BC Biomedical PS-2010 User manual

ECG PATIENT SIMULATOR
TEN LEAD
PS-2010
USER MANUAL


i
WARNINGS, CAUTIONS, NOTICES............................................................................ ii
DESCRIPTION............................................................................................................. 1
LAYOUT....................................................................................................................... 2
MANUAL REVISIONS.................................................................................................. 6
LIMITED WARRANTY.................................................................................................. 6
SPECIFICATIONS ....................................................................................................... 7
NOTES.......................................................................................................................... 8
BC BIOMEDICAL
PS-2010
TABLE OF CONTENTS
CALIBRATION INTERVAL
To ensure the accuracy of the PS-2010 Series,
BC Group International, Inc. recommends that it
be calibrated at least once every 12 months.
Calibration must be done by qualified personnel.
Contact BC Group International, Inc. for
calibration.

ii
WARNING - CONNECTIONS
All connections to patients must be removed
before connecting the DUT to the PS-2010. A
serious hazard may occur if the patient is
connected when testing with the PS-2010.
Do not connect any leads from the patient
directly to the PS-2010 or DUT.
CAUTION - SERVICE
The PS-2010 is intended to be serviced only by
authorized service personnel. Troubleshooting
and service procedures should only be
performed by qualified technical personnel.
WARNING - USE
The PS-2010 is intended for testing only and
should never be used in diagnostics, treatment
or any other capacity where it would come in
contact with a patient.
WARNING - USERS
The PS-2010 Series are for use by skilled
technical personnel only.
CAUTION - MODIFICATIONS
The PS-2010 is intended for use within the
published specifications. Any application
beyond these specifications or any unauthorized
user modifications may result in hazards or
improper operation.
CAUTION - INSPECTION
The PS-2010 should be inspected before each
use for obvious signs of abuse or wear. The
PS-2010 should not be used and should be
serviced if any parts are in question.

iii
CAUTION - CLEANING
Do not immerse. The PS-2010 should be cleaned
by wiping gently with a damp, lint-free cloth. A
mild detergent can be used if desired.
CAUTION - ENVIRONMENT
Exposure to environmental conditions outside
the specifications can adversely affect the
performance of the PS-2010. Allow the PS-2010
to acclimate to specified conditions for at least
30 minutes before attempting to operate it.
CAUTION - LIQUIDS
Do not submerge or spill liquids on the PS-2010
Series. Do not operate the PS-2010 Series if
exposed to fluid.
CAUTION - INSPECTION
The PS-2010 should be inspected before each
use for obvious signs of abuse or wear. The PS-
2010 should not be used and should be serviced
if any parts are in question.

iv

v
NOTICE –SYMBOLS
Symbol
Description
Caution
(Consult Manual for Further Information)
Center Negative
Per European Council Directive 2002/95/EC,
do not dispose of this product as unsorted
municipal waste.
CAT I
IEC Measurement Category I –CAT I
equipment designed to protect against
transients in equipment on circuits not directly
connected to MAINS. Under no
circumstances should the terminals of the
Analyzer be connected to any MAINS voltage
NOTICE –ABBREVIATIONS
AHA
American Heart Association
ANSI
American National Standards Institute
BPM
Beats Per Minute
C
Celsius
°
degree(s)
ECG
Electrocardiogram
F
Fahrenheit
Hz
hertz
IEC
International Electrotechnical Commission
Lbs
pounds
LED
Light Emitting Diode
mm
millimeter(s)
mV
millivolt(s)
NEDA
National Electronic Distributors Association
Ω
ohm(s)
USA
United States of America
V
Volts

vi
PS-2010 User Manual Copyright © 2021
www.bcgroupintl.com Made in the USA
12/21 Rev 06
NOTICE –CONTACT INFORMATION
BC BIOMEDICAL
BC GROUP INTERNATIONAL, INC.
3081 ELM POINT INDUSTRIAL DRIVE
ST. CHARLES, MO 63301
USA
1-800-242-8428
1-314-638-3800
www.bcgroupintl.com
NOTICE –DISCLAIMER
BC GROUP INTERNATIONAL, INC. RESERVES THE RIGHT TO
MAKE CHANGES TO ITS PRODUCTS OR SPECIFICATIONS AT
ANY TIME, WITHOUT NOTICE, IN ORDER TO IMPROVE THE
DESIGN OR PERFORMANCE AND TO SUPPLY THE BEST
POSSIBLE PRODUCT. THE INFORMATION IN THIS MANUAL HAS
BEEN CAREFULLY CHECKED AND IS BELIEVED TO BE
ACCURATE.HOWEVER,NO RESPONSIBILITY IS ASSUMED FOR
INACCURACIES.
NOTICE –DISCLAIMER
BC GROUP INTERNATIONAL, INC. WILL NOTBE RESPONSIBLE
FOR ANY INJURIES SUSTAINED DUE TO UNAUTHORIZED
EQUIPMENT MODIFICATIONS ORAPPLICATION OFEQUIPMENT
OUTSIDE OF THE PUBLISHED INTENDED USE AND
SPECIFICATIONS.

