Professional Documents
Culture Documents
Central Monitor
CNS-6201
Keep this manual near the instrument or in the reach of the operator and refer to it whenever the operation is unclear.
This product stores personal patient information. Manage and operate the information appropriately.
Patient names on the screen shots and recording examples in this manual are fictional and any resemblance to any
person living or dead is purely coincidental.
Copyright Notice
The entire contents of this manual are copyrighted by Nihon Kohden. All rights are reserved. No part of this document
may be reproduced, stored, or transmitted in any form or by any means (electronic, mechanical, photocopied, recorded,
or otherwise) without the prior written permission of Nihon Kohden.
Contents 1
2
GENERAL HANDLING PRECAUTIONS.............................................................................. i
3
WARRANTY POLICY.......................................................................................................... ii
EMC RELATED CAUTION...................................................................................................iii
4
Conventions Used in this Manual and Instrument.............................................................. vi
Warnings, Cautions and Notes................................................................................. vi 5
Text Conventions in this Manual............................................................................... vi
Related Documentation...................................................................................................... vi 6
6-1
Section 1 Installation and Connection.................................................. 1.1
Installing and Connecting each Instrument....................................................................... 1.2 6-2
Installation Flowchart.............................................................................................. 1.3
Attaching the Rubber Feet...................................................................................... 1.3 7
Installation Conditions....................................................................................................... 1.4
8
Connection Overview........................................................................................................ 1.5
Brief Overview........................................................................................................ 1.5
Detailed Overview.................................................................................................. 1.6
List of Connectors and Cables to be Connected.......................................... 1.7
Connecting Units to the PU-621R Central Monitor Processing Unit................................. 1.8
Connecting the LCD Display................................................................................... 1.8
Securing Cables........................................................................................... 1.9
Connecting Two LCD Displays (Dual Display Monitoring).................................... 1.10
Connecting the YL-611P/612P Alarm Indicator.................................................... 1.12
Connecting the WS-960P Recorder Unit.............................................................. 1.13
Connecting the Keyboard..................................................................................... 1.14
Connecting the Mouse.......................................................................................... 1.14
Securing the Cables (Central Monitor Processing Unit)....................................... 1.15
Secure the LAN and USB Cables............................................................... 1.15
Secure the Speaker and Alarm Indicator Cable......................................... 1.16
Connecting the Power Cord............................................................................................ 1.17
PU-621R Central Monitor Processing Unit........................................................... 1.17
Secure the Power Cord (Central Monitor Processing Unit)........................ 1.18
Cutting Off the Power Supply to the Central Monitor Processing Unit........ 1.19
LCD Display.......................................................................................................... 1.19
WS-960P Recorder Unit....................................................................................... 1.20
Section 6-1 Changing the System Setup Screen Settings for Administrator.... 6.1.1
System Configuration Settings...................................................................................... 6.1.2
System................................................................................................................. 6.1.2
Alarm................................................................................................................... 6.1.5
Alarm Events....................................................................................................... 6.1.7
Monitor Setting............................................................................................................... 6.1.8
Screen Composition............................................................................................ 6.1.8
Monitored Beds Setting....................................................................................... 6.1.9
Display Settings................................................................................................. 6.1.11
Bed Name Setting............................................................................................. 6.1.12
Parameter Setup.......................................................................................................... 6.1.14
Parameter Selection.......................................................................................... 6.1.14
Parameter Colors............................................................................................... 6.1.14
Alarm Master............................................................................................................... 6.1.15
Pre-registration............................................................................................................ 6.1.17
ORG Setting................................................................................................................ 6.1.18
ORG Setting...................................................................................................... 6.1.18
RSSI.................................................................................................................. 6.1.19
Alarm Level (Limits)........................................................................................... 6.1.19
Alarm Level (Arrhythmia)................................................................................... 6.1.20
Alarm Level (Technical)..................................................................................... 6.1.20
Patient Attribute Read Setting...................................................................................... 6.1.21
External Output............................................................................................................ 6.1.23
RS-232C............................................................................................................ 6.1.23
HL7.................................................................................................................... 6.1.23
Function Keys Setting.................................................................................................. 6.1.25
All Beds............................................................................................................. 6.1.25
Individual........................................................................................................... 6.1.25
Mouse Setting.............................................................................................................. 6.1.26
Remote Controller Setting........................................................................................... 6.1.28
Section 6-2 Changing the System Setup Screen Settings for Maintenance...... 6.2.1
Confirming Instruments Connected to the Network....................................................... 6.2.2
Checking the Keyboard Operation................................................................................. 6.2.3
Copying Settings to Other Beds or Registering Settings as Default Settings................ 6.2.4
Backing Up Settings...................................................................................................... 6.2.8
Exchanging Central Monitors.............................................................................. 6.2.8
Backing Up to a USB Thumb Drive...................................................................... 6.2.9
Restoring Settings on a Central Monitor............................................................ 6.2.11
Installing the Expansion Program Software................................................................. 6.2.13
Acquiring the Unlock Code................................................................................ 6.2.13
Installing the Expansion Program...................................................................... 6.2.13
Enabling/Disabling Screen Hard Copy Printing........................................................... 6.2.16
Printing a Screen Image (Screen Hard Copy)................................................... 6.2.17
Removing the USB Thumb Drive................................................................................. 6.2.18
Please read these precautions thoroughly before attempting to operate the instrument.
1. To safely and effectively use the instrument, its operation must be fully understood.
3. Before Operation
(1) Check that the instrument is in perfect operating order.
(2) Check that the instrument is grounded properly.
(3) Check that all cords are connected properly.
(4) Pay extra attention when the instrument is combined with other instruments to avoid misdiagnosis or other
problems.
(5) All circuitry used for direct patient connection must be doubly checked.
(6) Check that battery level is acceptable and battery condition is good when using battery-operated models.
4. During Operation
(1) Both the instrument and the patient must receive continual, careful attention.
(2) Turn power off or remove electrodes and/or transducers when necessary to assure the patient’s safety.
(3) Avoid direct contact between the instrument housing and the patient.
6. The instrument must receive expert, professional attention for maintenance and repairs. When the instrument is
not functioning properly, it should be clearly marked to avoid operation while it is out of order.
9. When the instrument is used with an electrosurgical instrument, pay careful attention to the application and/or
location of electrodes and/or transducers to avoid possible burn to the patient.
10. When the instrument is used with a defibrillator, make sure that the instrument is protected against defibrillator
discharge. If not, remove patient cables and/or transducers from the instrument to avoid possible damage.
WARRANTY POLICY
Nihon Kohden Corporation (NKC) shall warrant its products against all defects in materials and workmanship for one year
from the date of delivery. However, consumable materials such as recording paper, ink, stylus and battery are excluded
from the warranty.
NKC or its authorized agents will repair or replace any products which prove to be defective during the warranty period,
provided these products are used as prescribed by the operating instructions given in the operator’s and service manuals.
No other party is authorized to make any warranty or assume liability for NKC’s products. NKC will not recognize any
other warranty, either implied or in writing. In addition, service, technical modification or any other product change
performed by someone other than NKC or its authorized agents without prior consent of NKC may be cause for voiding
this warranty.
Defective products or parts must be returned to NKC or its authorized agents, along with an explanation of the failure.
Shipping costs must be pre-paid.
This warranty does not apply to products that have been modified, disassembled, reinstalled or repaired without Nihon
Kohden approval or which have been subjected to neglect or accident, damage due to accident, fire, lightning, vandalism,
water or other casualty, improper installation or application, or on which the original identification marks have been
removed.
CAUTION
United States law restricts this product to sale by or on the order of a physician.
The following describes some common interference sources and remedial actions:
1. Strong electromagnetic interference from a nearby emitter source such as an authorized radio station
or cellular phone:
Install the equipment and/or system at another location. Keep the emitter source such as cellular phone
away from the equipment and/or system, or turn off the cellular phone.
2. Radio-frequency interference from other equipment through the AC power supply of the equipment
and/or system:
Identify the cause of this interference and if possible remove this interference source. If this is not
possible, use a different power supply.
4. Electromagnetic interference with any radio wave receiver such as radio or television:
If the equipment and/or system interferes with any radio wave receiver, locate the equipment and/or
system as far as possible from the radio wave receiver.
5. Interference of lightning:
When lightning occurs near the location where the equipment and/or system is installed, it may induce
an excessive voltage in the equipment and/or system. In such a case, disconnect the AC power cord
from the equipment and/or system and operate the equipment and/or system by battery power, or use
an uninterruptible power supply.
If the above suggested remedial actions do not solve the problem, consult your Nihon Kohden
representative for additional suggestions.
In IEC 60601-1-2 Medical Electronic Equipment, Part 1: General Requirements for Safety, 2. Collateral
Standard: Electromagnetic compatibility-Requirements and test. Section 36. 202. 2 Radiated radio-
frequency electromagnetic fields, PATIENT COUPLED EQUIPMENT and/or SYSTEMS applicable
IMMUNITY test methods are under consideration at SC62A/WG13. The 3 V/m IMMUNITY level may be
inappropriate especially when measuring SpO2 because physiological signals can be much smaller than
those induced by a 3 V/m electromagnetic field.
When measuring SpO2, various interference may produce false waveforms which look like pulse
waveforms. SpO2 value and pulse rate may be measured from these false waveforms, causing the alarm to
function improperly.
When installing the monitor, avoid locations where the monitor may receive strong electromagnetic
interference such as radio or TV stations, cellular phone or mobile two-way radios.
The CE mark is a protected conformity mark of the European Community. Products with the CE mark
comply with the requirements of the Medical Device Directive 93/42/EEC.
This equipment complies with EUROPEAN STANDARD EN-60601-1-2: 1993 which requires EN-55011,
class A. Class A EQUIPMENT is allowed in domestic establishments when used under the jurisdiction of
a health care professional.
NOTE about Waste Electrical and Electronic Equipment (WEEE) Directive 2002/96/EEC
For the member states of the European Union only:
The purpose of WEEE directive 2002/96/EEC is, as a first priority, the prevention of waste electrical and
electronic equipment (WEEE), and in addition, the reuse, recycling and other forms of recovery of such
wastes so as to reduce the disposal of waste.
Contact your Nihon Kohden representative for disposal.
• Austria
• Belgium
• Cyprus
• Czech Republic
• Denmark
• Estonia
• Finland
• France
• Germany
• Greece
• Hungary
• Iceland
• Ireland
• Italy
• Latvia
• Liechtenstein
• Lithuania
• Luxembourg
• Malta
• The Netherlands
• Norway
• Poland
• Portugal
• Slovakia
• Slovenia
• Spain
• Sweden
• Switzerland
• The U.K.
Notice:
• Refer to “Restriction of Radio Equipment (European Union countries only)” in the “Specifications”
section for more details.
• This device is also authorized for use in Norway in accordance with regulation No.1399 of 20
December 2000.
As this equipment complies with Class 1.7 (Receive-only radio equipment), “Alert Sign” is not displayed.
This equipment complies with International Standard IEC 60601-1-2: 2001 and Amendment 1: 2004 which
require CISPR11, Group 1, Class B. Class B EQUIPMENT is equipment suitable for use in domestic
establishments and in establishments directly connected to a low voltage power supply network which
supplies buildings used for domestic purposes.
WARNING
A warning alerts the user to possible injury or death associated with the use or misuse of the instrument.
CAUTION
A caution alerts the user to possible injury or problems with the instrument associated with its use or
misuse such as instrument malfunction, instrument failure, damage to the instrument, or damage to other
property.
NOTE
A note provides specific information, in the form of recommendations, prerequirements, alternative methods or
supplemental information.
Related Documentation
The CNS-6201 Central Monitor comes with the following manuals in addition to the Operator’s Manual.
Administrator’s Guide
Describes how to install the central monitor. It also explains about the password protected settings which only an
administrator can change.
Service Manual
Describes information on servicing the central monitor. Only qualified service personnel can service the central monitor.
This section explains how to connect the power cord and connection cable and
precautions on installation. Install and connect this central monitor according to
this Administrator’s Guide. If the central monitor is set incorrectly, it may cause
serious problems such as mixing information of different patients.
WARNING
Install the central monitor outside the patient
environment (IEC 60601-1-1). If the central
monitor is installed inside the patient
environment, the patient or operator may receive
electrical shock or injury. For installation, contact
your Nihon Kohden representative.
CAUTION CAUTION
Connect only the specified instrument to the When installing, connecting and assembling the
central monitor and follow the specified central monitor, only use specified instruments
procedure. Failure to follow this instruction may and parts and follow the specified procedure.
result in electrical shock or injury to the operator, Otherwise, the operator may receive electrical
and cause fire or instrument malfunction. shock or injury.
CAUTION CAUTION
Before connecting or disconnecting instruments, Keep the cable out of the way by running it along
make sure that each instrument is turned off and the floor or wall. Otherwise people may trip over
the power cord is disconnected from the AC it, causing the instrument to fall and injure the
socket. Otherwise, the patient or operator may patient and operator.
receive electrical shock or injury.
The specified LCD display may be changed without notice. Contact your Nihon
Kohden representative before purchasing a display.
Installation Flowchart 1
1. Connect the YL-611P/612P alarm indicator, LCD display, WS-960P recorder
unit, keyboard and mouse to the PU-621R central monitor processing
unit. Prepare the RY-910PA remote controller. Refer to the this section. If
necessary, connect the LS2208 bar code reader. For connecting bar code
reader, refer to Section 3.
