(100 mm)

2.05

(52 mm)

.95

(24.25 mm)

3.15

(80 mm)

6.23

(163.20 mm)

3.94

(100 mm)

5.05

(128.20 mm)

4.99

(127 mm)

8.66

(220 mm)

Table of Contents

Warnings and Cautions .........................................................................2

Warnings ........................................................................................... 2

Cautions .................................... ........................................................ 3

Symbol Definitions ............................................................................5

Product Description and Intended Use ............................................... 6

Product Contents .............................................................................. 6

Setting Up the Monitor ..........................................................................8

System Interconnection ....................................................................8

Power Connection .............................................................................8

Operating the Monitor ...........................................................................9

Front Panel Controls .........................................................................9

Standard On-Screen Display (OSD) Operation ...............................10

Stryker Camera Preset Modes ........................................................10

OSD Function Description .............................................................. 11

Cleaning the Monitor .......................................................................12

Troubleshooting ..................................................................................13

Technical Specifications .....................................................................14

Classification and Approvals ...........................................................17

English

EN

Electromagnetic Compatibility ...........................................................16

Warranty ...............................................................................................22

Service and Claims .............................................................................. 22

Declaration of Conformity ..................................................................23

1

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:

arning The personal safety of the patient or physicia n may be

involved. Disregarding this information could result in
injury to the patient or physician.

arning A lightning bolt within a triangle is intended to warn of

the presence of hazardous volt age. Refer all servic e to
authorized personnel.

aution Special service procedures or precautions must be

followed to avoid damaging the instrument.

Note Special information to make maintenance easier or

important information more clear.

Warnings

Warning To avoid potential serious injury to the user and the

patient, and/or damage to this device, the user must:

1. Restrict this device to use by, or on the order of, a physician,
because of Federal law (United States of America).

2. Read the operating manual thoroughly and be familiar with its
contents prior to using this equipment.

3. Carefully unpack the unit and check if any damage occurred
during shipment.

4. Test this equipment prior to a surgical procedure. This monitor
was fully tested at the factory before shipment.

5. Do not place the monitor or any other heavy object on the power
cord. Damage to the cable can cause fire or electric shock.

6. Should any solid object or liquid fall into the panel, unplug the unit
and have it checked by qualified personnel before operating it
any further.

7. Unplug the unit if it is not to be used for an extended period of
time. To disconnect the cord, p ull it out by the plu g. Never pull the
cord itself.

2

8. To avoid electric shock, avoid removing control unit covers.

9. Do not attempt internal repairs or adjustments not specifically
detailed in this operating manual.

10. Pay close attention to the care and cleaning instructions in this
manual. A deviation may cause damage (refer to the Cleaning
section).

11. Do not sterilize the monitor.

12. Use appropriate caution to prevent contact with fluids, if the unit is
being used with a power supply in patient environments.

Cautions

1. The AC Adapter must be plugged into a grounded power outlet.

2. Use only the proprietary VISIONELECT (model 240-030-930)
power supply (model 240-030-931) for the VISIONELECT (model
240-030-930) monitor. Make a proper connection by ensuring
that the shrink tubing completely secures the connection between
the DC power cord and the extension cord.

3. Grounding reliability can only be achieved when the equipment is
connected to an equipment receptacle labeled “Hospital Only” or
“Hospital Grade.”

4. To connect to an international power supply, use an attachment
plug appropriate for the power outlet.

5. Turn power off when unit is not in use.

6. Remove the power module and connection when transporting the
unit.

7. Save the original carton and associated packing material. They
will be useful should you have to transport or ship the unit.

8. Handle the monitor with care. Do not strike or scratch the screen.

9. Never operate the unit right after having been transported from a
cold location directly to a warm location.

10. Do not expose the monitor to moisture or directly apply liquid
cleaners directly to the screen. Spray the cleaning solutio n into a
soft cloth and clean gently.

11. Allow adequate air circulation to prevent internal heat buildup.

12. Do not place the unit on surfaces (rugs, blankets, etc.) or near
materials (curtains, draperies) that may b lock the ventilat ion slots.
The monitor is cooled by natural convection and has no fan.