1
The Model PS-2010 is a Microprocessor based Patient Simulator. It provides ECG
Simulation with four waveforms with constant QRS duration and six machine performance
testing waveforms. The following are highlights of some of the main features:
•10 UNIVERSAL PATIENT LEAD CONNECTORS
•ECG: 30, 60, 120 AND 240 BPM
•SINE: 10, 60 AND 100 Hz
•SQUARE: 0.125 AND 2.000 Hz
•TRIANGLE: 2.000 Hz
•HIGH LEVEL OUTPUT (1 V p-p)
•AMPLITUDE ACCURACY: ± 2%
•FREQUENCY ACCURACY: ± 0.5% OF SETTING
•9 VOLT BATTERY POWER
•LOW BATTERY INDICATOR
•% BATTERY LIFE INDICATOR
•OPTIONAL BATTERY ELIMINATOR
•LEAD TEST FUNCTION
•HIGH IMPACT PLASTIC CASE
•LIGHT TOUCH KEYS
OPTIONAL ACCESSORIES:
•BC20-30103 SOFT-SIDED CARRYING CASE
•BC20-21114 BATTERY ELIMINATOR (Universal)
BC BIOMEDICAL
PS-2010
PATIENT SIMULATOR

2
•
This section looks at the layout of a PS-2010 and gives descriptions of the elements that
are present.
The unit is controlled by 4 light touch keys. They allow the user to select waveforms and
control the power for the unit. There is an audio click when a key is depressed.
There are 10 LEDs to provide the user with information about waveforms that are
generated; 1 LED for Lead Test confirmation and 1 LED for Low Battery Indication.
LAYOUT
High Level
Output (+)
Lead Test
Terminals
4 Light Touch
Keys for Power
and Waveform
Selection:
• On
• Off
• Up
• Down
Universal Patient
Lead Connectors:
• V2/C2
• V3/C3
• V4/C4
• V5/C5
• V6/C6
• RA/R
• LA/L
• RL/N (-)
• LL/F
• V1/C1
Lead Test
Indicator LED
Low Battery
Indicator LED
9V Battery
Compartment
(Back)
Battery
Eliminator
Receptacle (not
shown)
10 Waveforms with
LED Indicators for
Selection:
ECG Selection:
• 30, 60, 120, 240
BPM
Performance Wave
Selection:
• Sine:
10, 60, 100 Hz
• Square:
0.125, 2.000 Hz
• Triangle:
2.000 Hz

3
Universal Patient Lead Connectors
The 10 Universal Patient Lead Connectors allow for 12 lead ECG simulation with
independent outputs. AHA and IEC color-coded labels arelocatedonthefaceoftheunitto
aid in connecting the corresponding AHA and IEC Patient Leads.
High Level Output (+)
An additional Universal Patient Lead Connector is located on the top of the unit for
connecting the high level ECG output signal (1 Volt p-p ). The connection is between the
High Level (+) and RL/N (-) Patient Lead Connectors.
Waveform Selection
There are two keys and 10 LEDs in the Waveform Selection Control Section. The LEDs
indicate which waveform is generated. The keys sequentially select each
waveform. The microprocessor sends the stored waveform information of the selected
waveform to a Digital to Analog converter that generates an accurate analog
AHA Label
IEC Label
Description
RA
R
Right Arm
LA
L
Left Arm
RL
N
Right Leg
(reference or ground)
LL
F
Left Leg
V1
V2
V3
V4
V5
V6
C1
C2
C3
C4
C5
C6
V Leads (V1-V6)
(U.S. and Canada)
also referred to as pericardial,
precordial or unipolar chest
leads
Chest Leads (C1-C6)
(International)

4
representation. This waveform is then sent through a resistor network, developing the
appropriate signals on the output terminals.
Lead Test Terminals
There are two test terminals on the top of the unit that allow for a quick test of the
continuity of the lead cables. Connecting one end of the cable to one terminal and the
other end to the other terminal will test the cable. If the cable is OK (less than 1000
ohms), the LEAD TEST LED in the lower left of the face will light.
Power Keys
The keys control the power for the unit.
Auto Power Off
The unit will automatically turn off after 10 minutes of no key activity to conserve the
battery.
To override this feature and keep the unit on continuously, depress the key twice
after the unit is on. This will keep the unit on until it is manually turned off. The “Low Batt”
LED will illuminate for 3 sec to indicate that the AutoPower Off feature has beenturnedoff.
Percent of Battery Life Indicator
The unit provides an indication of the Percent of battery life left on the 9 Volt Alkaline
Battery. An analog to digital converter monitors the battery voltage. Continuously holding
down the key will change the 10 waveform LEDs into a Percent of Battery Life
display, with each LED representing 10% intervals. The indicator will strobe up to the

