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.