Seed 2_557-20-101 -5418654-1EN Rev 22.pdf

Pre-Installation Manual Revolution CT Family

5418654-1EN

Revision 22

General service documentation.

© 2023 GE HealthCare. GE is a trademark of General Electric Company used under trademark license.

Reproduction and/or distribution is prohibited.

This pre-installation manual covers the following products:

Product Name Configuration

Revolution CT • 160 mm detector (collimation)

• Performix tube

• Revolution CT Covers

• -61 PDU

Revolution CT ES • 80 mm detector (collimation)

• Performix tube

• Revolution CT Covers

• -61 PDU

Revolution Apex • 160 mm detector (collimation)

• Quantix tube

• Revolution Apex Covers

• -91 PDU or -92 PDU

Revolution CT with Apex Edition • 160 mm detector (collimation)

• Quantix tube

• -91 or -61 PDU or -92 PDU

Revolution CT ES with Apex Edition • 80 mm detector (collimation)

• Quantix tube

• -91 or -61 PDU or -92 PDU

Revolution Apex Select • 40 mm detector (collimation)

• Quantix tube

• Auto Patient Positioning Covers

• -91 or -61 PDU or -92 PDU

Revolution Apex Plus • 80 mm detector (collimation)

• Quantix tube

• Auto Patient Positioning Covers

• -91 or -61 PDU or -92 PDU

Revolution Apex Elite • 160 mm detector (collimation)

• Quantix tube

• Auto Patient Positioning Covers

• -91 or -61 PDU or -92 PDU

Revolution Apex Pro (China market) • 160 mm detector (collimation)

• Quantix tube

• Auto Patient Positioning Covers

• -61 PDU or -92 PDU

Revolution CT Power (China market) • 160 mm detector (collimation)

• Quantix tube

• Revolution CT Covers

• -61 PDU or -92 PDU

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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. GE HealthCare 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 GE HealthCare, 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.

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Contents 1 Introduction

1.1 Pre-Installation Manual Introduction

1.2 Document Purpose

1.3 Intended User

1.4 Who must consult this manual

1.5 Customer Responsibility

1.6 Form requirements

2 General Requirements

2.1 System Siting Requirements

2.2 Regulatory Requirements

2.3 Delivery and Handling

2.4 Shipping Dimensions and Weight

3 Equipment Specifications and Requirements

3.1 Intended Users

3.2 Gantry Dimensions

3.3 NG 2000 Patient Table Dimensions

3.4 NG2000V Patient Table Dimensions

3.5 NG1700V Patient Table Dimensions

3.6 Main Disconnect Panel (MDP) Dimensions

3.7 Power Distribution Unit (NGPDU) Dimensions

3.8 Uninterrupted Power Supply (UPS) Dimensions

3.9 Scanner Desktop II-IV Dimensions

3.10 System Cabinet Dimensions

3.11 Service Storage Cabinet Dimensions

4 Accessory Specifications and Requirements

4.1 Ceiling Requirements for Monitor-in-Room

4.2 Ceiling Requirement for Auto Patient Positioning Depth Camera

4.3 Remote Control Panel with Video Monitoring Mounting Requirements

5 Room Requirements

5.1 Flooring Requirements and Specifications

5.2 Floor Loading Data

5.3 Functional Scan Suite Layout Configuration

5.4 Work Space Requirements

5.5 Anchoring

Revolution CT Family Contents

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5.6 Electromagnetic Compatibility

5.7 Scatter Radiation Measurements

5.8 Vibration Isolation

5.9 Other Construction Considerations

6 Environmental Requirements (HVAC)

6.1 HVAC Requirements

7 Electrical Requirements

7.1 Power Requirements

7.2 Grounding

7.3 System Interconnection

7.4 System Cabling

7.5 Scan Room Warning Light and Door Switch

8 Communications Requirements

8.1 Network Requirements

9 System Connectivity Requirements

9.1 Edison HealthLink (EHL) Pre-Connectivity Checklist

9.2 Imaging Protocol Manager (IPM) Import/Export Criteria Checklist

9.3 McAfee ePO-Managed Antivirus

9.4 Remote Services Platform (RSvP) Connectivity

10 Appendicies

10.1 System Cabinet B7919AH

10.2 Scanner Desktop Dimensions

10.3 Install the Revolution CT Gantry on a Support Structure

Revision History

Language Policy

Revolution CT Family Contents

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1 Introduction

1.1 Pre-Installation Manual Introduction

(Applies to all sections within this chapter.)

1.2 Document Purpose

This preinstallation manual provides the necessary information to prepare a site for system installation. Specifically, this manual provides information:

1. To define system requirements and interactions.

2. For the effective arrangement and interconnection of system components.

3. The customer is responsible for:

3.1. Compliance with all local and national codes and regulations

3.2. Siting requirements for customer-specific site procedures (medical, CT, safety, and so on)

3.3. Any special architectural requirements (for example, seismic codes)

The implementation of all requirements and adherence to all specifications in this manual is the responsibility of the customer or its architect and engineers. Refer any questions to the GE HealthCare Project Manager of Installation (PMI).

1.3 Intended User

Roles and their responsibilities

Purchaser or Customer The entity that has entered into contract with GE HealthCare to purchase the system. See Section on Customer Responsibility below.

Customers Architectual Planner Oversees all aspects of the customers site for preparation of a successful installation. This includes but not limited to general contractor, structural, electrical, network and IT specialists, as well as HVAC.

General Contractor Customer contracted to coordinate all aspects of the installation.

Structural Engineer Customer contracted engineer consulting all aspects of the structural requirements for installation.

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Electrical Engineer Qualified (certified by a regulatory agency), in-house individual or entity contracted by the customer.

Responsible for electrical connections between customer power source and up to and including the final connection to the GE HealthCare product.

HVAC Design Engineer Customer contracted engineer consulting all aspects of the HVAC requirements for installation.

