03 Site Planning Electrical Information PDF

Elekta Oncology Products
Site Planning Electrical Information
Document ID: 1008404 03

Publication date: 2012–07
Language: English
Copyright and use of trademarks statement
Copyright ©2012 Elekta Limited. All rights reserved. Do not copy or use this document, or parts of
it, without written agreement from Elekta Limited. All trademarks and registered trademarks of
Elekta products are the property of the Elekta Group.
Registered trademarks of other manufacturers

Elekta acknowledges the trademarks and registered trademarks of other manufacturers that we use
in this document.
Related documents
Elekta does not supply all the documents that we refer to in this document with the equipment.
Elekta reserves the right to make the decision on which of the documents we supply with the
equipment.
Contact information:
WORLDWIDE PRODUCT MANUFACTURING CENTER – ONCOLOGY

ELEKTA LIMITED
Linac House
Fleming Way, Crawley
West Sussex RH10 9RR
United Kingdom
Tel +44 1293 544 422
Fax +44 1293 654 321
TECHNICAL HELP
Contact your local Elekta representative for technical help
1008404 03 Elekta Oncology Products

Page 2 Copyright ©2012 Elekta Limited. All rights reserved.
Field Change Order (FCO) record
When you receive an FCO, Elekta recommends that you:

• Put the FCO in the related section of this document
• Complete the FCO Record with:
– The FCO number.
– The date you added the FCO.
– Your signature.
• Use the information in your procedures.
FCO number Date Signature
Elekta Oncology Products 1008404 03

Copyright ©2012 Elekta Limited. All rights reserved. Page 3
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Table of contents
Table of contents
Section Description Page
1 General safety and regulatory information . . . . . . . . . . . . . . . . . . . . . . . . . . 9
2 Power supplies information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
3 Interlock information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
4 Cable information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51

Table of contents
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List of figures and tables

Figure 1.1 Conventions for the directions of the digital accelerator. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Figure 2.1 Treatment suite equipment locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Figure 2.2 Suggested layout of electrical items in the equipment room (plan view) . . . . . . . . . . . . . . . . . . . 21
Figure 2.3 Suggested layout of electrical items in the equipment room (elevation view) . . . . . . . . . . . . . . . 22
Figure 3.1 Suggested layout of interlock items in the treatment suite (plan view) . . . . . . . . . . . . . . . . . . . . . 36
Figure 3.2 CITB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
Figure 3.3 Connections to the client interface PCB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39
Figure 3.4 Client interface link label . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
Figure 3.5 Example of a fascia door interlock switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Figure 3.6 Typical emergency STOP switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Figure 4.1 Suggested layout of ducts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Table 2.1 Specification of three-phase mains electrical supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Table 2.2 Vacuum system specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Table 2.3 kV generator power requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Table 2.4 Voltage stabilizer input ranges. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Table 2.5 Specification for electrical outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Table 2.6 Electrical requirements of the laser alignment system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Table 2.7 Typical water cooling supply specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Table 3.1 Connections on the client interface PCB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Table 3.2 Client interface PCB links . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
Table 3.3 Time delay interlock operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
Table 4.1 The cable duct dimensions and routes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Table 4.2 Maximum cable lengths from the RIC to other equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Table 4.3 Maximum other cable lengths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
Table 4.4 Internal cable lengths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

Table 4.5 Interbay cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Table 4.6 Integrity R3.0 interbay cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Table 4.7 Remote detector retraction (RDR) cable kits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Table 4.8 Integrity R3.0 treatment room cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
Table 4.9 Treatment room cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

General safety and regulatory information
1 General safety and regulatory information

1.1 Function of this document. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

1.1.1 Intended audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.2 Important safety information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.3 Compliance. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.3.1 IEC safety standards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.4 Warnings, cautions and notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
1.5 Documentation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.6 Text formats . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.7 Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
1.8 Conventions for the directions of the digital accelerator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
1.9 Abbreviations and acronyms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14

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Function of this document
1.1 Function of this document
1.1.1 Intended audience

This document is intended for use by persons involved in site planning for the installation of Elekta
oncology products.
1.2 Important safety information

Elekta products strictly adhere to a set of safety standards. All medical electrical equipment must be
correctly installed, operated and maintained, particularly with regard to human safety.
For the safety of patients and users, you must always obey all safety procedures. Refer to the safety
information in the related product documentation.
1.3 Compliance
Elekta digital accelerators obey all related directives, regulations, international and national
standards and laws.
Contact Elekta Limited for more information on applicable international and IEC safety standards.
1.3.1 IEC safety standards

The equipment is in compliance with applicable IEC safety standards for medical devices.
1.4 Warnings, cautions and notes

This section shows how Elekta uses warnings, cautions, and notes in this document.
WARNING x.x
A warning is information about procedures, tasks, or conditions, where the
result can be fatal or serious injury, injury, or clinical mistreatment if you do
not obey the instructions.
CAUTION x.x
A caution is information about procedures, tasks, or conditions, where the
result can be damage to the equipment, data, or the environment if you do
not obey the instructions.
Note: A note gives more information about a related text. A note is not an instruction.

Documentation
1.5 Documentation
This document is a part of the Elekta Oncology Products - Site Planning Information. The documents
in the set are:
Elekta Oncology Products - Site Planning Introduction
Elekta Oncology Products - Site Planning Reference Information
Elekta Oncology Products - Site Planning Electrical Information
Elekta Oncology Products - Site Planning Construction Information
Elekta Oncology Products - Site Planning Environmental Information
Elekta Oncology Products - Site Planning Delivery Information
Elekta Oncology Products - Site Planning Computer Hardware, Software & Network Information
HexaPOD™ evo RT System Planning Guide (for use with Elekta Digital Accelerators).
1.6 Text formats

This is the convention for the text formats that you can find in this document.
Text Format Definition

Bold The text that shows on a VDU screen
Button labels
Screen (window) labels
Keyboard key legends
File names
Sequential selections
Important information
SMALL CAPS Signal names
courier Denotes text to be entered by the user, or paths
1.7 Conventions
This is the convention for terms that you can find in this document.
Term Convention
Authorized Person A person who is given the authority to do the work on the
equipment by the authority that controls the equipment.
Qualified Person A person that is recognized by a competent authority to have the
necessary knowledge and training to do specified tasks.

Conventions for the directions of the digital accelerator
1.8 Conventions for the directions of the digital accelerator

Figure 1.1 gives the conventions that Elekta uses to refer to the directions of the digital accelerator
in the treatment room. The conventions are applicable only when the patient is in the head first
(anatomical supine) position on the treatment table.
2 5
6
7
Figure 1.1 Conventions for the directions of the digital accelerator
(1) Treatment room ceiling (top) (5) Digital accelerator B-side (anatomical
(anatomical anterior) left)
(2) Digital accelerator gun (G-end) (6) Digital accelerator target (T-end)
(anatomical superior) (anatomical inferior)
(3) Digital accelerator A-side (anatomical (7) Treatment room floor (bottom)
right) (anatomical posterior)
(4) Machine isocenter
Note: The A and B positions in Figure 1.1 are correct with the gantry at 0° only. The A and B positions rotate
with the gantry. Therefore, with the gantry rotated 180°, A and B are opposite.

