The Eonis display presents crisp, razor-sharp, high-contrast images. To guarantee image consistency at
all times, it features a unique front sensor that automatically aligns image quality every time the display is
turned on. This image consistency enhances collaboration: images always appear exactly like they are
supposed to, on every display, which spurs confident clinical decisions. Furthermore, specialists looking
at X-ray images will appreciate the built-in DICOM settings.
One-click quality assurance
Like Barco’s entire medical display range, the Eonis display line comes with Barco’s online MediCal
QAWeb service for quality assurance and remote asset management. Proving its superior value in
hospitals around the world, MediCal QAWeb provides automated quality assurance checks and detailed
reports. It makes it easy for healthcare IT to centrally and remo
the healthcare organization. Also for private practices, QAWeb further strengthens image consistency
and allows you to easily personalize your image.
tely manage and configure displays across
Fully cleanable and smart design
The Eonis display carries all safety certifications required in clinical environments. It features an integrated cable management system, making it safe to use in hospitals and private practices. The multiple mounting options and connections further add to the smart design typical of Barco’s Eonis display.
Most unique, however, is the excellent cleanability of the white Eonis display thanks to the toughened and
scratch-proof glass. This display model can be disinfected, both front and back, with typical alcohol-based
cleaning agents.
Features
•Front sensor automatically aligns image quality
•IPS panel ensures wide viewing angle
•MediCal QAWeb suite for networked quality assurance, calibration and asset management all add to
the exceptional, consistent image quality of the Eonis display
•Toughened, scratch-proof front glass (white v
•Covered cables
•Medical-grade certifications
•Sockets for Kensington lock makes the Eonis display safe for use in clinical environments
•Flexible VESA mount for easy arm, wall or cart mounting
This manual further guides you through the different steps needed to install and use the Eonis display.
ersion only)
CAUTION: Read all the important safety information before installing and operating your
Eonis display. Please refer to the dedicated chapter in this user guide.
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1. Welcome!
1.2Symbols
Symbols in this document
The following symbols are used in this document:
Caution
Warning
Info, term definition. General info about the term
Note: gives extra information about the described subject
Tip: gives extra advice about the described subject
1.3What’s in the box
Overview
Your Eonis display comes with:
•this Eonis display user guide
•a documentation CD containing multilingual user documentation
•a system CD containing MediCal QAWeb Agent
•a (set of) AC power cord(s) (depending on the region of operation)
•aVGAcable
•aHDMIcable
•a USB cable
•an external power supply
•an accessory bag (cleaning cloth, velcro cable routing strap)
Keep your original pac kaging. It is designed for this display and is the ideal protection
during transport and storage.
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2. Parts, controls and connectors
2. PARTS,CONTROLSAND
CONNECTORS
2.1Front view
Overview
1276543
Image 2-1
1. Front sensor
2. USB downstream connector
3. Left / Decrease key
4. Right / Increase key
5. Menu / Enter key
6. Standby key
7. Power status LED
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2. Parts, controls and connectors
2.2Rear view
Overview
1
2
3
Image 2-2
1. Connector compartment cover
2. Kensington security slots
3. Opening for cable routing strap
4. Height mechanism lock screw
5. VGA input
6. HDMI audio line out
7. USB downstream connector
8. USB upstream connector
9. HDMI input
10. DisplayPort input
11. +12 VDC (
) power input
2
456 7 8 9 10 11
6
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3. Display installation
3. DISPLAY INSTALLATION
3.1Unlocking the height mechanism
To unlock the height mechanism
In the factory, the height mechanism in the stand of your Eonis display is locked to prevent damage during transportation. You’ll first have to unlock this mechanism before you can adjust your display height
position.
To unlock the height mechanism, unscrew the height mechanism lock screw and remove it from the d
stand.
Keep the lock screw in a known place for possible future transportation of your display.
Image 3-1
3.2Adjusting the display position
To adjust the display position
After unlocking the height mechanism, you can n
desired.
ow safely tilt, swivel, raise and lower your display as
isplay
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3. Display installation
Image 3-2
CAUTION: Do not try to pivot your display when a ttached to the stand. Trying to do so
could cause serious damage to your display and its stand.
3.3Removing t he cover
To remove the connector compartment cover
The connector compartment cover should be removed to get access to the connectors. To remove the
cover, gently slide the connector compartment cover upwards and remove it from the display.
