Nucletron Simulix-Evolution Imaging User manual

Simulix-Evolution Imaging
Service Manual
REF 112.912ENG-04
21f375 rev 02

How to contact Nucletron Offices
NUC-T380-13
HOW TO CONTACT NUCLETRON OFFICES
Unless otherwise stated the service dispatch call number is the main telephone number.
Head Office and Manufacturer:
Nucletron B.V.
PO Box 930
3900 AX VEENENDAAL
Waardgelder 1
3905 TH VEENENDAAL
The Netherlands
Tel.: [phone]
Fax: [phone]
Service: [phone]
E-mail [email protected]
Web site: www.nucletron.com
BeNeLux
Nucletron B.V.
PO Box 930
3900 AX VEENENDAAL
Waardgelder 1
3905 TH VEENENDAAL
The Netherlands
Tel.: [phone]
Fax: [phone]
Service: [phone]
E-mail [email protected]
Web site: www.nucletron.com
Germany
Theranostic Medizintechnik GmbH
Obere Dammstrasse 8-10
D-42653 Solingen
Tel.: [phone]
Fax: [phone]
Service: [phone]
E-mail: [email protected]
Web site: www.theranostic.de
France
Nucletron S.A.R.L.
Parc d’Activités l. Bernard Vergnaud
15 rue Paul Langevin
93274 SEVRAN Cedex
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
Italy
Nuclital srl
Viale Elvezia no. 2
20052 MONZA (Milan)
Tel.: [phone] / 323148
Fax: [phone]
E-mail: [email protected]
United Kingdom
Nucletron UK Ltd.
Nucletron House
Chowley Oak
Tattenhall
CHESTER CH3 9EX
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
Sweden
Nucletron Scandinavia AB
Box 1704
Klostergatan 12
SE–751 47 Uppsala
Sweden
Tel: [phone]
Fax: [phone]
E-mail: [email protected]
Spain
Nucletron S.A.
Avda. de Castilla, 2
Parque Empresarial San Fernando
Edificio Francia, Planta 2e, Esc. A
28830 San Fernando de Henares (Madrid)
Tel.: [phone]
Fax: [phone]
Service: [phone]
E-mail: [email protected]
Europe / Middle East and Africa
Poland
Nucletron Poland Sp. z o. o.
Oddzial w Warszawie
Al. Krakowska 285
02-133 Warszawa
Poland
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]

How to contact Nucletron Offices
NUC-T380-13
HOW TO CONTACT NUCLETRON OFFICES
Unless otherwise stated the service dispatch call number is the main telephone number.
USA
Nucletron Corporation
8671 Robert Fulton Drive
COLUMBIA, MD 21046
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
North and South
America
Canada
Nucletron Canada Inc.
411 Legget Drive, Suite 502
Kanata, Ontario
K2K 3C9
Canada
Tel: [phone]
Fax: [phone]
E-mail: [email protected]
Hong Kong
Nucletron Asia Pacific Ltd.
Room 1005, Tower 2, Silvercord,
30 Canton Road, Tsim Sha Tsui,
Kowloon, HONG KONG
Tel.: [phone] / 2684 / 3025
Fax: [phone]
E-mail: [email protected]
Australia
Nucletron Pty. Limited
Suite 4, 26 Sparkes Street
Camperdown. NSW. 2050
Sydney
Tel.: [phone]
Fax: [phone]
Email: [email protected]
China
Nucletron Asia Pacific Ltd.
Beijing Representative Office
Room 21D CITIC Building,
19 Jian Guo Men Wai Da Jie
Beijing, China
Post Code: 100004
Tel.: [phone] / 41
Fax: [phone]
E-mail: [email protected]
Web site: www.nucletron-china.com
India
Nucletron India Pvt Ltd.
No. 3, D’Silva Road
Mylapore
Chennai 600 004
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
Web site: www.nucletron-india.com
Nucletron Asia Pacific Ltd.
Shanghai Representative Office
Shanghai, China
Tel.: [phone] / 48
Fax: [phone]
E-mail: [email protected]
Web site: www.nucletron-china.com
Asia Pacific
Singapore
Nucletron Asia Pacific Ltd.
Singapore Representative Office
89 Science Park Drive
Rutherford # 03 - 06
Singapore 118261
Tel.: [phone]
Fax: [phone]
E-mail: [email protected]
Your Distributor / Agent

Preface
NUC-T374-02 v
Preface
Identification
Manuals are identified by a part number. The part number consists of three
parts:
Example:
The part number is printed on the right bottom side of the front page.
Numbers printed on other pages are for internal revision control and may
differ.
CE Classification
Manuals made for products that have been CE (Conformité Européenne)
marked have the CE mark on the front page. The number behind the CE
Mark defines the responsible notified body.
Nucletron systems are classified according to IEC 601-1 as Class I, type B.
Nucletron systems meet the relevant provisions of the European Medical
Device Directive 93/42/EEC or the European Active Implantable Medical
Device Directive 90/385/EEC; this is based on conformity of the products
and the quality system according to ISO 9001:2000 and ISO 13485:2003.
For this reason mark is used.