Zone Broadband Specialist GE HealthCare personnel responsible for providing IT expertise and maintaining records of specific network IT connectivity parameters that are required to properly configure the products’ connection to the broadband connection provided by the customer.

Network IT Personnel Dedicated customer site personnel affiliated with or contracted by the customer. Responsible for providing IT expertise necessary to ensure successful network IT connectivity between the GE HealthCare product and the facility.

GE HealthCare roles and their responsibility

Project Manager of Installation (PMI) GE HealthCare provided dedicated contact person working directly with the Project Site Coordinator.

Responsibilities include the overall project coordination and site planning of GE HealthCare products; manages activities cross-functionally with sales, customer, customer contractors, and local field teams to ensure customer site is designed and prepared to accept and install product in the facility.

GE HealthCare PMI must read and fully comprehend all chapters of the Pre-Installation Manual.

Prior to any construction or installation, a PMI must approve the completeness of all preliminary concepts, site plans, and final working drawings.

GE HealthCare Field Engineer (FE) GE HealthCare field personnel responsible for the actual assembly, installation, calibration of the product and verification of the proper operation and configuration of the GE HealthCare product. This may include the physical movement of the system and its subcomponents from the point of delivery to the scan suite.The FE will oversee coordinating any replacement of damage in-shipment items, and resolving missing in-shipment issues.

Revolution CT Family 1.3 Intended User

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1.4 Who must consult this manual

The following personnel must be aware of the content listed in the following sections:

Section

Personnel

Cu st om er

Ar ch ite ct

Ge ne ra l C on tr ac to r

St ru ct ua l E ng in ee r

El ec tr ic al E ng in ee r

H

VA

C En gi ne er

Zo ne

B ro ad ba nd S pe ci al is t

N et w or k

IT

P er so nn el

1 Introduction on page 6 X X X X X X X X

2.1 System Siting Require-

ments on page 12

X X X X X X X X

2.2 Regulatory Require-

ments on page 14

X

2.3 Delivery and Han-

dling on page 15

X X X

2.4 Shipping Dimensions and Weight X X

3 Equipment Specifications and Re-quirements on page 24

X X X X

4.1 Ceiling Requirements for Monitor-

in-Room on page 48

X X X

4.2 Ceiling Requirement for Auto

Patient Positioning Depth Cam-era on page 57

X X X

4.3 Remote Control Panel with

Video Monitoring Mounting Require-ments on page 63

X X X

5.1 Flooring Requirements and Speci-

fications on page 70

X X

5.2 Floor Loading Data on page 72 X X

5.3 Functional Scan Suite Layout Con-

figuration on page 74

X

5.4 Work Space Require-

ments on page 77

X

5.5 Anchoring X X

5.6 Electromagnetic Compatibili-

ty on page 96

X X

5.7 Scatter Radiation Measure-

ment on page 103

X X

Revolution CT Family 1.4 Who must consult this manual

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Section

Cu st om er

Ac hi te ct ic

Ge ne ra l C on tr ac to r

St ru ct ua l E ng in ee r

El ec tr ic al E ng in ee r

H

VA

C En gi ne er

Zo ne

B ro ad ba nd S pe ci al is t

N et w or k

IT

P er so nn el

5.8 Vibration Isolation on page 114 X X

5.9 Other Construction Considera-

tions on page 117

X X

6 Environmental Requirements (HVAC) on page 118

X X

7.1 Power Requirements X X

7.2 Grounding on page 129 X X

7.3 System Interconnection and Ca-

bling on page 131

X X

7.4 Scan Room Warning Light and

Door Interlock on page 141

X X

8 Network Requirements on page 143 X X X

9.1 Edison HealthLink (EHL) Pre-Con-

nectivity Checklist on page 145

X X X

9.2 Imaging Protocol Manager

(IPM) Import/Export Criteria Check-list on page 147

X X X

9.3 Remote Services Platform (RSvP)

Connectivity on page 149

X X X

10.1 System Cabinet

B7919AH on page 151

X X X

10.2 Scanner Desktop Dimensions X X X X

10.3 Install the Revolution CT Gantry

on a Support Structure on page 155

X X

Revolution CT Family 1.4 Who must consult this manual

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1.5 Customer Responsibility

Customer responsibility It is essential to verify all aspects of the site configuration before construction has begun, as subsequent changes can be costly or impractical. Consideration should be taken for future expansion or upgrades during the design phase of the site.

Planning and Design Work The customer will select the location of the site. All architectural, mechanical, and electrical drawings associated with the design and planning of the site are the responsibility of the customer. Any alterations or modifications to the drawings or to products not specifically included in the sales contract are the customer’s responsibility. The customer shall provide a clean and safe work environment including proper lighting. We recommend a minimum of 500 lux of illumination measured at the floor to ensure proper lighting to service the equipment. All floors, walls and ceiling should be in a finished state prior to installation, and all site construction and renovation is completed.

Regulatory Compliance The customer shall be solely responsible for all regulatory compliance.

All work shall comply with national, state and local regulatory and building codes for the location in which the installation occurs. This includes but is not limited to: permits, inspections, radiation licensing, fire control devices, earthquake regulations, international building codes, service, structural, flooring, vibration, HVAC, electrical, IT network, radiation protection, operational clearance requirements, and all applicable codes.

Electrical Requirements The customer shall be solely responsible for providing all electrical material and service required as outlined and illustrated in this publication. This includes but is not limited to: installation of all properly-sized junction boxes, outlets with covers, line safety switches, and fittings installed at the locations specified in the site design. Supplying electrical power of the required voltage, all necessary power supply cables and grounds, all necessary power cables and grounds to the PDU, and an Emergency-Off switch in the scan room.

NOTE

GE HealthCare does not provide or install conduits, junction boxes, or ducting illustrated in this publication. GE HealthCare only supplies some of the cabling and wiring used in this publication..

