GE T2100-ST1 User manual

GE Healthcare
T2100-ST1Treadmill, 110V / T2100-ST2 Treadmill, 220V
English
© 2016-2017 General Electric Company
All Rights Reserved
T2100-ST1
Treadmill, 110V
T2100-ST2
Treadmill, 220V
Operator’s Manual
2097937-001 Rev E

2 T2100-ST1 Treadmill, 110V / T2100-ST2 Treadmill, 220V 2097937-001 Rev E
12 June 2017
Publication Information
The information in this manual applies only to T2100-ST1 Treadmill, and T2100-ST2 Treadmill,. It does not
apply to earlier versions. Due to continuing product innovation, specifications in this manual are subject to
change without notice.
T2100-ST1, T2100-ST2, CASE, CardioSoft, and MAC are trademarks owned by GE Medical Systems Information
Technologies, Inc., a General Electric Company going to market as GE Healthcare. All other marks are the
properties of their respective owners.
This product complies with the regulatory requirements concerning medical devices from the following
bodies:
T2100-ST1 and T2100-ST2 treadmills meet the following safety and regulatory standards for FDA Class 1
motor operated physical medicine machines. They have been tested by Intertek Testing Services N.A Inc., and
are listed by Engineering Testing Laboratories (ETL). However, the ultimate conformance to IEC 6060-1 2005-
3rd edition is the responsibility of the system integrator when combined with other equipment. Additionally, all
motorized equipment is potentially dangerous if used incorrectly. Before using the T2100-ST1 or T2100-ST2
treadmill, follow all precautions listed in this manual and read the entire Operator’s Manual thoroughly. Use
the T2100-ST1 and T2100-ST2 treadmills only as described.
Revision History
The document part number and revision appear at the bottom of each page. The revision identifies the
document’s update level. The revision history of this document is summarized in the following table.
Revision
Publication Date
Description
A
20 August 2016
Internal release
B
9 September 2016
Initial public release
C
18 November 2016
Power cord configuration
D
30 March 2017
Authorized Representative Address Change
E
12 June 2017
Added power cord configuration
To access other GE Healthcare manuals, go to the Common Documentation Library (CDL), located at
www.gehealthcare.com/documents and click Cardiology.

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Contents
1Introduction............................................................................................................ 7
Intended User ...............................................................................................................................7
Indications for Use......................................................................................................................7
Prescription Device Statement..............................................................................................7
Regulatory and Safety Information ....................................................................................7
Safety Conventions ........................................................................................................8
Safety Hazards.................................................................................................................8
Classification of Medical Device ............................................................................ 10
Regulatory and Safety Conformance ................................................................. 11
Responsibility of the Manufacturer...................................................................... 12
Responsibility of the Customer .............................................................................. 12
Product and Package Information....................................................................... 14
Symbols ............................................................................................................................ 14
Equipment Identification....................................................................................................... 18
Product Label................................................................................................................. 18
Service Information................................................................................................................. 18
Service Requirements ................................................................................................ 18
Warranty Information ................................................................................................ 19
Additional Assistance ................................................................................................. 19
Manual Information ................................................................................................................ 19
Manual Purpose............................................................................................................ 19
Document Conventions............................................................................................. 19
Related Documents..................................................................................................... 20
Training......................................................................................................................................... 21
2Product Overview................................................................................................ 23
Safety Systems.......................................................................................................................... 24
Treadmill....................................................................................................................................... 24
Drive System............................................................................................................................... 24
Speed Range .............................................................................................................................. 24
Incline Range.............................................................................................................................. 24
Running Surface ....................................................................................................................... 24
Communication Ports ............................................................................................................ 25
Floor Surface Footprint.......................................................................................................... 25
Operating and Storage Condition Recommendations............................................ 25
Power Requirements .............................................................................................................. 25