5
present level and flash. This sequence will continue while the key is depressed.
Battery
The unit utilizes a 9 Volt Alkaline Battery in the rear battery compartment. When the unit
detects a LOW BATTERY, the LED in the lower right of the face will light, indicating the
need to change the battery.
Battery Eliminator Input –A 2.1mm receptacle is provided for theoptional9 VDC Battery
Eliminator power supply that may be used for continuous run applications. It bypasses the
internal battery when plugged in.
NOTE: The unit is shipped with a Red Battery Lock-Out plug installed into the line power
connector as shown below. Its purpose is topreventtheunitfrom accidentallybeing turned
on during handling and transport, subsequently depleting the battery. This plug must be
removed before any use.

6
Revision # Program # Revisions Made
Rev 01 DT7345CA Origination
Rev 02 DT7345CA Format and Pictures Updated
Rev 03 DT7345CA Misc. Edits, Format Updated, and Pictures Updated
Rev 04 DT7345CA Misc. Edits
Rev 05 DT7345CA Misc. Edits
Rev 06 DT7345CA Battery Eliminator Updated, Misc. Edits
MANUAL REVISIONS
LIMITED WARRANTY
WARRANTY: BC GROUPINTERNATIONAL,INC.WARRANTSITSNEWPRODUCTSTOBEFREE
FROM DEFECTS IN MATERIALS AND WORKMANSHIP UNDER THE SERVICE FOR WHICH THEY
ARE INTENDED. THIS WARRANTY IS EFFECTIVE FOR TWELVE MONTHS FROM THE DATE OF
SHIPMENT.
EXCLUSIONS: THIS WARRANTY IS IN LIEU OF ANY OTHER WARRANTY EXPRESSED OR
IMPLIED, INCLUDING, BUT NOT LIMITED TO ANY IMPLIED WARRANTY OF MERCHANTABILITY
OR FITNESS FOR A PARTICULAR PURPOSE.
BC GROUP INTERNATIONAL, INC. IS NOT LIABLE FOR ANY INCIDENTAL OR CONSEQUENTIAL
DAMAGES.
NO PERSON OTHER THAN AN OFFICER IS AUTHORIZED TO GIVE ANY OTHER WARRANTY OR
ASSUME ANY LIABILITY.
REMEDIES: THE PURCHASER'S SOLE AND EXCLUSIVE REMEDY SHALL BE: (1)THEREPAIROR
REPLACEMENT OF DEFECTIVE PARTS OR PRODUCTS, WITHOUT CHARGE. (2)ATTHEOPTION
OF BC GROUP INTERNATIONAL, INC., THE REFUND OF THE PURCHASE PRICE.

7
PATIENT SIMULATION
RATE
NORMAL SINUS
RHYTHM
30, 60, 120, 240 BPM
PERFORMANCE
WAVEFORMS
SINE
10, 60, 100 Hz
SQUARE
0.125, 2.0 Hz
TRIANGLE
2.0 Hz
ACCURACY
± 0.5 %
AMPLITUDE
LEAD 1
1.75 mV
LEAD 2
2.75 mV
LEAD 3
1.00 mV
ACCURACY
± 2 % Lead II
IMPEDANCE
LEAD TO LEAD
1000 Ω
LEAD TEST
< 1000 Ω
PHYSICAL & ENVIRONMENTAL
CONSTRUCTION
ENCLOSURE
ABS Plastic
FACEPLATE
Lexan, Back printed
SIZE
7.26 x 4.46 x 1.51 Inches
(184.4 x 113.3 x 38.4 mm)
WEIGHT
≤ 1 Lbs (0.45 kg)
OPERATING RANGE
15 to 40 °C (59 to 104 °F)
STORAGE RANGE
-20 to 65 °C (-4 to 149 °F)
ELECTRICAL
BATTERY
9 V Alkaline Battery
(ANSI/NEDA 1604A or equivalent)
BATTERY ELIMINATOR
(Optional)
9VDC, 50 mA
BC20-21114 (Universal)
SPECIFICATIONS

8
NOTES

9
NOTES

10
NOTES

Table of contents
Other BC Biomedical Test Equipment manuals