Accessory Installation Accessories ordered for use on the Revolution CT system come with their own service manual and installation instructions provided by the OEM (non-GE HealthCare) supplier. For items not installed by GE HealthCare Service, the customer must ensure that the accessory is installed per OEM specifications. For ceiling, wall or floor mounted accessories, ensure the item is mounted properly and will not be a hazard to users. GE HealthCare is not responsible for the contents and accuracy of the non-GE HealthCare supplied OEM installation manual.

For items installed by GE HealthCare Service but for which the pre-installation is under customer responsibility, the customer must ensure that the pre-installation work is performed per OEM specifications. For any ceiling, wall or floor support structure part of the pre-installation requirement, the customer must ensure those structures have been validated by a structural engineer. GE HealthCare is not responsible for the contents and accuracy of the non-GE HealthCare supplied OEM installation manual.

Revolution CT Family 1.5 Customer Responsibility

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1.6 Form requirements

Installation forms It will be the responsibility of the PMI to ensure the following forms are filled out completely and correctly by the proper personal and submitted prior to the end of the installation of the system. All forms are available on the Customer Potal Site by part number for download.

Form Part Number Description e4879 Installation Form BBGLY0389 The e4879 form is mandatory and must be submitted globally every time a system is installed or when certified component is re-placed. This is not a regulatory form but is required by GE HealthCare for all locations.

Note: If the system installation also includes Smart Subscription Option an additional e4879 form must be submitted.

Floor Levelness Measure-ment Form

DOC1766027 Used by Program Manager to record the floor levelness measurement prior to the installa-tion.

Pre-Installation Connectiv-ity Requirements

DOC2272544 This must be provided to the installation team prior to install. Only used with systems using Remote Services Platform (RSvP).

Revolution CT Family 1.6 Form requirements

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2 General Requirements

2.1 System Siting Requirements

System site print

A system installation, relocation, or move requires a site print.

The system site print, provided by GE HealthCare, is the overall layout of system, room components and egresses. The customer will ensure all equipment, storage cabinets, counter tops, and sinks appear on the site print, in their proper location. It is not to be used as a blue print for actual construction. If any discrepancies between actual room size, clearances, or egress is found on the site print, notify GE HealthCare PIM.

Facility Minimum clearance for doorways and hallways The scan room shall have at least one unobstructed clear doorway to move the scanner sub-systems in and out of the room. The customer is responsible for removing or protecting any doorway threshold (if one exists) in order to move the scanner sub-systems in and out of the room.

Table 2-1 Minimum doorway width requirements

Doorway Clear Opening Hallway

Minimum Width

1168.4 mm (46.0 in) No hallway or need to turn subsystems to enter the room

Minimum Width Needed to Turn Subsystem.**

1168.4 mm (46.0 in) 2438.4 mm (96.0 in)

1219.2 mm (48.0 in) 2119.3 mm (84.0 in)

1524.0 mm (60.0 in) 1802.4 mm (71.0 in)

**If there is enough room in the hallway to spin the system into the room, the minimum doorway width will be smaller. If the hallway is smaller in width, the doorway width must increase.

Table 2-2 Minimum height requirements

Doorway Clear Opening Hallway/Path to Room

1980.0 mm (78.0 in) 2438.5 mm (96.0 in)

Related hospital equipment clearances Check/verify the room layout for the necessary clearances required by any related hospital equipment.

Avoid compromising important system features by ensuring there is ample working space around the patient table for the hospital cart, emergency equipments, personnels, and so on.

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Steps for Site Readiness The PMI will work closely with the Customer and Architect in the advancement toward final site readiness. There will be sign offs at various steps towards final installation. These include but are not limited to:

• Site Readiness Completion and Verification

Installation cannot proceed until all site-readiness requirements have been completed and verified. A site is ready when all renovations/modifications have been completed and the scan suite meets all regulatory, code, and system requirements, system delivery needs, and all requirements for any options.

• Contractor’s Final Confirmation

Final confirmation of installation site readiness shall be made by all contractors associated with the project; structural engineer/architect, HVAC contractor, electrical contractor, qualified radiological health physicist, cleaning service, and so on.

• Schedule of Site-Ready Visit

To ensure timely system delivery and installation, the customer shall complete all necessary work listed in this Pre-Installation Manual and schedule a site-ready PMI visit prior to system delivery.

Revolution CT Family 2.1 System Siting Requirements

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2.2 Regulatory Requirements

Building codes, regulations and permits Building Codes and Regulations

The customer will ensure the scan suite meets all building codes and applicable local regulations.

Compliance to specifications defined in this manual as well as all federal, state, territory, province, city or local regulations (building codes, and so on.) shall be the responsibility of the customer. If a federal, state, territory, province, city, or local regulation is in conflict with a specification defined in this manual the most restrictive of the two specifications shall be applied.

Surface Penetration

Prior to drilling into the floor or other surface, an inspection is required to avoid drilling into any imbedded objects that may cause injury to the installer or cause damage to the site. For seismic active locations, there will be additional holes required in the floor to mount the other subsystems to the floor.

A GE HealthCare Surface Penetration Permit (DOC0741664) may be required to allow for GE HealthCare or GE HealthCare contracted personnel to drill into the concrete floor.

Clearance regulations Federal and National Association Regulations

Clearance regulations for all systems installed in the U.S. are determined by various federal agencies and the National Fire Protection Association (NFPA). The regulating publications are: Occupational Safety and Health Administration (OSHA) 29, Code of Federal Regulation (CFR) 1910, NFPA 70 (Standard for Electrical Safety in the Workplace), NFPA 101: (Life Safety Code), NFPA 99: (Standard for Health Care Facilities), and the ADA Amendments Act of 2008 (Americans with Disabilities Act). For countries outside the U.S., follow specific local country regulations.

Federal and Foreign Regulations

Ensure all systems installed within the U.S. and its territories comply with all GE HealthCare, federal, state, and local regulations. Compliance to specifications shall be the responsibility of the customer. If any regulation is in conflict with a specification defined in this manual, the most restrictive of the two specifications shall be applied.

