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GE Medical Systems

Technical Publication
Direction 2341917-100 REVISION 2 GE Medical Systems Discovery ST Pre-Installation

Copyright 2003 by General Electric Company, Inc. All rights reserved.

http://www.gemedical.com

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Published by GE Medical Systems FISE Manager Tim Erickson Program Integrators Paul Smith Editor-in-Chief Duane Delestienne Technical Editors and Writers Duane Delestienne Kris Pabliski Tom Mereen (Compuware) Phil Block (Compuware)

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GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

LEGAL NOTES
TRADEMARKS
Adobe, the Adobe logo, Acrobat, the Acrobat logo, Exchange, and PostScript are trademarks of Adobe Systems Incorporated or its subsidiaries and may be registered in certain jurisdictions. Microsoft is a registered trademark and Windows is a trademark of Microsoft Corporation. All other products and their name brands are trademarks of their respective holders.

COPYRIGHTS
All Material, Copyright 2003 by General Electric Company, Inc. All rights reserved.

Legal Notes

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GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2 End of Legal Notes

DISCOVERY ST PRE-INSTALLATION

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Legal Notes

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

IMPORTANT PRECAUTIONS
LANGUAGE
THIS SERVICE MANUAL IS AVAILABLE IN ENGLISH ONLY. IF A CUSTOMERS SERVICE PROVIDER REQUIRES A LANGUAGE OTHER THAN ENGLISH, IT IS THE CUSTOMERS RESPONSIBILITY TO PROVIDE TRANSLATION SERVICES. DO NOT ATTEMPT TO SERVICE THE EQUIPMENT UNLESS THIS SERVICE MANUAL HAS BEEN CONSULTED AND IS UNDERSTOOD. FAILURE TO HEED THIS WARNING MAY RESULT IN INJURY TO THE SERVICE PROVIDER, OPERATOR OR PATIENT FROM ELECTRIC SHOCK, MECHANICAL OR OTHER HAZARDS. CE MANUEL DE MAINTENANCE NEST DISPONIBLE QUEN ANGLAIS. SI LE TECHNICIEN DU CLIENT A BESOIN DE CE MANUEL DANS UNE AUTRE LANGUE QUE LANGLAIS, CEST AU CLIENT QUIL INCOMBE DE LE FAIRE TRADUIRE. NE PAS TENTER DINTERVENTION SUR LES QUIPEMENTS TANT QUE LE MANUEL SERVICE NA PAS T CONSULT ET COMPRIS. LE NON-RESPECT DE CET AVERTISSEMENT PEUT ENTRANER CHEZ LE TECHNICIEN, LOPRATEUR OU LE PATIENT DES BLESSURES DUES DES DANGERS LECTRIQUES, MCANIQUES OU AUTRES. DIESES KUNDENDIENST-HANDBUCH EXISTIERT NUR IN ENGLISCHER SPRACHE. FALLS EIN FREMDER KUNDENDIENST EINE ANDERE SPRACHE BENTIGT, IST ES AUFGABE DES KUNDEN FR EINE ENTSPRECHENDE BERSETZUNG ZU SORGEN. VERSUCHEN SIE NICHT, DAS GERT ZU REPARIEREN, BEVOR DIESES KUNDENDIENST-HANDBUCH NICHT ZU RATE GEZOGEN UND VERSTANDEN WURDE. WIRD DIESE WARNUNG NICHT BEACHTET, SO KANN ES ZU VERLETZUNGEN DES KUNDENDIENSTTECHNIKERS, DES BEDIENERS ODER DES PATIENTEN DURCH ELEKTRISCHE SCHLGE, MECHANISCHE ODER SONSTIGE GEFAHREN KOMMEN. ESTE MANUAL DE SERVICIO SLO EXISTE EN INGLS. SI ALGN PROVEEDOR DE SERVICIOS AJENO A GEMS SOLICITA UN IDIOMA QUE NO SEA EL INGLS, ES RESPONSABILIDAD DEL CLIENTE OFRECER UN SERVICIO DE TRADUCCIN. NO SE DEBER DAR SERVICIO TCNICO AL EQUIPO, SIN HABER CONSULTADO Y COMPRENDIDO ESTE MANUAL DE SERVICIO. LA NO OBSERVANCIA DEL PRESENTE AVISO PUEDE DAR LUGAR A QUE EL PROVEEDOR DE SERVICIOS, EL OPERADOR O EL PACIENTE SUFRAN LESIONES PROVOCADAS POR CAUSAS ELCTRICAS, MECNICAS O DE OTRA NATURALEZA.

Important Precautions

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GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

ESTE MANUAL DE ASSISTNCIA TCNICA S SE ENCONTRA DISPONVEL EM INGLS. SE QUALQUER OUTRO SERVIO DE ASSISTNCIA TCNICA, QUE NO A GEMS, SOLICITAR ESTES MANUAIS NOUTRO IDIOMA, DA RESPONSABILIDADE DO CLIENTE FORNECER OS SERVIOS DE TRADUO. NO TENTE REPARAR O EQUIPAMENTO SEM TER CONSULTADO E COMPREENDIDO ESTE MANUAL DE ASSISTNCIA TCNICA. O NO CUMPRIMENTO DESTE AVISO PODE POR EM PERIGO A SEGURANA DO TCNICO, OPERADOR OU PACIENTE DEVIDO A CHOQUES ELTRICOS, MECNICOS OU OUTROS. IL PRESENTE MANUALE DI MANUTENZIONE DISPONIBILE SOLTANTO IN INGLESE. SE UN ADDETTO ALLA MANUTENZIONE ESTERNO ALLA GEMS RICHIEDE IL MANUALE IN UNA LINGUA DIVERSA, IL CLIENTE TENUTO A PROVVEDERE DIRETTAMENTE ALLA TRADUZIONE. SI PROCEDA ALLA MANUTENZIONE DELLAPPARECCHIATURA SOLO DOPO AVER CONSULTATO IL PRESENTE MANUALE ED AVERNE COMPRESO IL CONTENUTO. NON TENERE CONTO DELLA PRESENTE AVVERTENZA POTREBBE FAR COMPIERE OPERAZIONI DA CUI DERIVINO LESIONI ALLADDETTO ALLA MANUTENZIONE, ALLUTILIZZATORE ED AL PAZIENTE PER FOLGORAZIONE ELETTRICA, PER URTI MECCANICI OD ALTRI RISCHI.

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Important Precautions

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent write Damage In Shipment on ALL copies of the freight or express bill BEFORE delivery is accepted or signed for by a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period. Call Traffic and Transportation, Milwaukee, WI (262) 785 5052 or 8*323 5052 immediately after damage is found. At this time be ready to supply name of carrier, delivery date, consignee name, freight or express bill number, item damaged and extent of damage. Complete instructions regarding claim procedure are found in Section S of the Policy And Procedures Bulletins. 14 July 1993

CERTIFIED ELECTRICAL CONTRACTOR STATEMENT


All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. In addition, electrical feeds into the Power Distribution Unit shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE Medical personnel. The products involved (and the accompanying electrical installations) are highly sophisticated, and special engineering competence is required. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GEs electrical work on these products will comply with the requirements of the applicable electrical codes. The purchaser of GE equipment shall only utilize qualified personnel (i.e., GEs field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.

IMPORTANT...X-RAY PROTECTION
X-ray equipment if not properly used may cause injury. Accordingly, the instructions herein contained should be thoroughly read and understood by everyone who will use the equipment before you attempt to place this equipment in operation. The General Electric Company, Medical Systems Group, will be glad to assist and cooperate in placing this equipment in use. Although this apparatus incorporates a high degree of protection against x-radiation other than the useful beam, no practical design of equipment can provide complete protection. Nor can any practical design compel the operator to take adequate precautions to prevent the possibility of any persons carelessly exposing themselves or others to radiation. It is important that anyone having anything to do with x-radiation be properly trained and fully acquainted with the recommendations of the National Council on Radiation Protection and Measurements as published in NCRP Reports available from NCRP Publications, 7910 Woodmont Avenue, Room 1016, Bethesda, Maryland 20814, and of the International Commission on Radiation Protection, and take adequate steps to protect against injury. The equipment is sold with the understanding that the General Electric Company, Medical Systems Group, its agents, and representatives have no responsibility for injury or damage which may result from improper use of the equipment. Various protective materials and devices are available. It is urged that such materials or devices be used.

OMISSIONS & ERRORS


Customers, please contact your GE Sales or Service representatives. GE personnel, please use the GEMS CQA Process to report all omissions, errors, and defects in this publication. Important Precautions Page 7

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

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Important Precautions

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Revision History
Revision 0 1 2 Date 03/14/03 04/11/03 05/19/03 Reason for change Initial release. Technical corrections. Updated floor loading equipment parameters. Revision History Page 9

Revision History

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

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Revision History

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

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List of Effected Pages


PAGES
1 through 116 1 through 116 1 through 118

REVISION
0 1 2

PAGES
All All All

REVISION

PAGES

REVISION

List of Effected Pages

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List of Effected Pages

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

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List of Effected Pages

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Preface Publication Conventions


Purpose: This section means to inform the reader on publication conventions used. So that the reader can identify safety and general material that is considered important by it format. This includes the interpretation of computer screen text as either input or output. There are a number of specific text and paragraph styles/conventions used within this section to accomplish this task. Please become familiar with the conventions used within this publication before proceeding.

1.1

Text and Character Representation


Within this publication, different paragraph and character styles have been used to indicated potential hazards. Paragraph prefixes, such as hazard, caution, danger and warning, are used to identify important safety information. Text (Hazard) styles are applied to the paragraph contents that is applicable to each specific safety statement. Words describe the type of potential hazard that may be encountered and are placed immediately before the paragraph it modifies. Safety information will normally include: Type of potential Hazard Nature of potential injury Causative condition How to avoid or correct the causative condition

EXAMPLES OF HAZARD STATEMENTS USED


A few examples are provided that have been adapted form GEMS global document standard (2119696-100). They include paragraph prefixes and modified text styles. CAUTION Pinch Points Loss of Data Sharp Objects Caution is used when a hazard exists which can or could cause minor injury to self or others if instructions are ignored. They include for example: Loss of critical patient data Crush or pinch points Sharp objects

DANGER EXCESSIVE VOLTAGE CRUSH POINT


WARNING ROTATING EQUIPMENT BARE WIRES

DANGER IS USED WHEN A HAZARD EXISTS WHICH WILL CAUSE SEVERE PERSONAL INJURY OR DEATH IF INSTRUCTIONS ARE IGNORED. THEY CAN INCLUDE: ELECTROCUTION CRUSHING RADIATION
WARNING IS USED WHEN A HAZARD EXISTS WHICH COULD OR CAN CAUSE SERIOUS PERSONAL INJURY OR DEATH IF INSTRUCTIONS ARE IGNORED. THEY CAN INCLUDE: Potential for shock Exposed wires Failure to Tag and lockout system power could allow for un-command motion. Preface Page 13

Preface

Section 1.0 Safety & Hazard Information

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2 NOTICE Equipment Damage Possible

DISCOVERY ST PRE-INSTALLATION

Notice is used when a hazard is present that can cause property damage but has absolutely no personal injury risk.They can include: Disk drive will crash Internal mechanical damage, such as to the x-ray tube Coasting the rotor through resonance.

Its important that the reader not ignore hazard statements in this document.

1.2

Graphical Representation
Important information will always be preceded by the exclamation point contained within a triangle, as seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be used to make you aware of specific types of hazards that could possibly cause harm.

ELECTRICAL

MECHANICAL

RADIATION

LASER

HEAT

PINCH

LASER LIGHT
Some others make you aware of specific procedures that should be followed.

AVOID STATIC ELECTRICITY

TAG AND LOCK OUT

WEAR EYE PROTECTION

TAG

&

LOCKOUT
Signed Date

EYE PROTECTION

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Preface

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DISCOVERY ST PRE-INSTALLATION

Section 2.0 Conventions Used For General Information


2.1 Document Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such as Purpose, Example, Comment and Note) are used to identify important but non-safety related information. Text styles are also applied to text within each paragraph modified by the specific prefix.

EXAMPLES OF PREFIXES USED FOR GENERAL INFORMATION


Purpose: Introduces and provides meaning as to the information contained within the chapter, section or subsection, Such as used at the beginning this chapter for example. Example: Comment: Used to make the reader aware that the paragraph(s) that follow are examples of information possibly stated previously. Represents additional information that may or may not be relevant. Preface Note: Conveys information that should be considered important to the reader.

2.2

Page Layout
Headers and footers in this publication are designed to allow you to quickly identify your location. The documents part number and revision number appears in every header on every page. Odd numbered page footers indicate the current chapter, its title and current page number. Even page footers show the current section and its title, as well current page number.

Section 3.0 Computer Screen Output and Input


Within this publication different character styles are used to indicate computer input and output text. Character (input, output, and variable) styles are used and applied to the text within a paragraph so as to indicate direction. Computer screen output and input is also formatted using mono (fixed width) spaced fonts. Example: Fixed Output Example: Variable Output This paragraph denotes computer screen fixed output. Its output is fixed from the sense that it does not vary from application to application. This paragraph denotes computer screen output that is variable. Its output varies from application to application. Variable output is sometimes found placed between greater than and lesser than operators. For example: <variable_ouput> This paragraph denotes fixed input. Its typed input that will not vary from application to application. This paragraph denotes computer input that can vary from application to application. Variable input will normally be found placed between greater than and lesser than operators. For example: <variable_input>

Example: Fixed Input Example: Variable Input

Preface

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GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

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Preface

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

PDF Publication Conventions


Purpose: This section means to inform the reader on electronic publication conventions used in PDF files. Please become familiar with the conventions used in this electronic publication before proceeding.

Section 1.0 Helpful Search Tips Within Adobe Acrobat Documents


PDF Preface Page 17

1.1

How to Locate Items


Display "Bookmarks" in the left panel of the Acrobat window. Use the "Find" function to select applicable search options. Use the "Table of Contents" bookmark. Use the Index" bookmark.

