Fluke Biomedical ProSim 8 Series Parts list manual

PN 3984515
January 2011, Rev. 3, 3/16
© 2011-2016 Fluke Corporation. All rights reserved. Specifications are subject to change without notice.
All product names are trademarks of their respective companies.
ProSim™8
Vital Signs Simulator

Warranty and Product Support
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.
7/07

Notices
All Rights Reserved
Copyright 2016, Fluke Biomedical. No part of this publication may be reproduced, transmitted, transcribed, stored in a retrieval
system, or translated into any language without the written permission of Fluke Biomedical.
Copyright Release
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 [e-mail] or call 1-800- 850-4608 or
1-440-248-9300. In Europe, email [email protected] or call [phone].
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.

Returns and Repairs
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 1-440-498-2560.
Repair and calibration:
To find the nearest service center, go to www.flukebiomedical.com/service or
In the U.S.A. and Asia:
Cleveland Calibration Lab
Tel: [phone] x2564
Email: [email protected]
In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel: [phone]
Email: [email protected]
To ensure the accuracy of the Product is maintained at a high level, Fluke Biomedical recommends the product be calibrated at least
once every 12 months. Calibration must be done by qualified personnel. Contact your local Fluke Biomedical representative for
calibration.

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 ProSim™ 8 Vital Signs Simulator is manufactured at Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A.

1
Introduction
The Fluke Biomedical ProSim™ 8 Vital Signs Simulator
(hereafter the Product) is a full-featured, compact,
portable simulator, used to measure the performance of
patient monitors.
Intended Use
The Product is intended to be used to test and verify the
basic operation of patient monitoring devices or systems
used to monitor various physiological parameters of a
patient, including ECG, Respiration, Invasive blood
pressure, Non-invasive blood pressure, Temperature, and
Cardiac output. Additionally, the Devices provide an
optical signal to verify that the electronics within the pulse
oximeter probe are functional.
The intended user is a trained biomedical equipment
technician who performs periodic preventative
maintenance checks on patient monitors in service. Users
can be associated with hospitals, clinics, original
equipment manufacturers and independent service
companies that repair and service medical equipment.
The end user is an individual, trained in medical
instrumentation technology.
This Product is intended to be used in the laboratory
environment, outside of the patient care area, and is not
intended for use on patients, or to test devices while
connected to patients. This Product is not intended to be
used to calibrate medical equipment. It is intended for
over the counter use.

ProSim™ 8
Getting Started Manual
2
Safety Information
In this manual, a Warning identifies hazardous conditions
and actions that could cause bodily harm or death. A
Caution identifies conditions and actions that could
damage the Product, the equipment under test, or cause
permanent loss of data.
XW Warnings
To prevent personal injury, use the Product
only as specified, or the protection supplied
by the Product can be compromised.
To prevent possible electrical shock, fire, or
personal injury:
•Read all safety Information before you use
the Product.
•Do not touch voltages >30 V ac rms,
42 V ac peak, or 60 V dc.
•Do not use the Product around explosive
gas, vapor, or in damp or wet
environments.
•Examine the case before you use the
Product. Look for cracks or missing
plastic. Carefully look at the insulation
around the terminals.
•Do not use the Product if it is damaged.
•Disable the Product if it is damaged.
•Use this Product indoors only.
•Do not connect directly to mains.
•Use the correct terminals, function, and
range for measurements.
•Do not use the Product if it operates
incorrectly.
•Use only current probes, test leads, and
adapters supplied with the Product.
•Remove all probes, test leads, and
accessories that are not necessary for the
measurement.

