System Requirements MX 6000/4000 CT

Author: J. Credico

MX 6000/4000 CT System Planning Data

Contents

1 INTRODUCTION ..................................................................................................................................... 4
1.1 History of the Document .......................................................................................................................... 4
1.2 Scope ....................................................................................................................................................... 4

2 SYSTEM CONFIGURATION ................................................................................................................... 4

2.1 Preferred Room Layout ........................................................................................................................... 4
2.2 Compatibility ............................................................................................................................................ 5
2.3 Attention Points ........................................................................................................................................ 5
2.4 Tips .......................................................................................................................................................... 5
2.5 Software Licensing................................................................................................................................... 6

3 ENVIRONMENTAL DATA ...................................................................................................................... 6

3.1 Equipment Heat Loads ............................................................................................................................ 6
3.1.1 Examination Room ............................................................................................................................... 6
3.1.2 Technical Room (optional) ................................................................................................................... 6
3.1.3 Control Room ....................................................................................................................................... 6
3.2 Heating, Ventilation & Air Conditioning .................................................................................................... 6
3.2.1 Examination Room ............................................................................................................................... 6
3.2.2 Technical Room (optional) ................................................................................................................... 7
3.2.3 Control Room ....................................................................................................................................... 7
3.2.4 CT Suite De-Humidification .................................................................................................................. 7
3.3 Acoustical ................................................................................................................................................. 7
3.3.1 Examination Room ............................................................................................................................... 7
3.3.2 Technical Room ................................................................................................................................... 7
3.3.3 Control Room ....................................................................................................................................... 7
3.4 Fringe Field & Magnetic Field .................................................................................................................. 7
3.5 Shielding X-ray......................................................................................................................................... 8
3.5.1 System Dose ........................................................................................................................................ 8
3.6 Liquid data ............................................................................................................................................... 8
3.7 Compressed Air ....................................................................................................................................... 8
3.8 Air Quality ................................................................................................................................................ 8
3.9 RF Immunity............................................................................................................................................. 9
3.10 regulatory compliance .......................................................................................................................... 9
3.11 recycling materials list .......................................................................................................................... 9

4 MANPOWER ........................................................................................................................................... 9
4.1 Manpower Requirements ......................................................................................................................... 9
4.2 Required Tools ......................................................................................................................................... 9

4598 002 32911 CSIP Level 1 1

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

4.3 Test Phantoms and Table Accessories .................................................................................................10

5 SITE SURVEY .......................................................................................................................................10

5.1 Planning Survey .....................................................................................................................................10
5.2 Network Survey......................................................................................................................................10

6 PRE-INSTALLATION ............................................................................................................................10
6.1 BU Reference ........................................................................................................................................10
6.2 GSS Responsibilities .............................................................................................................................10
6.3 Customer Responsibilities .....................................................................................................................11

7 SHIPPING & HANDLING ......................................................................................................................11

7.1 Transport & Delivery ..............................................................................................................................11
7.2 Rigging & Lifting .....................................................................................................................................12
7.3 Environmental Data (General) ...............................................................................................................12
7.4 Elevator lifts for patient couch................................................................................................................13

8 MECHANICAL / STRUCTURAL ...........................................................................................................13

8.1 Equipment weight, Sizes and Center of Gravity ....................................................................................13
8.1.1 Dimensions & Weights .......................................................................................................................13
8.1.2 Boundary / Space Considerations ......................................................................................................14
8.2 Floor .......................................................................................................................................................15
8.2.1 Loading ...............................................................................................................................................15
8.2.2 Vibration .............................................................................................................................................15
8.2.3 Leveling ..............................................................................................................................................15
8.2.4 Anchoring ...........................................................................................................................................15
8.3 Ceiling ....................................................................................................................................................16
8.4 Wall ........................................................................................................................................................16

9 ELECTRICAL DATA .............................................................................................................................16

9.1 Mains Supply & Quality mains supply....................................................................................................16
9.1.1 Power Conditioning & UPS (Uninterruptible Power Supply) ..............................................................18
9.2 Facility Wiring.........................................................................................................................................18
9.3 System Cables .......................................................................................................................................19
9.4 Cable Ducts & Raceways ......................................................................................................................19
9.5 Conduit pipes .........................................................................................................................................19
9.6 Lighting ..................................................................................................................................................19
9.6.1 Examination Room .............................................................................................................................19
9.6.2 Technical Room .................................................................................................................................19
9.6.3 Control Room .....................................................................................................................................19
9.7 Power Outlets / Sockets ........................................................................................................................20
9.7.1 Examination Room .............................................................................................................................20
9.7.2 Technical Room .................................................................................................................................20
9.7.3 Control Room .....................................................................................................................................20