Abbreviations and acronyms
1.9 Abbreviations and acronyms

This section gives the conventions for the abbreviations and acronyms that you can find in this
document.
Abbreviation Definition
BLD beam limiting device
BMDM beam monitor unit display module
BU business unit
CCTV closed circuit television
CITB client interface terminal box
CT computed tomography
DMLC Dynamic Micro Multileaf Collimator
EIM electrical interface module
EMC electromagnetic compatibility
EMR electronic medical record
ERT earth reference terminal
ESD electrostatic discharge
FKP function keypad
G-end digital accelerator gun end
Gy gray (the SI unit of absorbed dose)
HHC handheld controller
HP high pressure
HT high tension (high voltage)
iCom Elekta software protocol that enables the digital accelerator to interface
with third-party systems
iCom-Fx external field selection
iCom-Vx digital accelerator verification interface
IEC International Electrotechnical Commission
IMKM In-room Monitor, Keyboard and Mouse
IGRT image guided radiation therapy
IMRT intensity modulated radiation therapy
kV kilovolt (or kilovoltage)
LCD liquid crystal display
LED light emitting diode
Linac (digital) linear accelerator
LP low pressure
LV low voltage
MeV mega electron volts
MLC multileaf collimator

Abbreviation Definition
MRI Magnetic Resonance Imaging
MV megavolt (or megavoltage)
N/A not applicable
OIS Oncology Information System
PCB printed circuit board
PCDU power conditioning distribution unit
PET Positron Emission Tomography
psi pound-force per square inch (a non-SI unit of measure for pressure,
symbol is psi or lbf/in2)
PSU Power Supply Unit
PSS patient support system
R&V record and verify
RDR remote detector retraction
RF radio-frequency
RIC reeling interface cabinet
RT radiation therapy
SI international system of units
SWG standard wire gauge
T-end digital accelerator target end
TCC treatment control cabinet
TCS treatment control system (includes the TCC)
TPS Treatment Planning System
TRM treatment room monitor
UPS uninterruptible power supply
VDU visual display unit
VMAT volumetric intensity modulated arc therapy
XVI X-ray volume imaging

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Power supplies information
2 Power supplies information

2.1 Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
2.1.1 Responsibilities of the client for electrical supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
2.2 Location of electrical equipment. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
2.2.1 Treatment suite equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
2.2.2 Equipment room electrical items . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
2.3 Digital accelerator power supply and cabling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
2.3.1 Three-phase isolators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
2.3.2 Location of the three-phase isolator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
2.3.3 Responsibilities of the client for the three-phase cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
2.4 Vacuum system supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
2.4.1 Specification of vacuum system supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
2.4.2 Vacuum system isolator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
2.4.3 Location of vacuum system supply isolator. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
2.4.4 Responsibilities of the client for the vacuum system supply cables . . . . . . . . . . . . . . . . . . . . . 25
2.5 XVI power supply and cabling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
2.5.1 Responsibilities of the client for the three-phase supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
2.5.2 Responsibilities of the client for the three-phase cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
2.6 Voltage stabilizer (optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
2.6.1 Responsibilities of the client for the voltage stabilizer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
2.6.1.1 Grounding of the voltage stabilizer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
2.7 Power conditioning distribution unit (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28
2.8 Grounding (Earthing). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
2.8.1 Location of the earth reference terminal . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
2.8.2 Responsibilities of the client for grounding. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
2.8.2.1 Grounding of single-phase outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
2.8.3 Responsibilities of Elekta for grounding . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
2.9 Control, treatment, and equipment room supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
2.9.1 Control room outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
2.9.2 Treatment, and equipment room outlets. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
2.9.3 Specification for room electrical outlets. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
2.9.4 Responsibilities of the client for room electrical outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30
2.10 Laser alignment system supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
2.10.1 Specification of laser alignment system supply. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
2.10.2 Location of electrical outlet points for lasers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
2.10.3 Responsibilities of the client for the laser alignment supply . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
2.11 Water cooler supplies (optional). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
2.11.1 Specification of water cooler supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
2.11.2 Responsibilities of the client for water cooler supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
2.11.2.1 Responsibilities of the client for the three-phase cable . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
2.11.2.2 Remote starting of water cooler. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
2.12 Emergency power OFF switch. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32

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Overview
2.1 Overview
This document gives information about the electrical supplies necessary for the Elekta oncology
system. These are:
• Power supplies
• Interlock supplies
• Cable information
2.1.1 Responsibilities of the client for electrical supplies

It is the responsibility of the client to:
• Install a three-phase supply and isolator in the equipment room for the digital accelerator
• Install a three-phase supply and isolator in the equipment room for the XVI kV generator
• Install a single-phase supply and isolator in the equipment room for the digital accelerator
vacuum system
• Install a specified ERT in the equipment room
• Install and route the three-phase cables to the RIC for the digital accelerator
• Install and route the earth cable to the RIC from the ERT
• Install and route the three-phase cables to the XVI kV generator
• Install and route the earth cable to the XVI kV generator from the ERT
• Install and route the single-phase cable to the RIC for the digital accelerator vacuum
system
• Install a single-phase supply to the equipment room and treatment room wall sockets
• Install a single-phase supply to the control room wall sockets
• Install a single-phase supply to the warning lamps and CITB.
• Install a single-phase supply to the laser alignment system through the CITB
• Install and connect a three-phase supply and earth cable to the water cooler, including the
remote start/stop cable.
It is the responsiblity of Elekta to:
• Connect the three-phase cables to the RIC for the digital accelerator
• Connect the earth cable to the RIC from the ERT
• Connect the three-phase cables to the XVI kV generator
• Connect the earth cable to the XVI kV generator from the ERT
• Connect the single-phase cable to the RIC for the digital accelerator vacuum system.
All supplies installed by the client must be completed before the installation of the digital
accelerator, and have clear labels because of safety. If electrical supplies do not have clear labels,
delays to the installation can occur.

Location of electrical equipment
2.2 Location of electrical equipment
2.2.1 Treatment suite equipment

Refer to Figure 2.1 for the locations of the key items in the treatment suite that require electrical
power.
1 2
3
4
5
6
NOT TO SCALE 005241 ©2011 Elekta Limited
Figure 2.1 Treatment suite equipment locations
(1) CITB (4) RIC

(2) PCDU1 (5) XVI kV generator1
(3) Voltage stabilizer1 (6) Digital accelerator
1 This item is optional.
The location of the CITB must be in compliance with the laws and regulations of the region. The
location must also be above a duct that goes to the RIC.