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3Assembly and Setup ........................................................................................... 27
Safe Handling Guidelines...................................................................................................... 27
Initial Setup ................................................................................................................................. 28
Location........................................................................................................................................ 29
Final Setup - Running Belt Tracking Adjustment........................................................ 30
Final Setup - Running Belt Tension Adjustment ......................................................... 31
Final Setup - Drive Belt Tension Adjustment................................................................ 31
Final Setup - Test Plug Procedure..................................................................................... 31
Using the test plug................................................................................................................... 32
Communication Access Location ..................................................................................... 33
4Operating Instructions....................................................................................... 35
Electrical Safety Tests............................................................................................................. 35
Operating Controls .................................................................................................................. 35
Controlling the Treadmill....................................................................................................... 36
Power Switch.............................................................................................................................. 36
Emergency Stop Switch ........................................................................................................ 36
Emergency Stop Switch Check .......................................................................................... 36
Pull Tether Switch..................................................................................................................... 36
Pull Tether Switch Check....................................................................................................... 37
Adjustable Handrail Option ................................................................................................. 37
5Preventive Maintenance .................................................................................... 39
Daily Maintenance................................................................................................................... 39
Weekly Maintenance.............................................................................................................. 40
Monthly Maintenance ............................................................................................................ 40
Semiannual Maintenance .................................................................................................... 40
Belt Cleaning and Inspection.............................................................................................. 40
Running Belt Tracking Adjustment................................................................................... 41
Running Belt Tension Adjustment..................................................................................... 42
Drive Belt Tension Adjustment ........................................................................................... 42
Exterior Care............................................................................................................................... 43
Elevation Screw Lubrication................................................................................................ 43
Running Deck Maintenance ................................................................................................ 43
6Troubleshooting .................................................................................................. 45
Power Switch Will Not Illuminate ...................................................................................... 45
Facility Circuit Breaker Trips when Powering Up ....................................................... 46

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Treadmill Will Not Start.......................................................................................................... 46
Running Belt Slips When In Use......................................................................................... 46
Running Belt Is Off-Center.................................................................................................... 46
Internal Circuit Breaker Location and Resetting........................................................ 46
AMaintenance Log................................................................................................. 47

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1Introduction
This document describes the T2100-ST1 and T2100-ST2 treadmills
also referred to as the “system”, “device”, or “product”. The
document is intended to be used by clinical professionals.
This chapter provides general information required for the proper
use of the system and this manual. Familiarize yourself with this
information before using the system.
Intended User
This manual is geared for clinical professionals. Clinical
professionals are expected to have working knowledge of medical
procedures, practices, and terminology as required for completing
these examinations.
Indications for Use
The T2100-ST1 and T2100-ST2 treadmills are designed for cardiac
stress testing.
Prescription Device Statement
CAUTION:
United States federal law restricts this device to sale by, or on
the order of, a physician.
Regulatory and Safety Information
This section provides information about the safe use and regulatory
compliance of this system. Familiarize yourself with this
information, and read and understand all instructions before
attempting to use this system. The system was designed and
manufactured to the appropriate medical regulations and controls.

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NOTE:
Disregarding the safety information provided in this manual is
considered abnormal use of this system and could result in
injury, loss of data, and void any existing product warranties.
Safety Conventions
A Hazard is a source of potential injury to a person, property, or the
system.
This manual uses the terms DANGER, WARNING, CAUTION, and
NOTICE to point out hazards and to designate a degree or level of
seriousness. Familiarize yourself with the following definitions and
their significance.
Definition of Safety Conventions
Convention
Definition
DANGER
Indicates an imminent hazard, which, if not avoided, will result in
death or serious injury.
WARNING
Indicates a potential hazard or unsafe practice, which, if not
avoided, could result in death or serious injury.
CAUTION
Indicates a potential hazard or unsafe practice, which, if not
avoided, could result in moderate or minor injury.
NOTICE
Indicates a potential hazard or unsafe practice, which, if not
avoided, could result in loss or destruction of property or data.
Safety Hazards
The following messages apply to the system as a whole. Specific
messages may also appear elsewhere in the manual.
WARNING:
The T2100-ST1 and T2100-ST2 treadmills are manufactured to
exacting standards both in physical form and in component
selection. The components used in our products have been
selected with performance and medical safety in mind. The
treadmills have been engineered and certified to conform to
the list of medical and safety regulatory standards which
appear on the next page. Modification or part substitution of
any kind is strictly forbidden. Any deviation in component
replacement, physical or electrical modification will result in
loss of medical safety certification and warranty of this
product. Modifications to this equipment may put the patient
at risk of electrical shock or hardware malfunction.
Contact GE Healthcare Service department for all your repair
part needs.
WARNING:
The T2100-ST1 and T2100-ST2 treadmills must be grounded
to reduce the risk of electrical shock. If a malfunction occurs,

