Fluke Biomedical warrants this instrument against defects in materials and workmanship
for one year from the date of original purchase OR two years if at the end of your first
year you send the instrument to a Fluke Biomedical service center for calibration. You
will be charged our customary fee for such calibration. During the warranty period, we
will repair or at our option replace, at no charge, a product that proves to be defective,
provided you return the product, shipping prepaid, to Fluke Biomedical. This warranty
covers the original purchaser only and is not transferable. The warranty does not apply if
the product has been damaged by accident or misuse or has been serviced or modified by
anyone other than an authorized Fluke Biomedical service facility. NO OTHER
WARRANTIES, SUCH AS FITNESS FOR A PARTICULAR PURPOSE, ARE
EXPRESSED OR IMPLIED. FLUKE SHALL NOT BE LIABLE FOR ANY SPECIAL,
INDIRECT, INCIDENTAL OR CONSEQUENTIAL DAMAGES OR LOSSES,
INCLUDING LOSS OF DATA, ARISING FROM ANY CAUSE OR THEORY.
This warranty covers only serialized products and their accessory items that bear a
distinct serial number tag. Recalibration of instruments is not covered under the warranty.
This warranty gives you specific legal rights and you may also have other rights that vary
in different jurisdictions. Since some jurisdictions do not allow the exclusion or limitation
of an implied warranty or of incidental or consequential damages, this limitation of
liability may not apply to you. If any provision of this warranty is held invalid or
unenforceable by a court or other decision-maker of competent jurisdiction, such holding
will not affect the validity or enforceability of any other provision.
Fluke Biomedical agrees to a limited copyright release that allows you to reproduce manuals and other printed materials for use in
service training programs and other technical publications. If you would like other reproductions or distributions, submit a written
request to Fluke Biomedical.
Unpacking and Inspection
Follow standard receiving practices upon receipt of the instrument. Check the shipping carton for damage. If damage is found, stop
unpacking the instrument. Notify the carrier and ask for an agent to be present while the instrument is unpacked. There are no special
unpacking instructions, but be careful not to damage the instrument when unpacking it. Inspect the instrument for physical damage such
as bent or broken parts, dents, or scratches.
Technical Support
For application support or answers to technical questions, either email techservices@flukebiomedical.com or call 1-800- 850-4608 ext
2560 or 1-440-498-2560.
Claims
Our routine method of shipment is via common carrier, FOB origin. Upon delivery, if physical damage is found, retain all packing
materials in their original condition and contact the carrier immediately to file a claim. If the instrument is delivered in good physical
condition but does not operate within specifications, or if there are any other problems not caused by shipping damage, please contact
Fluke Biomedical or your local sales representative.
Standard Terms and Conditions
Refunds and Credits
Please note that only serialized products and their accessory items (i.e., products and items bearing a distinct serial number
tag) are eligible for partial refund and/or credit. Nonserialized parts and accessory items (e.g., cables, carrying cases,
auxiliary modules, etc.) are not eligible for return or refund. Only products returned within 90 days from the date of original
purchase are eligible for refund/credit. In order to receive a partial refund/credit of a product purchase price on a serialized product, the
product must not have been damaged by the customer or by the carrier chosen by the customer to return the goods, and the product
must be returned complete (meaning with all manuals, cables, accessories, etc.) and in “as new” and resalable condition. Products not
returned within 90 days of purchase, or products which are not in “as new” and resalable condition, are not eligible for credit return and
will be returned to the customer. The Return Procedure (see below) must be followed to assure prompt refund/credit.
Restocking Charges
Products returned within 30 days of original purchase are subject to a minimum restocking fee of 15 %. Products returned in excess of
30 days after purchase, but prior to 90 days, are subject to a minimum restocking fee of 20 %. Additional charges for damage and/or
missing parts and accessories will be applied to all returns.
Return Procedure
All items being returned (including all warranty-claim shipments) must be sent freight-prepaid to our factory location. When you return
an instrument to Fluke Biomedical, we recommend using United Parcel Service, Federal Express, or Air Parcel Post. We also
recommend that you insure your shipment for its actual replacement cost. Fluke Biomedical will not be responsible for lost shipments
or instruments that are received in damaged condition due to improper packaging or handling.
