Copyright 2007, Welch Allyn. All rights are reserved. No one is permitted to reproduce or duplicate, in any
form, this manual or any part thereof without permission from Welch Allyn.
Welch Allyn assumes no responsibility for injury or for any illegal or improper use of the product that may
result from failure to use this product in accordance with the instructions, cautions, warnings, or
indications for use published in this manual.
Welch Allyn
®
, Acuity®, Micropaq®, FlexNet® and Flexible Monitoring® are registered trademarks of Welch
Allyn, Inc.
Nellcor
®
is a registered trademark of Nellcor Puritan Bennett. Masimo® and SET® are registered trademarks
of Masimo Corporation.
Software in this product is Copyright Welch Allyn or its vendors. All rights are reserved. The software is
protected by United States of America copyright laws and international treaty provisions applicable
worldwide. Under such laws, the licensee is entitled to use the copy of the software incorporated within
this instrument as intended in the operation of the product in which it is embedded. The software may not
be copied, decompiled, reverse-engineered, disassembled or otherwise reduced to human-perceivable
form. This is not a sale of the software or any copy of the software; all right, title and ownership of the
software remain with Welch Allyn or its vendors.
For information about any Welch Allyn product, please call Welch Allyn Technical Support:
USA 800 535 6663
315 685 4560
Canada 800 561 8797China 86 21 6327 9631
European Call Center 353 46 9067790France 33 1 55 69 58 49
Germany 49 7477 9271 86Japan 81 3 3219 0071
Latin America 305 669 9003Netherlands 31 157 505 000
Singapore 65 6419 8100South Africa 27 11 777 7555
United Kingdom 44 1332 363812
Australia 61 2 9638 3000
800 074 793
Reorder Part Number 810-1464-XX
Manual Part Number 810-1177-06 Rev. A, 02/2007
Welch Allyn
8500 SW Creekside Place
Beaverton, Oregon 97008-7101
USA
The following table summarizes the new features that are implemented in this software
version 1.5. The version previously released was 1.4.
FeatureReference
Patient alarm tones are now discontinuous, and
life-threatening alarms beep at a faster pace than
other patient alarms.
If you press to silence a patient alarm tone
and a new patient vital sign alarm or equipment
alert occurs, a tone for the new alarm or alert will
break the silence period at the monitor.
Intended Use
The Micropaq™ monitor is intended to be used by clinicians for single or multiparameter
vital signs monitoring of ambulatory and nonambulatory pediatric and adult patients in
health care facilities. It is also intended for patient transport. The monitor is able to
withstand light rain exposure over short periods of time (uniform distribution of
approximately 1 mm of water/ minute for 10 minutes or less).
See “Respond to a Patient Alarm at
Monitor” on page 36.
The Micropaq monitor is intended to operate with an Acuity
wireless communication over Welch Allyn’s FlexNet
devices to the Acuity Central Station through hardwired Ethernet networks and Wireless
Local Area Networks (WLANs). If the Micropaq monitor is moved out of range or loses
communication with the FlexNet network, it continues to monitor the patient, display
patient data, and generate local patient alarms or alert messages.
•The ECG channel is intended primarily for five-lead ECG monitoring, although
three-lead ECG monitoring is supported.
•The Pulse Oximetry channel is intended for continuous noninvasive monitoring of
functional oxygen saturation of arterial hemoglobin (SpO
(measured by an SpO
sensor).
2
™
network. FlexNet connects multiple
®
Central Station through
) and pulse rate
2
2Chapter 1 General InformationWelch Allyn Micropaq Monitor
The most likely locations for patients monitored by this device are step-down units,
telemetry departments, general medical/surgical floors, emergency departments, and inhospital transport.
This guide was written for clinicians. Although this guide may describe some monitoring
techniques, Welch Allyn expects that the operator is a trained clinician who knows how to
take and interpret a patient’s vital signs.
Federal USA law restricts sale of the device identified in this manual to, or on the order of,
a licensed medical practitioner.
Symbols
Warning Warning statements in this manual identify conditions or practices that could result in personal
injury.
Caution Caution statements in this manual identify conditions or practices that could result in damage to the
equipment or other property.
The following symbols appear on the monitor or accessories.
