Fluke BP Pump 2 Operators User manual

BP Pump 2
NIBP Simulator and Tester
Operators Manual
PN 2196592
June 2007
© 2007 Fluke Corporation, All rights reserved. Printed in USA
All product names are trademarks of their respective companies.

Warranty and Product Support
Fluke Biomedical warrants this instrument against defects in materials and
workmanship for one year from the date of original purchase. During the war-
ranty 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 conse-
quential damages, this limitation of liability may not apply to you. If any pro-
vision of this warranty is held invalid or unenforceable by a court or other de-
cision-maker of competent jurisdiction, such holding will not affect the validity
or enforceability of any other provision.
07/07

Notices
All Rights Reserved
©Copyright 2007, Fluke Biomedical. No part of this publication may be reproduced, transmit-
ted, 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 physi-
cal 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- 648-7952 or
1-425-446-6945.
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 re-
salable 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 cus-
tomer. 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 acces-
sories 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 rec-
ommend 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 Authoriza-
tion (RMA) number, obtained from our Order Entry Group at 1-800-648-7952 or 1-425-446-
6945.
Repair and calibration:
To find the nearest service center, go to www.flukebiomedical.com/service, or
In the U.S.A.:
Cleveland Calibration Lab
Tel: [phone]
Email: [email protected]
Everett Calibration Lab
Tel: [phone]
Email: [email protected]
In Europe, Middle East, and Africa:
Eindhoven Calibration Lab
Tel: [phone]
Email: [email protected]m
In Asia:
Everett Calibration Lab
Tel: [phone]
mail: [email protected]
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 us-
ing 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 re-
sponsible for any injuries sustained due to unauthorized equipment modifications.
E

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 incorpo-
rated in new editions of the publication. No responsibility is assumed by Fluke Biomedi-
cal for the use or reliability of software or equipment that is not supplied by Fluke Bio-
medical, or by its affiliated dealers.
Manufacturing Location
The BP Pump 2 Non-invasive Blood Pressure Simulator and Tester is manufactured in
Everett, Washington by Fluke Biomedical, 6920 Seaway Blvd., Everett, WA, U.S.A.

i
Table of Contents
Chapter Title Page
1 Introduction and Specifications.............................................. 1-1
Introduction .......................................................................................... 1-3
Key Features ......................................................................................... 1-3
General Safety Considerations.............................................................. 1-4
Symbols ............................................................................................ 1-4
Warnings and Cautions..................................................................... 1-5
Instrument Familiarity .......................................................................... 1-7
Powering Up the Tester ........................................................................ 1-10
Specifications........................................................................................ 1-10
Accessories ........................................................................................... 1-12
2 Setup, Maintenance, and Support........................................... 2-1
Setting up the Tester ............................................................................. 2-3
Printer Output ................................................................................... 2-4
User-Defined Simulations................................................................. 2-5
Language .......................................................................................... 2-6
Units of Measure............................................................................... 2-6
Self Test............................................................................................ 2-8
Zero Pressure .................................................................................... 2-8
Enable ECG Signal ........................................................................... 2-9
Maintenance and Support ..................................................................... 2-10
Avoiding Damage ............................................................................. 2-10
Cleaning............................................................................................ 2-10
Service and Calibration..................................................................... 2-11
Packing Instructions.......................................................................... 2-11
3 Operation .................................................................................. 3-1
Introduction .......................................................................................... 3-3
Configurations for Devices Under Test (DUT)................................. 3-4
Conversion Factors ........................................................................... 3-7
Initializing Tests and Simulations..................................................... 3-7
Error Messages ................................................................................. 3-7

BP Pump 2
Operators Manual
ii
Pressure Tests....................................................................................... 3-8
Pressure Leak Test............................................................................ 3-8
Pressure Relief Test.......................................................................... 3-10
Pressure Source Test ........................................................................ 3-11
Pressure Gauge Test ......................................................................... 3-12
Simulations........................................................................................... 3-13
Standard BP...................................................................................... 3-14
Patient Conditions ............................................................................ 3-15
Arrhythmias...................................................................................... 3-16
Respiratory Artifacts ........................................................................ 3-18
Neonate ............................................................................................ 3-19
Wrist................................................................................................. 3-20
User-Defined .................................................................................... 3-21
Auto Sequences.................................................................................... 3-21
Editing Auto Sequences ................................................................... 3-22
Printing Auto Sequences .................................................................. 3-23
Running Auto Sequences ................................................................. 3-24
Pressure Gauge ............................................................................. 3-25
Leak Test...................................................................................... 3-25
Relief Valve Test.......................................................................... 3-26
Pressure Source ............................................................................ 3-26
Data Sheet Printout....................................................................... 3-27
BP Simulations............................................................................. 3-27
Remote Operation ................................................................................ 3-29
RS-232 Settings................................................................................ 3-29
Ansur Software Control.................................................................... 3-29
Appendices
A ECG Interface............................................................................... A-1
B Questions and Answers ................................................................ B-1
C Abbreviations ............................................................................... C-1
D Computer Control Commands...................................................... D-1

