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Brochure Monitor X2
Brochure Monitor X2
Brochure Monitor X2
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.
2
• 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 'QTc 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
and the Information Center. Information need only be entered once. • Yellow Alarms** indicate conditions violating preset vital signs
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.
3
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)
• The Support Tool helps technical personnel to The monitor complies with the EMC standards
- 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:
4
• 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°).
5
Performance Specifications
Monitor Performance Specifications
6
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
7
Measurement Specifications
X2 (M3002A) Compatible Devices
8
ECG/Arrhythmia/ST Performance Specifications
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 PA, 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
10
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 on60
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: d 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
12
SpO2 Performance Specifications SpO2 Performance Specifications
SpO2 Motion Masimo LNOP: Pulse Rate Measurement 25to 240 bpm
d,e Range
Accuracy Adt, Adtx, Pdt, Pdtx, Inf-L,
Neo, Neo-L, NeoPt, No motion 3 bpm
NeoPt-L, Neo Bridge,
accuracya,g
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
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
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)
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 :
high limit 0 to (0.5 kPa)
(resistive)
25 mmHg
Output Impedance:d3000 :
(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 d0.4% 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)
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).
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
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 @37qC 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)
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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
Cables M3002A
Application Options
MSL cable - 0.75 m SC1
20
Trunk Cables
Accessory M3002A
(5+5)
(6+4)
Intubated Pediatric Airway Adapter (ssCO2) N15
Mounting Information
3-Electrode Cable Sets
The Intellivue MP5 Roll Stand Mounting Kit (Order No.
989803002531) is compatible with the table top mount and the
standard mounting plate. For information on other mounting
AAMI Part
hardware, contact your local Philips sales representative. For GCX Description Length IEC Part No.
No.
mounting hardware information, see www.gcx.com/philips.
OR Grabber 1.0m M1675A M1678A
Documentation shielded
All documentation is available in .pdf format on documentation CD- ICU Grabber 1.0m M1671A M1672A
shielded
ROM. Additionally, a printed copy of the Instructions for Use and
Quick Guide ships with each monitor. ICU snap 1.0m M1673A M1674A
• Instructions for Use (printed) shielded
• Quick Guide (printed) ICU Clip non- 0.45m M1622A --
• Installation and Service Guide shielded
• Configuration Guide
ICU Clip non- 0.7m M1624A M1626A
• Documentation CD-ROM
shielded
• Training Guide (printed)
• Computer Based Training (optional)
5-Electrode Cable Sets
ECG Accessories
This symbol indicates that the cables and accessories are AAMI IEC Part
designed to have special protection against electric shocks Description Length
Part No. No.
(particularly regarding allowable leakage currents), and
are defibrillator proof. OR Grabber 1.0m/1.6m M1973A M1974A
shielded
21
6-Electrode Cable Sets One-piece Cables
ICU Snap, chest, 1.0m M1602A M1604A Set combiner 3-electrode M1501A
shielded 5-electrode M1502A
OR Grabber, 1.0m M1979A M1984A Set organizer for 3-electrode M1503A
chest, shielded shielded leadsets -
4-electrode M1664A
For Limb Leads see 5-electrode cable sets grabber and snap
5-electrode M1504A
22
Philips FAST SpO2 Accessories (for M3002A
Part Number Description Connector Type
#A01)
M1194A Adult/Pediatric Clip Philips 8-pin
Philips Reusable Sensors Sensor (ear) (1.5m
cable)
M1192A Small Adult/Pediatric Philips 8-pin M1196T Adult Clip Sensor Generic D-Sub
sensor (1.5m cable) (requires M1943A
(1.1m) or M1943AL
M1192AN Small Adult/Pediatric
(3m) adapter cable)
sensor (1.5m cable)
Nellcor OxiMax-
compatiblea a. only in combination with Philips FAST-SpO2 and Philips OxiMax-compatible patient
monitors.