"FIND" Function

Bookmarks

Figure 0-1 Acrobat "Find" Function

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

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Preface

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

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Table of Contents
Preface Publication Conventions ...................................................................................... 13
Section 1.0 Safety & Hazard Information ........................................................................... 13
1.1 1.2 Text and Character Representation................................................................................. 13 Graphical Representation ................................................................................................ 14 Table of Contents

Section 2.0 Conventions Used For General Information.................................................. 15


2.1 2.2 Document Paragraph and Character Styles .................................................................... 15 Page Layout..................................................................................................................... 15

Section 3.0 Computer Screen Output and Input ............................................................... 15

PDF Publication Conventions ...................................................................................... 17


Section 1.0 Helpful Search Tips Within Adobe Acrobat Documents .............................. 17
1.1 How to Locate Items ........................................................................................................ 17

Chapter 1 Introduction............................................................................................................ 29
Section 1.0 Responsibility of Purchaser............................................................................ 29 Section 2.0 Site Preparation Prior to Equipment Delivery ............................................... 29

Chapter 2 System Catalog...................................................................................................... 31


Section 1.0 Option Catalog Numbers ................................................................................. 31 Section 2.0 Base Scanner System...................................................................................... 32
2.1 2.2 Application ....................................................................................................................... 32 Configuration ................................................................................................................... 32

Table of Contents

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Table of Contents
Chapter 3 Room Planning ...................................................................................................... 33
Section 1.0 Recommended Layouts ................................................................................... 33
1.1 1.2 Injector Control ................................................................................................................ 35 Storage Cabinet .............................................................................................................. 35

Section 2.0 Component Dimensions .................................................................................. 36


2.1 2.2 2.3 2.4 2.5 Table and Gantry............................................................................................................. Power Distribution Unit.................................................................................................... Uninterruptable Power Supply......................................................................................... Operators Console ......................................................................................................... PET Host Computer Cabinet........................................................................................... 37 38 39 40 41

Section 3.0 Structural Requirements.................................................................................. 42


3.1 3.2 3.3 3.4 3.5 3.6 Suggested Ceiling Heights .............................................................................................. Table and Gantry Mounting Requirements ..................................................................... Floor Strength.................................................................................................................. Floor Levelness ............................................................................................................... Floor Vibration ................................................................................................................. Walls: Scan Window........................................................................................................ 42 42 43 43 43 44

Section 4.0 Network Connections....................................................................................... 44 Section 5.0 Radiation Protection......................................................................................... 44


5.1 5.2 X-ray Radiation Protection .............................................................................................. 44 Dose Rate from Radioactive Rod Source ....................................................................... 49

Chapter 4 Environmental Conditions.................................................................................... 53


Section 1.0 Temperature and Humidity Specifications..................................................... 53 Section 2.0 Temperature and Humidity Monitoring........................................................... 53 Section 3.0 Cooling Requirement ....................................................................................... 54 Section 4.0 Altitude .............................................................................................................. 54 Section 5.0 Electro-Magnetic Interference (EMI) ............................................................... 55
5.1 Page 20 Gantry.............................................................................................................................. 55 Table of Contents

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Table of Contents
5.2 5.3 5.4 5.5 5.6 5.7 5.8 Color Monitor ................................................................................................................... Console / Computer Equipment....................................................................................... Magnetic Media ............................................................................................................... PDU ................................................................................................................................. EMI Reduction ................................................................................................................. UPS ................................................................................................................................. Equipment EMI Envelopes ............................................................................................ 55 55 55 55 55 55 56

Chapter 5 Floor Loading and Weights .................................................................................. 57


Section 1.0 Floor Loading ................................................................................................... 57 Section 2.0 Mounting Data, Including Seismic.................................................................. 59

Chapter 6 Delivery Data.......................................................................................................... 71


Section 1.0 Van Delivery...................................................................................................... 71 Section 2.0 Delivery/Shipping Requirements & Considerations ..................................... 71 Section 3.0 Site Environmental Considerations................................................................ 73
3.1 3.2 Dust/Dirt Contamination................................................................................................... 73 Chemical Contamination.................................................................................................. 73

Section 4.0 For Crated Delivery .......................................................................................... 73 Section 5.0 Storage Requirements ..................................................................................... 74 Section 6.0 Gantry Considerations..................................................................................... 74 Section 7.0 Table Considerations....................................................................................... 78 Section 8.0 Console Considerations .................................................................................. 78

Table of Contents

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Table of Contents

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Table of Contents
Chapter 7 Power Requirements............................................................................................. 79
Section 1.0 Introduction....................................................................................................... 79 Section 2.0 System Input Power ......................................................................................... 79
2.1 2.2 2.3 2.4 2.5 2.6 2.7 2.8 2.9 Facility Source................................................................................................................. Main Disconnect Control ................................................................................................. Configuration ................................................................................................................... Rating .............................................................................................................................. Regulation ....................................................................................................................... Phase Imbalance............................................................................................................. Sags, Surges & Transients.............................................................................................. Microcuts ......................................................................................................................... Grounding........................................................................................................................ 79 80 80 80 80 80 80 81 81

Section 3.0 Recommended Power Distribution System ................................................... 82 Section 4.0 Uninterruptable Power Supplies (UPS) .......................................................... 83 Section 5.0 Power Audit....................................................................................................... 83 Section 6.0 Power Source Monitoring ................................................................................ 83 Section 7.0 Ground System ................................................................................................. 84

Chapter 8 Interconnection Data............................................................................................. 85


Section 1.0 Introduction....................................................................................................... 85 Section 2.0 Component Designators .................................................................................. 86 Section 3.0 Interconnect Runs, Wiring and Cables........................................................... 87
3.1 GEMS Supplied............................................................................................................... 3.1.1 Standard Length (Short) Cables......................................................................... 3.1.2 Non-Standard Length (Long) Cables ................................................................. Contractor (Customer) Supplied...................................................................................... 87 88 91 92

3.2

Section 4.0 Contractor Supplied Components .................................................................. 94


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GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

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Table of Contents
Section 5.0 UPS Interconnect ............................................................................................. 95
Table of Contents

Section 6.0 Typical Customer Supplied Wiring................................................................. 96


6.1 6.2 Primary Power Disconnect .............................................................................................. 96 Scan Room Warning Light & Door Interlock .................................................................... 97

Chapter 9 Final Pre-Installation Review................................................................................ 99


Section 1.0 Overview ........................................................................................................... 99 Section 2.0 Site Ready for Installation ............................................................................... 99
2.1 2.2 2.3 2.4 2.5 Dust/Dirt Contamination................................................................................................... 99 Chemical Contamination.................................................................................................. 99 Walls, Ceiling, and Floor.................................................................................................. 99 Phone Line....................................................................................................................... 99 Establish the Room Layout............................................................................................ 100

Section 3.0 Pre-Installation Checklist .............................................................................. 101

Chapter 10 Options and Accessories ................................................................................... 109


Section 1.0 CT Injectors..................................................................................................... 109
1.1 1.2 1.3 PercuPump CT Injection Systems............................................................................... 109 EnVision CT Injection Systems ................................................................................... 109 Liebel Flarsheim CT 9000 ADV Injectors .................................................................... 110

Section 2.0 Cameras & Imaging........................................................................................ 110


2.1 2.2 2.3 2.4 2.5 Kodak DryView PACS Link Laser Imaging .................................................................... Kodak DryView Laser Imaging System ......................................................................... AGFA Drystar 2000C Printers ....................................................................................... AGFA Drystar 3000 Dry Daylight Printer ....................................................................... Codonics NP-1660M Printer GEMS_AM ...................................................................... 110 111 111 111 112

Section 3.0 Print Camera Interface ................................................................................... 112 Section 4.0 Un-Interruptible Power Supplies (UPS)........................................................ 112
4.1 Powerware UPS ............................................................................................................ 112

Table of Contents

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DISCOVERY ST PRE-INSTALLATION

Table of Contents
Section 5.0 Slicker .............................................................................................................. 113

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Table of Contents

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Table of Figures
Figure 0-1 Acrobat "Find" Function ......................................................................................................... Figure 2-1 Discovery ST Base Scanner System ..................................................................................... Figure 3-1 Sample Room Layout, Cover Removal Clearances............................................................... Figure 3-2 DST System Service Clearances........................................................................................... Figure 3-3 Table and Gantry (Side View) .............................................................................................. Figure 3-4 Compact Power Distribution Unit (PDU) ................................................................................ Figure 3-5 Compact Power Distribution Unit (PDU) ................................................................................ Figure 3-6 Powerware 9330 UPS............................................................................................................ Figure 3-7 Operators Console / Computer (GOC1)................................................................................ Figure 3-8 PET Host Computer Cabinet (OC2)....................................................................................... Figure 3-9 Typical Scatter Survey (Head Filter) ...................................................................................... Figure 3-10 Typical Scatter Survey (Body Filter)....................................................................................... Figure 3-11 Location of Source Pin ........................................................................................................... Figure 3-12 Distance Measurement Locations.......................................................................................... Figure 4-1 Sample Room Layout, showing approximate EMI requirements ........................................... Figure 5-1 Typical Floor Anchor, Gantry and Table ................................................................................ Figure 5-2 Gantry - PET/CT CGs at Operating Position (SK4092003, Sheet 1, Rev 1) ......................... Figure 5-3 Gantry - PET/CT CGs at Service Position (SK4092003, Sheet 1, Rev 2)............................. Figure 5-4 Gantry - PET/CT CGs Entire Gantry (SK4092003, Sheet 1, Rev 3) ..................................... Figure 5-5 Gantry Leveler and Adjuster Locations - CT .......................................................................... Figure 5-6 Discovery ST PET Base......................................................................................................... Figure 5-7 Gantry Leveler and Adjuster Locations - PET........................................................................ Figure 5-8 Patient Table - Discovery ST ................................................................................................. Figure 5-9 Power Distribution Unit (PM).................................................................................................. Figure 5-10 Operators Console / Computer (GOC1)................................................................................ Figure 5-11 PET Host Computer Cabinet.................................................................................................. Table of Figures 17 32 33 34 37 38 38 39 40 41 45 46 49 52 56 59 60 61 62 63 63 64 65 66 67 68 Table of Figures

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GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Figure 5-12 Gantry/Table Mounting Dimensions ...................................................................................... 69 Figure 6-1 Gantry Strap Location............................................................................................................ 71 Figure 6-2 CT Gantry with Shipping Dollies and Side Rails.................................................................... 74 Figure 6-3 PET Gantry Base with Shipping Dollies and Side Rails ........................................................ 75 Figure 6-4 PET Gantry Image Ring with Shipping Dollies and Side Rails .............................................. 75 Figure 6-5 PET Gantry Trailer with Shipping Dollies and Side Rails ...................................................... 76 Figure 6-6 Table with Shipping Dollies ................................................................................................... 77 Figure 7-1 System Ground Map.............................................................................................................. 84 Figure 8-1 System Interconnect Diagram 2342229 SCH........................................................................ 89 Figure 8-2 Console Interconnect Diagram 2346059 SCH....................................................................... 90 Figure 8-3 Interconnection Runs............................................................................................................. 93 Figure 8-4 Typical UPS Interconnect ...................................................................................................... 95 Figure 8-5 Typical UPS ........................................................................................................................... 95 Figure 8-6 Primary Power Disconnect (A1) Fusible Disconnect and Magnetic Contactor ................... 96 Figure 8-7 Primary Power Disconnect (A1)............................................................................................. 97 Figure 8-8 Typical Customer Supplied Scan Room Warning Light Connection to PM ........................ 97 Figure 8-9 Typical Door Interlock ........................................................................................................... 98 Figure 9-1 Hole Locations ..................................................................................................................... 100

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Table of Figures

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Table of Tables
Table 2-1 System Options Catalog (Part) Numbers............................................................................... 32 Table 3-1 Equipment to be stored in storage cabinet............................................................................. 35 Table 3-2 Dimensions of Components ................................................................................................... 33 Table 3-3 Floor Loadings ....................................................................................................................... 42 Table 3-4 Shielding Requirements Scaling - Axial Imaging ................................................................... 47 Table 3-5 Shielding Requirements Scaling - Helical Imaging ................................................................ 48 Table 3-6 Dose Rate at Various Distances ............................................................................................ 51 Table 4-1 Cooling Requirements (Worksheet) ....................................................................................... 54 Table 5-1 Discovery ST System Floor Loading...................................................................................... 57 Table 6-1 Typical Crated Delivery Sizes and Weights ........................................................................... 73 Table 6-2 Size of CT Gantry & Dollies, with and without Side Rails ...................................................... 74 Table 6-3 Size of PET Gantry & Dollies, with and without Side Rails .................................................... 76 Table 6-4 Size of Table & Dollies ........................................................................................................... 77 Table 7-1 Facility Power Requirements ................................................................................................. 82 Table 8-1 Component Designators ........................................................................................................ 86 Table 8-2 GEMS Optional Cables (Short Length Run) - UL Information................................................ 88 Table 8-3 GEMS Supplied Cables (Long Run) - UL Information............................................................ 91 Table 8-4 Runs 1, 2, 3, 8 and 9 Connections......................................................................................... 92 Table 8-5 Contractor-Supplied Components.......................................................................................... 94 Table 9-1 Specific Site Requirements .................................................................................................. 101 Table 10-1 PercuPump CT Injection Systems ..................................................................................... 109 Table 10-2 EnVision CT Injection Systems.......................................................................................... 109 Table 10-3 Liebel Flarsheim CT 9000 ADV Injectors........................................................................... 110 Table 10-4 Kodak DryVIew PACS Link Laser Imaging .......................................................................... 110 Table 10-5 Kodak DryView Laser Imaging System................................................................................ 111

Table of Table

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Table of Tables

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Table 10-6 AGFA Drystar 2000C Printers ............................................................................................. Table 10-7 AGFA Drystar 3000 Dry Daylight Printers ........................................................................... Table 10-8 Codonics NP-1660M Printer GEMS_AM ............................................................................ Table 10-9 Print Camera Interface ........................................................................................................ Table 10-10 Powerware UPS .................................................................................................................. Table 10-11 Slicker ..................................................................................................................................

111 111 112 112 112 113

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Table of Table

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Chapter 1 Introduction
This direction contains physical and electrical data necessary for planning and preparing a site. Pre-installation work is defined as site preparation for installation of the GE Discovery ST scanner. It is the purchasers responsibility to arrange and pay for this work. Site Planning work includes: Installing electrical conduit, junction boxes, ducts, outlets, and line safety switches. Installing AWG stranded copper interconnection wiring. The electrical contractor shall ring out and tag all wires at both ends. Color-coded wires are recommended for easier identification. Wires shall be continuous without splices. Ground wires must conform to local codes. Any site renovation. Product alterations and modifications not specifically included in the sales contract. 1 - Introduction

All work must conform to local building and safety codes. Unless specifically mentioned, GE Medical Systems does not provide or install wires, conduits, junction boxes, and ducts as illustrated in this publication. Prior to construction or approval, all Discovery ST site plans, preliminary concepts and final working drawings must be reviewed by General Electric Headquarters Architectural Planning. For complete information regarding your site-specific room layout, contact your local General Electric sales representative.

Section 1.0 Site Readiness


The following MUST be completed before installation work can begin for a GE DST scanner: NOTICE Finished wall, ceiling, floors & millwork Active phone line and network connection

Power available to A1, w/provision for LOTO An improperly prepared site (i.e., one that is in a state of construction) can result in increased installation time. A DST scanner installed in a dirty environment is more prone to contamination, which can result in decreased reliability and increased scanner downtime.

Section 2.0 Purchasers Responsibilities


Site Planning is all work necessary to plan and prepare a site for equipment installation. To avoid delay, confusion, and waste of personnel resources, complete the following pre-installation work: Procure required materials. Prior to delivery of system components, install required material. Complete all alterations and modifications that are not specifically included in the sales contract.

Chapter 1 - Introduction

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Section 3.0 Site Preparation Prior to Equipment Delivery


Determine room dimensions and verify entry doors are large enough to bring scanner system through. Install table/gantry floor duct. Install junction boxes of correct size with covers at locations shown in installation plan. Install conduit, duct, and raceway. Install power supply of correct voltage output and adequate KVA rating. Install local disconnects, including proper over-current protection. Install Unistrut or other suitable support work for mounting equipment on walls or from ceiling. Broadband: To take maximum advantage of the GE Service remote diagnostic and services capabilities, a network connection (CAT 5) with internet access is preferred. This allows GE to better provide service and even perform proactive maintenance on your GE system. For more information on how GE can provide a secure connection using your facilitys internet connection, please inquire through your local GE Service or Sales representative. If a LAN connection is not available at your site, a voice grade analog telephone line will allow GE to connect to your system, however some capabilities may be limited due to bandwidth restrictions. Telephone: Supply 2 voice-grade telephone lines. One line must be a direct number from outside the facility do not route this line through a telephone switchboard. Telephone line operating charges are paid by customer. Complete the Pre-installation Check List in Chapter 9.