Use the original carton and packaging material for shipment. If they are not available, we recommend the following guide for
repackaging:
Use a double-walled carton of sufficient strength for the weight being shipped.
Use heavy paper or cardboard to protect all instrument surfaces. Use nonabrasive material around all projecting parts.
Use at least four inches of tightly packed, industry-approved, shock-absorbent material around the instrument.
Returns for partial refund/credit:
Every product returned for refund/credit must be accompanied by a Return Material Authorization (RMA) number, obtained from our
Order Entry Group at 1-800- 850-4608 ext 2560 or 1-440-498-2560.
Repair and calibration:
To find the nearest service center, go to www.flukebiomedical.com/service
In the U.S.A.:
Cleveland Calibration Lab
Tel: 1-800-850-4606
Email: globalcal@flukebiomedical.com
In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel: +31-402-675300
Email: ServiceDesk@fluke.com
In Asia:
Everett Calibration Lab
Tel: +425-446-6945
Email: mailto:service.international@fluke.com
, or
Certification
This instrument was thoroughly tested and inspected. It was found to meet Fluke Biomedical’s manufacturing specifications
when it was shipped from the factory. Calibration measurements are traceable to the National Institute of Standards and
Technology (NIST). Devices for which there are no NIST calibration standards are measured against in-house performance
standards using accepted test procedures.
WARNING
Unauthorized user modifications or application beyond the published specifications may result in electrical shock hazards or
improper operation. Fluke Biomedical will not be responsible for any injuries sustained due to unauthorized equipment
modifications.
Restrictions and Liabilities
Information in this document is subject to change and does not represent a commitment by Fluke Biomedical. Changes made
to the information in this document will be incorporated in new editions of the publication. No responsibility is assumed by
Fluke Biomedical for the use or reliability of software or equipment that is not supplied by Fluke Biomedical, or by its
affiliated dealers.
Manufacturing Location
The MPS450 Multiparameter Simulator is manufactured at Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A.
Applicable Testing Standards
Fluke Biomedical’s MPS450™ Multiparameter Simulator (hereafter referred to as the
MPS450) has been tested by an independent laboratory and meets the requirements listed
here.
Safety Requirements
nd
USA UL 61010-1 (2
Canada CAN/CSA C22.2 No. 61010 (2
Edition). General requirements.
nd
Edition), Safety
requirements for electrical equipment for measurement,
control and laboratory use.
EC Directive 2006/95/EC IEC/EN 61010-1:2001 (2
nd
Edition), safety requirement for
electrical equipment for measurement, control, and
laboratory use.
Electromagnetic Interference and Susceptibility
EN 61326-1:2006 Emissions Class A and Immunity
FCC Class A
Warning: Changes of modifications to this unit not expressly approved by the
Contents (continued)
manufacturer could void the user’s authority to operate the equipment.
This equipment has been tested and found to comply with the limits for a Class A digital
device.
These limits are designed to provide reasonable protection against harmful interference
when the equipment is operated in a commercial environment. Like all similar
equipment, this equipment generates, uses, and can radiate radio frequency energy, and,
if not installed and used in accordance with the instruction manual, may cause harmful
interference to radio communications. Operation of this equipment in a residential area is
likely to cause interference, in which case the user will be required to correct the
interference at his/her own expense.
Canadian Department of Communications Class A
This digital apparatus does not exceed Class A limits for radio emissions from digital
apparatus set out in the Radio Interference Regulations of the Canadian Department of
Communications.
Le présent appareil numérique n’excède pas des bruits radioélectriques dépassant les
limites applicables des appareils numériques de la Class A prescrites dans le Règlement
sur le brouillage radioélectrique édicté par le ministère des Communications du Canada.
Based on the testing standards below,
this device bears the
The system has been type tested by an independent, accredited testing laboratory and
found to meet the requirements of EN 61326-1:2006 for Radiated Emissions and Line
Conducted Emissions.
EN 61000-3-2 Harmonics Current Emissions
EN 61000-3-3 Voltage Fluctuations and Flicker
Immunity
The system has been type tested by an independent, accredited testing laboratory and
found to meet the requirements of EN 61326-1:2006 for immunity.