Vital Signs Simulator
Safety Information
3
•Remove all probes, test leads, and
accessories before the battery door is
opened.
•The battery door must be closed and
locked before you operate the Product.
•Replace the batteries when the low battery
indicator shows to prevent incorrect
measurements.
•Remove the batteries if the Product is not
used for an extended period of time, or if
stored in temperatures above 50 °C. If the
batteries are not removed, battery leakage
can damage the Product.
•Use only the mains power cord and
connector approved for the voltage and
plug configuration in your country and
rated for the Product.
•Replace the mains power cord if the
insulation is damaged or if the insulation
shows signs of wear.
•Use only the external mains power supply
included with the Product.
•Connect the battery charger to the mains
power outlet before the Product.
•Do not put metal objects into connectors.
•Do not connect the Product to a patient or
equipment connected to a patient. The
Product is intended for equipment
evaluation only and should never be used
in diagnostics, treatment, or any other
capacity where the Product would come in
contact with a patient.

ProSim™ 8
Getting Started Manual
4
•Batteries contain hazardous chemicals that
can cause burns or explode. If exposure to
chemicals occurs, clean with water and get
medical aid.
•Do not disassemble the battery.
•Do not disassemble or crush battery cells
and battery packs.
•Do not put battery cells and battery packs
near heat or fire. Do not put in sunlight.
•Do not short the battery terminals together.
•Do not keep cells or batteries in a
container where the terminals can be
shorted.
•Remove the input signals before you clean
the Product.
•Use only specified replacement parts.
•Have an approved technician repair the
Product.
XW Warnings
For safe operation and maintenance of the
Product:
•Repair the Product before use if the battery
leaks.
•Use only Fluke Biomedical approved
power adapters to charge the battery.

Vital Signs Simulator
Symbols
5
Symbols
Table 1 describes symbols used in association with the Product.
Table 1. Symbols
Symbol Description Symbol Description
WWARNING - RISK OF DANGER.
Consult user documentation. XWARNING. HAZARDOUS VOLTAGE. Risk of electric shock.
Magnetic Field "Input jack for the DC output of the AC-DC supply
connector.
PConforms to European Union
directives. )Certified by CSA Group to North American safety standards.
Conforms to relevant Australian EMC
standards. Complies with 47 CFR Part 15 requirements of the U.S. Federal Communications Commission.
ÃConforms to relevant South Korean
EMC Standards. 
Spent Lithium batteries should be disposed of by a qualified
recycler or hazardous materials handler per local
regulations. Contact your authorized Fluke Service Center
for recycling information.
~
This product complies with the WEEE Directive marking requirements. The affixed label indicates that you must
not discard this electrical/electronic product in domestic household waste. Product Category: With reference to
the equipment types in the WEEE Directive Annex I, this product is classed as category 9 "Monitoring and
Control Instrumentation" product. Do not dispose of this product as unsorted municipal waste.

ProSim™ 8
Getting Started Manual
6
Instrument Familiarization
Table 2 is a list of Product top-panel controls and connections shown in Figure 1.
F1 F2 F3 F4 F5
Top
14
13 10
11 98
7
6
5
4
2
3
15
16
18
17
1
12
glh034.eps
Figure 1. Top-Panel Controls and Connections

Vital Signs Simulator
Instrument Familiarization
7
Table 2. Top-Panel Controls and Connections
Item Name Description
ECG Posts Connection posts for Device Under Test (DUT) ECG leads.
ECG Function Accesses the ECG waveforms (adult, pediatric, and arrhythmias), and ECG test functions
(performance waves, QRS detection, Tall T wave rejection, and R wave detection).
NIBP Button Accesses the Non-Invasive Blood Pressure (NIBP) functions.
Special Functions Accesses the temperature, respiration, cardiac output, fetal simulation, autosequences, and
view memory functions.
SETUP Button Accesses the setup controls.
IBP Button Accesses the Invasive Blood Pressure (IBP) functions.
Navigation Buttons Cursor control buttons for navigating menus and lists.
Enter Button Sets the highlighted function.
Backlight Button Turns the display backlight on and off.
Power Button Turns the Product on and off.
SpO2 Button Accesses the SpO2 functions.
Function Softkeys Keys F1 through F5 are used to select from a number of selections that appear in the LCD
display above each function softkey.