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grounding provides a path of least resistance for an electric
current. Ungrounded connections must not be used.
No other equipment may be used on the electrical circuit with
the treadmills. Do not use extension cords. Using a shared or
unreliable circuit can also cause the treadmills to
unexpectedly shut off, potentially resulting in injury to the
patient.
Ensure the master power switch is in the off position before
plugging in the T2100-ST1 or T2100-ST2. A power surge could
damage the sophisticated electronic system of the treadmills.
WARNING:
Before permitting anyone to use the T2100-ST Series, do the
following:
Warn each user about the risk of falling while the belt is in
motion.
Stress the need for caution.
Demonstrate the proper mounting and dismounting
methods.
Show each user how to use the T2100-ST Series as
described in this manual.
Ask each user to perform a supervised "test usage" at
minimum belt speed to review and practice usage
techniques.
Observe all the precautions listed under “Responsibility of
the Customer“ on page 12 to reduce the possibility of
serious injury as a result of falls or loss of balance.
WARNING:
Serious injury or death could result from electrical shock. To
reduce the possibility of electrical shock, carefully observe
the following precautions.
To disconnect the treadmill, set the power switch to the OFF
position, and remove the plug from the outlet. When the
power is off, the green light on the power switch is dark.
Never operate the unit with a damaged power cord or plug.
Power cord should be routed through frame mounted clamp
and kept clear of the elevation mechanism.
Keep the power cord out of traffic areas and away from
heated surfaces.
Never use extension cords.
Never operate the unit when it is wet.

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Never operate the unit if it is not operating properly.
Always unplug the machine before service or maintenance is
performed.
Treadmill should be serviced by authorized technicians only.
Operator should report any electrical shock when touching
the treadmill and discontinue use immediately.
Never use the treadmill outdoors.
Immediately discontinue use and unplug the treadmill if you
smell the distinctive odor of hot electrical components.
WARNING:
Serious injury or death could result from electrical shock
occurring during defibrillation. Never allow patient or
operators near treadmill during defibrillation.
WARNING:
Consult your physician prior to using this appliance to
determine the patient’s physical readiness and capabilities.
Stop exercising immediately and seek medical attention if the
patient experience chest pain, dizziness or shortness of breath
or if you experience symptoms of overexertion.
WARNING:
Serious injury or death could result from operating the
treadmill in the presence of explosive or flammable vapors
and antiseptics.
WARNING:
The potential for foot crush injury at frontal end of treadmill at
lift mechanism (landing gear) when treadmill is descending.
Keep feet and hands away from this area at all times.
Potential foot crush injury at rearward side rail, rear of side rail
and rear roller exists when treadmill approaches full elevation.
Keep feet and hands away from this area at all times.
Classification of Medical Device
This device is classified as follows, according to IEC 60601-1:
Medical Device Classification
Category
Classification
Type of protection against electrical
shock
Class I motor operated physical
medicine machine.
Degree of protection against
electrical shocks
Type B external application applied
part.
Degree of protection against harmful
ingress or water
Ordinary equipment (enclosed
equipment without protection against
ingress of water).

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Category
Classification
Degree of safety of application in the
presence of a flammable anesthetic
mixture with air or with oxygen or
with nitrous oxide
Equipment is not suitable for use in the
presence of a flammable anesthetic
mixture with air or with oxygen or with
nitrous oxide.
Method(s) of sterilization or
disinfection recommended by the
manufacturer
Not applicable
Mode of operation
Continuous operation.
Regulatory and Safety Conformance
T2100-ST1 and T2100-ST2 treadmills meet the following safety and
regulatory standards for FDA Class 1 motor operated physical
medicine machines. They have been tested by Intertek Testing
Services N.A Inc., and are listed by Engineering Testing Laboratories
(ETL). However, the ultimate conformance to IEC 6060-1 2005-3rd
edition is the responsibility of the system integrator when combined
with other equipment. Additionally, all motorized equipment is
potentially dangerous if used incorrectly. Before using the T2100-
ST1 or T2100-ST2 treadmill, follow all precautions listed in this
manual and read the entire Operator’s Manual thoroughly. Use the
T2100-ST1 and T2100-ST2 treadmills only as described.
UL 1647
Issue: 2011/04/21 Ed: 5 UL Standard for Safety for Motor-Operated Massage and
Exercise Machines
CAN/CSA C22.2#68
Issue: 2009/09/01 Ed: 7 Motor-Operated Appliances (Household and Commercial)
General Instruction No.1: 2010/02/01 - General Instruction No.2: 2010/09/28
CSA C22.2#60601-1
Issued: 2008/02/01 Ed: 3 Medical Electrical Equipment - Part 1: General
Requirements for basic Safety and essential performance
ICES 003 Industry Canada (IC) Verification
Issue: 2004/01/01 Issue No.4 Interference-Causing Equipment Standard, Digital
Apparatus
IEC 60335-1 Low Voltage Directive for the European Union (EU)
Issued: 2004/07/01 Ed: 4.1 Household and Similar Electrical Appliances –Safety
Part 1: General Requirements; Corrigendum 1: 12/2005; Amendment 2: 05/2006;
Corrigendum: 08/2006
IEC 60601-1
Issued: 2005/01/01 Ed: 3 Medical electrical equipment Part 1: General
requirements for basic safety and essential performance Australia and Israel,
IEC 60601-1-2
Issued: 2007/03/01 Ed: 3.0 Medical Electrical Equipment - Part 1-2: General
Requirements for Basic Safety and Essential Performance - Collateral
Standard: Electromagnetic Compatibility - Requirements and Tests

