IntelliVue X2 Multi-Measurement

Module
Philips M3002A Technical Data Sheet

The IntelliVue X2 Multi-Measurement Module is the EASI method or with 10 electrodes using the
compact in size, ergonomic, and modular in design. conventional method.
It provides an easy-to-use touchscreen user • Multi-lead arrhythmia and ST segment analysis at
interface, is highly customizable and shares a the bedside on all available leads.
technological platform with the Philips IntelliVue • Mainstream or Sidestream CO2
MP5-MP90 patient monitors. • Choice of FAST SpO2 or Masimo SET SpO2
The IntelliVue series offers a complete monitoring • Invasive Pressure and Temperature measurement
solution that is flexible and modular, designed to • The monitor can operate using battery power for
suit a broad spectrum of monitoring needs. up to 3 hours with basic monitoring configuration
to let you safely and easily monitor patients during
in-hospital transfer.
Measurement Features • The X2 can be connected to a host monitor
• Compact, rugged, lightweight monitor with built in (IntelliVue MP20/30/40/50/60/70/80/90) via the
measurements MSL cable or directly to provide measurements,
trends and patient information. Alternatively, the
• ECG monitoring using any combination of three X2 can function as a standalone monitor, powered
to 10 electrodes. by an external power supply.
• 12-lead ECG monitoring with five electrodes using

PAD
Usability Features Main Components
• Touchscreen and hardkeys as input device.
• Intuitive user interface.
Monitor
• Simple menu hierarchy gives fast access to all basic monitoring tasks. The monitor has a color LCD TFT display with a wide viewing angle,
• Patient data management with tabular and graphic trends. providing high resolution waveform and data presentation.
• Settings “Profiles” for rapid case turnover. The display, processing unit and measurements are integrated into one
• Patented automatic alarm limits help clinicians provide care more device. An optional external power supply provides power for the
efficiently. monitor.
• 3.5" TFT flat panel display with QVGA
(320 x 240) resolution, wide viewing angle, large numerics, User Interface
permanently visible alarm limits, and up to three real-time waves.
• Capable of functioning in a wireless infrastructure (IIT) The user interface is designed for fast and intuitive operation. The
color graphical user interface ensures that clinicians quickly feel at ease
using the monitor.
Intended Use
Configurable SmartKeys with intuitive icons allow monitoring tasks to
The monitor is intended to be used for monitoring and recording of,
be performed quickly and easily, directly on the monitor screen.
and to generate alarms for, multiple physiological parameters of adults,
pediatrics, and neonates in a hospital environment and during patient Waves and numerics are color-coded.
transport inside and outside of hospitals. The monitor is intended for The monitor displays up to three measurement waves simultaneously.
use by health care professionals. For 12-lead ECG monitoring it can display 12 real-time ECG waves,
The monitor is only for use on one patient at a time. It is not intended with a rhythm strip and all ST values.
for home use. Not a therapeutic device. The X2 monitor is supplied with a resistive touchscreen.
Rx only: U.S. Federal Law restricts this device to sale by or on the
order of a physician. Simulated Keyboard
ST segment monitoring is intended for use with adult patients only and If alpha or numeric data entry is required, for example to enter patient
is not clinically validated for use with neonatal and pediatric patients. demographics, an on-screen keyboard will automatically appear on the
The ECG measurement is intended to be used for diagnostic recording screen.
of rhythm and detailed morphology of complex cardiac complexes
(according to AAMI EC 11). Mounting
EMC Environment: The mounting options available enable flexible, space saving placement
The monitor is suitable for use in all establishments incl. those directly of the monitors for an ergonomic work space. The monitor is shipped
connected to the public low-voltage supply network that supplies with a low cost mounting plate if not specified otherwise.
buildings for domestic purposes. When used with the M2741A
Sidestream CO2 sensor, the monitor can only be used in hospital Application Features
environments.

Critical and Cardiac Care Features

Upgradability
• The monitor performs multi-lead arrhythmia detection analysis
The X2 monitor allows new capabilities to be added in the future as on the patient’s ECG waveform at the bedside. It analyzes for
your monitoring requirements evolve. This upgradability gives the ventricular arrhythmias, calculates heart rate, and generates alarms,
including asystole, bradycardia, and ventricular fibrillation.
security of knowing that the monitors can be enhanced and updated as
practices and technologies advance, and it protects long-term • Up to 12 leads of ST segment analysis can be performed on adult
patients at the bedside, measuring ST segment elevation and
investments.
depression and generating alarms and events. The user can trend ST
changes, set high and low alarm limits, and set both ST and isoelectric
measurement points. Using ST Snippets, one-second wave segments
can be compared with a baseline segment for each measured ST lead.

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• optional ST Map application shows ST changes over time in two - Alarm Limit Reports
multi-axis spider diagrams. - Vital Signs
• QT/QTc interval monitoring provides the measured QT interval, - Graphic Trends
the calculated heart-rate corrected QTc value and a ΔQTc value, - Realtime Wave Reports
which tracks variation in the QT interval in relation to a baseline Report templates can be defined in advance, enabling print-outs
value. tailored to each hospital’s specific requirements to be started
• optional 12-lead ECG data can be measured, using either the EASI quickly. Reports can be printed on centrally-connected printers or
placement method with five standard electrodes or conventional via the IntelliVue PC Printing Solution, and they can be initiated
electrode placement with 10 electrodes.1 manually or automatically at user-defined intervals.
• 12 realtime ECG waveforms can be displayed simultaneously.
• The IntelliVue PC Printing Solution allows printing of reports,
• High performance pulse oximetry technologies perform accurately
waveform captures and trends from the X2 to a standard off-the
even in cases with low perfusion.
shelf printer or to an electronic file.
• Choice of sidestream or mainstream CO2 monitoring for high
quality measurements with intubated and non-intubated patients.
Alarms
Ease of Use The alarm system can be configured to present either the traditional
HP/Agilent/Philips alarm sounds or sounds compliant with the draft
• Screen layouts are easily adjustable, allowing flexible display of
measurement information. ISO/IEC 9703-2 Standard.

• Temperature, height, and weight can be configured either in metric Alarm limits are permanently visible on the main screen. The Alarm
or imperial units. Pressure measurements can be displayed in kPa or Limits page provides a graphic depiction of alarm limits in relation to
mmHg. Gases can be displayed in kPa, mmHg. the currently monitored measurement values and lets you adjust alarm
limits. It also lets you preview wide and narrow automatic alarm limits
Trends before you apply them.
• The trend database stores patient data from up to 30 When an alarm limit is exceeded, it is signalled by the monitor in the
measurement numerics. The measurement information can be following ways:
sampled every 12 seconds, one minute, or five minutes, and stored
for a period ranging from four to 48 hours. • an alarm tone sounds, graded according to severity
• Horizon Trends show the deviation from a stored baseline. • an alarm message is shown on the screen, color-coded according to
severity
• the numeric of the alarming measurement flashes on the screen
Transport Features
• alarm lamps flash for red and yellow alarms and are illuminated for
• The monitor’s portable design means it can be used for in and out-of- technical INOPs
hospital transport: a basic monitor weighs 1.5 kg.
If the monitor is connected via a network to a central monitoring
• The monitor can operate using battery power for up to 3 hours, to
station, alarming is simultaneous at the monitor and at the Information
let you safely and easily monitor patients during procedures or in-
hospital transfer. Center.

• Specially-designed mounting solutions let you quickly disconnect the Alarms are graded and prioritized according to severity:
monitor for transport and reconnect to the mount after transport.
• Red Alarms*** identify a potentially life threatening situation for a
• The Universal Admit, Discharge and Transfer (ADT) feature means patient .
that all ADT information is shared between the networked monitor
• Yellow Alarms** indicate conditions violating preset vital signs
and the Information Center. Information need only be entered once.
limits.
• Technical Alarms (INOPS) are triggered by signal quality
Patient Data Documentation
problems, equipment malfunction or equipment disconnect.
• An extensive range of Patient Reports can be printed:
The Silence/Pause Alarms function (equivalent to Silence/Suspend
- 12-lead ECG Reports
with previous monitor generations) allows the user to switch off
1.EASI-derived 12-lead ECGs and their measurements are approximations to conventional
alarm tones with one touch.
12-lead ECGs. As the 12-lead ECG derived with EASI is not exactly identical to the 12-
lead conventional ECG obtained from an electrocardiograph, it should not be used for
All alarms can be paused for a period of one, two, three, five, or 10
diagnostic purposes. minutes or turned off indefinitely.

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 Alarm strip recordings are available on a centrally-connected • MMS Extensions (M3012A, M3014A, M3015A, M3016A)1
recorder or via the IntelliVue PC Printing Solution. • an external power supply (M8023A)

Patented automatic alarm limits automatically adapt the alarm limits

to the patient’s currently measured vital signs within a safe margin Network Interface
defined individually for each patient. The network interface provides the system with networking capability
Visual and/or audible latching and non-latching alarm handling is via a wired or wireless network connection.
available.
Wireless Network (optional)
Profiles The monitor can function within a telemetry infrastructure compatible
Profiles are predefined configuration settings for Screens, with the Philips Cellular Telemetry System (CTS) in the WMTS and
measurement settings, and monitor settings. Each Profile can be ISM bands. Additional components are required to complete the
designed for a specific application area and patient category, for system. Please refer to the M3185A IntelliVue Clinical Network
example OR adult, or ICU neonatal. Profiles enable a quick reaction to Technical Data Sheet for further information.
patient and care location changes: activating a Profile with a particular
patient category (Adult, Pediatric or Neonatal) automatically applies
suitable alarm and safety limits and saves time usually spent carrying Monitor Specifications
out a complete set-up procedure.