Image 3-3
3.4Connecting t he cables
To connect the cables
1. Connect one or more of the video input connections of your display (VGA, HDMI or DisplayPort) to the
corresponding video outputs on your computer or any other video device.
2. If you want to make use of the
with the display’s USB upstream connector by means of the supplied USB cable.
3. Connect a speaker, amplifier, ... with the display’s audio line out if you want to use the internal sound
option of your display.
8
display’s USB downstream connectors, then connect your workstation
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3. Display installation
4. Connect the supplied external DC () power supply to the +12 VDC power input of your display.
5. Plug the other end of the external DC (
the proper power cord delivered with your display.
114
Image 3-4
231
) power supply into a grounded power outlet by means of
5
3.5Re-attaching the cover
To re-attach the connector compartment cover
Put the cover back in position by sliding it downwards so that it is fixed to the display again.
Pay attention that all cables stay in the cable channel while re-attaching the cover.
Image 3-5
3.6Routing the cab les
To route the cables
1. Slide the cable routing strap through the opening in the back of the stand.
2. Bundle all cables together so that they will fit in the strap.
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3. Display installation
3
2
3. Wrap and fix the cable routing strap around all cables.
Image 3-6
3.7Kensington security slots
To make use of the Kensington security slots
Your Eonis display has 2 Kensington slots available which allow you to secure the display to a desk or any
other fixed object. Moreover, when locking the display with the connector compartment cover attached,
you also prevent users from connecting/disconnecting any cables to/from the display.
Image 3-7
3.8VESA-mount installation
To mount the display on a VESA arm
The display panel, standard attached to a stand, is compatible with the VESA 75 mm standard.
1. Unscrew the four fixation screws to detach the panel from the stand.
2.Use4M4screwstoattachthep
screws is 10mm + VESA plate thickness (tolerance of +/- 1 mm).
10
anel to a VESA approved arm. Please make sure that the length of the
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Image 3-8
3. Display installation
CAUTION: Use an arm that can support a weight of at least 12 kg (26.50 lbs). Failure to
do so could make the panel fall, causing serious injury to a child or adult, and serious
damage to the equipment.
CAUTION: Never move a display attached to an arm by pulling or pushing the display
itself. Instead, make sure that the arm is equipped with a VESA approved handle and
use this to move the dis play. Plea se refer to the instruction manual of the arm for more
information and instructions.
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3. Display installation
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4. Daily operation
4. DAILY OPERATION
4.1Recommendations for d aily operation
Optimize the lifetime of your display
Enabling the Display Power Management System (DPMS) of your display will optimize its lifetime by automatically switching off the backlight when the display is not used for a specified period of time. By default,
DPMS is enabled on your display, but it also needs to be activated on your workstation. To do this, go to
“Power Options Properties” in the “Control Panel”.
Barco recommends setting DPMS activation after 20 minutes of non-usage.
Use a screen saver to avoid image retention
Prolonged operation of an LCD with the same content on the same screen area may result in a form of
image retention.
You can avoid or significantly reduce the occurrence of this phenomenon by using a screen saver. You
can activate a screen saver in the “Display properties” window of your workstation.
Barco recommends setting screen saver activation after 5 minutes of non-usage. A
good screen saver displays moving content.
In case you are working with the same image or an application with static image elements for several hours
continuously (so that the screen saver is not activated), change the image content regularly to avoid image
retention of the static elements.
Understand pixel technology
LCD displays use technology based on pixels. As a normal tolerance in the manufacturing of the LCD, a
limited number of these pixels may remain either dark or permanently lit, without affecting the performance
of the product. To ensure optimal product quality, Barco applies strict selection criteria for its LCD panels.
To learn more about LCD technology and missing pixels, consult the dedicated white
papers available at w
ww.barco.com/healthcare.
Maximize quality assurance
QAWeb guarantees optimum and stabilized image quality in every private practice.
The front sensor on the Eonis display works seamlessly with QAWeb to ensure a consistent image over
time. It automatically stabilizes the image from the moment you switch on the display. What’s more,
QAWeb provides you with instant feedback on the status of the display.
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4. Daily operation
4.2On/Off switching
To switch your display on or off
1. Shortly press the Standby ()key.
4.3Bringing up the OSD menus
About the OSD menu
TheOSDmenuallowsyoutoconfigure different settings to make your Eonis display fit your needs within
your working environment. Also, you can retrieve general information about your display and it
configuration settings through the OSD menu.