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AAMI ES60601-1
Issued: 2005/01/01 Medical electrical equipment Part 1: General requirements for
basic safety and essential performance.
IEC CISPR 11-1 EMC Directive for the European Union (EU)
Issued: A1:2010 Electromagnetic Compatibility Requirements for Household
Appliances, Electric Tools and Similar Apparatus Part 1: Emission Edition 5.0;
Federal Communications Commission (FCC) Verification for the
United States
FCC 47CFR 15A
Issued: 2011/04/21 Title 47 CFR Part 15 Subpart A General Radiators Class A
NOTE:
This equipment has been tested and found to comply with
the limits for a Class B digital device, pursuant to part 15 of
the FCC Rules. These limits are designed to provide
reasonable protection against harmful interference when
the equipment is operated in a commercial environment.
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 harmful
interference in which case the user will be required to
correct the interference at owner’s expense.
Responsibility of the Manufacturer
Full-Vision Inc. is responsible for the effects of safety, reliability, and
performance of the treadmill only if the following conditions are
met:
Assembly operations, extensions, readjustments, modifications,
or repairs are carried out by persons authorized GE Healthcare.
The electrical installation of the relevant room complies with
the requirements of the appropriate local, state, and other
government regulations.
The equipment is used in accordance with the instructions for
use.
Responsibility of the Customer
The customer is responsible for providing appropriate desks, chairs,
electrical wall outlets, network connections, and analog phone lines,
and for locating any of the system components described in this
manual in compliance with all local, state, and national codes.
The customer is solely responsible for the training, instruction,
supervision and safety of all users of the T2100-ST Series treadmill,
and to use it as intended by the manufacturer. This device is
intended to be used as a motion appliance to facilitate cardiac or
VO2 medical evaluation.

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Read this Operator’s Manual before operating the T2100-ST
Series Treadmill.
Assist in off-loading the patient in the event of abnormal or
unexpected operation of the treadmill.
If the treadmill is not responding properly, stop the treadmill,
assist in removing the patient off the running belt, unplug the
treadmill power supply, and seek factory authorized repair
before attempting to restart the treadmill.
Never allow children or pets near the machine without qualified
adult supervision.
Note the location of stop and/or emergency stop controls and
their operation before starting a test or workout.
This device is not intended for use by persons with reduced
physical, sensory or mental capabilities, or lack of experience
and knowledge unless they have been given supervision or
instruction concerning use of the appliance by a person
responsible for their safety.
Verify the Patient and Operator both know how to stop the
machine in the event of malfunction or emergency.
Patient should not wear loose fitting nylon material when
exercising on this treadmill to avoid generating Electro Static
Discharge.
Never attempt to remove any article of clothing while the
running belt is moving.
All persons on and around the treadmill must wear enclosed,
protective footwear. Shoe laces must be tight and not drape as
to cause a trip or catch hazard. Sandals, flip flops, slippers and
the like are not considered enclosed, protective footwear.
Walk in the center of the running belt. Contact with the side rail
and the moving belt could cause injury.
The Patient must always wear the Stop Tether lanyard wrist
strap while operating the T2100-ST Series Treadmill
Place the treadmill on a hard, level and unobstructed surface.
See Chapter 3“Assembly and Setup“ of this manual.
Check input power cord connection and location for hazardous
pinch points before use.
Check input communications cord connection (if equipped) for
proper interface with all equipment.
Keep all cords clear of patient to avoid trip hazards.