2.2.2 Equipment room electrical items

Figure 2.2 and Figure 2.3 show a suggested layout of electrical items in the equipment room.
1 2 3
Figure 2.2 Suggested layout of electrical items in the equipment room (plan view)
(1) XVI kV generator three-phase (5) Voltage stabilizer1

isolator1
(2) Digital accelerator three-phase (6) Digital accelerator
isolator and distribution board
(3) CITB (7) RIC
(4) PCDU1 (8) XVI kV generator1

1 2 3
6 5 4
Figure 2.3 Suggested layout of electrical items in the equipment room (elevation view)
(1) XVI kV generator three-phase (4) Duct

isolator1
(2) Digital accelerator three-phase (5) ERT
isolator and distribution board
(3) CITB (6) Vacuum system isolator

Digital accelerator power supply and cabling
2.3 Digital accelerator power supply and cabling

Table 2.1 gives information about the three-phase electrical supply necessary for the digital
accelerator. One more three-phase supply is necessary for the XVI system, which uses a kV
generator.
Table 2.1 Specification of three-phase mains electrical supply
Power required Peak 30 kVA

(maximum)
Power required Standby maximum 10 kVA
Typical 5.5 kVA
Radiating 18 kVA
Cosine power factor 0.9
Impedance Less than 0.3 Ω
Supply configuration Three-phase, neutral, and earth
Earth Direct from the client.

The earth connection must not be the armored screen of the mains supply cable. One
of the following must be used:
• 5-core armored cable
• A separate multi-strand copper earth wire in conjunction with a 4-core armored
cable.
Nominal voltage 380 V to 420 V
Voltage variation ±6% including when switching from no-load to 60 A per phase full load condition. If
variations are expected to exceed this level, a voltage stabilizer must be used.
Nominal frequency 50 Hz or 60 Hz
Fuse rating Fuse for 30 kVA max. load (nominally 45 A).

Slow-blow machine fuse.
Type D or similarly rated Type C.
Current Start surge (inrush) 60 A per phase
Supply source Direct from client mains supply. An isolation transformer is not normally required.
Safety A residual current detector must be placed in the three- phase supply line (as required
by local codes)
Earth leakage breaker The breaker must be a 30 mA residual current device for personal safety, with a load
current of at least 45 A, Class D, IEC 898 standard.
A suitable version can be supplied by Elekta on request (as required by local codes).

Digital accelerator power supply and cabling
2.3.1 Three-phase isolators

A three-phase isolator is required for the digital accelerator.
If an Elekta Synergy® Platform is ordered then a three-phase isolator is required for the kV generator.
The isolator must have a minimum contact separation of 3 mm. The direction of movement of the
actuator of the power supply isolator must be in compliance with IEC 60447.
The three-phase isolator must be fitted with a locking switch handle.
2.3.2 Location of the three-phase isolator

The three-phase isolators and cable connection points can be located on the wall in the equipment
room. The suggested location is shown in Figure 2.2 and a suggested layout is shown in Figure 2.3.
2.3.3 Responsibilities of the client for the three-phase cable

The client is responsible for supplying the three-phase tails from the isolator to the machine
(location of the reeling interface cabinet).
One of the following must be used:
• 5-core armored cable
• 4-core armored cable with external earth.
The suggested specification is:
• Tri-rated 16 mm2 cable

Vacuum system supply
2.4 Vacuum system supply

The waveguide is kept under high vacuum by electrical ion pumps installed on the digital
accelerator. These pumps operate constantly.
The electrical supply to the vacuum system must not be interrupted, as it can cause a loss of vacuum.
2.4.1 Specification of vacuum system supply

Table 2.2 lists the specification of the single-phase supply to the vacuum system, which is made up
of two power supply units.
Table 2.2 Vacuum system specifications
Power required 2 kVA

Supply configuration Single-phase, neutral and earth
Nominal voltage 230 V
Nominal frequency 50 Hz or 60 Hz
Fuse rating 13 A
Current Start surge (inrush 16 A)
Running 2 A
Supply source One phase of incoming three-phase supply taken before the
three-phase isolator or from the client emergency supply
Supplied by power conditioning distribution unit (PCDU)
(if used) in USA only
Supply control Isolated by switchable isolator or circuit breaker
2.4.2 Vacuum system isolator

The 10 VA single-phase vacuum system isolator must be permanently switched on while the digital
accelerator is in normal use. This supply can also be taken from the emergency supply of the client.
This configuration makes sure that the ion pumps stay on, even if the mains electrical supply fails.
This isolator must have a locking switch handle.
2.4.3 Location of vacuum system supply isolator

The three-phase isolators and cable connection points can be located on the wall in the equipment
room. The suggested location is shown in Figure 2.2 and a suggested layout is shown in Figure 2.3.
2.4.4 Responsibilities of the client for the vacuum system supply cables
Cabling from the vacuum system isolator to the interface cabinet must be supplied and fitted by the
client.
The cable must be three core, comprising one-phase, neutral and earth wires.

XVI power supply and cabling
2.5 XVI power supply and cabling

The XVI system uses a kV generator.
There are generators available rated at two voltages:
• 400 V generator for standard applications;
• 480 V generator for certain US sites.
The power requirements are listed in Table 2.3.
Table 2.3 kV generator power requirements
Power required Maximum power 32 kVA

Typical power 10 kVA1
Standby power 500 W
Supply configuration Three-phase and earth
Power factor 0.8
Nominal voltage 400 V to 440 V or 480 V
Voltage variation ±10%
Nominal frequency 50 or 60 Hz
Fuse rating 63 A circuit recommended
Impedance 0.27 Ω to 0.34 Ω or 0.40 Ω2
Supply source Direct from client mains supply
Safety A residual current detector must be placed in the
three-phase supply
1 Based on a prostate VolumeView™.
2 Ratings shown for 400 V to 440 V or 480 V.
The following equation can be used to work out the actual power used by the kV generator:
Actual power = Nominal power × Power factor
For example: 40 kVa x 0.8 = 32 kW
2.5.1 Responsibilities of the client for the three-phase supply

The additional three-phase supply must incorporate an isolator.
The isolator must have a minimum contact separation of 3 mm. The direction of movement of the
actuator of the power supply isolator must be in compliance with IEC 60447.
The client must make sure that if an Elekta Synergy® Platform is ordered with an upgrade in mind,
the three-phase supply and isolator are installed with the relevant cabling.
2.5.2 Responsibilities of the client for the three-phase cable

Cables from the isolator to the generator must be supplied by the client upon delivery of the
upgrade.

Voltage stabilizer (optional)
2.6 Voltage stabilizer (optional)

A voltage stabilizer must be used when variations in the local voltage supply exceed ±6%.
The purchased voltage stabilizer covers the following input voltage ranges.
The input voltage of either 380 V or 415 V must be specified at the time of order.
Table 2.4 Voltage stabilizer input ranges
Input Remarks Output

voltage
380 V For digital accelerator where mains 33 kVA nominal
fluctuations are likely to be in excess of
50 A/phase at 380 V output
±5%.
47 Hz to 65 Hz.
It gives a stable supply for mains
fluctuations of + 7.5% to - 17.5%.
(313 V to 408 V)
380 V For digital accelerator, where mains 33 kVA nominal
fluctuations are likely to be in excess of 50 A/phase at 380 V output
±5%.
47 Hz to 65 Hz.
(332 V to 427 V)
±5%.
47 Hz to 65 Hz.
(342 V to 446 V)
±5%.
47 Hz to 65 Hz.
(363 V to 467 V)
Note: When ordering a voltage stabilizer, state the absolute maximum and minimum supply voltage.