Profiles can be created directly on the monitor or remotely on a Safety Specifications

personal computer and transferred to the monitor using the IntelliVue The monitor complies with the Medical Device Directive 93/42/EEC
Support Tool. A selection of Profiles for common monitoring (CE0366) and with IEC 60601-1:1988 + A1:1991 + A2:1995; EN60601-
situations is provided with the monitor. These profiles can be changed, 1:1990 + A1:1993 + A2:1995; UL 60601-1:2003; CAN/CSA
added to, renamed, or deleted. C22.2#601.1-M90; JIS T 0601-1:1999; IEC 60601-1-1:2000; EN 60601-
1-1:2001.
Optional Networking Capabilities All applied parts are Type CF unless otherwise specified. They are
The monitor can operate as part of a wired or wireless hospital protected against damage from defibrillation and electrosurgery.
network system, using the Philips IntelliVue Clinical Network interface. The possibility of hazards arising from software errors was minimized
in compliance with ISO 14971:2000, EN60601-1-4:1996 + A1:1999
Service Features and IEC 60601-1-4:1996 + A1:1999.

The monitor complies with the EMC standards

• The Support Tool helps technical personnel to
- carry out configuration, upgrades and troubleshooting via the IEC 60601-1-2:2001; EN 60601-1-2:2001

network, or on an individual monitor This ISM device complies with Canadian ICES-001. Cet appareil ISM
- share configuration settings between monitors est conforme a la norme NMB-001 du Canada.
- back up the monitor settings. The X2 Multi-Measurement Module can be used in a transport
• A password-protected Service Mode ensures that only trained staff environment such as road ambulance, airplane or helicopter, except
can access service tests and tasks. when used with the M2741A Sidestream CO2 sensor. For this
• The Configuration Mode is password-protected and allows trained purpose, the monitor fulfills the following additional mechanical, EMC
users to customize the monitor configuration. and environmental requirements:

• Shock Tests according to IEC TR 60721-4-7, Class 7M3. Test

Device Connections procedure according to IEC/EN 60068-2-27 (peak acceleration up to
The monitor can be connected to: 100g).
• Random Vibration according to IEC TR 60721-4-7, Class 7M3. Test
• an Information Center (for example M3150B)
procedure according to IEC/EN 60068-2-64 (RMS acceleration 5g).
• a PC
• a host monitor of the IntelliVue family (MP20/30, MP40/50, MP60/70, 1.The MMS Extensions will only function when the monitor is connected to either the
MP80/90) via MSL cable external power supply or a host monitor.

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• Sinusoidal Vibration according to IEC TR 60721-4-7, Class 7M3. Environmental Specifications
Test procedure according to IEC/EN 60068-2-6 (acceleration up to
amplitude 2g).
• Bump Test according to IEC/EN60068-2-29 (peak acceleration 15g,
1000 bumps). Item Condition Range
• Free Fall Test according to EN1789 (covers also IEC TR 60721-4-7
Temperature Operating 0 to 40oC
and Class 7M3). Test procedure according to EN 60068-2-32 (height Range
0.75 m). (32 to 104 oF)
• Specification for degrees of protection provided by enclosures Storage -20 to 60oC
according to IEC/EN 60529: IP 32 (incl. Transport)
• EN 1789 +A1:2003 Medical vehicles and their equipment - Road (-4 to 140 oF)
ambulances (chapter 6 - Medical Devices). Temperature Operating 0 to 35oC
• Radiated susceptibility 20 V/m according to EN ISO 9919 (SpO2) Range when
and EN ISO 21647 (CO2). (32 to 95oF)
charging the
• Altitude Range from -500 to 3000 m operating and -500 to 4600 m battery
storage and transportation.
Humidity Range Operating 15% to 95% Relative
• Extended radiated susceptibility tests
Humidity (RH) (non
The X2 Multi-Measurement Module with its out-of-hospital parameter condensing)
set provides a general immunity level of 20 V/m with only few
Storage and 5% to 95% Relative
restrictions. Details are as listed below:
Transport Humidity (RH)
- GSM 900: Immunity at 900 MHz (uplink mobile phone), 20V/m,
Altitude Range Operating -500 m to 3000 m
duty cycle 1:8
(10000 ft)
- GSM 1800: Immunity at 1800 MHz (uplink mobile phone), 20V/m,
duty cycle 1:8. Storage and -500 m to 4600 m
- DECT: Immunity at 1800 MHz (digital cordless phone), 20V/m, Transport (15000 ft)a
duty cycle 1:24
Ingress Monitor IP32 (protected against
- AM: 1 kHz Immunity from 80 MHz to 2.5 GHz (any radio
Protection the ingress of solid
communication unit, broadcasting and TV transmitter), 20V/m, foreign objects 2.5 mm
modulation factor 80%. (ECG: 20 V/m except 0.8-1.2 GHz where in diameter or larger,
it is 10V/m) and the ingress of water
• Operating ambient temperature testing over the range from 0 to when the water is
40 °C (32 to 104 °F). dripping vertically and
• Operating ambient humidity testing up to 95% RH at 40 °C the monitor is tilted up
(104 °F), non condensing. to 15°).

External Power IP31(protected against

Physical Specifications Supply (M8023A) the ingress of solid
foreign objects 2.5 mm
in diameter or larger,
and the ingress of water
Product Max Weight WxHxD when the water is
dripping vertically) when
M3002A 1.5 kg < 188 x 99 x 86 mm
rested on its rubber feet
IntelliVue X2 (without (3.3 lb) (7.4 x 3.9 x 3.4 in)
on a flat, level surface.
options)
IP32 when mounted
with the connectors
facing downwards
a. sufficient for flight altitudes up to 12,000 m with pressurized cabins

5
Performance Specifications
Monitor Performance Specifications

Alarm Signal System delay less than 3 seconds

Monitor Performance Specifications Pause duration 1,2,3 minutes or infinite,

depending on
Power Power < 40W average, <65W configuration
Specifications consumption peak
Extended alarm 5 or 10 minutes
Line Voltage 100 to 240 V ~ pause
Current 1.3 to 0.7A Review Information: all alarms / inops, main alarms on/off,
Frequency 50/60 Hz Alarms alarms acknowledged and time of occurrence

Battery Operating Time Basic monitor capacity 500 items

Specifications (with new, fully configuration: 3 hours Real Time Range: from: January 1, 1997, 00:00 to: December
charged battery at Clock 31, 2080, 23:59
25 °C)
Accuracy: < 4 seconds per day (typically)
Charge Time WhenX2 is off: 2 h
Hold Time: infinite if powered by host monitor or
When X2 is in use and
external power supply; otherwise at least 48 hours
connected to MP20/30/
40/50/60/70/80/90 Buffered Contents: Active settings, trends, patient data,
without extensions: 12 h Memory realtime reports, review alarms
approx. Hold Time: infinite if powered by external power
When X2 is in use and supply; otherwise at least 48 hours
connected to the external Restart time: After power interruption, an ECG wave will be
power shown on the display after 30 seconds maximum.
Indicators Alarms Off red LED

Alarms red/yellow/cyan LED M8023A External Power Supply Performance

Specifications (optional)
On/Standby/Error green/red LED

AC Power green LED

Battery yellow (charging)/red M8023A External Power Supply Performance

blinking (empty) LED Specifications
External Power green LED
Power Power < 12 W average
Sounds Audible feedback for user input. Prompt tone. Specifications Consumption < 30 W peak
QRS tones, or SpO2 modulation tone. Four Line Voltage 100 to 240 V ~
different alarm sounds.
Current 0.7 to 0.4 A
Trends:
12, or 16 numerics @ 12 sec, 1 minute, 5 minute resolution. Frequency 50/60 Hz ~
Multiple choices of number of numerics, resolution and duration Indicators AC Power green LED
depending on trend option and application area.

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Interface Specifications

X2 (M3002A) Interface Specifications M8023A External Power Supply Interface Specifications

Measurement Connectors Female ODU (Proprietary) Measure- Connectors Male ODU (Proprietary)
Link (MSL) ment Link
Power 30 V to 60 V input Power 48 V output
(MSL)
Power Sync RS-422 compliant input Power Sync. RS-422 compliant output
78.125 kHz (typical 78.125 kHz (typical)

LAN signals IEEE 802.3 10-Base-T LAN signals IEEE 802.3 10-Base-T complaint
complaint Serial RS-422 compliant output
Serial signals RS-422 compliant signals 78.125 kHz (typical)

Local signals Provided for connecting MMS Local signals Not connected
extensions

ECG Sync Pulse Cable Yes

Output Detection
Display Specifications
Marker In No
Integrated Sweep 6.25, 12.5, 25 and 50 mm/s;
Wave No QVGA Speeds
Output Display
Resolution 320 x 240
Connector Binder Series 709/719
Refresh 60 Hz
Output Output low <0.8V @ I = - frequency
Levels 4 mA
Useful 72 x 54 mm (2.8 x 2.1 in)
Output high >2.4 V @ I= screen
4 mA
Pixel size 0.22 x 0.22 mm
Isolation None

Pulse Width 100 +/- 10 ms (high)

