1979257-Efficia CM Series

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Efficia CM Series
Patient Monitors
Release C.00
English
Ins
Installation and
11 in.
Configuration Guide
All manuals and user guides at all-guides.com
Efficia CM Series Patient Monitors
Installation and Configuration Guide
Release C.00
English
Notices
Proprietary Information
This document contains proprietary information, which is protected by copyright.
Copyright
Copyright © 2019 Koninklijke Philips N.V.
All Rights Reserved
Trademark Acknowledgements
Efficia is a registered trademark of Koninklijke Philips N.V. The following are registered
trademarks of Masimo Corporation: Masimo, SET, rainbow, and SpHb. RRA is a trademark of
Masimo Corporation. Other product names may be trademarks of their respective owners.
Manufacturer
Philips Medical Systems
3000 Minuteman Road
Andover, MA 01810-1085
(978) 687-1501
Document Number
453564623561 Rev C
Warranty Disclaimer
The information contained in this document is subject to change without notice. Philips
Medical Systems 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.
Philips Medical Systems 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.
ii Efficia CM Series Installation and Configuration Guide

Printing History
New editions of this document incorporate all material updated since the previous
edition. Update packages may be issued between editions and contain replacement and
additional pages to be merged by a revision date at the bottom of the page. Pages that
are rearranged due to changes on a previous page are not considered revised.
The documentation printing date and part number indicate its current edition. The
printing date changes when a new edition is printed. (Minor corrections and updates that
are incorporated at reprint do not cause the date to change.) The document part number
changes when extensive technical changes are incorporated.
Third Edition . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . September 2019
Efficia CM Series Installation and Configuration Guide iii

Conventions
This section describes the conventions used in this guide.
Text Formatting
The following typographical conventions are used in this guide.
Typeface Usage Example

Bold System keys Press the NBP key.
Special bold User interface text Open the System Menu.
Italic Variables, document • <product name>-<encryption

titles configuration>-<software version>.cfg
• Efficia CM Series Patient Monitors Instructions
for Use
Decimal Points
Because the Efficia CM Series monitor uses a period (.) to indicate a decimal point in decimal
numbers (for example, 10.0), all decimal numbers in this guide use a period as a decimal
point. Commas are not used as decimal points.
Notes, Cautions, and Warnings

This guide uses the following conventions for Notes, Cautions, and Warnings.
Note — A Note calls attention to an important point in the text.
Caution A Caution calls attention to a condition or possible situation that could damage or destroy
the product or the user’s work.
Warning A Warning calls attention to a condition or possible situation that could cause injury to
the user, patient, or both.
iv Efficia CM Series Installation and Configuration Guide

Explanation of Symbols
This section explains the symbols that appear on the monitor and its packaging.
Product labels have been redesigned to include UDI information, as required by USA
regulation. The UDI label contains a device identifier (DI) and a production identifier (PI).
The identifiers are machine and human readable.
• The Device Identifier (DI) is a unique GSI GTIN-12 number that has been registered
with the US FDA.
• The Production Identifier (PI) is a combination of Lot or Batch Number,
Manufacturing Dates, Serial Number and/or Expiration Date, as applicable for the
device.
Note: The symbols that appear on your monitor depend on the monitor model and its
configured options.
Documentation Symbol
The following symbol advises you to read the Instructions for Use.
Symbol Description Standard/Reference

Follow Instructions for Use ISO 7010* M002
(Blue safety symbol)
Packaging Symbols
The following symbols appear on the monitor’s packaging:
Symbol Name Standard/Reference

Keep upright International Air Transport
Association, 405B
* ISO 7000 Graphical symbols for use on equipment - Registered symbols

** ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labeling and information to be
supplied - Part 1: General requirements
Efficia CM Series Installation and Configuration Guide v

Fragile, handle with care ISO 15223-1** 5.3.1
Stacking limit by number ISO 7000* 2403
1014 hPA
Atmospheric pressure range for transport ISO 15223-1** 5.3.9
and storage
max
708 hPA
min
90%
Relative humidity range (non-condensing) ISO 15223-1** 5.3.8
for transport and storage
15%
Ambient temperature range ISO 15223-1**5.3.5

40°C
max
(non-condensing) for transport and
-20°C
min
storage
Keep dry ISO 15223-1** 5.3.4
CE mark: Product meets the requirements European Council Directive

of 93/42/EEC for Medical Devices 93/42/EEC of 14 June
distributed in the European Economic concerning Medical devices,
Area (EEA). Annex XII
Recycling Universal Recycling Symbol
* ISO 7000 Graphical symbols for use on equipment - Registered symbols

vi Efficia CM Series Installation and Configuration Guide

User-Control Symbols
The following symbols appear on and near the user-control buttons on the front of the
monitor:
On/Standby key IEC 60417* 5009
AC power LED IEC 60417* 5032
NBP key NA
Record key** NA
Home key** NA
Charging LED IEC 60417* 5546
Alarm silence key IEC 60417* 5576

IEC 60417* 5039
Freeze Waveform key NA
Trend key** IEC 60417* 5847
* IEC 60417 Graphical symbols for use on equipment

** CM10 and CM12 monitors only
Note — Not all monitors have all keys.
Efficia CM Series Installation and Configuration Guide

vii
Measurement Connector Symbols

The following symbols appear next to measurement connectors on the side of the monitor.

Gas input connector ISO 7000***-0794
Gas output connector ISO 7000***-0795
Mainstream CO2 connector NA

CO 2
Defibrillator Proof Type CF applied IEC 60417* 5336
part
ECG ECG connector NA
SpO2 connector NA
NBP connector NA
Caution ISO 15223-1** 5.4.4
IBP connectors NA
IBP I
IBP 2
Temperature connectors ISO 7000*** 0034
Masimo SET® and rainbow (red NA

and black symbol)
Nellcor OxiMax™ symbol NA

** ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labelling and information to
be supplied - Part 1: General requirements
*** ISO 7000 Graphical symbols for use on equipment - Registered symbols
viii Efficia CM Series Installation and Configuration Guide

Input/Output Connector Port Symbols

The following symbols appear next to the input/output ports on the rear panel of the
monitor:
Nurse call connector IEC 60417* 5336

IEC 60417* 5035
VGA Output NA
ECG Out port NA
USB port NA
Ethernet port NA
Rear Panel Label Symbols

The following symbols appear on the rear panel label of the monitor.
Catalog number ISO 15223-1* 5.1.6
Serial number ISO 15223-1* 5.1.7
Monitor key code NA

KC
Manufacturer’s name and address ISO 15223-1* 5.1.1
* ISO 15223-1 Medical devices - Symbols to be used with medical device labels, labeling and information to be supplied -
Part 1: General requirements
** IEC 60417 Graphical symbols for use on equipment
Efficia CM Series Installation and Configuration Guide ix

ICES-001 Canadian ISM requirement International Erosion Control

Systems
RF interference IEC 60417** 5140
RCM Mark Regulatory Compliance Mark for

electrical safety, EMC, EME, and
telecommunication requirements.
Compliance with WEEE standard Waste Electrical and Electronic

Equipment directive 2012/19/EU,
Article 14.4
100V-240V ~ 50Hz/60Hz 120VA Input power and fuse rating IEC 60417** 5016
2xT 1.6 AL 250V
Authorized EU Representative OK ISO 15223-1* 5.1.2

EC REP
Date of manufacture ISO 15223-1* 5.1.3
2019-02-08
Unique Device Identification (UDI) NA

UDI barcode
Option number NA
OPT
Rx Only Prescription Use Only (US Federal 21 CFR 801.109(b)(1) Prescription
Law) Devices
Ingress protection against IEC 60529, Ed. 2.2 Degrees of
vertically falling water drops protection provided by enclosures
(IP Code),
section 6
Caution, consult accompanying ISO 15223-1* 5.4.4

documents
x Efficia CM Series Installation and Configuration Guide

SGS mark SGS North America Listed Mark
Andover CE mark CE0123: Product European Council Directive

meets the requirements of 93/42/EEC of 14 June concerning
0123 93/42/EEC for Medical Devices Medical devices, Annex XII.
distributed in the European
The radio device used in the Efficia
Economic Area (EEA). CM10, CM12, CM100, CM120, and
CM150 monitors is in compliance
with the essential requirements
and other relevant provisions of
Directive 2014/53/EU (Radio
Equipment Directive).
Equipotential grounding post IEC 60417** 5021
Part number for label NA

PN
Internal Symbols
The following symbols are located inside the monitor:

Protective earth (ground) IEC 60417* 5032
Dangerous Voltage ISO 7010**, W012

(Yellow safety symbol)

++ ISO 7010 Graphical symbols - Safety colors and safety signs - Registered safety signs
Efficia CM Series Installation and Configuration Guide xi

Battery Symbols
The following symbols are located on the monitor batteries:

CE mark: Product meets the requirements of European Council Directive
93/42/EEC for Medical Devices distributed in the 93/42/EEC of 14 June
European Economic Area (EEA). concerning Medical devices,
Annex XII
Catalog number ISO 15223-1** 5.1.6
Serial number ISO 15223-1** 5.1.7
Date of manufacture ISO 15223-1** 5.1.3
Lot number ISO 15223-1** 5.1.5
Direct current IEC 60417* 5031
Ambient temperature range (non-condensing) for ISO 15223-1** 5.3.5

transport and storage
40°C
max
-20°C
min
Lithium-ion Charge Before Use NA
Lithium-ion Recycling mark Directive 2006/66/EC of the

European Parliament and of
the Council of 6 September
2006 on batteries and
accumulators and waste
batteries and accumulators
xii Efficia CM Series Installation and Configuration Guide

Do not dispose of this product (or any parts of it) Waste Electrical and
in industrial or domestic waste. The system may Electronic Equipment
contain materials or hazardous substances that directive 2012/19/EU, Article
can cause serious environmental pollution. The 14.4
system also contains privacy-sensitive
information. It is advisable to contact your service
personnel before disposing of this product.
This product contains certain hazardous Administrative Measure on
substances, and can be safely used during its the Control of Pollution
environmental protection use period of 5 years, Caused by Electronic
and should enter into the recycling system after its Information Products,
environmental protection use period. Chinese Ministry of
Information Industry,
2006-02-28, Decree No. 39
Product is certified to meet all applicable UL 61010-1 Safety

standards requirements Requirements for Electrical
Equipment for Measurement,
Control and Laboratory Use -
Part 1: General Requirements,
5.1
Product is certified to meet all applicable IEC 62133 Secondary cells
standards requirements. and batteries containing
alkaline or other non-acid
electrolytes - Safety
requirements for portable
sealed secondary cells, and
for batteries made from
them, for use in portable
applications.
Meets safety requirements for portable sealed CNS 15364 Bureau of
secondary cells for use in portable applications. Standards, Metrology and
Inspection of China
Product complies with Japan’s Electrical Ministry of Economy, Trade

Appliance and Material Safety Law. and Industry of Japan
Complies with FCC standards for home or office 47 CFR 15.19 (a)(3)
use.


xiii
Product meets requirements for certification by IS 16046 Secondary Cells

the Bureau of Indian Standards. and Batteries Containing
Alkaline or Other Non-Acid
Electrolytes -- Safety
Requirements for Portable
Sealed Secondary Cells, and
for Batteries made from
them, for use in Portable
Applications.
Accessory Symbols
The following symbols are located on the accessory packaging or on the accessory itself.
Symbol Description Standard/Reference

CapnoTrak
Contains or Presence of Phthalate
DEHP
Single Use
IPX4 Ingress protection against splashing water IEC 60529, Ed. 2.2 Degrees
of protection provided by
enclosures (IP Code),
section 6
IP44 Ingress protection against solid foreign IEC 60529, Ed. 2.2 Degrees
objects of 1.0 mm diameter and against of protection provided by
splashing water enclosures (IP Code),
section 6
xiv Efficia CM Series Installation and Configuration Guide