Power conditioning distribution unit (optional)
2.6.1 Responsibilities of the client for the voltage stabilizer

It is the responsibility of the client to supply electrical cable suitable for connecting the voltage
stabilizer to the mains supply and the mains isolator.
The maximum dimensions of cable to be supplied is 16 mm2. Larger cable dimensions are too large
to connect to the voltage stabilizer.
If the supply voltage is not in the range 380 V to 440 V phase to phase, the output windings of the
voltage stabilizer must be star-connected to give a neutral point.
A three-phase supply transformer can be supplied by the client. A transformer with an output
voltage of 400 V must be specified.
2.6.1.1 Grounding of the voltage stabilizer
The voltage stabilizer must be grounded to the connection that gives the lowest earth impedance.
This can be the host digital accelerator or the earth reference terminal.
2.7 Power conditioning distribution unit (optional)

The power conditioning distribution unit (PCDU) is mainly used in the U.S.A. or regions with a
110 V supply. If a contractor-supplied PCDU is used, the voltage stabilizer must be connected to the
output of the PCDU.

Grounding (Earthing)
2.8 Grounding (Earthing)

For safety, all of the main items of the digital accelerator must be effectively grounded.
2.8.1 Location of the earth reference terminal

The earth reference terminal (ERT) can be located next to the three-phase mains isolator in the
equipment room, (see Figure 2.3). If the ERT is to be housed within an enclosed cabinet, it must
have adequate apertures to allow for cable access. Alternatively the terminal strip may be wall
mounted without a cabinet.
2.8.2 Responsibilities of the client for grounding

The client must install an ERT, the impedance of which must be as low as possible to reduce the
possibility of inter-equipment interference.
2.8.2.1 Grounding of single-phase outlets
All single-phase electrical outlets must be properly earthed (grounded).
2.8.3 Responsibilities of Elekta for grounding

Elekta will supply and connect a 16 mm2 PVC insulated earth wire between the reeling interface
cabinet and the ERT. The resistance of this connection will be checked to make sure that it is less
than 0.1 Ω.

Control, treatment, and equipment room supplies
2.9 Control, treatment, and equipment room supplies

Additional electrical outlet points can be installed for convenience.
2.9.1 Control room outlets

It is recommended that a minimum of fifteen, single-phase electrical outlet points are installed in
the control room for test equipment and general hospital use. These outlets can be separated into
two or three individual circuits.
2.9.2 Treatment, and equipment room outlets

It is recommended that at least ten, single-phase electrical outlet points are installed in the treatment
room and equipment room. These are used for hand tools, test equipment, and general use.
If a KVM for iGUIDE® and a KVM for MOSAIQ®/SYNERGISTIQ™ are installed, more electrical
outlets will be necessary for connections in the treatment room.
2.9.3 Specification for room electrical outlets

Table 2.5 is the specification for the electrical outlets.
Table 2.5 Specification for electrical outlets
Supply Configuration Single Phase, Neutral, and Earth

Nominal voltage 230 V (115 V where applicable)
Nominal frequency 50 or 60 Hz
Fuse rating 13 A
Current 13 A
2.9.4 Responsibilities of the client for room electrical outlets

All electrical outlets in each room must be installed by the client according to local rules.

Laser alignment system supply
2.10 Laser alignment system supply

If a laser alignment system is to be fitted, electrical outlet points must be installed.
The electrical supply to the lasers can be switched by the digital accelerator through the CITB.
2.10.1 Specification of laser alignment system supply

The electrical supply to the laser alignment system depends on the type to be installed. Refer to your
local Elekta representative for the correct electrical supply specifications.
The specifications in Table 2.7 show an example of a typical laser.
Table 2.6 Electrical requirements of the laser alignment system
Power required 25 W
Supply configuration Single-phase, neutral and earth
Nominal voltage 230V
Nominal frequency 50/60 Hz
Mains resistance Not applicable
Fuse rating 3A
Current 0.08 A
2.10.2 Location of electrical outlet points for lasers

Electrical outlet points must be installed adjacent to each laser. These electrical outlet points can be
wired back to the CITB.
2.10.3 Responsibilities of the client for the laser alignment supply

Electrical supply, outlet points and cabling to the CITB must be installed by the client in accordance
with the information given in Table 2.6.

Water cooler supplies (optional)
2.11 Water cooler supplies (optional)

The water cooler is an option that can be supplied by Elekta. The cooler supplies cooled water to the
equipment.
If a water cooler is to be fitted, a local electrical supply must be installed.
2.11.1 Specification of water cooler supply

The electrical supply to the water cooler depends on the type of water cooling system to be installed.
Refer to your local Elekta representative for the correct electrical supply specifications.
Table 2.7 shows the specifications of a typical water cooler.
Table 2.7 Typical water cooling supply specifications
Power required 8 kVA

Supply configuration Three-phase, neutral and earth
Nominal voltage 380 to 440 V
Voltage variation ±6%
Nominal frequency 50 Hz (60 Hz available as special)
Mains resistance 0.2 Ω
Fuse rating 32 A
Current 14 A
2.11.2 Responsibilities of the client for water cooler supplies

The client must install a three-phase supply and isolator adjacent to the water cooler.
2.11.2.1 Responsibilities of the client for the three-phase cable
Cabling from the water cooler to the three-phase isolator must be supplied and installed by the
client.
2.11.2.2 Remote starting of water cooler

For remote starting of the water cooler, a two-core 0.75 mm2 cable must be installed from the water
cooler to the CITB.
2.12 Emergency power OFF switch

An emergency power OFF switch can be installed in the treatment, control and equipment room.
The switch cuts all electrical power, not just power to the equipment.

Interlock information
3 Interlock information
3.1 About this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35

3.1.1 Responsibilities of the client for interlock supplies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
3.2 The client interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
3.3 Client interface terminal box (CITB) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
3.3.1 Location of the CITB. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
3.3.2 Responsibilities of the client for the CITB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
3.3.3 Responsibilities of Elekta for the CITB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
3.4 Installing the CITB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
3.4.1 Client interface PCB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38
3.4.2 Configuring the client interface. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
3.5 Maze interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
3.5.1 Clinical use of the maze interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
3.5.2 Specification of the maze interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
3.6 Time delay interlock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
3.6.1 Clinical use of the time delay interlock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
3.6.2 Specifications of the time delay interlock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
3.6.3 Time delay interlock operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44
3.7 Fascia door interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
3.7.1 Clinical use of the fascia door interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
3.7.2 Responsibilities of the client for the fascia door interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
3.7.3 Specification of the fascia door interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
3.7.4 Area labelling in the equipment room . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
3.8 Interlocks for controlled areas. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
3.8.1 Examples of controlled areas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
3.8.2 Specifications of interlocks for controlled areas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
3.9 Emergency STOP switches. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.9.1 Clinical use of the emergency STOP switches. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.9.2 Specification of emergency STOP switches . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.9.3 Location of emergency STOP switches . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.9.4 Responsibilities of the client for emergency STOP switches. . . . . . . . . . . . . . . . . . . . . . . . . . . 47
3.10 Emergency power OFF system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
3.10.1 Clinical use of the emergency power OFF system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
3.10.2 Specification of emergency power OFF system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
3.10.3 Location of emergency power OFF system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 48
3.10.4 Responsibilities of the client for emergency power OFF switches . . . . . . . . . . . . . . . . . . . . . . 48
3.11 Warning lamps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
3.11.1 Conditions indicated by warning lamps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
3.11.2 Specification of warning lamps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
3.11.3 Location of warning lamps. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
3.11.4 Responsibilities of the client for warning lamps . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
3.12 Other client interfaces and interlocks. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
3.12.1 XVI kV generator interlocks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
3.12.2 Water cooler remote control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
3.12.3 Laser control. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
3.12.4 Room light control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50

