Eizo CuratOR SP1-24 User manual

Instructions for Use
Digital image and video viewing system
Important
Please read the safety information and all information delivered
with the product carefully to familiarize yourself with safe and
effective usage.

EIZO GmbH
Carl-Benz-Straße 3
76761 Rülzheim
Germany
1057449-003
02/2020 Technical data subject to change.
Copyright © EIZO GmbH 2020.
All rights reserved.
Legal information
Warning notice system
This manual contains notices you have to observe in order to ensure your personal safety, as well as to
prevent damage to property. The notices referring to your personal safety are highlighted in the manual
by a safety alert symbol, notices referring only to property damage have no safety alert symbol. These
notices shown below are graded according to the degree of danger.
DANGER
indicates that death or severe personal injury will result if proper precautions are not taken.
WARNING
indicates that death or severe personal injury may result if proper precautions are not taken.
CAUTION
indicates that minor personal injury can result if proper precautions are not taken.
NOTICE
indicates that material damage can result if proper precautions are not taken.
If more than one degree of danger is present, the warning notice representing the highest degree of
danger will be used. A notice warning of injury to persons with a safety alert symbol may also include a
warning relating to property damage.
Qualified personnel
The product/system described in this documentation may be operated only by personnel qualified for
the specific task in accordance with the relevant documentation, in particular its warning notices and
safety instructions. Qualified personnel are those who, based on their training and experience, are ca-
pable of identifying risks and avoiding potential hazards when working with these products/systems.
Use of EIZO products
WARNING
EIZO products may only be used for the applications described in the catalog and in the relevant tech-
nical documentation. If products and components from other manufacturers are used, these must be
recommended or approved by EIZO. Proper transport, storage, installation, assembly, commissioning,
operation and maintenance are required to ensure that the products operate safely and without any
problems. The permissible ambient conditions must be complied with. The information in the relevant
documentation must be observed.
Trademarks
All names identified by ® are registered trademarks of their respective owners. Please refer to the
trademarks listed in the appendix. The remaining trademarks in this publication may be trademarks
whose use by third parties for their own purposes could violate the rights of the owner.
Disclaimer of liability
We have reviewed the contents of this publication to ensure consistency with the hardware and soft-
ware described. Since variance cannot be precluded entirely, we cannot guarantee full consistency.
However, the information in this publication is reviewed regularly and any necessary corrections are
included in subsequent editions.

Table of contents
CuratOR Surgical Panel
Instructions for Use, 02/2020 3
Table of contents
Legal information ............................................................................................................. 2
1 Introduction....................................................................................................................... 4
1.1 Contents of this document ........................................................................................4
1.2 Intended use .............................................................................................................4
1.3 User ..........................................................................................................................4
2 Safety information ............................................................................................................ 5
2.1 General safety instructions .......................................................................................5
3 Description........................................................................................................................ 7
3.1 General information ..................................................................................................7
3.2 Design.......................................................................................................................8
4 Installation and start-up................................................................................................... 9
5 Operation......................................................................................................................... 10
5.1 Switching on and off ...............................................................................................10
5.1.1 Switch on .................................................................................................. 10
5.1.2 Shutdown .................................................................................................. 11
5.2 Avoiding image sticking ..........................................................................................11
5.3 Check for pixel defects ...........................................................................................12
5.4 Interfaces ................................................................................................................12
6 Cleaning and Maintenance ............................................................................................ 13
6.1 Cleaning..................................................................................................................13
6.2 Maintenance ...........................................................................................................14
7 Technical specifications ................................................................................................ 15
7.1 Power supply ..........................................................................................................15
7.2 Mechanical design ..................................................................................................15
7.3 Climatic conditions..................................................................................................15
7.4 CE marking .............................................................................................................16
7.5 Electromagnetic compatibility .................................................................................16
8 Appendix ......................................................................................................................... 18
8.1 Information on electromagnetic compatibility (EMC) ..............................................18
8.2 Markings and symbols ............................................................................................23
8.3 Environmental protection ........................................................................................23
8.4 Additional devices...................................................................................................23
8.5 Contact ...................................................................................................................24
8.6 Trademarks.............................................................................................................24

