Exact Arm 2.0 Reference Guide
Exact Arm 2.0 Reference Guide
Reference Guide
Introduction ................................................................................................................... 7
What is new in Exact Arm Reference Guide? ................................................................................... 7
Visual Cues ....................................................................................................................................... 7
Contact Varian Customer Support ..................................................................................................... 8
Abbreviations and Definitions ............................................................................................................ 8
Related Publications .......................................................................................................................... 9
Table of Contents 3
Using the Hand Pendant ID Utility ................................................................................................... 56
Using the Run Test Utility ................................................................................................................ 56
Index .......................................................................................................................... 69
Publication Title
Exact Arm Reference Guide
Abstract
This document provides reference information and procedures for using the Exact arm, version 2.0, in a treatment and
simulation environment.
This publication is the English-language original.
Trademarks
ARIA, Clinac, Exact, and VARiS are registered trademarks of Varian Medical Systems, Inc. Acuity BT, Acuity, PortalVision,
VARiS Vision, and Vision are trademarks of Varian Medical Systems, Inc.
Windows, Word, Windows NT and Windows XP, and Workstation are registered trademarks of Microsoft Corporation.
All other trademarks or registered trademarks are the property of their respective owners.
Copyright
© 2005–2014, 2020 Varian Medical Systems, Inc. All rights reserved. Published in Switzerland.
No part of this publication may be reproduced, translated, or transmitted without the express written permission of Varian
Medical Systems, Inc.
Notice
Information in this publication is subject to change without notice and does not represent a commitment on the part of
Varian. Varian is not liable for errors contained in this publication or for incidental or consequential damages in connection
with furnishing or use of this material.
Electronic Labeling
This symbol on the label indicates that the Instructions for Use for the corresponding product are available at
www.MyVarian.com. Access the Instructions for Use in electronic form by logging in with your assigned MyVarian user
credentials.
In compliance with Anvisa and EU regulations, Varian will send Brazil and EU customers a
free printed copy of the Instructions for Use within 7 days. Use the “Paper Publication Re-
quest” form provided on the Varian webpage to order your copy.
Legal Manufacturer
Varian Medical Systems, Inc.
3100 Hansen Way
Palo Alto, CA 94304
United States of America
CAUTION: US Federal law restricts this device to sale by or on the order of a physician.
Legal Information v
WHO
ICD-O codes and terms used by permission of WHO, from:
● International Classification of Diseases for Oncology, Third Edition.
ICD-10 codes and terms used by permission of WHO, from:
● International Statistical Classification of Diseases and Related Health Problems, Tenth Revision (ICD-10).
13485
Medical Device
2797
Visual Cues
This publication uses the following visual cues to help you find information:
Note: A note describes information that may pertain to only some conditions, readers, or
sites.
Tip: A tip describes useful but optional information such as a shortcut, reminder, or
suggestion, to help get optimal performance from the equipment or software.
Introduction 7
Contact Varian Customer Support
Varian Customer Support is available on the internet, by e-mail, and by telephone. Support
services are available without charge during the initial warranty period.
The MyVarian website provides contact information, product documentation, and other resources
for all Varian products.
Use MyVarian to report incidents. Any serious incident that has occurred while using the device
should be reported to the manufacturer and the competent authority of the Member State in which
the user or patient is established.
1. Go to www.MyVarian.com.
2. Choose an option:
● If you have an account, enter your user login information (e-mail and password).
● If you do not have an account, use the on-screen prompts to create one. Establishing an
account may take up to two working days.
3. To get customer support:
● To display contact information, click Contact Us at the top of the page.
● To access product information and other support options, click Documentation at the top
of the page, or use the menu on the top right side of the screen.
Introduction 9
Safety and Emergency
Care Required
WARNING: Incorrect use of a radiotherapy linear accelerator can cause serious
injury or death. Only trained personnel under the supervision of a
licensed physician should be authorized by the hospital or owner to
operate a clinical accelerator. The emergency and safety procedures
are described in the related Instructions for Use.
Careless handling or operating can result in poor performance, equipment and environmental
damage, potential fire hazards, and personal injury or death.
The equipment must be handled with care and kept in a good and safe condition as described in
the maintenance manuals.
Maintenance
For safety, best performance and long life of the equipment, regular cleaning and maintenance
work must be carried out as described in the maintenance manuals. This will keep the system in
proper working condition.
Deficiencies occurring during operation must be rectified immediately. The system must not be
operated while repair work is in progress.
