Huntleigh Smartsigns Liteplus User manual

2
Notice
This document contains proprietary information that is protected by copyright. All Rights
Reserved. Reproduction, adaptation, or translation without prior written permission is prohibited,
except as allowed under the copyright laws.
Warranty
The information contained in this document is subject to change without notice.
Huntleigh Healthcare Ltd makes no warranty of any kind with regard to this material, including,
but not limited to, the implied warranties or merchantability and fitness for a particular purpose.
Huntleigh Healthcare Ltd shall not be liable for errors contained herein or for incidental or
consequential damages in connection with the furnishing, performance, or use of this material.
Revision History
The documentation part number and revision number indicate its current edition. The revision
number changes when a new edition is printed in accordance with the revision history of the
documentation. Minor corrections and updates which are incorporated at reprint do not cause
the revision number to change. The document part number changes when extensive technical
changes are incorporated.

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Table of Contents
Contents
1. General Safety Information................................................5
1.1 Warnings.................................................................................................. 5
1.2 Cautions................................................................................................... 7
2. Introduction........................................................................8
2.1 Features of the Smartsigns®Liteplus....................................................... 8
2.2 Intended Use............................................................................................ 9
2.3 About This Manual................................................................................... 9
3. Description of Controls, Indicators, Symbols and
Displays ..............................................................................10
3.1 Identification of Front Panel Controls and Symbols................................. 10
3.2 Identification of Rear Panel Components and Symbols........................... 11
3.3 Description of Symbols/ Indicators........................................................... 12
3.4 Description of Controls............................................................................. 16
4. Setting up the Monitor........................................................17
4.1 Unpacking and Inspection........................................................................ 18
4.2 List of Components.................................................................................. 18
4.3 Power Cable Connections ....................................................................... 19
4.4 Measurement Cable Connections............................................................ 20
4.5 SpO2 Cables and Sensors ...................................................................... 20
4.6 Temperature Probes ................................................................................ 21
5. Battery Operation...............................................................22
5.1 Operating on Battery Power..................................................................... 22
5.2 Charging a Low Battery ........................................................................... 23
5.3 Low Battery Indication.............................................................................. 23
6. Using the Monitor...............................................................24
6.1 Turning on the Monitor............................................................................. 24
6.2 Performing Power On and Self-Test (POST)........................................... 25
6.3 Setting Date and Time............................................................................. 26
6.4 Setting Patient Type................................................................................. 28
6.5 Setting NIBP Units ................................................................................... 29
6.6 Setting Temperature Units and Modes..................................................... 30
6.7 Setting Pulse Tone Volume...................................................................... 31
6.8 Setting Alarm Volume .............................................................................. 32
6.9 Resetting to Factory Defaults................................................................... 33
7. NIBP Monitoring..................................................................34
7.1 General.................................................................................................... 35
7.2 Setup Connections................................................................................... 36
7.3 NIBP Measurement Modes...................................................................... 37
7.4 Description of NIBP Operation................................................................. 37
8. SpO2/Pulse Rate Monitoring...............................................41
8.1 General.................................................................................................... 42
8.2 Setup Connections................................................................................... 43
8.3 Description of Pulse Rate Operation........................................................ 44
8.4 Description of SpO2 Operation................................................................ 44
9. Temperature Monitoring.....................................................46
9.1 General.................................................................................................... 47
9.2 Setup Connections................................................................................... 47
9.3 Temperature Measurement Modes.......................................................... 48
9.4 Description of Temperature Operation..................................................... 48