EN 61000-4-2 Electrostatic Discharge
EN 61000-4-3 RF Electromagnetic Fields
EN 61000-4-4 Fast Transient/Burst
EN 61000-4-5 Surge Immunity
EN 61000-4-6 RF Common Mode Disturbance
EN 61000-4-11 Voltage Dips, Short interruptions and AC Variations
EC Directive 2006/95/EC Low Voltage
mark.
User Safety
The system has been type tested by an independent testing laboratory and found to meet
the requirements of EC Directive 2006/95/EC for Low Voltage. Verification of
compliance was conducted to the limits and methods of the following
EN 61010-1 (2001)
Safety Requirements for Electrical Equipment for Measurement Control and Laboratory
Use, Part 1:General requirements” (IEC 61010-1:2001, Mod).
Table of Contents
Chapter Title Page
1 Introduction and Specifications......................................................... 1-1
When the term “simulation” is used in connection with ECG, Respiration, Temperature,
IBP or Cardiac Output, the simulation is electrical.
The MPS450 Multiparameter Simulator (the MPS450) is an electronic signal source for
determining if patient monitors are performing within their operating specifications. The
MPS450 provides the following function categories:
• ECG Functions
• Arrhythmia Functions
• ECG-Performance Testing
• Respiration
• Blood Pressure
• Temperature
• Cardiac Output (Optional)
• Fetal/Maternal ECG and IUP (Optional)
The MPS450 is a lightweight, battery-powered unit that is portable enough to test a
patient monitor anywhere the monitor is being used. This device is not to replace clinical
testing of waveform detecting devices such as patient monitors.
The microprocessor control of the MPS450, combined with extensive digital memory,
assures rapid test and verification of cardiac-monitoring medical equipment. All
simulation settings are read easily on the clear, built-in LCD (liquid crystal display), with
adjustable viewing “angle” (contrast). Tests and simulations can be selected quickly and
easily, by choosing menu selections, by using front-panel keys to enter numeric codes for
actions, or by using computer control.
A cross-referenced listing of MPS450 actions, numeric codes, and remote-entry
commands is available in Chapter 4: “Remote Operations.”
MPS450 Features
The MPS450 provides control over the widest array of testing parameters, while also
providing simplicity in design and user interface. A keypad enables the easy entry of
functions, parameters, and codes; easy-access jacks simplify quick connection to
monitoring devices.
The wide variety of abnormal ECG waveforms replicated by the MPS450 can be used not
only for testing arrhythmia-detection systems, but also for training medical personnel,
hospital administrators, and staff. The MPS450 can be used to teach techniques for
recognizing normal and abnormal conditions in the heart, lungs, and circulatory system,
as well as techniques for CPR and defibrillation/cardioversion. Cardiac physiologists can
learn how to interpret ECG waveforms; respiratory physiologists can learn
pulmonary/respiratory analysis techniques.
The groupings in Table 1-1 list the main categories of MPS450 functions. Each of these
function groupings is explained in a corresponding section.
1-3
MPS450
Operators Manual
Table 1-1. MPS450 Functions
Function Category Function Description
ECG Functions
Arrhythmia Functions
ECG-Performance Testing
Normal sinus rhythm
ECG rate and amplitude
Adult / pediatric QRS
ST-segment elevation
ECG-artifact simulation
Pacemaker waveforms
Pacer amplitude and
width
Supraventricular
arrhythmia
Premature arrhythmia
Missed beat
Ventricular arrhythmia
Conduction defect
Square/pulse/triangle/sine
R waveforms
Wave amplitude
The MPS450 provides complete 3-, 5-, and
12-lead ECG simulation that includes seven
artificial pacemaker conditions. Normal sinus
rhythm is output over a range of heart rates
and voltage amplitudes.
ST-segment elevation is adjustable.
The MPS450 simulates 36 types of
arrhythmias, such as PVCs, tachycardia,
fibrillation, flutter, and asystole. Simulated
conduction defects include first-, second-, and
third-degree heart block; and left- and rightbundle-branch block.