Responsibility
● All persons who handle, use, or operate the system must read and understand the chapters
dealing with safety regulations and emergency procedures
● Only qualified and trained personnel are permitted to operate and maintain the system and
parts of it
● The hospital management shall establish emergency and safety procedures before operating
the system and all personnel must be trained in such procedures
● The system must only be run with its original and unmodified fittings and replacement parts
● No modifications to the system, its parts or the software are permitted without prior review
and approval from Varian
Varian cannot be held responsible for personal injury or equipment damage if:
● Changes or repairs are carried out that are not in accordance with the instructions contained
in any Varian manual for the system, or if spare parts, standards and procedures not
authorized in writing by Varian are used
● Safety devices are removed or changed
● Updates, modification or repair instructions occasionally issued by Varian are not complied
with
● The equipment is used for purposes other than those intended
● The periodic inspection and maintenance instructions are not complied with and records not
kept
● Operation or maintenance work is performed by unqualified persons
● The instructions and safety regulations are not complied with by the operators, maintenance
staff, or guests
● Local laws and regulations have not been complied with
● Anomalies during operation and maintenance are not reported to Varian immediately
● Legal and/or government regulations are not complied with
Further Regulations
These instructions do not render any further hospital and/or local, state or country regulations or
laws invalid. Such regulations must be complied with at any time.
Hazards
There are several hazards for the Exact arm:
● Electrical Hazards on page 12
● Mechanical Hazards on page 12
Electrical Hazards
Note: The emergency and safety procedures are described in the related Instructions for
Use.
Safety Precautions
● Only authorized and trained personnel are permitted to work on the system.
● The power supply must be properly shut off during maintenance, repair or inspection work on
the system as appropriate. Operators may be endangered if part of the equipment is
energized while work is being carried out. Take measures to prevent anyone from energizing
part of the equipment while work is being carried out. Adjacent parts that may be live must be
covered.
● Electric power must not be reapplied until after the persons working on any part of the system
have completed their task, are clear of moving parts, have reinstated the system to a safe
operating condition, and have personally reported on system clear and safe for energizing.
● Replace faulty cables immediately.
● Electrical equipment carries the risk of an electrical fire, which could lead to severe burns,
asphyxiation, other injuries or death.
● Only personnel trained in fire fighting procedures are allowed to attempt to put out an
electrical fire, using the correct type of fire extinguisher, not water.
Mechanical Hazards
Note: The emergency and safety procedures are described in the related Instructions for
Use.
The Exact arm is attached to the counterweight in the gantry and will intrude into the space
generally occupied by the treatment couch.
There is a risk of collision between the image detector unit, its arm, the patient and hospital
personnel whenever the Exact arm, the gantry, or the couch moves.
Safety Precautions
● Pay close attention to the patient's position, when mechanically moving the arm, gantry, and
couch.
● Immediately stop the motion if a collision appears possible.
● Stay out of hazardous areas while the system is in operation.
● Do not carry out maintenance or repair work unless the system is at standstill and has been
secured.
● Ensure that neither the calibration data nor the machine table is incorrect or corrupted, as this
may cause the Exact arm to drive to a point outside its limits.
Pinch Points
Note: The emergency and safety procedures are described in the related Instructions for
Use.
● Return the hand pendant to its holder at the end of the couch when you are not using it.
● Do not irradiate beyond the marked area of the cassette.
Mechanical Overload
The Exact arm is not designed to support weight other than the cassettes and its collision cover.
To prevent damage to the arm mechanisms, excess force on the cassette causes a mechanical
overload which interlocks clinical movements. Retraction is then possible only by BMC.
Only Varian service personnel can clear the overload interlock and reenable IDU movements.
CAUTION: Objects placed on the cassette could fall due to retraction of the Exact
arm or rotation of the gantry. This could result in injuries or equipment
damage. Any load on the cassette can affect its proper positioning.
Excess pressure on the cassette could trip the mechanical overload
interlock and result in damage to the arm mechanisms, causing in
unsafe operating conditions.
Emergency
In case of an emergency, do not panic or act in haste.
● Think before taking decisive action.
Emergency Procedures
There are several emergency procedures for the Exact arm:
● Overriding Motion Interlocks on page 15
● Retracting Manually by Backup Motion Controls (BMC) on page 16
● Power Failure on page 20
● Hand Pendant on Clinacs: Resolving Thumbwheel or Key Jams on page 20
Note: The override button on the Clinac collimator accessory I/F reenables the
interlocked motions of the Exact arm, gantry and couch. This override switch silences the
audible alarm. However, even a momentary collision requires that you press the Clinac
collimator accessory reset button to resume normal Clinac motion.
Collision detection is provided by touch guards in the following places, Figure 1 Collision
Detection on page 15:
● Cassette cover
● Both sides of the elbow joint
A motion interlock occurs when this collision detection system is activated. The motion interlock
disables all arm motion, gantry rotation, and treatment couch lift. It also activates an alarm that
sounds until you override or clear the collision condition.
CAUTION: The BMC function without software limits, but the motors speeds are
limited by hardware. Running into mechanical limits shall be
prevented, as this can result in the motor actuator shaft becoming
“stuck” against its internal end-stops. Always turn the BMC speed
selector slowly and never run the motor at full speed.
Note: The emergency and safety procedures are described in the related Instructions for
Use.