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Section 3.0 - Site Preparation Prior to Equipment Delivery

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Chapter 2 System Catalog


Section 1.0 Option Catalog Numbers
The following is a list of system options requiring site planning work for the Discovery ST system. For a complete list of system options, contact your local GE Medical Systems Sales representative or visit us at http://www.gemedical.com.

CATALOG NUMBER
Uninterruptible Power Supply P5051PS International Dolly Set CT - B7850LD PET - TBD Rear Cable Cover TBD GE Color Printer E7014LA Remote Color Monitors B7710WM B7530RC SmartScore Option B7850KC Performance Network Kits K9000L Switched Network Kit B7500PM Bar Code Reader B7540RB Options and Accessories CT Injectors Laser Cameras Seismic Kit CT - R4390JC PET - TBD

OPTION DESCRIPTION
Powerware 9330G 10KVA UPS For International customers, if dollies are required. 2 System Catalog

Optional rear cable cover for Discovery ST upgrades GE Color Printer includes Cassette Ultra LCD monitor. Remote 20 inch diagonal color monitor. EKG Monitor and Recording Device 6 Node, 10/100 Mbit Auto Sensing ConnectPro Option provides a direct interface to HIS/RIS Discovery ST Bar Code Reader See Chapter 10, Section 1.0 on page 109. See Chapter 10, Section 2.0 on page 110 Earthquake zones

Table 2-1 System Options Catalog (Part) Numbers

Chapter 2 - System Catalog

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Section 2.0 Base Scanner System


2.1 Application
The Discovery ST scanner system includes hardware and software to support patient data acquisition and image analysis for whole-body positron emission tomography and computed tomography.

2.2

Configuration
The base scanner system is configured as shown. All scan and analysis functions are controlled from the operator's console (not shown).

Figure 2-1 Discovery ST Base Scanner System

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DISCOVERY ST PRE-INSTALLATION

Chapter 3 Room Planning


Section 1.0 Recommended Layouts
To discuss specific needs, consult your local GE Sales and Service Representative. Figure 3-1 and Figure 3-2 show two of many possible room layouts (a third example is shown in Figure 4-1, on page 56). For exact equipment sizes, refer to Section 2.0. Remember, sufficient space must be maintained around equipment for full operation, service, and safety. Note: Other room arrangements are possible. Cable length is an important consideration in room layout. The Discovery ST system ships with a Long Cable set (2346968 cable collector). A set of shorter cables are available if needed.

Figure 3-1 Sample Room Layout, Cover Removal Clearances

Chapter 3 - Room Planning

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Figure 3-2 DST System Service Clearances Page 34 Section 1.0 - Recommended Layouts

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

COMMON DIMENSIONS AND CLEARANCES


System Service Back cover removal (rear clearance) Front/Back cover removal (side clearance) Gantry service side to obstruction Area around the PDU Area around the A1 breaker box Area between the table down foot end to obstruction 36.0" (913.5mm) 36.0" (913.5mm) 36.0 (913.5mm) 36.0 (913.5mm) 42.0 (1067mm) 36.0 (913.5mm)

Options Ceiling Pedestal mount lowest point to floor Injector or Monitor System Operation Finished ceiling to floor Table max extension head end with extender from Center Line Table extension head end with extender to obstruction Table in lowest position w/cradle at home position to Center Line Back of Console to wall Back of Console Host Cabinet to wall Back of Optional Storage Cabinet to wall Back of PDU to wall 108.0 (2743mm) 80.0 (2030.0mm) 6.0 (152.0mm) 126.5 (3209.0mm) 6.0 (152.0mm) 6.0 (152.0mm) 6.0 (152.0mm) 3 Room Planning 6.0 (152.0mm) 96.0 (2438.5mm)

Typicall Room Dimensions Scan Room Control Room 22 X 22 (6 m X 6 m) 110" X 126" (3.4 m X 3.8 m)

Additional dimensions are available in Figure 3-3 through Figure 3-7 of this document. Consult your local General Electric Installation Specialist for your appropriate room specifications.

1.1

Injector Control
It is recommended that a suitable work area be provided for the injector control that is within reach of the operator console.

1.2

Storage Cabinet
A storage cabinet is provided by GEMS to store all supplied service equipment. This 30 lb. storage cabinet (24" D x 26" W x 42" H) should be located in the scan room suite area, for easy service access. Refer to Figure 3-1. ITEM QA Phantom (water filled) 20CM Phantom 48CM Phantom Phantom Holder SIZE 20 x 15 cm 20 x 7 cm 48 x 7 cm 25 x 25 cm WEIGHT (TOTAL) 12 lb 13 lb 25 lb 8 lb

Table 3-1 Equipment to be stored in storage cabinet Chapter 3 - Room Planning Page 35

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2 ITEM Gantry Display FE Box (Purple) Rear Cover Dollies Front Cover Dollies Install Support Kit (box) Tube Hoist Kit Gantry Control Pad SIZE 62 x 13 cm 30 x 38 x 30 cm 158 x 82 cm 30 x 30 x 38 cm 77 x 8 cm and 38 x 15 cm 27 x 20 cm

DISCOVERY ST PRE-INSTALLATION WEIGHT (TOTAL) 2 lb 15 lb 25 lb 20 lb 20 lb 4 lb

85 x 20 cm and 85 x 15 cm 35 lb

Table 3-1 Equipment to be stored in storage cabinet (Continued)

Section 2.0 Component Dimensions


DESCRIPTION Discovery ST CT/PET System Gantry (PET/CT) Table Power Distribution Unit (PDU) Operator's Console/ Computer PET Host Computer Box Color Monitor Color Printer Powerware 9330 UPS MODEL/CATALOG WIDTH NUMBER INCH MM S9100LA (4 Slice) S9101LA (8 Slice) S9100LA (4 Slice) S9101LA (8 Slice) P5050RT P5050RD B7858CC Unknown (future) E7014LA (OPTION) 91.9 29.3 30 48 22 23 2297 740 762 1219 550 501 584 990 106.4 2659 136.5 3470 22 39 25 19.1 18 31 559 991 620 485 457 790 76.9 30 50 33.5 25.3 19.6 7 45 1923 760 1270 851 770 498 178 1140 DEPTH INCH MM HEIGHT INCH MM

B7850MM (OPTION) 19.7 P5051PS (OPTION) 39

Table 3-2 Dimensions of Components

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Section 2.0 - Component Dimensions

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2.1

Table and Gantry

Figure 3-3 Table and Gantry (Side View)

Chapter 3 - Room Planning

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2.2

Power Distribution Unit

NOTE: DIMENSIONS ARE IN INCHES (MILLIMETERS).

7.3 (185) 50 (1270) 22 (559) 14.5 (368)

4.5 (114) 4.7 (119) 7.3 (185) 3.94 (100) 30 (762)

Figure 3-4 Compact Power Distribution Unit (PDU)

MINIMUM AIR FLOW 6 CLEARANCE (152)


NOTES: DIMENSIONS ARE IN INCHES (MILLIMETERS).

22 (559)

INDICATES AIR FLOW (Convection):

36.0 (914) SERVICE AREA SERVICE AREA 30 (762) 24.0 (610)

72 (1829) 50 (1270)

Figure 3-5 Compact Power Distribution Unit (PDU) Page 38 Section 2.0 - Component Dimensions

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2.3

Uninterruptible Power Supply


The Powerware 9330 UPS has been selected for use with the Discovery ST scanner. For more information on this product, see the OEMs website at www.powerware.com.

Chapter 3 - Room Planning

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3 Room Planning

Figure 3-6 Powerware 9330 UPS

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

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2.4

Operators Console

INDICATES AIR FLOW

Figure 3-7 Operators Console / Computer (GOC1)

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Section 2.0 - Component Dimensions

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2.5

PET Host Computer Cabinet

Figure 3-8 PET Host Computer Cabinet (OC2)

Chapter 3 - Room Planning

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Section 3.0 Structural Requirements


3.1 Suggested Ceiling Heights
A ceiling height of 108" (2743mm) is recommended. A ceiling height of 90" (2286mm) is the absolute minimum acceptable height for gantry installation.

3.2

Table and Gantry Mounting Requirements


Note: It is the purchaser's responsibility to provide an approved support structure and mounting method. General Electric is not responsible for any failure of the support structure or method of anchoring. Table and gantry mounting dimensions are shown in Figure 3-3. Refer to Chapter 5 for additional details of floor loadings, component weights, and Gantry and Table installation and anchoring. Anchor gantry and table to floor by a means that will maintain their relative alignment and meet applicable building and other local codes, including seismic structural mounting requirements. Floor structure must be capable of withstanding the occupied weight of table and gantry, and the individual contact area loading of these components. Refer to Table 3-3 for each of the three (3) major components of the Discovery ST system. COMPONENT EFFECTIVE FLOOR MAXIMUM FOOT LOAD AREA * PAD PRESSURE ** Kgf/sq meter (lbf/sq ft) Sq meters (sq feet) MPa (psi) 1185 (243) 6180 (1266) 490 (100) 1.34 (14.4) 0.34 (3.7) *** 1.39 (15) 1.5 (212) 1.9 (280) 1.4 (196) FLOOR LOADING

CT Gantry PET Gantry Table (2 meter)

* Area bounded by outermost footpads (not stabilizers). ** Assumed floor pad area of 4.123 sq inches. *** Area bounded by four (4) front foot pads while gantry is in operating position. Table 3-3 Floor Loadings Any installation on a floor with a rating less than the values lilsted in Table 3-3 should be braced to bring it up to this requirement. Localized bracing to support the concentrated loads at the floor contact sections should also be provided. Support areas of the patient table and gantry must rest on solid concrete or other basic flooring, not resilient tile or carpeting which will slowly yield over a period of time and disturb alignment of table to gantry. Factors that could cause misalignment between gantry and table due to floor sag should be considered. The cradle can potentially carry a 450 lb (205 kilogram) patient. Center of gravity changes as cradle cantilevers. Take into consideration all other moving weights such as gurneys or personal equipment. Refer to Chapter 5 for gantry and table mounting details. No part of floor surface within table and gantry, nor the two interface areas between table and gantry, should be higher than the support area for table and gantry.

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Section 3.0 - Structural Requirements

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DISCOVERY ST PRE-INSTALLATION

A qualified person must verify that the site and method of anchoring are adequate to support loads and maintain table-to-gantry alignment. Location of supporting beams and columns may dictate position of table-to-gantry assembly. Use of flush floor duct or conduit in the floor may significantly affect floor strength. The method and placement of anchoring through bolts must not reduce structural strength of floor.

3.3

Floor Strength
Concrete floors must have a minimum strength of f'c = 2000 psi (1.4 X 107 Pa) at 28 days for mounting floor anchors. It is the responsibility of each customer to have appropriate tests performed to determine and measure concrete strength. Your GE Service representative can assist you. Consult GE Installation Support Services for further details.

3.4

Floor Levelness
The Discovery ST Room floor levelness requirement is important for accurate patient positioning. Floor levelness in the Scan Room must not be greater than 0.3125 (8mm) between depression and high spots over any 120 in. (3048 mm) distance within the area of the gantry and the area around the table (see the envelope shown in Figure 3-1 or Figure 3-2).

3.5

Floor Vibration
The Discovery ST equipment may be sensitive to vibration in the frequency range of 0.5 to 20 Hz depending on the amplitude of the vibration. It is the customers responsibility to contract a vibration consultant or qualified engineer to implement design modifications to meet the specific limits, However, it is ultimately the customer/architect/engineer responsibility to design the site solution.

3.5.1

Steady State Vibration


The maximum steady state vibration transmitted through the floor should not exceed 10-3 m/s2 rms maximum single frequency above ambient baseline from 0.5 to 80 Hz (measured in any 1 hour during a normal operating period).

3.5.2

Transient Vibration
The behavioral characteristics must be such that any measurable transient disturbance must also be minimized to less than 0.01 m/s2 peak-to-peak.

3.5.3

Equipment Location
To minimize the interference, the Discovery ST equipment should be placed on a solid floor, located as far as possible from the following vibration sources: Parking lots Roadways Subways Trains Hallways Elevators Heliports Hospital power plants containing pumps, motors, air handling equipment and air conditioning units Chapter 3 - Room Planning Page 43

3 Room Planning

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3.6

Walls: Scan Window


The recommended patient viewing window dimensions are 48 in. wide by 42 in. high (1219 mm x 1067 mm). The location of the window is dependent on the position of Operator Workspace position (see Figure 3-1). Note: The operator at the Operator Workspace must be able to view the patient during a scan.

Section 4.0 Network Connections


The Discovery ST system is connected to the network through the Console. A patch cable (not to exceed 10 feet) is used to connect the console to a wall box. Three IP addresses are required for CT host computer, PET host computer, and eNTEGRA workstation.

Section 5.0 Radiation Protection


Protective measures must be considered for the following: X-ray radiation from the CT equipment (see Figure 5.1) Gamma radiation from the PET radioactive rod source in the gantry (see Section 5.2)

Scanner-room shielding requirements should be reviewed by a qualified radiological health physicist taking into consideration equipment placement, weekly projected work-loads, and materials used for construction of walls, floors, ceiling, doors, and windows.

5.1

X-ray Radiation Protection


The main X-ray beam is collimated within the transaxial slice of the patient. During CT scanning there will be radiation in the Scan Room resulting from scattered radiation from the patient, and leakage from the X-ray housing. The scatter depends on the shape and size of the patient. The example plots shown in Figure 3-9 depicts measurable radiation levels within the scanning room while scanning a 32 cm CTDI phantom (body) and Figure 3-9 while scanning a 20 cm water phantom (head) with the technique shown. Note: All measurements have an accuracy of 20% because of measurement equipment, technique, and system-to-system variation.

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Section 4.0 - Network Connections

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2 Note:

DISCOVERY ST PRE-INSTALLATION

These measurements were performed without the PET gantry. The addition of the PET gantry minimally reduces the dose from the back of the CT gantry, but the dose around the front (table side) is unchanged.
HEAD PHANTOM ISO CONT OUR LEVELS: 0.0375, 0.075, 0.15, 0.305, mR/SCAN 100 mAs/scan, 140 kV, 4 x 5.00mm Scan Acquisition

.0375

.075

.15

.3 .3 .15 .075 .0375

50 Inches

HEAD PHANTOM ISO CONT OUR LEVELS: 0.0375, 0.075, 0.15, 0.30 mR/SCAN 100 mAs/scan, 140 kV, 4 x 5.00mm Scan Acquisition

.0375

.075

.15

.3

.3

.15

.075

.0375

50 Inches

Figure 3-9 Typical Scatter Survey (Head Filter) Chapter 3 - Room Planning

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BODY SCATTER PHANTOM ISO CONT OUR LEVELS: 0.075, 0.15, 0.3 AND 0.6 mR/SCAN 100 mAs/scan, 140 kV, 4 x 5.00mm Scan Acquisition

.075

.15

.3

.6

.6

.3

.15

.075

50 Inches

BODY SCATTER PHANTOM ISO CONT OUR LEVELS: 0.075, 0.15, 0.3 AND 0.6 mR/SCAN 100 mAs/scan, 140 kV, 4 x 5.00mm Scan Acquisition

.075

.15

.3

.6

.6

.3

.15

.075

50 Inches

Figure 3-10 Typical Scatter Survey (Body Filter)

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Section 5.0 - Radiation Protection

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Use the correction factors of Axial Imaging shown in Table 3-4 to adjust exposure levels to the usual scan technique at your site.