13. Do not install the unit near sunlight, excessive dust, mechanical
vibration or shock.

English

EN

3

14. The unit is designed for operation in a horizontal position. Do not
operate the unit in a vertical position.

15. Keep the unit away from equipment that uses strong magnets
(i.e., large loudspeakers).

16. Do not touch the patient with signal input or output connectors.
Equipment with SIP/SOP connectors should either comply with
IEC 60601-1 and/or IEC 60601-1-1 harmonized national
standards or the combination should be evaluated.

17. CAUTION: Changes or modifications not expressly approved by
the party responsible for compliance could void the user's authority
to operate the equipment.
NOTE : This equipment has been tested and found to comply
with the limit for a Cass B digital device, pursuant to Part 15 of
the FCC Rules. These limits are designed to provide resonable
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, which can
be determined by turning the equipment off and on, the user is
encourage 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 equipment.

• Connect the equipment to an outlet on a circuit different from

that to which the other device(s) are connected.

• Consult the manufacturer or field service technician for help.

18. To ensure electromagnetic compatibility, refer to the
“Electromagnetic Compatibility” section of this manual. The
VISIONELECT (model 240-030-930) monitor must be installed
and operated according to the EMC information provided in this
manual.

The VISIONELECT (model 240-030-930) monitor has been tested under
the UL 60601-1 standard and is UL listed for medical application.

The warranty is void if any of these warnings or cautions are
disregarded.

4

Symbol Definitions

The following symbols appear on the product, its labeling, or the product
packaging. Each symbol carries a special definition, as defined below

Dangerous: High Voltage

Consult accompanying documents.

Direct Current

Indicates protective earth ground.

For indoor use only.

DC power control switch

English

EN

SN

51LJ

Medical Equipment

E215822

Serial Number

Top - Bottom

Fragile

Do not get wet

Maximum Stacking

Manufacturer

European Authorized Representative

Indicates proof of conformity to applicable European Economic Community
Council directives and to harmonized standards pub lished in the of ficia l journal
of the European Communities.

Tested and certified by DEMKO in accordance with EN 60601-1 and
EN 60601-1-2.

Medical Equipment is in accordance with UL 60601-1 and CAN/CSA C22. 2 No.

601.1 in regards to electric shock, fire hazards, and mechanical hazards.

Tested to comply with FCC Class B standards.

This symbol indicates that the waste of electrical and electronic equipment
must not be disposed as unsorted municipal waste and must be collected
separately. Please contact the manufacturer or other authorized disposal
company to decommission your equipment.

5

Product Description and
Intended Use

The VISIONELECT (model 240-030-930) 21-Inch High Definition LCD
Monitor is an intelligent, microprocessor-based TFT-LCD monitor
intended for use in endoscopic surgical applications. It has an
ergonomically designed display and is compatible with most analog RGB
(Red, Green, Blue) display standards.

The VISIONELECT (model 240-030-930) monitor has the following
features:

• Advanced Viewing Solution (AVS): A sophisticated filter

extends the viewing angle of the screen image, without
sacrificing contrast ratio and brightness.

• Upgraded video cards or software will not require buying a new

monitor because of the wide auto-scanning compatibility range.

• The internal microprocessor digitally controls auto-scanning, for

horizontal scan frequencies between 31.47 KHz and 78.88 KHz,
and vertical scan frequencies between 50.0 Hz and 85.1 Hz. In
each frequency mode, the microprocessor-based circuitry allows
the monitor to function at the precision of a fixed frequency.

• The resident memory allows for storing factory default settings

and also additional user adjustment parameters.

• The maximum resolution achievable is UXGA (1600 × 1200,

be60Hz), st suited for Stryker cameras.

• The monitor is compliant with the VESA-DPMS power-

management standard. In order to save energy, the monitor
must be connected to a system compliant with the standard.

• The monitor is designed to mount an accessory (such as a

camera or speaker) with a 2 lbs (max) load per hole.

• The monitor is certified by UL International in accordance with

medical standard UL 60601-1. It is also CE marked for sale in
the European Community for integration or use with medical
products. It is certified by DEMKO according to EN 60601-1
and EN 60601-1-2 for sale to the medical market.

Product Contents

1. Carefully unpack the VISIONELECT (model 240-030-930)
monitor. Save the original carton and associated packing
material. They will be useful should you have to transport or ship
the unit.

6

2. Check the monitor and its accessories for any damage that may
have occurred during shipping. Immediately report any damage
to the shipping company.