To bring up the OSD menu
1. While the display is switched on, press the Menu/Enter ()key.
As a result, the OSD main menu comes up in the middle of the screen. If no further actions are taken
within the following 10 seconds however, the OSD menu will disappear again.
s current
4.4Navigating through the OSD menus
To navigate through the OSD menus
1. Use the Right/Down () and Left/Up () keys to move through the (sub)menus, change values or
make selections.
2. To go into a submenu or confirm adjustments and selections, use the Menu/Enter (
)key.
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5. Advanced operation
5. ADVANCED OPERATION
5.1Video input source selection
About video input source selection
By default, your Eonis display automatically detects and shows the connected video input source. However, when for instance more then one video input source is connected, it may be needed to manually
select the input source to be displayed.
The available video input source selections for your display are:
•Auto: This is the default setting and will automatically detect and display the connected video input
source.
•HDMI: This setting will display the video connected to the HDMI input.
•DisplayPort: This setting will display the video connected to the DisplayPort input.
•VGA: This setting will display the video connected to the VGA input.
To select a video input source
1. Bring up the OSD main menu.
2. Navigate to the Input Selection menu.
3. Select one of the available video input sources.
5.2Luminance adjustment
About luminance adjustment
The luminance of your Eonis display is adjustable over a predefined range. When you change the luminance, the display will adjust its backlight to reach the target.
To adjust the luminance
1. Bring up the OSD main menu.
2. Navigate to the Adjustments menu.
3. Enter the Luminance submenu.
4. Set a luminance value as desired and confirm.
5.3Gamma selection
About gamma selection
Native, uncorrected panels will display all grayscale/color levels with equal luminance increments. Studies
have shown however, that in medical images certain grayscale/color parts contain more relevant information than others. To respond to these conclusions, gamma functions have been defined. These functions
emphasize on these parts containing crucial information by correcting the native panel behavior.
The available gamma functions for your display are:
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5. Advanced operation
•Native:IfyouselectNative, the native panel behavior will not be corrected.
•sRGB:Thisisthedisplayfunctionasdefined in the sRGB specificationandisdesignedtomatch
typical home and office viewing conditions. It is widely used in most computer applications.
•DICOM: DICOM (Digital Imaging and Communications in Medicine) is an international standard that
was developed to improve the quality and communication of digital images in radiology. In short,
the DICOM gamma function results in more visible grayscales in the images. Barco recommends
selecting the DICOM gamma function for most medical viewing applications.
•Gamma 2.2: Select this function in case the display is to replace a CRT display with a gamma of 2.2.
•QAWeb: This gamma function will be automatically selected when gamma functions are defined by
MediCal QAWeb.
To select a gamma function
1. Bring up the OSD main menu.
2. Navigate to the Adjustments menu.
3. Enter the Gamma submenu.
4. Select one of the available gamma functions.
5.4Ambient light reading room selection
About ambient light reading rooms
The available ambient light reading rooms for your display are:
•Dark Room: Corresponds to light conditions in dark diagnostic reading rooms. This setting has the
lowest maximum ambient light.
•Office: Corresponds to light conditions in office rooms.
•Operation Room: Corresponds to light conditions in operating rooms. This setting has the highest
maximum ambient light.
•QAWeb: This setting will be automatically selected when ambient li
iCal QAWeb.
ght conditions are defined by Med-
To select an ambient light reading room
1. Bring up the OSD main menu.
2. Navigate to the Adjustments menu.
3. Enter the Ambient Light submenu.
4. Select one of the available reading rooms and confirm.
5.5White p oint selection
About white point selection
This setting allows you to modify the display white point, used as reference for all other colors to be displayed.
The available white point settings for your display are:
•Native: The native, unmodified color temperature of the LCD panel.
•6500K (sRGB): Corresponds to a color temperature of 6500 Kelvin (D65).
•QAWeb: This white point setting will be automatically selected when white point is defined by
MediCal QAWeb.
16
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5. Advanced operation
To select the white point
1. Bring up the OSD main menu.
2. Navigate to the Adjustments menu.
3. Enter the White Point submenu.
4. Select one of the available white point presets.
5.6Analog video settin gs
The following settings are only available when VGA video input source is selected.