Backup Motion Controls (BMC, Figure 14 Backup Motion Controls (BMC) on page 31) used for
manual retraction is a pendant-like device allowing to move the arm when the Exact arm
controller is inoperable. The controls perform a function similar to the controls on the Clinac
emergency pendant. The controls, which must be enabled by a switch, operate each motor
individually, allowing you to move each arm part separately (forearm, upper arm, wrist, hand).
The recommended sequence of motions for retraction using the BMC is:
1. Cassette laterally to center (in relation to the gantry).
2. Hand towards forearm.
3. Forearm towards upper arm.
4. Upper arm towards gantry.
To operate the BMC:
1. Remove the covers. For clinac types, Table 2 Clinac Types on page 15:
a. For HE Exact arms: Remove enough of the vertical black decorative strip on the center
right side of the clinac gantry (as viewed from the treatment couch) to expose the BMC
socket (unlabeled), Figure 2 HE BMC Socket at Gantry on page 17.
b. For LE Exact arms: Open the stand door to gain access, Figure 3 LE BMC Socket at
Stand on page 17.
2. Plug the connector of the BMC into the appropriate socket on the clinac gantry, Figure 2 HE
BMC Socket at Gantry on page 17 and Figure 3 LE BMC Socket at Stand on page 17.
CAUTION: Before you move the hand to the forearm, check that there is
enough clearance so that it will not hit the floor. A collision between
the cassette and the floor could cause serious damage to the
cassette.
1 2
1 2
1. Gantry
4. Move the hand towards the forearm until the mechanical limit is reached:
For the definition of the arm parts, Figure 9 Definition of Exact Arm Parts on page 23.
a. Turn the axis selector to Wrist.
b. Toggle the direction switch to control the direction of movement for the selected axis.
c. Press the motion enable button while turning the speed selector clockwise from the
neutral. Turning the speed selector increases the speed.
d. Move the hand slowly until the mechanical endstop is reached.
e. Release the motion enable button and return the speed selector to the neutral position,
by turning the speed selector counterclockwise.
If it is necessary to move the hand in the opposite direction toward the working position,
return the speed selector to the neutral position and toggle the direction switch.
CAUTION: Before you move the forearm towards the upper arm, check that
there is enough clearance so that it will not hit the cover of the
gantry. A collision between the cassette and the machine cover
could cause serious damage to the cassette.
1. Gantry
1. Gantry
CAUTION: When you retract the upper arm, stop before the arm is vertical
to check that the cassette is in the correct lateralposition for
retraction. A collision between the cassette and the sides of
thecounterweight could cause serious damage to both units.
6. Move the upper arm towards the counterweight, stopping to check the lateral position of the
cassette before it reaches the counterweight:
a. Turn the axis selector to Shoulder.
b. Toggle the direction switch to control the direction of movement for the selected axis.
c. Press the motion enable button while you turn the speed selector clockwise from the
neutral.
Turning the speed selector increases the speed.
d. Move the upper arm slowly until the IDU is about 5 cm from the gantry cover.
e. Release the motion enable button and return the speed selector to the neutral position,
by turning the speed selector counterclockwise.
If it is necessary to move the upper arm in the opposite direction toward an extended
position, release the motion enable button. Return the speed selector to the neutral position,
by turning the speed selector counterclockwise. Only than toggle the direction switch.
7. To fit the Image Detection Unit (IDU) into the space provided in the gantry, move the IDU
laterally, proceeding as follows:
a. Turn the axis selector to Hand.
b. Toggle the direction switch to control the direction of movement for the selected axis.
c. Press motion enable button while you turn the speed selector clockwise from the neutral.
Turning the speed selector increases the speed.
d. Move the IDU into central position.
CAUTION: After retracting the IDU, make sure that it is properly folded into the
base of the gantry.
1. Gantry
Power Failure
If there is a power failure during arm motion, you must recalibrate the arm. You must also
recalibrate it if the arm moves while the power is off.
If there is power to the Clinac but no power to the control rack (no LEDs lit), check the cable from
the power distribution of the machine.
Intended Use
The Exact arm is used to position an X-Ray source or a real-time imager to provide either high-
quality fluoroscopic/radiographic images or high energy treatment images of a specified area.
The Exact arm is compatible with other devices where their intended use is defined, see
Appendix: Intended Use Statements on page 57 in this manual.
1
2
3
7
5 6
All arm motion is fully motorized, with a separate drive assembly for each arm part: hand, upper
arm, and forearm. There is also a separate assembly for hand lateral motion.
● The shoulder, elbow and wrist drives move the corresponding arm parts so that the image
detection unit can reach every vertical and longitudinal position in its travel range.
● The lateral drive moves the image detection unit from side to side so that it can reach every
position in the lateral plane of its travel range.
The individual drives operate simultaneously, moving arm parts in order to position the image
detection unit along its three directional axes of motion: vertical, longitudinal, and lateral,
Figure 10 Directional Axes of Motion on page 24.