Introduction
1.1 Contents of this document
4
CuratOR Surgical Panel
Instructions for Use, 02/2020
1 Introduction
1.1 Contents of this document
This document explains the functions and proper use of the CuratOR Surgical Panel, which
is available in a number of project-specific and standard versions:
All information provided applies to standard conditions, and may differ depending on the op-
erating room and device configuration.
The contents of this document are neither part of a previous or existing agreement, commit-
ment or legal relationship, nor does it modify such.
Note
• Refer to the service manual for information regarding installation and start-up of the Cu-
ratOR Surgical Panel.
• The current electronic version of the instructions for use and the service manual can be
found on the EIZO GmbH home page www.eizo-or.com.
1.2 Intended use
EIZO CuratOR Surgical Panels are digital image and video viewing systems and are in-
tended for use in the OR or other medical environments. They are not suitable for direct
contact with patients or for use in the vicinity of the patient.
CuratOR Surgical Panels are merely intended for displaying patient-related data, images
and videos.
CuratOR Surgical Panels serve as central control platforms for video distribution, recording
and buffer storage of patient-specific data, images and videos.
CuratOR Surgical Panels serve as the physical interface between the operating room and
the IT infrastructure of a hospital.
1.3 User
User
In the following, healthcare personnel such as surgeons or medical technicians are referred
to as the "user".
Service / service personnel
"Service" or "Service personnel" identifies authorized personnel with knowledge of medical
imaging technology, local standards for image quality requirements, and safety of medical
products, for example a hospital technician or manufacturer of medical devices.
Cleaning staff
"Cleaning staff" refers to personnel responsible for cleaning medical devices.

Safety information
2.1 General safety instructions
CuratOR Surgical Panel
Instructions for Use, 02/2020 5
2 Safety information
2.1 General safety instructions
Careful operation is a prerequisite for correct and safe operation of the CuratOR Surgical
Panels.
The devices may only be used for applications for which they are commonly used.
For safety reasons, the following precautions must be observed:
DANGER
Please observe all warning information present on the device and in the instructions for use
There is a danger to life if warnings are not obeyed. Severe personal injury or damage to property
may occur.
Observe the safety requirements of EN 60601-1 (IEC 60601-1)
To prevent injury to patients and users, connect the electrical system in accordance with the safety
requirements of EN60601‑1 (IEC60601‑1) for “Safety requirements for medical electrical systems”.
Connecting the protective ground conductor
If the device is connected to the line power, the device must be connected to a protective ground
conductor. This is the only way to ensure that the touch leakage current in a first fault event does not
exceed 500 µA.
The interruption of the device's protective conductor is considered a first fault event in accordance
with EN 60601-1.
Use the following measures to ensure that the leakage currents remain below the specified limits:
• Separators for signal input unit or signal output unit.
• Use of a safety isolating transformer.
• Use of the additional protective ground terminal.
DANGER
No unauthorized opening of the device / no unauthorized service or maintenance work
The device may only be opened by qualified personnel authorized by EIZO. Likewise, service or
maintenance work may only be carried out by qualified personnel authorized by EIZO. There is a risk
of electric shock.
No liability is accepted for death and injury to persons or damage to property resulting from work car-
ried out by non-qualified personnel.
Do not touch components in the device
If the device is connected to the line power, components in the device are subjected to high voltages.
Touching the components may be fatal.
No contact between device and patients
The device is not suitable for direct contact with a patient. The device and patient must never be
touched simultaneously. Otherwise there is a danger to life and limb.
Do not insert any objects into the housing
Objects inserted into the housing may result in an electric shock or damage to the device.
Avoid penetration of liquid
Liquids seeping into the device may result in electric shock or device failure.

Safety information
2.1 General safety instructions
6
CuratOR Surgical Panel
Instructions for Use, 02/2020
CAUTION
Care of device / cleaning agents
• Remove water drops immediately.
• Only clean the surfaces using the cleaning agents referred to in the Instructions for Use.
What to do if the device is faulty
If the following conditions exist, the device must be disconnected from line power and checked by
qualified personnel:
• Damage to the device.
• After liquid seeps into the device.
• If the device does not function or if a fault cannot be eliminated using the Instructions for Use.
• If the device smells of burning or makes peculiar noises.
Be aware of the monitors aging
Note that monitors can fail as a result of aging, and that image properties such as brightness, con-
trast, and color value can change.