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This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

10 NETWORK DATA .................................................................................................................................20

10.1 System requirements .........................................................................................................................20
10.2 RSN (Remote Service Network) ........................................................................................................20
10.2.1 Remote Service Network Configuration .............................................................................................21

11 DOWNLOADS AND DRAWINGS .........................................................................................................21

Proprietary Notice CSIP Level 1:

This document and the information contained in it is strictly reserved for current Philips Medical Systems (“Philips”) personnel, Philips licensed representatives and Philips customers
who have purchased a valid service agreement for use by the customer’s designated in-house service employee on equipment located at the customer’s designated site. Use of this
document by unauthorized persons is strictly prohibited. This document must be returned to Philips when the user is no longer licensed and in any event upon Philips’ first written
request.
Liability / Warranty Disclaimer:
Philips provides this DOCUMENT without warranty of any kind, implied or expressed, including, but not limited to, the implied warranties of merchantability and fitness for a particular
purpose. Philips has taken care to ensure the accuracy of this document. However, Philips assumes no liability for errors or omissions and reserves the right to make changes without
further notice to any products herein to improve reliability, function, or design. Philips may make improvements or changes in the product(s) or program(s) described in this document at
any time.

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This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

1 INTRODUCTION
The MX 6000/4000 CT systems are advanced dual slice detector continuous-rotation tomographic scanner
systems. MX 6000D or MX 4000D versions have the same pre-installation and site planning requirements.
These systems are intended for an installation in smaller room areas as compared to other scanners.

1.1 HISTORY OF THE DOCUMENT

4598 002 32911 31/Jan/2012

This is an initial PRD release.

Previous version MX4000/6000 PRD documents that have been removed and now combined under 4598 002
32911:
 MX 6000/4000 CT Room Requirements – 4535 673 58692
 MX 6000/4000 CT System Planning Data - 4535 673 58683

1.2 SCOPE
This document provides site planning and pre-installation information on the MX 6000 Dual/ MX 4000 Dual/
MX 4000 CT system for all Philips GS&S and Key Market Drawing Offices and Project Managers worldwide to
apply. This is neither a construction document nor an installation manual.

2 SYSTEM CONFIGURATION
The MX 6000 Dual and MX 4000 Dual CT Systems consist of the following system components:

(1) Gantry and Patient Table.

(2) Operator Console/Table, Monitor, CT-Box, Keyboard, Microphone, Mouse.
(3) Computer Rack/Host, Network Switch, UPS option built inside of Computer Rack.
(4) Power Filter Box (IEC compliant) for export (standard) configuration.
(5) Power Protection Unit 50 kVA Hua Run Voltage Regulator for China only (non-IEC compliant) option.
(6) Teal LM Isolation Transformer 37 kVA (IEC compliant) option.

2.1 PREFERRED ROOM LAYOUT

The Preferred Room Layouts are examples of a most common CT suite. It is the responsibility of the GS&S/
Key Market Project Management and Drawing Office to verify: a) Space requirements meeting delivery,
4 CSIP Level 1 4598 002 32911
This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

installation, servicing and operation are met; b) Licensed electrical, mechanical and structural engineers hired
by the customer to meet facility requirements compatible with Philips equipment; c) Certified physicist to
determine room radiation protection, and; d) All national and local building codes have been met concerning
safety.

It is not allowed to place high voltage, UPS, VR or power conditioning equipment closer than 1.5 M (60
inches) from patient couch unless it is certified as a medical grade device. Philips strongly recommends that
these ancillary components be located in a Technical room (equipment closet) adjacent to the CT Exam room
or Control room. This provision may also protect the Philips Technician from radiation during equipment
installation and servicing. Philips UPS/VR equipment should never be located further than 61 M (200 ft.) from
the CT system. The Philips LM is to be located within 15.2M (50 ft.) from the CT.

See Downloads Section Z-11 Preferred & Minimum Room Layouts for drawing examples.

2.2 COMPATIBILITY
Note: Philips Medical Systems design and manufacturing practices comply with IEC and other regulatory
standards as approved medical imaging devices.

 The MX Workspace supports DICOM connectivity 3.0 compliant, PACS, scanners, workstations and
printers.

2.3 ATTENTION POINTS

A longer table top foot holder extension is being offered. All three options now available are as follows:
 Head holder
 Short foot extender

See revised drawings under Section 11 Downloads.