Regulatory and Safety Specifications

Declaration
The Efficia CM10, CM12, CM100, CM120, and CM150 monitors are Class IIb medical
devices and comply with the requirements of the Council Directive 93/42/EEC of 14
June 1993 concerning medical devices and carry CE-marking accordingly.
0123
The radio device used in the Efficia CM10, CM12, CM100, CM120, and CM150
monitors is in compliance with the essential requirements and other relevant
provisions of Directive 2014/53/EU (Radio Equipment Directive).
Authorized EU Representative
Philips Medizin Systeme Böblingen GmbH
EC REP Hewlett-Packard Str. 2
71034 Böblingen
Germany
Australian Sponsor
Philips Electronics Australia Ltd.
65 Epping Road, North Ryde, NSW
Australia 2113
Rx Only
Caution United States Federal Law restricts this device to sale by or on the order of a physician.
Safety Standards
Applicable Standards
IEC 60601-1:2005/A1:2012 IEC 60601-2-27:2011
IEC 60601-1-2:2014 IEC 80601-2-30:2018
EN 60601-1-2:2015 IEC 60601-2-34:2011
IEC 60601-1-6:2013 IEC 80601-2-49:2018
IEC 62366:2007/A1:2014 ISO 80601-2-55:2018
IEC 60601-1-8:2006/A1:2012 ISO 80601-2-56:2017
IEC 62304:2006/A1:2015 ISO 80601-2-61:2017
IEC 60601-2-26:2012
Parameter Specification
Protection Class Class I, internally powered equipment, per IEC 60601-1
Degree of Protection Type CF defibrillator-proof: per IEC 60601-1
IPX1 Ingress protection against vertically falling water drops
Mode of Operation Continuous
Protection Against Hazards of Equipment is not suitable for use in the presence of a
Ignition of Flammable Anesthetic flammable anesthetic mixture with air or oxygen or nitrous
Mixtures oxide, per IEC 60601-1.

xv
Safety
Anyone who connects additional equipment to the signal input port or signal output port
configures a medical system and is therefore responsible to ensure compliance with the
system requirements of IEC 60601-1. If in doubt, contact the Philips Customer Care Solutions
Center or your local Philips representative.
Warning If multiple instruments are interconnected or if multiple instruments are connected to a

patient, the sum of the leakage currents may exceed the limits given in EN/IEC 60601-1
system requirements.
Electromagnetic interference may cause disruption of performance. Protect the monitor
from sources of intense electromagnetic radiation. This device is designed to provide
resistance to electromagnetic interference; however, because of the proliferation of
radio-frequency transmitting equipment and other sources of electrical noise (such as
cellular phones, mobile two-way radios, and electrical appliances) in the health care
environment, it is possible that high levels of such interference due to close proximity or
strength of a source, may result in disruption of performance of this device. Disruption
may be evidenced by erratic readings, cessation of operation or other incorrect
functioning. If this occurs, the site of use should be surveyed to determine the source of
this disruption, and actions taken to eliminate the source. If you need assistance, contact
the Philips Customer Care Solutions Center or your local Philips representative.
External Displays
External displays should support the following resolutions:
• For the Efficia CM10, CM100, CM12, and CM120 monitors –1280 active pixels/line and
800 active lines/frame at 60Hz
• For the Efficia CM150 monitors – 1366 active pixels/line x 768 active lines/frame at
60Hz
Warning It is recommended that the user purchases a display that can be certified according to
EN/IEC 60950 for data-processing equipment or EN/IEC 60601-1 for electromedical
equipment. All combinations of equipment must be in compliance with the system
requirements of EN/IEC 60601-1. If selecting a display compliant to EN/IEC 60950, you
must also use a Medical Grade isolation transformer compliant to EN IEC 60601-1. The
system must be in compliance with the requirements of EN/IEC 60601-1.
xvi Efficia CM Series Installation and Configuration Guide

Contents
1. Introduction
Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
Efficia CM Series Documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
Navigation Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
2. Unpacking and Installing the Efficia Patient Monitor

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
Unpacking the Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
About the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Installing the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4
Installing the Optional Serial Interface Adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Removing the Insulator Sheath . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Installing the Optional Bed Rail Hooks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Starting the Monitor for the First Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Powering Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Charging the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Battery Status Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Changing the System Date and Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Loading the Recorder Paper . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-16
Testing Alarms on the Nurse Call System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17
3. Configuring the Monitor

Overview. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Accessing the System Menu Tabs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Configuring Administrative Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Changing the Administrator Password . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Selecting a Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Configuring the Line Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Configuring the Trend Display Timeout . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Configuring the Masimo® RRa™ Freshness Timeout . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8
Enabling Masimo Pulse Smart Tone . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9
Configuring Default Barometric Pressure (mmHg) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10
Configuring Patient ID Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10
Configuring Date and Time Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-14
Configuring Color Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-15
Configuring Night Mode Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-16
Exporting Configuration Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-20
Importing Configuration Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-22
Configuring Other Administrative Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-23
Configuring Alarm Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-24
Configuring the Alarm Tone . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-24
Configuring the Minimum Alarm Tone Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-25
Configuring the Audio Pause Duration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-26
Configuring the Minimum Nurse Call Alarm Priority . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-26
Configuring Alarm Reminder and Reminder Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-27
Latching Physiological Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-28
Restricting Alarm Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-29
Contents 1
Restricting Audio Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-29

Enabling an Audio Off Reminder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-30
Configuring the SpO2 Alarm Delay . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-31
Configure the Masimo RRa Alarm Delay . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-31
Configuring Arrhythmia Timeout Periods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32
Configuring NBP Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33
Configuring the Default NBP Interval . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-34
Aligning Measurement Intervals to the Clock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-34
Configuring the Default Initial Inflation Pressure (mmHg) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-35
Configuring the Default NBP VeniPuncture Pressure (mmHg) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-36
Configuring the Default NBP VeniPuncture Duration (seconds) . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-37
Configuring Profile Settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-37
Selecting a Default Profile . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-38
Saving Current Settings to a Profile . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-39
Renaming a Profile . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-40
4. Returning the Monitor

Submitting a Damage Claim . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Returning the Monitor For Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Disposing of the Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
A. Profile Settings
Profile Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-1
Contents 2
Introduction
Overview
This guide describes how to install and configure a standalone or networked Efficia
CM10, CM12, CM100, CM120, or CM150 patient monitor. These monitors shall be
referred to as the “Efficia CM Series patient monitors” or the “Efficia CM Series”
throughout this guide. The Efficia CM Series offers several configurations and optional
features. Measurements may include ECG, respiration, invasive blood pressure,
non-invasive blood pressure, heart rate, pulse rate, oxygen saturation (SpO2), carbon
dioxide (CO2), continuous temperature, cardiac output, arrhythmia analysis, and ST
analysis.
CM150
CM12 CM120
CM10 CM100
Intended Audience
This guide is for biomedical engineers or technicians responsible for installing and
configuring Philips patient monitoring systems.
Introduction
Efficia CM Series Patient Monitors Installation and Configuration Guide 1-1
Efficia CM Series Documentation
Efficia CM Series Documentation

Efficia CM Series documentation includes:
• Efficia CM Series Patient Monitors Instructions for Use: Provides information for
day to day operation of the Efficia CM Series monitors. Also includes safety
information, monitor specifications, and a list of compatible accessories.
Note — For information about purchasing additional copies of the Efficia CM Series
Patient Monitors Instructions for Use, contact the Philips Customer Care Center.
• Efficia CM10 and CM12 Quick Card and Efficia CM100, CM120, and CM150 Quick
Card: Provide brief descriptions of commonly used functions.
• Efficia CM Series with Masimo® Instructions for Use: Provides information for
operation of the Masimo SET® and Masimo rainbow® SET options on the Efficia CM
Series monitors. Includes safety information, alarm messages, specifications, and a
list of compatible accessories.
The Efficia CM Series documentation CD contains PDF versions of the following
documents:
• Efficia CM Series Patient Monitors Installation and Configuration Guide: Provides

instructions for unpacking, installing, and connecting all hardware. Includes initial
testing and configuration procedures. Also includes instructions for returning the
monitor.
• Efficia CM Series Patient Monitors Service Guide: Provides information about
maintenance, troubleshooting, diagnostics and performance verification testing of
the monitor.
• Efficia CM Series Patient Monitors Data Export Guide: Provides detailed
information about the syntax and structure of the HL7 messages that are exported
from the monitors.
• Efficia CM Series Patient Monitors Network Configuration Guide: Provides
instructions for configuring your monitor to connect to a network using a wired LAN
connection, a wireless LAN connection, or an RS-232 serial adapter.
Navigation Controls
Navigation on the Efficia CM Series patient monitors can be done using a touch screen or
a navigation wheel. The touch screen feature is standard on the CM100, CM120, and
CM150 models and is optional on the CM10 and CM12 models. All Efficia CM Series
patient monitors include a navigation wheel. The following table describes how to use
the navigation controls on all models.
Introduction
1-2 Efficia CM Series Patient Monitors Installation and Configuration Guide
Navigation Controls
Note — If the touch screen feature becomes disabled, the navigation wheel can still be
used to operate the monitor.
Screen
Action Description
Type
Select Touch Touch a button, menu, or list item on the touch screen to
select it.
Non-touch Rotate the wheel to highlight an item and then press the
wheel to select it.
Press Touch Press a front panel key or press the wheel.
Non-touch Press a front panel key or press the wheel.

Enter data Touch Touch the item to display the numeric keypad or the
using the keyboard. Touch the values, and then touch OK to close
keyboard the keypad or keyboard.
Non-touch Press the wheel to display a keyboard. Rotate the wheel

to highlight the text or value, and then press the wheel to
select the value. Select OK to close the keyboard.
Select or Touch Touch a check box to select or clear it.

clear
check Non-touch Rotate the wheel to highlight a check box and press the
boxes wheel to select or clear a check box.
Scroll Touch Touch a scroll bar arrow to scroll through the list one
segment at a time. Touch and hold the arrow to quickly
scroll through the list. (You can also use the wheel to
scroll and select items in the list.)
A scroll bar to the right of the list indicates the current
location in the list.
Touch an item to select it.
Non-touch Rotate the wheel to highlight a list and then press the
wheel.
To scroll through the list, rotate the wheel.
To select items in the list, press the wheel.
A scroll bar to the right of the list indicates the current
location in the list.
Introduction
Navigation Controls
Introduction
Unpacking and Installing the

Efficia Patient Monitor
Overview
This chapter describes how to:
• Unpack the monitor
• Install the battery
• Install the optional serial interface adapter
• Remove the insulator sheath
• Install the optional bed rail hooks
• Start the monitor for the first time
• Load recorder paper, if your monitor has the optional recorder
• Test the nurse call relay, if the monitor is used with the nurse call system in your
facility
Unpacking the Monitor

To unpack the monitor:
Step
1 Open the shipping container and remove the monitor from the container.
2 Examine the monitor for visible damage, such as broken components,

dents, or scratches on the surface of the equipment.
3 Store all documentation in an appropriate location.
4 Save the packaging material for possible reuse.
Unpacking and Installing the Efficia Patient Monitor

Unpacking the Monitor
Verify that you have received all of the following components:
• The Efficia CM Series patient monitor

• An accessories box, which contains:
– A battery (depending on the unit model and its options, the box may contain
two batteries).
– A power cord.
– CM Series Patient Monitors documentation CD.
If you purchased any of the following optional equipment, verify that these items are
included in the shipment:
• A starter set of accessories (SpO2 sensor, NBP cuff, ECG cable)

• Barcode scanner
• One roll of recorder paper, if you purchased the optional recorder
• Roll stand
• Wall mount
• Bed rail hooks
• Serial interface adapter
Warnings • Unless otherwise specified, hardware products and accessories not supplied by
Philips are not approved or supported for use with the Efficia CM Series monitors.
• The Efficia CM150 Patient Monitor cannot be mounted on a roll stand.