2. Secure the cables. Refer to the “Securing the Cables (Central Monitor
Processing Unit)”.
3. Connect the power cord and ground the PU-621R central monitor processing
unit. Refer to the “Connecting the Power Cord”.
Rubber foot
Screw
Screw
Installation Conditions
The system must be installed by qualified service personnel. When installing the
system, consult qualified service personnel. Observe the following important
points.
Install the monitor where the screen can be seen clearly and does not reflect light.
WARNING
Install the central monitor outside the patient
environment (IEC 60601-1-1). If the central
monitor is installed inside the patient
environment, the patient or operator may receive
electrical shock or injury. For installation, contact
your Nihon Kohden representative.
CAUTION CAUTION
Do not install the monitor where it will be exposed Avoid exposing the monitor to direct sunlight.
to water or chemical solutions. Avoid direct Otherwise, the temperature rises and it causes
sprinkling, spray or moist air from the nebulizer or malfunction and shortens the life of the monitor.
humidifier. These cause malfunction and shorten
the life of the monitor.
CAUTION CAUTION
Make sure that there is enough space between Do not place cables in the way or where people
the monitor and the wall for adequate ventilation. walk.
Otherwise the internal temperature of the monitor
rises, which leads to inaccurate operation and
CAUTION
shortens the monitor life.
Do not install the monitor in a dusty area.
• Leave more than 5 cm of space between the
wall and vent holes on the sides and rear
panels of the monitor. CAUTION
• When the monitor is surrounded, leave more Connect the power cord to an AC outlet which
than 10 cm of space above the monitor can supply sufficient AC current to the monitor.
for ventilation. Do not let the surrounding The monitor cannot function properly with low
temperature exceed 35°C (95°F) during current. Also the breaker trips and it causes
operation. electric power failure.
CAUTION CAUTION
When there is any problem with the monitor, turn Do not place blankets or cloth over the monitor. It
off the power immediately and disconnect the may affect monitoring.
power cord from the AC outlet. Take the monitor
out of service and check for damage.
1
Connection Overview
Brief Overview
YL-611P/612P alarm indicator
Main display
SC-611R WS-960P
power supply To wall AC outlet
LCD display
To wall AC outlet
To wall AC outlet
To network
Second display
Others
Mouse Keyboard
LCD display
Bar code reader
To wall AC outlet
Detailed Overview
YL-611P/612P YS-098P1/098P2
alam indicator additional alam indicator unit
AC adapter AC adapter
DVI cable 2.5 m/5 m
Speaker cable 2.5 m/5 m
USB cable 2.5 m/5 m
Wall AC outlet
Wall AC outlet
Wall AC outlet
PU-621R
central monitor
processing unit
front
Wall AC outlet
set (main)
Processing unit
Power connector AC adapter of the LCD display –––
COM 1 connector
Alarm indicator Alarm indicator cable
PS/2 mouse connector
RECORDER
RECORDER
unit
connector
Hospital network
LAN cable (CAT 5) LAN 2 connector
connector
2. Connect the DVI cable, speaker cable, power cord and USB cable in that
order.
3. Run the cables through the loop on the display in the above order.
4. Insert the lower tabs of the cable cover into the groove of the display and
attach the cover with a screw. Refer to “Securing Cables” on the next page.
WARNING
Make sure that the speaker cable is connected to the display and
processing unit. Otherwise the alarm sound cannot be heard.
NOTE
• Do not put any objects in front of the speaker. This may make it hard
to hear the alarm sound.
• Secure the cables so they do not become disconnected.
LCD display
PU-621R central monitor processing unit
2
3
1
4
AC adapter
Processing unit
DVI cable
DVI connector DVI connector
2
LCD display
Speaker cable
SOUND connector LINE-OUT connector
3
AC adapter
Power socket AC outlet
4
Securing Cables
Secure the cables to the LCD display by the following procedure.
1. Arrange the cable as shown in the illustration and connect the cables to the
LCD display.
Cable hook
NOTE
Hook the cables to the cable hook when securing cables. Otherwise,
tension on the cable may cause the cable to get disconnected.
3. Insert the lower tabs of the cable cover into the groove of the display and
attach the cover with a screw.
NOTE
Be sure to attach the cable cover. Otherwise, tension on the cable
may cause the cable to get disconnected.
Screw
Cover
Tab
WARNING WARNING
When monitoring with two displays, do not turn Do not turn off the display to which the speaker
off either display. Some monitored beds cannot cable is connected. The alarm sound cannot be
be monitored. heard.
NOTE
• Do not put any objects in front of the speaker. This may make it hard to
hear the alarm sound.
• Secure the cables so they do not become disconnected.
2
3
1
4 7
5 6
AC adapter
Wall AC outlet
USB cable
USB connector USB 0 connector
1
Processing unit
DVI cable
DVI connector DVI connector
Main display
LCD display
Speaker cable
SOUND connector LINE OUT connector
3
AC adapter
Power socket AC outlet
4
USB cable
Processing unit
RGB cable
RGB connector Analog VGA connector
6
AC adapter
Power socket AC outlet
7
NOTE
• YL-611P/612P alarm indicator is only for the PU-621R central
monitor processing unit. Do not connect this alarm indicator to other
instruments.
M2 × 6 tamper-proof screw • Make sure to fasten the alarm indicator connectors to the processing
unit with the M2 × 6 screws.
Processing unit
COM 1 connector
Alarm indicator cable
Alarm indicator
1
PS/2 mouse connector
After attaching the alarm indicator to the display, peel off the backing paper on
the back of the holder (provided with the alarm indicator) and attach the holder
to the rear of the display. Then attach the processing box of the alarm indicator to
the holder.
NOTE
Secure the cables so they do not become disconnected.
NOTE
Secure the cable so it does not become disconnected.
PU-621R central monitor processing unit
Keyboard
Processing unit
Keyboard cable
Keyboard PS/2 keyboard connector
1
NOTE
Secure the cable so it does not become disconnected.
PU-621R central monitor processing unit
Mouse
Mouse cable
Mouse USB 2 connector
1
NOTE
Secure the cables so they do not become disconnected.
Cable clamp
2. Put the USB cables into another slit of the cable clamp.
3. Press the cable clamp carefully to the processing unit so that it does not
interfere with the ferrite core of the mouse cable.
Ferrite core
Screw
4. Fasten the cable clamp to the processing unit with two PS3 × 6 screws.
1. Gather the speaker cable and two alarm indicator cables with a cable tie. Cut
off any extra tie length after securing it.
Speaker cable
Cable tie
Alarm indicator cables
2. Attach the cable tie to the processing unit with a PH3 × 8 screw.
PH3 × 8 screw
1
Connecting the Power Cord
CAUTION
Only use the provided power cord. Using other power cords may
result in electrical shock or injury to the operator.
CAUTION
Connect the power cord to an AC outlet which can supply sufficient
AC current to the monitor. The monitor cannot function properly with
low current. Also the breaker trips and it causes electric power
failure.
NOTE
Secure the cables so they do not become disconnected.
Wall AC outlet
Power cord
(Wall) AC outlet AC connector
1
NOTE
Surely secure the power cord.
1. Attach the cable fixing bar to the clamp of the central monitor processing
unit so that the serrated part is downward.
Clamp
Serrated part
2. Wind the cable clamp (standard accessory of the central monitor) around the
power cord in the direction of the illustration.
Cable clamp
3. Put the cable fixing bar through the hole of the cable clamp.
4. Slide the cable clamp and connect the power cord to the AC socket of the 1
central monitor processing unit.
Tighten the tabs again after
connecting the power cord.
Cutting Off the Power Supply to the Central Monitor Processing Unit
To cut off the power supply to the central monitor processing unit, disconnect
the power cord of the central monitor processing unit from the wall AC outlet.
When installing the central monitor processing unit, position the central monitor
processing unit so that it is easy to disconnect the power cord from the wall AC
outlet.
LCD Display
1. Connect the AC adapter provided with the LCD display to the power
connector of the LCD display.
2. Plug the 3-pin plug connector of the power cord provided with the LCD
display into the power connector of the AC adapter and connect the opposite
plug to a wall AC outlet. When you connect the 3-pin plug power cord to a
3-pin outlet with a grounding lead, the instrument is automatically grounded.
2. Plug the 3-pin plug connector of the power cord provided with the WS-960P
power supply into the power connector of the AC adapter and connect the
opposite plug to a wall AC outlet. When you connect the 3-pin plug power
cord to a 3-pin outlet with a grounding lead, the instrument is automatically
grounded. When the power is supplied, the power lamp of the AC adapter
lights.
PU-621R central monitor processing unit
WS-960P recorder unit
Wall AC outlet
Power lamp
Power cord
AC adapter of the SC-611R
WS-960P power supply
This section explains how to connect the central monitor to the network and
necessary settings after connection.
Overview
Connection Procedure
Connect the central monitor to the network according to the following procedure.
9. Assign the bed name, CNS name and group name to each instrument.
In the monitor network, the IP address is used as the name of each device in the
network communication. When a device sends a communication telegram to
another device, the device attaches the IP address of the receiving device to the
signal as an address. Receiving device recognizes the IP address and receives the
communication.
CAUTION
The network must be managed by the network administrator. Make
sure that each monitor in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a monitor to an already operating network, set the IP address
on the monitor before connecting the monitor to the network.
NOTE
Manually set the IP address if you have a network printer or remote
viewer in your computer.
The IP address of the PU-621R central monitor processing unit is set in Network
window of the System Setup screen. Refer to “Network Setting” in Section 6-1.
NOTE
• Contact your Nihon Kohden representative when changing the IP
address manually.
• To avoid communication trouble, do not connect the network cable to
each instrument before IP address setting is complete.
WARNING WARNING
Connect the central monitor to network as Do not use a damaged network cable. The patient
specified. Otherwise the patient and operator may or operator may receive electrical shock when the
receive electrical shock or injury. To connect the damaged part is touched.
network, contact your Nihon Kohden
representative.
CAUTION
The system should be used in a closed network
to prevent computer viruses and unexpected
software updates.
NOTE
• The time on this central monitor is automatically adjusted to match the
time of the network as long as the central monitor is connected to the
network.
• Secure the cables so they do not become disconnected. Refer to
“Securing Cables (Central Monitor Processing Unit)” in Section 1.
Connect the monitor to the network with the specified network cable.
PU-621R central monitor processing unit
1
To monitor network
2
To hospital network
Processing unit
LAN cable (CAT 5)
Monitor network connector LAN 0 connector
1
NOTE
Confirm that the “LINK” LED is lit on the hub and network connectors
for each instrument. If it is not lit when each instrument is turned on,
electrical connection is not complete. Confirm the wiring.
NOTE
• Changing the date and time settings affects the entire network.
• Date and time cannot be set on the multiple patient receiver.
When the date and time setting is changed on one of the instruments in a
network, the date and time settings of all instruments in the network change to
the same setting.
Set the date and time on the central monitor or bedside monitors on the network.
NOTE
Following bedside monitors do not have the function to set the date and
time of all the devices on the system. Set the date and time individually
on these monitors if necessary.
OEC-6401/6501/6102/6105/6120/8108/8120
Basically, a central monitor monitors and stores data of all beds in the same
group but it can also monitor and store data of beds in a different group. It is
recommended to only monitor and store data of beds in the same group as the
central monitor so that data will not be mixed or lost.
ICU group
Monitor network
CCU group
* The CNS-CCU1 central monitor can monitor and store data of beds in the ICU
group. However, it is recommended to monitor and store data of the CCU beds
in the CCU group so that data will not be lost.
CAUTION
The data of a bedside monitor cannot be stored on more than one 2
central monitor. If the data of the same bedside monitor is stored on
two central monitors, data communication cannot be properly
performed or the data may be lost. Make sure that the bedside
monitor data is saved only on one central monitor.
Before starting monitoring, confirm the settings on each window of the System
Setup screen and individual settings (Personal Setup, Parameter Setup and
Other Setup) and change them if necessary. Refer to Section 6-1 in this manual
and Operator’s Manual. If you change the units and date and time when the
network is in operation, the change on any instrument affects all instruments in
the network. Refer to “Setting the Date and Time of the Entire Network” in this
section.
To identify the monitors, each monitor has an instrument name (bed name/CNS
name) and a group name.
1. Each bed and central monitor on the network is identified by the bed name or
CNS name.
Bed name CNS name
CNS-ICU1
BSM-001 BSM-002 BSM-003
CNS
BSM BSM BSM
Monitor network
2. Several monitors form a group. Every bed and every central monitor belongs
to a group. When the group is large, set a group name to easily identify the
beds. Each bed and central monitor is identified by the combination of bed or
CNS name and group name.
OR group
Recovery group
Bed name of the Recovery group* CNS-Rec1
Rec-001 Rec-002 Rec-003 Rec-08
CNS
BSM BSM BSM BSM
3. The central monitor monitors and stores data of the beds in its group. The
central monitor can also monitor and store data of beds in other groups but
for identifying beds easily, only monitor and store data of the beds in the
same group as the central monitor.
ICU group
Monitor network
CCU group
* In this example, the CNS-CCU1 central monitor can monitor and store data of the beds in the
CCU and ICU groups but it is recommended to only monitor and store data of the beds in the CCU
group so that data will not be lost.
Central monitor:
Exit the central monitor program and assign a computer name in Windows as a
CNS name.
Bedside monitors:
Assign the bed name to bedside monitors on the SYSTEM SETUP screen/
window on each bedside monitor. Refer to the bedside monitor Operator’s
Manual. After the registration, you can change the name on the central monitor.