Delay from 20 ms maximum per AAMI

X2 (M3002A) Compatible Devices
R-wave peak EC13
to start of IntelliVue Instrument Telemetry Wireless Network
pulse (USA only)
Minimum 0.5 V Internal WMTS Technology compatible with Philips
required R- Adapter Cellular Telemetry System
wave (CTS), cellular infrastructure
amplitude
Frequency WMTS, 1395-1400 MHz and
Band 1427-1432 MHz

IntelliVue Instrument Telemetry Wireless Network

(except USA)

7
 Measurement Specifications
X2 (M3002A) Compatible Devices

Internal ISM Technology compatible with Philips ECG/Arrhythmia/ST/QT

Adapter Cellular Telemetry System
Complies with IEC 60601-2-25:1993 + A1:1999 /EN60601-2-25:1995
(CTS), cellular infrastructure
+ A1:1999, IEC 60601-2-27:2005/EN60601-2-27:2006, IEC 60601-2-
Frequency 2.4 GHz ISM 51:2003 /EN 60601-2-51:2003 and AAMI EC11/EC13:1991/2002.
Band

ECG/Arrhythmia/ST Performance Specifications

M4607A Battery Specifications Cardiotach Range Adult/pedi:

15 to 300 bpm
Physical Specifications Neo range:
WxDxH 66 mm (2.36 in) x 80 mm (3.15 in) x 15 to 350 bpm
20 mm (0.79 in)
Accuracy ±1% of range
Weight 160 g ±5% Resolution 1 bpm
Performance Specifications
Sensitivity ≥200 µVpeak
Nominal Voltage 10.8 Volt
PVC Rate Range 0 to 300 bpm
Rated Capacity at 1000 mAh (typical)
Resolution 1 bpm
discharge C/5
ST Numeric Range -20 to +20 mm
Environmental Specifications
Accuracy ±0.5 mm or 15%, whichever is
Temperature Range Discharge 0 to 60°C (32 to 122°F)
greater
Charge 0 to 60°C (32 to 122°F)
Storage and Transportation: -20 to Resolution 0.1 mm
65°C (-4 to 140°F)
QT Numeric Range 200 to 800 ms
Humidity Range Operating: 15 % to 95 % Relative
Accuracy ±30 ms
Humidity (RH)
Storage and Transportation: 5 % to Resolution 8 ms
95 % Relative Humidity (RH)
QTc Numeric Range 200 to 800 ms
Battery Type Lithium Ion Mangan, 10.8 V,
Resolution 1 ms
1000 mAh,
ΔQTc Numeric Range -600 to +600 ms
Safety complies with UL 1642 (UL
Recognized) Resolution 1 ms
Electromagnetic complies with the requirements for QT-HR Range - 15 to 300 bpm
Compatibility (EMC) FCC Type B computing Device, and Numeric adult
EN 61000-4-2 and EN 61000-3-2
Range - 15 to 350 bpm
Communication Standard complies with the SMBus specification pediatric
v1.1 and
neonatal

8
ECG/Arrhythmia/ST Performance Specifications

Sinus and SV Brady Adult: 15 to 60 bpm ECG/

Rhythm Ranges Pedi: 15 to 80 bpm Arrhythmia/
Range Adjustment
Neo: 15 to 90 bpm ST Alarm
Specifications
Normal Adult:60 to 100 bpm
Pedi: 80 to 160 bpm HR 15 to 300 bpm Adult:1 bpm steps (15
Neo: 90 to 180 bpm to 40 bpm)
maximum delay: 10
Tachy Adult: > 100 bpm seconds according to 5 bpm steps (40 to 300
Pedi: >160 bpm AAMI EC 13-1992 bpm)
Neo: >180 bpm standard Pedi/Neo:1 bpm steps
(15 to 50 bpm)
Bandwidth Diagnostic Adult/neo/pedi: 0.05 to 150Hz 5 bpm steps (50 to 300
Mode bpm)
Extended Neo/pedi: 0.5 to 150Hz Extreme Tachy Difference to high 5 bpm steps
Monitoring limit 0 to 50 bpm
Mode
Clamping at 150 to 5 bpm steps
Monitoring Adult: 0.5 to 40Hz 300 bpm
Mode Neo/pedi: 0.5 to 55Hz
Extreme Brady Difference to low 5 bpm steps
Filter Mode Adult/neo/pedi: 0.5 to 20Hz limit 0 to 50 bpm
Differential Input Impedance >2MΩ RA-LL leads (Resp) Clamping at 15 to 5 bpm steps
>5MΩ at all other leads (at 10Hz 100 bpm
including patient cable)
Run PVCs 2 PVCs Not adjustable by user
Common Mode Rejection Diagnostic mode: >86 dB (with a
Ratio 51 kΩ/47 nF imbalance). PVCs Rate 1 to 99 PVCs/minute 1 PVC
Filter mode: >106 dB (with a 51 Vent Tach HR 20 to 300 bpm 5 bpm
kΩ/47 nF imbalance).
Vent Tach Run 3 to 99 PVCs/minute 1 PVC
Electrode Offset Potential ±500mV
Tolerance Vent Rhythm 2 to 99 PVCs/minute 1 PVC
Run
Auxiliary Current Active electrode: <100 nA
(Leads off Detection) Reference electrode: <900 nA SVT HR 120 to 300 bpm 5 bpm

Input Signal Range ±5 mV SVT Run 3 to 99 SV beats 1 SV beat

ST High -19.8 to +20 mm 0.2 mm

ST Low -20 to +19.8 mm 0.2 mm

QTc High 200 ms to 800 ms 10 ms steps

ΔQTc High 30 ms to 200 ms 10 ms steps

9
 ECG/Arrhythmia/ST Supplemental Information as
required by AAMI EC11/13
ECG/Arrhythmia/ST Supplemental Information as
required by AAMI EC11/13 Heart Rate Meter Accuracy Ventricular bigeminy: 80 bpm
and Response to Irregular Slow alternating ventricular
Respiration Excitation Sinusoidal signal, 260 μA, 39 kHz
Rhythm bigeminy: 60 bpm
Waveform
Rapid alternating ventricular
Noise Suppression RL drive gain 44 dB max., max. bigeminy: 120 bpm
voltage 1.8 Vrms Bidirectional systoles: 90 bpm

Time to Vent Gain 0.5, Range 6.5 to 8.4 Accuracy of Input Signal Methods A and D were used to
Alarm for Tachycardia seconds, Average 7.2 seconds Reproduction establish overall system error
Tachycardia 1 mVpp,206 and frequency response.
Gain 1.0 Range 6.1 to 6.9
bpm
seconds, Average 6.5 seconds
Respiration
Gain 2.0, Range 5.9 to 6.7
seconds, Average 6.3 seconds

Vent Gain 0.5, Range 5.4 to 6.2 Respiration Performance Specifications

Tachycardia seconds, Average 5.8 seconds
2 mVpp,195b Respiration Range Adult/pedi: 0 to 120 rpm
Gain 1.0, Range 5.7 to 6.5 Rate Neo: 0 to 170 rpm
pm
seconds, Average 6.1 seconds
Accuracy at 0 to 120 rpm ±1 rpm
Gain 2.0, Range 5.3 to 6.1 at 120 to 170 rpm ±2 rpm
seconds, Average 5.7 seconds
Resolution 1 rpm
Tall T-Wave Rejection Exceeds ANSI/AAMI EC 13 Sect.
Capability 3.1.2.1(c) Bandwidth 0.3 to 2.5Hz (–6dB)
minimum recommended 1.2 mV Noise Less than 25mΩ (rms) referred to
T-Wave amplitude the input
Heart Rate Averaging Method Three different methods are
used:
Normally, heart rate is computed
by averaging the 12 most recent Respiration
RR intervals. Alarm Speci- Range Adjustment Delay
For runs of PVCs, up to 8 RR fications
intervals are averaged to
compute the HR. High Adult/pedi: under 20 rpm: 1 max. 14
If each of 3 consecutive RR 10 to 100 rpm steps seconds
intervals is greater than 1200 ms rpm over 20 rpm: 5
(that is, rate less than 50 bpm), Neo: 30 to rpm steps
then the 4 most recent RR 150 rpm
intervals are averaged to
Low Adult/pedi: 0 under 20 rpm: 1 for limits
compute the HR.
to 95 rpm rpm steps from 0 to
Response Time of Heart Rate HR change from 80 to 120 bpm: Neo: over 20 rpm: 5 20 rpm:
Meter to Change in Heart Range: [6.4 to 7.2 seconds] 0 to 145 rpm rpm steps max. 4
Rate Average: 6.8 seconds seconds
HR change from 80 to 40 bpm: for limits
Range: [5.6 to 6.4 sec] Average: above 20
6.0 seconds rpm: max.
14 seconds

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 Respiration SpO2 Performance Specifications
Alarm Speci- Range Adjustment Delay
fications SpO2* Accuracy NellcorPB® Sensors with
M1943A(L):
Apnea Alarm 10 to 40 5 second steps MAX-A, MAX-AL, MAX-P,
seconds MAX-I, MAX-N, D-25, D-20, I-
20, N-25, OxiCliq A, P, I, N:
Philips FAST SpO2 (M3002A #A01) 3% (70% to 100%)