About analog video settings
When the VGA video input source is active, a number of analog video settings will become available:
•Auto Adjust: The analog video setting will automatically be adjusted
•Geometry: Allows to manually adjust the geometry settings of the analog video (clock frequency, clock
phase, horizontal position, vertical position)
•Level: Allows to manually adjust the contrast and brightness levels of the analog video
To adjust the analog video settings
1. Bring up the OSD main menu.
2. Navigate to the Adjustments menu.
3. Enter the Analog submenu.
4. Adjust one of the available analog video settings as desired.
5.7OSD menu language
About the OSD menu language
By default, the OSD menu comes up in English. However, there’s a wide range of other languages available for the OSD menu of your Eonis display:
•English
•French
•German
•Spanish
•Italian
•Dutch
•Japanese
•Traditional Chinese
•Simplified Chinese
•Korean
To select the language of the OSD menu:
1. Bring up the OSD main menu.
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5. Advanced operation
2. Navigate to the Adjustments > Settings menu.
3. Enter the Language submenu.
4. Select one of the available languages.
5.8Power s tatu s LED
About the power status LED
By default, the power status LED has the following behavior:
•Green: Displayison
•Blinking green: Display is entering standby power-saving mode
•Orange: Display is in standby power-saving mode
•Off: Display is disconnected from the mains power
This default behavior can be changed so that the power status LED is also off when the display is on or
when the display is entering standby power-saving mode.
To change the behavior of the power status LED:
1. Bring up the OSD main menu.
2. Navigate to the Adjustments > Settings menu.
3. Enter the Power Status LED submenu.
4. Change the behavior of the power status LED as desired and confirm.
The orange standby power-saving state of the LED is not influenced by this setting. So,
when the display is in standby power-saving mode, the LED w ill turn orange, even if it
was switched off by this setting.
5.9DPMS mode
About DPMS mode
Enabling the Display Power Management System (DPMS) mode on your Eonis display will optimize the
displays’ lifetime by automatically switching off the backlight when no video signal is detected for approximately 10 seconds. The power status LED will then turn orange.
To enable/disable DPMS mode
1. Bring up the OSD main menu.
2. Navigate to the Adjustments > Settings > Power Save menu.
3. Enter the DPMS submenu.
4. Select On or Off as desired and confirm.
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5. Advanced operation
5.10Self calibration frequency
About self calibration
The front sensor of your Eonis display measures the output luminance of your screen and allows the
display to automatically stabilize its luminance for maximum image quality over the displays’ lifetime. This
self calibration is done at an adjustable, predefined frequency:
•1min
•1hr
•6hr
•24 hr
•Never
•QAWeb: This setting will be automatically selected when the self calibration frequency is defined by
MediCal QAWeb.
To adjust the self calibration frequency
1. Bring up the OSD main menu.
2. Navigate to the Adjustments > Settings menu.
3. Enter the Self Calibration Frequency submenu.
4. Select one of the available frequency presets.
5.11F actory reset
About factory reset
A factory reset allows you to fully restore the display to its original factory setting.
To perform a factory reset
1. Bring up the OSD main menu.
2. Navigate to the Adjustments > Settings menu.
3. Enter the Factory Reset submenu.
4. Select Yes or No as desired and confirm.
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5. Advanced operation
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6. Cleaning your display
6. CLEANING YOUR DISPLAY
6.1Cleaning instructions
To clean the display
Clean the display using a sponge, cleaning cloth or soft tissue, lightly moistened with a recognized cleaning product for medical equipment. Read and follow all label instructions on the cleaning product. In case
of doubt about a certain cleaning product, use plain water.
Do not use following products:
•Alcohol/solvents at higher concentration > 5%
•Strong alkalis lye, strong solvents
•Acid
•Detergents with fluoride
•Detergents with ammonia
•Detergents with abrasives
•Steel wool
•Sponge with abrasives
•Steel blades
•Cloth with steel thread
CAUTION: Take care not to damage or scratch the front glass or LCD. Be careful with
rings or other jewelry and do not apply excessive pressure on the front glass or LCD.
CAUTION: Do not apply or spray liquid directly to the display as excess liquid may cause
damage to internal electronics. Instead, apply the liquid to a cleaning cloth.
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6. Cleaning your display
22K5903049 EONIS 19/02/2014
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7. IMPORTANT INFORMATION
7.1Safety information
General recommendations
Read the safety and operating instructions before operating the device.
Retain safety and operating instructions for future reference.
Adhere to all warnings on the device and in the operating instructions manual.
Follow all instructions for operation and use.
Electrical Shock or Fire Hazard
To prevent electric shock or fire hazard, do n ot remove cover.
No serviceable parts inside. Refer servicing to qualified personnel.
Do not expose this apparatus to rain or moisture.