Refer to “Monitor Setting” in Section 6-1.
NOTE
Contact your Nihon Kohden representative for a maintenance
password.
5. Double-click System.
7. Click Change....
8. In the Computer name box, enter the CNS name (computer name) and then
click OK.
9. The “Restart your computer for the settings take effect” message appears.
Click OK.
11. The “You must restart your computer before the new settings will take effect.
Do you want to restart your computer now?” message appears. Click Yes.
Central monitor:
Set the group name on the [Network] → [Central] → [Group] window on the
central monitor. Refer to Section 6-1.
Bedside monitors:
Assign the group name to the bedside monitors on the SYSTEM SETUP screen/
window on each bedside monitor. Refer to the bedside monitor Operator’s
Manual.
If the group name does not appear on the monitoring/home screen on the bedside
monitors:
1. Turn the bedside monitor power off.
2. Wait for 30 seconds and display the monitoring/home screen. The group
name appears on the screen.
After you finish installation and connection of the central monitor and other
instruments, turn on the power of all instruments. When the system starts, check
the following items. If there is any problem, confirm that all installation and
connection are done correctly.
Surrounding Environment:
• No obstacle around the central monitor.
Connection:
• Power cord is connected properly.
• Equipotential grounding lead is connected properly when equipotential
grounding is required.
• The central monitor is connected to network properly.
Appearance:
• No damage to the keys, switch, lamps and panels.
• No scratches, damage or dirt on sensors and electrodes.
• The central monitor is not in a wet place.
LCD Display:
• After turning the power on, the central monitor system automatically starts and
the All Beds screen is displayed.
• The touch keys function properly. (When you use the central monitor for the
first time, you need to calibrate the touch keys before use.)
• No error message is displayed on the central monitor screen.
Keyboard:
• Input from the keyboard is recognized properly.
Mouse:
• The mouse and switches operate properly.
Do not use anything sharp to touch the LCD screen (touch screen), power
switches and other keys. It may damage the instrument.
• The connection must comply with IEC 60601-1-1 “General Requirements for
Safety of Medical Electrical Equipment”. Refer to the “General Requirements
for Connecting Medical Electrical Systems” in Section 8.
• For network connection, refer to the Network and System Installation Guide
which is available from your Nihon Kohden representative. The connection
must be done by qualified personnel in your hospital.
CAUTION
The network must be managed by the network administrator. Make
sure that each monitor in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a monitor to an already operating network, set the IP address
on the monitor before connecting the monitor to the network.
• The power of the central monitor to be added is turned off before connecting it
to the network. When the central monitor is properly connected to the network,
turn the central monitor power on.
• Assign the instrument name (bed name/CNS name) and group name to the
instrument. Refer to “Assigning the Bed Name, CNS Name and Group Name”
in this section.
CAUTION
When the instrument is connected to a central monitor network, set
the instrument name (Bed Name/CNS Name) and Group Name on
the instrument. Otherwise, the default settings are used for the bed
name, CNS name and group name and the bed may be incorrectly
identified on the central monitor.
• Check that the date and time and unit setting is the same as the other
instruments in the network.
Overview............................................................................................................................................................... 3.2
Connection Procedure................................................................................................................................ 3.2
Turning the Central Monitor Power Off................................................................................................................. 3.2
Connecting the Bar Code Reader to the PU-621R Central Monitor Processing Unit........................................... 3.3
Turning the Central Monitor Power On................................................................................................................. 3.3
Setting the Bar Code Reader............................................................................................................................... 3.4
Initializing the Bar Code Reader................................................................................................................. 3.6
Setting the Bar Code Reader Settings................................................................................................................. 3.7
Checking the Bar Code Reader Operation........................................................................................................... 3.7
This section explains how to install the LS2208 bar code reader and settings to
use the bar code reader.
You can use the bar code reader Symbol LS2208 from Motorola, Inc. For details
on using the bar code reader, refer to the manual provided with the bar code
reader. You can download the manual from http://support.symbol.com on the
Motorola website.
Overview
Connection Procedure
Connect the bar code reader according to the following procedure.
2. Connect the bar code reader to the USB 5 connector of the PU-621R central
monitor processing unit.
NOTE
Secure the cables so they do not become disconnected.
Attach the ferrite core to the bar code reader at 2 cm from the USB connector.
Connect the USB connector of the bar code reader to the USB 5 connector on the
front panel of the PU-621R central monitor processing unit.
PU-621R central monitor processing unit
LS2208 bar code reader
Ferrite core
1
Processing unit
Bar code reader cable
Bar code reader USB 5 connector
1
Following are the minimum settings of the bar code reader. Scan the following
bar codes in order. When scanning the bar code, there is one short high beep. For
further settings, refer to the Symbol LS2208 manual.
* This setting is a default value. You can skip scanning this bar code if you have
already used this bar code reader with the default value.
Beeper Volume
Low Volume
Prefix Values
Scan Prefix
3
3
Suffix Values
Scan Suffix
Enter
Enable/Disable Codabar
Enable Codabar
Set the patient attribute input device and data read settings. Refer to “Patient 3
Attribute Read Setting” in Section 6-1.
1. Set [Patient Attribute Input Device] to [Bar Code Reader] in Patient Attribute
Read Setting of the System Setup screen.
2. Read the patient bar code and display the information of the bar code. If the
data is not displayed, do the procedure of “Setting the Bar Code Reader”
section again.
3. For the following items, select whether or not to read the data and set the
data field.
• Patient ID
• Name
• Date of birth
• Gender
Scan the bar code of the patient on the Admit/Discharge window. Refer to
“Admitting a Patient” in Section 4 of the Operator’s Manual. Check that the
patient information is correctly scanned and displayed on the central monitor.
This section explains how to connect the printer to the network and how to install
the driver.
Overview
Connect the printer power cord to the wall AC outlet and turn the printer power
on. Refer to the printer manual.
In the monitor network, the IP address is used as the name of each device in
network communication. When a device sends communication to another device,
the device attaches the IP address of the receiving device to the communication
as the address. The receiving device recognizes the IP address and receives the
communication.
NOTE
Manually set the IP address of the printer.
CAUTION
The network must be managed by the network administrator. Make
sure that each instrument in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a printer to an already operating network, set the IP address
on the printer before connecting the printer to the network.
Explanation
A unique IP address is assigned to each Nihon Kohden monitor at shipment.
Therefore, there should be no duplicate IP addresses so usually the IP address
does not need to be changed.
When connecting the printer or other devices to the central monitor network, set
an IP address different than the above IP address.
2. Set the IP address of the printer. Refer to “Setting the IP Address of the
Printer”.
3. Connect the keyboard and mouse to the PU-621R central monitor processing
unit. Refer to “Connecting the Mouse” and “Connecting the Keyboard” in
Section 1.
4. Connect the PU-621R central monitor processing unit and printer to the
network.
NOTE
4
• When more than one central monitor uses the printer:
- Set the following settings on each central monitor.
- Set the printer share name setting to “Not Shared”.
• Connect the printer to each central monitor as a local printer, not as a
network printer.
NOTE
Contact your Nihon Kohden representative for a maintenance
password.
iv) Check that the “Press any key to continue...” message appears on the
Command Prompt window and press the Enter key on the keyboard.
5. To open Printers and Faxes, click Start and then click Control Panel.
8. Click Next>.
10. Click Create a new port. In the Type of port box, select Standard TCP/IP
Port and click Next>.
12. In the Printer Name or IP Address box, enter the printer IP address. Click
Next>.
13. Check that the adapter type is displayed on the Add Standard TCP/IP Printer
Port Wizard page. Click Finish.
Adapter Type
When the printer is recognized on the
network, Adapter Type is displayed.
If it is not displayed, the printer is not
recognized. Click Cancel, check the
IP address and subnet mask and do the
procedure from the beginning.
14. In the Manufacturer list, select HP. In the Printers list, select HP LaserJet
4100 Series PCL. (HP LaserJet 4100n, HP LaserJet 4250n, HP LaserJet
P4015n, HP LaserJet P4515n and HP LaserJet Enterprise 600 M602 use the
same driver.) Click Next>.
15. Click Replace existing driver and click Next>. This page might not be
displayed.
18. Check that the printer name and port name displayed on the page are correct.
Click Finish.
19. Files are copied and a test page is printed. After the test page is printed, click
Finish. If the test page fails to print, repeat steps 7 to 18.
20. To open Printers and Faxes, click Start, click Control Panel, and then
double-click Printers and Faxes. Check that HP LaserJet 4100 Series PCL
is added with a check mark. If no check mark is displayed, click the right
mouse button and set it as the default printer.
iv) Check that the “Press any key to continue...” message appears on the
Command Prompt window and press the Enter key on the keyboard.
23. After setup is complete, restart your computer. The CNS system program
starts.
• For network connection, refer to the Network and System Installation Guide
which is available from your Nihon Kohden representative. The connection
must be done by qualified personnel in your hospital.
CAUTION
The network must be managed by the network administrator. Make
sure that each instrument in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a printer to an already operating network, set the IP address
on the printer before connecting the printer to the network.
• The power of the printer to be added is turned off before connecting it to the
network. When the instrument is properly connected to the network, turn the
instrument power on.
This section explains how to connect the bedside monitor and settings.
Overview
Connection Procedure
1. Set the IP address of the bedside monitor.
9. Assign the bed name and group name of the bedside monitor.
CAUTION
The network must be managed by the network administrator. Make
sure that each monitor in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a monitor to an already operating network, set the IP address
on the monitor before connecting the monitor to the network.
NOTE
Manually set the IP address if you have a printer or remote viewer in your
computer.
You can check the network connection of the bedside monitor when the
central monitor is connected to the network. Refer to “Confirming Instruments
Connected to the Network” in Section 6-2.
You can set the date and time on the entire network when the central monitor is
connected to the network. Refer to “Date and Time” in Section 6-1.
You can set the bedside monitor as a monitored bed on the Monitor Setting
window of the System Setup screen when the central monitor is connected to the
network. Refer to “Monitor Setting” in Section 6-1.
You can change settings of System Setup screen and individual settings (Personal
Setup, Parameter Setup and Other Setup) on the central monitor when the central
monitor is connected to the network. Refer to Section 6-1 of this manual and
respective sections in the Operator’s Manual.
If you change the units and date and time when the network is in operation,
the change on any instrument affects all instruments in the network. Refer to
“Setting the Date and Time of the Entire Network” in Section 2.
You can assign a bed name and group name of the bedside monitor when the
bedside monitor is connected to the network. Refer to “Assigning the Bed Name,
CNS Name and Group Name” in Section 2. 5
• The connection must comply with IEC 60601-1-1 “General Requirements for
Safety of Medical Electrical Equipment”. Refer to the “General Requirements
for Connecting Medical Electrical Systems” in Section 8.
• For network connection, refer to the Network and System Installation Guide
which is available from your Nihon Kohden representative. The connection
must be done by qualified personnel in your hospital.
CAUTION
The network must be managed by the network administrator. Make
sure that each monitor in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a monitor to an already operating network, set the IP address
on the monitor before connecting the monitor to the network.
• The power of the bedside monitor to be added is turned off before connecting
it to the network. When the bedside monitor is properly connected to the
network, turn the bedside monitor power on.
• Assign the bed name and group name to the bedside monitor. Refer to
“Assigning the Bed Name, CNS Name and Group Name” in Section 2.
CAUTION
When the instrument is connected to a central monitor network, set
the instrument name (Bed Name/CNS Name) and Group Name on
the instrument. Otherwise, the default settings are used for the bed
name, CNS name and group name and the bed may be incorrectly
identified on the central monitor.
• Check that the date and time and unit setting is the same as the other
instruments in the network.
This section explains password protected settings in the System Setup screen.
On the System Setup screen, you can set how to operate the system.
NOTE
The shaded settings need an administrator password to access. These
settings must be set by authorized personnel in your hospital.
For Sound Control, Recording and Report settings, refer to the Operator’s Manual.
POWER OFF
Central monitor information
Refer to the Operator’s Manual.
When [System Setup] is assigned to the all beds function key, the Information
window of the System Setup screen can also be displayed with the function key.
Administrator Password
The administrator password allows access to the following windows of the
System Setup screen.
• System Configuration • Monitor Setting
• Parameter Setup • Alarm Master
• Pre-registration • ORG Setting
• External Output • Patient Attribute Read Setting
• Mouse Setting • Function Keys
• Group Name • Remote Controller
• Date & Time • Network
• Maintenance (window for changing the administrator password and displaying
monitored beds information only)
You can set a password which consists of four numbers. The factory default
setting is “1234”, but we recommend changing.
Maintenance Password
The maintenance password allows access to all settings on the System Setup
screen. Contact your Nihon Kohden representative for the password. You cannot
change the maintenance password.
When [System Setup] is assigned to the all beds function key, the Information
window of the System Setup screen can also be displayed with the function key.
2. Enter the password and touch the desired tab. To display the Maintenance
window, enter the maintenance password.
3. Display the setting window and set each item. A confirmation window may
be displayed depending on the setting.
2. Enter the item or numeric value with the keyboard or numeric key pad.
3. Touch [OK] to close the keyboard or numeric key pad. To cancel the setting,
touch the [Cancel] or close button [ ].
Example: Changing the alarm master name on the [Alarm Master] of the System
Setup screen.
On the System Configuration window, you can set system configuration settings
of the central monitor.
There are three tabs of system configuration settings. The windows can be
changed by touching the tab.