• Properly secure the monitor and cables when in use to avoid a tripping hazard
and/or injury to patient and staff. Use of a cable management kit is recommended.
Caution If your monitor is mounted on a roll stand, use the handle on the roll stand to move the
monitor. Do not use the monitor handle to move the monitor; doing so, creates stress on
the mounting bracket and could cause the monitor to fall off the roll stand.
Notes
• The weight of objects placed in the basket of the roll stand must not exceed
3.6 kg (8 lb).
• For information on mounting the monitor on the roll stand or wall mount, see
the Instructions for Use that comes with the mounting hardware.

About the Batteries
About the Batteries

The rechargeable lithium ion batteries used in the monitor are smart batteries with
built-in circuitry that communicates battery status information to the monitor. Two types
of batteries, a 3-cell and a 9-cell, can be used unless otherwise indicated.
The type of battery and number of batteries installed in your monitor depend on the
options purchased for your monitor. The CM10 and CM12 use either one or two 3-cell
batteries, or one or two 9-cell batteries. The CM100 monitor may contain one 9-cell
battery. The CM120 and CM150 monitors may contain one or two or 9-cell batteries. Your
monitor’s battery operating time depends on the number and type of batteries installed.
Notes
• The Efficia CM patient monitors do not support recording if only one 3-cell
battery is installed.
• When two batteries are installed, Philips recommends using batteries from the
same manufacturer for optimal performance. When using mixed batteries
from different manufacturers, the battery reconditioning function may not be
optimal.
Observe these guidelines:

• If a battery shows damage or signs of leakage, replace it immediately.
• Never use a faulty battery in the monitor.
• Never dispose of the battery in a normal waste container.
• Never leave a battery inside the monitor if it is not used for a long period of time.
• Never store a battery that is more than 50% charged.
For information about the battery status indicators, see the Efficia CM Series
Instructions for Use.

About the Batteries
Installing the Battery
Note — Depending on the unit model and its options, you may need to install two
batteries.
To install the battery:
Step
1 Insert a slotted screwdriver into the slot in the battery cover.
Slot
2 Hold one hand over the battery cover while you twist the screwdriver slightly
to release the battery cover from the case.
Warning
Twist the screwdriver slowly and gently to avoid expelling the battery cover
with enough force to cause personal injury.
3 Ensure that the retaining clip inside the battery compartment is positioned
out of the way in order to allow the battery to be inserted.
Note — For single-battery monitors, the retaining clip is at the bottom of the
battery compartment and must be rotated clockwise. For dual-battery
monitors, the retaining clip is on the left side of the battery compartment
and must be rotated counterclockwise.

About the Batteries
Step
4 Orient the battery so that the contacts and ribbon are on the left.
Ribbon
5 Push the battery until it is fully inserted into the battery slot. If you have a
second battery, repeat steps 2 and 3 to install the second battery.
6 Position the retaining clip so that it prevents the battery from being removed
(dual-battery model shown below).
Retaining Clip
Note — If the retaining clip is not properly positioned, you will not be able to
attach the battery compartment cover.

Installing the Optional Serial Interface Adapter
Step
7 Replace the battery cover.
8 The Charging LED on the front of the monitor should

light. The color of the LED depends on the charging
status. For more information see “Charging the Battery”
Charging LED on page 2-13.
Notes
• If you have inserted a battery that the monitor does not support,
the monitor generates an “Unsupported Battery” alarm.
• If you have installed only one 3-cell battery into a monitor with a
recorder, the monitor generates an “Unsupported Battery Config”
alarm.

You can use an optional USB to RS-232 serial interface adapter to export patient data
over a serial connection. For more information about configuring the monitor to export
patient data using the RS-232 serial interface adapter, see the Efficia CM Series Patient
Monitors Network Configuration Guide for your monitor.
Warning To ensure patient electrical isolation, use only the Philips serial interface adapter.
Caution Do not allow liquid to enter the connectors or the openings on the adapter. Wet
connectors could prevent connected devices from operating. If liquid spills on the
adapter, clean and dry it thoroughly before reuse. If you believe the liquid has entered
the adapter, verify the performance and safety of the adapter before returning it to use.

To install the serial interface adapter:
Step
1 Slide the serial interface adapter’s USB connector into a USB port on the
back of the monitor.
USB ports
2 Insert the other end of the USB connector into the adapter.

Step
3 Slide the insulator sheath over the adapter, wide end first, and push it down
to completely cover the adapter.
4 Attach the adapter to the RS-232 serial port of the receiving system.

Removing the Insulator Sheath
Removing the Insulator Sheath
Caution If you are using the optional serial interface adapter to export data and you disconnect
the adapter to move the monitor to a different location, make sure the black sheath
completely covers the RS-232 connector after you reconnect the cable.
To remove the adapter insulator sheath:
Step
1 Pull apart the wide side of the sheath with your fingers and push on the
adapter metal connector with your thumbs.
Metal Connector
2 Slide the adapter out of the sheath.

Installing the Optional Bed Rail Hooks
Installing the Optional Bed Rail Hooks

The optional bed rail hooks can be installed on the Efficia CM10, CM100, CM12, and
CM120 patient monitors.
To install the optional bed rail hooks:
Step
1 Using a T20 driver, remove the two screws located under the handle of the
monitor.
Screws
2 Slide a bed rail hook under the monitor handle so that the hole in the bed
rail hook aligns with the hole from which the screw was removed.
3 Insert a screw through the bed rail hook and tighten to hold the bed rail hook
in place. Recommended torque: 1.2Nm ±0.20
Bed rail hook
4 Repeat steps 2 and 3 for the second bed rail hook.

Starting the Monitor for the First Time

This section describes how to power up the monitor, charge the battery, and change the
system date and time.
Note — Before connecting the monitor to an AC power source, verify the following:
• Ensure that the AC outlet is properly grounded and supplies the specified
voltage and frequency (100 VAC – 240 VAC, 50 Hz – 60 Hz).
• If installing in the United States, a hospital-grade outlet is recommended.
• If your facility requires a separate potential equalization connection, use the

grounding post on the rear of the monitor. Connect a grounding cable from
the grounding post to the grounding system in your facility.
Warning To avoid impairing the performance of the monitor and its accessories, do not place the
monitor near heating or cooling sources.
Warning If an external display is to be used, it is recommended that the user purchases a display
that can be certified according to EN/IEC 60950 for data-processing equipment or
EN/IEC 60601-1 for electromedical equipment. All combinations of equipment must be
in compliance with the system requirements of EN/IEC 60601-1. If selecting a display
compliant to EN/IEC 60950, you must also use a Medical Grade isolation transformer
compliant to EN IEC 60601-1. The system must be in compliance with the requirements
of EN/IEC 60601-1.
Powering Up
The monitor can operate on AC power or battery power.
Note — Philips recommends that a battery is always installed in the monitor. If the
monitor loses AC power, it resorts to battery power. If an AC power failure occurs, and
the monitor does not contain a battery, monitoring is interrupted, no alarms sound, and
patient data may be lost.

To power up the monitor:
Step
1 Connect the power cord to the receptacle on the monitor’s rear panel.
Ensure that the power cord retainer clip is secured over the power cord.
2 Ensure that the AC outlet is properly grounded and supplies the specified
voltage and frequency (100 – 240 VAC, 50 – 60 Hz) and then connect to an
AC power source.
Note — Within the U.S., a hospital-grade outlet connected to back-up
power is recommended.
The green power LED on the front panel lights when the AC
power source is connected. Also, the battery indicator on the
Power LED front panel indicates the current battery status. For more
information, see “Charging the Battery” on page 2-13.
3 Press the On/Standby key.

The monitor powers up and performs a self-test.
During this self-test, the monitor tests the speaker; listen for an
On/Standby audible tone to confirm that the speaker is working properly.
Also observe that the monitor tests the alarm LED by lighting it
in blue, then yellow, and then red.
You may also be prompted to change the system date and time the first time
you power up the system. For more information, see “Changing the System
Date and Time” on page 2-15.

Charging the Battery

The type of battery and number of batteries installed in your monitor depend on the
model of your monitor and the options purchased for your monitor.
Any time the monitor is connected to AC power, the battery is being
charged. When you first receive the monitor, the battery charge may be
Charging LED
low. Connect the monitor to an AC power source and fully charge the
battery before using it on battery power alone.
Note — Philips recommends that you fully charge the battery before placing the monitor
into service.
If the monitor is connected to AC power, and the power cord is then disconnected, the
monitor automatically resorts to battery power, if the battery is sufficiently charged. All
alarm settings are preserved.
Note — To ensure that the battery is sufficiently charged, keep the monitor plugged in to
AC power when it is not in use.

Battery Status Indicators

The battery status pane and the Battery Info Menu provide information about the
battery charging status.
Battery Status Pane

The battery status pane on the bottom of the main screen indicates
battery status.
Battery Status
Note — If the monitor is plugged into AC power and no battery is installed or the battery
is dead, the blank battery status icon displays an AC plug icon.
The color of the battery status icon tells you how much charge remains on the battery:
• Green: The battery is at least 30% charged.
• Yellow: More than 20% charge, but less than 30%. This battery status triggers the
Low Batt technical alarm. The monitor will shut down in approximately 20 minutes,
depending on battery usage.
• Red: Less than 20% charged. This battery status triggers the Extreme Low Batt
technical alarm.The monitor will shut down in approximately 5 minutes, depending
on battery usage. Connect the monitor to AC power.
Battery Info Menu

The Battery Info Menu displays detailed information about the charging status for one
battery or for both batteries if your monitor has two:
• Battery 1 or Battery 2: Possible values include:

– Fully Charged: The specified battery is fully charged.
– Charging: If the monitor is plugged into AC power, the current charge level.
– Remaining: If the monitor is not plugged into AC power, the current charge
level.
– Not Present: If the specified battery slot is empty.
• <x.x> hours remaining (estimated): If the monitor is not plugged into AC power, the
approximate amount of time that you can continue to use the monitor before
recharging.
The remaining information in the Battery Info Menu may help your technical support
team to troubleshoot battery problems.
To open the Battery Info Menu:
• Select the battery status pane.
The Battery Info Menu opens and the current information is displayed.

Warning Dispose of used batteries in an environmentally responsible manner. Do not dispose of

the battery in normal waste containers. Consult your system administrator to find out
about local arrangements.
Changing the System Date and Time

Use the following procedure to change the system date and time. If the Date/Time Menu
is already open, skip to step 2.
Notes
• For details about synchronizing the time with the EHR server or the HL7
interface server and allowing the clock to automatically adjust for daylight
saving time, see the Efficia CM Series Patient Monitors Network Configuration
Guide and the Efficia CM Series Patient Monitors Data Export Guide.
• For details about allowing or restricting users from setting the date and time
on the monitor, see “Configuring Date and Time Settings” on page 3-14.
To change the system date and time:
Step
1 Select the Date/Time pane.
The Date/Time Menu appears.
2 Select the date and time values you want to change.
3 Use the wheel or soft keypad to change the values.
4 Select the Apply button to save your changes and close the menu.
You can change the date format (mm/dd/yyyy or dd/mm/yyyy) in the General tab of
the System Menu. For details, see the Instructions for Use supplied with your monitor.
Note — The monitor automatically adjusts for daylight saving time if you are in a
location that supports daylight saving time.

Loading the Recorder Paper
Loading the Recorder Paper

Caution Use only Philips-supplied paper. Using the wrong paper can damage the recorder. If the
paper is inserted incorrectly, data does not print.
To load the paper in the recorder:

Step
1 Press the paper eject button on the left side of the recorder door to open
the door.
Eject button
Recorder paper
Recorder door
If the door does not open completely, pull it toward you.
2 Remove the empty paper core.
3 Place a new roll in the holder so that the end comes from the back over the
top of the roll and slide the paper through the slot in the door.
Slide paper through

slot in door
4 Pull the loose edge to remove any slack and close the recorder door.