— Blank page —

About this chapter
3.1 About this chapter

This chapter gives information about the interlock supplies necessary for the digital accelerator.
3.1.1 Responsibilities of the client for interlock supplies

All cables and connections to the electrical equipment below must be installed by the client. These
include:
• room lights
• warning lamps
• emergency STOP interlocks
• emergency power OFF system
• room door interlocks.
It is the responsibility of the client to supply, fit, and test all interlock systems prior to the installation
of the digital accelerator, and to ensure that all interlocks satisfy local and national requirements.
All interlock systems, except the emergency power OFF system, must be terminated at the CITB.
The emergency power OFF system must be terminated at the client distribution board.
Interlocks must have a minimum wire size 32/0.2 standard wire gauge (SWG) or equivalent is to be
used for lengths up 100 m.
If a longer length is required then the wire resistance must be considered to make sure the
maximum voltage drop does not exceed 2 V.
The maximum resistance over each of these interlock circuits must be less than 3 Ω.
The type of wire to use must make sure that the maximum voltage drop does not exceed 2 V during
operation for each interlock.
For example:
Maximum voltage drop Maximum cable length Maximum cable length at

at 1 A 5 A to 7 A
3.76 V 175 m 23 m
3.2 The client interface

To prevent the irradiation of persons other than the patient, the treatment room must have safety
interlocks on all access ways. Figure 3.1 shows the location of some of the interlocks in operation in
the equipment, treatment, and control rooms.

The client interface
1 4 2 3 4 5 4 6
8 4 2 7 4
Figure 3.1 Suggested layout of interlock items in the treatment suite (plan view)
(1) Confirmation button (5) Room Door 2A switches (two)

(time delay interlock)
(2) Emergency power OFF control (6) CITB
(3) Room Door 1 switches (two) (7) Room Door 2B switches (two)
(4) Emergency STOP switch (8) Search button (time delay interlock)

Client interface terminal box (CITB)
3.3 Client interface terminal box (CITB)

The client interface printed circuit board (PCB) contains circuits to control voltages from the client,
such as control lighting, warning lights, and interlocks.
The client interface PCB is housed within the client interface terminal box (CITB). Both are
supplied by Elekta.
3.3.1 Location of the CITB

The CITB is usually installed on the wall in the equipment room. See Figure 3.1.
The CITB must be installed on a wall above the exit of the cable duct from the reeling interface
cabinet.
For the XVI system, the duct length between the CITB and kV generator must be less than 18 m.
3.3.2 Responsibilities of the client for the CITB

It is the responsibility of the client to install the necessary client connections, with correct voltages,
to the client interface.
Information about the connections must be supplied to the installation engineer.
The supply for the client interface must be the same as the supply to the warning lights.
3.3.3 Responsibilities of Elekta for the CITB

All connections from the client interface to the digital accelerator will be made by the installation
engineer.

Installing the CITB
3.4 Installing the CITB

There are holes on the back of the box for attaching it to the wall.
Cable access is available through a panel at the bottom of the box.
The box must be grounded.
Figure 3.2 CITB
3.4.1 Client interface PCB

The client interface PCB is in the CITB.
The client interface PCB is connected to the digital accelerator through a positronic socket
connection on the bottom of the PCB.
The client interface PCB must not be shifted from its central alignment in the CITB as this may not
accommodate the 9-way D-type connector, which connects to the kV generator. If deviations from
this are necessary, consult the Elekta representative.
The client electrical services are wired through screw terminal strips.
The client interface must be wired as shown in Figure 3.3.

Installing the CITB
Figure 3.3 Connections to the client interface PCB
Mains interlock
If the electrical mains supply to the client interface fails, the digital accelerator is inhibited. The
mains supply is wired to contacts 5, 6 and 7 of the client interface PCB and must be connected to the
same phase as that used for the radiation warning lights.

Installing the CITB
Table 3.1 Connections on the client interface PCB
Function Terminal Description

EXTERNAL 1,2 Stops radiation. MOSAIQ®/SYNERGISTIQ™ and
TERMINATE other external systems can connect to EXTERNAL
(OPTIONAL) TERMINATE.
EMERGENCY STOP 3,4 A normally-made circuit, which when opened stops
kV and MV radiation, and movements.
SUPPLY 5,6,7 Power for the client interface PCB power supply only.
It does not supply electrical power to the room lights,
lasers, etc.
SEARCH (OPTIONAL) 8,9 Time delay interlock feature used in conjunction with
Confirmation button. See Chapter 3.6.
CONFIRMATION 10,11 Time delay interlock feature used in conjunction with
(OPTIONAL) Search button. See Chapter 3.6.
ROOM DOOR 1 12,13,14,15 Treatment room main door interlock.
ROOM DOOR 2A 18,19,24,25 A-side equipment room door interlock.
ROOM DOOR 2B 16,17,22,23 B-side equipment room door interlock.
ROOM DOOR 3 26,27 Plant room, roof or under-floor access interlock.
(OPTIONAL) It is also used by HexaPOD™ evo.
NEUTRON DOOR 20,21 Treatment room maze neutron door interlock.
(OPTIONAL)
CONTROLLED AREA 30,31 Machine power on status indicator.
LAMP (OPTIONAL)
WATER COOLER 28,29 Water cooler remote control.
REMOTE START
RADIATION OFF LAMP 32,33 Radiation off status indicator.
RADIATION ON LAMP 34,35 Radiation on status indicator.
FLUORESCENT ROOM 36,37 Fluorescent lamp control.
LIGHTS
TUNGSTEN ROOM 38,39 Tungsten lamp control.
LIGHTS
LASERS VIA ROOM 40,41 Laser control.
LIGHTS
41,44
READY WARNING 42,43 System ready status indicator.
LAMP
kV RADIATION ON 45,46 XVI kV radiation status indicator.
LAMP
kV GENERATOR PL1 XVI kV generator connection to interlocks and
indicators.
Note: The contact rating of the contacts for all the warning lights, and room (laser) lighting is 230 Vac at 10 A
resistive load or 6 A inductive load.