• System
• Alarm
• Alarm Events
System
Touch the [System] tab on the System Configuration window.
Setting Range
Setting Item Description
( : Default)
System Language English (fixed) Settings for units and date display format. The ST Unit,
Temperature Unit Celsius, Fahrenheit CO2 Unit, Respiration Unit, tcPO2/PCO2 Unit and Date
Height Unit cm, inch Display Format settings only affect this central monitor.
Weight Unit kg, lb
Pressure Unit mmHg/cmH2O, NOTE
kPa/hPa Changing units (except ST Unit and Date Display
ST Unit mV, mm Format) affects the entire network. A changed units
Extended Units ON, OFF value takes effect the moment [Yes] is touched on
Blood Pressure mmHg, kPa the confirmation window.
Unit*
CO2 Unit* mmHg, kPa
Respiration Unit* cmH2O, hPa
tcPO2/PCO2 Unit* mmHg, kPa
Date Display YYYY/MM/DD,
Format MM/DD/YYYY,
DD/MM/YYYY,
YYYY-MM-DD
Admit Discharge Mode Discharge, Delete Selects the discharge mode on the Admit/Discharge
Data window.
• Discharge: When [Discharge] is touched, the
[Admit] key appears at the wave
area of the bed, and monitoring
ends. You can readmit a patient who
was discharged within the past 120
hours.
• Delete Data: When [Delete Data] is touched, all
data for the patient is deleted and
monitoring continues. The patient
cannot be readmitted.
Setting Range
Setting Item Description
( : Default)
Admit Auto Resume After OFF, 10 s, 30 s, 1 Selects when to resume monitoring of a temporarily
Pause min, 2 min, 3 min discharged patient at the central monitor after monitoring
resumes at the bedside monitor.*1 When [OFF] is set,
monitoring at the central monitor does not resume until
“Resume” is touched on the Admit/Discharge window.
WARNING
When the bed is set to automatically resume monitoring after pause,
check that monitoring is resumed at the central monitor when the
pause condition is ended. Monitoring might not resume if there is 6
network failure.
6-1
Pause Timer ON, OFF Selects whether or not to use the pause timer function.
Pause Timer Over ON, OFF Selects whether or not to give a sound when the pause
Time Notification timer function is used and the expected return time
Sound elapses. When [ON] is set, a 4-note melody (D-A-B-E)
plays for five seconds every two minutes.
Change Device ON, OFF Sets whether or not to allow moving the patient to a
different bedside monitor or multiple patient receiver.
Screen Screen Timeout OFF, 1 to 30 min When any screen other than the All Beds screen is
(Default: 5 min) displayed and there is no operation for a preset period, the
screen automatically returns to the All Beds screen. Enter
the value by touching the numeric keypad.
NOTE
After entering the period with the number keys on
the screen, touch “ENTER” to register the setting.
Display ECG ON, OFF This setting selects whether or not the “ECG
Measurement Key Measurement” key is displayed on the ECG window
of the Parameter Setup. When set to OFF, the “ECG
Measurement” key is not displayed on the ECG window.
Match QRS Sens to ON, OFF Selects whether or not to synchronize the ECG sensitivity
ORG and QRS detection sensitivity.
• ON: The ECG sensitivity and QRS detection
sensitivity are synchronized.
• OFF: The ECG sensitivity and QRS detection
sensitivity are not synchronized.
Recorder Recorder WS-960P (Display The connected recorder model is displayed.
only)
Security Channel Setting ON, OFF Selects whether or not password confirmation is needed
Protection when opening the Channel window.
Prohibit Duplicate ON, OFF Selects whether or not duplicate transmitter channels are
Channels*2 prohibited.
Even when set to [ON], if the patient is admitted on
another central monitor, the same channel can be set on
the other central monitor.
System Initialize Initializes the central monitor system settings. Refer to
“Initializing the PU-621R Central Monitor Processing
Unit”.
*1 Monitoring of the bed automatically resumes at the central monitor when the resume time is set at [Auto Resume After
Pause] and any one of the following conditions is met at the paused bed:
• Heart rate is continuously monitored for the selected time.
• SpO2 is continuously monitored for the selected time.
• PR from the invasive blood pressure (ART, ART2, RAD, DORS, AO, FEM, UA, LVP or P1 to 8) is continuously
monitored for the selected time at the bedside monitor or transmitter.
Monitoring of the bed automatically resumes at the central monitor when any one of the following conditions are met at
paused bed:
• NIBP is properly measured and the SYS, DIA or MAP value is displayed at the bedside monitor or transmitter.
• ASYSTOLE is generated (HR becomes 0).
*2 Available only when the maintenance password is entered.
Alarm
Touch the [Alarm] tab on the System Configuration window.
Setting Range
Setting Item Description
( : Default)
Alarm Limit Alarm Off ON, OFF Selects whether or not to display the limit alarm off mark [ ].
Mark ON: Displays the limit alarm off mark when either the upper and
lower limit is set to OFF at the bedside monitor.
OFF: Does not display the limit alarm off mark.
NOTE
When a bed is connected to the network directly, the condition
6
to display limit alarm off mark can be set on some bedside
6-1
monitor. In this case, the central monitor displays the limit
alarm off mark according to the bedside monitor setting.
Technical Icon ON, OFF Selects whether or not to display a technical icon. When ON is set, a
technical icon is displayed when the technical status becomes red or
yellow.
Communication Every Two Minutes, Selects the mode for communication loss alarm.
Loss Alarm Single Sound, Only Monitor’s Silencing the How the
Message behavior when communication loss communication
Setting
communication alarm loss alarm is reset
loss happens.
• Silence time is 2 Communication
minutes. loss alarm occurs
• Alarm sound stops. again if the same
Every • Highlighted alarm communication
message remains on loss still continues
Two
the screen. after two minutes
Minutes • Alarm suspend mark silence time
with remaining time elapses.
Communication is displayed on the
loss alarm screen.
(advisory level)
occurs. Alarm does
• Silence time is
not re-occur
indefinite (until
while the same
the end of the
communication
Single communication loss).
loss continues.
Sound • Alarm sound stops.
(Alarm occurs
• Alarm message
when a new
turns to white (non-
communication
highlighted).
loss happens.)
Only No alarm occurs. The “Communication Loss” message appears
Message in white (non-highlighted).
WARNING
When the [Communication Loss Alarm] is set to [Only Message],
there will be no communication loss alarm. When it is set to [Only
Message], always pay careful attention to the communication
status.
CAUTION
When the communication loss alarm in the [Single Sound] is
silenced, an alarm for the same alarm condition does not occur
again while communication is still lost. In [Single Sound], always
pay careful attention to the communication status.
Setting Range
Setting Item Description
( : Default)
Alarm Alarm Notice Icon ON, OFF Selects whether or not to display the alarm notice icon.
NOTE
Notice icons on the screen disappear when the Alarm Notice
Icon setting is changed.
Alarm Notice CRISIS, WARNING Selects the alarm level for which alarm notice icons are displayed.
Level or CRISIS, All CRISIS: The alarm notice icon is displayed when a CRISIS level
alarm occurs.
WARNING or CRISIS:
The alarm notice icon is displayed when a CRISIS or
WARNING level alarm occurs.
All: The alarm notice icon is displayed when a CRISIS,
WARNING or ADVISORY level alarm occurs.
NOTE
Notice icons on the screen disappear when the Alarm Notice
Level setting is changed.
Alarm Sound Type NK1, NK2, IEC Select the alarm sound standard.
Alarm sound
Setting
CRISIS WARNING ADVISORY
NK1 Continuous Continuous Single beep
pip sound bing bong every 20 or
sound 120 seconds*
NK2 Continuous Continuous Single beep
ping sound ding ding every 20 or
sound 120 seconds*
IEC ceg-gC ceg ec every 20 or
120 seconds*
* You can select the interval on the Advisory Alarm Sound Interval
setting.
Advisory Alarm Yellow, Cyan Selects the color of the alarm indicator, alarm message and frame of
Color waveform display area when the advisory and warning level alarm
occur.
Alarm Events
Touch the [Alarm Events] tab on the System Configuration window.
Setting Range
Setting Item Description
( : Default)
Status Display Measurement ECG Technical High, Middle, Sets the judgement conditions for the
Setting Status Low measurement status. The central monitor judges
Judgement the measurement status by counting the number
Condition of ECG Technical, SpO2 Technical and other
Technical alarms in the past one hour. You can set
the criteria on the Other window.
6
SpO2 Technical The judgement condition affects to the
measurement status as follows: 6-1
Default settings
Middle Sets the criteria for displaying a technical message. Enter the number
by touching the numeric keypad.
Low NOTE
After entering the number, touch the close button [ ] to set
the number.
Yellow High
Technical High Middle Low
message
Middle Red 2 to 997 3 to 998 4 to 999
Yellow 1 to 996 2 to 997 3 to 998
Monitor Setting
NOTE
The monitor settings must be set by qualified personnel in your hospital.
There are four tabs of monitor settings. The windows can be changed by
touching the tab.
• Screen Composition
• Monitored Beds Setting
• Display Settings
• Bed Name Setting
Screen Composition
Touch the [Screen Composition] tab on the Monitor Setting window.
Setting Range
Setting Item Description
( : Default)
Number of Displays*1 Single, Dual Selects the number of displays connected to the central
monitor.
Expand Individual Display*1 OFF, Main Display, Sets which screens are displayed on dual displays. This
Second Display setting is not available when the [Number of Displays] is set
to [Single].
You can monitor with dual displays and set both displays to
All Beds screen or one display to Expand Individual Bed
screen. To set this, select one of the following on [Expand
Individual Display] in the Monitor Setting.
Setting Range
Setting Item Description
( : Default)
Monitored bed Main Display Up to 32 beds* You must register a bed to monitor it on the central monitor. You can
register any bed in the network. Up to 300 beds can be registered.
NOTE
If you try to register a bed to a position where another bed is
already registered, a confirmation window asks if you want to
delete the other bed’s registration (stop monitoring the bed).
• Touch [Yes] to unregister the other bed and remove its data
from this central monitor.
• Touch [No] to cancel registration and keep the other bed’s
registration.
* You can register up to 32 beds with main and second display together.
NOTE
• Data for a bed can only be saved in one central monitor.
• If a bed’s data is not saved in any central monitor, the bed’s review data
cannot be displayed on any central monitor. Be sure to save a bed’s
data in one of the central monitors in the network.
• You can exchange the positions of two registered beds by touching the
two registered positions.
• You cannot save the data of a bed that is monitored through a CNS-
6201 central monitor on which [Extended Network] is set to [ON].
Stop Monitoring
Removes the monitored bed from the selected position.
Monitored beds
A bed is displayed in red or blue
depending on which central
monitor its data is saved in.
Display Settings
Touch the [Display Settings] tab on the Monitor Setting window.
Setting Range
Setting Items Description
( : Default)
All Beds Screen All Beds Numeric Area Normal, Wide Sets the size of the numeric area on the All
Beds screen.
Large
6-1
Normal
All Beds Numeric Size Normal, Large Sets the size of the numeric value on the All
Beds screen.
Large
Normal
Display Patient Name ON, OFF Selects whether or not to display the patient
name. When [OFF] is set, note entered on the
Admit/Discharge window cannot be displayed
even if the note is entered.
Large Patient Name ON, OFF Sets the size of the patient name on the All
Beds screen.
ON
OFF
All Beds Screen Transmitter Battery ON, OFF Selects whether or not to display the battery
Status level icon when the monitored bed is a
transmitter. The icon can only be displayed
only if the transmitter is compatible with the
transmitter battery status function.
Setting Range
Setting Items Description
( : Default)
Old NIBP Data Time Until NIBP Data 10 min, 30 min, 1 hour, 24 Selects how long to wait after NIBP
Display Is Old hours measurement to dim NIBP or delete NIBP and
display “---”.
Old NIBP Data Display Dim, --- Selects how to display the old NIBP data.
Dim: NIBP measurement is dimmed.
ECG Display Pacing Mark Position Above Wave, Overlap Wave Selects the pacing mark position on the ECG
waveform displays on the All Beds screen.
Above Wave: Pacing mark is displayed above
the wave.
Overlap Wave: Pacing mark is displayed
overlapping wave.
NOTE
Do not use the same bed name for more than one bed in a group.
You can also enter the bed name using the onscreen
Second Display keyboard.
Monitored beds
Touch the desired bed to change the name. For dual
displays, monitored beds are displayed on the Main
Display and Second Display separately.
6-1
Bed list
Select a monitored bed.
Registered beds on the Pre-
registration window are
displayed. Touch [ ] or
[ ] to scroll the list. If there
are no pre-registered beds, a
keyboard appears.
Every touch of the key toggles
between keyboard and bed list.
Parameter Setup
There are two tabs for parameter setting. The windows can be changed by
touching the tab.
• Parameter Selection
• Parameter Colors
Parameter Selection
Touch the [Parameter Selection] tab on the Parameter Setup window.
Parameter Colors
Touch the [Parameter Colors] tab on the Parameter Setup window.
Alarm Master
You can register three alarm masters (Alarm Master 1 to 3) on the Alarm Master
window. Touch the desired master and set the settings. For details, refer to the
Operator’s Manual.
The alarm master also gives the default alarm settings when the patient is
admitted.
• For a bedside monitor: Alarm Master 1 of the bedside monitor. 6
• For a bed monitored through an ORG-9100 series multiple patient receiver:
Alarm Master 1 of this central monitor (includes “arrhythmia analysis” and 6-1
“QRS detection type” settings)
Each alarm master has the following settings. The windows can be changed by
touching the tab.