Testing Alarms on the Nurse Call System
5 Select Record to verify that the paper is loaded correctly. If the

paper is loaded correctly, the recorder prints data. If the paper is
loaded incorrectly, data does not print or the paper may jam.

If your facility uses the nurse call function, test the system after installation and before
clinical use.
To perform this test, you need an NBP cuff and hose.
To perform the nurse call relay test:
Step
1 Plug the phono connector from your nurse call

system into the 3.5 mm nurse call connector on the
back of the monitor.
Nurse Call
Connector
2 Connect the NBP hose to the NBP input connector, but do not
place the cuff on your arm.
3 Press the NBP key on the front panel.
NBP Key
4 Check that an alarm message appears, an alarm tone sounds, and

the nurse call system signals an alarm.


Configuring the Monitor
Overview
This chapter describes how to configure the monitor settings using the System Menu.
The System Menu contains several tabs, including the General tab. Only the General tab
is user-accessible. The Admin, Alarm Settings, NBP Settings, and Profile tabs are
password-protected and should only be accessed by qualified service personnel.
Appendix A, "Profile Settings," contains worksheets that list the factory defaults. You
can
print these worksheets and record your facility’s default settings for your records.
Accessing the System Menu Tabs

To access the System Menu tabs:
Step
1 Select the System button in the toolbar to open the System Menu.
2 The General tab in the System Menu contains several system configuration settings and a
read-only section that provides information about the monitor.

Accessing the System Menu Tabs
Step
The read-only information in the General tab includes:

• Serial Number: The monitor’s serial number, which also appears on the back of the
monitor. The serial number is configured in the factory.
• Hardware ID: The version number of the monitor’s main board, front end board and
FPGA.
• Software Version: The unique identifier defining the software version installed on the
monitor.
• LAN MAC Address: The unique MAC address assigned to the monitor. The MAC
address is configured in the factory.
• LAN IP Address: The IP address currently assigned to the monitor.
• WLAN MAC Address: The unique WLAN MAC address assigned to the monitor. The WLAN
MAC address is configured in the factory (Note: this field is visible only if the wireless option is
purchased).
• WLAN IP Address: The WLAN IP address currently assigned to the monitor (Note: this field is
visible only if the wireless option is purchased).
• Language: The language currently configured on the monitor.
• Central Name: The name of the central station, if the monitor is connected to a
Central network.
• Current Profile: The name of the current profile configured as default settings.
Notes:
• The Efficia Central Station may not be available in all countries. Efficia CM
Series monitors only connect to the Efficia Central Station. For detailed
information, see the Efficia Central Station Instructions for Use.
• The SureSigns Dashboard is an optional service tool for biomedical
engineers to quickly view the status of your monitor, upgrade the monitor
software, and update configuration settings from a remote server. If the
monitor is connected to a SureSigns Dashboard server, the monitor can
receive requests to update configuration settings or upgrade the monitor
software over the network.
For more information on the General tab’s settings, see the Instructions for Use supplied
with your monitor.
3 Select the Admin, Alarm Settings, NBP Settings, or Profile tab.

A password request appears.

Configuring Administrative Settings
Step
4 In the Enter Password window, select the Password field and use the on-screen keyboard
to enter the current Administrator password.
Notes —
• The default Administrator password is 215. The password may have been
changed.
• If you have forgotten the Administrator password, contact your local Philips
representative.
5 Select the OK button on the keypad.
6 Select the OK button in the Enter Password window.

The selected tab appears.
Caution
These password-protected tabs remain unlocked for 1 minute after you close them. This
allows you to re-open the tab without having to re-enter the password. Do not leave
the monitor unattended during the unlock time.
7 Proceed to the appropriate configuration task:

• To configure administrative settings, see “Configuring Administrative Settings” on
page 3-3.
• To configure alarm settings, see “Configuring Alarm Settings” on page 3-24.
• To configure NBP settings, see “Configuring NBP Settings” on page 3-33.
• To configure profile settings, see “Configuring Profile Settings” on page 3-37.

This section provides details for configuring the administrative settings for your monitor.
Use the Admin tab to:
• Select a language
• Configure the line frequency (AC Power)
• Configure the trend display timeout
• Configure the Masimo® RRa™ Freshness timeout (optional)
• Enable Masimo pulse smart tone (optional)
• Configure BSA settings for monitors with Cardiac Output and Hemodynamic
Calculations
• Configure default barometric pressure

• Configure LAN and Wireless Settings

• Configure the connection to a Central Station (optional)
• Enabling Dashboard settings (optional)
• Configure data export
• Configure security and patient ID settings
• Configure date and time settings
• Configure color settings
• Configure night mode settings
• Upgrade software
• Configure import and export settings
• Run diagnostic tests
• View logs
• Enable or disable ADT
• Configure parameters for the Monitor and Efficia Rack (optional)
Changing the Administrator Password

The settings on the monitor are managed through password-protected menus. The default
Administrator password is set at the factory. To improve the security of the monitor settings,
Philips recommends that the user change the Administrator password upon first access, and
that the new password should follow the following rules:
• Have a minimum of 8 and up to at least 14 characters
• Use at least 3 of the following 4 types of characters:
– Uppercase characters
– Lowercase characters
– Numeric characters
– Special characters (e.g., #$%&)
The default Administrator password is 215.
Warning If you change the Administrator password, make note of the password and keep it in a safe
and secure place.
If you have forgotten the Administrator password, contact your local Philips representative.
Make sure that you reset the Administrator password to the default, 215, before returning
the monitor to Philips for any reason. Failure to reset the password to 215 may result in the
loss of data. For more information, see Chapter 4, “Returning the Monitor.”

To change the Administrator password:
Step
1 Select the System button in the toolbar to open the System

Menu.
2 Access the Admin tab as described in “Accessing the System Menu

Tabs” on page 3-1.
The Admin tab appears.
3 Select the Security button.

The Security Menu appears.
4 Select the Change Admin Password button.

The Change Admin Password screen appears.
5 Select the Old Password field.

A keyboard appears.
6 Enter the current Administrator password, and then select OK.

Note — The default Administrator password is 215. The password
may have been changed.
7 Select the New Password field.

A keyboard appears.
8 Enter a new password, and then select OK.

The password must be from 3 to 20 characters long. Any
characters on the keyboard may be used.
9 Select the Confirm Password field.

Re-enter the password you entered, and then select OK.

Step
10 Select OK on the Change Admin Password screen.

An error message is displayed if the value in the Old Password field
is incorrect or if the values in the New Password and Confirm
Password fields do not match.
11 In the confirmation window that appears, select OK.

The new password takes effect immediately.
Selecting a Language
You can specify the language used on the monitor. The default language is set at the time of
production per the ordering information.
Note — The System Menu is available in English only.
Caution Changing the language clears all patient data and resets all profile setting to defaults.
To change the language:
Step

Menu.

3 Select the Language option you want to use on the monitor.

A confirmation window appears, warning that changing the
language clears all patient data and restarts the monitor.
4 Select OK to change the language, clear all patient data, and

restart the monitor.
5 Close the window.

Configuring the Line Frequency

Select the power line frequency for the monitor to match the power line frequency for
your geographic region. This will allow for the cancellation of noise introduced by
fluorescent lights and other sources, which can improve signal quality.
Warning Ensure that the power line frequency on the monitor is set to the required operating
frequency for your country. If not set correctly, the monitor could experience extra
interference on SpO2 signals.
The default factory setting is either 50 Hz or 60 Hz, depending on the country.

To set the default AC power line frequency:
Step

Menu.

3 Select the default setting for AC Power.

The options are 50 Hz and 60 Hz.
4 Close the window.
Configuring the Trend Display Timeout

The trend display pop-up window partially obstructs your view of the monitor
parameters; however, you can control the time that the monitor displays trend data when
there is no user interaction.
Caution All parameters except ECG and HR are not visible during the trend display timeout
period.
The default time that the monitor displays trend data is 3 minutes. After this amount of
time, the trend display data disappears and the previous screen data reappears.

To set the trend display timeout:
Step

Menu.

3 Select the Trend Display Timeout – the time after which trend data
disappears.
The options are 1 minute, 2 minutes, 3 minutes, 5 minutes, No timeout.
4 Close the window.
Configuring the Masimo® RRa™ Freshness Timeout
Note — The Masimo RRa Freshness Timeout setting is available only if the monitor has Masimo
rainbow SET with the RRa option.
The Masimo RRa Freshness Timeout setting specifies the duration of time that, during
interference, the monitor will display the last known RRa value.
The default setting is 5 minutes.
To configure the Masimo RRa Freshness Timeout setting:
Step

Menu.

3 Select the Masimo RRa Freshness Timeout option.

The options are 0, 1, 5, 10, and 15 minutes.
4 Close the window.

Enabling Masimo Pulse Smart Tone

When Masimo Pulse Smart Tone is enabled, an audible tone sounds for each pulsatile
signal detected. If the Masimo Pulse Smart Tone setting is enabled, the audible pulse tone
notifies the clinician of changes in patient saturation and pulse rate during motion. This
can be useful if the clinician cannot observe the monitor display (for example, during
patient intubation or transport).
If the setting is disabled, the pulse tone is suppressed.
The default setting is unchecked.
Warning When HR/Pulse tone is enabled and the tone is from the ECG, there is no tone
modulation for changes in SpO2. If notification of subtle changes in SpO2 is needed,
adjust the SpO2 alarm limits to ensure alarm notification.
Notes
• The Masimo Pulse Smart Tone setting is only available if the monitor has the
Masimo
SpO2 option. Monitors with the Masimo SpO2 option display a Masimo logo at
the SpO2 connector site.
• The HR/Pulse Tone Volume setting in the Pulse Rate Menu must be greater than 0
to use the Masimo Pulse Smart Tone feature.
To enable or disable Masimo Pulse Smart Tone:
Step

Menu.

3 Select the Masimo Pulse Smart Tone check box to select or clear the
check box.
Masimo Pulse Smart Tone is On
NoMasimo Pulse Smart Tone is Off
Note — By default, the setting is unchecked.
4 Close the window.

Configuring Default Barometric Pressure (mmHg)
Note — This section applies only to monitors with the Mainstream CO2 module.
Default barometric pressure is set to sea level. However, you must configure the default
barometric pressure setting to the value appropriate for your facility’s altitude above or
below sea level. A correct barometric pressure setting is necessary for accurate monitoring
information.
Warning The mainstream CO2 module is not equipped with automatic barometric pressure
compensation. Before the CO2 measurement is used for the first time, the barometric
pressure must be set to the correct value. An incorrect barometric pressure setting will
result in incorrect CO2 readings.
The default setting is 760.

To configure the default Barometric Pressure (mmHg):
Step

Menu.

3 Select the Barometric Pressure (mmHg) field.

Use the up or down arrows to adjust the barometric pressure
setting.
The options are: 400 mmHg – 850 mmHg in 1 mmHg steps
4 Close the window.
Configuring Patient ID Settings

Use the Patient ID Settings Menu to:
• Select the input method used to enter patient information.
• Select the primary patient identification field.
• Specify the monitor’s default location.
• Configure the patient identification display settings.

To configure the Patient ID settings:
Step

Menu.

3 Select the Patient ID Settings button.

The Patient ID Settings Menu appears.
Selecting the Input Method

Use the Patient ID Settings Menu to specify whether the user enters patient ID information
using the barcode scanner or the on-screen keyboard. The options are:
• Manual: Enter patient information using the on-screen keyboard.

• Standard Barcode: Use a barcode scanner that reads each patient ID barcode, one at
a time.
• Programmed Barcode: The monitor automatically enters the scanned barcode data in
the patient ID fields.
The default setting is Manual.
Note — If the barcode scanner cannot read the barcode or does not function correctly,
users can unplug the scanner and use the on-screen keyboard to enter patient IDs. For
more information, see the Instructions for Use supplied with your monitor.