CHANGED PARAMETER
mAs 80 kV 120 kV 140 kV 4 x 3.75mm images 4 x 2.5mm images 4 x 1.25mm images 1 x 1.25mm images 2 x 0.625mm images

MULTIPLICATION FACTOR
new mAs/100 0.21 0.71 1.0 0.82 0.59 0.40 0.20 0.10

Table 3-4 Shielding Requirements Scaling - Axial Imaging Axial # scan seconds = (# images * gantry 360_rotation time)/4 (for 5mm images or less).

Chapter 3 - Room Planning

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Use the correction factors of Helical Imaging shown in Table 3-5 to adjust exposure levels to the scan technique at your site.

CHANGED PARAMETER
mAs 80 kV 120 kV 140 kV 15mm table travel/rotation (10/7.5/5mm image thickness @ premium IQ mode) 11.25m table travel/rotation (7.5/5/3.75mm image thickness @ premium IQ mode) 7.5mm table travel/rotation (5/3.75/2.5mm image thickness @ premium IQ mode) 3.75mm table travel/rotation (2.5/1.25mm image thickness @ premium IQ mode) 30mm table travel/rotation (10/7.5/5mm image thickness @ standard IQ mode) 22.5mm table travel/rotation (7.5/5mm image thickness @ standard IQ mode) 15mm table travel/rotation (5/3.75/2.5mm image thickness @ standard IQ mode) 7.5mm table travel/rotation (2.5/1.25mm image thickness @ standard IQ mode)

MULTIPLICATION FACTOR
new mAs/100 0.21 0.71 1.0 1 0.82 0.59 0.40 1 0.82 0.59 0.40

Table 3-5 Shielding Requirements Scaling - Helical Imaging Helical # scan seconds = ((# images* image thickness/table advance per rotation) + 1) * gantry 360_rotation time). Note: Premium Image Quality (IQ) mode requires 50-70% the mAs of standard IQ mode for comparable LCD and noise (dependent on image thickness and table advance per rotation). Values, in mR per scan, apply to both 50 Hz and 60 Hz operation.

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Section 5.0 - Radiation Protection

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5.2

Dose Rate from Radioactive Rod Source


Operation of the PET scanner requires the use of a single radioactive pin source. The source is stored in a shielded container inside the gantry, and remains within the gantry during use. The source is automatically withdrawn from its container before each use, and is automatically returned to the container after each use. Dose rates described in this document are estimates based on measurements taken under specific measurement conditions that are described in detail for each measurement. Since the measurement conditions vary at every scanner installation (due to differing room geometries, the presence of other equipment or shielding material, etc.), these measurements should be taken as guidelines only.

5.2.1

Radioactive Source Pin


PET images are generated by measuring radiation arising from electron positron annihilation events within the patient. No external radiation source is required to generate this data. The pin radiation source is never used for scanning a patient. However, the pin is required for the following functions: 1.) To calibrate the scanner detectors and electronics. 2.) To assess the relative performance of the scanners detector channels so that differences in individual detectors efficiency can be accounted for in the reconstruction process. 3 Room Planning To achieve these functions, the PET scanner uses a radioactive source, referred to as source pin. The pin contains Ge68, an isotope with a half-life of 287 days. The normalization source pin is referred to as "low activity pin." The pin has an initial activity level of 3mC. When not in use, the source pin is housed in a lead storage container located inside the PET part of the gantry. Facing the gantry from the table side, this storage container is in the lower middle back of the gantry (see Figure 3-11).

Source Storage Container Figure 3-11 Location of Source Pin When the pin is in use, it is located inside the gantry near the wall of the patient port. Depending on the task the pin is performing, it may be held in a fixed location or rotated around the circumference of the patient port at a speed of 20 revolutions per minute (one revolution per three seconds). The pin is transferred from the storage container to its position near the patient port, and returned to the storage container after use, by a mechanical system under software control. Radiation indicators are displayed on both the gantry control panels and the operators keypad when any pin source is removed from the storage container.

Chapter 3 - Room Planning

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5.2.2

Dose Rates with Pin Source Stored


When the pin is stored in the lead container, and no other sources are present in the scanner room, the maximum dose rates on Discovery ST are directly over the source loader. Only one pin is used, and this pin has only 3 mCi or less activity. The exposure rate at the cover is specified to be 2mR/ hr or less.

5.2.3

Dose Rates with Pin Source in Use


The dose rates were measured in the following conditions: 1.) Pin source rotating around the patient port. 2.) Patient table was lowered to its lower limit (55 cm above the floor). 3.) All measurements were performed at a height corresponding to the center of the patient port. The results of these experiments, measured along the central axis of the scanner, are summarized in Table 3-6 (distances are measured from the frontmost imaging slice; positive distance is in the direction towards the scanner table).

5.2.4

Gamma Ray Protection


A number of radioactive substances, of various levels of stability are used by the PET unit of the Discovery ST system. This material is necessary in imaging procedures. Before the suite is operational, unstable material may be on the premises. It is very important to recognize that clear and significant hazards from ionizing radiation may exist at the site, as it is undergoing preparation. Other equipment may be in place and operational at this time. This may include such equipment as X-ray systems and CT scanners (other than Discovery STs own CT unit). Calibration source may be on the site at some time during the preparation process, as well as after the PET imager has been put into operation. A cyclotron may be operational at the site. Definite steps should be taken to insure the safety of workers, patients, and visitors, during all phases of the construction, installation and operation of the facility.

Note:

By the time the site is ready to have radioactive material brought in, the licensing process must be complete. The site must be properly licensed before receiving radioactive material.

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Section 5.0 - Radiation Protection

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5.2.5

Protection of Equipment
It is important that background radiation be kept to a minimum. The coincidence detection used in a PET system allows a moderate amount of external singles events. The DST system has been found to have less than 1% deadtime if the external field is below 1 mR/hr from a single source. Because area background can be more general than a single source, a lower limit is appropriate. If the area dose rate is maintained to less than 0.2 mR/hr (due to 511 or lower energy gamma rays) at the covers, detector deadtime should not exceed 1%. Radioactive sources must be stored in approved shielded containers. It is recommended that any radioactive source not specifically designed to be housed in the gantry lead pig be stored in a separate room (hot lab) adjacent to, and accessible from, the Scan Room. This hot lab should be near the cyclotron (if used). Doses should be prepared in the same area. Consideration should be given to the placement of the gantry in relation to existing X-ray, Magnetic Resonance, or Nuclear diagnostic equipment. Magnetic interference above 1.0 gauss, at the surface of PET components, can adversely affect the image quality. Good shielding techniques must be implemented in order to avoid this type of interference. Some procedures involve the use of radioactive water. This will result in the patient exhaling radioactive carbon dioxide. This carbon dioxide must be contained in order to avoid adversely affecting the image quality. Some PET procedures require the use of radioactive gases. This too can result in compromising image quality if not properly controlled.

The escape of radioactive gases, if not properly confined, can cause unnecessary exposure to clinical staff. All sources must be properly stored in appropriate enclosures to provide adequate protection to all in the suite.

5.2.7

Barriers Partitions and Shielding


Appropriate barriers such as walls, lead-shielded glass, lead shields etc. must be installed to protect staff from unnecessary exposure to radiation. A qualified radiological health physicist must be consulted in the design of walls and safety barriers to assure proper attenuation. Keep in mind that patients become significant sources of radioactivity. Consideration should be given to maximize the distance between the patient and operator during the uptake and acquisition phases of scan procedures.

5.2.8

Sources of Radiation
A number of common radio nuclides will be used in the Discovery ST system. These radio nuclides will either be produced at the site, or brought to the site from an outside source. In either case, these devices have relatively short half-life (2 min. to 110 min. maximum) and as such decay to benign levels fairly quickly. Typical positron emitting isotopes include: Carbon-11, Nitrogen-13, Oxygen-15, and Fluorine-18. Table 3-6 shows the dose rate at various distances. The measurements have been taken at various locations around the equipment. These were measured without the CT gantry. Use the illustration in Figure 3-12 to understand the data in table Table 3-6.

DISTANCES
Dose rate per mCi mR/hr/mCi

-2m
0.13

-1m
0.77

Front Slice
3.20

+1m
0.40

+2m
0.11

+3m
0.04

Table 3-6 Dose Rate at Various Distances

Chapter 3 - Room Planning

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5.2.6

Protection of Personnel

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

D = 3M (910")

D = 2M (67")

D = 1M (34")

D = 0M

D = -1M (-34")

D = -2M (-67")

Figure 3-12 Distance Measurement Locations

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Section 5.0 - Radiation Protection

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Chapter 4 Environmental Conditions


Ratings and duty cycles of PET-CT subsystems apply if site environment meets the standards of this section. Maintain the environmental conditions listed below at all times; including, for example, overnight, weekends and holidays. If air conditioning is not working, shut down the Discovery ST system. When the system is shut down for major repair, air conditioning may be shut down also.

Section 1.0 Temperature and Humidity Specifications


Ambient Temperature: (Fahrenheit and Celsius) Scan Room: For patient comfort, maintain a temperature of 65 75 F (18 24 C). When the scan room is unoccupied, table and gantry temperature limitations are 60 75 F (15 24 C). Control Room (including Console/Computer): Maintain 60 75 F (15 24 C). Equipment Room: If a separate equipment room is used to house the PDU, the allowable temperature range is 60 84 F (15 29 C). 4 Environmental Conditions

Store media (cartridges) in long-term storage in same temperature range as host computer. Store media in the host computer environment for one-half hour before use. Maintain relative humidity of 30% 60% (non-condensing) during operation (all areas). The maximum temperature rate of change is 5 F/hr (3 C/hr). The maximum relative humidity rate of change is 5% RH/hr.

Section 2.0 Temperature and Humidity Monitoring


Locate computing subsystems in an area with the environment specified in Section 1.0, above. First, assess your environments heat and humidity. If necessary, temporarily install a temperature and humidity recorder close to where the gantry will be installed. Note readings before installation and again after installation to verify true temperature and humidity conditions for your environment. Consider your HVAC needs and redundancy. You may wish to consider an air conditioner with two compressor units rather than one. A backup (redundant) air conditioner permits PET-CT system operation during an extended repair of the primary air conditioner.

Chapter 4 - Environmental Conditions

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Section 3.0 Cooling Requirement


Use Table 4-1 to assist in cooling requirements planning. Over half the cooling used by your scanner is required for gantry operation. For patient comfort, locate a wall air-conditioning vent at floor level beside and behind gantry to meet both gantry cooling needs and provide patient comfort.

ROOM => SYSTEM COMPONENT SCANNER SYSTEM


1. Gantry minimum (See NOTE 1) Gantry recommended (See NOTE 1) Gantry growth (See NOTE 1) 2. Table 3. Power distribution unit 4. Operator's console/computer with two monitors SYSTEM TOTAL (MINIMUM) SYSTEM TOTAL (RECOMMENDED) SYSTEM TOTAL (GROWTH) (See NOTE 1)

SUITE BTU/HR WATT


24,400 31,000 41,000 1000 16,000 11,000 52,400 59,000 69,000 7150 9120 12000 290 4700 3240 8800 10,550 12,600

SELECTED OPTIONS
Powerware UPS Remote Color Monitor TV camera TV monitor 2500 1178 34 300 732 345 10 88

ROOM TOTAL (SEE NOTE 2)


NOTE 1: With 75 scan rotations per patient, minimum gantry cooling is enough for up to three patients per hour. Recommended cooling is enough for up to four patients per hour. Use growth BTU/hr. to size cooling for future, more powerful X-ray tubes. NOTE 2: Cooling requirements do not include cooling for room lighting, personnel or nonPET-CT equipment. Table 4-1 Cooling Requirements (Worksheet)

Please refer to Figure 3-3, Figure 3-5 and Figure 3-7, in Chapter 3, Section 2.0, for component air flow requirements.

Section 4.0 Altitude


System operating altitude is from mean sea level to 10,000 ft. (3050 meters).

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Section 5.0 Electro-Magnetic Interference (EMI)


5.1 Gantry
Locate gantry in ambient static magnetic fields of less than 10-4 tesla (1,000 milligauss) to guarantee specified imaging performance. Ambient AC magnetic fields must be below 10-6 tesla (10 milligauss) peak.

5.2

Color Monitor
Locate color monitors in ambient static magnetic fields of less than 5 x 10-5 tesla (500 milligauss) to guarantee color purity and display geometry. See Figure 4-1.

5.3

Console / Computer Equipment


Locate computer equipment in ambient static magnetic fields of less than 10-3 tesla (10,000 milligauss) to guarantee data integrity. See Figure 4-1.

Locate magnetic media in ambient static magnetic fields of less than 10-3 tesla (10,000 milligauss).

5.5

PDU
The PDU produces an electromagnetic field that radiates outward from its cabinet in all directions. Do not place sensitive electronics (e.g., console or computer equipment) within one meter (1m) of the Power Distribution Unit., in any direction (including above or below). See Figure 4-1.

5.6

EMI Reduction
If fields of excessive EMI are known or suspected to be present, consult GE Medical Systems Sales & Service for recommendations. Consider the following if you attempt to reduce EMI: External field strength decreases rapidly with distance from source of magnetic field. External leakage magnetic field of a three-phase transformer is much less than that of a bank of three single phase transformers of equivalent power rating. Large electric motors are a source of substantial EMI. High-powered radio signals are a source of EMI.

Maintain good shielding of cables and cabinets.

5.7

UPS
The Uninterruptable Power Supply (UPS) provides a consistent power supply to various electrical components of the system. Also, it continues to provide electrical power to components during a site-wide power outage so components can be safely shut down. Chapter 4 - Environmental Conditions Page 55

4 Environmental Conditions

5.4

Magnetic Media

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

5.8

Equipment EMI Envelopes

Range of PDU's EMI is 1m (39") in ALL directions. Do not place any electronics within this area!

UPS

GE Storage Cabinet

Slave Monitor (option) Laser Camera (option)

Power Distribution Unit

Operator's Console
Range of PDU's EMI is 1m (39") in ALL directions. Do not place any electronics within this area!

TV Monitor (not GE)

1m (3

9")

Injector Control (option)

Monitors are sensitive to EMI. Do not place an EMI source within 1m (39") of monitors, in ANY direction.

Patient Table

TV Camera (not GE) Supplied) (Not GE

Gantry

Note: Drawing is not to scale

Counter w/sink and Base Cabinets

Figure 4-1 Sample Room Layout, showing approximate EMI requirements

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Section 5.0 - Electro-Magnetic Interference (EMI)

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Chapter 5 Floor Loading and Weights


Section 1.0 Floor Loading
The Discovery ST system has a total floor load of approximately 11550 lbs (5239 kg). About 10088 lbs (4576 kg), including patient (450 lbs (205 kg)), is concentrated in the table-gantry assembly. Table 5-1 shows PET-CT components with size and weight, floor loading and normal mounting requirements
ITEM NET WEIGHT LB(KG) 3507 (1591) OVERALL WEIGHT/AREA WXD LB/SQ. FT. INCH (MM) (KG/M2) 88 x 43 (2235 x 1095) 41.5 x 64.5 (1050 x 1635) 243 (1185) LOAD PATTERN IN. (MM) CT effective load area is 27 x 77 (694 x 1937) with four round pads, each 2.5 (63.5) in contact with the floor. While in the imaging position, the effect PET load area is 19.2 x 24 (480 x 708) with 7 pads each 2.5 (63.5) as well as 2 pads that do not get anchored (support only) see Figure 5-7 Rectangular base 99 x 23 (2475 x 563) with four round pads, each 2.5 (63.5) in contact with the floor. NORMAL METHOD OF MOUNTING IN. (MM) (GE SUPPLIED)1 1/2" (12.7mm) diameter x 10" (254mm) long per P/N 2106573-2 at four leveling pads into concrete floor. Hilti Kwik-Bolt II 1/2in (12.7mm) diameter by 8in (203mm) long per P/N 2106573 at seven leveling pads into concrete floor.