Li++
Direct currentEnclosure Protection Drip proof: Classification
IPX1
IPX1 per EN60529: 1991
Alternating current (battery charger)Fuse
The CE Mark and Notified Body Registration
Number signify the device has met all essential
requirements of European Medical Device
Directive 93/42/EEC
Signifies the device has met all essential
requirements of European Medical Device
Directive 93/42/EEC for a Class 1 product
C
kj
This device has been tested and certified by
the Canadian Standards Association
International to comply with applicable U.S.
US
and Canadian medical safety standards.
Patient connections are Type CF, isolated for
direct cardiac application, and protected
against defibrillation
(battery charger)
Protective earth ground (battery charger)Protected during defibrillation
Lithium Ion batterySeparate batteries from other disposables for
recycling
Li++
Caution: Refer to Directions For Use and
For indoor use only (battery charger)
accompanying documentation
This way upKeep away from rain
Humidity limitStacking limit (by number)
FragileAltitude limit
Temperature limitsIATA/ICAO Hazard Class 9 Package
(International Air Transport Association/
9
International Civil Aviation Organization)
Non-ionizing electromagnetic radiationSingle use only
Directions for UseChapter 1 General Information3
Monitor Front Panel Keys
Select Key and Silence Patient Alarm/
Equipment Alert Key- Selects the choice
highlighted on the menu. During patient alarms,
silences the tone at the monitor and at Acuity (if
connected) for 90 seconds. During equipment
alerts, silences or acknowledges (dismisses) the
alert.
Nurse Call Key - When connected to Acuity,
pressing this key sends Acuity a Nurse Call
message.
Recycle the monitor and battery
separately from other disposables.
www.welchallyn.com/weee
Battery Charger Label and LEDs
Green LED on continuouslyBattery is fully charged.
Scroll Up Key and Reset Alarm Tone Key-
Scrolls up menus on the display. During patient
alarms, resets the tone at the monitor and at
Acuity (if connected).
Scroll Down Key and Main Menu Key- Pressing
this key scrolls down menus on the display, or
causes the Main Menu to appear if no menu is
displayed.
Green LED flashing
Green LED flashing very slowlyBattery detected and waiting to be charged.
Yellow LED on continuouslySomething is wrong with the battery or the
General Warnings and Cautions
Familiarize yourself with all warnings and cautions before using the monitor.
WARNING When considering a treatment protocol that involves wireless
communication of patient data, be sure to recognize some limitations inherent
in wireless communications. When the monitor is not connected to the
network:
•There are no patient alarms or alerts at the Acuity Central Station.
•Acuity does not perform arrhythmia and ST analysis on the patient data
and does not generate related alarms.
•Patient data is not saved.
•Pressing (Nurse Call) on the monitor does not cause any response
at Acuity.
kj
Battery is charging.
charger. (See
Response”
“Battery Status and Possible
on page 44.)
WARNING Do not try to monitor neonatal patients with the monitor. The
monitor is intended for adult or pediatric patients. It is not intended for use with
pediatric patients (or infants) weighing less than 22 lbs (10 kg).
4Chapter 1 General InformationWelch Allyn Micropaq Monitor
WARNING Always check the patient mode at Acuity when monitoring a new
patient. The patient mode determines default alarm limits and internal algorithm
settings.
WARNING The monitor may not meet its performance specifications if stored
or used outside the specified temperature and humidity ranges.
WARNING Do not connect more than one patient to a monitor. Do not connect
more than one monitor to a patient.
WARNING During defibrillation, keep the discharge paddles away from ECG
and other electrodes, as well as other conductive parts in contact with the
patient.
WARNING Do not operate this product in the presence of flammable
anesthetics or other flammable substances in combination with air, oxygenenriched environments, or nitrous oxide; explosion can result.
WARNING Do not use the monitor in a Magnetic Resonance Imaging (MRI)
suite or a hyperbaric chamber. Such use can cause fire or explosion resulting in
patient injury and monitor damage.
WARNING Electronic equipment that emits strong electromagnetic or radio
frequency signals can cause electrical interference with monitor operation. This
interference may distort the ECG signal, thereby preventing accurate rhythm
analysis. Avoid operating this device near equipment of this type.
WARNING Exposure to Radio Frequency (RF) radiation. To comply with Federal
Communications Commission (FCC) RF exposure requirements, this device
shall be used in accordance with the operating conditions and instructions
provided in this manual, including the section “Install the Carrying Pouch” on
page 28.