ProSim™ 8
Getting Started Manual
8
Table 2. Top-Panel Controls and Connections (cont.)
Item Name Description
LCD Display Color display.
SpO2 Connector Connector to the SpO2 accessory.
IBP Channel 2 Connector Connector to an IBP input of the patient monitor.
Cardiac Output Connector Connector to the Cardiac input of the patient monitor.
IBP Channel 1 Connector Connector to the IBP input of the patient monitor.
Temperature Connector Connector to the Temperature input of the patient monitor.

Vital Signs Simulator
Instrument Familiarization
9
Table 3 is a list of Product controls and connections shown in Figure 2.
Front Right
Back
1
4
7 8
5 6
23
glh035.eps
Figure 2. Back, Front, and Side Panel Connections

ProSim™ 8
Getting Started Manual
10
Table 3. Back, Front, and Side Panel Connections
Item Name Description
AC/DC Supply Connector Input jack for the DC output of the AC/DC supply connector.
Battery Charge LED Battery charges when LED shows red. Green shows battery charge is complete.
Battery Latch Locks the battery pack into the Product. Push down to remove the battery pack.
Mini B USB Device Port Used to connect to a PC for remote control or download test results data to a PC.
USB A Controller Port For external keyboard, barcode reader, or printer.
ECG BNC Connector High-level output of ECG signal.
Air Port Connector Pressure port for NIBP cuff and monitor.
Magnetic Holder for SpO2
Finger Module Holds the SpO2 Optical Emitter and Detector finger module in two orientations.

Vital Signs Simulator
How to Turn the Product On
11
How to Turn the Product On
After you unpack and inspect the Product, fully charge the
battery before the first use. Afterwards, charge the battery
when the Product shows the low battery message. See
the Users Manual for detailed instructions.
Push on the front panel to turn the Product on. The
startup screen shows on the display. When the self test is
complete and no errors are sensed, the Home screen
shows in the display. The Product is ready to use. See
the Users Manual for detailed instructions.
General Specifications
Temperature
Operating ............................................................10 °C to 40 °C (50 °F to 104 °F)
Storage................................................................-20 °C to +60 °C (-4 °F to +140 °F)
Humidity.................................................................10 % to 90 % non-condensing
Altitude...................................................................3000 meters (9843 ft)
Size (L x W x H)......................................................30.22 cm x 14.48 cm x 8.64 cm (11.9 in x 5.7 in x 3.4 in)
Display....................................................................LCD Color Display
Communication
USB Device Upstream Port.................................Mini-B connector for control by a computer
USB Host Controller Port ....................................Type A, 5 V output, 0.5 A max load. Connector for keyboard, barcode reader, and printer
Wireless...............................................................IEEE 802.15.4 for control by a computer
USB Device Virtual COM Port Settings
Baud Rate .......................................................115 200 bps
Data bits..........................................................8 data bits
Stop Bits..........................................................1 stop bit
Flow Control....................................................Hardware (RTS/CTS)

ProSim™ 8
Getting Started Manual
12
Power .....................................................................Lithium-Ion rechargeable, 7.2 V, 31 Wh battery, 4300 mAh
Battery Charger.....................................................100 V to 240 V, 50/60 Hz input, 15 V/2.0 A output. For best performance, the battery
charger should be connected to a properly grounded ac receptacle
Battery Life ............................................................9 hours (minimum), 100 NIBP cycles typical
Weight....................................................................1.81 kg (4 lb)
Wireless Radio
Frequency Range ...............................................2412 MHz to 2462 MHz
Output Power......................................................<1 mW
Safety .....................................................................IEC 61010-1: Overvoltage Category II, Pollution Degree 2
Electromagnetic Compatibility (EMC)
International ........................................................IEC 61326-1: Portable Electromagnetic Environment CISPR 11: Group 1, Class A
Group 1: Equipment has intentionally generated and/or uses conductively-coupled radio frequency energy that is necessary for the
internal function of the equipment itself.
Class A: Equipment is suitable for use in all establishments other than domestic and those directly connected to a low-voltage power
supply network that supplies buildings used for domestic purposes. There may be potential difficulties in ensuring electromagnetic
compatibility in other environments due to conducted and radiated disturbances.
Emissions that exceed the levels required by CISPR 11 can occur when the equipment is connected to a test object. The equipment
may not meet the immunity requirements of this standard when test leads and/or test probes are connected.
Korea (KCC) .......................................................Class A Equipment (Industrial Broadcasting & Communication Equipment)
Class A: Equipment meets requirements for industrial electromagnetic wave equipment and the seller or user should take notice of it.
This equipment is intended for use in business environments and not to be used in homes.