Gantry CT

Gantry

PET

4631 (2101)

1266 (6180)

Patient Table

29.73 x 1950 (886) 109.65 Includes 450 (205) (628 x 2785) Patient

100 (490)

Hilti Kwik-Bolt II 1/2in (12.7mm) diameter by 8in (203mm) long per P/N 2106573 at three leveling pads into concrete floor.

Power Distribution Unit

800 (363)

30 x 22 (762 x 559)

180 (82)

Four Casters or support Casters are for positioning area of 30 x 22 (762 x 559). and service. Set on floor. May be anchored to floor using angle brackets in seismic zones. Four Casters or Leveling Casters are for positioning. Feet support area of 46 x 19 Set on floor. Four leveling (1168 x 483). pads may be anchored to floor using angle brackets in seismic zones.

Operator's console/ computer

662 (300)

48 x 39 (1219 x 991)

50 (23)

Notes: 1.) Use the GE Supplied mounting hardware ONLY IF APPROVED by qualified personnel. [See statements in 3.2 - Table and Gantry Mounting Requirements, on page 42.] 2.) Angle brackets are included in the OPTIONAL Seismic Kit (R4390JC) only.

Table 5-1 Discovery ST System Floor Loading

Chapter 5 - Floor Loading and Weights

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5 Floor Loading

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2


ITEM NET WEIGHT LB(KG) 150 (68) OVERALL WEIGHT/AREA WXD LB/SQ. FT. INCH (MM) (KG/M2) 30 x 22 (770 x 550) 39 (17.5)

DISCOVERY ST PRE-INSTALLATION
LOAD PATTERN IN. (MM) NORMAL METHOD OF MOUNTING IN. (MM) (GE SUPPLIED)1 Four Casters or Leveling Casters are for positioning. Feet support area of 28 x 20 Set on floor. Four leveling (711 x 508). pads may be anchored to floor using angle brackets in seismic zones.

Operator's console/ Option Cabinet Notes:

1.) Use the GE Supplied mounting hardware ONLY IF APPROVED by qualified personnel. [See statements in 3.2 - Table and Gantry Mounting Requirements, on page 42.] 2.) Angle brackets are included in the OPTIONAL Seismic Kit (R4390JC) only.

Table 5-1 Discovery ST System Floor Loading

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Section 1.0 - Floor Loading

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DISCOVERY ST PRE-INSTALLATION

Section 2.0 Mounting Data, Including Seismic


Standard mounting meets seismic requirements. See Figure 5-1 However, customer is responsible for seismic mounting. Refer to all applicable codes in your area.

Figure 5-1 Typical Floor Anchor, Gantry and Table The following pages show center-of-gravity information for system components: Gantry: Figure 5-2, Figure 5-3, Figure 5-4 Table: Figure 5-8 Power Distribution Unit: Figure 5-9 Operator's Console/Computer: Figure 5-10 5 Floor Loading

Floor mounting hole locations for components that don't have templates are also in this section.

Chapter 5 - Floor Loading and Weights

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Figure 5-2 Gantry - PET/CT CGs at Operating Position (SK4092003, Sheet 1, Rev 1) Page 60 Section 2.0 - Mounting Data, Including Seismic

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Figure 5-3 Gantry - PET/CT CGs at Service Position (SK4092003, Sheet 2, Rev 1) Chapter 5 - Floor Loading and Weights Page 61

5 Floor Loading

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Figure 5-4 Gantry - PET/CT CGs Entire Gantry (SK4092003, Sheet 3, Rev 1) Page 62 Section 2.0 - Mounting Data, Including Seismic

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Anchor Location #2 Redundant Anchor Location


Back

Anchor Location #3 Redundant Anchor Location

Rear Aux Levelers

Left
Inside Levelers

Right

Front Aux Levelers

Front

Redundant Anchor Location Anchor Location #1

Redundant Anchor Location Anchor Location #4

Note: Adjusters are used at each anchor location. Anchor hole ID is 1" (2.5 cm). Void between adjuster and anchor must be filled according to local building codes for siesmic application.

Figure 5-5 Gantry Leveler and Adjuster Locations - CT 5 Floor Loading Figure 5-6 Discovery ST PET Base Chapter 5 - Floor Loading and Weights Page 63

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Figure 5-7 Gantry Leveler and Adjuster Locations - PET

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Figure 5-8 Patient Table - Discovery ST Chapter 5 - Floor Loading and Weights Page 65

5 Floor Loading

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2


MINIMUM AIR FLOW CLEARANCE 6 (152)

DISCOVERY ST PRE-INSTALLATION

Notes: Dimensions are in inches (millimeters) Indicates Center of Gravity

14.5 (368)

14.75 (375)

22 (559)

36.0 (914) SERVICE AREA SERVICE AREA 30 (762) 24.0 (610)

72 (1829) 50 (1270) 14.75 (375) 1.34 (34) FRAME THRU HOLES 4 LOCATIONS 0.3125 (8) 4.85 (123) 19.3 (490) Seismic Mounting Holes
Note: Mounting brackets not shipped with system. Order Seismic Kit R4390JC.

14.5 (368)

21.75 (552)

21.75 (552)

Figure 5-9 Power Distribution Unit (PM)

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Figure 5-10 Operators Console / Computer (GOC1)

Chapter 5 - Floor Loading and Weights

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5 Floor Loading

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Figure 5-11 PET Host Computer Cabinet

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Figure 5-12 Gantry/Table Mounting Dimensions

Chapter 5 - Floor Loading and Weights

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Section 2.0 - Mounting Data, Including Seismic

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DISCOVERY ST PRE-INSTALLATION

Chapter 6 Delivery Data


WARNING SOME ASSEMBLIES ARE TOP-HEAVY. BE CAREFUL NOT TO TIP.

Section 1.0 Van Delivery


The Discovery ST system is packed for van shipment with minimum tear-down of components. It consists of approximately 20 shipping containers which include dollies, skids and boxes without skids.

Section 2.0 Delivery/Shipping Requirements & Considerations


The Discovery ST system is not designed to tolerate excessive mishandling, including dropping, shock, vibration, tipping or hoisting. The Gantry, Console, Table and PDU must NEVER be dropped. A drop from a height greater than one half inch () may induce structural damage to the frame or other major components. Damage resulting from a drop (e.g., bent frame, misalignment) may not be obvious until after system installation is complete. To avoid dropping the Gantry, Dock to Dock shipment is recommended. Other methods are acceptable, provided that the system is not dropped or otherwise mishandled. For example, the system may be moved via flat-bed wrecker or by rolling it across SMOOTH sidewalks or other paved surfaces. When moving Gantry off of a flat-bed wrecker, attach the straps to the lowest point possible on the dolly. Lower the Gantry at the slowest reasonable rate. See Figure 6-1.

Figure 6-1 Gantry Strap Location

Chapter 6 - Delivery Data

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The Discovery ST Systemincluding Gantry, Console, Table and PDUis not designed to tolerate any excessive shock or vibration that may occur during unloading. For example, rolling the Console across a washboard style ramp may vibrate components, causing loosened or broken connections, etc. Damage resulting from shock or vibration (e.g., monitor, CD-ROM, hard-drive or Octane failure) may not be evident until after system installation is complete. All system components must remain upright at all times, and must not be tipped. Likewise, do not hoist the Gantry. Move the Gantry only by rolling it on its dollies. During transit through hallways, doorways, elevators, etc., do not tip or lift the Gantry.

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Section 2.0 - Delivery/Shipping Requirements & Considerations

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Section 3.0 Site Environmental Considerations


3.1 Dust/Dirt Contamination
The Discovery ST systems (consisting of: Console, PDU, Table and Gantry) are highly susceptible to airborne contaminants, especially concrete and drywall dust. Due to the possibility of contamination, these systems should NEVER be installed in a construction site. Any site with unfinished floors, walls or ceilings is considered a construction site, and is not suitable for system installation.

3.2

Chemical Contamination
Wet film processors must never be installed in the same room as the scanner, due to the possibility of chemical contamination of Discovery ST components. Such chemicals can contribute to increased equipment failures, increased system downtime, and decreased reliability. Film processor equipment installation must meet the manufacturers requirements (e.g. ventilation specifications) and all applicable national and local codes. Also, consideration should be given to the location of this equipment and chemical fumes relative to human contact as it relates to locating this equipment and chemicals in the control room.

Section 4.0 For Crated Delivery


The Discovery ST system is packed for air shipment in 6 packages including the chair. Total weight of the basic system, including pre-installation kit, is 11,869 lbs (5384 kg). It is shipped in wooden crating. Note: The information in Table 6-1 is estimated, due to lack of experiential shipping information as of the release date of this document.

CRATE #
1 2 3 4 5 6

HEIGHT IN (CM)
87 (221.5) 80 (203) 60 (158) 51 (130) 62 (157.5) 68.5 (174)

WIDTH IN (CM)
57.5 (145.5) 38.5 (97.5) 37 (94) 57.5 (146) 52.75 (134) 53 (134.5)

DEPTH IN (CM)
97.75 (248) 103 (262) 40.5 (103) 63 (159.5) 53 (134.5) 53 (134.5)

WEIGHT LB (KG)
4533 (2056) 1481 (672) 953 (432) 992 (450) 656 (298) 3254 (1476)

Table 6-1 Estimated Crated Delivery Sizes and Weights

Chapter 6 - Delivery Data

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Section 5.0 Storage Requirements


If the Discovery ST system is to be stored before installation, store in a warehouse. Protect from weather, dirt and dust. Storage temperature should not exceed -20 to +100 F (-30 to +50 C). Maintain relative humidity (non-condensing) between 0 and 80%. Do not store Discovery ST systems for more than 90 days.

Section 6.0 Gantry Considerations


The gantry is shipped with most covers installed. The assembly is mounted between two dollies. See Figure 6-2. Two side rails are bolted to the dollies to stabilize dollies and protect gantry. Use dolly elevating casters to lift gantry off its base and roll it into position.

Figure 6-2 CT Gantry with Shipping Dollies and Side Rails

CONFIGURATION
Dollies On, Side Rails On Dollies On, Side Rails Removed

LENGTH IN (CM)
114 (290) 114 (290)

WIDTH IN (CM)
51 (129) 42 (107)

HEIGHT IN (CM)
79 (200) 79 (200)

Table 6-2 Size of CT Gantry & Dollies, with and without Side Rails

Page 74

Section 5.0 - Storage Requirements

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DISCOVERY ST PRE-INSTALLATION

Figure 6-3 PET Gantry Base with Shipping Dollies and Side Rails

Figure 6-4 PET Gantry Image Ring with Shipping Dollies and Side Rails Chapter 6 - Delivery Data Page 75

6 Delivery Data

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DISCOVERY ST PRE-INSTALLATION

Figure 6-5 PET Gantry Trailer with Shipping Dollies and Side Rails

CONFIGURATION
PET Base with Dollies PET Base without dollies PET Image Ring with Dollies PET Image Ringe without Dollies PET Trailer with Dollies PET Trailer without Dollies

LENGTH IN (MM)
88.5 (2248) 64.5 (1639) 110 (2794) 81.5 (2070) 96 (2439) 71.5 (1816)

WIDTH IN (MM)
41.5 (1054) 41.5 (1054) 41.5 (1054) 36 (914) 41 (1042) 32.75 (832)

HEIGHT IN (MM)
43.5 (1105) 10.5 (267) 73.5 (1867) 73.5 (1867) 55.5 (1410) 55.5 (1410)

WEIGHT LB (KG)
1430 (649) 1070 (485) 2935 (1331) 2210 (1002) 1415 (642) 730 (331)

Table 6-3 Size of PET Gantry, with and without Dollies

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Section 6.0 - Gantry Considerations

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DISCOVERY ST PRE-INSTALLATION

Figure 6-6 Table with Shipping Dollies

CONFIGURATION
Dollies On Dollies Off

LENGTH IN (MM)
122 (3099) 110 (2794)

WIDTH IN (MM)
37.4 (950) 37.4 (950)

HEIGHT IN (CM)
44.5 (1130) nominal 44.5 (1130) nominal

WEIGHT
LB (KG)

1323 (600)

Table 6-4 Size of Table & Dollies

Door Openings. Clear door openings for moving equipment into building must be 42 X 82 in. (1067 X 2083 mm) minimum, if there is an 8 ft. (2439 mm) corridor width. 6 Delivery Data Elevator requirements. To move gantry from receiving location to scanning room, consider elevator capacity and size. By removing side rails and one dolly after gantry is placed in elevator, gantry width/length and elevator depth requirements are reduced. Contact a representative of elevator manufacturer if gantry weight exceeds elevator capacity. Minimum hallway and door size for gantry with covers and dollies attached, but side rails removed, is 40 inches (101.6 cm). For alternative lifting arrangements and instructions, contact GE Installation Support Services. Dollies: Typically, dollies are used on the gantry, table, and console for domestic shipments. Once the gantry, table and console are installed at the site, return dollies to GE using the shipping document located in Box #1. Dollies can be purchased for international shipments (B7850LD) to be used at the customer site. After the system has been removed from the crates, dollies shipped with international shipments only are not to be shipped back to GE in Milwaukee, WI, USA, but to be retained to the local GE office or warehouse.

Chapter 6 - Delivery Data

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Section 7.0 Table Considerations


The table is shipped without side covers installed. Covers are shipped in four separate boxes. The table is mounted between two dollies. Table dimensions are shown in Table 6-4. These dimensions do not include shipping crates or packaging materials.

Section 8.0 Console Considerations


The console is shipped without the keyboard table installed. Keyboard table is shipped in one of the two boxes shipped with the console. The console is shipped between two dollies. Console shipping dimensions are 55" (140 mm) long, 39" (99 mm) wide, and 41" (104 mm) high. Note: Note: The width changes to 25.5" (65 mm) when the skid is removed. Two boxes are shipped with the console. The first box shipping dimensions are 71" (180 mm) long, 26.5" (67 mm) wide, and 11" (28 mm) high. The second box shipping dimensions are 61" (55 mm) long, 22" (55 mm) wide, and 11" (28 mm) high.

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Section 7.0 - Table Considerations

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Chapter 7 Power Requirements


Section 1.0 Introduction
The Power Distribution Unit (PDU) supplied with the Discovery ST systems transforms and distributes power to all system components. The PDU is the only power entry point required to operate the system. Power wiring between the facility main distribution panel and the PDU should be kept as short as possible. This minimizes voltage regulation effects. Carefully consider advantages and disadvantages of conduits, floor ducts and surface raceways for running cables. Make cable passageways large enough to install any cable with all other cables already installed. When routing power cables, all three phase wires and ground must be run in the same conduit or raceway duct-work. Power cables should be routed separately from system control cables (for example, use a separate trough in duct).