Complies with EN ISO 9919:2005 (except alarm system; alarm system Masimo Reusable Sensors®
complies with IEC 60601-2-49:2001). with LNOP MP12 or LNC
MP10:
Measurement Validation: The SpO2 accuracy has been validated in
LNOP DC-I, LNOP DC-IP,
human studies against arterial blood sample reference measured with a
LNOP YI, LNCS DC-I, LNCS
CO-oximeter. Pulse oximeter measurements are statistically
DC-IP, LNCS TF-I:
distributed, only about two-thirds of the measurements can be 2% (70% to 100%)
expected to fall within the specified accuracy compared to CO-
LNOP TC-I, LNCS TC-I:
oximeter measurements. Display Update Period: Typical: 2 seconds,
3.5% (70% to 100%)
Maximum: 30 seconds. Max. with NBP INOP suppression on: 60
seconds. Masimo Disposable
Sensors® with LNOP MP12
SpO2 Performance Specifications or LNC MP10:
LNOP Adt, LNOP Adtx, LNOP
SpO2* Range 0 to 100% Pdt, LNOP Pdtx, LNOP Inf-L,
LNCS Adtx, LNCS Pdtx, LNCS
Accuracy Philips Reusable Sensors:
Inf-L: 2% (70% to 100%)
M1191A, M1191AL,
LNOP Neo-L, LNOP NeoPt-L,
M1191ANL, M1191B,
LNCS Neo-L, LNCS NeoPt-L:
M1191BL, M1192A, M1192AN:
3% (70% to 100%)
2% (70% to 100%)
M1193A, M1193AN, M1194A, Resolution 1%
M1194AN, M1195A, Pulse Range 30 to 300 bpm
M1195AN, M1196A:
Accuracy ±2% or 1 bpm, whichever is
3% (70% to 100%)
greater
Philips Reusable Sensors
Resolution 1 bpm
with M1943A(L):
M1191T, M1192T, M1193T Sensors Wavelength range: 500 to 1000
(Adult), M1196T: nm
3% (70% to 100%) Emitted Light Energy: ≤ 15mW
M1193T (Neonate): Information about the
4% (70% to 100%) wavelength range can be
especially useful to clinicians
Philips Disposable Sensors (for instance, when
with M1943A(L): photodynamic therapy is
M1132A, M1133A (adult/ performed)
infant): 2%
M1131A, M1133A (neonate), Pulse Oximeter Calibration 70 - 100%
M1901B, M1902B, M1903B, Range
M1904B: 3% (70% to 100%)
*The specified accuracy is the root-mean-square (RMS) difference between the measured
values and the reference values

11
 Masimo SET SpO2/Pulse Rate Specifications
(M3002A #A03)
SpO2 Alarm
Complies with EN ISO 9919:2005 (except alarm system; alarm system
Specifica- Range Adjustment Delay
complies with IEC 60601-2-49:2001)
tions

SpO2 Adult: 50 to 100% 1% steps (0, 1, 2, SpO2 Performance Specifications

Pedi/Neo: 30 to 3,... 30)
100% +4 SpO2a Range 1to 100%
seconds No Motion Masimo LNOP:
Desat Adult: 50 to Low 1% steps
alarm limit Accuracyb,c,e Adt, Adtx, Pdt, Pdtx, Neo-
Pedi/Neo: 30 to L (Adult), Inf-L, Hi-Fi Neo/
Low alarm limit adult (Adult), Hi-Fi Inf/ped
(Pedi), DC-I, DC-IP, YI
Pulse 30 to 300 bpm Adult: max. 14 (Adult / Pedi), DC-195, TF-
1 bpm steps seconds I:
(30 to 40 bpm) 2% (70% to 100%)
5 bpm steps
Neo, NeoPt, Neo-L (Neo),
(40 to 300
NeoPt-L, Neo Bridge,
bpm)
NeoPt Bridge, YI (Neo),
Pedi/Neo:
Hi-Fi Neo/adult (Neo), Hi-
1 bpm steps
Fi Inf/ped (Infant):
(30 to 50 bpm)
3% (70% to 100%)
5 bpm steps
TC-I: 3.5% (70% to 100%)
(50 to 300
bpm) Blue Inf:
3.3% (70% to 100%),
Tachycardia Difference to high 5 bpm steps max. 14 3% (80% to 100%),
limit 0 to 50 bpm seconds 4% (60% to 80%)
Clamping at 150 to 5 bpm steps Masimo LNOPv:
300 bpm Ad, In: 2% (70% to 100%)
Bradycardia Difference to low 5 bpm steps max. 14 Ne: 3% (70% to 100%)
limit 0 to 50 bpm seconds Masimo LNCS:
Adtx, Pdtx, Inf-L, Neo-L
Clamping at 30 to 5 bpm steps
(Adult), DC-I, DC-IP, TF-I:
100 bpm
2% (70% to 100%)
Neo-L (Neo), NeoPt-L:
3% (70% to 100%)
TC-I: 3.5% (70% to 100%)

12
SpO2 Performance Specifications SpO2 Performance Specifications

SpO2 Motion Masimo LNOP: Pulse Rate Measurement 25to 240 bpm
Accuracyd , e Adt, Adtx, Pdt, Pdtx, Inf-L, Range
Neo, Neo-L, NeoPt, No motion 3 bpm
NeoPt-L, Neo Bridge, a,g
accuracy
NeoPt Bridge, Hi-Fi Neo/
adult, Hi-Fi Inf/ped, DC-I, Motion 5 bpm
DC-IP, YI, DC-195: accuracyc,h
3% (70% to 100%)
Low perfusion 3 bpm
Masimo LNOPv:
accuracyd,i
Ad, In, Ne:
3% (70% to 100%) Pulse Rate 1 bpm
Masimo LNCS: Resolution

Adtx, Pdtx, Inf-L, Neo-L, Sensors Wavelength range:

NeoPt-L, DC-I, DC-IP: 500 to 1000 nm
3% (70% to 100%) Emitted Light Energy:
Low Perfusion Masimo LNOP: ≤ 15mW
Accuracye,f: Adt, Adtx, Pdt, Pdtx, Inf-L, Information about the
Neo-L (Adult), Hi-Fi Neo/ wavelength range can be
adult (Adult), Hi-Fi Inf/ped especially useful to
(Pedi), DC-I, DC-IP, DC- clinicians (for instance,
195, TF-I : when photodynamic
2% (70% to 100%) therapy is performed)
Blue Inf, Neo, NeoPt, Neo- Numeric Update Range Typical: 1 second
L (Neo), NeoPt-L, Neo Maximum for all numerics
Bridge, NeoPt Bridge, Hi-Fi from this parameter:
Neo/adult (Neo), Hi-Fi Inf/ 30 seconds
ped (Infant):
a. The specified accuracy is the root-mean-square (RMS) difference between the measured
3% (70% to 100%) values and the reference values
TC-I: 3.5% (70% to 100%) b.Masimo SET technology with LNOP and LNCS sensors have been validated for no
motion accuracy in human blood studies on healthy adult volunteers in induced hypoxia
Masimo LNOPv: studies in the range of 70 to 100% SpO2 against a laboratory CO-oximeter and ECG
monitor. This variation equals plus or minus one standard deviation, which encompasses
Ad, In: 2% (70% to 100%) 68% of the population.
Ne: 3% (70% to 100%) c. Masimo SET technology with LNOP Blue sensors have been validated for no motion
accuracy in human blood studies on neonatal, infant and pediatric patients with congenital
Masimo LNCS: cyanotic cardiac lesions in the range of 60%-100% SpO2 against a laboratory CO-oximeter.
This variation equals plus or minus one standard deviation, which encompasses 68% of the
Adtx, Pdtx, Inf-L, Neo-L population.
(Adult), DC-I, DC-IP, TF-I: d.Masimo SET technology with LNOP and LNCS sensors have been validated for motion
2% (70% to 100%) accuracy in human blood studies on healthy adult volunteers in induced hypoxia studies
while performing rubbing and tapping motions, at 2 to 4 Hz at an amplitude of 1 to 2 cm
Neo-L (Neo), NeoPt-L: and a non-repetitive motion between 1 to 5 Hz at an amplitude of 2 to 3 cm in induced
hypoxia studies in the range of 70-100% SpO2 against a laboratory CO-oximeter and ECG
3% (70% to 100%) monitor. This variation equals plus or minus one standard deviation, which encompasses
TC-I: 3.5% (70% to 100%) 68% of the population.
e. Masimo SET technology has been validated for low perfusion accuracy in bench top
Resolution 1% testing against a Biotek Index 2 simulator and Masimo's simulator with signal strengths of
greater than 0.02% and a % transmission of greater than 5% for saturations ranging from 70
to 100%. This variation equals plus or minus one standard deviation, which encompasses
68% of the population.
f. 1% has been added to the saturation accuracy for neonates to account for the effects of
fetal hemoglobin.