Codes, clearances, and service space regulation Federal, State, and Local Codes The diagrams and dimensions used throughout this manual, detail required clearances for proper system operation and servicing only. The customer shall be responsible for ensuring all federal, state, and local county codes and clearances are followed and maintained, regarding facility egress and all other related requirements.

Revolution CT Family 2.2 Regulatory Requirements

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2.3 Delivery and Handling

Contents of this section include:

• GE HealthCare Project Manager Task List on page 15

• Delivery types and system lifting and rigging restrictions on page 16

• Shipping and receiving on page 18

• Storage on page 20 Construction sites on page 20

GE HealthCare Project Manager Task List

NOTICE

This document should be reviewed by the GE HealthCare Project Manager of Installation (PMI) and site service personnel a minimum of 6 weeks prior to the actual installation.

NOTICE

It is highly recommend that the PMI review the product installation manual prior to starting an installation to ensure no major changes to the install process requires additional pre-work.

Task Description

Site dimensions PMI shall measure and verify all site dimensions to ensure the facility can accommodate the delivery of the system (and any related com-ponents or equipment), from the delivery drop-off point to the scan suite.

Delivery type PMI shall determine type of delivery: loading dock or ground level.

Ground level delivery may require a fork truck.

Delivery equipment PMI shall determine if delivery requires special dollies, lifting crates, or riggers. PMI shall order any additional delivery equipment and all necessary delivery personnel.

NOTE

The CT gantry or its sections cannot be lifted or trans-ported by any means other than pallet or the dolly sys-tem which it was delivered. Otherwise, serious damage to the gantry could result.

Revolution CT Family 2.3 Delivery and Handling

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Identify delivery route PMI shall identify the delivery route, which may include any eleva-tors, doorways, and hallways necessary to accommodate the deliv-ery of all system components.

NOTE

The customer's structural engineer of record is responsi-ble for making sure the floor material and design along the delivery route (loading dock, halls and rooms) meets the forces and weight requirements for the delivery of the individual sub-systems to the final installation loca-tion within the facility.

Non-Construction-Zone route to scan suite PMI shall verify an accessible, dust-free, non-construction-zone de-livery route to the scan suite.

Packaging requirements PMI shall order any construction site packaging requirements prior to shipment. Packaging cannot be modified once the system is ship-ped.

Floor protection PMI shall determine if floor protection is required along facility deliv-ery route and communicates requirement to delivery company/per-sonnel.

Consult the Shipping Dimensions and Weight for details on each system component and carts.

Delivery types and system lifting and rigging restrictions

DANGER

PERSONAL INJURY OR DEATH, EQUIPMENT DAMAGE. TIP HAZARD.

Gantry is very heavy and may tip over if tilted past 10 degrees.

When transporting a system to the final destination, do not exceed tilt angle equal to, or greater than 10 degrees in either direction of axis.

• Loading Dock Deliveries (Preferred method): Facilities with a loading dock in the receiving areas can generally accommodate delivery of the system by semi-tractor trailer. This is the preferred method for system delivery. Dock-to-dock shipment minimizes the possibility of dropping the gantry or damaging other sub-systems during the transition from the trailer to the facility. This method also allows for the most efficient packing and unpacking of the system.

• Ground (Non-Loading Dock) Deliveries: Facilities without a loading dock require a lift-gate or forklift. Such deliveries require unloading the system components from the truck bed to ground level and then transported to the facility over a smooth surface such as a concrete sidewalk or driveway or paved area. These paved surfaces must be able to support the weight of the sub-systems. It may be necessary to protect these surfaces as well.

• Lift-Gate Truck: The delivery truck requires a lift-gate rated for at least a 2722.0 kg (3.0 tons) capacity. When the gantry or table is lowered to ground level, lower it at a steady rate using the slowest speed as possible to minimize G-loads until the lift-gate reaches the ground. Keep the gantry or table level when moving to avoid flipping. Failure to smoothly transition the table and gantry to ground level may cause serious damage to the table, gantry or their transport dollies.

Delivery of the system by tilt-bed truck is no longer an approved delivery method due to EHS safety risks of tipping the system over. If a loading dock is not available, use an appropriately sized forklift truck.

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Rigging

The CT gantry assemblies shall not be lifted by their dollies. The CT gantry assemblies shall not be transported across any surface by any means other than the dollies provided by GE HealthCare. The CT gantry assemblies have no lifting points on them and are not designed to be lifted by any special rigging attached to the gantry assemblies themselves.

DANGER

POSSIBLE SEVERE PERSONAL INJURY OR DEATH.

The dollies are not designed to be used as an attachment point for any method of lifting the subsystems.

Attaching lifting straps, cables or mechanisms to the dolly handles or any other part of the dolly is strictly prohibited.

NOTICE

If it is determined that the sub-systems must be lifted by crane or other lifting method the PMI or person responsible for local siting of the system shall NOT proceed with the installation without consulting with GE HealthCare Engineering. The GE HealthCare PMI is responsible for getting consultation.

Lifting the sub-systems by crane or other lifting method should always be avoided. All alternate methods of delivery should be evaluated including the removal of any obstructions, doorways, walls, and windows.

If lifting is still required, see Shipping Dimensions and Weight:

1. The entire gantry assembly and both gantry transport side dollies must be placed on a lifting platform. GE HealthCare does not provide a lifting platform.

The Stationary Assembly shall be lowered to its transport position with the gantry base in contact with the platform. The Rotating Assembly shall be lowered to its transport position resting on the dolly transport pads in contact with the platform.

NOTE

If the platform has limited space, the gantry transport side dollies may be removed during the lift. Once the lift is completed, the gantry transport side dollies must be installed back on the gantry assembly.

2. The entire patient table must be on its dollies and lifted while sitting on a lifting platform.

The patient table on its dolly shall be lowered to its transport position so the table base is in contact with the platform.

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3. The platform must be designed such that no lifting straps or cables come in contact with any part of the gantry or table sub-systems or its side dollies.