- Lng +
-
Lat +
+ Vrt
-
Actual value increases in the + direction
Actual value decreases in the - direction
1. Gantry
Hand Pendant
All communication between the operator and the Exact arm control system is through the hand
pendant display and controls. The hand pendant is an infrared device that is powered by a
rechargeable battery.
The display shows position values and status information sent by the control system.
The controls on the hand pendant move the Exact arm. There are directional controls that
position the image detection unit vertically, longitudinally, and laterally. Other controls move the
arm to predefined positions.
Clinical Mode
The clinical mode is used to position the imager for clinical image acquisition.
There are two different types of motion:
● Point-to-point motion
Movement to a predefined position using the position controls on the hand pendant.
● Directional motion
Movement using the variable speed controls on the hand pendant.
The speed of motion in the vertical, longitudinal and lateral direction ranges from approximately 3
mm/s (or slower) to 40 mm/s. The speed of motion to a predefined position is higher than the
speed of motion in a single direction.
For the vertical, longitudinal and lateral travel range, Figure 11 Vertical, Longitudinal and Lateral
Travel Range (Isocenter not Calibrated) on page 25.
MV
Detector’s Collimator
Reference Point Isocenter
Z
(vert.)
[X, +50, +25] [X, -50, +25]
+200
Gantry
-200
Y
(long.)
-200
-400
Coordinates in [X, Y, Z] mm
where X = [-lat max to +lat max]
= 323 mm @ any position in
the travel field
-600
[X, 0, -820]
Figure 11 Vertical, Longitudinal and Lateral Travel Range (Isocenter not Calibrated)
The total lateral travel range is 323 mm from ‑Lat (‑143 mm) to +Lat (+180 mm).
Non-Clinical
Used to service the Exact arm.
● Mechanical Axis Velocity mode
This is motion of one arm part at a time by direct velocity control over one motor.
● Mechanical Axis PWM mode
This is motion of one arm part at a time by direct PWM control over one motor and without
software supervision of mechanical limits.
1. Gantry
2. Electronics
The type of detector is configured in the Exact arm Control system. For more details, see the
Exact Arm Data Book.
1. Infrared device
2. Paddle
3. Thumbwheels
4. Handle
5. Enable bars
6. Hand position guides
7. Keys
8. Display
Infrared The infrared device is located in the head of the hand pendant. It is the communica-
Device tion link between the hand pendant and the control system.
The device receives information from the control system and sends information to it.
Display The display is an LCD with LED backlight. The display is active only while you hold
the enable bars (and for a few seconds after you release them).
The display shows position values for the three directionalaxes of motion, as well as
status information.
Point-to-Point Motion
1 4
5
1. Speed selector
2. Motion enable button
3. BMC mode switch
4. Direction switch
5. Axis selector
Note: For a description how to perform the manual retraction procedures, Retracting
Manually by Backup Motion Controls (BMC) on page 16.
1. Infrared receiver
The hand pendant and the Exact arm system communicate by receivers and transmitters. The
receivers and transmitters reside inside the top part of the hand pendant and besides the Clinac
counterweight.
The enable bars on the hand pendant energize the infrared diodes activating the display and
enabling motion.
The communication range of hand pendant and infrared diodes differs with each installation. The
range is affected by the size of the treatment room, its color, the building material and so on.
Being on the edge of the range, information on the display will be incomplete.
To use the hand pendant:
1. Point the hand pendant toward one of the infrared devices in the counterweight.
2. To activate the display on the hand pendant, press the enable bars on either side of the hand
pendant.
After releasing the enable bars, the display remains on for a few seconds, until it times out.
3. To move the arm, hold the enable bars and perform one of the following steps:
● For directional motion, deflect a thumbwheel (VRT, LNG or LAT) until the arm reaches the
position you want. You stop the motion when you release the thumbwheel (or the enable
bars).
● For point-to-point motion, press one of the keys (OUT, LAST, P1 through P5, AUTO GO,
and RETR). In order to start the motion you either have to press the key for more than 2
seconds or you have to press it twice in a row. If you choose the latter, after the first
button press the target position is shown and after the second press the motion starts.
The arm then moves automatically to the selected position and “Actual” is shown on the
top line of the menu, when the move is complete. You can interrupt the move by pressing
any key or by releasing the enable bars.
Note: If a motion is aborted by either pressing a key or by releasing the enable bars,
the hand may not be in a level position, that is, the IDU may not be perpendicular to
the beam axis.
OUT Moves the arm to a semi-retracted (out of the way) position which provides more clear-
ance around the couch and patient area.
LAST Moves the arm to the last position in the travel range where it came previously to a com-
plete stop.
Moving to the last position is helpful for AP/PA setups (A = Anterior, P = Posterior), as
illustrated by the following example:
a. After treating with the AP setup, move the arm to the OUT position.
b. Rotate the gantry to the PA position.
c. Use the LAST key to position the arm for the PA setup.
Note: If the last position was a predefined position, you can use the LAST key again to
return to the “last” position.