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Never attempt to remove the motor pan hood or do electrical
repairs yourself. Repairs should only be done by a factory
authorized repair provider.
Always unplug the T2100-ST Series Treadmill when servicing,
inspecting or cleaning the treadmill.
Routinely inspect the treadmill for loose parts.
Inspect handrails and ensure they will support the patient
properly.
Always start the running belt at its slowest speed before
starting the patient test.
Do not step onto belt when it is moving.
Always slow the running belt to its minimum speed before
stopping.
Keep hands, feet, and clothing away from any moving parts.
Verify no one is near the elevation mechanism before
operating. Never put any part of the body under any part of a
running treadmill.
Never drop or insert objects into any opening.
Never drape garments, hook-up leads, or other equipment over
the side rails or drop objects on the belt while the T2100-ST
Series Treadmill is running.
Do not allow moisture or oils to accumulate on equipment,
creating a slip hazard.
Product and Package Information
This section describes the location of the labels used on your device
and its packaging. It also describes the symbols used on the labels.
Symbols
The following symbols may appear on the device or its packaging.
Familiarity with these symbols assists in the safe use and disposal
of the equipment. For equipment symbols not shown, refer to the
original equipment manufacturers (OEM) manuals.
Symbols are used to convey warnings, cautions, prohibitions,
mandatory actions, or information. Any hazard symbols on your
device or packaging with markings in color indicates there is certain
danger and is a warning. Any hazard symbols on your device or
packaging that is in black and white indicates a potential hazard
and is a caution.

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Symbols
Symbol
Description
Catalog or Orderable Part Number
Indicates the manufacturer's catalog or part number.
Serial Number
Indicates the manufacturer's serial number.
Date of Manufacture (Year-Month)
Indicates the original manufacture date for this device.
Manufacturer Name and Address
Indicates the name and address for the manufacturer of this
device.
CAUTION:
CONSULT ACCOMPANYING DOCUMENTS - There may be
specific warnings or precautions associated with the
device that are not otherwise found on the label.
Consult the accompanying documentation for more
information about safely using this device.
CAUTION:
ELECTRIC SHOCK - Indicates the presence of hazardous
energy circuits or electric shock hazards.
To reduce the risk of electric shock hazards, do not open this
enclosure. Refer servicing to qualified personnel.
Reading of the Owner’s Manual is mandatory.
Upper Temperature Limit
Indicates the maximum temperature for transportation and
handling of this package.
Temperature Limits
Indicates the upper and lower temperature limitations for the
transportation and handling of this package.
European Union Disposal Requirements
This equipment complies with the EU WEEE marking
requirement for proper disposal of electrical and electronic
waste in accordance with the European Directive 2011/65/EE.
This directive calls for separation and recovery or reuse of
used electrical or electronic equipment upon end of life EEE
disposal.
The T2100 must not be disposed of as unsorted municipal
waste. Electrical or electronic components must be collected
separately and disposed of in accordance with your local
requirements and sources. The EEE program minimizes any
potential effects on the environment and user health by
eliminating the potential presence of hazardous substances in
the waste stream. Customers should contact their local
authorities or T2100 Distributor for guidance in complying
with the directive.

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Symbol
Description
Keep Dry
Indicates that you need to keep the container away from rain
and other sources of moisture.
CE Mark
Indicates the device or product conforms with applicable EU
(European Union) directives.
Eurasian Conformity mark
Conformity to applicable technical regulations of Customs
Union.
Electrical Testing Laboratories
Indicates the device or product has been tested by an
accredited third-party testing laboratory and meets
applicable safety standards for sale and distribution within
North America.
PCT (GOST-R) Mark
Indicates the device or product conforms with applicable
Russian Gosstandard technical and safety standards.
Protective earth (ground).
Alternating current.
Device is suitable for the external application of the type “B”
applied parts.
Label Locations
This section identifies the labels and their locations on the product
and packaging.