4. The lifting platform shall bear the entire load. No part of the sub-system shall bear any load during the lift.

NOTE

If delivery requires vertical or horizontal lifting, the PMI needs to add the necessary identifier to the order.

Shipping and receiving Handling Restrictions

• Shock Restrictions: The system cannot tolerate shock or vibration. System components cannot be tipped, dropped, or hoisted. The PMI shall communicate these restrictions to everyone involved with handling the system components.

• Rolling on Surfaces: System components shall be rolled across smooth surfaces (sidewalks, parking lots, tile flooring, and so on.) only. If a smooth surface is not available (for examples, a sidewalk or driveway has cracks or uneven joints, or a tiled floor has deep or rough joint lines), then floor protection shall be used to move the system across the uneven surface.

• Shipping Crate/Packaging Integrity: Do not damage or puncture the shipping crate or packaging.

Floor Protection

To protect the floor during delivery, floor protection shall be used along the entire delivery path and throughout the scan suite, where necessary.

Door Threshold Not Allowed The customer is responsible for removing any doorway threshold (if one exists), in order to move the scanner sub-systems in and out of the room.

Floor Load Along Delivery Route The customer’s structural engineer of record is responsible for making sure the floor material and design along the delivery route (loading dock, halls and rooms) meets the forces and weight requirements for the delivery of the individual sub-systems to the final installation location within the facility.

• Evaluate the flooring along the path from where the system will be delivered and installed in the scan suite. For finished floors, adequate space must be present to lay down sheets of fiberboard (masonite) with a minimum thickness of 6.35 mm (1/4 in) in front of the subsystem dolly wheels as they are moved through the facility.

DO NOT move any subsystem from the loading dock or unloading platform location unless the finished floor is protected. This is the responsibility of the delivery company. Use of protective sheets of fiber board (masonite) is required to roll and move subsystem components to the scan suite.

Dollies, Installation and Shipping Carts

• U.S. Installations — Shipments within the United States typically involve the use of dollies (pre-installed on the gantry sections and table) for moving the gantry sections and table to the suite, and the use of installation and shipping carts and pallets for other parts. After completing the installation, return all dollies, the gantry shipping cage, and installation and shipping carts to UMI using the shipping document found in box #1. http://www.umi-dollyshop.com. Pallets are not re-usable.

• Installations Outside U.S. — For shipments outside the United States, customers may purchase dollies at: http://www.umi-dollyshop.com. DO NOT return dollies, the gantry shipping cage, or installation and shipping carts to the U.S. Instead, forward dollies, cage, and installation and

5418654-1EN Revision 22 Pre-Installation Manual 18/171 shipping carts to the local GE HealthCare office or warehouse. The gantry sections and table subsystems are shipped with dollies attached placed on a pallet for transport. Pallets are not re-usable.

• Installations China Only — For system installations in China, dollies and shipping carts are returned to: GE HealthCare Renewable Resources (Tianjin) Co., Ltd.

Address: No 266-1 Jingsan Road Airport Economic Zone Tianjin City

Important Returning toxic materials, chemicals of any type, paints or food waste items in the shipping carts is prohibited. With the exceptions noted below, table/gantry dollies and their associated shipping cages, as well as shipping carts, can eventually be returned to UMI Inc. DollyShop Division. Go to their website for instructions on where and how to return the dollies; http://www.umicompany.com/umimobility/

Exceptions: For tables shipped with yellow transport dollies: If the table was delivered in a wooden crate with yellow transport dollies already attached, both the crate and yellow dollies are single-use and must be discarded or recycled. They are not returnable.

• The square footage required for the installation and shipping carts storage can be calculated based on the dimensions in GE HealthCare Project Manager Task List on page 15.

Delivery Temperature and Humidity Tolerance

When transporting the system, excluding any scanner desktop LCD display monitors, water-filled calibration/IQ phantoms and covers, the temperature shall be maintained within the range of -40 to +70° C (-40 to +158° F), inclusive.

When transporting the system, excluding water-filled calibration/IQ phantoms, all packing material shall remain intact and the relative humidity shall be maintained within the range of 5% to 95% (non-condensing), inclusive.

NOTE

See the table below for the shipping temperature and humidity ranges of excluded items.

Table 2-3 Shipping temperature and humidity ranges for excluded items

Items Temperature Humidity

NOTE

Relative hu-midity (non-condensing)

LCD monitors -20 to +60° C (-4 to +140° F) 5% to 95%

Covers -40 to +50° C (-40 to +122° F) 5% to 95%

Water-filled calibration/IQ phantoms +5 to +70° C (+41 to +158° F) 5% to 95%

After delivery to the scan suite and before unpacking any system components, allow 12 hours for the equipment to adjust to room temperature to avoid condensation or rapid temperature change. This 12 hour warm up period is not required if the shipping environment meets the same temperature and humidity requirement as the scan room and the system components are already at steady room temperature.

Unpacking System

Do not remove any protective wrapper or packaging from any system component until all construction is complete and all construction dust is removed from the installation site.

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Do not remove the scanner desktop from the shipping skid until after the unit has been delivered to the scan suite location.

Storage If storing a system prior to installation, the system shall be stored in its original packaging in a temperature and humidity controlled environment protected from water and dust. It is advised that storage of the system be no longer than six months. If storage is going to exceed six months, contact your PMI for long-term storage procedures.

Table 2-4 Humidity and ambient temperatures for storage**

Ambient temperature shall be maintained within a range of: +4 to +27° C (+40 to +80° F)

Maximum rate of change in the temperature shall be no greater than: 3° C per hour (+5.4° F)

Relative humidity (non-condensing) shall be maintained within a range of: 20 to 60% RH

Maximum rate of change in the relative humidity shall be no greater than: 5% RH per hour

** Delivery van/truck storage shall meet these same requirements.

The estimated floor footprint of all the packages shipped with a standard Revolution CT system takes up an area approximately 45.5 feet (1386.8 cm) long by 8.5 feet (259.1 cm) wide by 7.0 feet (213.4 cm) high.