The MPS450 generates square, pulse,
triangle, sine, and R waveforms for
performance testing. Wave amplitude is
adjustable, as well as R-wave rate and width.
R-wave rate and width
Respiration
Blood Pressure
Temperature Temperature settings The MPS450 provides four preset
Respiration lead
Baseline (impedance)
Respiration rate
Respiration amplitude
Apnea simulation
BP sensitivity
BP zeroing
Static-pressure levels
Dynamic BP waveforms
BP respiration artifact
Swan-Ganz simulation
Calibrated respiration rates are generated
from 15 to 120 BrPM (breaths per minute),
including four respiration-impedance
selections, with two different lead selections
(LA or LL). The output-impedance level is
adjustable to 500, 1000, 1500, or 2000 ohms.
The MPS450 generates apnea pauses (0
BrPM) of 12, 22, and 32 seconds, as well as a
continuous-apnea condition.
The MPS450 simulates static and dynamic
invasive pressures, providing complete bloodpressure simulation. The MPS450 also
provides calibrated static pressures and
dynamic waveforms to simulate signals such
as pulmonary-artery, left- and right-ventricle
and Swan Ganz (RA-RV-PA-PAW) pressures.
temperature simulations: 0 °C, 24 °C, 37 °C,
and 40 °C. All temperature simulations are
compatible with Yellow Springs, Inc. (YSI)
Series 400 and 700 thermistors.
1-4
Introduction and Specifications
MPS450 Package Contents 1
Table 1-1. MPS450 Functions (cont.)
Function Category Function Description
Cardiac Output
Thermodilution method,
(Option)
(Option)
Injectate temperature
Injectate flow
Faulty-injectate curve
Left-to-right-shunt curve
Calibrated pulse
Fixed/periodic FHR Fetal / Maternal ECG
IUP simulation
RS-232 serial port Remote Operations
RS-232 serial port
The MPS450 simulates cardiac-output
waveforms for testing the accuracy and
sensitivity of cardiac-output computational
devices equipped with Baxter-Edwards-type
catheters. Injectate temperature can be set
either to “iced” or room-temperature
conditions, with adjustable flow rate (in liters
per minute). The MPS450 also simulates a
faulty-injectate curve, as well as a left-to-rightshunt curve which is a function of temperature
(Y-axis) and time (X-axis) curve, instead of a
pressure curve.
The MPS450 simulates a combined fetal and
maternal ECG occurring during labor, as well
as a selection of pressure waveforms
produced by uterine contractions. The
contraction period is adjustable and includes a
manually generated waveform.
MPS450 features include a built-in RS-232
serial port that, when connected to a
computer, enables instrument control through
remote commands. In addition, a special
command can be used to operate the
MPS450 remotely in the numeric-control
mode.
WWarning
To prevent personal injury, use the Simulator in the manner
specified in this manual or the protection provided by the
Simulator may be impaired.
MPS450 Package Contents
Standard Equipment
• MPS450 Multiparameter Simulator
Standard Accessories
• MPS450 Operators Manual (P/N 2243350)
• Registration card
• Two 9-volt alkaline batteries (minimum 8 hours continuous use)
• Cardiac-output adapter box (P/N 2226608, standard with Cardiac-Output Option)
Optional Accessories
• Carrying case (P/N 2248623)
• Blood-pressure cables (See your local Fluke Biomedical Representative for
The date of manufacture of the MPS450 unit appears on a label on the back of the
instrument, for example, JAN-03.
Unpack the MPS450 and accessories from the shipping carton and insert the batteries.
Inspect the unit carefully for damage, such as cracks, dents, scratches, or bent parts. If
any physical damage is apparent, please call Fluke Biomedical for assistance, and notify
the carrier if the damage appears to be the result of a shipping mishap.
Storage and Maintenance
As with most electronic equipment, the MPS450 should be operated in a dry area within
normal temperature limits (10 °C to 40 °C).
There are no unique storage requirements. However, when storing the unit, maintain the
storage temperature between -25 °C and 50 °C. Remove the batteries if the unit will be
stored for a long period.