New Vibration specifications and graph chart have been provided. See Download Z-2.6 for the chart.

Updates applied to Networking Data have been provided under Section 10.2 and 10.2.1

Individual radiation dose maps have been created. See Download Z-7

New wood shipping crate and pallet design for gantry has been developed.

Patient Table floor anchor hole locations now resemble MX16.

Some information and options described in this PRD may not apply to systems sold directly in China.

The Philips/Teal LM Transformer option is required and must be ordered at additional cost for sites not having
380/220V, 4 wire (neutral) wye configurations, or where only 3 wire delta configurations are present and
grounding isolation is absent not meeting Philips specifications for any voltage between 200-480V. The LM
should be located within the CT suite with cable runs no further than 15.2M (50 ft.) from the CT gantry input
connections.

For sites not requiring the LM transformer, a 380/220V, 50/60 Hz, three-phase, wye supply with neutral wire is
required from the facility power supply, along with an isolated ground wire from the same N/G reference point.
See Section 9 Electrical Data and Downloads Z-14 Cable Data for mains connection schematics and
diagrams.

2.4 TIPS

Power Filter Box is provided as standard equipment for non-IEC compliant site locations and required 380V,
wye configuration with grounded neutral from the power supply source.

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This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

The Philips/Teal LM Isolation Transformer input voltage range is from 200 to 480V and output having
380/220V feeding the CT system is both 50 and 60 Hz compatible. The LM is required to meet IEC or when
supply source does not meet Philips requirements.

The LM Isolation Transformers may be used in combination with the Full System UPS or VR, in order to
provide the proper input voltage to the CT system.

2.5 SOFTWARE LICENSING

Product licensing is managed through Commercial Order Management (COM). Each system is delivered with
the options licenses according to the sales records.
http://pww.hfa.ms.philips.com/homepage/CustomerSupport.
On this page you have to select: License Utility, MX16/4000/6000 option key generator.

3 ENVIRONMENTAL DATA
3.1 EQUIPMENT HEAT LOADS
3.1.1 Examination Room
Heat emission
MX6000 Scanner Gantry : 5.7 KW (19,500 BTU/hr)
MX4000 Scanner Gantry : 4.09 KW (14,000 BTU/hr)
Either/Or 1.5 kW (5,123 BTU/hr) – Standby

3.1.2 Technical Room (optional)

Heat emission
Power Filter Box : Negligible. Note: May be located in exam room
LM Isolation Transformer : 0.65 KW (2,210 BTU/hr) Note: May be located in exam room.
(option)
Full System UPS and/or V.R. : 1.9 KW (7,000 BTU/hr) – estimated. Usually remotely located
(option)

3.1.3 Control Room

Heat emission
Operator Workstation & : 0.75 KW (2,561 BTU/hr)
Computer Rack
Console UPS (option) : 0.11 KW (375 BTU/hr) [inside Computer Rack]

3.2 HEATING, VENTILATION & AIR CONDITIONING

3.2.1 Examination Room
 The gantry requires air-conditioning and good air flow. Additional capacity and circulation must be
considered when other equipment is located in this area including, but not limited to, other Philips
system cabinets or power conditioning equipment.
 The ideal stable room temperature for the gantry during operation and including patient comfort is 22
degrees C (72 F). Under no instances shall the temperature be allowed to drop below 20 C (68 F) or
rise above 24 C (75 F). Relative humidity 30% to 60% (non-condensing).
 The above conditions must be maintained at all times including overnight, weekends and holidays.
 Location of room air-conditioning supply vents must not discharge directly over patient table and
treatment area causing discomfort to patient.
 See Downloads Section Z-2 interface Data for gantry air flow circulation directions.

6 CSIP Level 1 4598 002 32911

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

3.2.2 Technical Room (optional)

Power conditioning equipment should be located in a Technical or Equipment room to prevent interference of
its noise with the patient intercom system. See Control room Requirements below.

3.2.3 Control Room

 The Operator Workstation/ Computer Rack require air-conditioning and good air flow. Additional
capacity and circulation must be considered when other equipment is located in this area including,
but not limited to, UPS, EBW and monitoring equipment.
 The ideal stable room temperature for the equipment during operation and including technician
comfort is 22 degrees C (72 F). Relative humidity 30% to 60% (non-condensing). Under no instances
shall the temperature be allowed to drop below 20 C (68 F) or rise above 24 C (75 F).
 The above conditions must be maintained at all times including overnight, weekends and holidays.
 Power conditioning equipment should be located outside of the control room, in order to help
eliminate heat concerns and prevent noise interference with the patient intercom.