3. Check the contents of the accessories package with the following
list to make sure all components have been included. In addition
to this manual, you should find:

(a) 1 DVI cable
(b) 1 VGA HDDB15 cable
(c) 1 AC adapter (Stryker P/N 240-030-931)
(d) 1 Hospital-grade AC power cord
(e) 4 M4 x 10mm VESA screws (not shown)
(f) 1 BNC cable
(g) 1 S-Video cable
(h) 1 15’ or 75’ extension cable with heat shrink tubing, for

connection to the DC power cord (optional, not shown)

(i) Power supply bracket (optional, not shown)

English

EN

(d)

(b)

(a)

(c)

(f)

(g)

7

System Interconnection

Signal Output
DVI
RGBHV
S-Video
C-Video

:

VISIONELECT

VISIONELECT

(Model 240-030-930)

Video Input Signals

Video Peripheral

eg:

SDC

SIDNE

VIDEO PRINTER

DVD/VCR

etc...

Power Connection

Hospital-grade
power cord

Heat-shrink tubing between the
DC power cord and extension cord

8

Power Supply
240-030-931

Video Sources:
Camera (1188 Series,
1088 Series, 988 Series)

Ground to
Cart Chassis

240-030-722 or
240-030-932

VISIONELECT

(model 240-030-930)

Operating the Monitor

Front Panel Controls

Operate the monitor using the rotary control located on the front panel. A
list of the monitor controls and their functions is provided below.

.

English

EN

Power LED
Power Switch

Figure 1: The VISIONELECT LCD Monitor front panel controls.

1. Power LED: Indicates menu current status. Displays green if
monitor is powered on, blinks orange if monitor is in Standby
mode.

2. Power Switch: Turns the power ON or OFF.

3. Rotary Control (Turn Right): With the on-screen display menu
activated, increases the value of the selected parameter. With the
on-screen display deactivated, activates the video source
selection menu.

4. Rotary Control (Turn Left): With the on-screen display menu
activated, decreases the value of the selected parameter. With
the on-screen display deactivated, activates the video source
selection menu.

5. Rotary Control Switch (Push): Accesses/selects on-screen
display menu.

6. Rotary Control Switch (Push and Hold): Exits on-screen
display menu.

Rotary
Control

9

Standard On-Screen Display (OSD) Operation

The monitor provides an on-screen display to help navigate through the
various monitor-adjustment menus.

1. Press the Rotary Control to activate the on-screen display (OSD)
menu.

2. Rotate the Rotary Control to move up or down thro ugh 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 different
options.

5. T o 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 for a time
period, the OSD automatically times out.

6. While the OSD menu is deactivated, rotate the Rotary Control to
activate the input signal selection menu. The current input signal
will be highlighted with a dot. Rotate the rotary control to select
the preferred input signal.

Stryker Camera Preset Modes

Camera Resolution

(H x V)

988 1024 x 768 49.09 59.90

988i 1024 x 768 41.25 50.00

1088/SDC Pro2 1024 x 768 50.03 60.00

1088i/SDC Pro2 1024 x 768 41.10 50.00

1088/1188/SDC HD 1280 x 1024 64.02 60.10

1088i/1188i/SDC HD 1280 x 1024 59.99 50.00

Horizontal

Frequency

(KHz)

10

Vertical

Frequency

(Hz)

OSD Function Description

Item Function Description Range

Specialty

Color Temperature
RGB adjustment is
available only for
Standard, Arth and
Lap settings)

Red Red balance 0-255
Green Green balance 0-255
Blue Blue balance 0-255
Gamma Gamma value 1.6-2.4

Setting

Brightness Increase or decrease the brightness 0-100
Contrast Increase or decrease the contrast 0-100
Phase* Increase or decrease the Phase level 0-100
Chroma* Increase or decrease the Chroma level 0-100
Image Sharpness Set image sharpness from 1 to 10 1-10
Video Sharpness* Increase or decrease the video sharpness 0-100

Image Effect

Scale Mode Choose scale mode between fill screen, V-fill, H-fill, or one to one
Mirror Enable or Disable mirror image
Freeze Frame Enable or Disable freeze frame
Zoom/Pan Enable zoom-in and pan function
PIP Enable PIP (Picture in Picture) function

Advanced

OSD position Control Control OSD Menu Position, Background, and Timeout
Screen Control** Control and adjust Horizontal, Vertical, Frequency, Phase
DPMS Choose DPMS (Display Power Management Signaling)
Auto Source Select Adjust Auto Source Select between on and off.
Recall Factory Default Set to factory default
Key lock Set to Key lock mode

Information

User Name Entry Enter custom username display for boot-up display
Serial Number Display monitor serial number
Runtime Display current run time of monitor
Input Format Display current input format

Actual on-screen display values may vary with updated versions of the firmware and user setting.
* Only available under S or C video input.
** Only available under VGA input.