The MPS450 should be recalibrated once a year by a qualified technician. For safety
reasons, although the power output from the MPS450 is not potentially dangerous, only
an experienced technician should open the unit to access the inner electronics.
The MPS450 operates continuously for 8 or more hours on two 9-volt alkaline batteries,
which should be replaced regularly. The message “Low Battery” displays on the LCD
whenever the batteries need to be replaced.
When the LCD screen displays a message warning that batteries are low,
replace the two batteries immediately. The battery compartment is located
at the back of the unit, toward the bottom. Use only two new 9-volt
batteries.
Note
1-6
Introduction and Specifications
Powering Up the MPS450 1
Powering Up the MPS450
1. Power up the system by pressing the power-on/off key (the green key located on the
keypad of the unit, bottom/right). After one short beep, the LCD screen displays the
following startup message:
2. After a three-second display test, the following top menu displays:
Note
Once you have the MPS450 up and running, please fill out the Registration
Card and mail it to Fluke Biomedical.
gje001.eps
gje002.eps
1-7
MPS450
Operators Manual
Connection the MPS450
Figure 1-1. MPS450 Patient Simulator
The right side of the MPS450 features connections for linking to blood-pressure, cardiacoutput, and temperature monitors. In addition, there is an auxiliary connection for future
expansion. The bottom of the MPS450 features an RS-232 serial port and a connection
for a battery eliminator. Prewired cables compatible with all major manufacturers’
monitors are available for simulating functions related to blood pressure, temperature,
and cardiac-output injectate. (Call your sales representative for a complete list.)
The left side of the MPS450 features a full set of universal ECG jacks, enabling the
connection of any 3-, 5-, or 12-lead ECG device. AHA and IEC color-coded dots run
along the left side of the face of the unit as an aid in connecting the corresponding U.S.
and international patient leads to the proper universal ECG jacks on the MPS450:
Table 1-2. ECG Jack Labeling
Label Meaning
RA or R Right arm
LA or L Left arm
RL or N Right leg (reference or ground)
LL or F Left led
gje041.eps
1-8
V1, V2, V3, V4, V5, and V6 V Leads (U.S. and Canada). Also referred to as
pericardial, precordial, or unipolar chest leads.
C1, C2, C3, C4, C5, and C6 Chest leads (International)
Introduction and Specifications
Using the MPS450 1
Using the MPS450
The MPS450 offers a wide array of simulations, functions, and adjustments that are easy
to use. During operation, press the MODE key (the yellow key located on the keypad
near the bottom of the unit) to enable either the menu-control or numeric-control mode.
In menu mode, simply press the top-menu key for a function group (labeled in yellow just
above the corresponding number key as shown in the Table 1-3), and then press one of
the four function keys (the blue keys located on the keypad just beneath the LCD) to
select from options displayed on the screen. In numeric mode, simply press the number
keys to enter the three-digit numeric code for the desired function, and select RUN.
Adjust injectate temperature and flow for CO test.
Simulate injectate failure.
Simulate left-to-right shunt.
Simulate output from a calibrated pulse signal.
Simulate ECG artifact.
Set fixed fetal heart rate.
Simulate intrauterine-pressure (IUP) wave.
Adjust IUP-wave period.
1-9
MPS450
Operators Manual
Table 1-3. MPS450 Button Description (cont.)
Number Key /
Key
Select option displayed on LCD screen.
Menu Label Menu Functions
Set respiration lead and baseline (impedance).
SETUP
Switch between menu control and numeric control.
View current parameters.
Return to previous or top menu.
Set blood-pressure sensitivity.
Adjust viewing angle (contrast) for LCD screen.
Set beeper mode.
Viewing Current MPS450 Parameters
The current settings for adjustable parameters—such as heart rate and BP static-pressure
levels—are available for display at any time on a series of LCD screens that are accessed
by pressing the VIEW key.
(When the MPS450 is turned off, the parameters reset to defaults, with the exception of
settings that can be stored, i.e., respiration lead and baseline, BP sensitivity, view angle,
and beeper mode. Power-on default settings for functions are listed in the
“Specifications” section later in this chapter.)