3.2.4 CT Suite De-Humidification

2
Exam Room Size (M ) Air-Conditioning Capacity (HP) De-humidify (Watts)
Less than 20 2 5,000 *
More than 20 3 2 x 5,000 *
Operator Room Not more than 2.5
Ceiling Height: 2.8M
* Suggested that all sites with high humidity provide one dehumidifier unit for small room and two units for
larger room. Moderate humidity site locations can apply one dehumidification unit.

3.3 ACOUSTICAL
3.3.1 Examination Room
Audible noise
Scanner Gantry : 68 dB @ 1 meter typical
Note: If transformers or power conditioning equipment is placed in the exam room it should be positioned as
far away from the gantry (within limitations of distance safety regulations and cable lengths) or located within a
dedicated closet enclosure, in order to prevent interference of its noise with the patient intercom.

3.3.2 Technical Room

Audible noise
LM Isolation Transformer : 50 dB @ 1 meter typical
(option)

3.3.3 Control Room

Audible noise
Operator Workstation & : 55 dB @ 1 meter typical
Computer Rack

3.4 FRINGE FIELD & MAGNETIC FIELD

The external field strength at scanner and all other system components must be less than 1 gauss
( 0.1mT).

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This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

3.5 SHIELDING X-RAY

Room shielding requirements for CT scanners can be unique for any particular scanner installation. Scanner
placement within the scan room as well as specifics about the scan room and the spaces surrounding the
scan room should be considered in order to develop a proper scan room shielding design.

Scanner room shielding should therefore be designed and/or at least reviewed and approved by a qualified
radiological health physicist or the facility’s radiation safety officer. The completed shielding design should
also be inspected and verified to meet industry standards before clinical scanning begins (see NCRP report
#147 entitled “Structural Shielding design for Medical X-ray Imaging Facilities”). Other guidelines must be
followed as determined by local or country codes and regulations.

The primary and required input from manufacturers for determining the required shielding design is found in
the IEC Stray Radiation Dose Map(s) for a particular system. This map presents near worst-case room
scatter values in a horizontal plane containing the system’s axis of rotation. The map may also be rotated
about its symmetry axis (i.e. the scanner’s axis of rotation) to obtain room scatter values in the vertical
direction. From this scatter data and other detailed information about the scanner operation and the site, an
adequate and proper shielding design can be developed.

Additional information that could be useful in producing a successful radiation shielding design:

 Materials used in the construction of the existing walls, floors, doors and ceilings of the room and
surrounding spaces.
 Occupancy information (contents and usage) of the surrounding rooms and spaces.
 Anticipated operating workload for the scanner to be sited. Some busy modern scanners can
experience workloads approaching 1,000,000 mAs/week or more.
 Room scatter varies approximately linearly with collimated beam width if other factors remain
unchanged. For example, a 20 mm collimated beam width will produce approximately 50% of the
room scatter values as that of a 40 mm collimated beam width for a 140 kVp x-ray beam. Like
wise an 80 mm collimated beam will produce roughly twice the room scatter as a 40 mm beam
width.
 The scattered radiation falls off approximately as the square of the distance from the scattering
source. For example, the scattered dose at 2 meters is approximately 6.35 mm (¼ inch) the value
at 1 meter.
 Second and third order scatter from the air in the scanner room can result in a measurable and
significant dose behind adequate primary scatter barriers. CT control rooms should always be
surveyed to verify compliance with NCRP #147 guidelines.
 Typical shielding requirements for modern multi-slice scanner rooms can vary from 1.58 mm (1/16
inch) to 3.17 mm (1/8 inch) lead equivalency, depending on the site specifics mentioned above.

3.5.1 System Dose

See Downloads Section Z-7 Miscellaneous for drawing dose maps emitted from the MX16 gantry.

3.6 LIQUID DATA

N/A

3.7 COMPRESSED AIR

N/A

3.8 AIR QUALITY

Airborne contaminants must be minimized once the Philips medical equipment is placed in the clinic/ hospital
facility staging area or CT suite. All major room construction must be completed eliminating concrete and
drywall dust. Refer to appropriate Room Ready Checklists for more details and level of acceptance.

8 CSIP Level 1 4598 002 32911

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

Once the CT system has been fully installed and turned-over to the customer, air quality must be maintained
throughout the life of the system. Common use and change of linens and blankets around the patient exam
room area can cause dust to clog gantry air intake filters.