Section 2.0 System Input Power


2.1 Facility Source
Power to the system should be supplied by a dedicated feeder from the nearest Main Distribution Panel (MDP). A protective disconnect device must be provided in the power line supplying the PDU in accordance with National Electric Code and applicable local codes. Note: Lockout/tagout provision required The disconnect device must be located within forty feet of the PDU, visible to PDU service personnel, and must have provision for tagout / lockout. It is identified as A1 in the interconnection schematic diagrams. The GE part number for the disconnect is P5050RB. The rating of the disconnect device depends on the nominal line voltage. It must provide overcurrent protection and have a low voltage release, with multi-point remote control capability. Refer to Section 3.0: Recommended Power Distribution System, for minimum rated capacity requirements and suggested device.

Chapter 7 - Power Requirements

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2.2

Main Disconnect Control


Customer-supplied emergency off buttons are to be mounted in the PET-CT Room near each exit 60 in. (1424 mm) from the floor and connected to the protective disconnect device in order to disable the power to all Discovery ST system equipment in emergency situations. This button is to be clearly labeled Emergency Off and visible to personnel in the PET-CT Room. It is important that the button be labeled off and not stop since there exists an Emergency Stop button in the Discovery ST system that disables output power to the Discovery ST system equipment in the patient area of the PET-CT system. An additional emergency button should be mounted in the computer/ equipment room near the exit door. Customer supplied main disconnect controller (MDC) must be lockable to meet OSHA requirements for power Lockout/Tagout requirements. An optional MDC is available from GE providing for the disconnect of the facility power to the PDU, including the emergency buttons, and contacts for an interlock to the air-conditioning units in the computer/equipment room. The Main Disconnect Control Panel must be UL or other nationally recognizes testing organization listed and labeled in accordance with 1999 National Electrical Code (NEC) Article 110-2.

2.3

Configuration
The Discovery ST systems are designed to operate on three-phase, four-wire wye power. A ground referenced wye source produces the lowest leakage currents and is preferred. However, the neutral wire does not need to be run to the system, i.e., four-wire connection. (A dummy terminal is provided for `parking' the neutral wire in the event a five-wire service is already installed at the site.)

2.4

Rating
Catalog Number: P5050RD (NGPDU) Voltage Capacity Frequency Note: 380 to 480 VAC (see note, below) 90 KVA momentary 20 KVA average 50 or 60 Hz (47 to 53 or 57 to 63 Hz)

The absolute range of line voltage at the input to the PDU must remain within one of the ranges shown in Table 7-1 at all times.

2.5

Regulation
The size of the facility transformer and feeder wires determine load regulation presented to the system. Total load regulation as measured at the PDU input terminals must not exceed 6%.

2.6

Phase Imbalance
The difference between the highest line-to-line voltage and lowest line-to-line voltage must not exceed 2% of the lowest line-to-line voltage.

2.7

Sags, Surges & Transients


Sags and surges of the power line must not exceed the absolute range limits shown in Table 7-1.

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Section 2.0 - System Input Power

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DISCOVERY ST PRE-INSTALLATION

2.8

Microcuts
The Discovery ST systems are generally unaffected by microcuts.

2.9

Grounding
The ground to the PET-CT system shall originate at the system power source, (i.e., transformer or first access point of power into a facility) and be continuous to the PET-CT system power disconnect in the room. A dedicated 1/0 (55mm2) or larger insulated copper ground wire must be run with the phase wires from the main distribution panel to the PDU. These grounds can be spliced with High Compression Fittings and should be terminated at each distribution panel it passes through. When the ground is broken for a connection to a panel, it shall be connected into an approved non-insulated grounding block with the incoming and outgoing ground in this same grounding block, which is then connected to the steel panel, never using the steel or other material of the panel as the block. The resistance between the PDU ground and the facility earth ground must not exceed 0.5 ohm. In addition, the total resistance between the PDU ground and earth must not exceed 2 ohms. Resistance between any two grounded devices must not exceed 0.1 ohm to ensure equal potential ground system within the PET-CT Room.

Chapter 7 - Power Requirements

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Section 3.0 Recommended Power Distribution System


A single-unit installation where the distribution transformer and feeder are dedicated to the Discovery ST system is recommended. In this case, the minimum recommended transformer size is 112.5 KVA, rated 3.2% regulation at unity power factor. The minimum recommended feeder size and over-current protection device ampacity based on line voltage is shown in Table 7-1. Maximum power demand = 90 kVa @ 0.85 PF at a selected technic of 140 kV, 380 mA. Average (continuous) power demand at maximum duty cycle = 20 kVa. Maximum allowable total source regulation = 6%.

CATALOG > P5050RD (DISCOVERY ST PDU)


Nominal Line Voltage (VAC) Voltage Range (VAC) +/- 8% Average Line Current (A) Momentary Line Current (A) @ Nominal Line Voltage Maximum Line Current (A) @ Low Line Voltage Primary Disconnect Device (A1) Over-current Protection (A) 6 Feeder Length (MDP to A1) 1 0-100 ft (0-30.5 m) 100-250 ft (30.5-76 m) 2 (35)3 1 (45)3 2 (35)3 2 (35)3 2 (35)3 2 (35)3 2 (35)3 2 (35)3 1 (45)3 2 (35)3 2 (35)3 1 (45)3 2 (35)3 2 (35)3 2 (35)3 1 (45)3 380 350-410 30 137 149 110 400 368-432 29 130 141 110 420 27 124 135 110 440 26 118 128 110 460 25 113 123 110 480 24 108 117 110 386-454 405-475 423-497 442-518

251-300 ft (77-91 m) 2/0 (70)3 1/0 (55)3 1/0 (55)3

301-350 ft (92-106 m) 3/0 (85)3 2/0 (70)3 2/0 (70)3 1/0 (55)3 1/0 (55)3

351-400 ft (107-122 m) 3/0 (85)3 3/0 (85)3 2/0 (70)3 2/0 (70)3 1/0 (55)3 1/0 (55)3 Sub-Feeder Length (A1 to PDU) 0-40 ft (0-12 m)
Notes: 1.) The feeder table above is based on the use of copper wire, rated 75C and run in steel conduit. Wire size is in AWG (mm2). Ampacity is determined in accordance with the National Electric Code (NFPA 70), Table 310-16 (1999). 2.) The wire size shown is the minimum allowable for the specified over-current protection rating. 3.) The feeder is sized to contribute 2.4% maximum regulation. 4.) A minimum 1/0 (55 mm2) ground wire is required. 5.) A neutral wire is not required and, if present, is not used. 6.) The Primary Disconnect (A1) must have provision for tagout/lockout. Figure 8-7, on page 97, shows the primary power disconnect (A1 - P/N P5050RB) using a combination fusible disconnect and magnetic contactor.

1 (45)2

2 (35)2

2 (35)2

3 (30)2

3 (30)2

3 (30)2

Table 7-1 Facility Power Requirements

Page 82

Section 3.0 - Recommended Power Distribution System

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

If the Discovery ST system must be powered from an existing distribution transformer and secondary feeder, such as the equipment distribution panel of an X-ray department, installation with other X-Ray equipment which use rapid film changers should be avoided. These changers use a large number of high powered, closely spaced exposures which may coincide with a PET-CT scan and produce image artifacts. In all cases, qualified personnel must verify that the transformer and feeder, at point of take-off, plus the run to Discovery ST meets all the requirements. Power Systems for X-Ray Rooms, Direction 46-013833, is available for additional information on power requirements for X-ray systems.

Section 4.0 Uninterruptable Power Supplies (UPS)


Uninterruptable Power Supplies (UPS) are recommended for areas or sites with known power issues. Consult your local power provider for power quality data in your area. UPS is standard equipment on all mobile units. Filter and surge protectors are not needed with Discovery ST systems. For use with Discovery ST Systems, the PowerWare 9330 UPS (catalog number P5051PS) is recommended.

Section 5.0 Power Audit


A site power audit is required for the Discovery ST family of products. This site power audit can be arranged with the GE Power Quality team, or through your sales person. A sample audit form is located in the back of Chapter 9.

Note: Perform a power audit first.

A power line analyzer should be used to check the proposed Discovery ST site power for average line voltage, surges, sags, reclosures, impulses, frequency and microcuts. A period that includes two weekends should be used to simulate several days of normal use. Analysis of the data and site history of any previous power problems with other X-ray systems or computer installations should be reviewed with your Power and Ground representative. Verify brown-out (low voltage) conditions, which may occur during summer months, will not exceed the allowable range shown in Table 7-1. Some analyzer models that are suitable for power line monitoring are: Dranetz Model 658 Dranetz Model 656A BMI 3630 RPM

Chapter 7 - Power Requirements

Page 83

7 Power Reqs

Section 6.0 Power Source Monitoring

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Section 7.0 Ground System


Discovery ST has been designed to use an equal potential grounding system. The required ground system is shown in Figure 7-1. There are three primary grounding points: A system power ground point located in the PM (Power Module). A reference ground point located between gantry and table base. A patient ground point located at the front of the table base.

All exposed metal surfaces in patient vicinity are grounded to the reference ground point. For additional information, refer to Electrical Safety Equipment, Direction 46-014505. [
TO POWER VAULT GROUND NOTES: SHIELD / SIGNAL GROUNDS ARE NOT SHOWN. A1 POWER DISCONNECT = GROUND WIRE IN SUPPLIED CABLE. DISK UNITS ARE LOCATED IN CC1 AND SCU. GANTRY (CT2) ROTATING ASSEMBLY FRAME TILT MECH FRAME

GANTRY (PT1)

#1/0 POWER DISTRIBUTION UNIT (PM)

G #1/0

TABLE/GANTRY JUNCTION RACEWAY T #2 Part of Gantry

TABLE (CT1)

Ground Braid (Part of Gantry)

#2

IN-ROOM MONITOR (OPTION) TO CONSOLE (OC1) VIDEO PRINTER COLOR (OPTION) TO CONSOLE (OC1)

OPERATOR'S CONSOLE/ COMPUTER (OC1)

PET Host Computer Cabinet (OC2)

Figure 7-1 System Ground Map

Page 84

Section 7.0 - Ground System

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Chapter 8 Interconnection Data


Section 1.0 Introduction
Figure 8-3 shows interconnection runs for a 50/60 Hz system. Table 8-1 shows component designators for supplied equipment and options and wall power outlets. Table 8-4 lists customer-installed wiring and supplied cables. Actual length of each run is less than the length of supplied cables to allow for routing inside equipment. Cable diameters and sizes of connectors are provided to aid in sizing conduit and access plates. Table 8-2 and Table 8-3 list details for connection to Discovery ST equipment, using standard (short) length and non-standard (long) length cables, respectively. Details are listed for the following types of runs as appropriate: Flush-floor duct Computer floor Through-wall bushing Junction box Surface floor duct Through-floor duct Wall duct Conduit

Need for additional junction boxes is minimized by use of either a cable raceway system or a raised computer floor. Discovery ST use prefabricated cables with large plugs. Therefore, conduit or pipe is not recommended for cable runs.

Chapter 8 - Interconnection Data

Page 85

8 Interconnects

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Section 2.0 Component Designators


DESIGNATOR APPLIES TO
A1 CT1 CT2 PT1 ITL LP OC1 OC2 PM SEO SM WL DS XCVR Primary power disconnect Patient table Gantry - CT - PET InSite telephone lines Line printer Operator's console/computer PET Host Computer Cabinet Power distribution unit System emergency off Slave monitor X-ray on warning light Door Interlock Switch Ethernet transceiver Contractor supplied Option System System System Contractor supplied Option Contractor supplied Contractor supplied System

SOURCE
Contractor supplied System System

Table 8-1 Component Designators

Page 86

Section 2.0 - Component Designators

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2 DISCOVERY ST PRE-INSTALLATION

Section 3.0 Interconnect Runs, Wiring and Cables

3.1

GEMS Supplied

Chapter 8 - Interconnection Data

Page 87

8 Interconnects

3.1.1

Short Length Run (Optional) Cables UL CABLE INFORMATION


Dia. mm (inch) Temp. Rating (C) Size AWG # of Cond UL Style

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

Voltage Rating

Voltage Actual

RUN #

LENGTH, ACTUAL (USABLE)


ft 43 (35) 43 (35) 40 (35) 42 (35) m

Flammability Rating

PART # DESCRIPTION

PULL SIZE MM (INCHES)


15.8 (0.62) Dia 19.8 (0.78) Dia 56.4 (2.22) Dia 16.8 (.66) Dia

13.2 2275844-3 Ground - PDU to (10.67) CT1

1284

VW-1 (FT-1) FT-4 FT-4

600 600 600

0 + 350 VDC 208Y/120 440Y/254

105 90 90 90

15.5 1 (.608) 19.0 2 (.751) 13.8 5 (.542) 15.3 4 (.604)

1/0 6 8 12

13.2 2267642-2 HVDC - PDU to CT2 2587 (10.67) 12.3 2266880-2 Power - PDU to CT2 2587 (10.67) 12.9 2267644-2 HVDC - PDU to CT2 Flexible (10.67) Motor Supply Cable 13.2 2344446-2 Power - PDU to PT-1 2587 (10.67) 16.9 2266879-2 Power - PDU to OC1 2587 (15.24) 17.8 2275844-4 Ground - PDU to (15.24) OC1 13.2 2266014-2 Signal - PDU to (10.67) Gantry STC 17.8 2271060-2 Signal - Console to (15.24) Gantry STC (CT2) 16.7 2266887-3 Signal - LAN (15.24) Console to CT2 16.9 2117848-6 Fiber Optic - Console (15.24) to CT2 16.9 2215028(15.24) 10 Signal - LAN Console to PT-1 CAT 5 1283 UL UL

Chapter 8 - Interconnection Data Page 88

FT-4 TC 1000

43 (35) 2 55 (50) 58 (50) 3 4 43 (35) 58 (50) 55 (50) 55 (50) 55 (50)

FT-4 FT-4 VW-1 (FT-1) FT-4 FT-4

600 600 600 300 300 1900 NA

208Y/120 208Y/120 0 <30VDC <30VDC <30VDC NA <30VDC

90 90 105 80 80

13.8 5 (.542) 12.3 4 (.483) 11.9 1 (.467)

8 10 2

56.4 (2.22) Dia 56.4 (2.22) Dia 12.2 (.48) Dia 20 x 75 (.78 x 2.95) 20 x 51 (.79 x 2.01) 17 x 58 (.68 x 2.30) 19 x 51 (.75 x 2.01) 15 (.59) Dia 10 (.39) Dia 15 (.59) Dia DISCOVERY ST PRE-INSTALLATION

13.3 37 22 (.525) 11.2 25 22 (.440) 5.9 1 (.234) 1 5.9 1 (.234) 19 NA 19

UL FT-4 (RG-223/U)

FT-4

1900

Table 8-2 GEMS Optional Cables (Short Length Run) - UL Information

8 Interconnects

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

Extender cables installed for service. 2352381

P1

Front Cover 2336637 SCH

CAN Terminator used when Rear Control Panel option not installed. All terminators used when removed for service and no extender cables installed. J1 P1 P1 J1 J2 P2

Rear Cover 2336638 SCH


(2353596SCH Productivity upgrade)

Cable Bundles

J1

P1

J2 Cardiac/Resp Input

Cable Retractor
2301800 [SUB] J1 J2 J3 J4 J5 J6 J8 J9 J10 P1 P2 P3 P4

ESTOP Terminator 2275843

CAN ESTOP Terminator Terminator 2295965 2275843

GOB
2351851-2 optional install kit, cabling comes with kit

Cable Bundles

J1

Table-1.5m 2338513
ETC Backplane

P5 P6 P8 P9 P10

CT Gantry 2336576

PET Gantry 2337134 SCH


2346122-2 (-3)

J1 P2

10/100 LAN ECG/ RESP Motion Enable

J11 J12 J13 2295969 [SUB]

P11 P12 P13 existing cable braid 2309058 [SUB]

2346946 J10 J16 J6

P3
Power Panel

Chapter 8 - Interconnection Data Page 89

2275854-2 [SUB] 46-297428P1 [SUB] 2261425-10 [SUB]

Power Panel
DC+ DC-

relay

STC Backplane

J1

L3

L2

2267644(-2) [SUB]

2267642(-2) [SUB]

L1 G

2266880(-2) [SUB]

J2

2266014(-2) [SUB]

J8

J7

2275844-5

2344446 (-2)

2275844(-3) [SUB]

P1

TS1

TS2

Fiber

KB Box

Phone Line Gantry

J4

DC+

DC-

Light

Door

J2

L3

L2

L1 G

1 2 3 4

1 2

TS1
HVDC

TB1
440VAC 120VAC

Hospital LAN

Controls

Input

PDU 2335370 SCH

J6
TS2
6 5 4 3 2 1 120VAC 2271060 (-2) [SUB] 2117848-2 (-6) [SUB] 2266887(-2) [SUB] 2266879(-2) [SUB]

PET LAN

10/100 RJ45

J5
120VAC

J20
Fiber
CT LAN 10 Base2 Coax

Console 2346059 SCH

L3 L2 L1 G

from A1 Panel
2275844-2(-4) [SUB]

P1

NOTES: 1. all cables marked (SUB) are structured and kitted at sub-assembly level. 2. cables showing additional (- #), are kitted options that include alternate lengths.