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Table of Contents
10. Alarms And Limits ............................................................54
10.1 General.................................................................................................... 54
10.2 Setting Alarm Limits................................................................................. 55
10.3 Alarm Silence........................................................................................... 61
10.4 Verifying Visual and Audible Alarm Indication.......................................... 61
11. Reviewing Patient Data ....................................................62
11.1 General.................................................................................................... 62
11.2 Displaying Stored Patient Data................................................................ 62
11.3 Printing Stored Patient Data (Optional Printer Installed).......................... 64
11.4 Erasing Patient Data................................................................................ 64
12. Printing..............................................................................65
12.1 General.................................................................................................... 65
12.2 Selecting Manual or Stream Printing type................................................ 65
12.3 Printing Patient Data (Manual Mode)....................................................... 66
12.4 Print Out Configuration ............................................................................ 67
13. RS232 Interface................................................................70
13.1 Overview.................................................................................................. 70
13.2 Cable Connection .................................................................................... 70
13.3 Nurse Call Interface................................................................................. 71
14. Maintenance .....................................................................72
14.1 General.................................................................................................... 72
14.2 Returning the Smartsigns®Liteplus and System Components................ 72
14.3 Service..................................................................................................... 72
14.4 Periodic Safety Checks............................................................................ 72
14.5 Cleaning................................................................................................... 73
14.6 Battery maintenance................................................................................ 73
14.7 Replacement of Printer Paper.................................................................. 74
15. Troubleshooting................................................................75
15.1 General.................................................................................................... 75
15.2 Corrective Action...................................................................................... 76
15.3 EMI (Electromagnetic Interference)......................................................... 77
15.4 Obtaining Technical Assistance............................................................... 78
16. Factory Defaults ...............................................................79
16.1 General.................................................................................................... 79
16.2 Parameter Ranges and Default Settings ................................................. 79
17. Specifications ...................................................................80
17.1 Physical.................................................................................................... 80
17.2 Electrical .................................................................................................. 80
17.3 Environmental.......................................................................................... 80
17.4 Measurement Parameters ....................................................................... 81
17.5 Compliance.............................................................................................. 83
17.6 Manufacturer’s Declaration...................................................................... 86
.... Service Returns ....................................................................................... 90

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1. General Safety Information
This section contains important safety information related to general use of the
Smartsigns®Liteplus vital signs monitor. Other important safety information appears
throughout the manual
Important! Before using this equipment, please study this manual carefully and
familiarise yourself with the controls, display features and operating techniques.
Ensure each user fully understands the safety and operation of the unit, as
misuse may cause damage to the unit or injury to the user or patient.
1.1 Warnings
Warnings are identified by the WARNING symbol shown and alert you to potential
hazards.
WARNING: In the USA, do not connect to an electrical outlet controlled by a
wall switch as the device may be accidentally turned off.
WARNING: If in doubt about the integrity of the AC power source, the
monitor must be operated from its internal battery.
WARNING: Do not disconnect a power cord before the system shuts down
as monitor settings may be lost.
WARNING: As with any medical equipment, carefully route patient cabling to
reduce the possibility of patient entanglement or strangulation.
WARNING: Do not touch the monitor when a defibrillator is being discharged
(electrified), as doing so may cause electric shock. NIBP monitoring only in
this monitor is protected against the discharge of a defibrillator. The other
functions (SPO2, TEMP) are not protected. Please be sure of no other patient
connections, except NIPB, before using the defibrillator.
WARNING: If the monitor does not shut down properly, the settings return to
factory defaults.
WARNING: Check the equipment prior to use and ensure its safe and proper
use.
WARNING: Do not autoclave the monitor.
WARNING: Explosion hazard. Do not use the unit in the presence of
flammable anesthetics or gases. Do not operate in a hyperbaric chamber,
in oxygen-enriched environments, or in any other potentially explosive
environment.
WARNING: Before use, carefully read sensor or probe directions for use,
including all warnings, cautions, and instructions.
General Safety Information

6
WARNING: Do not use damaged cuffs, sensors and other cables. Do not
immerse cuffs, sensors and other cables completely in water, solvents, or
cleaning solutions as the connectors are not waterproof. Do not sterilize
cuffs, sensors and other cables by irradiation, steam, or ethylene oxide.
Refer to each cleaning instructions in the directions for use.
WARNING: If the battery shows any signs of damage, leakage, or cracking, it
must be replaced immediately, by a qualified service person, and only with a
battery approved by the manufacturer.
WARNING: The monitor is intended only as an adjunct in patient assessment.
It must be used in conjunction with clinical signs and symptoms.
WARNING: The measurement of vital signs can be affected by patient
conditions, motions, sensors, environmental condition and electromagnetic
external condition.
WARNING: It is possible that any radio frequency transmitting equipment
and other sources of electrical noise such as cellular phones, due to close
proximity or strength of a source, may result in disruption of performance.
WARNING: To ensure patient safety, do not place the monitor in any position
that might cause it to fall on the patient.
WARNING: Disconnect the monitor and sensors during magnetic resonance
imaging (MRI) scanning. Use during MRI could cause burns or adversely
affect the MRI image or the monitor’s accuracy. Also, to avoid burns, remove
the sensors from the patient before conducting MRI.
WARNING: During prolonged and continuous SpO2monitoring, check the
sensor site at least once every 4 hours. Inspect the patient’s skin integrity
and circulation, and relocate the sensor if necessary. Tissue damage can
result from improper or prolonged sensor attachment.
WARNING: Do not lift the monitor by a sensor cable or a power cord because
the cable could disconnect from the monitor, causing the monitor to drop on
the patient.
WARNING: The unit may not operate effectively on patients who are
experiencing convulsions or tremors.
WARNING: To avoid burns, the temperature probe must remain in the probe
well when turning the monitor on or off.
WARNING: Do not connect more than one patient to the monitor. Do not
connect more than one monitor to a patient.
General Safety Information