13
g. Masimo SET technology with LNOP and LNCS sensors have been validated for pulse
rate accuracy for the range of 25 -240 bpm in bench top testing against a Biotek Index 2
NBP
simulator. This variation equals plus or minus one standard deviation, which encompasses
68% of the population. Complies with IEC 60601-2-30:1999/EN60601-2-30:2000.
h.Motion performance does not apply to LNOP Blue Inf, LNOP TF-I, TC-I and LNCS TF-I,
TC-I sensors
i. Low perfusion performance does not apply to LNOP YI
NBP Performance Specifications

Measure- Systolic Adult: 30 to 270 mmHg (4 to 36

ment kPa)
SpO2 Alarm Ranges Pedi: 30 to 180 mmHg (4 to 24 kPa)
Specifica- Range Adjustment Delay Neo: 30 to 130 mmHg (4 to 17 kPa)
tions
Diastolic Adult: 10 to 245 mmHg (1.5 to 32
SpO2 Adult: 50 to 100% 1% steps (0, 1, 2, kPa)
Pedi/Neo: 30 to 3,... 30) Pedi: 10 to 150 mmHg (1.5 to 20
100% +4 kPa)
seconds Neo: 10 to 100 mmHg (1.5 to 13
Desat Adult: 50 to Low 1% steps kPa)
alarm limit
Pedi/Neo: 30 to Mean Adult: 20 to 255 mmHg (2.5 to 34
Low alarm limit kPa)
Pedi: 20 to 160 mmHg (2.5 to 21
Pulse 30 to 300 bpm Adult: max. 14 kPa)
1 bpm steps seconds Neo: 20 to 120 mmHg (2.5 to 16
(30 to 40 kPa)
bpm)
5 bpm steps Pulse Rate Adult:40 to 300
(40 to 300 Pedi: 40 to 300
bpm) Neo: 40 to 300
Pedi/Neo: Accuracy Max. Std. Deviation: 8 mmHg (1.1
1 bpm steps kPa)
(30 to 50 Max. Mean Error: ±5 mmHg (±0.7
bpm) kPa)
5 bpm steps
(50 to 300 Pulse Rate Measurement 40 to 100 bpm: ± 5 bpm
bpm) Accuracy 101 to 200 bpm: ± 5% of reading
Tachycardia Difference to high 5 bpm steps max. 14 201 to 300 bpm: ± 10% of reading
limit 0 to 50 bpm seconds (average over NBP measurement
cycle)
Clamping at 150 to 5 bpm steps
300 bpm Heart Rate Range 40 to 300 bpm

Bradycardia Difference to low 5 bpm steps max. 14 Measurement Time Typical at HR > 60bpm
limit 0 to 50 bpm seconds Auto/manual: 30 seconds (adult)
Clamping at 30 to 5 bpm steps 25 seconds (neonatal)
100 bpm Stat: 20 seconds
Maximum time: 180 seconds (adult/
pediatric)
90 seconds (neonates)

14
 NBP Performance Specifications

Cuff Inflation Time Typical for normal adult cuff: Less NBP Alarm
Range Adjustment
than 10 seconds Specifications
Typical for neonatal cuff: Less than 2
seconds Systolic Adult: 30 to 270 mmHg 10 to 30 mmHg: 2
(4 to 36 kPa) mmHg (0.5 kPa)
Initial Cuff Inflation Adult: 165 ±15 mmHg > 30 mmHg: 5
Pressure Pedi: 130 ±15 mmHg Pedi: 30 to 180 mmHg (4
mmHg (1kPa)
Neo: 100 ±15 mmHg to 24 kPa)

Auto Mode Repetition 1, 2, 2.5, 3, 5, 10, 15, 20, 30, 45, 60 Neo: 30 to 130 mmHg
Times or 120 minutes (4 to 17 kPa)

STAT Mode Cycle Time 5 minutes Diastolic Adult: 10 to 245 mmHg

(1.5 to 32 kPa)
Venipuncture Mode Inflation
Pedi: 10 to 150 mmHg
Inflation Adult 20 to 120 mmHg (3 to 16 kPa) (1.5 to 20 kPa)
Pressure
Pediatric 20 to 80 mmHg (3 to 11 kPa) Neo: 10 to 100 mmHg
Neonatal 20 to 50 mmHg (3 to 7 kPa) (1.5 to 13 kPa)

Automatic Adult/ 170 seconds Mean Adult: 20 to 255 mmHg

deflation pediatric (2.5 to 34 kPa)
after Pedi: 20 to 160 mmHg
Neonatal 85 seconds
(2.5 to 21 kPa)
Measurement Validation: In adult and pediatric mode, the blood Neo: 20 to 120 mmHg
pressure measurements determined with this device comply with the (2.5 to 16 kPa)
American National Standard for Electronic or Automated
Sphygmomanometers (ANSI/AAMI SP10 - 1992) in relation to mean
error and standard deviation, when compared to intra-arterial or
auscultatory measurements (depending on the configuration) in a
NBP Overpressure Settings
representative patient population. For the auscultatory reference the
5th Korotkoff sound was used to determine the diastolic pressure. Adult > 300 mmHg (40 kPa) not user adjustable
In neonatal mode, the blood pressure measurements determined with > 2 sec
this device comply with the American National Standard for Electronic Pedi > 300 mmHg (40 kPa)
or Automated Sphygmomanometers (ANSI/AAMI SP10 - 1992 and > 2 sec
AAMI/ANSI SP10A -1996) in relation to mean error and standard
Neo > 150 mmHg (20 kPa)
deviation, when compared to intra-arterial measurements in a
> 2 sec
representative patient population.

15
Invasive Pressure and Pulse
Complies with IEC 60601-2-34:2000/EN60601-2-34:2000.
Invasive
Pressure
Invasive Pressure Performance Specifications Range Adjustment Delay
Alarm
Measurement Range –40 to 360 mmHg Specifications

Pulse Rate Range 25 to 350 bpm Pressure –40 to 360 -40 to 30 max. 12
mmHg mmHg seconds
Accuracy ±1% Full Range
(–5.0 to 48 2 mmHg (0.5
Resolution 1 bpm kPa) kPa)
> 30 mmHg
Input Sensitivity Sensitivity:5µV/V/mmHg (37.5µV/V/
5 mmHg (1
kPa)
kPa)
Adjustment range:±10%
Extreme High Difference to 5 mmHg steps
Transducer Load Impedance:200 to 2000 Ω
high limit 0 to (0.5 kPa)
(resistive)
25 mmHg
Output Impedance:≤3000 Ω
(resistive) Clamping at - 5 mmHg steps
40 to 360 (1.0 kPa)
Frequency Response dc to 12.5 Hz or 40 Hz
mmHg
Zero Range ±200 mmHg (±26 kPa)
Extreme Low Difference to 5 mmHg steps
Adjustment
Accuracy ±1 mmHg (±0.1 kPa) low limit 0 to (0.5 kPa)
25 mmHg
Drift Less than 0.1mmHg/°C (0.013 kPa/
°C) Clamping at 5 mmHg steps
40 to 360 (1.0 kPa)
Gain Accuracy ±1%
mmHg
Accuracy
Drift Less than 0.05%/°C
Pulse 25 to 300 bpm Adult:
Non Error of ≤ 0.4% FS (@CAL 1 bpm steps (25
linearity 200 mmHg) to 40 bpm)
and 5 bpm steps (40
Hysteresis to 300 bpm)
Pedi/Neo:
Overall (including ± 4% of reading or ± 4 mmHg (± 0.5
1 bpm steps (25
Accuracy transducer) kPa), whichever is greater
to 50 bpm)
Volume displacement 0.1 mm3 /100 mmHg 5 bpm steps (50
of CPJ840J6 to 300 bpm)

Tachycardia Difference to 5 bpm steps max. 14

high limit 0 to seconds
50 bpm

Clamping at 5 bpm steps

150 to 300
bpm

16
 CO2
Invasive
Pressure The CO2 measurement in the monitor, M3014A and M3015A
Range Adjustment Delay
Alarm complies with EN ISO 21647:2004 + Cor.1:2005 (except alarm system;
Specifications alarm system complies with IEC 60601-2-49:2001).

Bradycardia Difference to 5 bpm steps max. 14

M3015A Microstream CO2 Performance Specifications
low limit 0 to seconds
50 bpm CO2 Range 0 to 98 mmHg (0 to 13 kPa), or
Clamping at 25 5 bpm steps 13 % CO2, whichever is lower
to 100 bpm
Accuracy Up to 5 minutes during warmup:
±4 mmHg or 12 %, whichever is
Temp greater
After 5 minutes warmup:
Complies with EN 12470-4:2000
0 to 40 mmHg (0 to 5.3 kPa):
±2.2 mmHg (±0.3 kPa)
Temp Performance Specifications Above 40 mmHg (5.3 kPa):±(5.5 % +
(0.08 %/mmHg above 40 mmHg)) of
Temp Range –1 to 45 °C
reading
(30 to 113 °F)
These specifications are valid for
Resolution 0.1 °C (0.2 °F) 21 % O2 and N2 balance, up to 35°C
ambient temperature, up to 60 rpm
Accuracy ±0.1 °C (±0.2 °F)
in adult mode and 100 rpm in
Average Time Constant Less than 10 seconds neonatal mode. Outside of these
Alarms Range –1 to 45 °C (30 to 113 °F) conditions the accuracy reaches at a
minimum ±4 mmHg or ±12 % of the
Adjustment -1 to 35 °C (30 to 95 °F): 0.5 °C reading, whichever is greater.
(1.0 °F) steps
Resolution Numeric: 1.0 mmHg (0.1 kPa)
35 to 45 °C (95 to 113 °F): 0.1 °C
Wave: 0.1 mmHg (0.01 kPa)
(0.2 °F) steps
Stability Included in Accuracy specifications

awRR Range 0 to 150 rpm

Temp Alarm Accuracy 0 to 40 rpm: ±1 rpm

Range Adjustment 41 to 70 rpm: ±2 rpm
Specifications
71 to 100 rpm: ±3 rpm
Temp High/ –1 to 45 ºC (30 -1 to 35 °C (30 to 95 °F), 0.5 >100 rpm: ±5 % of reading
Low Alarms to 113 ºF) °C (1.0 °F) steps
Warm-up Time 5 minutes for full accuracy
35 to 45 °C (95 to 113 °F),
specification
0.1 °C (0.2 °F) steps
Rise Time 190 ms for neonatal mode
(measured with FilterLine H for
neonatal)
240 ms for adult mode
(measured with FilterLine H for
adult)