REVISIONS REV MADE BY DATE 11-10-02 PCN NO. DESCRIPTION


MADE CHECK APPR OTHER

APPROVALS electronic

DD/MM/YY TITLE

Hosp Ethernet

Phone

Jim Malaney

NA

Engineering release

FIRST MADE FOR:

Road Warrior CT-PET System Assy A


TBD

REV

DISCOVERY ST PRE-INSTALLATION

GE MEDICAL SYSTEMS MILWAUKEE, WI

2342229 SCH 1 SHEET

OF 1

Figure 8-1 System Interconnect Diagram 2342229 SCH

8 Interconnects

term

CD-R MOD

2350049

SCSI

Ethernet

Rx Mon

Display

KeyBD

Mouse

Service Key

SCSI

CT HOST
Serial 2

Service Key /Bulkhead Power Switch


Modem1

2350049

2347061 2361012

HD50

Monitor

J20 Fiber CT LAN GND

J20 Fiber
10 Base 2 Txcvr

KeyBD

Mouse

2271060 (-2) [REF] 2117848-2 (-6) [REF]

Monitor

2266887(-2) [REF]

CT Console Assembly 2341104 (B7858GC)


DC Converter Recon Chassis RIP BD Ethernet

Ethernet 0 Ethernet 1

Ethernet 0 Ethernet 1

Serial 1

Serial 1

2275844-2(-4) [REF]

SCSI

Console Power Panel


2266879(-2) [REF]

PET Host (Linux)

SCSI

Entegra

2142226 1

115VAC

5VDC 5vDC

P1

115V

115V

115V

8 Port Ethernet Switch

2354735
PET LAN
2346122-2(-3) [REF]

(see note 1) 2346122-5

2346122-5 2346122-5

2330676

2323733 (P5020JA)

Hosp LAN
5vDC 5VDC

2346122-5 2346122-5
DC Converter 115VAC

8 Port Ethernet Switch

2354735 2142226 NOTES: 1. Connect PET LAN cable to uplink port (#1) on Ethernet switch. Make sure port #1 switch is set to crossover. Remaining port positions are not critical. 2. All cables marked (REF) are shown for reference only and are structured at alternate assembly level. 3. Some details of internal power and signal cabling for CT console assembly are not shown.

2285747
REVISIONS REV MADE BY DATE 11-21-02 PCN NO. DESCRIPTION
MADE CHECK APPR OTHER

APPROVALS electronic

DD/MM/YY TITLE

KeyBD

Mouse

Page 90 Section 3.0 - Interconnect Runs, Wiring and Cables

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

46-328475P1
Phoneline Multiplexer

2245773
Modem2
Trackball

Rx Monitor

2333243 or 2254212 (B7850MM)

Display Monitor Mouse

RW SCIM

port1

port2

2336374

2318316

2318316
KVM Switch

2318318

Mouse

2142759

2275756

Ethernet 0

Ethernet 1

Serial 1

Road Warrior Console Assembly


FIRST MADE FOR:

REV

Jim Malaney

NA

Engineering release

TBD

A
1
OF 1

DISCOVERY ST PRE-INSTALLATION

GE MEDICAL SYSTEMS MILWAUKEE, WI

2346059 SCH SHEET

Figure 8-2 Console Interconnect Diagram 2346059 SCH

3.1.2

Standard Length Run (Long) Cables UL CABLE INFORMATION


Dia. mm (inch) Temp. Rating (C) Size AWG # of Cond UL Style

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

Voltage Rating

Voltage Actual

RUN #

LENGTH, ACTUAL (USABLE)


ft 63 (55) 63 (55) 60 (55) 62.5 (55) m

Flammability Rating

PART # DESCRIPTION
Ground - PDU to CT1

PULL SIZE MM (INCHES)


15.8 (0.62) Dia 19.8 (0.78) Dia 56.4 (2.22) Dia 16.8 (.66) Dia

19.3 2275844 (16.76) 19.3 2267642 (16.76) 18.5 2266880 (16.76) 19.0 2267644 (16.76)

1284

VW-1 (FT-1) FT-4 FT-4

600 600 600

0 + 350 VDC 208Y/120 440Y/254

105 90 90 90

15.5 1 (.608) 19.0 2 (.751) 13.8 5 (.542) 15.3 4 (.604)

1/0 6 8 12

HVDC - PDU to CT2 2587 Power - PDU to CT2 2587 HVDC - PDU to CT2 Flexible Motor Supply Cable Power - PDU to PT-1 2587 Power - PDU to OC1 2587 Ground - PDU to OC1 Signal - PDU to Gantry STC Signal - Console to Gantry STC (CT2) Signal - LAN Console to CT2 Fiber Optic - Console to CT2 Signal - LAN Console to PT-1 CAT 5 1283 UL UL

Chapter 8 - Interconnection Data Page 91

FT-4 TC 1000

60 (55) 2 80 (75) 83 (75) 3 4 63 (55) 83 (75) 80 (75) 80 (75) 80 (75)

18.5 2344446 (16.76) 24.5 2266879 (22.86) 25.5 2275844 (22.86) 19.3 2266014 (16.76) 25.5 2271060 (22.86) 24.3 2266887 (22.86) 24.3 2117848 (22.86) 24.3 2215028(22.86) 10

FT-4 FT-4 VW-1 (FT-1) FT-4 FT-4

600 600 600 300 300 1900 NA

208Y/120 208Y/120 0 <30VDC <30VDC <30VDC NA <30VDC

90 90 105 80 80

13.8 5 (.542) 12.3 4 (.483) 11.9 1 (.467)

8 10 2

56.4 (2.22) Dia 56.4 (2.22) Dia 12.2 (.48) Dia 20 x 75 (.78 x 2.95) 20 x 51 (.79 x 2.01) 17 x 58 (.68 x 2.30) 19 x 51 (.75 x 2.01) 15 (.59) Dia 10 (.39) Dia 15 (.59) Dia DISCOVERY ST PRE-INSTALLATION

13.3 37 22 (.525) 11.2 25 22 (.440) 5.9 1 (.234) 1 5.9 1 (.234) 19 NA 19

UL FT-4 (RG-223/U)

FT-4

1900

Table 8-3 GEMS Supplied Cables (Long Run) - UL Information

8 Interconnects

3.2

Contractor (Customer) Supplied

Page 92 Section 3.0 - Interconnect Runs, Wiring and Cables 3 1 1 3 1 1 2 1 2 2 *

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

CUSTOMER INSTALLED WIRING QTY SIZE AWG (MM2)

DESCRIPTION

CABLES SUPPLIED

PLUG PULLING DIMENSIONS

WIRE & CABLE PIGTAILS FT. (M) FROM TO

PART NO

LENGTH FT. (M)

DIA. IN (MM)

FROM

TO

RUN NO. 1 FROM PRIMARY POWER SOURCE TO FACILITY DISCONNECT (POWER SOURCE - A1) Maximum Run Length * * 1/0 (50) * * 1/0 (50) * 14 (2) 14 (2) 14 (2) POWER GROUND NEUTRAL POWER GROUND NEUTRAL POWER GROUND WARNING LIGHT 24 VOLT CONTROL A3J2-1,2,3,4 3 (1) 3 (1) 3 (1) 3 (1) 3 (1) 3 (1) 6 (2) 6 (2) 3(1) 3 (1) 3 (1) 3(1) 3 (1) 3 (1) 6 (2) 6 (2)

RUN NO. 2 FROM FACILITY DISCONNECT TO POWER MODULE (A1 - PM) MAXIMUM RUN LENGTH *

RUN N0. 3 FROM FACILITY DISCONNECT TO SYSTEM EMERGENCY OFF (A1 - SEO)

RUN NO. 8 POWER MODULE TO WARNING LIGHT CONTROL (PM - WL)

RUN NO. 9 POWER MODULE TO SCAN ROOM DOOR INTERLOCK (PM - DOOR SWITCH) 14 (2) SCAN ROOM DOOR INTER LOCK A3J6-1,2

DISCOVERY ST PRE-INSTALLATION

REFER TO FOR AWG (MM2) WIRE SIZES.

Table 8-4 Runs 1, 2, 3, 8 and 9 Connections

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

g
SEO (Emergency OFF) A1(Main Disconnect) WL(Warning Light) DS (Door Interlock)

PM (PDU)

Minimum 63 (2.5 inch) Conduit

Laser

Telephone System Power Run #2

Minimum 63 (2.5 inch) Conduit

Power Run #1

Signal Run #3 PET Host (OC2) CT Operators Console (OC1)

Minimum 78 (3.0 inch) Conduit

Table (CT1)

Signal Run #4

CT Gantry (CT2)

PET Gantry (PT1)

Minimum 78 (3.0 inch) Conduit

Figure 8-3 Interconnection Runs

Chapter 8 - Interconnection Data

Page 93

8 Interconnects

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Section 4.0 Contractor Supplied Components


REFERENCE A1 (50-60 Hz) ASSOCIATED EQUIPMENT Main Disconnect Control (MDC) MATERIAL/LABOR SUPPLIED BY CUSTOMER USA VENDOR / CAT NO. CONTRACTOR GE CATALOG 480VAC, Surface or Flush Mount, On/Off Control Main Disconnect Control, 480VAC, Surface Mount with Flush Mount Kit included, two remote Push Button Switches. (Catalog No. P5050RB)

ITL

In-suite Broadband/ Broadband: To take maximum advantage of the Telephone Lines GE Service remote diagnostic and services capabilities, a network connection (CAT 5) with internet access is preferred. This allows GE to better provide service and even perform proactive maintenance on your GE system. For more information on how GE can provide a secure connection using your facilitys internet connection, please inquire through your local GE Service or Sales representative. If a LAN connection is not available at your site, a voice grade analog telephone line will allow GE to connect to your system, however some capabilities may be limited due to bandwidth restrictions. Telephone: Supply 2 voice-grade telephone lines. One line must be a direct number from outside the facility do not route this line through a telephone switchboard. Telephone line operating charges are paid by customer.

MFC

GE LaserCam HQ System Components

See Chapter 10, Section 2.0, for listings of Camera part numbers and descriptions. Reference the system installation drawings supplied by Installation Support Services within your geographic area.

Table 8-5 Contractor-Supplied Components

Page 94

Section 4.0 - Contractor Supplied Components

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Section 5.0 UPS Interconnect


Console 2230VAC (2266879)

UPS Supplied Cable

Scan Int'l (2271060) Supplied with UPS

Gantry 117VAC (2266880) 4 Feeders (Customer Supplied)

Figure 8-4 Typical UPS Interconnect

Figure 8-5 Typical UPS

Chapter 8 - Interconnection Data

Page 95

8 Interconnects

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Section 6.0 Typical Customer Supplied Wiring


6.1 Primary Power Disconnect

Figure 8-6 Primary Power Disconnect (A1) Fusible Disconnect and Magnetic Contactor Page 96 Section 6.0 - Typical Customer Supplied Wiring

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Figure 8-7 Primary Power Disconnect (A1)

6.2

Scan Room Warning Light & Door Interlock

GE-SUPPLIED
A3J2 A3K3 1 Hi FUSE

CUSTOMER-SUPPLIED

Line 24 V Secondary Neutral

Lo 2
8 Interconnects

Hi 3

Lo 4 Room Warning Lamp

Figure 8-8 Typical Customer Supplied Scan Room Warning Light Connection to CPDU

Chapter 8 - Interconnection Data

Page 97

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

GE-SUPPLIED

CUSTOMER-SUPPLIED

A3 J6 1,2 TO RELAY CONTROL CIRCUIT BOARD J3 46,50

N.O. Switch

Figure 8-9 Typical Door Interlock

Page 98

Section 6.0 - Typical Customer Supplied Wiring

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Chapter 9 Final Pre-Installation Review


Section 1.0 Overview
Before the Discovery ST system can be installed, all pre-installation requirements must be complete.

Section 2.0 Site Ready for Installation


Site-specific items must be verified before the installation can begin:

2.1

Dust/Dirt Contamination
The Discovery ST systems (consisting of: Console, PDU, Table and Gantry) are highly susceptible to airborne contaminants, especially concrete and drywall dust. Due to the possibility of contamination, these systems should NEVER be installed in a construction site. Any site with unfinished floors, walls or ceilings is considered a construction site, and is not suitable for system installation.

2.2

Chemical Contamination
Wet film processors must never be installed in the same room as the scanner, due to the possibility of chemical contamination of Discovery ST components. Such chemicals can contribute to increased equipment failures, increased system downtime, and decreased reliability. Film processor equipment installation must meet the manufacturers requirements (e.g. ventilation specifications) and all applicable national and local codes. Also, consider the location of this equipment and chemical fumes relative to human contact as it relates to locating this equipment and chemicals in the control room.

2.3

Walls, Ceiling, and Floor


All walls, ceiling, and flooring must be completed before installation can begin.

2.4

Phone Line
Phone line(s) must be installed and operational.

Chapter 9 - Final Pre-Installation Review

Page 99

9 Review

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

2.5

Establish the Room Layout


CT The Discovery ST systems use adjustable leveling pads to support the gantry and table. The gantry has four (4) primary leveling pads and six (6) auxiliary leveler pads located just inside the gantry base, and two each on the front and rear support frame. The auxiliary pads are sometimes referred to as Jig-feet and/or inside levelers. The table has five (5) pads used for leveling it. PET The Pet base is "T" shaped and has 7 "leveler" pads that are anchored. It also has two additional pads that are used as load bearing only and are not anchored. Using the GE print to establish the room layout, make sure all the operating and service clearances shown on the print are observed. Using the supplied template, locate the anchor holes. Make sure they clear structural interferences in the floor. Clean the area. Free the mounting surface of any material that may interfere with the positioning and leveling of the system. 1.) Lay out the 2 floor templates. 2.) Start with the Gantry template and align per the GE print. 3.) Place the table template over the top of the Gantry template. Align the scan and table centerlines and secure the templates to the floor. Make sure there are no potential clearance issues. 4.) Check the level of the floor (See Figure 9-1) across the templates. Note: Tiles (or other resilient flooring) around all holes will be cut during the installation process.