Choose between color temperatures for Default, Standard, Arth, or Lap

English

EN

11

Cleaning the Monitor

Caution Do not expose the monitor to moisture or directly

apply liquid cleaners directly to the screen. Spray the
cleaning solution into a soft cloth and clean gently.

No specific liquid or chemical is necessary for cleaning this
VISIONELECT (model 240-030-930) LCD monitor . Use only n on-abrasive
cloths and cleaning solutions to clean similar equipment used in hospitals.

1. Clean the panel with a dry soft cloth, or a soft cloth lightly
moistened with mild detergent solution. Do not use any type of
solvent, such as alcohol or benzine, which might damage the
finish.

2. Apply alcohol to glass surfaces with soft cotton applicator to aid in
cleaning and drying without leaving spots or streaks.

3. Dry thoroughly with soft towel or gauze surgical sponge.

Acceptable cleaning agents for bezel cleaning include:

• Cidex (2.4% glutaraldehyde solution)

• Sodium Hypochlorite (bleach) 10%

• 0.5% Chlorhexidine in 70% isopropyl alcohol

70% isopropyl alcohol is recommended for the screen surface.

12

Troubleshooting

Before returning your LCD monitor for service, consult the
troubleshooting list below

Problem Current Status Remedy

English

EN

No Picture

Abnormal

Picture

LED ON

LED OFF

LED Blinking

Oversized or
undersized display;
missing display;
center shift

Using the OSD, adjust the brightness and contrast
to maximum, or reset them to their default
settings.

Check the power switch.
Check if the AC power cord is properly connected

to the AC adapter.
Check if the video signal cable is properly

connected at the back of the monitor.
Check if the power to the computer system is ON.
Using the Auto Setup button, adjust CLOCK,

CLOCK-PHASE, H-POSITION, and V-POSITION
with non-standard signals.

Wait for a few seconds after adjusting the size of
the image before changing or disconnecting the
signal or powering OFF the monitor.

13

Technical Specifications

Display

LCD Monitor Panel 21 inches (533.4mm)

(s/w TFT Active matrix LCD)
Synchronization 2.5 - 5.0 Vpp separated sync
Pixel Pitch 0.270mm
Response Time <25ms
View Angle +/-85° (L/R) × +/-85° (U/D)
Display Colors 16 million colors
Native Resolution 1600 dots × 1200 dots
Input Signal Composite video; S-video;

Analog RGB; DVI
Maximum Pixel Clock 135 MHz × 1

Electrical

Power Adapter AC 100-240V; DC 24V
Power Consumption 90W (max)
Current Direct

Dimensions

Dimensions (W × H × D) 499.66 x 428.88 x 104.25mm
Weight 17 lbs.
VESA Mounting Interface VESA 100mm × 100mm

Operating Conditions

Operating Temperature 41 to 90°F (5 to 32.2°C)
Relative Humidity 10 to 60%
Electrical Input Rating 24V DC 3.75A

Tran sport & Storage Conditions

Storage (-4 to 140°F) -20 to 60°C
Relative Humidity Range 10 to 85%
Atmospheric Pressure Range 500 to 1060 hPa

14

Classification and Approvals

51 LJ

Medical Equipment

E215822

Class I Equipment
Medical equipment with respect to electric shock, fire and mechanical

hazards only in accordance with UL 60601-1 and CAN/CSA C22.2
No. 601.1.

IPX1 Water Ingress Protection
Continuous operation

Warning This equipment is not suitable for use in the presence

of a FLAMMABLE ANESTHETIC MIXTURE WITH AIR, or
WITH OXYGEN OR NITROUS OXIDE.

This monitor is intended for use on Health Care Facilities model
240-030-930.

No user serviceable parts inside. Ask qualified personnel before
accessing internal components.

English

EN

Caution For disposal of waste product, follow the requirement

of the local code.