Sample Flow Rate 50 + 15/-7.5 ml/minute

17
 M3015A Microstream CO2 Performance Specifications

Gas Sampling Delay Time Typical:2.3 seconds M3014A Sidestream CO2 Performance Specifications

Maximum:3 seconds
CO2 Range 0 to 150 mmHg (0 to 20.0 kPa)
Sound Pressure Acoustic noise: <45 dBA
Accuracy after 2 minutes warmup:
Total System Response The total system response time is For values between 0 and 40 mmHg:
Time the sum of the delay time and the ±2.0 mmHg (±0.29 kPa)
rise time. For values from 41 to 70 mmHg: ±5 %
of reading
For values from 71 to 100 mmHg:
±8 % of reading
M3014A Mainstream CO2 Performance Specifications For values from 101 to 150 mmHg:
±10 % of reading
CO2 Range 0 to 150 mmHg (0 to 20.0 kPa) At respiration rates above 80 rpm, all
ranges are ±12 % of actual. The
Accuracy after 2 minutes warmup: specifications are valid for gas mixtures
For values between 0 and 40 mmHg: of CO2, balance N2, dry gas at
±2.0 mmHg (±0.29 kPa)
760 mmHg within specified operating
For values from 41 to 70 mmHg: ±5 %
temperature range.
of reading
For values from 71 to 100 mmHg: Resolution Numeric: 1.0 mmHg (0.1 kPa)
±8 % of reading Wave: 0.1 mmHg (0.01 kPa)
The specifications are valid for
Stability:
standard gas mixtures, balance air, fully
Short term ±0.8 mmHg over four hours
hydrated at 35°C, Pabs = 760 mmHg,
drift Accuracy specification will be
flow rate = 2 l/min.
Long term maintained over a 120 hour period
Resolution Numeric: 1.0 mmHg (0.1 kPa) drift
Wave: 0.1 mmHg (0.01 kPa)
awRR Range 2 to 150 rpm
Stability:
Accuracy ±1 rpm
Short term ±0.8 mmHg over four hours
drift Accuracy specification will be Warm-up Time 2 minutes with CO2 sensor attached
Long term maintained over a 120 hour period for full accuracy specification
drift
Sample Flow Rate 50 ±10 ml/minute
awRR Range 2 to 150 rpm
Total System Response 3 seconds
Accuracy ±1 rpm Time

Warm-up Time 2 minutes with CO2 transducer Operating Temperature 0 to 40°C (32 to 104°F)
attached for full accuracy specification
M3002A/M3014A Mainstream and Sidestream CO2 Humidity
Response Time Less than 60 ms (with adult or infant
Correction Factor
reusable or disposable adapter)
Either BTPS or STPD can be selected as the humidity correction factor
for the CO2 readings. The formula for the correction calculation is:
P abs
P STPD = P BTPS ⋅ ---------------------------
P abs – P H2O

Where p = partial pressure, Pabs = absolute pressure, and PH2O = 42

mmHg @35°C and 100 % RH.

18
 M3016A Mainstream CO2 Performance Specifications CO2 Alarm Adjust-
Range Delay
Specifications ment
CO2 Range –4 to 150 mmHg (-0.5 to 20.0 kPa)
etCO2 High 20 to 1 mmHg M3002A/
Accuracy after 20 minutes warmup and
95 mmHg (2 (0.1 kPa) M3014A/
calibration:
to 13 kPa) M3016A: less
For values between 0 and 40 mmHg:
than 14 seconds
±2.2 mmHg (±0.29 kPa) etCO2 Low 10 to
M3015A: less
For values between 40 and 76 mmHg: 90 mmHg (1
than18 seconds.
±5.5 % of reading to 12 kPa)
The specifications are valid for 45 %
imCO2 High 2 to steps of M3002A/
O2 and N2 or N2O balance. Outside
20 mmHg 1 mmHg M3014A/
these conditions the accuracy reaches
(0.3 to (0.1 kPa) M3016A: less
at a minimum the requirements of
3.0 kPa) than 14 seconds
EN864/ISO9918.
M3015A: less
Resolution Numeric: 1.0 mmHg (0.1 kPa) than18 seconds.
Wave: 0.1 mmHg (0.01 kPa)
awRR High Adult/pedi: under M3002A/
Stability ±1.0 mmHg over a 7 day period 10 to 20 rpm: 1 M3014A/
100 rpm rpm steps M3016A: less
awRR Range 0 to 150 rpm
Neo: 30 to over than 14 seconds
Accuracy ±2 rpm 150 rpm 20 rpm:5 M3015A: less
rpm steps than18 seconds.
Warm-up Time 20 minutes with CO2 transducer
attached for full accuracy specification awRR Low Adult/pedi: M3015A:
0 to 95 rpm settings
Response Time Less than 125 ms (for step from 10 % Neo: 0 to <20 rpm: less
to 90 %) 145 rpm than 8 seconds
>20 rpm: less
Mainstream CO2 Humidity Correction Factor than 18 seconds
Either BTPS or STPD can be selected as the humidity correction factor M3002A/
for the Mainstream CO2 readings. The formula for the correction M3014A/
calculation is: M3016A
settings
<20 rpm: less
P abs than 4 seconds
P STPD = P BTPS ⋅ ---------------------------
P abs – P H2O >20 rpm: less
than 14 seconds
Where p = partial pressure, Pabs = absolute pressure, and PH2O =
47 mmHg @37°C and 100 % RH. Apnea delay 10 to 5 second set apnea delay
40 seconds steps time + 4 seconds
(M3002A/
M3014A/
M3016A) or
8 seconds
(M3015A)

19
Ordering Information Interface Options
Ordering information for the M3002A Multi-Measurement Module is
given here.
Interfaces M3002A
Basic Functionality M3002A
Instrument Telemetry 1.4 GHz J45
Order one Axx option
Instrument Telemetry 2.4 GHz J47
FAST SpO2 A01

Masimo SpO2 Algorithm A03 System Cables

Cables M3002A
Application Options
MSL cable - 0.75 m SC1

MSL cable - 2.0 m SC2

Application Options M3002A MSL cable - 4.0 m SC4

12-Lead ECG Application (conventional) C12

Sensors and Disposables
Measurement Options

Parameter Add-ons M3002A Accessory M3002A

Press & Temp C06 5-lead Accessories Bundle ICU-AAMI H06

Respironics CO2- ready C14 5-lead Accessories Bundle ICU-IEC H07

5-lead Accessories Bundle OR-AAMI H08

Hardware Options 5-lead Accessories Bundle OR-IEC H09

Accessories Bundle Neonatal-AAMI H14

Accessories Bundle Neonatal-IEC H15

Hardware Add-Ons M3002A
3-lead Accessories Bundle ICU-AAMI H16
Handle E31
3-lead Accessories Bundle ICU-IEC H17
Anti-slip pad E18
3-lead Accessories Bundle OR-AAMI H18
MMS Mount E20
3-lead Accessories Bundle OR-IEC H19
Add 1X Lithium-Ion battery E24
CO2 Mainstream Sensor N01
Add 2X Lithium-Ion battery E26
Reusable Adult Airway Adapter (msCO2) N02
Power and Network Adapter E27
Reusable Infant Airway Adapter (msCO2) N03
SN3 ECG Sync Cable SN3
Single Use Adult Airway Adapter (msCO2) N04

Single USe Infant Airway Adapter (msCO2) N05

20
 Accessory M3002A Trunk Cable for 3-Electrode Cable Set

CO2 Sidestream Sensor N11 Length AAMI Part No. IEC Part No.

Non-intubated Adult Airway Adapter (ssCO2) N12 2.7m M1500A M1510A

Non-intubated pediatric Airway Adapter (ssCO2) N13

Intubated Adult Airway Adapter (ssCO2) N14

Trunk Cable
Intubated Pediatric Airway Adapter (ssCO2) N15
for 5-Electrode for 10-Electrode
Cable Set Cable Set
Related Products
Length
M3086A Support Tool AAMI IEC AAMI/IEC
Part No. Part No. Part No.
Mounting Information 0.9m M1560C M1570C n/a
The Intellivue MP5 Roll Stand Mounting Kit (Order No. 2.7m M1520A M1530A M1949A
989803002531) is compatible with the table top mount and the
standard mounting plate. For information on other mounting
hardware, contact your local Philips sales representative. For GCX
mounting hardware information, see www.gcx.com/philips. 3-Electrode AAMI IEC
Length
Cable Sets Part No. Part No.
Documentation
OR 1.0m M1601A M1611A
All documentation is available in .pdf format on documentation CD-
ROM. Additionally, a printed copy of the Instructions for Use and ICU Grabber 1.0m M1603A M1613A
shielded
Quick Guide ships with each monitor.