iii
List of Tables
Table Title Page
1-1. Symbols ................................................................................................ 1-4
1-2. Top and Side Panel Components .......................................................... 1-8
1-3. Number Key Functions......................................................................... 1-9
1-4. Standard Accessories ............................................................................ 1-12
1-5. Optional Accessories ............................................................................ 1-12
3-1. Conversion Factors ............................................................................... 3-7
3-2. Standard Blood Pressure Simulations ................................................... 3-15
3-3. Patient Condition Simulations .............................................................. 3-16
3-4. Arrhythmia Simulations........................................................................ 3-17
3-5. Respiratory Artifact Simulations .......................................................... 3-18
3-6. Neonate Simulations ............................................................................. 3-19
3-7. Wrist Simulations ................................................................................. 3-20
D-1. Computer Control Commands .............................................................. D-1

BP Pump 2
Operators Manual
iv

v
List of Figures
Figure Title Page
1-1. Tester Top and Side Panel Components ............................................... 1-7
3-1. Tester Pneumatic Block Diagram ......................................................... 3-3
3-2. Connecting Tester to Single-hose NIBP Monitor (Int Cuff) ................. 3-4
3-3. Connecting Tester to Double-hose NIBP Monitor (Int Cuff)................ 3-5
3-4. Connecting Tester to Single-hose NIBP Monitor (Ext Cuff) ................ 3-5
3-5. Connecting Tester to Double-hose NIBP Monitor (Ext Cuff)............... 3-6
3-6. Connecting Tester to Single-hose NIBP Wrist Monitor (Ext Cuff) ...... 3-6
3-7. Sample Auto Sequence Test Printout.................................................... 3-24
3-8. Sample Data Sheet Printout .................................................................. 3-28
A-1. Optional ECG Interface Adapter........................................................... A-1

BP Pump 2
Operators Manual
vi

1-1
Chapter 1
Introduction and Specifications
Contents Page
Introduction .................................................................................. 1-3
Key Features................................................................................. 1-3
General Safety Considerations ..................................................... 1-4
Symbols .................................................................................... 1-4
Warnings and Cautions............................................................. 1-5
Instrument Familiarity.................................................................. 1-7
Powering Up the Tester................................................................ 1-10
Specifications ............................................................................... 1-10
Accessories................................................................................... 1-12

BP Pump 2
Operators Manual
1-2

Introduction and Specifications
Introduction
1
1-3
Introduction
The Fluke Biomedical BP Pump 2 Non-Invasive Blood Pressure Simulator and
Tester, hereafter known as the “Tester”, is a multi-purpose test instrument for
use with oscillometric Non-Invasive Blood Pressure Monitors (NIBPMs). The
Tester provides dynamic blood pressure simulations, static calibration,
automated leak testing, and pressure relief valve testing. The following
models are available:
•BP Pump 2L (Basic Model)
•BP Pump 2M (High-Accuracy Model)
The Tester allows you to verify the performance claims of different blood
pressure monitors. You can quickly recall the fixed onboard simulations or
define your own. With its internal pump, the Tester can generate pressures up
to 400 mmHg (53.3 kPa) for leak testing, pressure sourcing, and relief valve
testing.
In addition, you can define auto sequences that automate the sequencing of
tests and NIBP simulations and provide an optional printed report.
Key Features
Key features of the Tester include:
•Pressure leak testing on cuff, tubing, and connections
•Relief valve testing on the patient monitor
•Pressure gauge measurements
•Pressure source capability
•NIBP simulations including adult, neonate, arrhythmias, and respiratory
artifacts
•Auto sequences with optional reports
•Internal Adult and Neonatal Cuff simulation
Tester capabilities can be extended with optional accessories that allow:
•ECG synchronization with non-invasive output
•External wrist cuff simulations