WARNING Pacemaker signals can differ from one pacemaker to the next. The
Association for Advancement of Medical Instrumentation (AAMI) cautions that
“in some devices, rate meters may continue to count the pacemaker rate during
occurrences of cardiac arrest or some arrhythmias. Do not rely entirely upon rate
meter alarms. All pacemaker patients should be kept under close or constant
observation.” See “ECG Specifications” on page 50 for disclosure of the
pacemaker pulse rejection capability of this instrument.
WARNING For patients with a pacemaker, position the monitor to maintain a
minimum 6-inch distance between the monitor and pacemaker. Immediately
turn the monitor off and provide appropriate patient care if you have any reason
to suspect that the monitor is interfering with the pacemaker. The Health
Industry Manufacturers Association recommends this minimum 6-inch distance
between a hand-held wireless radio and a pacemaker, which is consistent with
the independent research by, and recommendations of, Wireless Technology
Research.
Directions for UseChapter 1 General Information5
WARNING Make frequent electrical and visual checks on cables, sensors, and
electrode wires. All cables, sensors, and electrode wires must be inspected and
properly maintained and in proper working order to allow the equipment to
function properly and protect patient safety.
WARNING Avoid electrosurgery burns at monitoring sites by ensuring proper
connection of the electrosurgery return circuit so that the return paths cannot be
made through monitoring electrodes and probes.
WARNING Use of ECG cables not specified by Welch Allyn may negate
defibrillator protection and risk patient injury due to shock.
WARNING To ensure patient safety, the conductive parts of the ECG
electrodes (including associated connectors) and other patient-applied parts
should not contact other conductive parts, including earth ground, at any time.
WARNING Motion artifact can affect the accuracy of patient vital sign
measurements. Minimize patient motion whenever possible.
WARNING For best product performance and measurement accuracy, use only
accessories supplied by Welch Allyn or recommended in the Welch Allyn
Products and Accessories booklet (810-0409-XX). Use accessories according to
your facility’s standards and the manufacturer’s recommendations. Always refer
to the manufacturer’s Directions for Use.
WARNING As with all medical equipment, carefully route the patient cabling to
reduce the possibility of patient entanglement or strangulation. Use the supplied
garment clips to secure the cable properly.
WARNING When positioning the monitor pouch on the patient, make sure the
straps do not entangle the patient’s neck or cause choking. Make sure the straps
do not restrict the movement of the patient’s limbs or create a hazard when
walking or moving.
WARNING If a product has been dropped or severely abused, send it to a
qualified service person to confirm proper operation.
Caution Do not autoclave the monitor. Autoclave accessories only if the
manufacturer’s instructions clearly approve it. Many accessories can be severely
damaged by autoclaving.
It is possible for the monitor to detect a problem that prevents the monitor from operating
properly. If this occurs, the monitor displays an error message and error number. Report
such errors to Welch Allyn. The monitor should be serviced only by a Welch Allyn service
technician while under warranty. Contact Welch Allyn for information about post-warranty
period service.
6Chapter 1 General InformationWelch Allyn Micropaq Monitor
Introducing the Monitor
The monitor is a patient-worn vital signs monitor for use by adult or pediatric ambulatory
patients.
•One or two ECG channels displayed
•Up to 2 ECG leads displayed at the monitor:
I, II, III, V, aV
•Up to 7 ECG leads displayed at Acuity:
I, II, III, V, aV
•One ECG lead displayed at the monitor and
at Acuity: Fixed lead II with 3-lead cable, or
5-lead cable with only RA, LA and LL
electrodes attached.
•Pulse oximetry (SpO
404 only)
•Two-way wireless communication within
Welch Allyn’s FlexNet network
•LCD for display of ECG waveforms, SpO
and heart rate/pulse rate data, and
messages from Acuity
•Standalone operation with patient alarms
when out of range of the network
•Patient alarm limits that can be set at the
monitor or at Acuity
•Configurable formats for single- or dual-waveform ECG display
•Internal antenna
•Nurse call key
•Lightweight (slightly more than 1 pound with battery)
•Rugged and tolerant of brief water exposure
•Rechargeable battery
•Sleep mode to extend battery life
, aVL, or aVF with 5-lead cable
R
, aVL, or aVF with 5-lead cable
R
) monitoring (Model
2
2
Model 402
Model 404
ECG monitoring
ECG monitoring and either one of two pulse oximetry (SpO2) monitoring options:
•SpO
•SpO
with Masimo® SET® technology
2
with NELLCOR® OxiMax™ technology
2
Directions for UseChapter 1 General Information7
Understanding the Monitor and the FlexNet Network
The monitor is intended to operate with an Acuity® Central Station as part of Welch Allyn’s
FlexNet network. FlexNet allows multiple devices to communicate through hardwired
Ethernet networks and Wireless Local Area Networks (WLANs). The Acuity Central
Station provides the primary display and entry of patient data for a patient connected to
the monitor.