This product is considered electronic equipment. It must not be disposed
of as unsorted municipal waste, and must be collected separately. Please
contact the manufacturer or other authorized disposal company to
decommission your equipment.

15

Electromagnetic Compatibility

Like other electrical medical equipment, the VISIONELECT (model 240­030-930) monitor requires special precautions to ensure electromagnetic
compatibility with other electrical medical devices. To ensure
electromagnetic compatibility (EMC), the VISIONELECT (model
240-030-930) monitor must be installed and operated according to the
EMC information provided in this manual.

Note The VISIONELECT (model 240-030-930) mo nitor has been

designed and tested to comply with IEC 60601-1-2:2003
requirements for EMC with other devices.

Caution The VISIONELECT (model 240-030-930) monitor may

be interfered with by other equipment, including
portable and mobile RF communication equip m ent,
even if such equipment meets the applicable
emissions requirements.

Warning Do not use cables or accessories other than those

provided with the VISIONELECT (model 240-030-930)
monitor, as this may result in increased
electromagnetic emissions or decreased immunity to
such emissions.

Warning If the VISIONELECT (model 240-030-930) monitor is

used adjacent to or stacked with other equipment,
observe and verify normal operation of the
VISIONELECT (model 240-030-930) monitor in the
configuration in which it will be used prior to using it in
a surgical procedure. Consult the tables below for
guidance in placing the VISIONELECT (model 240-030-

930) monitor

Warning When this device is connected with other electrical

equipment, leakage currents may be additive. To
minimize total leakage current per patient, ensure that
all systems are installed according t o the requirement s
of IEC 60601-1.

16

Guidance and Manufacturer's Declaration: Electromagnetic Emissions

VISIONELECT (model 240-030-930) monitor is intended for use in the ele ctromagnetic environment
specified below. The customer or the user of VISIONELECT (model 240-030-930) monitor should
ensure that it is used in such an environment.

Emissions test Compliance Electromagnetic Environment - guidance

English

EN

RF emissions
CISPR11

RF emissions
CISPR11

Harmonic emissions
IEC61000-3-2

Voltage Fluctuations/
flicker emissions
IEC61000-3-3

Group 1

Class B

Class A

Complies

The VISIONELECT (model 240-030-930)
monitor must emit electromagnetic energy in
order to perform its intended function. Nearby
electronic equipment may be affected.

VISIONELECT (model 240-030-930) monitor is
suitable for use in all establishments, including
domestic establishments and those directly
connected to the public low-voltage power
supply network that supplies buildings used for
domestic purposes.

17

Guidance and Manufacturer's Declaration: Electromagnetic Immunity

VISIONELECT (model 240-030-930) monitor is intended for use in the elect romagnetic environment
specified below. The customer or the user of VISIONELECT (model 240-030-930) monitor should
ensure that it is used in such an environment.

Immunity Test

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 field
IEC 61000-4-8

IEC 60601 Test

Level

±6kV contact
±8kV air

±2kV for power
supply lines
±1kV for input/
output lines

±1kV differential
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.

3 A/m N/A

Compliance Level

±2,4,6kV contact
±2,4,8kV air

±2kV line to ground
±1kV line to line

±0.5, 1kV
differential mode
±0.5, 1, 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.

Electromagnetic

Environment:

Guidance

Floors should be
wood, concrete, or
ceramic tile. If floors
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
VISIONELECT
(model 240-030-

930) monitor
requires continued
operation during
power mains
interruptions, it is
recommended that
VISIONELECT
(model 240-030-

930) monitor be
powered from an
uninterruptible
power supply or a
battery.

Power-frequency
magnetic fields
should be at levels
characteristic of a
typical location in a
typical commercial
or hospital
environment.

18

Guidance and Manufacturer's Declaration: Electromagnetic Immunity

VISIONELECT (model 240-030-930) monitor is intended for use in the elect romagnetic environment
specified below. The customer or the user of VISIONELECT (model 240-030-930) monitor should
ensure that it is used in such an environment.

NOTE: Ut is the AC mains voltage prior to application of the test level.

Guidance and Manufacturer's Declaration: Electromagnetic Immunity

VISIONELECT (model 240-030-930) monitor is intended for use in the electromagnetic environment
specified below. The customer or the user of VISIONELECT (model 240-030-930) monitor should
ensure that it is used in such an environment.