7. Important information
Type of protection (electrical):
Display with external power supply: Class I equipment.
Degree of safety (flammable anesthetic mixture):
Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen
or nitrous oxide.
Non-patient care equipment
•Equipment primarily for use in a health care facility that is intended for use where contact with a patient
is unlikely (no applied part).
•The equipment may not be used with life support equipment.
•The user should not touch the equipment, nor its signal input ports (SIP)/signal output ports (SOP)
and the patient at the same time.
Power connection – Equipment with external 12 VDC power supply
•Power requirements: The equipment must be powered using the delivered medical approved 12 VDC
(
) power supply.
•The medical approved DC (
•The power supply is specified as a part of the ME equipment or combination is specified as a ME
system.
•To avoid the risk of electric shock, this equipment mu
protective earth.
•The equipment should be installed near an easily accessible outlet.
•The equipment is intended for continuous operation.
) power supply must be powered by the A
st only be connected to a supply mains with
C mains voltage.
Transient over-voltage
If the device is not used for a long time, disconnect it from the AC inlet to avoid damage by transient
over-voltage.
To fully disengage the power to the device, please disconnect the power cord from the AC inlet.
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7. Important information
Power cords:
•Utilize a UL-listed detachable power cord, 3-wire, type SJ or equivalent, 18 AWG min., rated 250 V
min., provided with a hospital-grade type plug 5-15P configuration for 120V application, or 6-15P for
240V application.
•Do not overload wall outlets and extension cords as this may result in fire or electric shock.
•Mains lead protection (U.S.: Power cord): Power cords should be routed so that they are not likely to
be walked upon or pinched by items placed upon or against them, paying particular attention to cords
at plugs and receptacles.
•The power supply cord should be replaced by the designated operator only at all time.
•Use a power cord that matches the voltage of the power outlet, which has been approved and complies
with the safety standard of your particular country.
External equipment
External equipment intended for connection to signal input/output or other connectors, shall comply with
relevant UL/ EN/ IEC standard (e.g. UL/EN/IEC 60950 for IT equipment and UL/EN 60601-1 / IEC 60601
series for medical electrical equipment). In addition, all such combinations -systems- shall comply with the
standard IEC 60601-1-1, safety requirements for medical electrical systems. Equipment not complying
with UL/EN / IEC 60601-1 shall be kept outside the patient environment, as defined in the standard.
Equipment not complying with IEC 60601 must be kept outside the patient environment, as definedinthe
standard as at least 1.5 meters from the patient or the patient support.
Any person who connects external equipment to signal input, signal output, or other connectors has formed
a system and is therefore responsible for the system to comply with the requirements of IEC 60601-1-1.
If in doubt, speak with a qualified technician.
In locations where 240 V outlets are used, connect this display only on a center-tapped, 240 V, singlephase supply .
Water and moisture
Never expose the device to rain or moisture. Never use the device near water - e.g. near a bathtub,
washbasin, swimming pool, kitchen sink, laundry tub or in a wet basement.
IP-x level for MDRC-2122 BL: Ordinary
IP-x level fo r MDRC-2122 WP: Prote ction glass, IP32
Ventilation
Do not cover or block any ventilation openings in the cover of the set. When installing the device in a
cupboard or another closed location, heed the necessary space between the set and the sides of the
cupboard.
Installation
Place the device on a flat, solid and stable surface that can support the weight of at least 3 devices. If you
use an unstable cart or stand, the device may fall, causing serious injury to a child or adult, and serious
damage to the device.
This apparatus conforms to:
CE (MDD 93/42/EEC class I product), CE - 2004/ 10
TION), IEC 60601-1 2ND ED:1988 + A1:1991 + A2:1995, UL 60601-1 1ST EDITION, CAN/CSA-C22.2
NO. 601.1-M90:2005, IEC 60601-1:2005 + A1:2012, ANSI/AAMI ES 60601-1:2005 + C1:2009 + A1:2012,
CAN/CSAC22.2 No. 60601-1-08:2008, DEMKO - EN 60601- 1:2006, EN 60601-1-2:2007, CCC - GB92542008 + GB4943-2001 + GB17625.1-2003, KC, VCCI, FCC class B, ICES-001 Level B, FDA Class I device, RoHS
8/EC, IEC 60950-1:2005 + A1:2009 (2ND EDI-
National Scandinavian Deviations for CL. 1.7.2:
Finland: "Laite on liitettävä suojamaadoituskoskettimilla varustettuun pistorasiaan"
24
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7. Important information
Norway: "Apparatet må tilkoples jordet stikkontakt"
Sweden: "Apparaten skall anslutas till jordat uttag"
Essential performance
Barco states that the Eonis display is only used for reviewing medical digital images. These reviews are
done in rooms where the equipment is unlikely to be in contact with patients. With this information, if
the display fails, the patient is not in direct danger for harm. If, by some reason, the display would fail
there would be no danger towards the operator working with it. Also the Eonis display has no artificial
intelligence and doesn’t manipulate the image information. If something would fail in the display, ex. no
image on the screen, the medical staff will notice this directly. Some other risks are less obvious, for
example image artifacts introduced by the display. However, as the display is only intended to be u
for reviewing medical digital images, indirect danger towards the patient isn’t there. With this information,
the Eonis display has no essential performance.