Description
3.1 General information
CuratOR Surgical Panel
Instructions for Use, 02/2020 7
3 Description
3.1 General information
Each CuratOR Surgical Panel is adapted to the specific requirements of the operating room
(OR). Consequently, the powder-coated stainless steel housing is available in a wide variety
of sizes and colors, with the inner workings protected by an anti-reflective single-layer safety
glass pane (ESG) or a front panel made of metal (whichever is used varies from design to
design). The front can be fully disinfected and can be incorporated into the cleaning plan for
the OR.
See also Cleaning [}13].
The inner workings of the Surgical Panels, comprising a monitor system and IT and video
management components, always correspond to the current state of the art.
By default, the Surgical Panel comes with a Microsoft Windows operating system. Follow
the information in the corresponding documentation.
If you are using EIZO Caliop software, please follow the information in the software docu-
mentation.
Input devices include a medical silicone keypad with or without touch pad, which is fit into a
purpose-built holder, and a medical silicone mouse. The tilt of the keypad holder and special
mouse pad ensure ergonomic working conditions.
Various video and USB inputs as well as suitable accessories can be integrated into the
front in addition to the main switch and system switch.
The following standard versions of the Surgical Panels are available:
Standard version Description
CuratOR Surgical Panel SP1-24
CuratOR Surgical Panel SP1-24T
Nurse Station with 24" panel.
Nurse Station with 24" Touchscreen.
CuratOR Surgical Panel SP1-49
CuratOR Surgical Panel SP1-49T
Viewing Station with 49" panel.
Viewing Station with 49" Touchscreen.
CuratOR Surgical Panel SP2-24 HIS/PACS Station with two 24" panels.
CuratOR Surgical Panel SP2-24-49
CuratOR Surgical Panel SP2-24T-49
HIS/PACS Station with 24" panel and 49" panel.
HIS/PACS Station with 24" Touchscreen and 49" Panel.

Description
3.2 Design
8
CuratOR Surgical Panel
Instructions for Use, 02/2020
3.2 Design
The CuratOR Surgical Panel has the following components as standard:
• Monitor panel
• PC module
• Keyboard holder with or without mouse pad and palm rest
• Silicone keyboard and silicone mouse
• USB ports
• Main switch and system switch
• Input and output interfaces
Examples
Fig.: CuratOR Surgical Panel SP2-24-49 / SP2-24T-49
Fig.: CuratOR Surgical Panel SP1-49

Installation and start-up
3.2 Design
CuratOR Surgical Panel
Instructions for Use, 02/2020 9
4 Installation and start-up
The CuratOR Surgical Panel is suited to surface-mounted or flush-mounted installation
depending on the individual design.
In addition to mounting on the wall or in a niche, installation includes connection to power
and the IT network.
Start-up includes the first intended use of the CuratOR Surgical Panel.
CAUTION
Installation and start-up
• The CuratOR Surgical Panel may only be installed and put into operation by EIZO em-
ployees or by personnel authorized by EIZO.
• The CuratOR Surgical Panel must be installed in accordance with all applicable national
directives and regulations currently in effect.
Note
Refer to the service manual for information regarding installation and start-up.

Operation
5.1 Switching on and off
10
CuratOR Surgical Panel
Instructions for Use, 02/2020
5 Operation
5.1 Switching on and off
Observe the device switching on sequence for devices with an integrated PC.
5.1.1 Switch on
1. Use the switch labeled “Power Switch” to turn on the system.
ðOperating voltage is turned on.
2. Wait until the border of the switch labeled “PC on/off” illuminates green.
ðThe system is ready for operation after approx. 5 seconds.
3. Press the green-bordered switch labeled “PC on/off”.
ðThe IT system boots.
4. Wait until the IT system has fully booted.
ðThe system is fully operational after approx. 10 seconds.