BP Pump 2
Operators Manual
1-4
Tester pressure accuracy can be improved by upgrading to a high-accuracy
pressure transducer. This is a factory service upgrade and is provided to
customers wanting to meet the DIN EN 1060 requirements for pressure
measurement accuracy. For more information, refer to “Setup, Maintenance,
and Support: Maintenance and Support.”
General Safety Considerations
This Tester complies with safety and technical requirements described in the
following directives:
•UL 3101-1, Electrical Equipment for Laboratory Use; Part 1: General
Requirements.
•CAN/CSA C22.2 No. 1010.1 (1992), Safety Requirements for Electrical
Equipment for Measurement, Control and Laboratory Use, Part 1: General
Requirements.
•EC 73/23/EEC (Amended 93/68/EEC) EN61010-1:2001, Safety
requirement for electrical equipment for measurement, control and
laboratory use, Part 1: General Requirements.
Symbols
Table 1-1 describes symbols used in association with the Tester.
Table 1-1. Symbols
Symbol Description Symbol Description
WRisk of danger. Important
information. See manual. XHazardous voltage. Risk of electrical shock.
Œ
Intertek Electrical Test
Laboratory listed.
Conforms to relevant
Canadian and U.S.
standards.
PConforms to European
Union directives
~
Do not dispose of this
product as unsorted
municipal waste. Contact
Fluke or a qualified
recycler for disposal.

Introduction and Specifications
General Safety Considerations 1
1-5
Warnings and Cautions
Users are advised to read the manual carefully, observing all warnings and
cautions, before attempting to set up and operate the Tester.
A Warning identifies hazardous conditions and actions that could cause
bodily harm or death.
A Caution identifies conditions and actions that could damage the Tester or
the equipment under test, or cause permanent loss of data.
WXWarning
To avoid possible electric shock or personal injury, follow
these guidelines:
•Read the Users Manual before operating the Tester.
•Use this Tester only in the manner specified by the
manufacturer or the protection provided may be
impaired.
•Do not connect the Tester to a patient or equipment
connected to a patient. The Tester is intended for
equipment evaluation only and should never be used
in diagnostics, treatment or in any other capacity
where the Tester would come in contact with a patient.
•Do not use the product in wet locations, around
explosive gases or dust.
•Never open the Tester case, because dangerous
voltages are present. There are no user replaceable
parts in the Tester.
•The Tester must be properly earthed. Only use a
supply socket that has a protective earth contact. If
there is any doubt as to the effectiveness of the supply
socket earth, do not connect the Tester.
•Do not use a two-conductor adapter or extension cord;
this will break the protective ground connection.
•Ensure that the external power source is properly rated
for the system.

BP Pump 2
Operators Manual
1-6
•Always connect the system power cord directly to a
three-prong receptacle with a functional ground. Never
use a two-prong plug adapter to connect primary
power to the Tester, thereby disconnecting the utility
ground.
•Disconnect the Tester from the power source before
changing the supply voltage. The Tester operates at a
range of 100 to 240 volts.
WCaution
To avoid damage to the Tester or adverse affects on its
performance, follow these guidelines:
•Allow only qualified technical personnel to service the
Tester.
•Do not expose the system to temperature extremes.
Ambient temperatures should remain between 15° C
and 40° C. System performance may be adversely
affected if temperatures fluctuate above or below this
range.
•Clean the Tester only by gently wiping down with a
clean, lint-free cloth dampened with a mild detergent
solution. Do not immerse the unit.
•Do not apply pressures greater than 400 mmHg (53
kPa) to the pressure port.

Introduction and Specifications
Instrument Familiarity
1
1-7
Instrument Familiarity
Figure 1-1 shows the Tester. The top and side panel components are described
in Table 1-2 and the number key functions are described in Table 1-3.
BP Pump 2
NON-INVASIVE BLOOD PRESSURE MONITOR ANALYZER
PRESSURE
LEAK
1
PRESSURE
RELIEF
TESTS AND SIMULATIONS
2
STATIC
PRESSURE
3
STANDARD BP
NEONATEWRIST
PRESSURE PORT
USER DEFINED
ARRHYTHMIAS
4
PATIENT
CONDITIONS
56
9
8
RESPIRITORY
ARTIFACT
7
0
ENT
12
45
8
3
9
7
6
fas10.eps
Figure 1-1. Tester Top and Side Panel Components

BP Pump 2
Operators Manual
1-8
Table 1-2. Top and Side Panel Components
Label Name Function
A Home Key Returns the operator to the Main Menu.
B Soft Keys 1 - 4 Makes dynamic assignments based on
the current screen.
C Number (Test and
Simulations) Keys
Allows the operator to perform auto
sequences and simulations using
numeric keys.
D Enter Key Advances to the next menu or
saves/selects options.
E Pulse Indicator
LED blinks in synchronization with
beeper, indicating that the pump is
generating a simulated blood pressure
pulse.
F ECG Interface Port Allows connection of optional ECG
accessory (refer to Appendix, ECG
Option).
G Printer Port Provides D-25 female connector for
external parallel printer.
H RS-232 Serial Port Provides serial D-9 female connector for
bi-directional computer control.
I Pressure Port
Connects to the Non-Invasive Blood
Pressure Monitor for all pressure
simulations and tests.