Position 1 - Moves the arm to predefined or user defined positions. Each of the five predefined
5 positions can be used as a standard setting for different types of treatment fields.
They can also be used as starting points for adjusting the arm to the appropriate
position for an individual field.
To display the target position values for a P1-P5 key without causing motion,
press and release the key quickly.
For the procedure of assigning target positions to the keys, see section Save Po-
sition Utility on page 47.
RETRACT Moves the arm to the retracted position. The retract position folds the arm into the
base of the gantry.
Note: The out position is an alternative to retracting the arm when you have not yet
finished with it for the day. It takes less time to move to a working position from the out
position than from the retracted position.
Operating Procedures 35
About Hand Pendant Menus
This section describes the various hand pendant menus during clinical operation.
For descriptions of the menus for the utility functions, Safety and Emergency on page 10.
There are the following main menus:
● Standard menu (no motion)
● Movement control menu (directional motion)
Each menu provides the following information:
● What kind of motion is occurring, such as Pos 1, Actual MOVE, and Actual (no motion)
● Actual or target position values (vrt, lng, lat)
● When there is motion toward a predefined position (+ -)
● Notations about system conditions, such as interlocks, collisions, etc.
Note: Position values are shown in centimeters with one decimal digit (+/-xx.x cm).
Menu Timeout
The standard menu is the default hand pendant menu. It is shown until you press a hand pendant
control.
Most other menus, including the utility menus, have a time limit. If you do not press a key during
this time limit, the timeout results in navigating to the standard menu.
If you release the enable bars on the hand pendant, the display will go off after a few seconds.
Menu Languages
The following menu languages are available:
● English
● German
● French
● Italian
The language is set in the utility Using the Languages Utility on page 55.
Info Menu
While pressing the enable bar and powering on the arm, an Info menu is shown for about 2
seconds. Thereafter it is shown whenever you press the CLR key. If a sub menu is displayed, you
have to press the CLR key several times until the Info menu is shown. The Info menu generated
by the control system software is as follows:
Varian service personnel may ask you for the software version number from the bottom line of the
Info menu.
However, if there is no link to the control system of the hand pendant during power ON the hand
pendant software generates the following:
To go to the info menu from the standard or retracted menu, press the CLR key. To return to the
standard menu, press the CLR key or wait for the timeout.
Standard Menu
Actual
Vrt - 10.0 cm
Lng + 5.0 cm
Lat - 2.0 cm
The standard menu is shown when the arm is extended but not moving. It is identified by the label
“Actual” and gives the actual (current) position of each directional axis of motion.
● Press the CLR key to go to the Info menu.
Retracted Menu
When you activate a hand pendant with the arm retracted, the following is displayed:
Arm Retracted
When the arm is retracted, you can use only the keys to extend it; you cannot use the directional
keys until the point-to-point motion has completed.
● Press the CLR key to go to the Info menu.
Operating Procedures 37
Position Control Menu
Pos 1
Vrt - 10.0 cm +
Lng + 5.0 cm -
Lat - 2.0 cm
The position control menu is shown whenever you press a point-to-point motion control once.
A position control menu can be identified by the label on the top line. In the example above, the
label “Pos 1” represents the P1 key.
The point-to-point motion controls and their labels in the menu are:
Key Display
P1 - P5 Pos 1 - Pos 5
RETR Retract
AUTO GO Auto Go
The values shown on a position menu are the target values for the predefined position. Actual
position values are not shown until the arm has reached its target position.
You can display the target position for P1-P5 without moving the Exact arm by pressing the key
briefly. Keeping the key pressed enables motion. After motion begins you can release the key.
A plus (+) or minus (-) after the positional value is displayed to indicate the direction of motion:
When you interrupt point-to-point motion by pressing any key (while holding the enable bars), the
standard menu returns immediately.
No position values are displayed while the arm is being retracted. Instead, an asterisk (*) moves
across the display to indicate that the arm is moving toward the retracted position:
Retracting
*------>
Arm Retracted
When you interrupt the retract or unfold motion outside of the travel range by pressing any key
(while holding the enable bars), the display changes to:
Transition
When you interrupt the retract or unfold motion inside of the travel range by pressing any key
(while holding the enable bars), the display changes to:
Not Ready
Vrt - 30.0 cm
Lng + 24.0 cm
Lat - 2.0 cm
Operating Procedures 39
Directional Motion Menu
Actual MOVE
Vrt - 30.0 cm
Lng + 24.0 cm *
Lat - 2.0 cm
This menu, with the label “Actual MOVE”, is shown whenever you request directional motion
with the VRT, LNG, or LAT keys.
The values on the directional motion menu are the actual position values, and they are updated
while motion occurs.
An asterisk (*) indicates that the arm has reached the operating limit of motion for this directional
axis and cannot travel any further. It must be moved using another position or directional key.