Figure 9-1 Hole Locations

Page 100

Chapter 9 - Final Pre-Installation Review

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Section 3.0 Pre-Installation Checklist


GE Y N CUST Y N DATES

Project schedule verified with contractor, facilities department, and GE? Can you meet the committed site ready date? Construction completion date matches delivery date? Power & Ground survey complete, date _____________Hospital contact_______________ Delivery date is scheduled for: _____________ First Use date is scheduled for:_____________ Does the delivery and / or installation date need to be adjusted? Applications dates: On Site scheduled for:__________, Education Center Training:___________ Have all required Radioactive Material Licenses and approvals been obtained for the equipment and facility?

GE Y N

CUST GENERAL / SITE REQUIREMENTS Y N Must be completed 5 week prior to the delivery

Final drawings distributed to the contractors and reviewed with GE? Have any additional requirements or questions of the install been discussed with GE? Final print(s) signed off that approve equipment layout / orientation? Person assigned to review and verify that all installation requirements are met? Have the specific site requirements been discussed with the contractor? Refer to the GE final drawings specifications. (See Table 9-1, below) Has the responsibility of cabling, installing, interfacing accessories not on the order been discussed? (Refer to service price pages for GEs support of 3rd party accessories) All 3rd party vendors identified, notified and scheduled? (i.e., Netcom, 3M, Kodak, Medrad, etc.) Will existing network, modem, and camera cable drops reach new locations / requirements? Has a radiological health physicists review of shielding requirements been obtained? 9 Review

Requirements? Air Conditioning Electrical Structural Other site

All work by contractors must be completed prior to GE delivery Table 9-1 Specific Site Requirements Chapter 9 - Final Pre-Installation Review Page 101

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

GE Y N

CUST EQUIPMENT Y N Must be completed 5 weeks prior to the delivery



Order reviewed for completeness and compatibility with existing equipment. Accessories on the order verified for compatibility (i.e. DASMs, cable lengths, laser cameras, AWW work station, injector and other NL items, etc.) Interfaces to existing and/or new accessories ordered and planned for accordingly. Has the location of any peripherals been determined and planned accordingly with GE representatives? EKG monitor___ Injector control___ Laser camera ___ UPS ___ 2nd Monitor___ Have any additional services to be provided by GE been discussed and agreed upon? Remote monitors ____ AWW relocation ____ Wall mounted accessories ____

GE Y N

CUST NETWORKING Y N Must be completed 5 weeks prior to the delivery



Have IP addresses and Host Names been obtained?____ Will a network camera be used?____ PET-CT service telephone line identified and installed for the InSite (Electrical, mechanical, etc.) Network installed? _____ Network jacks installed and tested? Network options ordered ____HIS RIS option ___ DICOM print ___ AWW ____ Test network connections.

GE Y N

CUST OTHER Y N Must be completed prior to the delivery



Arrangements made in the schedule to allow for remodeling, if required. (i.e., wall, floor, or ceiling repair work, painting, other cosmetic finishes) Have arrangements been made to clean the floor after equipment removal and prior to reinstall? Is de-installation required? No__ Yes ___ Is there a trade-in of existing equipment? Delivery route identified, and verified with the proper hospital personal? _________ Appropriate arrangements made with traffic for delivery? Will acceptance testing or Bio-Medical testing be required? Trash bins available for the removal of papers/ boxes/ etc. during the installation. PET-CT removal date _______

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Chapter 9 - Final Pre-Installation Review

Pre-Installation Block Diagram


Order Placed
Check order integrity

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

GE Sad - 8
Pre-Install Checks Delivery Facility Work
12 hr max

Sad -5 Call
Environmental Work

Customer Sad -8 to

Sad -1
Customer Contractors

Power Review

~ 4 - 10 hr.

Responsibility GE Complete GE
check list

Responsibility GE Leadership GE

Responsibility

Responsibility

Responsibility GE Leadership

Responsibility GE Leadership

Send copy to
vendor

Chapter 9 - Final Pre-Installation Review

GE P & G Audit Follow-up Summary Communication Leadership Review Options Review Cables
Purchaser Complete check list & focus on risk Order Options AWW / network Purchaser Trash disposal Contractors onsite Vendors onsite Options onsite

Movers Dimensions Elevator Weight Delivery Route Floor Protection

Purchaser Electrical contractor Facility mgr. Power company

Purchaser Equipment Layout Floor Loading Radiation protection Equipment Mounting Seismic Room Renovation Contractors review meeting

Purchaser HVAC Humidity Magnetic interference Environmental cleanliness Patient comfort

Purchaser Mechanical Electrical HVAC Filming Bio- MedPatient Monitor Injector Networks / pacs Radiation Therapy

SAD - 1 Final site review with customer. SAD - 0 Customer Delivery Starts

Is Site READY?
Rev 9

DISCOVERY ST PRE-INSTALLATION

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9 Review

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

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Chapter 9 - Final Pre-Installation Review

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Power & Grounding Survey


Customer Name:

System FDO: (last 5 digits)

System ID: (if available)

Modality: PET-CT MR NM US X-Ray

Zone: Central Central Atlantic HCS Latin American NorthEast SouthEast West

LCT:

Type for Audit: Pre-Install or Reactive

Auditors name:

Completion date: MM DD YY

Chapter 9 - Final Pre-Installation Review

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9 Review

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

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Chapter 9 - Final Pre-Installation Review

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

POWER & GROUNDING SURVEY ENTRY


Customer Name: System ID: Equipment: VOLTAGE (RMS) Phase A - Neutral Phase B - Neutral Phase C - Neutral Phase A - B Phase B - C Phase C - A Phase A - Ground Phase B - Ground Phase C - Ground Neutral - Ground Date of Audit: Location: VOLTAGE (RMS) Phase A Phase B Phase C Neutral Ground CURRENT (A RMS)

Ground Currents to Load:


Ground Current at MDC (A1) Power off: Ground Current at MDC (A1) Power on: mA mA

Grounding Electrode:
Location: Ground impedance: Current measured:

Chapter 9 - Final Pre-Installation Review

Page 107

9 Review

ohms

mA

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION Test Equipment Used: (list only equipment used in the audit) 150amp Clamp-On Amp Probe 1000amp Clamp-On Amp Probe Fluke 41 Fluke 43 AEMC 3730 (Ground rod impedance meter) AEMC 3710 (Ground rod impedance meter) Amprobe CT-326B Circuit Tracer True RMS Digital Volt Meter

Other Connected Loads: (Describes other connected loads.)

Areas of concern that could affect the operation of the imaging equipment:

Imaging Equipment Electrical Service Summary:

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Chapter 9 - Final Pre-Installation Review

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Chapter 10 Options and Accessories


Section 1.0 CT Injectors
This chapter covers the more common options and accessories. For a complete list of options and accessories, consult your GE sales representative.

1.1

PercuPump CT Injection Systems


INJECTOR
Part Num E8005C Description PercuPump Touch Screen CT Injection System. Floor Stand with Casters. PercuPump Touch Screen CT Injection System Part Num E9999ER

OPTIONS
Description Operator and Installation Manuals

E8005CA

E8005CE E8005CF E8005CG E8005CH

Wall Mount Accessory. Ceiling Mount Accessory - Short Ceiling Mount Accessory - Medium Ceiling Mount Accessory - Long

Table 10-1 PercuPump CT Injection Systems

1.2

EnVision CT Injection Systems


INJECTOR
Part Num Description E8007KA Medrad EnVision CT Injection E8007KE System, Adjustable Pedestal Head Mount included Medrad EnVision CT Injection System, Overhead Counterpoise Mount included "Medrad EnVision CT Injection System for International. Same as E8007KA Medrad EnVision CT Injection System for International. Same as E8007KB E8007KG

OPTIONS
Part Num Description Head Extension Cable 50 ft. (15.2 M) Head Extension Cable 100 ft. (30.5 M) Medrad EnVision Wall Mounted Counterpoised System "Medrad EnVision Height Adjustable Pedestal. #EHP 700," 10 Options

E8007KB

E8007LA

E8007LE

E8007LB

E8007LG

Table 10-2 EnVision CT Injection Systems

Chapter 10 - Options and Accessories

Page 109

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

INJECTOR
Part Num Description E8007LC Medrad EnVision CT Injection System for International. Same as E8007KC E8007LJ

OPTIONS
Part Num Description "Short Mobile Ceiling Mount Counter-poise Length ranges between 19-25 in." EnVision CT Injector System Installation Manual EnVision Counterpoise System Installation and Service Manual

E9999JC E9999JD Table 10-2 EnVision CT Injection Systems (Continued)

1.3

Liebel Flarsheim CT 9000 ADV Injectors


INJECTOR
Part Num E8006LC Description CT 9000 ADV Fixed Ceiling Mounted Injector System with medium/long column E8006LM

OPTIONS
Part Num Description Wall Mount Bracket for Electronics

E8006LD

CT 9000 ADV Fixed Ceiling E8006MH 100 ft. Powerhead Cable. #800111 Mounted Injector System with Short column

Table 10-3 Liebel Flarsheim CT 9000 ADV Injectors

Section 2.0 Cameras & Imaging


2.1 Kodak DryView PACS Link Laser Imaging
CAMERA
Part Num Description E8201PL E8201PM E8201PP DryView 8300 PACS Link Laser Imager. DryView 8100 PACS Link Laser Imager. DryView 8700 PACS Link Laser Imager. E8201SP

OPTIONS
Part Num Description DryView 8300 PACS Link Print Connection.

Table 10-4 Kodak DryVIew PACS Link Laser Imaging

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Chapter 10 - Options and Accessories

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

2.2

Kodak DryView Laser Imaging System


CAMERA
Part Num Description E8201SL Kodak DryView 8100 Mobile Analog Laser Imager. One Analog Direct Print Connection. E8201PT

OPTIONS
Part Num Description PACS Link Setup for Third-Party. Required for each Third-party DICOM 3.0 (i.e. OEM). PACS Link Laser Imager Upgrade Package. Does not include PACS Link Print connection.

E8201PS

Kodak PACS Link Print Connection. E8201PY Converts modality to DICOM 3.0 Print.

Table 10-5 Kodak DryView Laser Imaging System

2.3

AGFA Drystar 2000C Printers


CAMERA
Part Num Description E8202A Drystar 2000C includes One Video Network ready for Ethernet. Can be upgraded. Drystar 2000C DICOM. Print class. Must specify DICOM print. Drystar 2000C Point-to-Point, 2 Video connections. NO DIGITAL connection. Drystar 2000C Dual (1). Double [2]. Point-to-Point Video connections and DICOM print. E9999EK

OPTIONS
Part Num Description Installation and Service Manual for DS200C. Operators Manual for DS200C. DICOM Print Class Upgrade Kit.

E8202AN E802AM

E9999EL E8202AY

E8202AR

Table 10-6 AGFA Drystar 2000C Printers

2.4

AGFA Drystar 3000 Dry Daylight Printer


CAMERA
Part Num Description E8202CB Drystar 3000 Network (DICOM) E8202CD con-figuration with built-in transceiver for network connection.

OPTIONS
Part Num Description DICOM 3.0 package for Drystar 3000. 10 Options

E8202CM Drystar 3000 Point-to-Point Interface. Table 10-7 AGFA Drystar 3000 Dry Daylight Printers

Chapter 10 - Options and Accessories

Page 111

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

2.5

Codonics NP-1660M Printer GEMS_AM


PRINTER
Part Num Description E8200C E8200CA Codonics 1660M DICOM Printer connections to AW, PET-CT. Codonics 1660M PostScript Printer for connections to AW, PET-CT. E8200D

OPTIONS
Part Num Description PostScript Key for Codonics 1660M Printer.

Table 10-8 Codonics NP-1660M Printer GEMS_AM

Section 3.0 Print Camera Interface


INTERFACE
Part Num Description B7700L Digital/LCAM Camera Interface Table 10-9 Print Camera Interface

OPTIONS
Part Num Description

Section 4.0 Un-Interruptible Power Supplies (UPS)


4.1 Powerware UPS
UPS
Part Num Description P5051PS Powerware 9330 Un-interruptible Power Supply for Discovery ST system.

OPTIONS
Part Num Description

Table 10-10 Powerware UPS

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Chapter 10 - Options and Accessories

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DISCOVERY ST PRE-INSTALLATION

Section 5.0 Slicker


OPTIONS
Part Num E8016AC Description Metalless CT Slicker protective table cover. Includes table cover, extender cover, and bag holder.

Table 10-11 Slicker

Chapter 10 - Options and Accessories

Page 113

10 Options

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

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Chapter 10 - Options and Accessories

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2

DISCOVERY ST PRE-INSTALLATION

Index
A
Air Cooling Requirements and Specifications Area Designators 86 53

I
Injector Control 35 Interconnection Runs Diagram 89, 90, 93

B
Base Scanner System, Illustration 32

L
Line-to-line Voltage 80

C
Cables, Supplied Pull Size 88, 91 UL Information 88, 91 Catalog Numbers 31 Ceiling Heights, Suggested 40 Clearances, Common 35 Options 34 System Service 34 Component Dimensions 36 Interconnection Runs 89, 90, 93 Concrete 41

M
Maximum Transient Voltage Mounting Requirements Description 40 80

P
Power Input Configuration 80 Power Audit 83 Power Disconnect Diagram Fusible Disconnect and Magnetic Contactor Power Line Analyzer 83 Power Requirements Distribution Transformer 82 Grounding 81, 84 . Diagram 84 Line Monitor 87 Regulation 80

96

D
Delivery Data Gantry 74 Delivery, Crated 73 Delivery, Van 71

E
Electro-Magnetic Interference EMI 55 55

R
Radiation HSA Standard Tube Scatter Survey . Using Body Filter 43 Protection 42 Resistance to Ground 81 Room Dimensions, Typical 35 Room Door Interlock, Typical Switch and Connection 97 Room Layout, Sample 33, 34, 56 Room Warning Light, Typical Control Circuit and Connection 97S Scan Window 41 Seismic Data Center-of-gravity Information for Specific Components 58 Shielding Requirements Radiation Protection 42 Space Planning Gantry 37 Operators Console/Computer 39, 40, 51 Index Page 115

F
Facility Source 79 Floor Loading . Summary 57 Strength Of 41 Floor Levelness 41 Floor Vibration 41

Humidity Air, Cooling Requirements and Specifications

53

Index

GE MEDICAL SYSTEMS DIRECTION 2341917-100, REVISION 2 Power Distribution Unit 38, 48 Table 37 Storage Media 53 System, Prior to Installation 74 Storage Cabinet 35 System Components 31 System Options 31

DISCOVERY ST PRE-INSTALLATION

T
Temperature and Humidity Specifications Transformer Size 82 53

U
UPS Interconnect 95

Page 116

Index

CT

GE MEDICAL SYSTEMS
GE MEDICAL SYSTEMS-AMERICAS: FAX 414.544.3384 P.O. BOX 414; MILWAUKEE, WISCONSIN 53201-0414, U.S.A. GE MEDICAL SYSTEMS-EUROPE: FAX 33.1.40.93.33.33 PARIS, FRANCE 118 GE MEDICAL SYSTEMS-ASIA: FAX 65.291.7006

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