Construction sites The site for delivery and installation must be a dust-free, occupancy-ready state. If the site is under construction or adjacent construction, the system and all its components must be packaged for construction site. Determine if the system will be stored or installation at this site.

1. Construction Site Storage

• Construction site packaging must be ordered and the system shipped packaged for storage.

• Do not damage or puncture the shipping crate.

• Do not remove packaging until the completion of all construction at the site and the removal of all dust created by the construction.

• Maintain a storage temperature within the range outlined in the Pre-installation Manual.

• Maintain a relative humidity as outlined in the Pre-Installation Manual.

2. Construction Site Installations

A construction installation describes installations at sites without an occupancy permit, or ongoing construction. In general, construction sites fail to meet the required specifications for system delivery, and GE HealthCare does not recommend such installations, as they can result in delays, increased costs, and possible damage to the system. When construction-site delivery proves unavoidable, the installation falls into one of two categories:

• Full construction site with completed radiology area

This type of site consists of a finished, dust-free, occupancy-ready radiology suite at a site with ongoing construction in other areas, but with no remaining construction in or around the scan suite area. At the time of delivery such sites feature:

2.1.1. Dust control measures deployed in the radiology suite area.

2.1.2. Scan suite access limited to a single entrance.

2.1.3. Radiology suite sealed off from the remaining construction area.

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2.1.4. Operational HVAC, with a positive air pressure within the radiology suite.

In addition, the radiology suite at such a site REMAINS in a dust-free, occupancy-ready state after delivery and throughout the remaining construction phase.

• Full construction site with limited delivery access

This type of site allows delivery during ongoing construction of the radiology suite area.

Construction site packaging must be ordered and the system is delivered packed for construction site storage. Packaging cannot be added during the delivery.

At full construction sites, delivery occurs prior to site completion, but the product remains stored until the completion of a finished, dust-free, occupancy-ready radiology suite area.

This system is delivered in sealed packages with dollies. Delivery to the storage area requires a lift truck or riggers. Installation work can begin only when the site reaches the completed, dust-free, occupancy-ready radiology suite requirement.

2.4 Shipping Dimensions and Weight

Gantry Shipping Dimensions and Weight

Gantry Height mm (in.)

Length mm (in.)

Width/

Depth mm (in.)

Weight kg (lb)

Stationary assembly (with two (2) gantry transport side dollies and upper and lower cross bars) *Assume the lowest point of its bottom is 101 mm (4 in) above the floor.

Adjust the vertical dimension with transporting dollies to desire height if necessary.

**Width becomes 925 mm (36.4 in) if cross bars are removed.

*2049.0 (80.7)

2753.0 (108.4)

**1149.0 (45.2)

1738.8 (3830.0)

Rotating assembly (with gantry transport cage plus two (2) gan-try transport side dollies)

NOTE

Assume the transport cage is raised so the lowest point of its bottom is 97.0 mm (3.8 in) above the floor.

1905.0 (75.0)

2878.0 (113.3)

1018.0 (40.1)

1681.6 (3704.0)

Gantry transport side dolly -- (Two (2) for stationary assembly and two (2) for rotating assembly)

NOTE

Does not include cross-bars.

1360.0 (53.5)

328.0 (12.9)

870.0 (34.3)

95.3 (210.0) [190.7

(420.0)]

Gantry cross-bars (4) N/A N/A N/A 45.4 (100.0)

Gantry transport cage 1552.0 (61.1)

2377.0 (93.6)

925.0 (36.4)

564.8 (1244.0)

Gantry covers and cover brackets N/A N/A N/A 331.4 (730.0)

Revolution CT Family 2.4 Shipping Dimensions and Weight

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Patient Table Shipping dimensions and weight

Patient Table Height mm (in)

Length mm (in)

Width/ Depth mm

(in)

Weight kg (lb)

NG-2000 table with shipping dolly

NOTE

Table is fully lowered (550.0 mm (21.7 in) ) and in Home position for shipping *Estimated weight.

1244.6 (49.0)

3866.4 (155.2)

863.6 (34.0)

*1257.6 (2770.0)

NG-2000 Table at mechanical shipping height with four (4) trans-porting dollies/extension brackets *Height can be adjusted by table elevation.

**Estimated length, bulkhead included.

***Estimated weight

*1230.0 (48.4)

**3149.6 (124.0)

1120.0 (44.1)

***866.0 (1905.0)

NG-2000V Table with shipping dolly 1244.6 (49.0)

3866.4 (155.2)

863.6 (34.0)

1280.0 (2816.0)

NG-2000V Table at mechanical shipping height with four (4) transporting dollies and extensions

*1230.0 (48.4)

(117.0)

1120.0 (44.1)

737.2 (1622.0)

NG-1700V Table with shipping dolly 1244.6 (49.0)

3866.4 (155.2)

863.6 (34.0)

1108.0 (2438.0)

NG-1700V Table at mechanical shipping height with four (4) transporting dollies and extensions

*1230.0 (48.4)

(105.2)

1120.0 (44.1)

(1430.0)

Scanner Desktop Shipping dimensions and weight

Scanner Desktop Height mm (in)

Length mm (in)

Width/ Depth mm

(in)

Weight kg (lb)

Scanner Desktop IV 660.0 (26.0)

670.0 (26.4)

600.0 (23.6) 29.5 (65)

Scanner Desktop (I-III) computer (with shipping crate) 769.6 (30.3)

1219.2 (48.0)

1016.0 (40.0)

85.9 (189.2)

Operator workspace table (option) (with shipping crate) N/A 1520.0 (59.8)

915.0 (36.0)

74.9 (165.0)

System Cabinet Shipping dimensions and weight

System Cabinet Height mm (in)

Length mm (in)

Width/ Depth mm

(in)

Weight kg (lb)

System Cabinet VII 1219.2 (48) 1346.2 (53) 863.6 (34) 256.2 (565)