Installing the CITB
3.4.2 Configuring the client interface

The client interface has ten links. The configurations of the links are shown on the link
configuration label on the door of the CITB. See Figure 3.4.
Figure 3.4 Client interface link label

Installing the CITB
A fitted link overrides the associated function.
Link configuration record

When the links on the client interface have been configured, the link positions and date must be
recorded on the label on the inside of the door of the box (see Figure 3.4).
Table 3.2 Client interface PCB links
Function Link Description

External terminate LK1 Remove this if the EXTERNAL TERMINATE interlock is
connected.
Timer override LK2 Remove this for the timer function to operate with
Search and Confirmation.
Confirmation LK3 Remove this if the Confirmation button is connected.
Room door 2A LK6 Remove this if room door 2A interlock is connected.
Neutron door LK7 Remove this if the neutron door interlock is
connected.
Room door 2B LK9 Remove this if room door 2A interlock is connected.
Room door 3 LK10 Remove this if room door 3 interlock is connected.
Room lights LK11 Room lighting control. They configure the room light
switching relative to the machine supply. Links LK 11
LK12
and LK 12 are mutually exclusive - one must be
removed.
kV Radiation lamp LK13 Remove this if the kV radiation on lamp is installed in
the treatment suite.
HexaPOD™ evo
For systems with HexaPOD™ evo, the HexaPOD™ evo interlock is connected into Room Door 3.
LK10 must be removed.
MOSAIQ®/SYNERGISTIQ™
For systems with MOSAIQ®/SYNERGISTIQ™, the MOSAIQ®/SYNERGISTIQ™ radiation interlock is
connected into EXTERNAL TERMINATE. LK1 must be removed.

Maze interlocks
3.5 Maze interlocks
3.5.1 Clinical use of the maze interlocks

During treatment, it may be necessary to enter the treatment room quickly. The maze entrance must
be fitted with an interlock device connected to the client interface PCB at Room Door 1. This will
stop the radiation from the digital accelerator when a person attempts to enter the treatment room.
3.5.2 Specification of the maze interlocks

The interlock devices can be photoelectric, electro-mechanical or of another type, but must:
• Operate when the door is opened by no more than 75 mm
• Be capable of switching 7.5 A at 24 Vac
• Be fail safe. This means that it must fail open circuit.
Note: If a neutron door is fitted in the maze, an additional interlock switch must be fitted to this door and
connected to the client interface PCB at Neutron Door. This interlock is used to check that the neutron
door is in the correct position for the prescribed treatment.

Time delay interlock
3.6 Time delay interlock
3.6.1 Clinical use of the time delay interlock

Time delay or 'last man out' interlocks can be fitted in the treatment room to make sure that
personnel have vacated the room prior to radiation treatment.
This section describes the principle of a time delay interlock.
Note: In some regions, time delay interlocks are a mandatory legal requirement.
3.6.2 Specifications of the time delay interlock

The time delay period must be set for each installation according to the local rules.
Note: The Search (timer set) and Confirmation buttons must be momentary-action devices.
The contacts must be rated at 7.5 A and 24 Vac.
3.6.3 Time delay interlock operation

If a time delay interlock is fitted, the parameters must be set to ensure the clinical operation of the
interlock as described in Table 3.3.
When the Search button is pressed, the Room Door 1 interlock circuit must be completed in the set
time. If a timer Confirmation button is fitted, the Room Door 1 interlock circuit is armed when the
Confirmation button is pressed before the timer period has expired.
Table 3.3 Time delay interlock operation
Step Action Result

1 Press Search button in treatment room Timer is started
2 Vacate treatment room Timer is running
3 Close treatment room door to complete
maze interlock
4 Press Confirmation button outside maze
entrance
If timer is still running Room Door 1 circuit is complete and
radiation will be enabled
If timer has expired Room Door 1 circuit is not complete and
radiation will be disabled
5 If radiation is disabled, steps 1 to 4 must be repeated within the set time delay to
permit radiation
TDR1 on the client interface PCB can be adjusted to change the time delay. TDR1 is preset to
30 seconds but can be adjusted between 0 seconds and 60 seconds to give personnel sufficient time
to leave the treatment room. This must be set to enable the user to make the Room Door 1 interlock
circuit as described in Table 3.3.
A physical link can be added between terminals 9 and 11 on the client interface PCB if this function
is used.

Fascia door interlocks
3.7 Fascia door interlocks
3.7.1 Clinical use of the fascia door interlocks

The fascia doors must be connected to the client interface PCB at the Room Door 2A and
Room Door 2B connections.
WARNING 3.1
If this interlock circuit is connected incorrectly, it can allow the gantry to be
rotated by automatic set up (ASU) when the fascia doors are open. If you
ignore this warning, it can cause fatal injury.
If the doors to the equipment room are to be configured differently, local procedures must prevent
against possible accidents.
3.7.2 Responsibilities of the client for the fascia door interlocks

It is the responsibility of the client to:
• Make sure that only authorized personnel have access to the equipment room
• Supply, fit, and test two separate sets of fail safe interlock switches to each door fitted,
• Supply lockable fascia door(s) which are NOT self closing.
Note: If self closing doors must be installed to satisfy local rules, a time delay interlock system must be
installed.
Figure 3.5 Example of a fascia door interlock switch

Interlocks for controlled areas
3.7.3 Specification of the fascia door interlocks

The interlock devices can be photoelectric, electro-mechanical or of another type, but must:
• Operate when the door is opened by no more than 75 mm
• Be capable of switching 7.5 A at 24 Vac
• Be fail safe. This means that it must fail open circuit.
3.7.4 Area labelling in the equipment room

The equipment room must be labelled as a restricted access area, it is mandatory under IEC rules.
3.8 Interlocks for controlled areas

Interlocks and barriers must be installed at the entrance to any area which is unsafe to enter as
defined by the local rules. This section gives information about these interlocks.
3.8.1 Examples of controlled areas

Some examples of areas which may be unsafe are:
• A basement under the treatment room
• The roof of the treatment room
• Any other room designated as a restricted area by the client or their advisors.
3.8.2 Specifications of interlocks for controlled areas

Doors to controlled areas must be lockable and fitted with interlock switches.
Provision for the inclusion of additional interlock switches is made in the CITB at Room Door 3
(see Figure 3.3).
A controlled area warning must be displayed. This can be a warning lamp connected to the CITB at
Controlled Area Lamp.

Emergency STOP switches
3.9 Emergency STOP switches
3.9.1 Clinical use of the emergency STOP switches

The function of an emergency STOP switch is to stop kV and MV radiation, and movements. The
switch removes electrical power from many, but not all, electrical circuits.
Emergency STOP switches must be installed in the treatment room and the control room.
3.9.2 Specification of emergency STOP switches

An emergency STOP switch must:
• Be prominent and easily recognizable as an emergency STOP switch
• Be of a latching type that requires manually resetting
• Be rated at 7.5 A and 24 Vac
• Have earthed cases
Be wired in series from and to the CITB.
Figure 3.6 Typical emergency STOP switch
3.9.3 Location of emergency STOP switches

For suggested locations of emergency STOP switches in a typical installation, see Figure 3.1.
3.9.4 Responsibilities of the client for emergency STOP switches

It is the responsibility of the client to supply, install, and test a sufficient number of emergency STOP
switches in the correct locations to satisfy local requirements.