Immunity

Test

Conducted RF
IEC 61000-4-6

IEC 60601 Test

Level

3 Vrms
150 kHz to 80 MHz

Compliance

Level

3 V

Electromagnetic Environment:

Portable and mobile RF communications
equipment should be used no closer to
any part of the VISIONELECT (model
240-030-930) monitor system, including
its cables, than the recommended
separation distance calculated fr om the
equation applicable to the frequency of
the transmitter.

Recommended Separation Distance

d1.17P=

Guidance

English

EN

Radiated RF
IEC 61000-4-3

NOTE 1: At 80
MHz and 800
MHz, the
higher
frequency
range applies.

3 V/m
80MHz to 2.5 GHz

3 V/m

d1.17P=

d2.33P=

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 fixed RF transmitters,
as determined by an electromagnetic site

survey
compliance level in each frequency

range
Interference may occur in the vicinity of
equipment marked with the following
symbol:

80 MHz to 800 MHz
800 MHz to 2.5 GHz

(a)

, should be less than the

(b)

.

19

Guidance and Manufacturer's Declaration: Electromagnetic Immunity

VISIONELECT (model 240-030-930) monitor is intended for use in the electromagnetic environment
specified below. The customer or the user of VISIONELECT (model 240-030-930) monitor should
ensure that it is used in such an environment.

NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects, and people.

(a) Field strengths from fixed 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
fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field
strength in the location in which theVISIONELECT (model 240-030-930) monitor system is used
exceeds the applicable RF compliance level above, the VISIONELECT (model 240-030-930) monitor
system should be observed to verify normal operation. If abnormal performance is observed,
additional measures may be necessary, such as reorienting or relocating the VISIONELECT monitor
VISIONELECT (model 240-030-930) monitor unit.
(b) Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

20

Recommended Separation Distances Between Portable and Mobile RF Communications

Equipment and the VISIONELECT (model 240-030-930) monitor System

The VISIONELECT (model 240-030-930) monitor system is intended for use in an electromagnetic
environment in which radiated RF disturb ances ar e controll ed. The user of the VI SIONELECT (model
240-030-930) monitor system can help prevent electromagnetic interferen ce by maintaining a
minimum distance between portable and mobile RF communications equipment (t ransmitters) and
the VISIONELECT (model 240-030-930) monitor system 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

0.01 0.12 0.12 0.23

0.1 0.37 0.37 0.74

11.171.172.33
10 3.70 3.70 7.37
100 11.70 11.70 23.30
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 ap plicable 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 affected by

absorption and reflection from structures, objects, and people.

150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz

d1.17P= d1.17P=

d2.33P=

English

EN

21

Warranty

This Stryker Endoscopy prod uct is warr anted to the or iginal pu rchaser for
a period of one year from the date of purchase to be free from defects in
material and workmanship.

This warranty extends to all purchases and is limited to the repair or
replacement of the product without charge when returned in the original
shipping case to:

Stryker Endoscopy
5900 Optical Court
San Jose, CA 95138
USA

Stryker Endoscopy cannot accept responsibility for returns or
replacements which have not been authorized. This warranty does not
cover damages caused by misuse or by failure to follow the procedures
outlined in this manual or demonstrated by Stryker Endoscopy
representatives.

There are no other expressed warranties.

Service and Claims

Do not attempt to service this product yourself. If service is needed either
during or after the warranty period, contact Stryker Endoscopy at
1-800-624-4422, or phone your local Stryker Endoscopy sales
representative.

22

Declaration of Conformity

Manufacturer:

Stryker Endoscopy
5900 Optical Court
San Jose, CA 95138
USA
1-800-624-4422
1-408-754-2000

Product Designation: VISIONELECT (model 240-030-930) 21" High
Definition LCD Monitor

The above product complies with the requirements of EC Directive 93/42/
EEC. This declaration is based on compliance testing to:

EN 60601-1/08-90
EN 60601-1 A1/05-93
EN 60601-1 A2/06-95

This document is on file.
The CE mark will be affixed based on directive 93/42/EEC.

Stryker European Representative
Regulatory Manager, Stryker France
ZAC Satolas Green Pusignan
Av. de Satolas Green
69881 MEYZIEU Cedex, France

Stryker and Stryker Endoscopy are registered trademarks of Stryker Corporation.

23

24

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

2006/05 www.stryker.com 1000-400-895 A