• Alarm Limits
• Arrhythmia Alarm
• ST Alarm
You can change the master name by touching [ ] of the selected alarm
master.
Pre-registration
There are six tabs of Pre-registration settings. The windows can be changed by
touching the tab.
• Bed Name
• Group Color
• Pause 6
• Channel
• Hospital Name 6-1
NOTE
After entering the items, touch [ENTER] to register the setting. Then,
touch [OK] to close the window.
ORG Setting
Set the settings for the ORG-9100 multiple patient receiver. These settings
can only be set at the central monitor that monitoring through the ORG-9100
multiple patient receiver.
NOTE
• The ORG setting must be set by qualified personnel in your hospital.
• This settings are only available for monitored beds.
There are five tabs of ORG setting. The windows can be changed by touching the
tab.
• ORG Setting
• RSSI
• Alarm Level (Limits)
• Alarm Level (Arrhythmia)
• Alarm Level (Technical)
ORG Setting
Select the desired ORG and touch ORG Setting.
Setting Range
Setting Items Description
( : Default)*
Group Select from groups in the Sets the name of the group the ORG belongs to.
network (Default: General)
Channel 1001-6080, 7001-7997, Sets the channel band the ORG belongs to. When the channel is
A000-C0FE, 8001-8009, changed, a confirmation message appears and registered channel
9001-9479 is reset.
Antenna Antenna-1, Diversity Selects the antenna type.
• Antenna-1: ORG uses antenna 1 to receive signals.
• Diversity: ORG uses antennas 1 and 2 to receive signals.
Telemetry Alarm 1 min, 2 min, 3 min Sets the alarm silence time for the beds through the multiple
Silence Time patient receiver.
Arrhythmia Type Standard, Extended Selects the arrhythmia type. This setting is available only when
the multiple patient receiver corresponds to the function.
ZR Setting Bed Name Select from the registered Sets the bed name. Touch [ ] of the desired bed and enter the
bed names (Up to 64 bed) bed name.
Type A, C (display only) Selects the transmitter type, A or C, for each bed.
RSSI
Select the desired ORG and touch [RSSI].
Setting Range
Setting Items Description
( : Default)
RSSI Mode ON, OFF Selects whether or not to display the trendgraph of the registered beds through
the multiple patient receiver. When [ON] is set, the RSSI trendgraph is
displayed for up to 30 minutes and the field strength value is displayed on the
All Beds screen and Individual Bed window. The trendgraph has 16 levels ( 0
to 15) and is updated every three seconds. The default setting depends on the
multiple patient receiver.
6
6-1
Alarm Level (Limits)
Select the desired ORG and touch [Alarm Level (Limits)].
Setting Range
Setting Items Description
( : Default)
HR CRISIS, WARNING, ADVISORY Sets the alarm level of each vital sign and ST alarm. The
PR default setting depends on the multiple patient receiver
ST setting.
SpO2
RR
PRESS
NIBP
TEMP CRISIS, WARNING, ADVISORY
APNEA(T) CRISIS, WARNING, ADVISORY
ETCO2
Setting Range
Setting Items Description
( : Default)
EXT TACHY CRISIS, WARNING, ADVISORY Sets the alarm level of each arrhythmia alarm. The
EXT BRADY default setting depends on the multiple patient receiver
VPC RUN*1 CRISIS, WARNING, ADVISORY setting.
V BRADY*2
SV TACHY*2
TACHYCARDIA
BRADYCARDIA
PAUSE*2
COUPLET CRISIS, WARNING, ADVISORY
EARLY VPC
MULTIFORM
V RHYTHM*2
BIGEMINY
TRIGEMINY*2
FREQ VPC
IRREGULAR RR*2
PROLONGED RR
NO PACER PULSE*2
PACER NON-CAPTURE*2
*1 When the arrhythmia type for the multiple patient receiver is set to Standard, the default setting of VPC RUN is
ADVISORY.
* Only available when the arrhythmia type for the multiple patient receiver is set to Extended.
2
Set the settings to read the patient information with a bar code reader.
Setting Range
Setting Items Description
( : Default)
Patient Attribute Input Device OFF, Bar Code Selects whether or not to read patient information
Reader with a bar code reader. When Bar Code Reader is
selected, patient information items are displayed.
Touching [Delete] deletes read information. 6
Patient ID Read Patient ID Enable, Disable Selects whether or not to read the patient ID. When
reading the patient ID, touch [Enable] → [SETUP] 6-1
and set the data area of the patient ID. The data area
of the patient ID is displayed in cyan.
SETUP Offset 0 to 259 Sets the patient ID data area. Touch [ ] of the
start position or length and set them.
NOTE
Length 0 to 16 After entering the numeric value, touch [OK] to
close the window.
NOTE
After entering the division, touch [OK] to close
the window.
Setting Range
Setting Items Description
( : Default)
Date of Read Date of Birth Enable, Disable Selects whether or not to read the date of birth.
Birth When reading the date of birth, touch [Enable] →
[SETUP] and set the data area of the date of birth.
The data area of the date of birth is displayed in
green.
Settings Year Offset 0 to 259 Set the date of birth data area. The procedure is the
Length 4 (fixed) same for patient ID.
Month Offset 0 to 259
Length 2 (fixed)
Day Offset 0 to 259
Length 2 (fixed)
Gender Read Gender Enable, Disable Selects whether or not to read the gender. When
reading the gender, touch [Enable] → [SETUP] and
set the data area of the gender. The data area of the
gender is displayed in purple.
Settings Gender Offset 0 to 259 Sets the gender data area. The procedure is the same
Length 1 (fixed) for patient ID.
Identification Male 0 to 8 M Sets the identification code of gender. Touch the
Code [ ] of the Separation Code and enter the code.
Female F
NOTE
After entering the separation code, touch
Unknown U [ENTER] to register the setting. Then, touch
[OK] to close the window.
External Output
Set the communication settings for RS-232C and HL7 on the External Output
setting.
There are two tabs of External Output settings. The windows can be changed by
touching the tab.
• RS-232C
• HL7 6
6-1
RS-232C
Touch [RS-232C] tab on the External Output window and set the settings.
Setting Range
Setting Items Description
( : Default)
Baud Rate 2400, 4800, 9600, 14400, 19200, Sets the RS-232C communication settings according to
38400 the external instrument which is connected to the USB 3
Data Bits 7, 8 connector.
Parity None, Even, Odd
Stop Bits 1, 1.5, 2
Flow Control None, Xon/Xoff, Hardware, Hardware
XON/XOFF
Communication Mode NK Protocol, Off
HL7
Touch the [HL7] tab on the External Output window and set the settings. Touch
[OK] on the confirmation window to restart the HL7 service.
Setting Range
Setting Items Description
( : Default)
ORU Use ORU ON, OFF Selects whether or not to output the ORU (current
numeric) data.
ORU Port 1024 to 65535 (Default: 7998) Sets the port number to use for ORU data output.
No. (ORU/ Touch [ ] of the port number and enter the
ACK-R01) number.
NOTE
After entering the port number, touch [OK] to
close the window.
ORU 1 min, 5 min, 10 min, 30 min, 60 min Sets the interval to output the ORU data. Touch
Sample [ORU Sample Interval] and select the time.
Interval
ORF Use ORF ON, OFF Selects whether or not to output the ORF (old
numeric) data.
ORF 1024 to 65535 (Default: 9004) Sets the port number to use for ORF data output.
Port No. Touch [ ] of the port number and enter the
(QRY∧R02/ number.
ORF∧R04) NOTE
After entering the port number, touch [OK] to
close the window.
Administrator’s Guide CNS-6201 6.1.23
6. SYSTEM SETUP SCREEN
Setting Range
Setting Items Description
( : Default)
QRY Use QRY ON, OFF Selects whether or not to request patient
information.
HIS IP Set depending on the hospital Sets the IP address of the HIS server.
Address network. (Default: 0.0.0.0)
Touch [ ] of the each number and enter the IP
address.
NOTE
After entering the IP address, touch [OK] to
close the window.
Patient 1024 to 65535 (Default: 7997) Sets the port number that is used by HIS server for
QRY Port receiving patient information. Touch [ ] of the
(QRY/ port number and enter the number.
ADR-A19)
NOTE
After entering the port number, touch [OK] to
close the window.
ADT Use ADT ON, OFF Selects whether or not to output the admit and
Admit/ 1024 to 65535 (Default: 9005) discharge, patient information update and presence
Discharge check information.
Port
(ADT-A04/ • Admit/Discharge Port
A02) Sets the port number for admitting or discharging
Patient Info 1024 to 65535 (Default: 9006) a patient from an external system.
Update Port
(ADT∧A08) • Patient Info Update Port
Sets the port number for entering the patient
Patient List 1024 to 65535 (Default: 9007)
information including patient ID from an
QRY Port
external system.
(QRY∧R02)
• Patient List QRY Port
Sets the port number for requesting the admit
condition of a patient from an external system.
NOTE
After entering the port number, touch [OK] to
close the window.
MSH Segment HL7 ––– (Display only) Displays the HL7 version.
Version
Character ASCII, JIS, UNICODE UTF-8 Sets the character code type. Touch the character
Set code key and select the character code.
Sending Up to 180 characters Sets the names in the HL7 telegram.
Application (Default:
Sending • Send Application Name Touch [ ] of the each item and enter the name.
Facility NIHON KOHDEN
Receiving • Send Facility Name
NOTE
Application NIHON KOHDEN
• Receive Application Name After entering the name, touch [OK] to close
Receiving
CLIENT APP the window.
Facility
• Receive Facility Name
CLIENT FACILITY)
Set the keys for All Beds and Individual Patient function keys.
There are two tabs of function keys setting. The windows can be changed by
touching the tab.
• All Beds
• Individual
6
Setting Range
Setting Items Description
( : Default)
All Beds Function Keys (7 keys) • Screen Selects the function or window for
Overview, Discharged Patients List, all beds function keys of the All Beds
System Setup, All Beds Alarm Events, All screen. Touch the desired key and
Beds Limits select the function or window.
• Operation
Touchkeys Setting, Touchkeys Off, Alarm When [Reset] is touched, a
Check, Record All confirmation window is displayed.
• None Touch [Yes] to return the setting to the
factory default setting.
Individual
Setting Range
Setting Items Description
( : Default)
Individual Function Keys (6 keys) • Screen Set the individual function keys to
Individual Waveforms display on the All Beds screen when
• Personal Setup [ » ] of each bed is touched. Touch the
Admit/Discharge, Alarm Limits, desired key and select the function or
Arrhythmia Alarm, ST Alarm window.
• Other Setup
All Beds Screen Setup, Individual When [Reset] is touched, a
Bed Screen Setup, Parameter Priority, confirmation window is displayed.
Function Keys, Recording, Report Touch [Yes] to return the setting to the
• Parameter Setup factory default setting.
ECG, RESP, SpO2, NIBP, PRESS, TEMP
• Review
Trend, Tabular Trend, Full Disclosure,
Expanded Waveform, ST Recall,
Arrhythmia Recall, Hemodynamics List,
ECG 12 Lead Analysis, Event List, Alarm
Events, Review*
• Operation
NIBP Measurement, Learn ECG
• None
* The Review window that is displayed when [Review] on the Individual Bed window is touched is displayed. (Default:
Custom Review).
Mouse Setting
The mouse setting must be set on the central monitor to which the mouse is
connected.
* Up to 6 central monitors which are controlled by one mouse and their position is displayed. You can move the cursor
from the mouse controller to other central monitors as allowed in the following screen.
Applicable Display
Returns to the applicable
display when mouse controller
Display Placement Image
is touched.
Applicable display is displayed in green.
Mouse Controller
Selects the mouse controller.
Find Cursor
Returns the mouse cursor
to the center of the display. 6
Mouse Controller
Displays in blue frame.
6-1
Central Monitor List
Touch applicable display
Not used
of the display placement
Leave the place unselected.
image and select the central
monitor.
Sets the channel of the remote controller. The remote controller is only available
when the YL-611P/612P alarm indicator is connected to the central monitor.
CAUTION
• Set the remote control channel on the monitor to prevent the
remote control from operating a different monitor.
• When several monitors are installed close together, check that the
remote control operates only the desired monitor. If the remote
control operates a different monitor, recheck the channel setting.
NOTE
This setting must be set by qualified personnel in your hospital.
Network Setting
There are three tabs of network setting. The windows can be changed by
touching the tab.
• Network
• Central
• Extended Network
Network
Touch the [Network] tab on the Network Setting window.
CAUTION
The network must be managed by the network administrator. Make
sure that each monitor in the network has a different IP address.
Otherwise, data communication cannot be performed properly. When
adding a monitor to an already operating network, set the IP address
on the monitor before connecting the monitor to the network.
NOTE
• Contact your Nihon Kohden representative when changing the IP
address manually.
• To avoid communication trouble, do not connect the network cable to
each instrument before IP address setting is complete.
• When a monitored bed is registered, do not change the IP address. The
data may be lost.
Central
Touch the [Central] tab on the Network Setting window.
Extended Network 6
Touch [Extended Network] tab on the Network Setting window.
6-1
WARNING
Do not diagnose a patient based on alarm information of an
instrument which can view the data by setting [Extended Network] to
ON. There is a time delay. Confirm the alarm information on this
central monitor.
Set the date and time. These are displayed at the lower right of the screen.
NOTE
Changing the date and time affects the all central monitors and bedside
monitors in the network.