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Refer to the previous illustrations for the locations of the labels
identified in the following table. For detailed descriptions of the
symbols that appear on the labels, refer to “Symbols” on page 12.
Item
Label
Location
Description
1
Front of
device
Identifies the product model.
2
Front of
device
Identifies Listing Standards
3
Front of
device
Contains the European Union
disposal requirements.
4
Front of
device on
Hood
Identifies the Caution
Electrical shock hazard.
5
On Power
Cord
Identifies DC Hi-Pot Caution.
6
Front of
device
Identifies Power switch.
7
Shipping
Package
Identifies the following
information for shipping:
Model number
Reference number
Serial number
Storage conditions
Regulatory compliance
Country of origin
EC Representative
information

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Equipment Identification
Product Label
Product Label Format
Item
Name
Description
1
Manufacture
Full Vision Inc.
2
Private Label Manufacture
GE Medical Systems
Information Technologies, Inc.
3
Model Number
Identifies model of treadmill
4
Manufacture Model Number
Identifies manufactures model of treadmill
5
Serial Number
Manufactures assigned serial number
6
REF
GE Medical Systems reference part number
7
Manufacture Part Number
Manufactures part number
8
Manufacture Date
Manufactures date code
9
Voltage
Specifies operating voltage of treadmill
10
Hertz
Specifies the electrical hertz of treadmill
11
Amps
Specifies amperage of treadmill
12
Type B Equipment
Device is suitable for the external application
of type “B” applied parts
Service Information
This section provides information pertaining to the maintenance
and servicing of the system. Familiarize yourself with this
information before requesting service from GE Healthcare or its
authorized representatives.
Service Requirements
Failure on the part of the responsible individual, hospital, or
institution using this equipment to implement a satisfactory
maintenance schedule may cause undue equipment failure and
possible safety hazards.

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Regular maintenance, irrespective of usage, is essential to ensure
that the components of this system are always functional when
required.
Warranty Information
This device is considered GE Healthcare-supplied hardware. Only
authorized GE Healthcare service personnel should service the
device. Any unauthorized attempt to repair equipment under
warranty voids that warranty. It is the user's responsibility to report
the need for service to GE Healthcare or to one of their authorized
agents.
Additional Assistance
GE Healthcare maintains a trained staff of application and technical
experts to answer questions and respond to issues and problems
that may arise during the installation, maintenance, and use of this
system.
Contact your local GE Healthcare representative to request
additional assistance.
Manual Information
This section provides information for the correct use of this manual.
Keep this manual with the equipment at all times and periodically
review it. You should request training assistance from GE
Healthcare, if needed.
Manual Purpose
This manual provides information necessary for the configuration
and safe operation of this equipment in accordance with its
function and intended use. It is not intended as a replacement for,
but a supplement to, thorough product training. Keep it with the
equipment at all times. Additional manuals may be ordered by
contacting GE Healthcare.
Refer to the service manual for technical information related to the
maintenance and repair of the equipment.
Document Conventions
This document uses the following conventions.
Typographical Conventions
The following table identifies the typographical conventions used in
both this document and GE Healthcare Diagnostic Cardiology
product documents.

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Convention
Description
Bold Text
Indicates keys on the keyboard, text to enter, or hardware
items such as buttons or switches on the equipment
Italicized Bold
Text
Indicates software terms that identify menu items, buttons,
or options in various windows.
KEY1+KEY2
Indicates a keyboard operation. A plus (+) sign between the
names of two keys indicates that while holding the first key,
you should press and release the second key. For example,
Press CTRL+ESC means to press and hold the CTRL key and
then press and release the ESC key.
<space>
Indicates that you must press the spacebar. When
instructions are given for typing a precise text string with
one or more spaces, the point where you must press the
spacebar is indicated as: <space>. This ensures that the
correct number of spaces are inserted in the correct
positions within the literal text string. The purpose of the <>
brackets is to distinguish the command from the literal text
within the string.
Enter
Indicates that you must press the Enter or Return key on
the keyboard. Do not type Enter.
>
The greater than symbol, or right angle bracket, is a concise
method to indicate a sequence of menu selections.
For example, the statement “From the main menu, select
System>Setup>Options to open the Option Activation
window” replaces the following:
1. From the main menu, select System to open the
System menu.
2. From the System menu, select Setup to open the
Setup menu.
3. From the Setup menu, select Options to open the
Option Activation window.
Illustrations
All illustrations in the document are provided as examples only.
Notes
Notes provide tips or additional information that, while useful, are
not essential to the correct operation of the tools. They are called
out from the body text through a flag word and indentation, as
follows:
NOTE:
The tip or additional information appears indented below the
NOTE flag word.
Related Documents
The following documents are referenced in this manual and provide
additional information that may be helpful in the installation,
configuration, maintenance, and use of this product.