Action in the Menu-Control Mode
1. Press the white key labeled VIEW to display the VIEW PAGE 1 screen—the ECG
page—which indicates current ECG settings:
The types of parameters displayed on VIEW PAGE 1 depend on which group of
ECG waves is running. In this example (the ECG-NSR-wave group), the settings
displayed include NSR rate (90 BPM), patient type (ADULT), ST-segment elevation
(+.30 mV), NSR amplitude (2.00 mV), and ECG artifact (50 HZ).
Four other types of ECG-wave groups display different parameter types on VIEW PAGE 1, and three other VIEW PAGE screens display parameters for respiration,
blood-pressure, and temperature/cardiac-output functions. Table 1-4 lists the
parameters available for viewing on the four pages:
gje003.eps
1-10
Introduction and Specifications
Viewing Current MPS450 Parameters 1
Table 1-4. Parameter Viewing List
View
Page
1
2 Respiration Respiration rate, amplitude, lead, and baseline
3 Blood Pressure BP sensitivity; and settings BP1, BP2, BP3, BP4
ECG R-wave detection R-wave rate, width, and amplitude
ECG Arrhythmia Arrhythmia and ECG artifact
Fetal/maternal IUP wave, IUP period, and fetal heart rate
Temperature/Cardiac Output Temperature, thermistor, cardiac-output wave, and
CO-injectate temperature and flow
2. Select < or > to cycle through the other three VIEW pages, which display as screens
similar to the following:
gje004.eps
gje005.eps
gje006.eps
3. To exit viewing, press the VIEW key again, or press the ESC key to return to the
previous control mode.
4. While viewing settings, the MODE key is inactive. Press the ESC key to exit
viewing before changing modes.
1-11
MPS450
Operators Manual
Setting the MPS450 View Angle
Action in the Menu-Control Mode
The MPS450 offers eight preconfigured settings to customize the preferred degree of
contrast (brightness) for the angle at which the LCD screen is being viewed.
1. Press the top-menu key labeled SETUP to display the LCD screen:
2. Select VIEW to scroll to the LCD screen SET VIEW ANGLE, which displays the
current screen-contrast setting (in this example, 4):
3. To adjust the LCD screen’s contrast, scroll to the preferred setting, from 1 (lowest) to
8 (highest). The setting is active when displayed and remains active until the setting
is changed.
4. To store the contrast setting beyond the current session, select STORE. On the LCD
screen, Storing blinks on momentarily to indicate the value is being saved.
5. Press the ESC key to return to the top menu SETUP.
Adjusting the MPS450 Beeper
If not turned off, the MPS450 beeper sounds on power-up and whenever a key is pressed.
A double-beep sounds for an invalid key.
gje007.eps
gje008.eps
1-12
The MPS450 offers three preconfigured settings to customize the beeper sound: off,
short, or long.
Action in the Menu-Control Mode
1. Press the top-menu key labeled SETUP to display the LCD screen.
2. Select > to display the following LCD screen:
Introduction and Specifications
Navigation in the MPS450 1
3. Select BEEP to scroll to the LCD screen SET BEEPER MODE, which displays the
current setting (in this example,
4. Scroll to the desired beeper mode. The setting is active when displayed and remains
active until the setting is changed.
5. To hear the audible beep as currently set, select TEST.
6. To store the beeper setting beyond the current session, select STORE. On the LCD
screen, Storing blinks on momentarily to indicate the value is being saved.
7. Press the ESC key to return to the top menu SETUP.
Navigation in the MPS450
Press the MODE key (the yellow key located on the keypad near the bottom of the unit)
to enable either the menu-control or numeric-control mode. The control mode can be
switched at any time, except while viewing current parameters on a VIEW page; press
the VIEW key to exit back to the mode you were in previously.
SHORT):
gje009.eps
gje010.eps
Action in the Menu-Control Mode
1. To navigate in menu-control mode, press the top-menu key for a function group,
labeled in yellow just above the corresponding number key. (Available functions in
each of the menu categories are listed in the “Using the MPS450” section earlier in
this chapter.)
2. Press one of the four function keys (the blue keys located on the keypad just beneath
the LCD) to select from options displayed on the screen.