Operation
5.2 Avoiding image sticking
CuratOR Surgical Panel
Instructions for Use, 02/2020 11
5.1.2 Shutdown
üAll work in progress with the system is ended, so that it can be shut down and, for ex-
ample, important data is not lost.
1. To shut down the IT system press the green-bordered switch labeled “PC on/off”.
2. Wait until the green border of the switch labeled “PC on/off” goes off.
ðMake sure the system has shut down properly.
3. Use the blue-bordered switch labeled “Power Switch” to turn off the system.
4. All components are disconnected from the operating voltage.
NOTICE
Note the sequence during shutdown
The blue-bordered switch labeled “Power Switch” may not be turned off until the border of
the switch labeled “PC on/off” is off.
Of necessity, any other sequence will cause the IT components to be abruptly discon-
nected from the power supply, which can result in hardware damage such as hard drive
failure.
5.2 Avoiding image sticking
Image sticking may occur with LCD monitors. Image sticking is an effect whereby a faint im-
age of the previous screen contents can be seen after the display contents have changed.
The following measures can reduce or prevent image sticking:
• Use a screen saver with regularly changing images
• Switch off the device when it is no longer needed.

Operation
5.3 Check for pixel defects
12
CuratOR Surgical Panel
Instructions for Use, 02/2020
5.3 Check for pixel defects
Pixel defects (small bright or dark dots) can occur in LCD monitors. During the manufactur-
ing process, all monitors are checked for the permitted number of defective pixels.
Defective pixels cannot be corrected.
5.4 Interfaces
USB
Two USB ports are integrated in the front of the CuratOR Surgical Panel as standard. They
are intended for connecting a mouse and a USB data medium.
Note
Data medium
Use trusted data media only. Observe the facility's applicable security guidelines.
Video
Video interfaces are integrated into the front of the device depending on the customer-spe-
cific design. They are used to connect any devices (modalities) with suitable video signal
output.
NOTICE
Connecting devices
• During connection of devices, make sure the socket will not be damaged when inserting
the connector.
• All devices connected to the Surgical Panel have to meet the respective national safety
standards.

Cleaning and Maintenance
6.1 Cleaning
CuratOR Surgical Panel
Instructions for Use, 02/2020 13
6 Cleaning and Maintenance
6.1 Cleaning
Cleaning agent
External cleaning of the protective front pane and housing should be incorporated into the
OR cleaning plan. Use a soft cloth for cleaning to prevent scratching painted parts and the
protective front pane.
A more thorough cleaning may only be provided through wiping with a damp cloth. Make
sure the liquids do not seep into the device near the operating elements or any other loca-
tion. When cleaning only use agents that will not form explosive mixtures with oxygen during
evaporation.
Do not use any cleaning agents containing the following ingredients:
Prohibited cleaning agents
More than 10% alcohol Gasoline mixtures containing benzene
Stain remover Perchloroethylene
Trichloroethylene Ethyl alcohol
Carbolic acid Petroleum
White spirit Carbon tetrachloride
More than 40% hydrogen peroxide in water All phenols and phenol derivatives
Disinfectants
The responsible hospital hygiene officer should establish the requirements regarding disin-
fection of the device, disinfection interval, and the selection of agent and procedure, in a
cleaning and disinfection plan (hygiene plan).
A suitable disinfectant and procedure in accordance with the disinfectant list of the German
Society for Hygiene and Microbiology (DGHM) should be used to disinfect the device.
We recommended an aldehyde mixture for disinfection.
For disinfection, rub surfaces with slight pressure and a suitable quantity of disinfectant (wet
wiping).

Cleaning and Maintenance
6.2 Maintenance
14
CuratOR Surgical Panel
Instructions for Use, 02/2020
6.2 Maintenance
WARNING
Maintenance
• Maintenance may only be performed by EIZO or personnel authorized by EIZO.
• Maintenance may not take place in the presence of patients.
• Information on maintenance can be found in the service manual.
Note
• Perform maintenance and inspection at least once per year, including the protective
conductor test.
• Perform a visual inspection every four weeks, for example for paint chips.
• Individual service and maintenance contracts can be negotiated. For detailed informa-
tion, please contact your EIZO partner.
www.eizo-or.com/de/eizo-gmbh/kontakt/