Setting Range 6
Setting Items Description
( : Default)
Time Setting Mode Manual, Synchronized to Select whether to set the date and time
6-1
NTP Server manually or synchronize it to the NTP server
in the network.
• Manual
Set the date and time manually. Touch the
desired setting and enter the number.
Password
To access some windows of the System Setup screen, you need an administrator
password. You can set a password which consists of four numbers. The factory
default setting is “1234”, but we recommend that you change this password.
2. Enter the new password twice. The password is displayed as “*” for
protection.
NOTE
After entering the password, touch [Set] to set the password.
Set
Set the entered password.
You can check the information of the monitored beds on the Revision window of
the Maintenance window. Touch [Revision] tab on the Maintenance window.
6
Registered bed information
• Bed: Bed name
• Group: Group name 6-1
• Device: Model name
• Revision: Software revision
• IP Address: IP address
• Arrhythmia: Arrhythmia version
Use the following procedure to initialize the PU-621R central monitor processing
unit to the factory default settings.
NOTE
Initializing the central monitor deletes all data saved in the central monitor
and returns all settings to the factory default settings. Before initialization,
make sure that all necessary data is backed up.
3. Touch [OK] to initialize the system. The system is initialized, the Windows
screen appears, then the CNS-6201 central monitor program starts.
List of instruments
in the network
The registered bed
columns are filled in
blue.
For setting the IP address of the PU-621R central monitor processing unit
manually, refer to “Setting the IP Address of PU-621R Central Monitor
Processing Unit Manually” in Section 2.
NOTE
The ALT key is not displayed.
NOTE
This operation must be done by qualified personnel in your hospital.
You can copy settings from one bed to other beds or to a USB thumb drive. This
function is useful when you start using a new central monitor and want to set the
same settings for all beds. A USB thumb drive can also be the copy source or
copy destination.
You can also register the desired bed settings or removable disk settings to the
default settings of the central monitor. The registered default settings are applied
to the default settings of the new admitted bed.
Setting items that can be copied by this operation are listed in “Factory Default
Settings” in Section 7.
NOTE
• Patient information and review data cannot be copied.
• When copying the bed settings from the USB thumb drive, the software
version of the copy source and copy destination must be the same.
When a USB thumb drive is the copy source or destination, do steps 1 to 10.
When a USB thumb drive is not used, do steps 6 to 10.
1. Touch [Menu] on the left lower corner of the screen → [System Setup] to
display the Information window of the System Setup screen.
When [System Setup] is assigned to an all beds function key, the Information
window of the System Setup screen can also be displayed with the function
key.
3 6-2
4. Insert a USB thumb drive into the USB connector on the PU-621R central
monitor processing unit.
NOTE
• Insert only one removable media into the central monitor at a time.
• Use a removable media with enough free space.
• A USB hard disk cannot be used.
• Do not insert a removable media into the central monitor during
monitoring. This may cause communication loss.
7. Select the source (bed) and destination (bed) and touch [Copy]. You can
select two or more destination (beds).
NOTE
• If bed settings are already in the USB thumb drive, copying
overwrites them.
• If the software version of the copy source and copy destination are
different, [Removable Disk] cannot be selected.
Source Destination
All registered beds are displayed. All monitored beds are displayed and two or more destinations
You can select only one bed including can be selected. [ALL] copies the settings to all the monitored
removable disk. [Removable Disk] is beds. [Removable Disk] copies the settings to the removable
used when the setting is copied to the disk. [Default Settings] registers the source bed settings to the
removable disk. default settings of the central monitor.
To copy the settings to another bed, touch [Yes] and repeat step 7.
To end copying, touch [No]. The confirmation window appears.
9. Touch [Yes]. When copying is finished, the “Bed settings copied” message
appears.
ii) Remove the USB thumb drive from the central monitor.
NOTE
• Follow the procedure above to remove the USB thumb drive from
the central monitor. Otherwise it may cause instrument trouble and
data may be damaged.
• If the “The USB device cannot be stopped right now.” message
appears, touch [Other Settings] to change the window and then
touch [Unplug Device]. For details, refer to “Removing the USB
Thumb Drive” in this section.
6-2
Backing Up Settings
NOTE
• This operation must be done by qualified personnel in your hospital.
• When exchanging the central monitor, check the following conditions.
Otherwise the central monitor might not operate correctly.
- The central monitors are the same model.
- The software version of the new central monitor is the same as the
current central monitor.
- The new central monitor is initialized.
When you exchange the central monitor for another one, first back up the settings
of the current central monitor to a USB thumb drive. Use the USB thumb drive
to transfer the settings to the new central monitor.
For setting items you can back up by this operation, refer to “Factory Default
Settings” in Section 7.
NOTE
Patient information and review data cannot be backed up.
1. Back up the settings of the current central monitor on a USB thumb drive.
Refer to “Backing Up to a Removable Media”.
NOTE
Do not set the IP address after registering monitored beds.
4. Restore the settings you saved at step 1 on the new central monitor. For the
procedure, refer to “Restoring Settings on a Central Monitor” in this section.
5. Confirm that the new central monitor can perform the same monitoring as
the previous central monitor.
1. Touch [Menu] on the left lower corner of the screen → [System Setup] to
display the Information window of the System Setup screen.
When [System Setup] is assigned to an all beds function key, the Information
window of the System Setup screen can also be displayed with the function
key.
6
2. Enter the maintenance password and touch [ENTER].
NOTE
• Insert only one USB thumb drive into the central monitor at a time.
• Use a USB thumb drive with enough free space.
• A USB hard disk cannot be used.
• Do not insert any removable media into the central monitor during
monitoring. This may cause communication loss.
NOTE
If settings of the same central monitor are already saved in the
removable media, they are overwritten.
8. Touch [Yes]. Backup starts and the “Saving data” message appears.
The “The data is saved to the USB thumb drive.” message appears when
backup is finished.
9. Touch [OK].
10. Remove the USB thumb drive from the central monitor.
i) The “The USB device can now be safely removed from the system.”
message appears. Touch [OK] to complete the backup.
ii) Remove the USB thumb drive from the central monitor.
NOTE
• Follow the procedure above to remove the USB thumb drive from
the central monitor. Otherwise it may cause instrument trouble and
data may be damaged.
• When the “The USB device cannot be stopped right now.” message
appears, touch [Other Settings] to change the window and then
touch [Unplug Device]. For details refer to “Removing the USB
Thumb Drive” in this section.
NOTE
Check that the new central monitor is initialized.
1. Touch [Menu] on the left lower corner of the screen → [System Setup] to
display the Information window of the System Setup screen.
6
When [System Setup] is assigned to an all beds function key, the Information
window of the System Setup screen can also be displayed with the function
key.
6-2
2. Enter the maintenance password and touch [ENTER].
NOTE
• Insert only one USB thumb drive into the central monitor at a time.
• Use a USB thumb drive with enough free space.
• A USB hard disk cannot be used.
• Do not insert any removable media into the central monitor during
monitoring. This may cause communication loss.
9. Touch [Yes]. Restoring the settings starts and the “Restoring data” message
appears. The “The restore is complete.” message appears when restoring the
settings is finished.
11. Remove the USB thumb drive from the central monitor.
i) The “The USB device can now be safely removed from the system.”
message appears. Touch [OK] to complete restoring the settings.
ii) Remove the USB thumb drive from the central monitor.
NOTE
• Follow the procedure above to remove the USB thumb drive from
the central monitor. Otherwise it may cause instrument trouble and
data may be damaged.
• When the “The USB device cannot be stopped right now.” message
appears, touch [Other Settings] to change the window and then
touch [Unplug Device]. For details, refer to “Removing the USB
Thumb Drive” in this section.
iii) The “The system will shut down and return to Windows.” message
appears. Touch [OK]. The Windows restarts and then central monitor
program starts automatically.
6.2.12 Administrator’s Guide CNS-6201
6-2. CHANGING THE SYSTEM SETUP SCREEN SETTINGS FOR MAINTENANCE
6-2
2. Fill in the registration form on the back page of this guide and send it to your
Nihon Kohden representative.
Input Password
Touch to display the Input Password window. This key is disabled
when the number of monitored bed is already 32 beds.
4. Touch the keyboard icon ( ) to display the keyboard. Enter the unlock
code acquired from Nihon Kohden and touch [OK].
NOTE
It is not necessary to restart the central monitor after installing the
expansion program.
6-2
NOTE
• This setting becomes “Disable” whenever you restart the central monitor
program.
• Use the screen hard copy function for maintenance only. The waveform
might not be displayed correctly.
Printing example
6-2
If you could not remove the USB thumb drive when copying bed settings or
backing up the central monitor settings, do the procedure below to safely remove
the USB thumb drive.
NOTE
Follow the procedure below to remove the USB thumb drive from the
central monitor. Otherwise it may cause instrument trouble and data may
be damaged.
2. Touch [Unplug Device] in [USB Device]. The “The USB device can now be
safely removed from the system.” message appears.
NOTE
The “Please confirm connection of the USB memory” message appears
when the USB thumb drive was already in a condition where it can be
safely removed.
The factory default settings of the System Setup screen are listed below. Other
default settings are listed in the Section 16 “Factory Default Settings” of the
Operator’s Manual.
OK: The copy settings and backup settings are available. When changing the
monitor for a bed whose data is saved on another central monitor, the
setting is maintained.
NO: The copy settings and backup settings are not available. When changing
the monitor for a bed whose data is saved on another central monitor, the
setting returns to default setting.
–: The displayed setting is the setting maintained on the bed. When changing
the monitor for a bed whose data is saved on another central monitor, the
settings are changed to new bed settings.
System Configuration
Factory
Copy Backup
Setting Item Setting Range Default
Settings Settings
Setting
Language English (fixed)
Temperature Unit Celsius, Fahrenheit Celsius
Height Unit cm, in (inch) cm
NO
Weight Unit kg, lb kg
Pressure Unit mmHg/cmH2O, kPa/hPa mmHg/cmH2O
ST Unit mV/mm mV
Extended Units ON, OFF OFF
System Blood Pressure
mmHg, kPa mmHg
Unit*
CO2 Unit* mmHg, kPa mmHg
Respiration Unit* cmH2O, kPa cmH2O
System
Factory
Copy Backup
Setting Item Setting Range Default
Settings Settings
Setting
Screen Timeout OFF, 1 to 30 min 5 min
Display ECG
Screen ON, OFF ON
Measurement Key
Match QRS Sens
ON, OFF OFF
System
to ORG
Recorder WS-960P WS-960P (Display only)
Channel Display
ON, OFF OFF
Protection
Security
Prohibit Duplicate
ON, OFF ON
Channels
Limit Alarm Off
ON, OFF ON
Mark
Technical Icon ON, OFF OFF
Every Two Minutes,
Communication 7
Single Sound, Only Single Sound
Loss Alarm
Message
Alarm Notice Icon ON, OFF ON
Alarm Notice CRISIS, WARNING or WARNING or
Alarm
ECG Technical
Status Display Setting
Judgement Condition
Measurement Status
Other Technical
Measurement
Display
Status
Other
Monitor Setting
Factory
Copy Backup
Setting Item Setting Range Default
Settings Settings
Setting
Number of Displays Single, Dual Single
OFF, Main Display, Second
Expand Individual Display OFF
Display
32 Patients*,
24 Patients*,
16 Patients*,
Main Display 12 Patients,
Screen 10 Patients,
Composition Number of
8 Patients (4 × 2),
Patients on 8 Patients
8 Patients (8 × 1),
All Beds (4 × 2)
6 Patients (3 × 2),
Screen
6 Patients (6 × 1),
Second Display 4 Patients (2 × 2),
4 Patients (4 × 1),
2 Patients (1 × 2),
2 Patients (2 × 1)
Monitored Monitored Main Display Up to 32 patients with main and second display
Beds Setting Bed Second Display together NO OK
All Beds Numeric
Normal, Wide Normal
Area
All Beds Numeric
Normal, Large Normal
Size
All Beds Display Patient
ON, OFF ON
Screen Name
Large Patient
ON, OFF ON
Display Name
Settings Transmitter Battery
ON, OFF ON
Status
Time Until NIBP 10 min, 30 min, 1 hour, 24
Old NIBP 10 min
Data Is Old hours
Data
Old NIBP Data
Display Dim, --- Dim
Display
ECG Pacing Mark
Above Wave, Overlap Wave Above Wave
Display Position
Monitored Main Display
Bed Name
Beds Bed Name (up to 10 characters) ― ―
Setting Second Display
Setting
* Optional software to expand the number of patients is required.
Parameter Selection
Copy Backup
Setting Item Setting Range Factory Default Setting
Settings Settings
All parameters that can be
Parameter Selection displayed on this central All unselected
monitor
White: RESP, P5, CO2, O2,
FLOW, VOL, Paw, tcPO2/
PCO2 (EXT), CO2 (GAS),
GAS, PiCCO (EXT)
Beige: FLOW (GAS), Paw
(GAS), VENT (EXT)
Red: ART, ART2, RAD,
DORS, AO, FEM, UA,
LVP, P1
Blue: UV, CVP, RVP, P2,
N2O, Delta SpO2, DES
(GAS)
7
Green: ECG, P7, O2
NO OK
All parameters that (GAS), EEG1, EEG2, PR
Parameter
can be displayed on 32 colors Yellow: PAP, RAP, LAP,
Colors
this central monitor ICP, ICP 2 to 4, P3, P4,
Trect, Tcore, Tnaso, Teso,
Ttymp, Tblad, Taxil, T2,
T4, T8, Delta T, Delta T2,
Delta T3, Delta T4, SEV
(GAS)
Violet: EXT 1 to 4
Orange: BIS, Tskin,
Tskin2, Tskin3, T1, T3,
T5, T7, Tb, Tb (CCO), Tb
(EXT), CCO, ENF (GAS)
Cyan: SpO2, SpO2-2
Pink: NIBP, P6
Purple: P8
Alarm Master
Factory
Copy Backup
Setting Item Setting Range Default
Settings Settings
Setting
All
parameters
Alarm Limits which have Set for each parameter
alarm limits
setting
Arrhythmia Refer to “Alarm
Alarm Master 1 to ON, OFF
Analysis Master” in NO OK
Alarm Master 3
QRS Section 6-1.