Actual TRP
Vrt - 10.0 cm
Lng + 5.0 cm
Lat - 2.0 cm
TRP indicates that the hardware motion interlock is active. To correct the problem:
● Press the Trip Reset switch. Or, perform a power down/up cycle on the Exact arm.
CAL indicates that the arm must be calibrated. You cannot move the arm with a directional key or
to a predefined position until it is calibrated. For additional information, see Utilities for Clinac
Version with Hand Pendant on page 46.
1. To bring the arm to its calibration position, use the Using the Mech Axis Vel Utility on
page 51.
2. To calibrate the arm, use the Using the Mech Axis Cal Utility on page 52.
FLT indicates that there is a non-collision FLT (fault).
To acknowledge it, proceed to the Using the Faults Utility on page 50, as follows:
1. Press the MODE key, then press the P2 key for clinical utility menu 2.
2. Press the P2 key to select the Fault utility.
3. Press the CLR key for more than 1 second to acknowledge the faults and exit to the standard
menu. For fault classes and descriptions, see Appendix: Intended Use Statements on
page 57.
COL indicates that there is a collision condition but no non-collision interlocks. To correct this,
move the equipment out of the collision condition (for additional information, see Safety and
Emergency on page 10):
Operating Procedures 41
1. Hold the touch guard reset button on the Clinac collimator.
2. Use the Clinac and/or Exact arm hand pendant keys to move the equipment out of the
collision condition.
BAT indicates that the battery needs to be recharged. For more information, Recharging the
Hand Pendant Battery on page 44.
NL
Actual
Vrt - 10.0 cm
Lng + 5.0 cm
Lat - 2.0 cm NL
The no link (NL) indication at the bottom right of any display is generated by the hand pendant to
indicate that it is no longer receiving data and that, therefore, the display might not be accurate.
Indicators of IDU Level
The hand pendant display will indicate the following items when the arm is standing still:
● Actual is displayed on the top line of the display when the hand is less than 0.2° off level.
● Actual //// is displayed on the top line of the display when the hand is more than 0.2°, but less
than 2.0° off level. This condition can occur if a point-to-point or directional motion is aborted.
● Not Ready is displayed on the top line of the display when the hand is more than 2.0° off
level. This condition can occur if a point-to-point or directional motion is aborted.
Transition
Transition is displayed on the top line of the display when motion to or from the retracted position
is aborted outside of the travel range and stopping the arm in this in-between position. You can
use only the position keys to correct this condition; you cannot use the directional keys.
CAUTION
THUMBWHEEL XXX
IS JAMMING
<CLR>
where “XXX” is a thumbwheel on the hand pendant handle: VRT, LNG, LAT, or ANG.
CAUTION
KEY XXX
IS JAMMING
<CLR>
where “XXX” is a key on the hand pendant paddle: OUT, RETR, AUTO GO, LAST, P1-P5, MODE,
or, CLR.
This caution indicator is displayed if a key or thumbwheel switch is stuck “on”, when power is
enabled to the hand pendant. The hand pendant cannot communicate with the Exact arm
controller until the switch has been reset to its neutral position and the display cleared.
For the hand pendant, you can maintain power to the display by keeping the enable bars pressed
while you reset the switch. You must then press the CLR key. Otherwise, you can release the
enable bars, reset the switch, and then reenable power.
Operating Procedures 43
Recharging the Hand Pendant Battery
CAUTION: Do not overcharge the battery.
Note: When the battery power is so low that the display cannot be enabled, the hand
pendant is not transmitting data and should be immediately recharged.
CAUTION: Do not recharge the battery before the “BAT” message is displayed. Do
not store the hand pendant in the battery charger station when you are
not recharging it. Over time, recharging before battery power drops to
the warning level will result in a reduction of battery capacity.
When the hand pendant battery power drops to a low level, either of two indications are displayed
depending on whether there is enough power for the hand pendant to communicate with the
control system. If there is, then the system state “BAT” notation is displayed in the upper right
corner of the standard menu. When this message is displayed, there is enough power for you to
complete the treatments for the day. Press any key to communicate with the control system. If
there is not enough power to communicate, the following message is displayed when you press
the enable bars:
BATTERY LOW
PLEASE CHARGE
NL
Note: Leaving the hand pendant in the battery charger station for more than 12
hours, such as over a weekend, will not cause any damage.
Operating Procedures 45
Utilities for Clinac Version with Hand Pendant
Overview
The utilities are the support and diagnostic functions for the Exact arm. Most utilities are used for
diagnostic and test purposes.
The four kinds of utilities ‐ clinical, physics, and service ‐ are organized in five menus. You use
the MODE key on the hand pendant paddle to display the menus.
● For the Physics and Service menus you must enter a four‐digit access code.
● The Service menu is always in English. The other menus are displayed in the language
selected in the Physics menu.
<MODE>
xxxxxxxxxxxxx
xxxxxxxxxxxxx
xxxxxxxxxxxxx
(You can exit from this display to the previous display by pressing the CLR key or waiting for
the timeout).