Technical specifications
7.1 Power supply
CuratOR Surgical Panel
Instructions for Use, 02/2020 15
7 Technical specifications
Note
Technical specifications / product information
• Specifications regarding the CuratOR Surgical Panel such as data on the housing,
panel, as well as dimensions of the standard versions can be found on our website
www.eizo-or.com.
• The product brochures with additional information can also be found on our website.
7.1 Power supply
Line voltage 100 to 240 V
Line frequency 50 to 60 Hz
Current consumption 4 to 2 A
7.2 Mechanical design
Housing components Powder-coated stainless steel and protective
glass pane
Ventilation openings No fan, thermal output through housing
Degree of protection according to EN60529 IPX4 up to IP65
7.3 Climatic conditions
In operation
Temperature range +5 °Cto+40 °C ambient temperature
Temperature gradient Max. 10 K/h, no condensation
Humidity 10to90%, non-condensing, at 25°C
Air pressure 700to1060 hPa
During transport and storage (packed)
Temperature range -20°Cto+60°C ambient temperature
Temperature gradient Max. 20 K/h, no condensation
Humidity 10to90%, non-condensing, at 25°C
Air pressure 200to1060 hPa

Technical specifications
7.4 CE marking
16
CuratOR Surgical Panel
Instructions for Use, 02/2020
7.4 CE marking
This product has been assigned a CE marking in compliance with the stipulations of EU di-
rectives 2014/30/EU, 2014/35/EU, and 2011/65/EU.
Conformity
Safety standards IEC 60950:2005/AMD1:2009/AMD2:2013
EN 60950:2006+A11:2009 +A1:2010 + A12:2011 +A2:2013
EN 62368:2014
CAN/CSA-C22.2 No.60950-1:2007/A2:2014-10
Protection class Protection class I
7.5 Electromagnetic compatibility
Electromagnetic compatibility
Interference immunity/interference
emissions
• IEC 60601-1-2:2014, EN 60601-1-2:2015
• EN 55032:2015 Class A
• RCM
– CISPR32:2015, Class A
– EN55022:2010+AC:2011, ClassA
– IEC 61000-3-2:2009, EN 61000-3-2:2014
• VCCI/JEITA
– CISPR32:2015, Class A
– EN 55032:2015, Class A
– IEC 61000-3-2:2009, EN 61000-3-2:2014
Electrostatic discharge on housing
parts(ESD)
IEC61000-4-2 Ed.2.0 (2008)
EN61000-4-2:2009-03
Nominal voltage 240V/50Hz 1/60nsec
Contact 2, 4, 6, 8 kV (direct and indirect discharge), air 2, 4, 6,
8, 15 kV (direct)
HF radiation IEC61000-4-3 Ed.3.2 (2010-04)
EN61000-4-3/A2:2010-07
80 MHz -2700 MHz
10 V/m 80 % AM with 1kHz
Burst on power cables IEC 61000-4-4:2012, EN 61000-4-4:2012
Testing with 100V/60Hz and 240V/50Hz nominal voltage
2, 3kV, 5/50nsec; coupling to power supply cables
Burst on signal line IEC 61000-4-4:2012, EN 61000-4-4:2012
± 2 kV on signal lines