7.2Environmental information
Disposal Information
Waste Electrical and Electronic Equipment
sed
This symbol on the product indicates that, under the European Di
waste from electrical and electronic equipment, this product must not be disposed of with other municipal
waste. Please dispose of your waste equipment by handing it over to a designated collection point for the
recycling of waste electrical and electronic equipment. To prevent possible harm to the environment or
human health from uncontrolled waste disposal, please separate these items from other types of waste
and recycle them responsibly to promote the sustainable reuse of material resources.
For more information about recycling of this product, please contact your local city office or your municipal
waste disposal service.
For details, please visit the Barco website at: h
ttp://www.barco.com/en/AboutBarco/weee
rective 2012/19/EU governing
Tu rkey RoHS compliance
Türkiye Cumhuriyeti: AEEE Yönetmeliğine Uygundur.
[Republic of Turkey: In conformity with the WEEE Regulation]
According to the “China Administration on Control of Pollution Caused by Electronic Information Products”
(Also called RoHS of Chinese Mainland), the table below lists the names and contents of toxic and/or
hazardous substances that Barco’s product may contain. The RoHS of Chinese Mainland is included in
the MCV standard of the Ministry of Information Industry of China, in the section “Limit Requirements of
toxic substances in Electronic Information Products”.
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7. Important information
零件项目(名称)
Component name
印制电路配件
Printed Circuit Assemblies
液晶面板
LCD panel
外接电(线)缆
External Cables
內部 线路
Internal wiring
金属外壳
Metal enclosure
塑胶外壳
Plastic enclosure
散热片(器)
Heatsinks
电源供应器
有毒有害物质或元素
Hazardous substances and elements
铅
Pb
X
X
X
OO O O OO
OO O O OO
OO O O OO
OO O O OO
X
汞
Hg
OOOOO
OOOOO
OOOOO
OOOOO
镉
Cd
六价铬
Cr6+
多溴联苯
PBB
多溴二苯
醚
PBDE
Power Supply Unit
风扇
Fan
文件说明书
Paper Manuals
光盘说明书
CD manual
O: 表示该有毒有害物质在该部件所有均质材料中的含量均在 SJ/T 11363-2006 标准规定的限量要求以下.
O: Indicates that this toxic or hazardous substance contained in all of the homogeneous materials for
this part is below the limit requirement in SJ/T11363-2006.
X: 表示该有毒有害物质至少在该部件的某一均质材料中的含量超出 SJ/T 11363-2006 标准规定的限量要求.
X: Indicates that this toxic or hazardous substance contained in at least one of the homogeneous
materials used for this part is above the limit requirement in SJ/T11363-2006
All Electronic Information Products (EIP) that are sold within Chinese Mainland must comply with the
“Electronic Information Products Pollution Control Labeling Standard” of Chinese Mainland, marked with
the Environmental Friendly Use Period (EFUP) logo. The number inside the EFUP logo that Barco uses
(please refer to the photo) is based on the “Standard of Electronic Information Products Environmental
Friendly Use Period” of Chinese Mai
OO O O OO
OO O O OO
OO O O OO
nland.
10
26K5903049 EONIS 19/02/2014
Page 29
7. Important information
7.3Regulatory compliance information
Indications for use
This display is an AMLCD display designed for viewing medical X-ray images. This unit should not be
used near patients (where patients are likely to be in unconscious condition) and should be kept outside
of 1.83 m perimeter and 2.29 m vertical.
This display is not cleared for primary diagnosis. Any use for primary diagnosis is the sole responsibility
of the user.
FCC class B
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
(1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.