To select the input method:
Step
1 Open the Patient ID Settings Menu.
2 Select the Patient ID Input field and select the method to use to
enter patient information.
The options are:
• Manual
• Standard Barcode
• Programmed Barcode
Selecting the Primary Identification Field

Use the Patient ID Settings Menu to specify the patient ID input fields that correspond to the
patient record requirements for your facility and EHR system. Select the primary field that
your facility and EHR system uses to identify a patient. The Primary Identification options are:
• MRN: Medical Record Number. A unique number used to track and identify a patient.
The maximum length is 20 characters.
• Transaction ID: Also known as the visit ID, the transaction ID is a unique number used to
track a single patient visit. The maximum length is 20 characters.
• Location ID: Typically, a description of the physical location of the Efficia CM Series
monitor, for example, a room number. The maximum length is 20 characters.
Note — When your monitor is connected to a central station, the Location ID cannot be
used as a
Primary Identification.
The field you designate as the Primary Identification appears in the Admit Patient Menu within
brackets (for example, [MRN]) and appears in the patient pane.
Only records that have a primary patient ID can be exported over a LAN network. If a record
does not contain a primary ID (ID Unknown appears in the record), the data is not exported.
If your monitor is connected to an RS-232 serial connection, a record that does not have a
primary patient ID can be exported.
Caution When you change the patient Primary Identification field, the patient data and trend data is
cleared.

To select the primary identification field:
Step
1 Open the Patient ID Settings Menu.
2 Select the Primary Identification field.

The options are:
• MRN
• Transaction ID
• Location ID
Specifying the Default Location ID

If the monitor remains in one location, you can enter the Default Location ID (for
example, the room number) so that users do not have to manually enter a Location ID
each time they start a new patient.
Caution Enter a Default Location ID only if the monitor always remains in the same location.
Configuring Patient ID Display Settings

Use the Patient ID Settings Menu to configure which identifiers are required, enabled, or
disabled. For example, if your facility uses a medical record number (MRN) as the primary
method for identifying patients, you can designate the MRN as the Primary Identification
and then further specify if users are required to enter the new patient’s MRN to save the
patient record.
Note — If the user does not enter data in the field that you designate as the Primary
Identification field, ID Unknown appears in the patient record. If no ID is supplied, the
records cannot be exported to an EMR system.
• Enable indicates the field will appear in the Admit Patient Menu but is not required.
The user can enter and change text.
• Required indicates the field is required and the user must enter data in the field to
save the patient identification information. Use this option to ensure that users fill in
the field you designate as the Primary Identification field. An asterisk appears next to
all required fields in the Admit Patient Menu. Users cannot save the patient record
until all required input fields are complete.
• Disable indicates the field is not accessible to the user. The field appears on the
Admit Patient Menu but text cannot be entered or changed. This setting is not
available if the field is designated as the Primary Identification field.

To configure the Patient ID Settings and confirm the settings:
Step
1 Open the Patient ID Settings menu.
2 Configure the following patient identification settings. The options are

Enable, Required, and Disable.
• MRN
• Transaction ID
• First Name
• Middle Name
• Last Name
• Location ID
• Operator ID
• Gender
• Age
• Date of Birth
• Height
• Weight
• Department
• Admit Time
3 To close the Patient ID Settings menu the changes saved, select the Apply
button.
4 To confirm that patient ID settings appear as expected, select the Manage

Patient button on the main screen, and then select the Admit Patient
button.
The Admit Patient Menu appears.
5 Confirm that all settings appear as expected.
Configuring Date and Time Settings

Use the Date/Time Settings Menu to allow users to change the monitor’s date and time. For
other date/time options (synchronization), refer to the Efficia CM Series Patient Monitors
Network Configuration Guide.

To configure date and time settings:

Step
2 Access the Admin tab as described in “Accessing the System Menu Tabs”
on page 3-1. The Admin tab appears.
3 Select the Date/Time Settings button.

The Date/Time Settings Menu appears.
4 Select the Disable Date/Time Menu check box.

Users cannot change the monitor’s date and time
NoUsers are allowed to change the monitor’s date and time
Note — The monitor will adjust for Daylight Saving Time if selected time
zone observes Daylight Saving Time.
5 Select the Apply button to save the change and close the Date/Time
Settings Menu.
Configuring Color Settings

The color of active measurements can be configured to pre-defined colors. Use the Color
Settings Menu to change the colors of active measurements.
Step
on page 3-1.
3 Select the Color Settings button. The Color Settings Menu appears.

Step
4 Use the drop down menus to select colors for each measurements.
Note: The colors for the optional Gas module are not configurable, so they will
not be displayed on the Color Settings Menu.
5 Select one of the following options:

• Select Apply to save the colors of the measurements according to
the current color setting on the menu.
• Select Restore Default to restore the default colors.
• Select Cancel to return the changes of the menu since the last time
it was open.
The default color settings are as follows:
Measurement Color Measurement Color

ECG/HR Green PAP Yellow
RESP Yellow Ao Red
SpO2/Pulse Cyan ABP Red
SpCO Dark Orange ICP Magenta
SpOC Light Purple UAP Red
SpHb Red LAP Cyan
RRa Light Blue RAP Cyan
NBP/Pulse Red UVP Cyan
T1/T2 Green BIS L Yellow
CO2 Yellow BIS R Magenta
C.O. Pink NMT Yellow
ART Red EEG Yellow
CVP Cyan Vent Cyan
P Red
Configuring Night Mode Settings

Use the Night Mode Settings Menu to enable or disable the night mode feature and to change
the monitor’s brightness level, minimum alarm tone volume, and minimum HR/pulse tone
volume when the night mode feature is used.
Note — Set the minimum alarm tone volume before configuring night mode settings because
the minimum alarm tone volume setting dictates the lowest setting for the Alarm Tone Volume
on the Night Mode Settings Menu. For more information, see “Configuring the Minimum Alarm
Tone Volume” on page 3-25.

Use the Night Mode Settings Menu to:
• Enable or disable the night mode feature.

• Set the monitor’s brightness level when the night mode feature is used.
• Set the monitor’s minimum alarm tone volume when the night mode feature is used.
• Set the monitor’s minimum HR/pulse tone volume when the night mode feature is
used.
To configure Night Mode settings:
Step
on page 3-1.
3 Select the Night Mode button.

The Night Mode Settings Menu appears.
Patient ID Settings
Patient ID Input: Manual
Primary Identification: MRN
Default Location ID:
Please select the input fields you want to include in the New Patient Menu.
MRN:
Transaction ID:
First Name:
Enabling or disabling the Night Mode Feature

Use the Night Mode Settings Menu to specify whether the night mode feature is enabled or
disabled.
The options are:
• Enable: Allows the use of the night mode feature.
• Disable: Prevents the use of the night mode feature.

The default setting is Disable.

To enable or disable the night mode feature:
Step
1 Open the Night Mode Settings Menu.
2 Select the Night Mode field and select Enable or Disable.
3 Select the Apply button to save the change.
Note — When the night mode feature is enabled, the Night Mode
button appears on the system toolbar.

Setting the Monitor’s Brightness Level for Night Mode

Use the Night Mode Settings Menu to set the monitor’s brightness level for night mode.
The options are: 1-8. The default setting is 1.
To set the monitor’s brightness level for Night Mode:
Step
2 Select the Brightness Level field.
Note — The Night Mode field must be set to Enable in order for the
Brightness Level field to be activated.
Up and down arrows appear next to the Brightness Level field.
3 Select the up or down arrow to increase or decrease the brightness level.
Setting the Monitor’s Minimum Alarm Tone Volume for Night Mode
Use the Night Mode Settings Menu to set the monitor’s minimum alarm tone volume for
night mode.
The options are: 1-8.
The default setting reflects the current default minimum alarm tone volume. Set the
minimum alarm tone volume before configuring night mode settings because the
minimum alarm tone volume setting dictates the lowest setting for the Alarm Tone Volume
on the Night Mode Settings Menu. For more information, see “Configuring the Minimum
Alarm Tone Volume” on page 3-25.
To set the monitor’s alarm tone volume for Night Mode:
Step
2 Select the Alarm Tone Volume field.
Note — The Night Mode field must be set to Enable in order for the Alarm
Tone Volume field to be activated.
Up and down arrows appear next to the Alarm Tone Volume field.
3 Select the up or down arrow to increase or decrease the alarm tone

volume level for night mode.

Setting the Monitor’s HR/Pulse Tone Volume for Night Mode

Use the Night Mode Settings Menu to set the monitor’s HR/pulse tone volume for night mode.
The options are: 0-8.
The default setting is 0.

To set the monitor’s HR/pulse tone volume for Night Mode:
Step
2 Select the HR/Pulse Tone Volume field.
Note — The Night Mode field must be set to Enable in order for the
HR/Pulse Tone Volume field to be activated.
Up and down arrows appear next to the HR/Pulse Tone Volume field.
3 Select the up or down arrow to increase or decrease the HR/pulse tone

volume level for night mode.
Exporting Configuration Settings

Use the Export Settings option to:
• Save a copy of your monitor’s configuration settings to a USB flash drive.
• Import the configuration settings into other monitors with the same hardware
configuration and software revision.
• Import these settings back into the original monitor after service.
Cautions • To import configuration settings from one monitor to another, ensure that both monitors
have the same hardware configuration and software version. The General tab displays
the current monitor hardware and software details.
• Importing configuration settings from another monitor clears patient data and trend
data.
• After importing configuration settings, review the settings to ensure they are correct.
When you export the settings to a USB flash drive, the file is saved in the following format:
<product name >_<encrypted configuration>_<software version>.cfg

What Is Exported
When you export the monitor’s configuration settings, only the settings that can be
shared among multiple monitors are exported. This allows you to configure multiple
monitors with the same settings instead of having to configure those settings individually
on each monitor.
The settings that are exported include:
• Default alarm limits and alarm settings

• Default NBP settings
• Default date and time settings
• General tab settings (except for Monitor Name)
• Admin tab settings

• All trend settings
• Data Export Menu settings (including the Server Port number if the associated Export
Port to cfg File check boxes are selected).
• Certificates and their associated passwords

• Security settings
• Recorder settings
• Current settings – other than alarm limits (depending on monitor options
purchased) – in the following measurement menus:
– General
– HR
– Pulse
– SpO2
– NBP
– RESP
– IBP
– Temp
– CO2
– C.O.
– RRa
What Is Not Exported

Patient-specific and monitor-specific configuration settings are not exported because
they are unique to each monitor and should not be copied to other monitors. For
example, alarm settings that are specific to an individual patient are not exported. The
monitor name is not exported because it only applies to the specific monitor.
The settings that are not exported include:
• Current patient settings.

• Monitor-specific settings such as the monitor’s name, default location, language
setting, and IP address settings.
For information about importing the exported settings into another monitor, see
“Importing Configuration Settings” on page 3-22.

To export configuration settings:
Step
1 Insert a USB flash drive into the USB port.

Menu.

4 Select the Export Settings button.

The monitor searches for the USB flash drive and a message
appears displaying the name of the exported file.
5 Select OK.
6 Close the window.
Importing Configuration Settings

Use the Import Settings option to import configuration settings from one monitor to another
monitor. Use the USB flash drive that contains the exported settings in the following format:
<product name >_<encrypted configuration>_<software version>.cfg
For more information about exporting settings, see “Exporting Configuration Settings” on
page 3-20.
The monitor restarts after importing configuration settings.
Cautions • To import configuration settings from one monitor to another, ensure that both monitors
have the same hardware configuration and software version. The General tab displays
the current monitor hardware and software details.
• Importing configuration settings from another monitor clears patient data and trend
data.
• After importing configuration settings, review the settings to ensure they are correct.
Note — The Language setting is not included in the exported configuration file. When you
import configuration settings, the selected language remains the same as it was before the
import process.