Technical specifications
7.5 Electromagnetic compatibility
CuratOR Surgical Panel
Instructions for Use, 02/2020 17
Electromagnetic compatibility
Surge on power cables IEC 61000-4-5:2014, EN 61000-4-5:2014
Testing with 100V/60Hz and 240V/50Hz nominal voltage
Hybrid generator values: 1.2/50-8/20μsec.
0.5, 1, 2kV symmetrical;
0,5, 1, 2, 3kV asymmetrical at 0, 90, 180, 270 degrees
Input on power supply lines
Magnetic fields IEC 61000-4-8 (2009-09)
EN 61000-4-8 Edition 2010-02
Alternating fields Nominal voltage 100V/50Hz and 60Hz
Standard: 30A/m
10A/m at 100V/60Hz
10A/m at 240V/50Hz
Voltage fluctuations IEC 61000-4-11:2017, EN 61000-4-11:2017
a) Nominal voltage 240V/50Hz
b) Nominal voltage 100V/60Hz
Requirements according to IEC standard
Dips at nominal voltage 240V / 50Hz, each
• 70% for 25 periods of malfunction criterion B
• 0% for 0.5 periods, malfunction criterion B at 0°, 45°, 90°,
135°, 180°, 225°, 270°, 315°
• 0% for 1 periods of malfunction criterion C
• 0% for 250 periods (5 sec.) of malfunction criterion C.
Dips at nominal voltage 100V / 60Hz, each
• 70% for 30 periods of malfunction criterion B
• 0% for 0.5 periods, malfunction criterion B at 0°, 45°, 90°,
135°, 180°, 225°, 270°, 315°
• 0% for 1 periods of malfunction criterion C
• 0% for 300 periods (5 sec.) of malfunction criterion C.
Recovery time > 1s each
Line reaction to harmonics IEC 61000-3-2:2009, EN 61000-3-2:2014
Nominal voltage 240V/50Hz (-30%); measurement accord-
ing to Class D
GB17625.1
Line reaction to voltage fluctuations IEC 61000-3-3:2013, EN 61000-3-3:2014
Nominal voltage 240V/50Hz (-30%)

Appendix
8.1 Information on electromagnetic compatibility (EMC)
18
CuratOR Surgical Panel
Instructions for Use, 02/2020
8 Appendix
8.1 Information on electromagnetic compatibility (EMC)
CuratOR Surgical Panel is a digital image and video viewing system and is intended for use
in the OR or other medical environments.
NOTICE
Special EMC provisions are required for use of the CuratOR Surgical Panel. Installation,
assembly, and use must take place in compliance with the following instructions:
• Do not position any portable or mobile RF communication devices in the immediate
vicinity of the CuratOR Surgical Panel. Otherwise, problem-free function of the device
cannot be guaranteed.
• The CuratOR Surgical Panel should not be positioned or used in the immediate vicinity
of other devices. If devices have to be operated in the immediate vicinity of one an-
other, the Surgical Panel must be monitored to ensure proper operation for the defined
configuration.
• Persons connecting additional devices to the signal input or output for configuring a
medical system are responsible for ensuring compliance with standard IEC/
EN60601-1-2.
Electromagnetic radiation
The CuratOR Surgical Panel is intended for use in the electromagnetic environments noted below.
Customers and users of the CuratOR Surgical Panel have to ensure that the device is used in such
an environment.
Radiation test Conformity Information regarding the electromagnetic environment
RF radiation
CISPR11/EN 55011
Group 1 The CuratOR Surgical Panel uses RF radiation for internal
operation only. For this reason, the RF radiation is very low
and is therefore unlikely that the device will cause interfer-
ence in electronic devices in the immediate vicinity.
RF radiation
CISPR11/EN 55011
GB9254
Class B The CuratOR Surgical Panel is approved for use in a number
of environments. This includes residential areas and areas
connected directly to the public low-voltage grid, such as pri-
vate homes.
Harmonic currents
IEC/EN 61000-3-2
GB17625.1
Class D
Voltage fluctuations /
flicker
IEC/EN 61000-3-3
fulfilled