Emergency power OFF system
3.10 Emergency power OFF system
3.10.1 Clinical use of the emergency power OFF system

The function of an emergency power OFF system is to remove all electrical power, not just power to
the equipment. The switch removes all electrical power from the digital accelerator, kV generator,
vacuum supply and the mains sockets in the treatment room, equipment room and control room.
The switch can be used to test the system when necessary, during installation and maintenance.
3.10.2 Specification of emergency power OFF system

An emergency power OFF system must:
• Be prominent and easily recognizable as an emergency power OFF system
• Be in compliance with local regulations
3.10.3 Location of emergency power OFF system

The emergency power OFF system must be installed in a different place to the emergency STOP
switches. One emergency power OFF control should be provided in the treatment room, control
room and the equipment room wall. See Figure 3.1 for a suggested location.
3.10.4 Responsibilities of the client for emergency power OFF switches

It is the responsibility of the client to supply, install, and test an emergency power OFF system with
the correct color and in a location according to local rules.

Warning lamps
3.11 Warning lamps

Warning lamps are used to indicate the radiation state of the digital accelerator and XVI system.
3.11.1 Conditions indicated by warning lamps

The switching of the warning lamps must make it possible to indicate the following machine
conditions:
• Radiation ON - machine radiating
• Radiation OFF - machine not radiating
• Ready - machine ready to radiate
• kV radiation ON (where applicable)
Note: Some local rules require that the RADIATION ON warning must flash. In this event, it is the
responsibility of the client to supply the flashing system.
3.11.2 Specification of warning lamps

A warning lamp must:
• Be prominent and easily recognizable as warning lamp
• Be in compliance with location regulations
• Be of filament type for immediate illumination
• Be wired in to the CITB
3.11.3 Location of warning lamps

It is recommended that warning lamps are positioned:
• Adjacent to the maze entrance
• Adjacent to basement entrances
• Adjacent to entrances of any other restricted areas.
Before positioning any warning lamps, consult the local rules.
3.11.4 Responsibilities of the client for warning lamps

It is the responsibility of the client to supply, install, and test warning lamps in prominent positions
to satisfy local rules.
Note: If the bulbs are to be rated at a voltage other than that of the mains, then the client must install a
suitable supply.

Other client interfaces and interlocks
3.12 Other client interfaces and interlocks

The CITB can be used for systems where remote control or interlock connection is necessary:
• XVI kV generator interlock
• Water cooler remote control
• Laser control
• Room light control
3.12.1 XVI kV generator interlocks

The XVI kV generator must be connected to the interlock circuits. This will enable the the kV
radiation ON lamp to be lit when the kV generator operates. It will also enable the kV generator to
be shut down when the applicable interlock is triggered.
The XVI kV generator must be connected to the client interface PCB at kV generator.
3.12.2 Water cooler remote control

The water cooler can be connected to the CITB to provide remote control.
The water cooler provides 24 Vac to a relay on the client interface PCB. Remote control is enabled
when the relay is closed, providing a remote signal from the CITB.
The client must install a two core 0.75 mm2 cable between the CITB and the water cooler.
For remote control, make a connection to the client interface PCB at Water Cooler Remote Start.
3.12.3 Laser control

The lasers can be connected to the CITB to provide remote control. This will enable the HHC Laser
or Room Lights buttons.
For remote control of the lasers, make a connection to the client interface PCB at
Lasers Through Room Lights.
3.12.4 Room light control

The room lights can be connected to the CITB to provide remote control. This will enable the HHC
Room Lights button.
For remote control of the room lights, make a connection to the client interface PCB at
Room Lights.
The CITB provides changeover contacts for room lighting capable of switching between fluorescent
of tungsten lighting. The switch between terminals 36 and 37 is normally closed.

Cable information
4 Cable information
4.1 About this chapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53

4.2 Treatment suite ducts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
4.3 Duct dimensions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
4.4 Maximum cable lengths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56
4.5 Cable order process . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
4.5.1 Fixed length cable kits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58
4.5.2 Measuring the cables. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59
4.5.3 Ordering the cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 59

Cable information
— Blank page —

Cable information
About this chapter
4.1 About this chapter

The electrical cabling necessary for Elekta oncology products can be divided into three categories:
• Cables supplied by the client
• Cables supplied with parts (such as the UPS)
• Cables supplied by Elekta.
It is necessary to measure the routing of the cables supplied by Elekta before installation. The
procedure is given in Section 4.4.
For information about cables for the HexaPOD™ evo, refer to HexaPOD™ evo RT System Planning
Guide.

Cable information
Treatment suite ducts
4.2 Treatment suite ducts

Cable ducts are necessary to keep cables between items in an environment with low-interference
and protection from damage.
The ducts can be below the floor or in the walls. They must be in compliance with maximum cable
lengths for the equipment.
Figure 4.1 shows the suggested layout of ducting for an .

Figure 4.1 Suggested layout of ducts
(1) EIM (6) Gantry base duct exit

(2) CITB (7) Precise Treatment Table duct
(3) RIC duct side exit (8) Precise Treatment Table pit
(4) RIC duct main exit (9) IMKM
(5) XVI kV generator1 (10) Duct to control room
This duct layout is compatible with US seismic codes.

Cable information
Duct dimensions
4.3 Duct dimensions

Refer to Table 4.1 for the dimensions and routes of treatment suite cable ducts.
Table 4.1 The cable duct dimensions and routes
From To Recommended size Minimum size Maximum

W x D (mm) W x D (mm) length (m)
Reeling interface Gantry base 100 × 200 100 × 200 1.5

cabinet
Precise Treatment Table pit1 100 × 100 100 × 50 3.0
XVI kV generator 200 × 150 150 × 150 4.0
EIM 100 × 200 100 × 200 6.0
CITB 200 × 150 200 × 100 13.0
iViewGT™ control cabinet 100 × 200 100 × 200 22.0
Service terminal box 200 × 150 200 × 150 22.5
Peripheral tie tray 200 × 150 200 × 150 22.5
MDU 200 × 150 200 × 150 28.0
Treatment control cabinet 200 × 150 200 × 150 29.0
XVI control cabinet 100 × 200 100 × 200 33.0
Water cooler 200 × 150 200 × 100 50.0
XVI control cabinet TRM line receiver 200 × 150 150 × 100 29.0

(TRM line driver)
XVI control cabinet kV generator 100 × 200 100 × 200 32.0

1 Can be 100 mm diameter tube.
The gantry base duct can contain cables to:

• Gantry base
• TRMs
• EIM
• Apex™ control box
• HexaPOD™ evo ControlBox

Cable information
Maximum cable lengths
4.4 Maximum cable lengths

Refer to Table 4.2 and Table 4.3 for the list of maximum cable lengths.
Table 4.2 Maximum cable lengths from the RIC to other equipment
To Maximum cable length

(m)
Gantry motor 4.5
EIM 8.0
TRM 3 (optional) 8.5
XVI kV generator (optional) 10.5
IMKM (optional) 15.0
CITB 15.0
iViewGT™ control cabinet (optional) 26.5
TCC 30.0
Service terminal box 30.0
MDU 30.0
FKP 30.0
XVI control cabinet (optional) 30.0
Table 4.3 Maximum other cable lengths
From To Maximum cable length