To import configuration settings:
Step
1 Insert a USB flash drive containing exported settings into the USB
port.

Menu.

4 Select the Import Settings button.

The monitor searches for the file on the USB flash drive and a
message appears asking you to confirm the file to import.
5 Select Yes.
When the import is complete, the monitor displays the message,
System will restart now.
6 Select OK to restart the monitor.
Configuring Other Administrative Settings

See the following table for details on where to locate instructions for configuring other
settings on the Admin tab.
For details on this Admin tab option See the following

• LAN Efficia CM Series Patient Monitors
• Wireless Network Configuration Guide
• Data Export
• Security
• Central Central Installation and Configuration
Guide
• Dashboard Dashboard Installation and Configuration
Guide
• Diagnostics1 Efficia CM Series Patient Monitors Service
• Upgrade Software Guide
• View Logs
1.
The Diagnostics pane allows the technician to configure hardware configurations, view the status and errors
for the patient monitor and connected modules.

Configuring Alarm Settings

This section provides details for configuring the alarm settings for your monitor.
Warning A potential hazard can exist if different alarm settings are used for the same or similar
equipment in any single area.
Use the Alarm Settings tab to:

• Configure the alarm tone pattern
• Configure the minimum alarm tone volume
• Configure the duration of Audio Pause mode
• Configure nurse call alarm priority
• Enable an alarm reminder
• Latch physiological alarms
• Restrict alarm settings
• Restrict audio settings
• Enable an audio off reminder
• Configure the SpO2 alarm delay
• Configure the Masimo RRa alarm delay (available only if the monitor has Masimo
rainbow SET with the RRa option)
• Configure arrhythmia timeout 1st
• Configure arrhythmia timeout 2nd
Configuring the Alarm Tone
The Alarm Tone setting controls the pattern of audible sounds during alarms. You can change
the Alarm Tone setting so that your monitor sounds different from other monitors in your care
area.
The default setting is Philips.
To set the alarm tone:
Step

Menu.

Step
2 Access the Alarm Settings tab as described in “Accessing the

System Menu Tabs” on page 3-1. The Alarm Settings tab appears.
3 Select the default setting for the Alarm Tone.

The options are Philips and IEC.
4 Close the window.
Configuring the Minimum Alarm Tone Volume

You can specify a minimum alarm volume, which prevents users from setting the alarm
volume below the specified level.
Note — Set the minimum alarm tone volume before configuring night mode settings
because the minimum alarm tone volume setting dictates the lowest setting for the Alarm
Tone Volume on the Night Mode Settings Menu.
Caution Set the minimum volume based on the environment and ambient noise levels where the
monitor will be used. Alarm volume should be loud enough to be heard within a room or
through an open door.
The default setting is 2 for the GW and ICU profiles. The default setting is 1 for the OR
profile.
To set the minimum alarm tone volume:
Step

Menu.

2 Access the Alarm Settings tab as described in “Accessing the System

Menu Tabs” on page 3-1.
The Alarm Settings tab appears.
3 Select the default setting for the Minimum Alarm Tone Volume.
The options are 1 – 8.
4 Close the window.
Configuring the Audio Pause Duration

If the user presses the Alarm Silence key twice within one second, the monitor enters Audio
Pause mode. A white box displays the message Audio Paused, and a timer shows the
remaining seconds until Audio Pause mode ends. When Audio Pause mode ends, all currently
active alarms become audible.
When alarms are paused, the nurse call signal does not alarm and alarms do not sound at
the central station. Audio Pause does not affect the monitor’s visual alarm indication methods.
The default setting is 120 seconds. To set the Audio Pause duration:
Step

Menu.

System Menu Tabs” on page 3-1.
3 Select the default setting for Audio Pause Duration.

The options are Off, 30, 60, 90,120, 180 seconds.
4 Close the window.
Configuring the Minimum Nurse Call Alarm Priority

The nurse call signal is a physical connection on the monitor that can connect to a variety of
external signals. For example, lights, alarm buzzers, or paging systems. When any alarm
condition exists, the nurse call signal activates.
You can configure the alarm priority that triggers the nurse call signal. Acknowledging (or
turning off) alarms turns off the nurse call signal. The nurse call alarm priority is the minimum
alarm priority level that triggers the nurse call signal. The priority level selected is inclusive.
For example, if the priority is Medium, then medium and high priority alarms will trigger the
nurse call signal, but a low priority alarm will not. The default is Low.

Note — Pausing or silencing alarms will cause the nurse call alarm not to trigger,
regardless of the priority setting.
To set the nurse call alarm priority:
Step

Menu.

3 Select the Minimum Nurse Call Alarm Priority.

The options are Low, Medium, or High.
4 Close the window.
Configuring Alarm Reminder and Reminder Time

You can set an audible reminder for alarm conditions that remain active after you have
acknowledged the alarm. This reminder can take the form of a repeat alarm tone for a
limited time, or an unlimited repetition of the alarm tone (same as a new alarm).
Note: Arrhythmia red alarms (high priority) are always included in an Alarm Reminder.
When Arrhythmia is set to Basic or Advanced, Yellow Arrhythmia Alarms are NOT
reminded by the Alarm Reminder. Instead they follow Arrhythmia Timeouts as
described on page 3-32.
To set the alarm reminder and reminder time:
Step
2 Access the Alarm Settings tab as described in “Accessing the System Menu

Step
3 Select the Alarm Reminder.

The options are On, ReAlarm, or Off.
On = If the alarm condition is still present after the alarm has been
acknowledged, the alarm will be reminded for a short period (6 seconds)
after the reminder interval time and remind again in the next reminder
period.
ReAlarm = If the alarm condition is still present after the alarm has been
acknowledged, the alarm’s status will be reset to active and continue to
play alarm sound after the reminder timeout, as if this alarm has never
been silenced.
Off = If the alarm is silenced, the alarm will NOT be played until it is
restored. In this case, the Reminder Time does not work.
4 Select the Reminder Time.

If you have selected On or ReAlarm in the Alarm Reminder field, select one of
the available Reminder Times.
The options are 1 minute, 2 minutes, and 3 minutes.
5 Close the window.
Latching Physiological Alarms

You can choose to latch all physiological alarms. A latched alarm continues even after the
condition that caused the alarm has resolved itself. For more information, see the
Instructions for Use supplied with your monitor.
To latch all physiological alarms:
Step
2 Access the Alarm Settings tab as described in “Accessing the System Menu

Step
3 Select the Latch Physiological Alarms check box to select or clear the check
box.
Physiological alarms are latched
NoPhysiological alarms are not latched
4 Close the window.
Restricting Alarm Settings

You can control whether a user can disable audible alarms for individual measurements.
By default, the monitor allows users to disable audible alarms. Visual alarms would not
be disabled.
To specify whether or not a user can disable audible alarms:
Step

Menu.

3 Select the Allow Alarm Disable check box.

Users are allowed to disable audible alarms for individual
measurements
NoUsers cannot disable audible alarms for individual
measurements
4 Close the window.
Restricting Audio Settings

You can control whether a user can silence all audible alarms indefinitely (or until
manually activated). By default, the monitor does not allow users to use the Audio Off
mode.

To specify whether or not a user can silence all audible alarms:
Step

Menu.

3 Select the desired Allow Audio Off option:

• Disabled - prevent the option to turn the audio off
• All - Provides the ability to turn alarms off on the monitor and
the Central Station (if available).
• Central Audio On - If your facility uses a Central Station and
this option is selected, you will be able to turn audio off on the
monitor and allow just the Central station to sound alarms.
4 Close the window.
Enabling an Audio Off Reminder

You can enable the monitor to play a reminder signal every three minutes when the monitor
is in Audio Off mode.
To enable an audio off reminder:
Step

Menu.

3 Select the Audio Off Reminder check box to select or clear the check
box.
Audio Off Reminder is enabled
NoAudio Off Reminder is disabled
4 Close the window.

Configuring the SpO2 Alarm Delay

Use the SpO2 Alarm Delay settings to configure the amount of time (in seconds) that the
averaged SpO2 value is above or below the corresponding alarm limit before an alarm is
activated. You can specify the time for the High/Low SpO2 alarm delay and the Desat
SpO2 alarm delay.
The default setting for both alarm delays is 0 (zero) seconds.

To specify the SpO2 Alarm Delay settings:
Step

Menu.

2 Select the SpO2 Alarm Delay setting for High/Low and Desat.
The options for both settings are 0 to 30 seconds.
3 Close the window.
Configure the Masimo RRa Alarm Delay
Note — The Masimo RRa Alarm Delay setting is available only if the monitor has Masimo
rainbow SET with the RRa option.
If you configure an RRa alarm delay time, the monitor does not sound an audible alarm
for the specified number of seconds.
The default setting is 30 seconds.
To configure the Masimo RRa Alarm Delay time:
Step

Menu.

Menu Tabs” on page 3-1. The Alarm Settings tab appears.
2 Select the Masimo RRa Alarm Delay setting.

The options are:
• Off
• 10 seconds
• 15 seconds
• 30 seconds
• 60 seconds
3 Close the window.

Configuring Arrhythmia Timeout Periods

Normally, arrhythmia alarms are announced when an alarm condition is detected. If multiple
alarm conditions are present, announcing all of the detected alarms might be confusing and
may hide a more serious condition. However, you can configure timeout periods in which the
audible and visible indications of alarms are inhibited even though the alarm condition was
detected.
Arrhythmia alarms are grouped according to priority/severity. During the configured timeout
period, only the highest priority alarm condition in each group is announced. Lower priority
alarms in the same group are not announced.
You can configure the arrhythmia timeout period for both first- and second-priority
arrhythmia alarms. First-priority (more severe) alarms have shorter timeout period options,
whereas second-priority (less severe) alarms have longer timeout period options. For more
information about arrhythmia alarm priorities, see the Instructions for Use supplied with your
monitor.
Configuring Arrhythmia Timeout 1st

For first-priority arrhythmia alarms, the default timeout period is 3 minutes.
To configure the Arrhythmia Timeout 1st:
Step

Menu.

2 Select the Arrhythmia Timeout 1st setting.

The options are:
• 0 minute
• 1 minute
• 2 minutes
• 3 minutes
• 4 minutes
• 5 minutes
3 Close the window.

Configuring NBP Settings
Configuring Arrhythmia Timeout 2nd

For second-priority arrhythmia alarms, the default timeout period is 10 minutes.
Note — The Arrhythmia Timeout 2nd setting cannot be less than the Arrhythmia Timeout 1st
setting.
To configure the Arrhythmia Timeout 2nd:
Step

Menu.

2 Select the Arrhythmia Timeout 2nd setting.

The options are:
• 0 minute
• 1 minute
• 2 minutes
• 3 minutes
• 4 minutes
• 5 minutes
• 10 minutes
• 15 minutes
Note — Only the options that are equal to or greater than the
Arrhythmia Timeout 1st setting are displayed.
3 Close the window.

This section provides details for configuring the NBP settings for your monitor.
Use the NBP Settings tab to:
• Configure the default NBP interval

• Align measurement intervals to the clock
• Configure the default initial inflation pressure (mmHg)
• Configure the default NBP VeniPuncture pressure
• Configure the default NBP VeniPuncture duration

Configuring the Default NBP Interval

Use the Default NBP Interval option to specify that the monitor automatically start an NBP
measurement each time a user turns on the monitor, starts a new patient, or changes the
patient type.
The default is Off.
To configure the default NBP interval value:
Step

Menu.
2 Access the NBP Settings tab as described in “Accessing the System

The NBP Settings tab appears.
3 Select the Default NBP Interval.