Design of the facility HV/AC system must always consider common dust and dirt problems affecting internal
equipment sub-components, air flow and system reliability. Air vents (supply, return, positive, negative,
pressurized, or otherwise) should be fully ducted and must never be distributed through open interstitial ceiling
spaces exposed to dust, asbestos and other contaminants. Chemical contamination must also be considered,
in order to avoid corrosion to internal and external equipment parts and connections.

3.9 RF IMMUNITY
N/A

3.10 REGULATORY COMPLIANCE

N/A

3.11 RECYCLING MATERIALS LIST

The following list is an estimate of the total MX 6000/4000 CT system by material and weight content. Contact
the CT BU for additional information and documentation on this topic when required.

Material Content (global) Weight Material Content (global) Weight

(KG) (KG)
Lead (Pb) 25.151 Printed Circuit Boards 6.874
Iron (Fe) 1259.57 Tungsten (W) 2.183
Aluminum (Al) 563.69
Copper (Cu) 15.828 All other material types 336.704

4 MANPOWER
4.1 MANPOWER REQUIREMENTS
Installation Activity Hours FSEs Total Labor
Hours
Unpacking and Positioning System Components 4 2 8
Gantry Final Leveling and Anchoring 2 2 4
Connection System Components 2 2 4
Preparing the system for operation 1 1 1
First time system operation and functional checks 3 1 3
Calibration & Acceptance test 1 1 1
Network installation, configuration 1 1 1
Installing license keys and verifying options 1 1 1
Preparing System for Clinical operation 1 1 1
Sub Totals 24
First year learning curve 1 4
Totals 28

4.2 REQUIRED TOOLS

All tools listings can be obtained from the CSPP (Customer Support Product Plan). Contact the Helpdesk for
more information.

4598 002 32911 CSIP Level 1 9

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

4.3 TEST PHANTOMS AND TABLE ACCESSORIES

Test phantoms for imaging calibration system and patient accessory attachments are provided with each CT.
Preferred storage location for these various devices should be within the immediate CT suite for easy access
to the Philips FSE and customer’s Physicist. Never store phantoms in areas where temperature approach
freezing.

5 SITE SURVEY
5.1 PLANNING SURVEY
See General column of the PRD website for the Site Inspection/ Pre-installation Checklist from CT Service
Innovations. Also refer to General column of the Ingenuity CT webpage module for helpful links.

5.2 NETWORK SURVEY

See General column of the PRD website for the Site Inspection/ Pre-installation Checklist from CT Service
Innovations. Refer to the Connectivity section for networking, including RSN.

6 PRE-INSTALLATION
6.1 BU REFERENCE
CT BU references available to GS&S / Key Market offices:
 PRD (Planning Reference Data).
 Pre-installation and Site Planning Checklists
 Pre-installation and Installation tools & kit catalogs
 Operator and User Instructions
 Installation Manuals.
 Safety Guideline Manuals.
 RSN website (managed by Global Customer Services).

Most of the above data is available on InCenter as follows:

http://incenter.medical.philips.com/Default.aspx?tabit=43&PTLLObjld=356730

Note: InCenter requires log in with user ID (your e-mail – [email protected]) and password
(IST password).

6.2 GSS RESPONSIBILITIES

GS&S / Key Market Pre-installation Responsibilities:
 Completion of Pre-installation or Site Planning Checklists.
 Power line surveys and monitoring (see Section 9).
 RSN connectivity arrangements.
 Providing calculations to customer for seismic compliance.
 Meeting service and access clearances around equipment.
 Room preparation & site ready acceptance.
 Hiring of 3 party contractors as required.
rd

 Delivery instructions and rigging needs.

 Delivery schedules and release, or pre-release, of Philips equipment and kits.
 Coordination and release of vendor’s equipment and startup or commissioning.
 Coordination of all national and local building codes & regulations with customer.
 Coordination of all safety requirements with customer.
 Preparation of Site Planning Guides translated and produced in local country language.
 Preparation of site specific Site Planning Drawings in local country language.
 Turn-Key contract agreements and language.