This device 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 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. However, there is no guarantee that interference will not occur in a particular
installation. If this device does cause harmful interference to ra
determined by turning the device off and on, the user is encouraged to try to correct the interference by
one or more of the following measures:
dio or television reception, which can be
•Reorient or relocate the receiving antenna.
•Increase the separation between the device and receiver.
•Connect the device into an outlet on a circuit different from that to which the receiver is connected.
•Consult the dealer or an experienced radio/TV technician for help.
Changes or modifications not expressly approved by the party responsible for compliance could void the
user’s authority to operate the equipment.
Canadian notice
This ISM device complies with Canadian ICES-001.
Cet appareil ISM est conforme à la norme NMB-001 du Canada.
7.4EMC notice
General information
No specific requirement on the use of external cables or other accessories except power supply.
With the installation of the device, use only the delivered power supply or a spare part provided by the
legal manufacturer. Using another can result in a decrease of the immunity level of the device.
Electromagnetic emissions
The Eonis display is intended for use in the electromagnetic environment specified below. The customer
or the user of the Eonis display should assure that it is used in such an environment.
only for its internal function.
Therefore, its RF emissions are
very low and are not likely to
cause any interference in nearby
electronic equipment.
Page 30
7. Important information
Emissions test
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/ flicker
emissions
IEC 61000-3-3
This Eonis display complies with appropriate medical EMC standards on emissions to, and interference
from surrounding equipment. Operation is subject to the following two conditions: (1) this device may n
cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.
Interference can be determined by turning the equipment off and on.
If this equipment does cause harmful interference to, or suffer from harmful interference of, surrounding
equipment, the user is encouraged to try to correct the interference by one or more of the following mea
sures:
•Reorient or relocate the receiving antenna or equipment.
•Increase the separation between the equipment and receiver.
•Connect the equipment into an outlet on a circuit different from that to which t
•Consult the dealer or an experienced technician for help.
Compliance
Class B
Class D
Complies
Electromagnetic environment –
Guidance
The Eonis display 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.
ot
he receiver is connected.
-
Electromagnetic immunity
The Eonis display is intended for use in the electromagnetic environment specifi
or the user of the Eonis display should assure that it is used in such an environment.
Immunity test
Electrostatic discharge
(ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC61000-4-5
IEC 60601
Test levels
± 6kV contact
±8kVair
± 2kV for power supply
lines
± 1kV for input/ output
lines
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
Compliance level
± 6kV contact
±8kVair
± 2kV for power supply
lines
± 1kV for input/ output
lines
± 1 kV line(s) to line(s)
±2kVline(s)toearth
ed below. The customer
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
28K5903049 EONIS 19/02/2014
Page 31
7. Important information
Immunity test
Voltage dips, short
interruptions and voltage
variations on power
supply input lines
IEC 61000-4-11
Power frequency (50/60
Hz) magnetic field
IEC 61000-4-8
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
IEC 60601
Test levels
<5%U
U
T
40% U
1
(> 95% dip in
T
) for 0.5 cycle
(60%dipinUT)
T
for 5 cycles
70% U
(30%dipinUT)
T
for 25 cycles
<5%U
U
) for 5s
T
(>95% dip in
T
3A/m
3Vrms
150 kHz to 80 MHz
3V/m
80 MHz to 2.5 GHz
Compliance level
<5%U
U
) for 0.5 cycle
T
40% U
(> 95% dip in
T
(60% dip in UT)
T
for 5 cycles
70% U
(30% dip in UT)
T
for 25 cycles
<5%U
U
)for5s
T
Not applicable
(>95% dip in
T
2
3V
3V/m
Electromagnetic
environment –
guidance
Mains power quality
should by that of a typical
commercial or hospital
environment. If the user
of the Eonis display
requires continued
operation during power
mains interruptions, it is
recommended that the
Eonis display 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.
Portable and mobile
RF communications
equipment should be
used no closer to any
part of the Eonis display,
including cables, than
the recommended
separation distance
calculated from the
equation applicable
to the frequency
of the transmitter.
Recommended
separation distance
1. is the a.c. mains voltage prior to application of the test level.
2. Eonis display doesn’t contain susceptible components to magnetic fields
d=1.2√P
d=1.2√P 80 MHz to 800
MHz
d=2.3√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
fixed RF transmitters,
as determined by an
electromagnetic site
survey,
3
should be less
than the compliance
K5903049 EONIS 19/02/201429
Page 32
7. Important information
Immunity test
IEC 60601
Test levels
At 80 MHz and 800 MHz, the higher frequency range applies.