Vital Signs Simulator
Detailed Specifications
13
USA (FCC) ..........................................................47 CFR 15 Intentional Radiators: This device complies with part 15 of the FCC Rules.
Operation is subject to the following two conditions:
(1) This device may not cause harmful interference.
(2) This device must accept any interference received, including interference that may cause undesired operation. (15.19).
Changes or modifications not expressly approved by Fluke could void the user's authority to operate the equipment. (15.21)
Detailed Specifications
Normal-Sinus-Rhythm Waveform
ECG Reference ......................................................The ECG amplitudes specified are for Lead II (calibration), from the baseline to the peak
of the R wave. All other leads are proportional.
Normal Sinus Rhythm...........................................12-lead configuration with independent outputs referenced to right leg (RL). Output to
10 Universal ECG Jacks, color-coded to AHA and IEC Standards.
High-Level Output .................................................0.5 V/mV ±5 % of the ECG amplitude setting available on a BNC connector.
Amplitude...............................................................0.05 mV to 0.5 mV (0.05 mV steps); 0.5 mV to 5.0 mV (0.25 mV steps). Other leads are
proportional to Lead II (reference lead) in percentage per:
Lead I ..................................................................70
Lead II .................................................................100
Lead III ................................................................30
Lead V1...............................................................24
Lead V2...............................................................48
Lead V3...............................................................100
Lead V4...............................................................120
Lead V5...............................................................112
Lead V6...............................................................80

ProSim™ 8
Getting Started Manual
14
Amplitude Accuracy .............................................±(2 % of setting + 0.05 mV)
ECG Rate ...............................................................10 BPM to 360 BPM in 1 BPM steps
Rate Accuracy.......................................................±1 % of setting
ECG Waveform Selection.....................................Adult (80 ms) or pediatric (40 ms) QRS duration
ST-Segment Elevation.......................................... Adult mode only. -0.8 mV to +0.8 mV (0.1 mV steps)
Additional steps: +0.05 mV and -0.05 mV
Power-On Default..................................................60 BPM, 1.0 mV, adult QRS and ST-segment elevation of 0 mV
Pacemaker Waveform
Pacer-Pulse
Amplitude ..........................................................0 mV (off), ±2 mV, ±4 mV, ±6 mV, ±8 mV, ±10 mV, ±12 mV, ±14 mV, ±16 mV, ±18 mV,
±20 mV, ±50 mV, ±100 mV, ±200 mV, ±500 mV, and ±700 mV for lead II (reference lead)
Accuracy
Reference lead II.............................................±(5 % setting + 0.2 mV)
All other leads .................................................±(10 % setting + 0.4 mV)
Pacer-Pulse Width ................................................0.1 ms, 0.2 ms, 0.5 ms, 1.0 ms, and 2.0 ms ±5 %
Paced Arrhythmias ...............................................Atrial 80 BPM
Asynchronous 75 BPM
Demand with frequent sinus beats
Demand with occasional sinus beats
Atrio-Ventricular sequential
Noncapture (one time)
Nonfunction
Power-On Default..................................................Amplitude 10 mV, width 1.0 ms, atrial waveform