Arrhythmia
Detection Adult, Child, Neonate
Alarm
Type
Arrhythmia
Set for each arrhythmia
Alarm Limits
ST (all lead) Set for each lead
Alarm
Alarm Item Lower Limit Upper Limit Unit
Master
SYS
mmHg
PRESS P1 to 8 DIA Master 1 to 3 OFF OFF
(kPa)
MEAN
Tskin, Tskin2 to 3,
Master 1, 2 38.0 (100.4)
Tcore, Trect, Teso,
TEMP Ttymp, Tblad, Taxil, OFF
Tnaso, T1, T2, T3, T4, Master 3 39.0 (102.2)
T5, T6, T7, T8 °C (°F)
Delta T, Delta T2,
Delta T Master 1 to 3 OFF OFF
Delta T3, Delta T4
Master 1, 2 38.0 (100.4)
Tb OFF
Master 3 39.0 (102.2)
O2 (I) 18 OFF
O2 Master 1 to 3 %
O2 (E) OFF OFF
Master 1, 3 OFF
CO2 (I) ― mmHg
CO2 Master 2 3 (0.4)
(kPa) 7
ETCO2 OFF OFF
N2O (I) (GAS) 80
N 2O OFF
N2O (E) (GAS) OFF
HAL (I) (GAS) 4.0
HAL OFF
HAL (E) (GAS) OFF
ISO (I) (GAS) 5.0
ISO OFF
ISO (E) (GAS) OFF
Master 1 to 3 %
ENF (I) (GAS) 5.0
ENF OFF
ENF (E) (GAS) OFF
SEV (I) (GAS) 6.0
SEV OFF
SEV (E) (GAS) OFF
DES (I) (GAS) 12.0
DES OFF
DES (E) (GAS) OFF
CCO OFF OFF
Master 1, 2 4.0 10.0 L/min
MV
Master 3 OFF OFF
Master 1, 2 26 (26)
Ppeak OFF
Master 3 OFF cmH2O
Master 1, 2 10 (10) (hPa)
PEEP OFF
Master 3 OFF
BIS 40 OFF ―
SEF (EEG1), SEF
OFF OFF Hz
(EEG2) Master 1 to 3
EEG
TP (EEG1), TP
OFF OFF nW
(EEG2)
Master 1, 2 80 (10.7) 180 (24.0) mmHg
SYS
Master 3 50 (6.7) 100 (13.3) kPa
CNIBP
DIA OFF OFF mmHg
Master 1 to 3
MEAN OFF OFF kPa
*1 Only available when the Arrhythmia Type is set to Extended on the bedside
monitor.
*2 The settings are synchronized with the HR alarm limits settings. The values
cannot be set on the Arrhythmia Alarm Master setting window.
ST Alarm Master
The factory default settings are the same as those on the ST Alarm window.
Alarm
Alarm Item Lower Limit Upper Limit Unit
Master
ST Master 1 to 3 OFF OFF mV
Pre-registration
Factory
Copy Backup
Setting Item Setting Range Default
Settings Settings 7
Setting
Up to 10 alphanumeric
Bed Name BED-001 to 064
characters
Up to 8 alphanumeric Refer to “Pre-
Group Name
Group Color characters registration” in
Group Color 32 colors Section 6-1.
Up to 8 alphanumeric
Pause Reason ―
characters
15 min, 30 min, 1 hour, 2 NO OK
Pause hours, 3 hours, 4 hours, 5 Refer to “Pre-
Pause Time hours, 6 hours, 8 hours, 10 registration” in
hours, 12 hours, 24 hours, Section 6-1.
Free
4 alphanumeric characters
Channel ―
(A to F, 0 to 9)
Up to 20 alphanumeric
Hospital Name ―
characters
ORG Setting
Factory
Copy Backup
Setting Item Setting Range Default
Settings Settings
Setting*1
Select from 16 groups in the
Group General
network
1001-6080, 7001-7997, A000- ― ―
Channel 1001-6080
C0FE, 8001-8009, 9001-9479
Antenna Antenna-1, Diversity Antenna-1
ORG Setting Telemetry Alarm
1 min, 2 min, 3 min 2 min NO OK
Silence Time
Arrhythmia Type Standard, Extended Standard
Select from the registered bed names (Up to 64
Bed Name
ZR Setting bed) or up to 10 alphanumeric characters
Type A, C (display only)
RSSI RSSI Mode ON, OFF OFF
HR, PR, ST, SpO2,
RR, PRESS, NIBP, CRISIS, WARNING, WARNING
Alarm Level (Limits)
APNEA(T), ETCO2 ADVISORY
TEMP ADVISORY
EXT TACHY
CRISIS
EXT BRADY
VPC RUN*2
V BRADY*3
SV TACHY*3
WARNING
TACHYCARDIA
BRADYCARDIA
PAUSE*3 ― ―
COUPLET
Alarm Level EARLY VPC CRISIS, WARNING,
(Arrhythmia) MULTIFORM ADVISORY
V RHYTHM* 3
BIGEMINY
TRIGEMINY*3
ADVISORY
FREQ VPC
IRREGULAR RR*3
PROLONGED RR
NO PACER PULSE*3
PACER NON-
CAPTURE*3
ECG Check Electrode WARNING, ADVISORY ADVISORY
SpO2 Probe Off WARNING, ADVISORY ADVISORY
Alarm Level (Technical)
ECG Noise WARNING, ADVISORY WARNING
Signal Loss WARNING, ADVISORY ADVISORY
* The default settings depend on the multiple patient receiver except for the [Telemetry Alarm Silence Time] setting.
1
*2 When the multiple patient receiver is not correspond to “Extended”, the default setting of VPC RUN is ADVISORY.
*3 Available when the arrhythmia type of the multiple patient receiver is “Extended”.
Factory
Copy Backup
Setting Item Setting Range Default
Settings Settings
Setting
Patient Attribute Input Device OFF, Bar Code Reader OFF
Read Patient ID Enable, Disable Disable
Patient ID Offset 0 to 259
SETUP 0
Length 0 to 16
Read Patient Name Enable, Disable Disable
Offset 0 to 259
0
Settings Length 0 to 16
Name
Char Code ASCII (fixed)
ON, OFF OFF
Name Division Code
ON: 00 to FF 0
Read Date of Birth Enable, Disable Disable
Offset 0 to 259 0 NO OK 7
Year
Length 4 (fixed)
Date of
Offset 0 to 259 0
Birth Settings Month
Length 2 (fixed)
Offset 0 to 259 0
Day
Length 2 (fixed)
Read Gender Enable, Disable Disable
Offset 0 to 259 0
Gender
Length 1 (fixed)
Gender
Settings Male M
Identification
Female 0 to 8 F
Code
Unknown U
External Output
Copy Backup
Setting Item Setting Range Factory Default Setting
Settings Settings
• Screen
Overview, Discharged
Patients List, System
Overview, Discharged
Setup, All Beds Alarm
Patients List, Touchkeys Off,
All Beds Function Events, All Beds Limits
All Beds All Beds Alarm Events, All NO OK
Keys • Operation
Beds Limits, Alarm Check,
Touchkeys Setting,
Record All
Touchkeys Off, Alarm
Check, Record All
• None
• Screen
Individual Waveforms
• Personal Setup
Admit/Discharge, Alarm
Limits, Arrhythmia Alarm, 7
ST Alarm
• Other Setup
All Beds Screen Setup,
Individual Bed Screen
Setup, Parameter Priority,
Function Keys, Recording,
Report
Admit/Discharge, Alarm
• Parameter Setup
Limits, All Beds Screen
Individual ECG, RESP, SpO2, NIBP,
Individual Setup, Tabular Trend, NO OK
Function Keys PRESS, TEMP
Arrhythmia Recall, Event
• Review
List
Trend, Tabular Trend, Full
Disclosure, Expanded
Waveform, ST Recall,
Arrhythmia Recall,
Hemodynamics List,
ECG 12 Lead Analysis,
Event List, Alarm Events,
Review*
• Operation
NIBP Measurement, Learn
ECG
• None
* The Review window that is displayed when [Review] on the Individual Bed window is touched is displayed. (Default:
Custom Review)
Mouse Setting
Copy Backup
Setting Item Setting Range Factory Default Setting
Settings Settings
Default: This central monitor is set as the mouse controller
on the lower center of the display placement image.
Mouse Controller
When the central monitor is set to dual display, the central
monitor is set on the lower center and right. NO OK
After setting mouse controller, set the place of other central
Applicable Display monitors that is controlled by the mouse.
Default: vacant
Copy Backup
Setting Item Setting Range Factory Default Setting
Settings Settings
Channel ch-1 to ch-9, ALL ALL NO OK
Group Name
Copy Backup
Setting Item Setting Range Factory Default Setting
Settings Settings
General, CCU, CCU-1,
CCU-2, ER, ICU, ICU-1,
Group Name Up to 8 alphanumeric letters ICU-2, OR, Post CCU, NO OK
Recovery, Tele-1, Tele-2,
Tele-3, Tele-4, Tele-5
Network Setting
Copy Backup
Setting Item Setting Range Factory Default Setting
Settings Settings
IP
Address Set according to the network
Monitor Subnet which is connected to LAN
0.0.0.0
Network Mask 0 connector of the central
Default monitor.
Gateway
Network NO
IP
Address Set according to the network
Hospital Subnet which is connected to LAN
0.0.0.0
Network Mask 2 connector of the central
Default monitor.
Gateway NO
General, CCU, CCU-1,
CCU-2, ER, ICU, ICU-1,
Select from registered 16
Central Group ICU-2, OR, Post CCU,
group
Recovery, Tele-1, Tele-2,
Tele-3, Tele-4, Tele-5
Extended Network ON, OFF OFF OK
Extended
Set according to the network
Extended Network
IP which is connected to LAN
Network 1 to 0.0.0.0
Address 0 connector of the central
Extended
monitor.
Network 4
Copy Backup
Setting Item Setting Range Factory Default Setting
Settings Settings
Manual, Synchronized to
Time Setting Mode Manual OK
NTP Server
Year
Month
Day
Manual Settings Any value Current time NO
Hour
NO
min
sec
Synchronized to NTP Server IP Set depending on the NTP
0.0.0.0
NTP Server Address server
Specifications....................................................................................................................................................... 8.3
Function...................................................................................................................................................... 8.3
Display............................................................................................................................................. 8.3
Full Disclosure Window.................................................................................................................... 8.4
Arrhythmia Recall Window............................................................................................................... 8.4
ST Recall Window............................................................................................................................ 8.4
Trend Window................................................................................................................................... 8.4
Hemodynamics List Window............................................................................................................ 8.4
ECG 12 Lead Analysis Window....................................................................................................... 8.5
Report Window................................................................................................................................. 8.5
Overview Bed Window..................................................................................................................... 8.5
Alarm................................................................................................................................................ 8.5
8
Recording......................................................................................................................................... 8.5
Printing............................................................................................................................................. 8.6
Operation......................................................................................................................................... 8.6
Sound and Light Output................................................................................................................... 8.6
Data Output...................................................................................................................................... 8.6
Network............................................................................................................................................ 8.6
System Settings............................................................................................................................... 8.6
Saving Data...................................................................................................................................... 8.6
Performance..................................................................................................................................... 8.7
LCD Display..................................................................................................................................... 8.7
Environment..................................................................................................................................... 8.7
Power Requirements........................................................................................................................ 8.7
Acoustic Energy (noise)................................................................................................................... 8.8
Mechanical Strength........................................................................................................................ 8.8
Dimensions and Weight (approximate, without protrusion).............................................................. 8.8
Safety Standard............................................................................................................................... 8.8
Electromagnetic Compatibility.......................................................................................................... 8.9
Electromagnetic Emissions............................................................................................................ 8.10
Electromagnetic Immunity.............................................................................................................. 8.10
Recommended Separation Distances between Portable and Mobile RF Communications
Equipment...................................................................................................................................... 8.12
System Composition for EMC Test................................................................................................. 8.12
Restriction of Radio Equipment (European Union countries only)................................................. 8.13
European Community CE Notice................................................................................................... 8.13
General Requirements for Connecting Medical Electrical Systems................................................................... 8.14
Connector Pin Assignment................................................................................................................................. 8.16
PU-621R Central Monitor Processing Unit............................................................................................... 8.16
DVI Connector................................................................................................................................ 8.16
Analog VGA Connector.................................................................................................................. 8.16
LAN 0 to 2 Connector..................................................................................................................... 8.16
USB 0 to 5 Connector.................................................................................................................... 8.17
Specifications
Function
Display
All Beds screen
Number of patients: Up to 32 patients
Number of waveform traces: More than 1 trace/patient (Up to 16 patients)
Sweep speed: 6.25, 25, 50 mm/s (when 24 inch LCD display is used)
Waveform selection: Maximum 16 traces/auto
Waveform display: ECG, IBP, respiration wave, EEG, ETCO2, external input, pulse wave (SpO2),
FLOW/Paw, others depends on the connected bedside monitor or transmitter
Number of numeric data: More than 3 parameters/patient (less than 3 parameters are also available)
Numerical selection: Up to 17 parameters/auto
Numeric data display: Heart rate, VPC rate, respiration rate, pulse rate, IBP (systolic, diastolic, mean),
NIBP (systolic, diastolic, MAP), temperature, ΔT, blood temperature, ETCO2,
tcPO2, tcPCO2, SpO2, ST level, O2, CO, CCO, PiCCO, ventilator, anesthetic gas, 8
BIS, others depends on the connected bedside monitor or transmitter
Numeric data display size: Numeric data display size depends on the parameters
Waveform and numeric data display color: 32 colors
Alarm indication: Displays for each bed. Frame of alarmed bed lights or blinks*, highlighted
message for arrhythmia (when arrhythmia is detected)*, highlighted numeric
data (when vital signs alarms are generated)*, alarm sound* (Volume can be
adjusted.* Minimum volume is more than 45 dB. Minimum volume can be set
by the administrator.), alarm indicator lights
* Essential performance in EMC standard
Alarm silence: Displays alarm silence mark or silence mark with remaining minutes.