7
1.2 Cautions
CAUTION: U.S. Federal law restricts this device to sale by or on the order of a
licensed healthcare practitioner.
CAUTION: Alert you to exercise care necessary for the safe and effective use of
Smartsigns®Liteplus monitor. Inaccurate data may be measured if operated or
stored at conditions outside the stated ranges, or subjected to excessive shock or
dropping.
CAUTION: Grounding reliability can only be achieved when equipment is connected
to an equivalent receptacle marked ‘Hospital Only’ or ‘Hospital Grade’.
CAUTION: The accuracy of the monitor may degrade if the monitor is connected to
secondary I/O devices when the monitor is not connected to earth reference.
CAUTION: Never place fluids on the monitor. In case of fluid spilling on the monitor,
disconnect power cord, wipe clean immediately and have the monitor serviced to
ensure that no hazard exists.
CAUTION: The monitor may display error codes when outside of the measurable
range occur.
CAUTION: Accessory equipment connected to the monitor’s data interface must be
certified according to IEC60950 for data processing equipment or IEC60601-1 for
electromedical equipment. All combinations of equipment must be in compliance
with IEC60601-1-1 system requirements. Anyone who connects additional
equipment to the signal input or signal output port configures a medical system and
is therefore responsible that the system complies with the requirements of
IEC60601-1-1 and the electromagnetic compatibility standard IEC60601-1-2. If in
doubt, contact Huntleigh Healthcare Technical Services Department.
General Safety Information

8
2. Introduction
WARNING: The Smartsigns®Liteplus is intended only as an adjunct in
patient assessment. It must be used in conjunction with clinical signs and
symptoms.
This manual contains information about the Smartsigns®Liteplus vital signs monitor. The
Smartsigns®Liteplus is available in the following configurations:
Config. Features
NB Standard (NIBP + Pulse Rate + Ni-MH Battery)
NSB Standard + SpO2
NTB Standard + Temperature
NSTB Standard + SpO2+ Temperature
NPB Standard + Printer
NSPB Standard + SpO2+ Printer
NTPB Standard + Temperature+ Printer
NSTPB Standard + SpO2+ Temperature + Printer
Note: Refer to Specification Section for more information about each configuration.
All information in this manual, including the illustrations, are based on a monitor
configured with the NIBP, Temperature, SpO2, and Printer options. If your monitor
configuration lacks any of these options, certain information in this manual does
not apply.
2.1 Features of the Smartsigns®Liteplus
Physical
The Smartsigns®Liteplus vital signs monitor is a lightweight and compact vital signs
monitor measuring 130×180×284 (mm) (H×D×W) and weighing 2.7 kg. Its carrying handle
is designed for instrument transport while battery-powered monitoring.
Electrical
The monitor is powered by a Ni-MH type of internal battery pack. The batteries are
continuously recharged when AC power (100-240 VAC, 50-60 Hz) is connected to the
monitor. Details are described in the Battery Operation section.
Introduction

9
Display
The monitor has an LED display which shows numeric patient information as well as
alphanumeric status conditions and error codes.
Auxiliary Outputs
The monitor provides RS-232 I/O port for software upgrade or nurse call system. Refer to
the RS-232 Interface section for additional information.
2.2 Intended Use
The purpose and function of the Huntleigh Healthcare Smartsigns®Liteplus vital signs
monitor is to monitor non-invasive blood pressure (systolic, diastolic, and mean arterial
pressures), functional arterial oxygen saturation, pulse rate for adult, pediatric and
neonate patients and temperature for adult and pediatric patients in all hospital areas
and hospital-type facilities. It may be used during hospital transport and in mobile, land-
based environments, such as ambulances, within the specification of the environmental
characteristics.
Note: Hospital use typically covers such areas as general care floors, operating
rooms, special procedure areas, intensive and critical care areas, within the
hospital plus hospital-type facilities. Hospital-type facilities include physician
office based facilities, sleep labs, skilled nursing facilities, surgicenters, and
sub-acutecenters.
Note: Intra-hospital transport includes transport of a patient within the hospital or
hospital-type facility.
Note: The medically skilled and trained user can be clinicians like doctors and
nurses who know how to take and interpret a patient’s vital signs. These
clinicians must take direct responsibility for the patient’s life. This can include
care-givers or medically trained interpreters who are authorised under the
appropriate clinical facility procedures to support patient care. Any
inappropriate setting, especially the alarm limit or alarm notification settings,
can lead to a hazardous situation that injures, harms or threatens the patient’s
life. This equipment should only be operated by trained users who can adjust
the settings of the patient monitor.
2.3 About This Manual
This manual explains how to set up and use the Smartsigns®Liteplus vital signs monitor.
Important safety information relating to general use of the monitors appears before this
introduction. Other important safety information is located throughout the text where
applicable.
All users should read this manual thoroughly. More experienced users of the
Smartsigns®Liteplus will be able to go to the topics for the information they require.
Read the entire manual including the Safety Information section, before you operate the
monitor.
Introduction