2. Press the P key for the menu you want.
3. If required, enter the access code.
4. When the utility menu is displayed, press the P key for the selection you want.
3. Press the P key that you want to program with the current position.
If the arm position is valid, the following is displayed:
Actual position
saved as:
Pos X
Actual position
can not be
saved!
Reposition the arm so that it is within the travel range, then select the Save Position utility
again.
4. To exit to the standard menu, press the CLR key or wait for the timeout.
Note: Interlocks are cleared by means of the Faults utility. If there is no fault, there
are no interlocks either.
Faults
xx xx xx xx xx
xx xx xx xx xx
Note: The emergency and safety procedures are described in the related
Instructions for Use.
2. To acknowledge the faults, press the CLR key for more than one second.
To exit to the standard menu, press the CLR key for less than half a second or wait for the
timeout.
The list of active faults can be browsed forward by pressing P5, and backwards by pressing the
P4 key. To exit the browse function, press the CLR key, or wait for the timeout.
Note: If you must enter the passcode for using the Mech Axis Vel utility, press the P1
key four times.
The Mech Axis Velocity utility allows you to use the directional keys on the hand pendant handle
to move each mechanical axis individually (shoulder axis, elbow axis, wrist axis, hand lateral axis)
close to its calibration position, Figure 20 Mechanical Calibration Position on page 52.
If a mechanical axis is calibrated, it can be moved with maximal speed. The axis will stop
automatically before reaching its mechanical limit of motion.
If the mechanical axis is not calibrated, motion is limited to a slow speed. In this case, it can be
moved to its mechanical limits of motion.
To use Mech Axis Vel utility:
1. Select the Mech Axis Vel utility (MODE - P3 - P2).
The following is displayed:
2. Use the VRT, LNG, LAT or ANG thumbwheels to move each axis.
It is not possible to move several axes simultaneously.
VRT moves the shoulder axis.
left = up
right = down
LNG moves the elbow axis.
left = in (towards the gantry)
right = out (away from the gantry)
LAT moves wrist axis.
left = up
right = down
ANG moves the hand lateral axis from side to side.
left = left (as you face the gantry)
right = right (as you face the gantry)
This utility is used by Varian service personnel during installation of the Exact arm. You do not
have to recalibrate after installation unless there is a power failure while the arm is moving or if
the arm moves while the power is off. Also certain faults can force a decalibration, see
Appendix: Interlocks, Faults and Error Codes on page 58. The notation “CAL” is displayed on
the hand pendant if calibration is necessary.
The calibration of a mechanical axis gives the system the accurate mechanical position of this
axis.
To use Mech Axis Cal utility:
1. Use the Mech Axis Vel utility to position the axes at their corresponding calibration positions.
These are as follows:
● Shoulder - upper arm horizontal (mechanical axis position = 180°)
● Elbow - forearm vertical (mechanical axis position = 90°)
● Wrist - IDU horizontal (mechanical axis position = 270°)
● Hand Lat - slide at mech center pos (mechanical axis position = 0 mm). There are two
notches (white) on the bottom side of the toothed rack.
Note: The position of the axes must lie within ±1° or ±1 mm respectively, for the
calibration to succeed. Use water level to verify the axis angles.
1
270°
90° 180°
1. Gantry
Note: If you must enter the passcode for using the Isocenter Cal Utility, press the P1 key
four times.
The calibration procedure involves positioning the arm at isocenter (vertical distance to isocenter
is measured at the surface of the sensitive area of the cassette, beneath the plastic cover).
1 2 3 4
11.0 mm
1,000.0 mm
5 6 7 8
12.0 mm
1. LIC IDU
2. LIC isocenter
3. LIC sensitive layer
4. LIC detector surface
5. a-Si IDU
6. a-Si isocenter
7. a-Si sensitive layer
8. a-Si detector surface
Calibrating IDU
Succeeded
4. Possible causes for a calibration failure are not calibrated mechanical axes or an implausible
isocenter position.
This utility is used by Varian service personnel during installation of the Exact arm to select the
language used for the hand pendant menus.
To use Languages utility:
1. Select the Languages utility (MODE - P3 - P4).
2. When the list of languages is displayed, press the P key that corresponds to the display
language that you want (English, German, French, or Italian).
3. To exit to the standard menu, press the CLR key until you reach the standard menu or wait
for the timeout.
This utility uses the directional keys on the hand pendant handle individually to move each axis in
open loop mode to its mechanical limit of motion. This is similar to the Mech Axis Vel utility except
that the velocity controller is bypassed, making the PWM signal to the motor driver directly
proportional to the deflection of the thumbwheel. To reduce the force and speed of an axis, the
PWM value is limited to a maximum value of 25%.
To use Mech Axis PWM utility:
1. Press the MODE key.
2. Press the P4 key.
3. Enter the access code.
4. Press the P1 key.
Each hand pendant has a unique ID (1-15). This utility gives service personnel an easy way to
determine that hand pendant ID.