3. To scroll through screens while in the menu mode, select PREV or NEXT. (Selecting
PREV from the first selection—or NEXT from the last selection—in a menu usually
results in a double-beep. Press the ESC key to return to the previous menu, or press
another top-menu key.)
4. To scroll through the adjustment options, select DOWN or UP.
5. Some menu selections are active when displayed. For others, RUN must be selected
to execute the option. (Instructions are provided in this manual for each function.)
When selected, RUN or RUNNING flashes on the LCD screen to indicate the
selection is active.
1-13
MPS450
Operators Manual
Action in the Numeric-Control Mode
6. Some simulations run continuously until terminated; others run as one-time events
and must be selected again to repeat. (Again, instructions are provided for each
function.)
1. To navigate in numeric-control mode, press the number keys to enter the three-digit
numeric code for the desired function. (Numeric codes for functions are listed in each
section after the menu-control instructions. A complete list of MPS450 numeric
codes for actions, arranged by category and cross-referenced to remote-control-entry
codes, is available in the “Remote Operations” Chapter.)
2. The LCD displays a screen similar to the following:
gje011.eps
3. Select RUN. (On the LCD screen, RUN does not flash while the selection is active as
it does in the menu-control mode.)
4. To scroll through screens while in the numeric-control mode, select DOWN or UP;
screens are available in chronological numeric order. (Inactive numeric-control codes
are skipped automatically.) Alternatively, simply press the number keys for another
numeric selection.
5. The screen for a numeric entry appears only after the entire numeric code is entered.
6. As the numbers for a three-digit code are entered, each number on the screen shifts
one place to the left. This means that the function identifications for other key codes
appear briefly on the screen during the entry process.
For example, from the ASYSTOLE numeric screen (in the example shown in this
section), if you begin to enter 382 for the PAROXYSMAL ATR TACH screen,
when you press 3, the LCD displays the screen [333] R WAVE WIDTH 150 MS;
and when you press 8, the LCD displays the screen [338] R WAVE WIDTH 200
MS. The ASYSTOLE screen does not appear until the entire code 382 is entered.
1-14
Introduction and Specifications
General Specifications 1
General Specifications
Power ..................................................................... Two 9-V alkaline batteries (minimum 8 hours continuous power).
Size......................................................................... 6 in x 7.5 in x 2 in (15.2 cm x 19 cm x 5 cm)
Weight .................................................................... 1 lb 8 oz (0.7 kg)
Temperature
Storage ............................................................... -25 °C to +50 °C
Operation ............................................................ 10 °C to 40 °C
Maximum Humidity ............................................... 80 % relative humidity
Battery Replacement ............................................ Warning for low-battery condition. The batteries must be replaced at
Optional battery eliminator: 9 Vdc, 50 mA
this time.
Detailed Specifications
Normal-Sinus-Rhythm Waveform
ECG Reference...................................................... The ECG amplitudes specified are for Lead II (calibration), from the
Normal Sinus Rhythm .......................................... 12-lead configuration with independent outputs referenced to right leg
High-Level Output................................................. 0.2 V/mV ±5 % of the ECG amplitude setting available on the BP3
Amplitude .............................................................. 0.05 mV to 0.5 mV (0.05 mV steps); 0.5 mV to 5.5 mV (0.5 mV steps)
Amplitude Accuracy ............................................. ±2 % of setting Lead II
nodal contraction (PNC); PVC1 left ventricular; PVC1 left ventricular,
early; PVC1 left ventricular, R on T; PVC2 right ventricular; PVC2 right
ventricular, early; PVC2 right ventricular, R on T; and multifocal PVCs
1-15
MPS450
Operators Manual
Ventricular Arrhythmia......................................... PVCs 6, 12, or 24 per minute; frequent multifocal PVCs; bigeminy;
Conduction Defect ................................................ First-, second-, or third-degree heart block; and right- or left-bundle-
Radial artery: 120/80
Left ventricle: 120/00
Right atrium (central venous or CVP): 15/10
Right ventricle: 25/00
Pulmonary artery: 25/10
Pulmonary-artery wedge: 10/2
Left atrium: 14/4