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This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

6.3 CUSTOMER RESPONSIBILITIES

Customer Pre-installation Responsibilities:
 Acceptance of Philips room layout and equipment delivery path.
 Site accommodations and approvals to accept Philips equipment delivery.
 Meeting site ready dates agreed upon with Philips.
 Compliance to Philips Site Planning drawings and equipment specifications.
 Clean room preparations for installation of Philips equipment.
 Supply & install all electrical, mechanical, structural and environmental facility apparatus.
 Supply and install all wiring, over-current protection and EPO switches.
 Supply and install all raceways, troughs, junction boxes and conduit pipes.
 Hiring of licensed electrical, mechanical and structural contractors or engineers.
 Facility meeting Philips safety and equipment performance specifications.
 Installation and wiring of all Philips supplied power protection equipment and safety switches.
 Networking infrastructure, Broadband connectivity and jack connections (See Section 10)
 Determine room radiation protection by a certified physicist according to local regulations.
 Handling and removal of hazardous materials.
 Other requirements agreed with Philips GS&S or local Key Market representative.
 Compliance to all national and local building codes & regulations.
 Networking connections and IT setup

7 SHIPPING & HANDLING

7.1 TRANSPORT & DELIVERY

Floor loading and clearances must be determined as acceptable by the customer along the entire delivery
path with, but not limited to, doorways, corridors, ramps, elevators and the CT exam room. Philips supervision
(or by a trained and approved Philips representative) is required during the entire delivery and handling
process for all CT system equipment or heavy UPS and power conditioning equipment. Use of elevator lifts to
move CT equipment to another floor level within building must be first approved by the customer’s facility
engineer or elevator service provider prior to equipment delivery. Allowable load limits will vary depending on
elevator classification for passenger and freight use. If CT gantry is not permitted for elevator lift due to
exceeding weight limits, elevator use may still be permitted for the CT patient couch. See Section 7.4 for more
information.

Domestic:
Defined as shipments delivered from factory in China directly to customer site or depot transported by truck.

International:
Defined as shipments delivered from factory in China transported in crate by ocean, air and/or truck (outside
of China) to a depot prior to arrival at customer site. For shipments to North America the system will be
delivered to a Philips warehouse facility and uncrated there. Gantry wheels will be provided with system
delivered to customer and attached on site. Couch wheels will be attached at warehouse for delivery to
customer. See 7.2 defining when the full gantry crate is required for crane lift operations.

All international shipments are in wooden crate without transportation kit. It is recommended that the local KM
office, which handles the delivery of these scanners, order a minimum of one kit with their first scanner. These
returnable Gantry and Patient Table Casters can also be ordered through Service Parts and maintained by
the KM after installation is completed.

All delivery trucks used to transport the CT system must have shock absorbers as the minimum requirements.
Air-ride suspension is preferred. The CT system components must remain in its original packaging from the
factory to the warehouse or (in some instances) directly to customers’ delivery door.

Forklift Specifications:

4598 002 32911 CSIP Level 1 11

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

4500 kg minimum capacity capable of balancing load that is 2.4 M long with center of gravity at
midpoint when lowering gantry and wooden crate from delivery truck.
 Fork thickness: 184 mm wide by 57 mm high.
 Fork length: 1524 mm long (min).
 Fork spread: 610 mm apart (center to center).
Note: Wood pallet skid must remain attached to bottom of gantry for all forklift operations.

Refer to the following gantry delivery weight combinations to determine a specific configuration:
 2000 kg = Configuration for crated delivery: Gantry (no side covers) inside full wooden shipping crate
with pallet skid.
 2035 kg = Configuration for mainly North America delivery: Gantry (no side covers) with wooden
pallet skid. Lift forks must penetrate at least 1475 mm through length of skid.
 1938 kg = Configuration for moving through hospital building: Gantry (no side covers) with dolly
wheels attached.

Refer to the following list for a breakdown on individual components to itemize from:
 1850 kg = Gantry without covers
 2000kg = Full wooden shipping crate including pallet skid with gantry
 185 kg = Wooden shipping pallet skid only
 88 kg = Dolly wheel set (4 individual wheel assemblies provided)
Note: For elevator lifts, it may be possible to reduce gantry weight by temporarily removing the dolly wheels.
Contact the HelpDesk for more information and direction as needed.

Once the wooden shipping crate is dismantled, the pallet skid under the gantry can be removed by using the
dolly wheels as jacks to raise the gantry. Never attempt to move or push the gantry without either the
dolly wheels or wooden shipping pallet skid. Gantry and Couch dolly wheels must be ordered by the
GS&S or Key Market Office when not provided from factory with the CT system delivery.