Preface
vi NUC-T374-02
Directive WEEE
Symbol Meaning Remarks
Location: Near or on
the type identification
plate.
Symbol for separated collection of
electrical and electronic equipment per
Directive 2002/96 of the European
Parliament and the Council of the
European Union (Directive on Waste of
Electrical and Electronic Equipment). If
applicable to the type of device, it
indicates legally imposed obligations
within EU member states, Iceland,
Norway and Switzerland when the
equipment is disposed of, at the end of
its life-time.
Owners of marked equipment should
contact the organization that imported
the equipment into their country, when
they want to dispose of the equipment,
at the end of its lifetime. The Directive
prioritizes re-use of equipment over re-
use of components over re-use of
materials over disposal as waste. Article
5 part 2d allows producers to decline the
return of any used equipment that is or
may be biologically or radiologically
contaminated.
Conventions
Throughout this manual certain conventions are used. These are Warnings,
Cautions and Notes. They provide a means of prioritizing information to be
brought to the attention of the user. They are given as follows:
Warning: Designates a possibly dangerous situation. Non-observance may lead
to death or the most severe injuries
Caution: Designates a possibly harmful situation. Non-observance may lead to
minor injuries or damage to the product.
Note: Designates a possibly harmful situation. Non-observance may lead to
damage to the product or the environment.
Precautions
The user is expected to use the product (soft and hardware) in accordance
with the instructions given in this manual, which must be read before the
system is used. Any unauthorized deviation from the procedures laid down
in this manual can affect the contractual obligations between purchaser and
vendor.
Warning: Do not modify any part of Nucletron supplied computer's hardware,
software or software configuration. Installing or running an appli-
cation that has not explicitly been approved by Nucletron may
compromise patient safety and will result in termination of all
warranty and service contracts.

Preface
NUC-T374-02 vii
Warning: The Nucletron products are designed for use and maintenance using
only parts available from Nucletron. No liability for failure can be
accepted by Nucletron through the use of parts obtained from other
suppliers unless written permission is obtained from Nucletron.
Copyright
All rights reserved. No part of this manual may be reproduced or transmitted
in any form whatsoever, including photocopying and recording without
written permission of the copyright holder: Nucletron B.V., PO Box 930,
3900 AX VEENENDAAL, The Netherlands.
Concerning this Publication
Information contained in this publication is subject to change without
notice. Whenever the equipment is delivered with a documentation medium
such as a CD or DVD, the user shall always check the medium for latest
information. This information is part of Release Notes and Document
Upgrade files.
Neither Nucletron B.V. and its subsidiaries nor anyone else who has been
involved with the development, production or delivery of the documentation
be liable for any special, incidental or consequential damages, whether
based upon breach of warranty, breach of contract, negligence, strict
liability in tort or any other legal theory.

Preface
viii NUC-T374-02

Table of Contents
112.912ENG-04 Simulix-Evolution Imaging –Service Manual ix
Table of Contents
1. Introduction 1-1
1.1 Intended Audience ............................................................................................................. 1-1
1.2 Related Documents............................................................................................................ 1-1
2. Safety Instructions 2-1
2.1 General Information............................................................................................................ 2-1
2.2 Safety Features .................................................................................................................. 2-1
2.2.1 Basic Safety Features for All Simulix Systems ................................................... 2-1
2.2.2 Oncentra Simulation ........................................................................................... 2-1
2.2.3 Anti-virus Software.............................................................................................. 2-2
2.2.4 Simulix Error Messages ...................................................................................... 2-3
2.2.5 Door Interlock Switch (X-ray Safety)................................................................... 2-3
2.2.6 Data Integrity and Security.................................................................................. 2-3
2.3 Electrical Safety.................................................................................................................. 2-3
2.3.1 Classification ....................................................................................................... 2-3
2.3.2 Power Supply ...................................................................................................... 2-4
2.4 Fire Safety .......................................................................................................................... 2-4
2.5 Fluid Safety......................................................................................................................... 2-4
2.6 Radiation Safety ................................................................................................................. 2-4
2.7 X-Ray Exposure Interlocks................................................................................................. 2-5
2.8 Electromagnetic Safety ...................................................................................................... 2-5
2.8.1 Electromagnetic Emissions................................................................................. 2-6
2.8.2 Electromagnetic Immunity................................................................................... 2-7
2.8.3 Separation Distance............................................................................................ 2-9
2.9 Emergency .......................................................................................................................2-10
2.9.1 Emergency Stop Buttons .................................................................................. 2-10
2.10 Collision Safety................................................................................................................. 2-10
2.10.1 Collision Avoidance System.............................................................................. 2-10
2.10.2 Collision Touch Guards..................................................................................... 2-11
3. Flat Panel Detector and Interface Box 3-1
4. Drawings 4-1
5. Service Procedures 5-1
5.1 Cleaning ............................................................................................................................. 5-1
5.1.1 Vacuum Cleaning................................................................................................ 5-1
5.1.2 Wiping ................................................................................................................. 5-1
5.2 Touch Guard Check ........................................................................................................... 5-1
5.3 Preventive Maintenance..................................................................................................... 5-2
5.4 Corrective Maintenance ..................................................................................................... 5-2
5.5 Fuse Replacement ............................................................................................................. 5-2
5.6 Backup and Restore........................................................................................................... 5-3
5.7 Cone Beam CT................................................................................................................... 5-3
5.7.1 Cone Beam CT Air-scan Calibration................................................................... 5-3

Table of Contents
x Simulix-Evolution Imaging – Service Manual 112.912ENG-04
5.7.2 Calibrations for Cone Beam CT Isocenter Calibration........................................ 5-5
6. Spare Parts List 6-1
7. Smoothbase Service Manual 7-1
8. Additional Information 8-1