The options are Off, 1, 2, 3, 5, 10, 15, 30, 60, 90, 120 minutes.
4 Close the window.
Aligning Measurement Intervals to the Clock

You can specify whether to align NBP measurement intervals to the clock. For example, if the
Align Interval to Clock option is enabled and the user sets the interval to 10 minutes, and
presses the NBP key at 10:17 to start the auto interval, the monitor records the first
measurement at 10:17. The next NBP measurement will begin at 10:20, then 10:30, 10:40, and

so on. If the Align Interval to Clock option is disabled, the measurements in the example
will occur at 10:17, 10:27, 10:37, and so on.
To align NBP measurement intervals to the clock:
Step

Menu.

3 Select the Align Interval to Clock setting.

The options are Yes or No.
Note — The default setting is Yes.
4 Close the window.
Configuring the Default Initial Inflation Pressure (mmHg)
Caution Consider the typical patient population when determining what the default initial
inflation pressure setting should be for the device. The setting will be used unless the
user changes it for an individual patient.
You can specify the default initial inflation pressure value for Adult, Pediatric, and
Neonatal patients. The monitor uses this default value when a new patient is started.
When the monitor is in NBP Interval mode, the cuff inflates to the Default Initial Inflation
Pressure (mmHg) setting for the first NBP measurement, and then the monitor adjusts the
inflation value based on the patient’s Systolic measurement.
The default settings for each patient type are:

• Adult: 160 mmHg (21.3 kPa).
• Pediatric: 140 mmHg (18.7 kPa).
• Neonatal: 100 mmHg (13.3 kPa).
To configure the default initial inflation pressure:
Step
2 Access the NBP Settings tab as described in “Accessing the System Menu

Step
3 Select the Default Initial Inflation Pressure (mmHg) setting for Adult, Pediatric, or
Neonate. Use the up or down arrows to adjust the values.
The options are:
• Adult: 100 mmHg – 280 mmHg in 10 mmHg steps
(13.3 kPa – 37.3 kPa in 1.3 kPa steps).
• Pediatric: 80 mmHg – 190 mmHg in 10 mmHg steps
• Neonate: 60 mmHg – 140 mmHg in 10 mmHg steps
4 Close the window.
Configuring the Default NBP VeniPuncture Pressure (mmHg)

You can specify the default NBP venipuncture pressure value for Adult, Pediatric, and
Neonatal patients.

• Adult: 60 mmHg (8.0 kPa).
• Pediatric: 40 mmHg (5.3 kPa).
• Neonatal: 30 mmHg (4.0 kPa).
To configure the default NBP venipuncture pressure:
Step
2 Access the NBP Settings tab as described in “Accessing the System Menu
3 Select the Default NBP VeniPuncture Pressure (mmHg) setting for Adult, Pediatric,
or Neonate. Use the up or down arrows to adjust the values.
The options are:
• Adult: 20 mmHg – 120 mmHg in 5 mmHg steps
• Pediatric: 20 mmHg – 80 mmHg in 5 mmHg steps
• Neonate: 20 mmHg – 50 mmHg in 5 mmHg steps
4 Close the window.

Configuring Profile Settings
Configuring the Default NBP VeniPuncture Duration (seconds)

You can specify the default NBP venipuncture duration value for Adult, Pediatric, and
Neonatal patients.
• Adult: 170 seconds.
• Pediatric: 170 seconds.
• Neonatal: 85 seconds.
To configure the default NBP venipuncture pressure:
Step

Menu.

3 Select the Default NBP VeniPuncture Duration (seconds) setting for

Adult, Pediatric, or Neonate. Use the up or down arrows to adjust
the values.
The options are:
• Adult: 30 seconds – 170 seconds in 5-second steps
Pediatric: 30 seconds – 170 seconds in 5-second steps
Neonate: 30 seconds – 85 seconds in 5-second steps
4 Close the window.

Profiles are predefined monitor configurations that can be used for different monitoring
situations and care areas. Efficia CM monitors support up to six profiles. This section
provides details for configuring the profile settings for your monitor.
Use the Profile tab to:
• Select the default profile

• Save current settings to a profile
• Rename a user-configured profile

Selecting a Default Profile

The monitor returns to the default profile settings when a patient is admitted or discharged.
When the default profile is changed, the current patient under monitoring is discharged and
all trend data are cleared.
The monitor ships with the following three default profiles that cannot be modified by the
user:
• Operating Room (OR)
• General Ward (GW)
• Intensive Care Unit (ICU)
Note — Because users cannot modify profiles, ensure that you select the correct profile for
the care area in which the monitor will be used.
The remaining profiles are customizable:

• Profile 1
• Profile 2
• Profile 3
For a complete list of each profile’s default configurations, see “Profile Settings” .
Note — The factory default configurations for Profile 1, Profile 2, and Profile 3 are the same as
those for the GW profile.
To select a default profile:

Step
2 Access the Profile tab as described in “Accessing the System Menu Tabs” on
page 3-1. The Profile tab appears.

Step
3 Select the default profile from the Select Default Profile list.
The options are OR, ICU, GW, Profile 1, Profile 2, Profile 3.
Note — The options listed for Profile 1, Profile 2, and Profile 3 may differ if they
have been renamed. For more information, see “Renaming a Profile” on
page 3-40.
A confirmation window appears.
4 Select OK to load the selected profile and discharge the current patient.
5 Close the window.
Saving Current Settings to a Profile

You can configure the monitor for use in a specific care area. To do so, make all of your
changes to the monitor’s settings, save the changes to a profile, and then rename the
profile. You can select one of the three customizable profiles to be updated with the
monitor’s current settings.
To save the monitor’s current settings to a profile:
Step

Menu.
2 Access the Profile tab as described in “Accessing the System Menu

The Profile tab appears.
3 Make your changes to the monitor’s settings.
4 Select the Save Current Settings button.

A window appears, prompting you to select a profile to update.
5 Select a profile from the Select a Profile field.
6 Select OK to save the monitor’s current settings to the profile.
7 Close the window. To rename the profile, proceed to “Renaming a

Profile” on page 3-40.

Renaming a Profile
After you have saved the monitor’s settings to one of the customizable profiles (Profile 1,
Profile 2, or Profile 3), you should rename the profile.
To rename a profile:
Step

Menu.
2 Access the Profile tab as described in “Accessing the System Menu

The Profile tab appears.
3 Select the Rename Profile button.

A window appears, prompting you to select a profile to rename.
4 Select a profile from the Select Profile field.
5 Select the New Name field.

A keyboard appears.
6 Enter a new name for the profile, and then select OK.
The maximum number of characters for the new name is 10. Any
characters on the keyboard may be used.
The New Name field displays the entry.
7 Select OK.
The renamed profile appears in the Select Default Profile list.
8 Close the window.

Returning the Monitor
Submitting a Damage Claim

If there is physical damage when you receive your monitor, or if an item does not meet
specified operational requirements, notify the carrier and the nearest Philips Customer
Care Solutions Center. Philips will arrange for immediate repair or replacement of the
damaged/inoperative part.
Returning the Monitor For Service

To return the monitor for service, call the Philips Customer Care Solutions Center or
your local Philips representative for a Returned Materials Authorization (RMA) number.
Have all equipment serial numbers available when calling. Mark the shipping carton
and any shipping documents with the RMA number.
Warning Before returning any equipment to Philips:
• Back up the configuration. For more information, see “Exporting Configuration

Settings” on page 3-20.
• Clean and disinfect it. For detailed information, see the Instructions for Use
supplied with your monitor.
• Delete all patient data. For detailed information, see the Service Guide supplied
with your monitor.
• If you changed the administrator password from the factory default, return the
password to 2-1-5. Failure to do so may result in the loss of data.
• Remove the battery. For detailed information, see the Service Guide supplied with
your monitor.

Disposing of the Monitor
To pack the monitor for return, disconnect all cables. It is not necessary to return
accessories or the power cord. If available, use the original carton and packing materials.
Ensure that the monitor is transported within the following specifications:

• Temperature: -20°C to +40°C (-4°F to 104°F).
• Humidity: 15% to 90%.
• Atmospheric Pressure: 1013 hPA to 701 hPA.
To return the monitor in the original packaging:
Step
1 Place the monitor in the original packaging.
2 Seal the carton with packaging tape.
3 Label the carton with the shipping address, return address, and
RMA number.
If the original carton is not available, use the following procedure to pack the monitor:
Step
1 Place the monitor in a plastic bag.
2 Locate a corrugated cardboard shipping carton with at least 200

psi (pounds per square inch) bursting strength.
3 Fill the bottom of the carton with at least 2 inches of packing

material.
4 Place the bagged unit on the layer of packing material and fill the
box completely with packing material.
5 Seal the carton with packaging tape.
6 Label the carton with the shipping address, return address, and
RMA number.

For disposal of parts and accessories, where not otherwise specified, follow local
regulations regarding disposal of hospital waste.

Warning Before disposing of an Efficia CM Series monitor, delete all patient information. For
more information about deleting patient data, see the Service Guide supplied with your
monitor.
Do not dispose of this product (or any parts of it) in industrial or domestic waste. The
system may contain hazardous substances that can cause serious environmental
pollution. The system also contains sensitive privacy information. Philips recommends
that you contact your Philips Customer Care Solutions Center before disposing of this
product.
To avoid contaminating or infecting personnel, the environment or other equipment,
disinfect and decontaminate the monitor before disposing of it in accordance with your
country’s laws. For more information, see the resources listed below.
Philips Healthcare gives support for:
• Recovery of reusable parts
• The recycling of useful materials by competent disposal companies
• Safe and effective disposal of equipment
For advice and information, contact your Philips Customer Care Solutions Center and
see
http://www.healthcare.philips.com/main/about/sustainability/recycling/index.wpd for
more information.
If this product is to be passed on to another user who is to use it for its intended
purpose, then it should be passed on in its complete state. In particular, the existing
user should make sure that all the product support documentation - including all
Instructions for Use - are passed on to the new user. A new user should be made aware
of the support services that Philips Customer Care Solutions Center provides for
installing, commissioning and maintaining the equipment or system, and for the
comprehensive training of operators. Existing users must bear in mind that passing on
medical electrical equipment to new users may present serious technical, medical,
privacy and legal risks. The original user may remain liable even if the equipment is
given away.
Existing users are strongly advised to seek advice from their local Philips Customer Care
Solutions Center representative before agreeing to pass on any equipment.
Once the equipment has been passed on to a new user, the previous user may still
receive important safety-related information, such as bulletins and field change orders.
In many jurisdictions there is a clear duty on the previous user to communicate such
safety-related information to new users.
Previous users who are not able or prepared to do this should inform the Philips
Customer Care Solutions Center about the new user, so that Philips Customer Care
Solutions Center can provide the new user with safety-related information.