• Instructions for Use (printed) ICU Snap shielded 1.0m M1605A M1615A
• Quick Guide (printed) ICU Clip non- 0.45m M1608A M1618A
• Installation and Service Guide shielded
• Configuration Guide
ICU Clip non- 0.7m M1609A M1619A
• Documentation CD-ROM
shielded
• Training Guide (printed)
• Computer Based Training (optional)

ECG Accessories 5-Electrode AAMI IEC

Length
This symbol indicates that the cables and accessories are Cable Sets Part No. Part No.
designed to have special protection against electric shocks
OR Grabber 1.0m/1.6m M1621A M1631A
(particularly regarding allowable leakage currents), and
shielded
are defibrillator proof.
ICU Grabber 1.0m/1.6m M1623A M1633A
shielded

Trunk Cable for 3-Electrode Cable Set ICU Snap shielded 1.0m/1.6m M1625A M1635A

ICU Clip non- 0.7m/1.3m M1629A M1639A

Length AAMI Part No. IEC Part No.
shielded
0.9m M1540C M1550C

21
 Set Combiners and Organizers Part No.

10-Electrode Cable AAMI IEC Set organizer Shielded 3-electrode M1503A

Length
Sets Part No. Part No.
Shielded 5-electrode M1504A
OR grabber - 1.0m/ M1973A M1974A
Bedsheet clip M1509A
extremities 1.6m

OR grabber - chest 1.0m M1979A M1984A

Philips FAST SpO2 Accessories (for M3002A
ICU extremities 1.0m/ M1968A M1971A #A01)
1.6m (grabber) (grabber)

ICU chest 1.0m M1976A M1978A Philips Reusable Sensors

(grabber) (grabber)

Part Number Description Connector Type

3-Electrode One Piece
Length Part No.
Cables M1191A/B Adult Sensor Philips 8-pin
(2m cable)
AAMI
M1191AL/ Adult Sensor
OR Grabber 1.9m M1970A
BL (3m cable)
ICU Snap 1.9m M1972A
M1191ANL Adult Sensor
IEC (3m cable)
Nellcor OxiMax-
OR Grabber 1.9m M1980A
compatiblea
ICU Grabber 1.9m M1981A
M1191T Adult Sensor Generic D-Sub
(requires M1943A
(1.1m) or M1943AL
(3m) adapter cable)
5-Electrode One Piece
Length Part No.
Cables
M1192A Small Adult/Pediatric Philips 8-pin
AAMI sensor (1.5m cable)
OR Grabber 2.5m M1975A M1192AN Small Adult/Pediatric
ICU Snap 2.5m M1977A sensor (1.5m cable)
Nellcor OxiMax-
IEC compatiblea
OR Grabber 2.5m M1985A
M1192T Small Adult Pediatric Generic D-Sub
ICU Grabber 2.5m M1986A sensor (requires
M1943A (1.1m) or
M1943AL (3m)
adapter cable)
Set Combiners and Organizers Part No.

Set combiner 3-electrode M1501A

5-electrode M1502A

22
 Philips Disposable Sensors
Part Number Description Connector Type

M1193A Neonatal Hand/Foot Philips 8-pin

Sensor (1.5m cable)
Part Number Description Connector Type
M1193AN Neonatal Hand/Foot
Sensor (1.5m cable) M1131A Adult/Pediatric Generic D-Sub
Nellcor OxiMax- Sensor (requires
M1943A (1.1m) or
compatiblea
M1943AL (3m)
M1193T Neonatal Sensor Generic D-Sub adapter cable)
(requires M1943A
M1132A Infant Sensor Generic D-Sub
(1.1m) or M1943AL
(requires M1943A
(3m) adapter cable)
(1.1m) or M1943AL
(3m) adapter cable)
M1194A Adult/Pediatric Clip Philips 8-pin
Sensor (ear) (1.5m
M1133A Adult/Infant/ Generic D-Sub
cable)
Neonatal Sensor
M1194AN Adult/Pediatric Clip (requires M1943A
Sensor (ear) (1.5m (1.1m) or M1943AL
cable) (3m) adapter cable)
Nellcor OxiMax-
compatiblea NELLCOR® Disposable Sensors1:
M1195A Infant Sensor (1.5m Philips 8-pin Purchase Nellcor OxiCliq sensors and adapter cables directly from
cable) Tyco Healthcare.
M1195AN Infant Sensor (1.5m
cable)
Nellcor OxiMax-
Philips
compatiblea
Product Number Description Part
M1196A Adult Clip Sensor Philips 8-pin Number
(3m cable)
OxiMax MAX-A a Adult Sensor M1904Bb

OxiMax MAX-AL a Adult Sensor n/a

(long cable)
M1196T Adult Clip Sensor Generic D-Sub
(requires M1943A OxiMax MAX-P a Pediatric Sensor M1903Bb
(1.1m) or M1943AL
(3m) adapter cable) OxiMax MAX-I a Infant Sensor M1902Bb

OxiMax MAX-N a Neonatal Sensor M1901Bb

a. only in combination with Philips FAST-SpO2 and Philips OxiMax-compatible patient
monitors.
Oxisensor II D-25 a Adult Sensor n/a

Oxisensor II D-20 a Pediatric Sensor n/a

Oxisensor II I-20 a Infant Sensor n/a

1.Nellcor, OxiMax and OxiCliq are trademarks of Nellcor Puritan Bennett Inc., a part
of Tyco Healthcare.

23
 MASIMO LNOP® Disposable Adhesive Sensors:
Philips
Product Number Description Part
Number Product Philips
Description
Number Part Number
Oxisensor II N-25 a Neonatal Sensor n/a
LNOP Adt Adult Sensor 989803140231
OxiCliq A c Adult Sensor n/a
LNOP Adtx Adult Sensor n/a
Oxicliq P c Pediatric Sensor n/a LNOP Pdt Pediatric Adhesive 989803140261
Sensor
OxiCliq I c Infant Sensor n/a
LNOP Pdtx Pediatric Sensor n/a
OxiCliq N c Neonatal Sensor n/a
LNOP INF-L Neo/Infant 989803140311
a. Requires M1943 A(L) adapter cable Adhesive Sensor
b.not available from Philips in the U.S.A.
c. Requires M1943 A(L) and OC3 adapter cables LNOP NEO-L Neo Adhesive 989803140291
Sensor
MASIMO LNOP®1 Reusable Sensors: LNOP NEOPT- Neo Pre-Term 989803140301
L Sensitive Skin
Product Philips Adhesive Sensors
Description
Number Part Number

LNOP DC-I Adult Sensor 989803140321 MASIMO LNCS® Disposable Adhesive Sensors:

LNOP DC-IP Pediatric Sensor 989803140331

Product Philips
Description
LNOP-YI Reusable Multi-Site n/a Number Part Number
Sensor
LNCS Adtx Adult Finger 989803148231
LNOP TC-I Tip Clip reusable 989803140341 Sensor
Sensor
LNCS Pdtx Pediatric Finger 989803148241
Sensor
MASIMO LNCS®1 Reusable Sensors:
LNCS INF-L Infant Toe Sensor 989803148251

Product Philips LNCS NEO-L Neo Foot Sensor 989803148271

Description or Adult Finger
Number Part Number
Sensor
LNCS DC-I Adult Sensor 989803148281
LNCS NEOPT-L Neo Pre-Term 989803148261
LNCS DC-IP Pediatric Sensor 989803148291 Sensitive Skin
Adhesive Sensors
LNCS-TC-I Reusable Ear 989803148301
Sensor
The Philips M3002A option A01 uses Masimo
LNCS TF-I Reusable Forehead 989803148311 certified pulse oximetry for reduced noise and low
Sensor perfusion performance with Masimo Sensors under
the Masimo NR&LP protocol available from
Masimo.

1.LNOP and LNCS are federally registered trademarks of Masimo Corporation

24
Extension/Adapter Cables:
Description a/
Product Philips Order
Preferred Application
Part Number Description Name Number
Site
M1941A Extension Cable (2m) (8-pin to 8-pin)
YI Only available from Reusable Multi-site
M1943A Adapter Cable (1.1m) for Philips and Masimo Sensor:
Nellcor disposable sensors foot (alternative sites:
(8-pin to 9-pin D-Sub) hand, toe, finger) for
patients between 1 kg
M1943AL Adapter Cable (3m) for Philips and and 3 kg
Nellcor disposable sensors toe, for patients more
(8-pin to 9-pin D-Sub)
than 3 kg
OC3 Adapter cable for OxiCliq Sensors TC-I 989803140341 Reusable Ear Sensor
(available from Nellcor only) ear lobe, for patients
LNOP MP12 LNOP MP Series Patient Cable (3.6 m) more than 30 kg
(451261000761) Adapter Cable for Masimo LNOP DC-195 Only available from Reusable Finger Sensor:
Sensors Masimo finger, for patients
LNC MP10 LNCS MP Series Patient CAble (3.0 m) more than 30 kg
(989803148221) Adapter Cable for Masimo LNCS TF-I Only available from Reusable Forehead
Sensors Masimo Sensor:
forehead, for patients
more than 30 kg
Masimo SET SpO2 Accessories (for M3002A #A03)
Some of the sensors listed below must be ordered directly from Masimo LNOP disposable adhesive sensorsb
Masimo.
Adt 989803140231 Adult Adhesive Sensor:
finger, for patients
Masimo LNOP Reusable Sensors more than 30 kg

Adtx Only available from Adult Adhesive Sensor:

Masimo finger, for patients
Description a/ more than 30 kg
Product Philips Order
Preferred Application Pdt 989803140261 Pediatric Adhesive
Name Number
Site Sensor:
finger, for patients
Masimo LNOP reusable sensorsb between 10 kg and 50
kg
DC-I 989803140321 Reusable Finger Sensor:
finger, for patients Pdtx Only available from Pediatric Adhesive
more than 30 kg Masimo Sensor:
finger, for patients
DC-IP 989803140331 Reusable Pediatric
between 10 kg and 50
Finger Sensor:
kg
finger, for patients
between 10 kg and 50 Inf-L 989803140311 Infant Adhesive Sensor:
kg great toe, for patients
between 3 kg and 20 kg