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3. Description of Controls, Indicators,
Symbols and Displays
3.1 Identification of Front Panel Controls and
Symbols
SYS
DIA
MAP
%SpO
2
/min
°F
°C M
mmHg
kPa
BP
1
smartsignsLitePlus
®
1 Blood Pressure Unit Indicators 15 %SpO2Display
2 Systolic Blood Pressure Display 16 Mode Button
3 Patient Type Indicators 17 Pulse Amplitude Indicator
4 Diastolic Blood Pressure Display 18 Alarm Silence Indicator
5 Pulse Rate Display 19 Up/Down Selection Button
6 MAP (Mean Arterial Pressure) Display 20 Alarm silence button
7 Print Setting Indicators 21 NIBP start/stop button
8 Print Button 22 Temperature Unit/Mode Indicators
9 Alarm Button 23 Temperature Display
10 Auto Indicator 24 Power Button
11 Auto Cycle Display 25 Battery Indicator
12 Auto Button 26 Charging/AC in Indicator
13 Pulse Tone/Alarm Volume Setting Indicators 27 Time Display
14 Review Button 28 Review Indicator
Figure 1. Front Panel Controls and Symbols
28
27
26
25
24
23
22
21
20
8 9 10 11 12 13 14 15 16 17 18 19
1
2
3
4
5
6
7
Description of Controls, Indicators, Symbols and Displays

11
3.2 Identification of Rear Panel Components and
Symbols
1 Handle 4 Equipotential (Ground)
2 Air Ventilator 5 Battery Cover (Replacement)
3 AC Power Connector 6 Battery Label
7 RS-232 Data Interface
Figure 2. Rear Panel Components and Symbols
3 4 5 6 7
1
2
Description of Controls, Indicators, Symbols and Displays
NiMH

12
3.3 Description of Symbols/ Indicators
The symbols and Indicators are described as follows:
Table 1. Display Symbols/Indicators
Symbols Description
Attention, consult accompanying documents.
Type BF applied part
Type BF – Defibrillator proof
Equipotentiality
Data interface
Review Indicator
is lit when the user select the Review button to see the patient history.
Auto Indicator
is on whenever NIBP automatic timed cycles are enabled.
Charging/AC in Indicator
is on whenever AC power is present from the wall (even if the monitor is off
and is not under battery charging).
The Charging/AC in indicator flashes while the battery is charging, and then
remains illuminated once the battery is maintained with a trickle charge.
Description of Controls, Indicators, Symbols and Displays

13
Symbols Description
Battery Indicator
indicates the state of the battery. This indicator is on when the monitor
uses battery power. This indicator will be flashing when the battery needs
charging. It is not reset unless AC power cord has been plugged in for
battery charging.
Alarm Silence Indicator
is on continuously whenever the unit is in Alarm Silence mode.
Temperature in degrees Fahrenheit
is configured to display temperature in degrees Fahrenheit.
Temperature in degrees Celsius
is configured to display temperature in degrees Celsius.
Temperature in Monitor mode
is configured to take temperature in the monitor mode. This indicator is off
when the temperature is being taken using the predictive method.
Patient type: Adult
is on when the Patient type is adult.
Patient type: Paediatric
is on when the Patient type is paediatric.
Patient type: Neonatal
is on when the Patient type is neonatal.
NIBP unit: mmHg
is on when the NIBP unit setting is mmHg.
NIBP unit: kPa
is on when the NIBP unit setting is kPa.
Description of Controls, Indicators, Symbols and Displays