For shipments from factory to outside of China, the CT system will first be transported to a depot/warehouse
from Customs in a wooden crate. The gantry may be uncrated at the warehouse and then delivered to the
customer’s site, or possibly uncrated at the customer’s site. Wood pallet skid must remain attached under
gantry until all forklift operations have been completed. Gantry dolly wheels will not be provided with the CT
system delivery. See description above for North America procedures.

See Downloads Section Z-5 Transport Data for all crating dimensions, moving and lifting clearance distances.

7.2 RIGGING & LIFTING

Philips supervision is required during the entire delivery and handling process of the CT system. For overhead
lifting with a crane, the wooden shipping crate must remain attached to the gantry. Nylon straps will wrap
around the bottom of the crate’s lower pallet skid. Minimum roof hatch opening must be predetermined prior to
delivery for the entire crate to fit through the building facility. Never tip the gantry or attempt to lay it flat to
compensate for low overhead clearances.

7.3 ENVIRONMENTAL DATA (GENERAL)

Stock / Transport
Temperature in °F (C) -4 / + 131
(See Note 1) (-20 / + 55)
Temperature in °F (C) /hour 7.2 (5)

Humidity in % (non-condensing) 10 / 90
Gradient °F (C) /hour (See note 2)
Vibrations Frequency range in Hz 1 – 150
Vibrations / Shock Amplitude in mm 0 – 0.75
Vibrations / Acceleration in grms 0 – 10
Shock Acceleration in g 0 – 10
12 CSIP Level 1 4598 002 32911
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copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

Shock Pulse Duration in msec 6 – 10

Air pressure in kPa (10 mbar) 50 - 106
Note 1: These temperatures do not apply to phantoms which contain water, which will freeze at temperatures
from 0 C (32 F) or lower. Batteries should not be exposed above 25 C (77 F) for extended periods.
Note 2: Do not unpack until the product has acclimated to the ambient temperature at least 24 hours.

7.4 ELEVATOR LIFTS FOR PATIENT COUCH

Size and weight rating capacities for elevator lifts will vary. In most instances the weight of the CT patient
couch will not exceed those load limits; however, couch length must be considered to determine fit. Other
methods may be required and must be determined by Philips and the rigging company hired by the customer.
Contact the CT Helpdesk for more information and instructions.

8 MECHANICAL / STRUCTURAL
8.1 EQUIPMENT WEIGHT, SIZES AND CENTER OF GRAVITY
See Downloads Section Z-2 Interface for overall dimensions, center of gravity displacement and weights for
MX16 system equipment components and accessory or options.

8.1.1 Dimensions & Weights

Notice: Refer to Installation and Service Manuals for this product on equipment handling and safety
considerations.
Crate / Box Dimension mm (inches) Weight kg (pounds)
Length Width Height
Packed 2370 1030 2250 2000
Gantry (in (93.3) (40.5) (88.6) (4409)
wooden crate)
Transport Gantry 3063 984 1920 1938
with wheels (120.6 (38.7) (75.6) (4273)
(bottom of gantry
spaced 30 mm
above floor)
Installed 2210 890 1890 1720
Gantry (87) (35) (74.5) (3792)
Packed Patient 2570 970 1230 475
Table Couch (in (101.2) (38.2) (48.5) (1047)
wooden crate)
Transport Patient 2300 885 870 383
Table Couch (with (90.6) (34.9) (34.3) (845)
caster wheels)
Installed Patient 2440 575 1100 343
Table Couch (96.1) (22.7) (43.3) (756)
(extended) (Maximum)

Packed Console Located on accessories pallet

Table Desk
Installed 1400 700 740 35
Console Table (55.2) (27.6) (29.2) (77)
Desk (Monitor &
Acc.)
Packed LCD 570 370 575 11.5
19” Monitors (ea.) (22.4) (14.6) (22.7) (26)
Installed LCD 488 221 495 8
19” Monitor (19.2) (8.7) (19.5) (18)
Packed Host Located on accessories pallet

4598 002 32911 CSIP Level 1 13

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

Computer
Installed Host 660 620 720 32
Computer Rack (26) (24.4) (28.3) (71)
(without US)

Packed CCT 1320 770 800 92

Cart (52) (31) (32) (203)
Installed CCT 637 645 1571 34
Monitor & Cart (25) (25.5) (62) (75)
Accessories 1850 1090 1400 225
Pallet (73) (43) (55) (495)

Couch covers 1850 1090 580 59

(73) (43) (23) (131)

Gantry Side 1850 1090 580 66

Covers (73) (43) (23) (145)

989605200861 Philips (Teal) LM Isolation Transformer (50/60 Hz)

Input: 200 to 480 VAC
Output: 380/220 VAC
(This option is required for all non-380Vsites or for IEC compliance)
Packed LM 940 740 890 352
Isolation (37) (29) (35) (775)
Transformer
Installed LM 516 552 712 274
Isolation (20.3) (21.7) (37) (604)
Transformer
Power Filter Box Option (50Hz)
Packed Filter Box 480 170 650 45
(18.9) (6.7) (25.6) (99)
Installed Filter 420 138 590 200
Box (16.5) (5.4) (23.3) (66)

Refer to Installation manuals and User/Operation instructions for information describing all Philips
factory approved power conditioning and UPS equipment not listed in the chart above.