23
MASIMO LNOP®2 Reusable Sensors:
Part Number Description Connector Type
Philips
MASIMO LNCS®1 Reusable Sensors:
Product Number Description Part
Number Product Philips
Description
Number Part Number
OxiMax MAX-A a Adult Sensor M1904Bb
LNCS DC-I Adult Sensor 989803148281
OxiMax MAX-AL a Adult Sensor n/a
(long cable) LNCS DC-IP Pediatric Sensor 989803148291
1.Nellcor, OxiMax and OxiCliq are trademarks of Nellcor Puritan Bennett Inc., a part
of Tyco Healthcare. 2. LNOP and LNCS are federally registered trademarks of Masimo Corporation
24
MASIMO LNOP® Disposable Adhesive Sensors: Extension/Adapter Cables:
The Philips M3002A option A01 uses Masimo DC-IP 989803140331 Reusable Pediatric
Finger Sensor:
certified pulse oximetry for reduced noise and low
finger, for patients
perfusion performance with Masimo Sensors under
between 10 kg and 50
the Masimo NR&LP protocol available from
kg
Masimo.
25
Description a/ Description a/
Product Philips Order Product Philips Order
Preferred Application Preferred Application
Name Number Name Number
Site Site
TF-I Only available from Reusable Forehead NeoPt-L 989803140301 Sensitive Skin Neonate
Masimo Sensor: Adhesive Sensor:
forehead, for patients foot, for patients less
more than 30 kg than 1 kg
Masimo LNOP disposable adhesive sensorsb Neo Bridge Only available from Neonate Adhesive
Masimo Sensor:
Adt 989803140231 Adult Adhesive Sensor: great toe, for patients
finger, for patients less than 10 kg
more than 30 kg
NeoPt Bridge Only available from Sensitive Skin Neonate
Adtx Only available from Adult Adhesive Sensor: Masimo Adhesive Sensor:
Masimo finger, for patients great toe, for patients
more than 30 kg less than 1 kg
Pdt 989803140261 Pediatric Adhesive Hi-Fi Neo/ Only available from High Fidelity Adhesive
Sensor: adult Masimo Sensor:
finger, for patients foot, for patients less
between 10 kg and 50 than 3kg
kg finger, for patients
more than 30 kg
Pdtx Only available from Pediatric Adhesive
Masimo Sensor:
finger, for patients Hi-Fi Inf/ped Only available from High Fidelity Adhesive
between 10 kg and 50 Masimo Sensor:
kg great toe, for patients
Inf-L 989803140311 Infant Adhesive Sensor: between 3 kg and 10 kg
great toe, for patients finger, for patients
between 3 kg and 20 kg between 10 kg and 30
kg
26
Description a/ Description a/
Product Philips Order Product Philips Order
Preferred Application Preferred Application
Name Number Name Number
Site Site
Blue Inf Only available from Neonate, Infant and Masimo LNCS disposable adhesive sensorsc
Masimo pediatric sensor for
patients with congenital Adtx 989803148231 Adult Adhesive Sensor:
cyanotic cardiac lesions: finger, for patients
great toe or thumb, for more than 30 kg
patients between 2.5 kg
Pdtx 989803148241 Pediatric Adhesive
and 20 kg
Sensor:
Masimo LNOPvTM disposable adhesive sensorsb finger, for patients
between 10 kg and 50
Ad Only available from Disposable Adult kg
Masimo Sensor:
Inf-L 989803148251 Infant Adhesive Sensor:
finger, for patients
great toe, for patients
more than 30 kg
between 3 kg and 20 kg
In Only available from Disposable Infant
Neo-L 989803148271 Neonate Adhesive
Masimo Sensor:
Sensor:
big toe, for patients foot, for patients less
between 3 kg and 20 kg than 3kg
Ne Only available from Disposable Neonate finger, for patients
Masimo Sensor: more than 40 kg
27
Extension/Adapter Cables:
Multi-Patient Comfort Cuffs and Disposable Cuffs Adult 27.5 - 36.5 13.5 cm M4556A
X-long 5.3 inches
Patient Category Disposable cuff Reusable cuff (navy blue)
Adult (Thigh) M1879A M1576A Large Adult 35.5 - 46.0 17.0 cm M4557A
(burgundy) 6.7 inches
Large Adult M1878A M1575A
Large Adult 35.5 - 46.0 17.0 cm M4558A
Adult M1877A M1574A
X-long 6.7 inches
Small Adult M1876A M1573A (burgundy)
28
Temperature Accessories
Adult/Pediatric Soft Single Patient Single-Hose Disposable
Cuffs
Temperature Probes Part No.
Disposable
Patient Limb Bladder Reusable
cuff
Category Circumference Width
Part No. General purpose probe 21075A
Reusable
29
Pressure Transducers and Accessories Part No.
30
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
Latin America
Tel: +55 11 2125 0764
0366