Appendix
8.1 Information on electromagnetic compatibility (EMC)
CuratOR Surgical Panel
Instructions for Use, 02/2020 19
Electromagnetic interference immunity
The CuratOR Surgical Panel was tested with the following compliance levels in accordance with the
test requirements for professional healthcare facilities, as established in IEC/EN 6061-1-2.
Customers and users of the device have to ensure that the device is used in such an environment.
Interference im-
munity test
Measurement
level
Compliance level Information regarding the electromag-
netic environment
Electrostatic dis-
charge (ESD)
IEC/EN
61000-4-2
±8 kV contact
±15 kV air
±8 kV contact
±15 kV air
As described in the CuratOR Surgical
Panel service manual, the device is
suited to surface mounting or flush
mounting depending on the individual
version.
In addition to mounting on the wall or in a
niche, installation includes connection to
power and the IT network inside of the
device.
Fast transient
electric distur-
bances (bursts)
IEC/EN
61000-4-4
±2 kV power lines
±1 kV input / out-
put lines
±3 kV power lines
±2 kV input / out-
put lines
The power supply quality has to corre-
spond to that of typical industrial environ-
ments or hospitals.
Surge voltage
IEC/EN
61000-4-5
±1 kV line
against line
±2 kV line against
ground
±2 kV line against
line
±4 kV line against
ground
The power supply quality has to corre-
spond to that of typical industrial environ-
ments or hospitals.
Voltage dips,
brief interrup-
tions, and fluctu-
ations of power
supply lines
IEC/EN
61000-4-11
0% VT for 0.5pe-
riods and 1 period
70% VT for 25 /
30 periods at 50 /
60Hz
0 % VT for 250 /
300 periods at
50 / 60Hz
0% VT for 0.5peri-
ods and 1 period
70% VT for 25 pe-
riods at 50Hz
0 % VT for 250 pe-
riods at 50Hz
The power supply quality has to corre-
spond to that of typical industrial environ-
ments or hospitals.
If the device has to continue operation
even if the power supply is interrupted, it
is recommended to connect the device to
an uninterruptible power supply or bat-
tery.
Magnetic fields
with energy
technology fre-
quencies
IEC/EN
61000-4-8
30 A/m
(50 / 60 Hz)
30 A/m
(50 Hz)
The magnetic fields with energy technol-
ogy frequencies must be in an area that
is representative of a typical location in a
typical industrial environment or hospi-
tals.
This product should be used at least 15
cm away from the source of magnetic
fields with energy technology frequen-
cies.
Note: VT is the alternating current voltage before application of the measurement level.

Appendix
8.1 Information on electromagnetic compatibility (EMC)
20
CuratOR Surgical Panel
Instructions for Use, 02/2020
Electromagnetic interference immunity
The CuratOR Surgical Panel was tested with the following compliance levels in accordance with the
test requirements for professional healthcare facilities, as established in IEC/EN 6061-1-2.
Customers and users of the device have to ensure that the device is used in such an environment.
Interference
immunity test
Measurement
level
Compli-
ance level
Information regarding the electromagnetic envi-
ronment
Line-based dis-
turbances
caused by RF
fields
IEC/EN
61000-4-6
3 Vrms
150 kHz to 80
MHz
6 Vrms Portable and mobile RF communications devices
may only be operated in the vicinity of the device
and its components (including cables) when in com-
pliance with the recommended minimum distance. It
is determined using the formula for calculating the
frequency of the transmitter.
Recommended minimum distance
d = 0.6 √P, 150 kHz to 80 MHz
d = 2 √P, ISM bands between 150 kHz and 80 MHz
d = 0.35 √P, 80 MHz to 800 MHz
d = 0.7 √P, 800 MHz to 2.7 GHz
In this case, “P” stands for the measured maximum
nominal output power in watts (W) of the transmitter
recommended by the transmitter manufacturer, and
“d” for the recommended minimum distance in me-
ters (m).
The field strengths of fixed transmitters according to
electromagnetic location measurementa) have to be
less than the compliance level in each individual
frequency range.
Interference can occur when used in the vicinity of
devices identified with the following symbol.
6 Vrms
ISM bands be-
tween 150kHz
and 80MHz
6 Vrms
Electromagnetic
RF fields
IEC/EN
61000-4-3
3 V/m
80 MHz to 2.7
GHz
10 V/m
Note: The higher frequency range applies at 80 MHz and 800 MHz.
Note: Guidelines with respect to line-based interference due to RF fields or electromagnetic RF
fields may not apply in all situations. Absorption and reflection by structures, objects, and people im-
pact the propagation of electromagnetic waves. .
a) The field strengths of fixed transmitters, for example the base station for cordless and mobile tele-
phones, radio, land mobile radio, ham radio, and television cannot be determined precisely in ad-
vance. To evaluate the electromagnetic environment using fixed transmitters, an electromagnetic lo-
cation measurement should be included. If the measured field strength in the environment where the
device is used exceeds the applicable RF compliance level, observe the device to ensure its proper
operation. If improper operation is observed, in some circumstances additional measures may be
necessary, such as reorienting or repositioning the device.