25
 Description a/ Description a/
Product Philips Order Product Philips Order
Preferred Application Preferred Application
Name Number Name Number
Site Site

Neo 989803140271 Neonate Adhesive Blue Inf Only available from Neonate, Infant and
Sensor: Masimo pediatric sensor for
great toe, for patients patients with congenital
less than 10 kg cyanotic cardiac lesions:
great toe or thumb, for
NeoPt 989803140281 Sensitive Skin Neonate
patients between 2.5 kg
Adhesive Sensor:
and 20 kg
foot, for patients less
than 1 kg Masimo LNOPvTM disposable adhesive sensorsb
Neo-L 989803140291 Neonate Adhesive
Ad Only available from Disposable Adult
Sensor:
Masimo Sensor:
foot, for patients less
finger, for patients
than 3kg
more than 30 kg
finger, for patients
more than 40 kg In Only available from Disposable Infant
Masimo Sensor:
NeoPt-L 989803140301 Sensitive Skin Neonate
Adhesive Sensor: big toe, for patients
foot, for patients less between 3 kg and 20 kg
than 1 kg Ne Only available from Disposable Neonate
Neo Bridge Only available from Neonate Adhesive Masimo Sensor:
Masimo Sensor:
great toe, for patients foot, for patients less
less than 10 kg than 3kg

NeoPt Bridge Only available from Sensitive Skin Neonate Masimo LNCS reusable sensorsc
Masimo Adhesive Sensor:
great toe, for patients DC-I 989803148281 Reusable Finger Sensor:
less than 1 kg finger, for patients
more than 30 kg
Hi-Fi Neo/ Only available from High Fidelity Adhesive
adult Masimo Sensor: DC-IP 989803148291 Reusable Pediatric
foot, for patients less Finger Sensor:
than 3kg finger, for patients
finger, for patients between 10 kg and 50
more than 30 kg kg

TC-I 989803148301 Reusable Ear Sensor

Hi-Fi Inf/ped Only available from High Fidelity Adhesive ear lobe, for patients
Masimo Sensor: more than 30 kg
great toe, for patients TF-I 989803148311 Reusable Forehead
between 3 kg and 10 kg Sensor:
finger, for patients forehead, for patients
between 10 kg and 30 more than 30 kg
kg

26
 Extension/Adapter Cables:
Description a/
Product Philips Order
Preferred Application
Name Number Part Number Description
Site
LNOP MP12 LNOP MP Series Patient Cable (3.6 m)
Masimo LNCS disposable adhesive sensorsc (451261000761) Adapter Cable for Masimo LNOP
Sensors
Adtx 989803148231 Adult Adhesive Sensor:
finger, for patients LNC MP10 LNCS MP Series Patient CAble (3.0 m)
more than 30 kg (989803148221) Adapter Cable for Masimo LNCS
Sensors
Pdtx 989803148241 Pediatric Adhesive
Sensor:
finger, for patients
Non Invasive Blood Pressure Accessories
between 10 kg and 50
kg These cuffs and tubings are designed to have special
protection against electric shocks (particularly regarding
Inf-L 989803148251 Infant Adhesive Sensor:
allowable leakage currents), and are defibrillator proof.
great toe, for patients
between 3 kg and 20 kg

Neo-L 989803148271 Neonate Adhesive

Multi-Patient Comfort Cuffs and Disposable Cuffs
Sensor:
foot, for patients less
Patient Category Disposable cuff Reusable cuff
than 3kg
finger, for patients Adult (Thigh) M1879A M1576A
more than 40 kg
Large Adult M1878A M1575A
NeoPt-L 989803148261 Sensitive Skin Neonate
Adult M1877A M1574A
Adhesive Sensor:
foot, for patients less Small Adult M1876A M1573A
than 1 kg
Pediatric M1875A M1572A
a. For more details on application site, refer to the Instructions for Use provided with the
sensors. Infant M1874A M1571A
b.Adapter cable LNOP MP12 required
c. Adapter cable LNC MP10 required Tubing: Use M1598B or M1599B

Reusable Cuff Kits Part No.

Infant, pediatric, small adult, adult M1577A

Small adult, adult, large adult, thigh M1578A

Infant, pediatric, small adult, adult, large M1579A

adult, thigh

27
 Adult/Pediatric Soft Single Patient Single-Hose Disposable
Cuffs
Adult/Pediatric Antimicrobial Coated
Reusable cuffs Disposable
Patient Limb Bladder
cuff
Single- Category Circumference Width
Cuff Size Circumference Bladder Part No.
Hose Part
(color) (cm) Width
No. Adult 27.5-36.5 cm 13.1 cm M4575A

Infant 9.0 - 14.8 5.4 cm M4552A Small Adult 20.5-28.5 cm 10.4 cm M4574A
(orange) 2.1 inches Pediatric 15.0-21.5 cm 8.0 cm M4573A
Pediatric 13.8 - 21.5 8.0 cm M4553A
Infant 9.0-15.0 cm 5.6 cm M4572A
(green) 3.1 inches
Tubing: Use M1598B or M1599B
Small Adult 20.5 - 28.5 10.6 cm M4554A
(royal blue) 4.2 inches

Adult 27.5 - 36.5 13.5 cm M4555A

(navy blue) Neonatal/Infant Cuffs (Disposable, non-sterile)
5.3 inches

Adult 27.5 - 36.5 13.5 cm M4556A Limb Bladder

Cuffs Part No.
X-long 5.3 inches Circumference Width
(navy blue)
Size 1 3.1 to 5.7 cm 2.2 cm M1866A
Large Adult 35.5 - 46.0 17.0 cm M4557A
Size 2 4.3 to 8.0 cm 2.8 cm M1868A
(burgundy) 6.7 inches
Size 3 5.8 to 10.9 cm 3.9 cm M1870A
Large Adult 35.5 - 46.0 17.0 cm M4558A
X-long 6.7 inches Size 4 7.1 to 13.1 cm 4.7 cm M1872A
(burgundy)
Tubing: Use M1596B or M1597B
Thigh 45 - 56.5 21.0 cm M4559A
(grey) 8.3 inches

Tubing: Use M1598B or M1599B

Cuff Tubing

Adult 1.5 m /4.9’ M1598B

3.0 m/9.8’ M1599B

Adult/Pediatric Soft Single Patient Single-Hose Disposable
Cuffs Neonatal 1.5 m /4.9’ M1596B

3.0 m/9.8’ M1597B

Disposable
Patient Limb Bladder
cuff
Category Circumference Width
Part No.

Adult (Thigh) 45.0-56.5 cm 20.4 cm M4579A

Large Adult 35.5-46.0 cm 16.4 cm M4578A

X-long

Large Adult 35.5-46.0 cm 16.4 cm M4577A

Adult 27.5 to 36.5 cm 16.4 cm M4576A

X-long

28
Temperature Accessories
Pressure Transducers and Accessories Part No.

Temperature Probes Part No. Transducer holder for CPJ840J6 CPJ84046

(pack of 4)
Reusable
IV pole mount for CPJ840J6 CPJ84447
General purpose probe 21075A
Disposable (EU/EFTA only. Not available in USA)
Small flexible vinyl probe 21076A
(Infant/Pediatric) Single channel disposable sensor kit (20) M1567A

Attachable surface probe 21078A Dual channel disposable sensor kit (20) M1568A

Disposable Transducer holder for M1567/8A M2271A

General purpose probe M1837A IV pole mount for M1567/8A M2272C

Skin probe 21091A Adapter cable for disposable sensor kit, 3.0m, M1634A
for M1567/8A
Esophageal/Stethoscope Probe 21093A
(12 French)

Esophageal/Stethoscope Probe 21094A

(18 French)

Esophageal/Stethoscope Probe 21095A

(24 French)

Foley Catheter Probe M2255A

(12 French)

Foley Catheter Probe 21096A

(16 French)

Foley Catheter Probe 21097A

(18 French)

Adapter cable 1.5m/4.9’ 21082B

Adapter cable 3.0m/9.8’ 21082A

PRESS Accessories
These transducers and accessories are designed to have
special protection against electric shocks (particularly
regarding allowable leakage currents), and are defibrillator proof.

Pressure Transducers and Accessories Part No.

Reusable

Reusable pressure transducer CPJ840J6

5 μV/V/mmHg sensitivity

Sterile disposable pressure domes for CPJ84022

CPJ840J6 (pack of 50)

29
Philips Medical Systems is part of
Royal Philips Electronics

Interested?
Would you like to know more about our
imaginative products? Please do not hesitate to
contact us. We would be glad to hear from you.

On the web
www.medical.philips.com

Via e-mail
medical@philips.com

By fax
+31 40 27 64 887

By mail
Philips Medical Systems
Global Information Center
P.O Box 1286
5602 BG Eindhoven
The Netherlands

By phone
Asia
Tel: +852 2821 5888

Europe, Middle East, Africa

Tel: +49 7031 463 2254

Latin America
Tel: +55 11 2125 0764
0366

North America M3002A complies with the requirements of the

Tel: +1 800 229 6417 Council Directive 93/42/EEC of 14 June 1993
(Medical Device Directive).

S
© 2007 Koninklijke Philips Electronics N.V.
All rights are reserved.
Philips Medical Systems Nederland B.V. reserves the right to make changes in specifications and/or to discontinue any product at any time without notice
or obligation and will not be liable for any consequences resulting from the use of this publication.
Printed in The Netherlands.
4522 962 26711 AUG 2007