System Cabinet VI 1536.7 (60.5)

1485.9 (58.5)

977.9 (38.5)

404.7 (892.2)

System Cabinet V (with shipping brackets and crate) 1536.7 (60.5)

1485.9 (58.5)

977.9 (38.5)

404.7 (892.2)

System Cabinet IV (with shipping brackets and crate) 1536.7 (60.5)

1485.9 (58.5)

977.9 (38.5)

478.54 (1055)

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System Cabinet Height mm (in)

Length mm (in)

Width/ Depth mm

(in)

Weight kg (lb)

System Cabinet III (with shipping brackets and crate) 1536.7 (60.5)

1485.9 (58.5)

977.9 (38.5)

352.8 (777.0)

PDU Shipping dimensions and weights

Power Distribution Unit (PDU) Height mm (in)

Length mm (in)

Width/ Depth mm

(in)

Weight kg (lb)

NGPDU-61 (with shipping crate) 1214.2 (47.8)

1219.2 (48.0)

1219.2 (48.0)

374.6 (825.0)

NGPDU-91 (with shipping crate) 1222.0 (48.1)

975.0 (38.0)

635.0 (25.0)

480.8 (1060.0)

NGPDU-92 (with shipping crate) 1222.0 (48.1)

975.0 (38.0)

635.0 (25.0)

551.5 (1215.9)

Other components dimensions and weight

Miscellaneous Components Height mm (in)

Length mm (in)

Width/ Depth mm

(in)

Weight kg (lb)

Service storage cabinet (option) (with shipping crate) 1206.5 (47.5)

977.9 (38.5)

673.1 (26.5)

61.3 (135.0)

UPS (If equipped) (with shipping crate) 1358.9 (53.5)

1219.2 (48.0)

1016.0 (40.0)

297.4 (655.0)

Shipping Cart dimensions and weight

Shipping Carts Height mm (in)

Length mm (in)

Width/ Depth mm

(in)

Weight kg (lb)

Installation Cart #1 1403.4 (55.3)

1308.1 (51.5)

781.1 (30.8)

168.0 (370.0)

Installation Cart #2 1403.4 (55.3)

1308.1 (51.5)

781.1 (30.8)

174.8 (385.0)

Installation Cart #3 (frames and brackets) 1410.0 (55.5)

1315.0 (51.8)

790.0 (31.1)

220.0 (484.6)

Revolution Cover Cart #4 (front cover and rear bezel) 2095.0 (82.5)

2360.0 (92.9)

740.0 (29.1)

250.0 (550.7)

Revolution Cover Cart #5 (covers) 1670.0 (65.7)

2120.0 (83.5)

890.0 (35.0)

190.0 (418.5)

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3 Equipment Specifications and Requirements

3.1 Intended Users

(Applies to all sections within this chapter.)

3.2 Gantry Dimensions

Gantry dimensions and weight

Figure 3-1 Gantry dimensions

Gantry Height mm (in)

[1] Length mm (in)

[2]

Width/Depth mm (in)

[3] Weight kg (lb)

Assembled gantry for all Revolution gan-tries (without covers or cover brackets)

1938.0 (76.3) 2059.0 (81.1) 1041.4 (41.0) 2544.7 (5605.0)

Assembled gantry for Revolution CT, Revo-lution CT ES and Revolution CT with Apex Edition (with covers installed)

2005.0 (78.9) 2365 (93.1) 1427.5 (56.2) Revolution CT:

2874.5 (6335) Revolution CT

ES: 2820.4

(6218)

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Figure 3-2 Gantry dimensions for Revolution Apex Select

NOTE

Dimension of assembled gantry depth is measured when both front and back top LCD displays in open position.

Gantry Height mm (in)

[1] Length mm (in)

[2]

Width/Depth mm (in)

[3] Weight kg (lb)

Revolution Apex Elite, Plus, Select gantry (with covers installed) 2036.5 (80.2) 2300.0 (90.6) 1331.4 (52.4) 2676.2 (5900)

Revolution Apex gantry (with covers instal-led) 2029.5 (79.9) 2293.6 (90.3) 1331 (52.4) 2798.7 (6170)

Gantry open cover dimensions The figure below shows the maximum height of the front cover during installation and during service.

Note: the exact dimensions in both figures are different, more hieght is required for installation.

Anything from the ceiling must stay above these heights or there will be a collision with the top cover.

Note, the change in placement of the maximum height location.

Revolution CT Family 3.2 Gantry Dimensions

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Figure 3-3 Maximum height at installation and during service

Figure Height Length (from ISO center)

Gantry front cover installa-tion

(1) 2252 mm (88.6 in) (2) 1760 mm (69.2 in)

Gantry front cover service (3) 2126 mm (83.7 in) (4) 1097 mm (43.2 in)

Air Flow: Intake air pulled through side covers. Exhaust air pushed through top covers.

Figure 3-4 Air flow for Revolution CT, Revolution ES and Revolution Apex

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Gantry Center of Gravity

Figure 3-5 Gantry Center of Gravity (all gantry models)

1907 mm (75.1 in)

954 mm (37.5 in)

837 mm (32.9 in)

837 mm (32.9 in)

937 mm (36.9 in)

937 mm (36.9 in) m m

(1 5.

in

) 76 m m

(3 0.

in

1873 mm (73.7 in)

837 mm (32.9 in)

737 mm (29 in)

737 mm (29 in)

737 mm (29 in)

737 mm (29 in)

837 mm (32.9 in)

954 mm (37.5 in)

NOTE

CG-Y from floor at nominal feet height is 963 mm (37.9 in.).

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3.3 NG 2000 Patient Table Dimensions

Patient Table Height mm

(in) Length mm

(in) Width/Depth mm (in) Weight kg (lb)

NG-2000 table (only) 1230.0 (48.4) 2971.8 (117.0) 609.6 (24.0) 799.0 (1760.0)

NG-2000 table foot pedal unit 209.0 (8.2) 733.0 (28.9) 574 (22.6) 33.0 (72.7)

NOTE

The weight of the patient table does not include patient load.