Alarm can be silence for each patient.
Recording: Alarm recording, manual recording, all beds recording
Alarm recording starts when an alarm is generated even which screen is
displayed.
Sync sound: Displays QRS sync mark at the selected patient data display area. Sync sound is
generated from the speaker (volume can be adjusted). Sync sound is generated
even which screen is displayed. Alarm indicator lights.
Alarm silence: Displays alarm silence mark or silence mark with remaining minutes.
Alarm can be silence for each bed.
Patient settings: Patient information can be entered when admitting or discharging the patient.
Receiving channel number can be set when using the multiple patient receiver.
Alarm settings can be changed.
Recording: 10 seconds of waveforms (on the network printer), manual recording
ST Recall Window
Display formats: ST file display, comparison display
Number of recall files: Up to 120 hours/bed
ST recall file recording: Recorder, network printer
Trend Window
Display formats: Trendgraph, tabular trend
Display times: Up to 120 hours/bed
Zoom in display: 1, 2, 4, 8, 12, 24, 48, 96 or 120 hours
Display interval: 1, 2, 5, 10, 15, 30, 60 minutes at NIBP measurement
Parameters: Depends on the connected bedside monitor
Trend recording: Network printer
Tabular trend recording: Network printer
NIBP trend recording: Network printer
Report Window
Printing: Network printer
Printing type: Manual, periodic
Printing items: Bed name, patient information, comment, tabular trend, trendgraph, full
disclosure waveform, expanded waveform, event list, arrhythmia
recall, ST recall, hemodynamics list, ECG 12 lead analysis, alarm event
Printing settings: Interval, printing start time, printing end time 8
Alarm
Alarm indication: Frame of alarmed bed lights or blinks*, highlighted message*, highlighted
numeric data*, alarm sound* and alarm indicator
* Essential performance in EMC standard
Alarm type: Arrhythmia, vital signs, technical
Setting method: Default setting applies unless the setting is changed. Settings can be changed on
the Alarm Master window. A group of alarm items can be set all together to one
group of preset setting.
Alarm silence: Alarm silence key is available on each screen.
Alarm On/Off: Available on each bed
Alarm setting range: Depends on the connected bedside monitor
Alarm history: Displayed by event list
Alarm volume: 45 to 85 dB (A) (Requirement of IEC 60601-2-49: 2001) (at 1 m in front of
central monitor) Crisis ≥ Warning ≥ Advisory
Alarm delay time
Delay between alarm occurrence on the central monitor and output of the alarm signal from a device that generates
alarm in the network: ≤4s
Recording
Record unit: WS-960P Recorder Unit
Record type: Manual recording, automatic alarm recording, periodic recording, remote
recording
Recorded items: Patient information, 3 traces of waveforms, waveform information, measurement
data, date and time, recording type and paper speed
Record color: Monochrome
Printing
Print device: Network printer
Print type: Manual recording or periodic recording
Printed items: Patient information, up to 16 traces of waveforms, waveform information,
measurement data, date and time, print type, paper speed
Print color: Monochrome, color
Operation
Touch panel (touch panel/LCD display with speaker), keyboard (option) and
mouse (option)
Data Output
Available through network
Network
This central monitor has a LS-NET interface and connect to other LS-NET
communication devices and display patient data. Through the LS-NET interface,
data can be output. The communication method complies with the Ethernet
standard.
System Settings
Information: Displays the version and password window.
Environment: Settings for the system such as unit settings.
Bed composition: Select the bed to be monitored always or only displays waveform.
ORG: Settings for the ORG-9100 series multiple patient receiver.
Recorder: Settings for recording.
Mouse: Setting the available range of network mouse.
Parameters: Selecting parameters.
Name registration: Editing the group name.
Waveform color: Setting for waveform display color.
Alarm master: Registering or changing the alarm master.
Function keys: Assigning functions to function keys.
Alarm volume: Setting for the alarm volume.
QRS sync sound: Setting for the QRS sync sound.
Touch panel: Calibrating the touch panel.
Date & Time: Setting for the date and time.
Maintenance: Displays the Maintenance window.
Saving Data
When monitoring a bedside monitor with several central monitors, the data is saved in the one central monitor and other
central monitor refer the data from the central monitor.
Performance
Display type: 24 inch LCD
Resolution (Maximum): 1920 × 1200 dots
Sweep speed: 6.25, 25, 50 mm/s
Memory: More than 1 GB
Processor: Core2Duo 2.2 GHz or better
Bulit-in display interface (compatible with WUXGA)
Built-in USB interface
Built-in sound interface
Built-in network interface
Large-capacity HDD: More than 160 GB
3-ch Recorder (option)
Recording paper: 50 mm width
Paper speed: 25, 50 mm/s
Number of channels: 3
Network printer
Paper size: A4, letter
USB I/F: Touch panel, mouse, bar code reader, USB-serial conversion cable 8
COM I/F: Alarm indicator, 3-ch recorder
PS/2 I/F: Keyboard
OS: Windows XP Embedded
Keyboard, mouse and bar code reader: Available as an option
LCD Display
LCD display: Local purchase
Environment
Operating environment
Temperature: 10 to 40°C (50 to 104°F)
Humidity: 30 to 85%
30 to 80% (PU-621R)
(10 to 40°C, noncondensing)
Atmospheric pressure: 700 to 1060 hPa
Transport and storage environment
Temperature: –20 to +65°C (–4 to +149°F)
–20 to +60°C (PU-621R) (–4 to +140°F)
–15 to +55°C (recording paper) (5 to 131°F)
Humidity: 10 to 95%
10 to 90% (noncondensing) (PU-621R)
Atmospheric pressure: 700 to 1060 hPa
Power Requirements
Line voltage: AC 100 to 240 V
Line frequency: 50, 60 Hz
Power consumption: 180 VA
Rated current: 4.8 to 1.9 A
Mechanical Strength
STATIONARY type
Safety Standard
Safety standard: IEC 60601-1-1: 2000
IEC 60950-1: 2005*1
IEC 60601-1: 1988*2
IEC 60601-1 Amendment 1: 1991*2
IEC 60601-1 Amendment 2: 1995*2
IEC 60601-1-2: 2001
IEC 60601-1-2 Amendment 1: 2004
IEC 60601-1-4: 1996
IEC-60601-1-4 Amendment 1: 1999
IEC 60601-1-6: 2004
IEC 60601-1-8: 2006
CAN/CSA C22.2 No.60950-1-07*3
CAN/CSA C22.2 No.601-1 M90: 1990*4
CAN/CSA C22.2 No.601-1 1S1-94: 1994*4
CAN/CSA C22.2 No.601-1B-98*4
*1 IEC 60950-1: 2005 applies to the following items.
• PU-621R Central Monitor Processing Unit (Op No. 21K)
• YL-611P/YL-612P Alarm Indicator
• YS-098P1/YS-098P2 Additional Alarm Indicator Unit
• YS-097P5/YS-097P6 VL Cable Set (Main)
• YS-097P8/YS-097P9 VL Cable Set (Second)
*2 IEC 60601-1: 1988, IEC 60601-1 Amendment 1: 1991 and IEC 60601-1
Amendment 2: 1995 applies to the following items.
• WS-960P Recorder Unit
• SC-611R WS-960P Power Supply
*3 CAN/CSA C22.2 No.60950-1-07 applies to the following items.
• PU-621R Central Monitor Processing Unit (manufactured by PFU
LIMITED, Op No. 21A)
• YL-611P/YL-612P Alarm Indicator
• YS-098P1/YS-098P2 Additional Alarm Indicator Unit
• YS-097P5/YS-097P6 VL Cable Set (Main)
• YS-097P8/YS-097P9 VL Cable Set (Second)
*4 CAN/CSA C22.2 No.601-1 M90: 1990, CAN/CSA C22.2 No.601-1 1S1-94:
1994 and CAN/CSA C22.2 No.601-1B-98 applies to the following items.
• WS-960P Recorder Unit
• SC-611R WS-960P Power Supply
Electromagnetic Compatibility
IEC 60601-1-2: 2001
IEC 60601-1-2 Amendment 1: 2004
Electromagnetic Emissions
This Model CNS-6201 is intended for use in the electromagnetic environment specified below.
The customer or the user of the CNS-6201 should assure that it is used in such an environment.
Electromagnetic Immunity
This Model CNS-6201 is intended for use in the electromagnetic environment specified below.
The customer or the user of the CNS-6201 should assure that it is used in such an environment.
Immunity test IEC 60601 test level Compliance level Electromagnetic environment - guidance
Electrostatic discharge ±6 kV contact ±6 kV contact Floors should be wood, concrete or ceramic
(ESD) ±8 kV air ±8 kV air tiles. If floors are covered with synthetic
IEC 61000-4-2 material, the relative humidity should be at least
30%.
Electrical fast ±2 kV for power ±2 kV for power Mains power quality should be that of a typical
transient/ burst supply lines supply lines commercial or hospital environment.
IEC 61000-4-4 ±1 kV for input/output ±1 kV for input/output
lines lines
Surge ±1 kV differential ±1 kV differential Mains power quality should be that of a typical
IEC 61000-4-5 mode mode commercial or hospital environment.
±2 kV common mode ±2 kV common mode
Voltage dips, short <5% UT (>95% dip in <5% UT (>95% dip in Mains power quality should be that of a typical
interruptions and UT) for 0.5 cycles UT) for 0.5 cycles commercial or hospital environment.
voltage variations on If the user of the CNS-6201 requires continued
power supply input 40% UT (60% dip in 40% UT (60% dip in operation during power mains interruptions, it
lines UT) for 5 cycles UT) for 5 cycles is recommended that the CNS-6201 be powered
IEC 61000-4-11 from an uninterruptible power supply or a
70% UT (30% dip in 70% UT (30% dip in battery.
UT) for 25 cycles UT) for 25 cycles
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
*1 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 CNS-6201 is used exceeds the applicable RF
compliance level above, the CNS-6201 should be observed to verify normal operation. If abnormal performance is
observed, additional measures may be necessary, such as re-orienting or relocating the CNS-6201.
*2 Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
When more than one electrical instrument is used, there may be electrical
potential difference between the instruments. Potential difference between
instruments may cause current to flow to the patient connected to the
instruments, resulting in electrical shock (micro shock). Therefore, electrical
instruments must be appropriately installed as specified in IEC 60601-1-1: 2000
Second edition.
KEY TO TABLE
• Additional protective earth: If necessary, provide additional protective
earthing, which is permanently connected (see also 58.201).
NOTE Equipment modification may be required.
• Separating transformer: If necessary, limit the ENCLOSURE LEAKAGE
CURRENT, by using an additional separating transformer according to annex
EEE.
NOTE 1 No equipment modification is required.
NOTE 2 A separating transformer is a transformer with one or more input
winding(s) separated from the output winding(s) by at least basic insulation
[IEC 60989].
• SEPARATION DEVICE: If necessary, apply SEPARATION DEVICE.
• IEC 60601: MEDICAL ELECTRICAL EQUIPMENT in compliance with IEC
60601.
• IEC XXXXX: Non-medical equipment in compliance with relevant IEC safety
standards.
LAN 0 to 2 Connector
Connection cable: Network cable (CAT 5)
8 Pin Assignment:
USB 0 to 5 Connector
Connection cable:
1
• USB 0 connector: USB cable in the VL cable set (main)
• USB 1 connector: USB cable in the VL cable set (sub)
4
• USB 2 connector: Mouse cable
• USB 3-5 connector: Bar code reader cable
Pin Assignment:
LINE-OUT Connector
Connection cable: Speaker cable of the VL cable set (main)
Pin Assignment:
Thank you for purchasing the QP-625P 16 Patient Software, QP-626P 24 Patient
Software or QP-627P 32 Patient Software. The unlock code is required to use
this software. We will send you the unlock code within three days after we
receive your registration form.
To confirm the registration code or install the software, refer to Section 6-2
“Installing the Expansion Program Software”.
Please complete the following form. Otherwise, Nihon Kohden cannot send you
the unlock code.
Hospital/Institution
Address
Phone Number
Fax Number
Date of Purchase