To use Hand Pendant ID utility:
1. Select the Hand Pendant ID utility (MODE - P4 - P3)
The ID of this hand pendant is displayed.
2. To exit to the Service Menu, press the CLR key or wait for the timeout.
On-Board Imager
The On-Board Imager device is used for verification of correct patient position in relation to
isocenter and verification of the treatment fields in relation to anatomical and/or fiducial
landmarks.
Acuity
The Acuity Radiation Therapy Simulator is to be used in radiation therapy simulation, using a
fluoroscopic and/or radiographic x-ray system for visualizing the volume to be exposed during
radiation therapy and confirming the position and size of the therapeutic irritation field to be
applied. The Acuity ConeBeam Computed Tomography (CBCT) is intended to assist the
Radiation Oncologist in acquiring 3D “multislice” planning data in patient set-ups for the purpose
of radiation therapy treatment planning and patient positioning.
F Fatal. The application is stopped, movements are disabled. It may be necessary to restart
the Exact arm.
C Critical. Any movements are stopped. Clinical movements are disabled until the fault is re-
moved.
W Warning. The system detected the presence of a fault condition that is noteworthy to the
user. However, ongoing motion is not aborted, nor are clinical movements disabled.
Note: In general the supervisory system does query for faults on a periodical basis. (In
some exceptional conditions the application may not able to respond to such requests. In
this case some fault id is shown on a local display and logged in an exception log).
Interlocks none means that the particular node does not impose an interlock. However, the
Supervisor may impose an interlock on its level.
Object Identifiers
0 Not used
1 Not used
2 Not used
3 Not used
4 Mechanical shoulder
Object
Identifier
Fault 41 A mechanical axis C/P H/W: 50 ms The applica- Perform an ‘Axis
has lost its cali- tion discards Calibration’ on the
Mechan- - None
bration or has any IDU failing axis.
ical axis
never been cali- S/W: movement
not cali-
brated. command,
brated - Stop mo-
including re-
tion
Object tract and un-
Identifier fold. The ap-
plication dis-
cards any
mechanical
axis position
movement
command.
Mechanical
axis velocity
limited to
25% of max-
imum ve-
locity.
Fault 42 The QDEC value C/TL H/W: 50 ms The applica- Perform a recali-
of a mechanical tion discards bration. If fault re-
Encoder - None
axis did not match any IDU appears Perform
index
the expected S/W: movement fault analysis by
pulse
value when an command, using PWM axis
check - Initiate
index pulse oc- including re- moves to check
failed fault 'Me-
curred. tract and un- the PRO/SPRO
chanical
Object fold. readout system.
axis not cali-
Identifier Fix / replace faulty
brated'
device. Perform a
calibration.
Index 69
Not Ready 41 mechanical overload 13
Info, menu 36 menu
infrared diode 34 hand pendant 36
intended use Info 36
Acuity ConeBeam Computed Tomography Languages 36
57 Position Control 38
Acuity Radiation Therapy Simulator 57 Retracted 37
Exact arm 22 Standard 37
On-Board Imager 57 Timeout 36
PortalVision Advanced Imaging 57 minus sign 38
interlock MODE key 28
motion 15 motion
interlocks 50 aborted 41
isocenter calibration 54 arm 24
MV detector 54 motion interlock
couch 15, 20
override 15
K MyVarian 8
key jam 20
keys 27 N
NL 8
L NL notation 41
languages 55 no link 8
languages, menu 36 notations 41
LAST key 28
LAT 8 O
LAT key 29
lateral 8 On-Board Imager
lateral motion 16 intended use 57
LCD 8 online customer support 8
LED 8 ordering product documents by phone 8
LIC 8 OUT key 28
light emitting diode 8 overload, mechanical 13
liquid crystal display 8 override
liquid ion chamber 8 button 15
LNG 8 motion interlock 15
LNG key 29
longitudinal 8
P
M P1-P5
key 28
mech axis position 35
calibration 52 plus sign 38
passcode 52, 55 PortalVision Advanced Imaging
PWM 55 intended use 57
Mech Axis Cal 50 position
Mech Axis Vel 50 mechanical calibration 52
mechanical calibration position 52 Position Control, menu 38
V
R
Varian customer support 8
radiation effect on electronics 13 vertical 8
related publications 9 visual cues 7
RETR key 28 VRT 8
retract position 35 VRT key 29
Retracted, menu 37
W
S
wireless 27
secondary position read out 8
service monitor 48
SPRO 8
standard, menu 37
support e-mail addresses 8
system self test 56
system state 41
T
technical support 8
thumbwheel 27
jamming 20
Timeout, menu 36
touch guard reset button 41
transition 41
travel range uncalibrated 24
TRP notation 41
U
uncalibrated travel range 24
utilities
accessing 46
Utility
Faults 50
Hand Pendant ID 56
Hand Pendant Test 49
Interlocks 50
Isocenter Cal 54
Languages 55
Mech Axis Cal 52
Index 71