(m)
TCC Treatment sheet printer (USB) 5.0
TCC Daily record printer (USB) 5.0
Integrity R1.1 and earlier TCC Radiotherapy workstation 1.5 (standard)
15.0 (with KVM extender)
Integrity R1.1 and earlier TCC Radiotherapy workstation 1.5 (standard)
optional monitor 15.0 (with VGA extender)
Integrity R3.0 TCC Radiotherapy workstations 30.0
Integrity R3.0 TCC Radiotherapy workstation 30.0
optional monitor
Integrity R3.0 TCC BMDM 30.0
MOSAIQ®/SYNERGISTIQ™ CITB (External Terminate) 30.0
computer

Cable information
Maximum cable lengths
The dimensions in Table 4.4 can be used to calculate the necessary length of cable from the duct exit
point to the connection inside the item.
Table 4.4 Internal cable lengths
Item Internal cable length (m)

CITB 0
Peripheral tie tray 0
TRM line receiver 0
Reeling interface cabinet (RIC) 2.0
Service terminal box 2.0
Treatment control cabinet 2.0
MOSAIQ®/SYNERGISTIQ™ computer 2.0
kV generator 2.0
XVI control cabinet 2.0
iViewGT™ control cabinet 2.0
kV X-ray tube (on digital accelerator) 10.0

Cable information
Cable order process
4.5 Cable order process

This section is applicable only to the cables for the digital accelerator.
This section describes how to measure and order cables that are supplied by Elekta.
Cables supplied by Elekta are sent to site at least six weeks before the start of the installation of the
machine.
4.5.1 Fixed length cable kits

The cable kits are fixed length cable kits that give all the necessary cables at the selected length.
Table 4.5 Interbay cable kits
Cable kit Length (m) Part number

Interbay cable kit 10.0 1026758
15.0 1026769
20.0 1023406
25.0 1023408
30.0 1023477
Table 4.6 Integrity R3.0 interbay cable kits

Integrity R3.0 and later interbay 10.0 1026849
cable kit
20.0 1026847
(RIC to TCC)
30.0 1026845
Table 4.7 Remote detector retraction (RDR) cable kits

RDR cable kit 20.0 1024485
25.0 1024694
30.0 1024158
Table 4.8 Integrity R3.0 treatment room cable kits

Integrity R3.0 and later treatment 10.0 1026848
room cable kit
20.0 1026846
(TCC to control room)
30.0 1026843
Table 4.9 Treatment room cable kits

Treatment room cable kit 5.0 1023832
10.0 1023833
15.0 1023840

Cable information
Cable order process
4.5.2 Measuring the cables

Using Figure 4.1, and Table 4.5 to Table 4.9 as a guide measure the lengths of the applicable the
cable routings.
All measurements are to be made from connection to connection of each item, along the exact cable
routing, including distances for lengths and depths of cable ducts, not by the shortest distance
between the equipment parts.
The distances between the items of equipment must be accurately measured because it is not
possible to coil large lengths of extra cable in the ducts.
For certain sites where maximum stated cable lengths are exceeded, non-standard requests (NSRs)
are necessary. Contact the local Elekta representative
4.5.3 Ordering the cables

The necessary cable kit is ordered using the Cable & Water Hose Order Form. See Site Planning
Delivery Information for an example of the Cable & Water Hose Order Form.
The Cable & Water Hose Order Form is available from your Elekta representative.
The completed form is necessary for Elekta to send the correct cables at the correct lengths to the
site.
Select one length from each of the cable kits shown in Table 4.5 to Table 4.9. This will be the longest
length measured out of all cable routings in each kit. For example, if one cable needs to be 25 m, and
all other cables are 20 m, then the 25 m cable kit must be ordered.
The completed form must be sent to Elekta at least six weeks prior to the expected start of
installation.
If the form is not sent back on time, there will be cable shortages and the start of installation will be
late.
It is the responsibility of the Elekta business unit (BU) or agent to complete and send back the form
to Elekta.
The cables will then be sent from Elekta to the Delivery Name at the Delivery Address stated on the
form.

Cable information
Cable order process
— Blank page —

— Blank page —
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Elekta AB (publ) North America Europe, Middle East, Africa, Asia Pacific
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Elekta Oncology Products

Site Planning Electrical Information

Document ID: 1008404 03

Registered trademarks of other manufacturers

WORLDWIDE PRODUCT MANUFACTURING CENTER – ONCOLOGY

1008404 03 Elekta Oncology Products

When you receive an FCO, Elekta recommends that you:

FCO number Date Signature

Elekta Oncology Products 1008404 03

1008404 03 Elekta Oncology Products

Section Description Page

1 General safety and regulatory information . . . . . . . . . . . . . . . . . . . . . . . . . . 9

2 Power supplies information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

Elekta Oncology Products 1008404 03

1008404 03 Elekta Oncology Products

List of figures and tables

Figure 2.1 Treatment suite equipment locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20

Figure 3.2 CITB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 38

Figure 3.3 Connections to the client interface PCB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 39

Figure 3.4 Client interface link label . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41

Figure 3.5 Example of a fascia door interlock switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45

Figure 3.6 Typical emergency STOP switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47

Figure 4.1 Suggested layout of ducts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54

Table 2.1 Specification of three-phase mains electrical supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23

Table 2.2 Vacuum system specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

Table 2.3 kV generator power requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26

Table 2.4 Voltage stabilizer input ranges. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27

Table 2.5 Specification for electrical outlets . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30

Table 2.6 Electrical requirements of the laser alignment system . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31

Table 2.7 Typical water cooling supply specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32

Table 3.1 Connections on the client interface PCB . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40

Table 3.2 Client interface PCB links . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42

Table 3.3 Time delay interlock operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 44

Table 4.1 The cable duct dimensions and routes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55

Table 4.3 Maximum other cable lengths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 56

Table 4.4 Internal cable lengths . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57

Elekta Oncology Products 1008404 03

Table 4.5 Interbay cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Table 4.6 Integrity R3.0 interbay cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Table 4.7 Remote detector retraction (RDR) cable kits. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Table 4.8 Integrity R3.0 treatment room cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

Table 4.9 Treatment room cable kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 58

1008404 03 Elekta Oncology Products

1 General safety and regulatory information

1.1 Function of this document. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

Elekta Oncology Products 1008404 03

1008404 03 Elekta Oncology Products

1.1 Function of this document

1.1.1 Intended audience

1.2 Important safety information

1.3.1 IEC safety standards

1.4 Warnings, cautions and notes

Elekta Oncology Products 1008404 03

1.6 Text formats

Text Format Definition

1008404 03 Elekta Oncology Products

1.8 Conventions for the directions of the digital accelerator

Figure 1.1 Conventions for the directions of the digital accelerator

Elekta Oncology Products 1008404 03

1.9 Abbreviations and acronyms

1008404 03 Elekta Oncology Products

Elekta Oncology Products 1008404 03

1008404 03 Elekta Oncology Products