To Other Acuity
Central Stations
Acuity Central Station
Access Points
H
R
S
p
O
2
80
97
H
R
S
p
O
2
80
97
H
R
S
p
O
2
80
97
Micropaq monitors
H
R
80
S
p
O
2
97
To Other
Access
Points
FlexNet Network
Each patient-worn monitor supports two-way communication with an Acuity Central
Station through an access point in the FlexNet network. The access point is a digital radio
transceiver that connects to the FlexNet network. During monitoring, the monitor sends
the patient data to Acuity. Acuity and the monitor continuously analyze the data. Acuity
provides appropriate alarm or alert messages at the Central Station and other network
devices such as a hallway message panel and the monitor itself. Acuity also stores the
patient data for viewing or report printing.
If the monitor is moved out of range or loses communication with the FlexNet network
and Acuity, it continues to monitor the patient and display patient data. While not
communicating with Acuity, the monitor continues to generate local patient alarms or
alert messages. Patient data is not stored and Acuity does not perform waveform analysis
or generate arrhythmia messages while the monitor is not communicating with Acuity.
When the monitor is returned to within range of the FlexNet network, it automatically
reconnects to Acuity.
8Chapter 1 General InformationWelch Allyn Micropaq Monitor
Monitor Features
Controls and Connectors
SpO2 Connector
ECG Connector
Visual Alarm Indicator
Liquid Crystal Display
Select Key and
Silence Patient Alarm/
Equipment Alert Key
Scroll Up Key and Reset Patient Alarm Tone Key
Scroll Down Key and Main Menu Key
Nurse Call
Key
Battery pack latch
Battery
Back
Directions for UseChapter 1 General Information9
Visual Alarm Indicator
GreenFlashes slowly during normal operation.
RedFlashes during patient alarm, remains on continuously when alarms
are silenced or suspended.
YellowFlashes during an equipment alert or while not connected to the
network.
Remains on continuously if the operator suspends an alert at Acuity
for 90 seconds or acknowledges (dismisses) a low battery alert from
the monitor or Acuity.
Note
The flashing green LED indicates that the monitor is connected to the network
but not necessarily connected to a patient. If the monitor is actively monitoring a
patient, the green LED indicates no alarms or alerts are detected.
Audible Alarm Indicator
Beeps to indicate a patient alarm, and beeps faster for life-threatening arrhythmia
alarms (see “Patient Alarm and Equipment Alert Specifications” on page 55).
Beeps to indicate when the equipment needs attention. This beep tone is slower than
patient alarm tones (see “Patient Alarm and Equipment Alert Specifications” on
page 55).
Volume can be configured as high, low, or off (configured at Acuity).
Volume can be configured differently for network connection or stand-alone operation
(configured at Acuity).
Nurse Call Key
When connected to Acuity, pressing this key sends a Nurse Call message to Acuity.
Depending on how Acuity is configured, this will cause Acuity to:
Generate a Nurse Call Alert at the Acuity Central Station.
Print a “snapshot” of the patient waveform at the Acuity Central Station.
Scroll Up Key and Reset Patient Alarm Tone Key
Scrolls up menus on the display.
Resets a silenced patient alarm tone.
10Chapter 1 General InformationWelch Allyn Micropaq Monitor
Scroll Down Key and Main Menu Key
Scrolls down menus on the display.
Displays the Main Menu.
Select Key and Silence Patient Alarm/Equipment Alert Key
Selects the choice highlighted on the menu.
During patient alarms, silences the tone at the monitor and Acuity (if connected) for
90 seconds. During equipment alerts, silences or acknowledges (dismisses) the alert
at the monitor and Acuity.
Battery
Insert the battery to turn on power. Remove the battery to turn off power. (While the
battery is removed, the monitor does not perform patient monitoring.)
Recharge the battery while it is removed from the monitor. (See “Recharge a Battery”
on page 43.)
To order a new battery, see “Battery Status and Possible Response” on page 44.
Directions for UseChapter 1 General Information11
Display
Although the Acuity Central Station is the primary location for viewing patient data, the
monitor provides information to support patient care.