Profile Settings
Profiles are predefined monitor configurations that can be used for different
monitoring situations. The monitor ships with the following three default profiles:
• Operating Room (OR)

• General Ward (GW)
• Intensive Care Unit (ICU)
The default profile settings cannot be changed, however, you can create up to three
customized profiles for different care settings.
Profile Configurations
The following table lists the default configurations of the default profiles, GW, ICU, and
OR. The default configuration for the customizable profiles are the same as the GW
default configuration. If you create a customized profile to be used as your facility’s
default profile, print this table and record your settings in the Facility Default column.
Facility
Parameter GW ICU OR
Default
Tone Volume Alarm 4 4 2
Minimum 2 2 1
HR/Pulse 0 0 3
Profile Settings
Efficia CM Series Patient Monitors Installation and Configuration Guide A-1
Facility
Parameter GW ICU OR
Default
Alarm Audio pause duration 120 seconds 120 seconds 120 seconds
Latch physiological alarms Off Off Off
Allow alarm disable On On On
Allow audio off Disabled Disabled Disabled
Audio off reminder Off Off Off
Alarm Reminder On On On
Reminder Time 3 minutes 3 minutes 3 minutes
Record on alarm Off Off Off
Display alarm limits On On On
All alarm limits See “The following table lists the default
configurations of the default profiles, GW,
ICU, and OR. The default configuration for the
customizable profiles are the same as the GW
default configuration. If you create a
customized profile to be used as your
facility’s default profile, print this table and
record your settings in the Facility Default
column.” on page A-1.
Recorder Speed 25.0 mm/s 25.0 mm/s 25.0 mm/s
ECG Gain 10.0 mm/mV 10.0 mm/mV 10.0
mm/mV
Waveform length 7 seconds 7 seconds 7 seconds
Real-time wave selection 1 1 1
Real-time wave 1 Primary ECG Primary ECG Primary
ECG
Real-time wave 2 NA/blank NA/blank NA/blank
Full disclosure wave selection 2 2 2
Full disclosure wave 1 ECG II ECG II ECG II
Full disclosure wave 2 SpO2 SpO2 SpO2
Full disclosure wave 3 NA/blank NA/blank NA/blank
Full disclosure wave 4 NA/blank NA/blank NA/blank
Profile Settings
A-2 Efficia CM Series Patient Monitors Installation and Configuration Guide
Facility
Parameter GW ICU OR
Default
ECG Sweep speed 25.0 mm/s 25.0 mm/s 25.0 mm/s
Scale 0.5 cm/mV 0.5 cm/mV 0.5 cm/mV
Filter mode Monitoring Monitoring Filtered
Notch filter Off Off On
Lead set 3-Lead 3-Lead 3-Lead
Primary lead ECG II ECG II ECG II
Secondary lead NA/Blank NA/Blank NA/Blank
HR alarm audible Yes Yes Yes
Arrhythmia analysis Adult: Adult: Adult:
Enhanced (if Enhanced (if Enhanced
available) or available) or (if available)
Basic Basic or Basic
Pediatric: Pediatric: Pediatric:
Basic Basic Basic
Neonatal: Neonatal: Neonatal:
Cardiotach Cardiotach Cardiotach
Analysis mode Single lead Single lead Single lead
ECG waveform selection for I, II, III I, II, III I, II, III
alarm history
Arrhythmia TimeOut 1st 3 minutes 3 minutes 3 minutes
Arrhythmia TimeOut 2nd 10 minutes 10 minutes 10 minutes
AFib/IHR Reminder 30 minutes 30 minutes 30 minutes
ST analysis Adult: On Adult: On Adult: On
Pediatric: Off Pediatric: Off Pediatric:
Neonatal: Off Neonatal: Off Off
Neonatal:
Off
ST Audible alarm Yes Yes Yes
ISO/J point detection Auto Auto Auto
ISO Point -80 ms -80 ms -80 ms
J Point 48 ms 48 ms 48 ms
ST Offset 60 ms 60 ms 60 ms
Profile Settings
Facility
Parameter GW ICU OR
Default
Impedance Impedance resp Enable Enable Disable
respiration Sweep speed 6.25 mm/s 6.25 mm/s 6.25 mm/s
Scale x1 x1 x1
Detection mode Auto Auto Auto
Threshold 1 ohm (or 1 ohm (or 1 ohm (or
64 LSB at 64 LSB at 64 LSB at
x1 scale) x1 scale) x1 scale)
Audible alarm Yes Yes Yes
Apnea alarm 20 seconds 20 seconds Off
SpO2 Sweep speed 25.0 mm/s 25.0 mm/s 25.0 mm/s
SpO2 Audible alarm Yes Yes Yes
SpHb Audible alarm Yes Yes Yes
SpCO Audible alarm Yes Yes Yes
SpO2 high/low alarm delay 0 second 0 second 0 second
SpO2 desat alarm delay 0 second 0 second 0 second
SpO2 response Normal Normal Normal
Perfusion indicator On On Off
Profile Settings
Facility
Parameter GW ICU OR
Default
NBP Default NBP interval Off Off Off
Align interval to clock Yes Yes Yes
Default initial inflation Adult: Adult: Adult:
pressure 160 mmHg 160 mmHg 160 mmHg
140 mmHg 140 mmHg 140 mmHg
Default VeniPuncture pressure Adult: Adult: Adult:
Default VeniPuncture duration Adult/ Adult/ Adult/
170 seconds 170 second 170 second
85 seconds 85 seconds 85 seconds
Limit display Sys Sys Sys
Auto print NBP Off Off Off
NBP pressure units mmHg mmHg mmHg
NBP audible alarm Yes Yes Yes
NBP list display mode Graphical Graphical Graphical
NBP list time scale 1 hour 1 hour 1 hour
Profile Settings
Facility
Parameter GW ICU OR
Default
IBP IBP1 label ABP ABP ABP
IBP2 Label PAP PAP PAP
IBP3 Label CVP CVP CVP
IBP4 Label P P P
Sweep Speed
ABP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
Ao Sweep Speed 25 mm/s 25 mm/s 25 mm/s
ART Sweep Speed 25 mm/s 25 mm/s 25 mm/s
CVP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
ICP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
LAP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
P Sweep Speed 25 mm/s 25 mm/s 25 mm/s
PAP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
RAP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
UAP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
UVP Sweep Speed 25 mm/s 25 mm/s 25 mm/s
Overlap IBP Sweep speed 25 mm/s 25 mm/s 25 mm/s
Scale
ABP Scale 0-150 mmHg 0-150 mmHg 0-150
mmHg
Ao Scale 0-150 mmHg 0-150 mmHg 0-150
mmHg
ART Scale 0-150 mmHg 0-150 mmHg 0-150
mmHg
CVP Scale 0-30 mmHg 0-30 mmHg 0-30
mmHg
ICP Scale 0-30 mmHg 0-30 mmHg 0-30
mmHg
LAP Scale 0-30 mmHg 0-30 mmHg 0-30
mmHg
P Scale 0-150 mmHg 0-150 mmHg 0-150
mmHg
PAP Scale 0-30 mmHg 0-30 mmHg 0-30
mmHg
RAP Scale 0-30 mmHg 0-30 mmHg 0-30
mmHg
UAP Scale 0-150 mmHg 0-150 mmHg 0-150
mmHg
Profile Settings
Facility
Parameter GW ICU OR
Default
Temperature Audible alarm Yes Yes Yes
(T1 and T2)
Temperature units °C °C °C
CO2 Sweep speed 6.25 mm/s 6.25 mm/s 6.25 mm/s
Scale 0 mmHg – 0 mmHg – 0 mmHg –
CO2 audible alarm Yes Yes Yes
awRR audible alarm Yes Yes Yes
awRR apnea alarm 20 seconds 20 seconds 20 seconds
CO2 pressure units mmHg mmHg mmHg
CO2 On/Standby Standby Standby Standby
Max hold 20 seconds 20 seconds 20 seconds
Humidity correction BTPS BTPS BTPS
(Sidestream)
Balance gas (Mainstream) Room air Room air Room air
O2 Compensation 16% 16% 16%
(Mainstream)
Anesthetic agent (Mainstream) 0.0% 0.0% 0.0%
Gas temperature (Mainstream) 35 °C 35 °C 35 °C
Cardiac Tblood audible alarm Yes Yes Yes
output
Layout Default Adult/ Adult/ 8 waveform
Pediatric: Pediatric:
5 waveform 5 waveform
Neonatal: Neonatal:
OxyCRG OxyCRG
Layout configure See the Changing the Layout chapter in the
Efficia CM Series Monitor Instructions for Use.
Short Trend Layout Time Scale 15 minutes 15 minutes 15 minutes
Profile Settings
Facility
Parameter GW ICU OR
Default
Trend Tabular trend display interval 15 minutes 5 minutes 15 seconds
Tabular trend display HR, NBP, HR, NBP, HR, NBP,
parameter selection SpO2, Pulse, SpO2, Pulse, SpO2,
RESP, etCO2, RESP, etCO2, Pulse,
awRR, ABP, awRR, ABP, RESP,
PAP PAP etCO2,
awRR, ABP,
PAP
NBP trend display parameter HR, NBP, HR, NBP, HR, NBP,
selection SpO2, Pulse, SpO2, Pulse, SpO2,
PAP PAP etCO2,
awRR, ABP,
PAP
Graphic trend display time 8 hours 8 hours 4 hours
scale
Graphic trend display HR, NBP, HR, NBP, HR, NBP,
parameter selection SpO2, Pulse, SpO2, Pulse, SpO2,
PAP PAP etCO2,
awRR, ABP,
PAP
Alarm history waveform 25 mm/s 25 mm/s 25 mm/s
sweep speed
Alarm history display ECG II, SpO2, ECG II, SpO2, ECG II,
waveform selection RESP RESP SpO2, ABP
Full disclosure waveform 25 mm/s 25 mm/s 25 mm/s
sweep speed
Full disclosure display ECG II, SpO2, ECG II, SpO2, ECG II,
waveform selection RESP, CO2, RESP, CO2, SpO2,
ABP, PAP ABP, PAP RESP, CO2,
ABP, PAP
Pulse Audible alarm Yes Yes Yes
Pulse source Auto Auto Auto
Profile Settings
© 2019 Koninklijke Philips N.V.

All rights are reserved. Reproduction or transmission in whole or in part, in any form or by any means, electronic, mechanical or otherwise, is prohibited
without the prior written consent of the copyright owner.
Printed in China
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*453564623561*
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All manuals and user guides at all-guides.

Efficia CM Series Patient Monitors

Installation and Configuration Guide

ii Efficia CM Series Installation and Configuration Guide

Efficia CM Series Installation and Configuration Guide iii

Typeface Usage Example

Italic Variables, document • <product name>-<encryption

Notes, Cautions, and Warnings

Note — A Note calls attention to an important point in the text.

iv Efficia CM Series Installation and Configuration Guide

Symbol Description Standard/Reference

Symbol Name Standard/Reference

* ISO 7000 Graphical symbols for use on equipment - Registered symbols

Efficia CM Series Installation and Configuration Guide v

Symbol Name Standard/Reference

Fragile, handle with care ISO 15223-1** 5.3.1

Stacking limit by number ISO 7000* 2403

Ambient temperature range ISO 15223-1**5.3.5

Keep dry ISO 15223-1** 5.3.4

CE mark: Product meets the requirements European Council Directive

* ISO 7000 Graphical symbols for use on equipment - Registered symbols

vi Efficia CM Series Installation and Configuration Guide

Symbol Name Standard/Reference

On/Standby key IEC 60417* 5009

AC power LED IEC 60417* 5032

Charging LED IEC 60417* 5546

Alarm silence key IEC 60417* 5576

Freeze Waveform key NA

Trend key** IEC 60417* 5847

* IEC 60417 Graphical symbols for use on equipment

Note — Not all monitors have all keys.

Efficia CM Series Installation and Configuration Guide

Measurement Connector Symbols

Symbol Name Standard/Reference

Gas output connector ISO 7000***-0795

Mainstream CO2 connector NA

ECG ECG connector NA

Caution ISO 15223-1** 5.4.4

Masimo SET® and rainbow (red NA

Nellcor OxiMax™ symbol NA

* IEC 60417 Graphical symbols for use on equipment

viii Efficia CM Series Installation and Configuration Guide

Input/Output Connector Port Symbols

Symbol Name Standard/Reference

Nurse call connector IEC 60417* 5336

ECG Out port NA

* IEC 60417 Graphical symbols for use on equipment

Rear Panel Label Symbols

Symbol Name Standard/Reference

Catalog number ISO 15223-1* 5.1.6

Serial number ISO 15223-1* 5.1.7

Monitor key code NA

Efficia CM Series Installation and Configuration Guide ix

Symbol Name Standard/Reference

ICES-001 Canadian ISM requirement International Erosion Control

RCM Mark Regulatory Compliance Mark for

Compliance with WEEE standard Waste Electrical and Electronic

Authorized EU Representative OK ISO 15223-1* 5.1.2