Figure 3-6 NG-2000 table component dimensions and Center of Gravity

5765 ± 10 mm (227 ± 0.4 in)

2270 mm (89.4 in)

2793 mm (110 in)

545 mm (21.5 in) m

(4

0.

in

2045 mm (80.5 in)

2459 mm (96.8 in)

1155 mm (45.5 in)

407 mm (16 in)

225 mm (8.9 in)

Item Description Dimensions

1 Capacity table 227 kg (500 lb) 688 mm (27.1 in)

Capacity table 306.7 kg (675 lb) 725 mm (28.5 in)

2 Center of gravity

3 ISO center

4 Transporter Travel

NOTE

CG calculations include the maximum patient weight listed, on the end of the cradle when fully extended at maximum elevation.

Revolution CT Family 3.3 NG 2000 Patient Table Dimensions

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Figure 3-7 NG-2000 patient table Center of Gravity

1948 mm (76.7 in)

S P

P

P

S

S

P

S

P

S

L

S P

1997 mm (78.6 in)

994 mm (39.1 in)

843 mm (33.2 in) m m

(8 .7 in m m

(1 7.

in

145 mm (5.7 in) m m

(1 7.

in m m

(8 .6 in

140 mm (5.5 in) 140 mm (5.5 in)

47 mm (1.9 in)

68 mm (2.7 in)

145 mm (5.7 in)

13 x Ø72 mm (13 x Ø3 in)

Item Description Dimensions

1 Capacity table 227 kg (500 lb) 171 mm (6.7 in)

Capacity table 306.7 kg (675 lb) 341 mm (13.4 in)

Revolution CT Family 3.3 NG 2000 Patient Table Dimensions

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3.4 NG2000V Patient Table Dimensions

(in) Length mm

(in) Width/Depth mm (in) Weight kg (lb)

NG2000V table (only) 1232 (48.5) 2960.4 (116.5) 600.2 (23.6) 670.0 (1474.0)

NG2000V table foot pedal unit 216 (8.5) 591 (23.3) 594 (23.4) 34 (74.8)

NOTE

The weight of the patient table does not include patient load.

Figure 3-8 NG2000V table component dimensions and Center of Gravity

5746 ± 10 mm (226.2 ± 0.4 in)

2470 mm (97.2 in)

2793 mm (110 in)

2020 mm (79.5 in)

770 mm (30.3 in)

1792 mm (70.6 in)

1033 mm (40.7 in)

407 mm (16 in) in

2 3

Item Description Dimensions

1 Capacity table 227 kg (500 lb) 795 mm (31.3 in)

Capacity table 306.7 kg (675 lb) 796 mm (31.3 in)

2 Center of gravity

3 ISO center

4 Transporterless — no travel

NOTE

CG calculations include the maximum patient weight listed, on the end of the cradle when fully extended at maximum elevation.

NOTE

NG1700V and NG2000V have identical COG data.

Revolution CT Family 3.4 NG2000V Patient Table Dimensions

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Figure 3-9 NG2000V patient table Center of Gravity

1226 mm (48.3 in) 1189 mm (46.8 in) 1151 mm (45.3 in)

839 mm (33 in)

764 mm (30.1 in) m m

(1 7.

in m m

(1 7.

in m m

(1 1.

in

87 mm (3.4 in)

2 3

Item Description Dimensions

1 Capacity table 227 kg (500 lb) 197 mm (7.8 in)

Capacity table 306.7 kg (675 lb) 362 mm (14.3 in)

2 Primary anchor locations

3 Secondary anchor locations

Revolution CT Family 3.4 NG2000V Patient Table Dimensions

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3.5 NG1700V Patient Table Dimensions

(in) Length mm

(in) Width/Depth mm (in) Weight kg (lb)

NG1700V table (only) 1233.0 (48.5) 2660.5 (104.7) 600.2 (23.6) 650.0 (1430.0)

NG1700V table foot pedal unit 216 (8.5) 591 (23.3) 594 (23.4) 34 (74.8)

NOTE

The weight of the patient table does not include patient load.

Figure 3-10 NG1700V table dimensions

5146 ± 10 mm (202.6 ± 0.4 in)

2170 mm (85.4 in)

2493 mm (98.1 in)

1720 mm (76.7 in)

770 mm (30.3 in)

1792 mm (70.6 in)

1033 mm (40.7 in)

407 mm (16 in) in

Item Description Dimensions

1 Capacity table 306.7 kg (675 lb) 794 mm (31.2 in)

2 Center of gravity

3 ISO center

4 Transporterless — no travel

NOTE

CG calculations include the maximum patient weight listed, on the end of the cradle when fully extended at maximum elevation.

NOTE

NG1700V and NG2000V have identical COG data.

Revolution CT Family 3.5 NG1700V Patient Table Dimensions

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Figure 3-11 NG1700V patient table Center of Gravity

1226 mm (48.3 in) 1189 mm (46.8 in) 1151 mm (45.3 in)

839 mm (33 in)

764 mm (30.1 in) m m

(1 7.

in m m

(1 7.

in m m

(1 1.

in

87 mm (3.4 in)

2 3

Item Description Dimensions

1 Capacity table 306.7 kg (675 lb) 362 mm (14.3 in)

2 Primary anchor locations

3 Secondary anchor locations

Revolution CT Family 3.5 NG1700V Patient Table Dimensions

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3.6 Main Disconnect Panel (MDP) Dimensions

MDP details in this section are intended for seismic calculations and does not fully represent all variations available.

MDP E4502BG (200 kVA)

216 mm (8.5 in)

210 mm (8.25 in) 229 mm (9.5 in)

368 mm (14.5 in) 424 mm (16.7 in)

89 mm (3.5 in)

424 mm (16.7 in)

19 mm (0.75 in)

19 mm (0.75 in)

Ø10 mm (Ø0.4 in) m m

(3 0.

in…