Dashed lines indicate the
monitor detects a pacemaker
Waveform scale is
selectable
ECG lead is selectable
HR indicates the heart
rate is from ECG.
PR (pulse rate) is
displayed if SpO
and ECG is not (pulse rate
is derived from SpO
If the monitor detects
a vital sign outside
the measurable range,
- - - (below the range)
+ + + (above the range).
Indicates the monitor
is connected to
This symbol indicates the monitor is not
communicating with Acuity:
Flashing indicates the monitor is associated
with an access point, but not communicating
with Acuity.
Continuous on indicates the monitor is not
communicating with an access point or Acuity.
is active
2
it displays:
Acuity.
).
2
signal (display of pacer
detection can be enabled or
disabled at Acuity)
Indicates one or
more patient alarms
are disabled (off).
Patient name as entered at
Acuity.
If the patient name has not
been entered, the monitor
displays the last four digits of
the monitor serial number, such
as:
ID:6472
Symbol is displayed at the
monitor whenever the Nurse
Call key is pressed.
ECG waveform is displayed
when active.
SpO2 numeric data is a
percentage value.
SpO2 pulse amplitude indicator
(not proportional to pulse
volume)
Low battery icon flashes to
indicate monitor will shut off in
30 minutes or less.
Display Sleep Mode
In order to extend battery life, the display becomes blank after two minutes if no keys are
pressed. The display becomes active again if an alarm or alert occurs, a key is pressed,
the initial Acuity connection occurs, a cable is inserted, or an electrode is attached.
The display will not become blank if a patient alarm is occurring, an Acuity message is
displayed, or the monitor is in Demo mode or Service mode.
12Chapter 1 General InformationWelch Allyn Micropaq Monitor
Main Menu
When you first press , the Main Menu appears:
Press to move through the menu.
Press to select or change the highlighted choice.
EXITExit the Main Menu (the menu disappears).
ACUITY...Access the Acuity Menu with network options. The Acuity Menu
is only accessible while connected to Acuity.
EXITExit all menus and return to the monitoring
screen.
END TELEDiscontinue monitoring a patient.
NEW ROOMReassign a patient to a new room in the same
unit.
TRANSFERTransfer a patient to a new room in a new unit.
NEW PATIENTAssign the monitor to a new patient.
PATIENT INFODisplay patient information such as ID, name,
unit and room.
Whenever the monitor is connected to Acuity and you select
ACUITY... from the Main Menu, the monitor displays the message
ACUITY CONTACTED to confirm that Acuity has been contacted.
The monitor continues to display this message until Acuity
responds, or you press to acknowledge the message and clear
the screen. If the monitor detects an alarm or alert, it clears the
screen to display the appropriate alarm or alert message. The
length of time required for Acuity to respond to your selection at
the monitor can vary widely depending on the amount of network
traffic and other conditions.
ECG LEAD...Access a menu to change the ECG 1 or ECG 2 lead selection (I, II,
III, aV
, aVL, aVF, or V). Available vectors depend on the
R
connected electrodes.
Directions for UseChapter 1 General Information13
ECG SCALE...Change the scale of the ECG waveform. If two waveforms are
displayed, both have the same scale.
1 WAVEFORMThere are four possible ECG waveform display selections:
1 WAVEFORMthe default selection
2 WAVEFORMS
5 SECONDS
FULL SCREEN
Pressing changes to the next selection. This change does not
take effect until after you exit the Main Menu. See “Display” on
page 11 for descriptions.
LIMITS...Enter the Alarm Limits Menu (“Customize Patient Alarm Limits at
the Monitor” on page 37) and change alarm limits.
SYSTEM
INFORMATION
Display information about the network connection and SpO
module.
SERVICE MENU Enter Service Mode for a demonstration mode (Demo, see
“Demonstration Mode” on page 16) or service functions for
technicians. Service Mode is not available if any cables are
plugged in.
Note
To restrict access to the Main Menu, a Menu Lock option can be configured for
the monitor at the Acuity Central Station. When the Menu Lock is enabled, the
operator must press and hold down and for two seconds to gain access
to the Main Menu. The Menu Lock is disabled if the monitor loses
communication with Acuity.
2
14Chapter 1 General InformationWelch Allyn Micropaq Monitor
Waveform Options
There are four ECG waveform options as shown:
1 Waveform
The single ECG 1 (lead II)
waveform is displayed.