14
Symbols Description
Target Pressure Setting Indicator
is flashing when the NIBP target inflation pressure is under the setting for
NIBP measurement.
Time Indicator
is on when the actual time is displayed on the time/date numeric display
area. It is flashing when it is selected to set the time in configuration mode.
Date Indicator
is on when the actual date is displayed on the time/date numeric display
area. It is flashing when it is selected to set the date in configuration mode.
Manual Print Indicator
is on when the print setting is set to Manual Print.
Stream Print Indicator
is on when the print setting is set to Stream Print.
Pulse Tone Volume Setting indicator
is flashing when the pulse tone volume setting is selected in setting mode.
Alarm Volume Setting Indicator
is flashing when the alarm volume setting is selected in setting mode.
Network Indicator
is flashing when the monitor is set to software upgrade mode.
AC Power Rating Input
Disposal Instructions
Description of Controls, Indicators, Symbols and Displays

15
Symbols Description
Manufacturer
Date of Manufacture
CE Mark
PATIENT MONITOR
32MX
E252514
UL60601-1
CAN/CSA C22.2 No.601.1
UL Mark
IPX2 Dust and Water Resistance
REF Reference Number
SN Serial Number
500-1060 hPa
Environmental shipping / storage temperature limitations
50 C
o
-20 C
o
Fragile - Handle with Care
This Way Up
Keep Dry
Description of Controls, Indicators, Symbols and Displays

16
3.4 Description of Controls
Table 2. Controls
Controls Description
Power Button
turns the monitor on or off when pressed for over 1 second.
NIBP start/stop button
initiates NIBP measurement when pressed. If the NIBP start/stop button is
pressed again during the measurement, it will cancel the current reading.
Alarm Silence Button
allows you to silence a patient alarm temporarily and also is used to
acknowledge (cancel) other non-patient alarms.
Up/Down Selection Buttons
allows you to select items within a particular settable feature in several
different modes. If the Up or Down selection button is pressed and held,
the unit will scroll through the available selections as if the button is being
pressed repeatedly while the button is held in.
Print Button (Option)
sends the data to the printer and prints current onscreen readings if a
printer is installed in the monitor. Pressing the Print button during print-out
stops printing.
Review Button
allows the user to review or to erase measurement data in the memory.
If pressed and held for more than 3 seconds, the monitor will erase the
data.
Auto Button
puts the monitor in Auto interval selection mode, allowing the user to take
automatic blood pressures at a selected increment.
Alarm Button
puts the monitor into Alarm Set mode, allowing the user to set alarm limits
for Systolic, Diastolic, MAP, Pulse rate and SpO2.
Mode Button
puts the monitor into the Settings or Configuration mode. Once the
monitor is in one of these modes, the Mode button will be used to cycle
through the configuration options of the specific menu mode.
Description of Controls, Indicators, Symbols and Displays

17
4. Setting up the Monitor
WARNING: The Smartsigns®Liteplus is a prescription device and is to be
operated by qualified personnel only. It is designed for use by medical
clinicians. Although this document might illustrate medical monitoring
techniques, the monitor must be used only by trained clinicians who know
how to take and interpret a patient’s vital signs.
WARNING: In the USA, do not connect to an electrical outlet controlled by a
wall switch because the device may be accidentally turned off.
WARNING: As with all medical equipment, carefully route patient cabling to
reduce the possibility of patient entanglement or strangulation.
WARNING: To ensure patient safety, do not place the monitor in any position
that might cause it to fall on the patient.
WARNING: Do not lift the monitor by the sensor cables or power cord
because the cable could disconnect from the monitor, causing the monitor to
drop on the patient.
WARNING: Disconnect the monitor and sensors/cables during magnetic
resonance imaging (MRI) scanning. Using the monitor during MRI may cause
burns or adversely affect the MRI image or the monitor’s accuracy.
WARNING: To ensure accurate performance or prevent device failure do not
subject the monitor to extreme moisture, such as direct exposure to rain.
Such exposure may cause inaccurate performance or device failure
WARNING: Do not use the Smartsigns®Liteplus vital signs monitor, SpO2
sensors, temperature probes or connectors that appear damaged.
WARNING: Discarded battery may explode during incineration. Follow local
government ordinances and recycle instructions regarding disposal or
recycling of device components, including batteries.
WARNING: Do not touch the monitor when a defibrillator is being discharged
(electrified), as doing so may cause electric shock. NIBP monitoring only in
this monitor is protected against the discharge of a defibrillator. The other
functions (SPO2, TEMP) are not protected. Please be sure of no other patient
connections, except NIPB, before using the defibrillator.
WARNING: Ensure that the speaker is clear of any obstruction. Failure to do
so could result in an inaudible alarm tone.
CAUTION: If the Smartsigns®Liteplus is to be stored for a period of 2 months or longer, it
is recommended to notify service personnel to remove the battery from the monitor prior to
storage. Recharging the battery is strongly recommended when the battery has not been
recharged for 2 or more months.
CAUTION: Recycle used batteries properly. Do not dispose of batteries in refuse
containers.
Setting up the Monitor