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from s tructures, objects and people.
Recommended separation distance
Compliance level
Electromagnetic
environment –
guidance
level in each frequency
4
range.
Interference may occur in
the vicinity of equipment
marked with symbol:
The Eonis display is intended for use in an electromagnetic environment in which radiated RF disturbances
are controlled. The customer of the user of the Eonis display can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment
(transmitters) and the Eonis display as recommended below, according to the maximum output power of
the communications equipment.
Rated maximum output
power of transmitter
W
Separation dis tance according to frequency of transmitter
5
150kHz to 80MHz
d=1.2√P
80MHz to 800MHz
d=1.2√P
800MHz to 2.5GHz
d=2.3√P
0.010.120.120.23
0.10.380.380.73
11.21.22.3
103.83.87.3
100121223
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
3. 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 the Eonis display is used exceeds the applicable RF compliance level above, the Eonis display should be observed
to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or
relocating the Eonis display.
4. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than3V/m.
5. 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.
30K5903049 EONIS 19/02/2014
Page 33
These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection form structures, object and people.
7.5Exp lanation of symbols
Symbols on the device
On the device or p ower supply, you may find the following symbols (nonrestrictive list):
Indicates compliance with the Directive 93/42/EEC as Class I device
Indicates compliance with the Directive 93/42/EEC as Class II device
7. Important information
Indicates compliance with Part 15 of the FCC rules (Class A or Class B)
Indicates the device is approved according to the UL regulations
Indicates the device is approved according to the UL regulations for Canada
and US
Indicates the device is approved according to the UL Demko regulations
Indicates the device is approved according to the CCC regulations
Indicates the device is approved according to the VCCI regulations
Indicates the device is approved according to the KC regulations
Indicates the device is ap
Indicates the USB connectors on the device
Indicates the DisplayPort connectors on the device
K5903049 EONIS 19/02/201431
proved according to the BSMI regulations
Page 34
7. Important information
Indicates the manufacturing date
Indicates the temperature limitations6for the device to safely operate within specs
Indicates the device serial no.
Warning: dangerous voltage
Caution
Consult the operating instructions
Indicates this device must not be thrown in the trash but must be recycled,
according to the European WEEE (Waste Electrical and Electronic Equipment)
directive
Indicates Direct Current (DC)
Indicates Alternating Current (AC)
Stand-by
Equipotentiality
Symbols on the box
On the box of the device, you may find the following symbols (nonrestrictive list):
Indicates a device that can be broken or damaged if not handled carefully when
being stored.
Indicates a device that needs to be protected from moisture when being stored.
Indicates the storage direction of the box. The box must be transported, handled
and stored in such a way that the arrows always point upwards.
15
6. Values for xx and yy can be found in the technical specifications paragraph.
32K5903049 EONIS 19/02/2014
n
or
Indicates the maximum number of identical boxes which may be stacked on each
other, where “n” is the limiting number.
Page 35
20 - 30 Kg
7. Important information
Indicates that the box should be carried with two persons.
Indicates that the box should not be cut with a knife, a cutter or any other sharp
object.
yy
xx
-20 °C
+60 °C
85 %
yy
being stored.
Indicates the range7of humidity to which the device can be safely exposed when
being stored.
Indicates the temperature limits7to which the device can be safely exposed when
x
5 %
yyy
106 kPa
Indicates the range7of atmospheric pressure to which the device can be safely
exposed when being stored.
xx
50 kPa
7.6Legal disclaimer
Disclaimer notice
Although every attempt has been made to achieve technical accuracy in this document, we assume no
responsibility for errors that may be found. Our goal is to provide you with the most accurate and usable
documentation possible; if you discover errors, please let us know.
Barco software products are the property of Barco. They a
Barco, Inc., for use only under the specific terms of a software license agreement between Barco N.V. or
Barco Inc. and the licensee. No other use, duplication, or disclosure of a Barco software product, in any
form, is authorized.
re distributed under copyright by Barco N.V. or
The specifications of Barco products are subject to change without notice.
Trademarks
All trademarks and registered trademarks are property of their respective owners.
Copyright notice
This document is copyrighted. All rights are reserved. Neither this document, nor any part of it, may
be reproduced or copied in any form or by any means - graphical, electronic, or mechanical including
photocopying, taping or information storage and retrieval systems - without written permission of Barco.