5 Seconds
ECG 1 (lead II) cascades from
one line to the other.
The single ECG 1 (lead II) waveform is
allowed to occupy most of the screen.
2 Waveforms
ECG 1 (lead II) and ECG 2
(lead V) are both displayed.
Full Screen
To change the waveform selection during operation:
1.Press to display the Main Menu.
2. Press as needed to highlight the current waveform selection. Then press as
needed to select the desired display.
Directions for UseChapter 1 General Information15
Messages from Acuity
The monitor displays messages sent from Acuity as needed, including patient alarms and
equipment alerts. When Acuity messages are displayed, they temporarily override
information displayed on the lower half of the monitor screen.
sensors (Masimo or Nellcor)Micropaq Directions For Use
2
WARNING For best product performance and measurement accuracy, use only
accessories supplied by Welch Allyn or recommended in the Welch Allyn
Products and Accessories booklet (810-0409-XX). Use accessories according to
your facility’s standards and the manufacturer’s recommendations. Always refer
to the manufacturer’s Directions for Use.
Operating Settings
The following monitor operating settings can be set at the monitor or at the Acuity Central
Station:
•Patient alarm limit settings (ECG and SpO
•ECG lead and scale selection
•ECG display format
Many other monitor operating settings (such as patient mode and alarms volume) can
only be set at the Acuity Central Station. See “Operating Settings” on page 49 for a list of
all settings and where they are set.
).
2
16Chapter 1 General InformationWelch Allyn Micropaq Monitor
Default Settings
When the monitor connects to Acuity for a new patient, the Acuity Central Station
downloads the appropriate default settings stored at Acuity. While the monitor is
connected to Acuity, settings can be changed either at the monitor or at the Acuity Central
Station.
If the monitor is temporarily disconnected from Acuity and the operator changes settings
at the monitor, those settings are transmitted to and stored at Acuity when the monitor
reconnects.
Demonstration Mode
You can practice using the monitor with the Demo mode of operation, including
connection to Acuity.
The Demo mode cannot be activated while you are monitoring a patient or if any cables
have been plugged into the monitor. During the Demo mode, the monitor and Acuity
display the message SIMULATION.
To practice with the monitor in Demo mode:
1.Disconnect all patient cables connected to the monitor.
2. Remove the battery (if installed).
3. Insert the battery and watch for the Power-Up screen.
Power-Up Screen
4. After the Power-Up screen disappears, press to display the Main Menu.
Main Menu
Directions for UseChapter 1 General Information17
5. Press to highlight SERVICE MENU, then press to display the Service Menu.
Service Menu
6. Press to highlight DEMO MENU, then press to display the Demo Menu.
7.Press to highlight DEMO 1 or DEMO 2, then press to start.
SIMULATION indicates the
Demo mode is active.
A simulated waveform and
numerics are displayed.
Demonstration Mode
Demo Mode Display Values and Alarm Limits
DisplayDemo 1Demo 2
ECG WaveformNormal sinus rhythm,
normal ST
ECG Heart Rate
SpO2 Pulse Rate
Saturation%9788Lower 90
SpO
2
a. Demo 2 will cause patient alarms.
80125Lower 50
a
Normal sinus rhythm,
normal ST
Alarm Limits (On)
(not applicable)
Upper 120
Upper 100
8. While in Demo mode you can practice changing settings such as ECG lead selection
and alarm limit adjustment. (These changes only affect the Demo mode and are
erased when you exit the Demo mode.)
18Chapter 1 General InformationWelch Allyn Micropaq Monitor
9. To change to the other Demo selection, press to display the menu, then scroll
down to highlight TOG GLE DE MO MOD E and press .
10. To exit the Demo mode, either insert a patient cable or remove and insert the battery.
The monitor restarts and enters the normal monitoring mode.
19
2
Monitoring
Connect a New Patient
Connect to the Network
1.Insert a battery into the monitor to turn it on. After a few seconds the monitor PowerUp Screen is replaced by an initial monitoring screen.
The monitor is
searching for a
network
connection.
2. After the network connection is established, the monitor may prompt you to select an
Acuity Unit (if your facility has more than one Acuity unit):
If any patient cables are
connected, there will be
some patient data displayed.
The format depends on the
monitor default settings.
Example of Initial Monitor Screen
Possible Acuity Unit
selections.
Press to view more.
Example of Acuity Unit Selection
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