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4.1 Unpacking and Inspection
The Smartsigns®Liteplus vital signs monitor is shipped in one carton. Examine the carton
carefully for evidence of damage. Contact Huntleigh Healthcare Ltd Technical Services
Department immediately if any damage is discovered. Return all packing material and
monitor. Refer to the Maintenance section for instructions on returning damaged items.
Set the monitor to the user’s intended position where the user can easily recognise the
visual and audible monitoring conditions. Normally it is recommended to set at a distance
of 1 metre from the user. Also, the viewpoint is at any point within the base of a cone by
an angle of 30° to the centre of the monitoring display.
4.2 List of Components
Quantity Item
1 Smartsigns®Liteplus Vital signs monitor
1 NIBP Cuff adult (23 - 33 cm)
1 NIBP Cuff small adult (17 - 25 cm)
1 NIBP Cuff child (12 - 19 cm)
1 NIBP Hose adult/paediatric
1 Temperature Probe with Temperature option configured
1 Temperature Probe Cover with Temperature option configured
1 SpO2Sensor with SpO2option configured
1 Pulse Oximetry Cable with SpO2option configured
1 Operator’s Manual
1 Power Cord (applicable to country of sale)
1 pack Printer Paper with Printer option configured
A range of additional accessories are available for the Smartsigns®Liteplus.
Please contact the Customer Services Department for more information.
Setting up the Monitor

19
4.3 Power Cable Connections
WARNING: In the USA, do not connect to an electrical outlet controlled by a
wall switch because the device may be accidentally turned off.
CAUTION: For the safety of patients, use only a Huntleigh Healthcare Ltd supplied
power cord. Using a non approved power cord can damage the monitor, and will
void the product warranty. If in doubt about the integrity of the AC power source,
the monitor must be operated from its internal battery.
AC Power
Ensure that the AC outlet is properly grounded and that it is the specified voltage
and frequency (100-240 VAC, 50-60 Hz).
Figure 3. AC Power Connection
1. Connect the female connector end of the AC power cord to the monitor rear
panel connector.
2. Plug the male connector end of the AC power cord into a properly grounded
AC outlet.
3. Verify that the Charging/AC in Indicator is lit. This indicator will be flashing if
the battery needs charging.
4. If necessary, connect the grounding wire. Connect the grounding wire
connector to the equipotential terminal on the rear panel. Attach the clip end
of the grounding wire to the medical equipment grounding terminal on the wall.
Note: If the Charging/AC in Indicator is not lit, check:
• the power cord
• the AC power inlet
AC Power Connector
Setting up the Monitor

20
4.4 Measurement Cable Connections
WARNING: Do not lift the monitor by the sensor cables, or power cord
because the cable could disconnect from the monitor, causing the monitor
to drop on the patient.
NIBP Hoses and Cuffs
SYS
DIA
MAP
%SpO
2
/min
°F
°C M
mmHg
kPa
BP
1
smartsignsLitePlus
®
Figure 4. NIBP Cable Connections
1. Select the appropriate size cuff for the patient (Refer to the NIBP Monitoring
section) and apply the cuff to the selected site.
2. Connect the hose to the right panel NIBP connector (see Figure 4).
Note: For the safety of patients, and to ensure the best product performance
and accuracy, use only a cuff and a hose provided with the Smartsigns®
Liteplus, or a cuff and hose recommended by Huntleigh Healthcare Ltd
Technical Services.
4.5 SpO2 Cables and Sensors
Figure 5. SpO2Sensor/Cable Connections
1. Select an appropriate sensor for the patient and desired application.
2. Apply the sensor to the selected site.
3. Connect the sensor to the cable.
4. Connect the cable to the right panel SpO2 connector (see Figure 5).
NIBP Cuff Hose Connector
SpO2Sensor/ Cable Connector
Setting up the Monitor