8.1.2 Boundary / Space Considerations

Apply the following space distances mm (inches) around CT equipment as described. Local codes may
exceed these requirements:

Host Computer Rack:

 914 (36”) front for service
 102 (4”) sides for air flow
 100 (4”) rear for air flow and cables. Note: Good air flow needed when located under counter top or
2
shelf. Provide 5 x 46 cm (2” x 18”) opening on counter top near wall or area of 232 cm (36 sq in).

Gantry Couch:
 914 (36”) sides for safe service access
 Front and rear distances are usually dictated by table travel and patient access. Note: Minimum
distance from gantry isocenter to rear wall is 1890 (74.5”) for use with long table top extension.
 Ceiling height: Recommended 2.43M (8’-0”); Minimum for air flow 2.3M (7’-6”)

LM Isolation Transformer:

14 CSIP Level 1 4598 002 32911

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copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

 914 (36”) front for service

 610 (24”) above for service
 152 (6”) sides for air flow
 203 (8”) rear for air flow and cable bending

8.2 FLOOR
8.2.1 Loading
Gantry
Concrete load area: .65 Sq. M (6.9Sq. Ft.)
Floor area: 1.7 Sq. M (18.3 Sq. Ft.)

Patient Couch
Concrete load area: .07 Sq. M (.75 Sq. Ft.)
Floor area: .75 Sq. M (8 Sq. Ft.)

See Downloads Section Z-3 Floor Plate Base Structure for equipment floor loading displacement and
dimensions in relationship to floor contact locations.

8.2.2 Vibration
Operation Operation
Gantry & Couch Rest of System
Vibrations Frequency range in Hz 1 – 150 1 – 150
Vibrations / Shock Amplitude in mm 0.15 0.15
(peak to peak)
Vibrations Acceleration in grms See Note 1 0–2
Shock Acceleration in g 0–2 0–2
Steady State Vibration See Note 1 xxx
Air Pressure in kPa (10 mbar) 70 – 110 70 – 110
Note 1: See Downloads Section Z-2 Interface for Floor Vibration Amplitude Limit profile chart.

8.2.3 Leveling
See Downloads Section Z-2 Interface for equipment floor levelness and waviness tolerances within given
equipment perimeters.

When shim stock is applied exceeding 6.3mm (1/4”) in thickness to compensate for un-level floor surfaces,
improper anchor engagement may occur using the standard mounting hardware supplied with the CT system.
Local Philips Service representative to determine alternative solutions with customer, such as: deeper
anchors, longer studs, through bolting, grout pad, etc.

8.2.4 Anchoring
Gantry
 Sleeve anchor with 4000 psi (27.6 MPa) normal weight concrete:
 123 mm long M14 mm diameter with 75 mm embedment
 Tension = 3300 lbs (14.7 kN) ultimate anchor value
 Shear = 4580 lbs (20.4 kN) ultimate anchor value
 Torque = 22 ft-lbs (30 Nm)

Patient Couch
 Sleeve anchor with 4000 psi (27.6 MPa) normal weight concrete:
 110 mm long M12 mm diameter with 80 mm embedment
 Tension = 3300 lbs (14.7 kN) ultimate anchor value
4598 002 32911 CSIP Level 1 15
This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

 Shear = 4580 lbs (20.4 kN) ultimate anchor value

 Torque = 22 ft-lbs (30 Nm)

See Downloads Section Z-2 Interface for equipment floor anchor hardware provided by Philips indicating
required drill-hole methods.

8.2.4.1 Seismic
Seismic calculations are to be provided through a third-party licensed engineering firm hired by the Philips
GS&S or local Key Market office in compliance with state or country regulations. The Philips Factory will
provide the equipment mounting hole diameters and locations at the floor, along with equipment weight and
center of gravity displacement in the X, Y, Z directions. Availability of Philips seismic mounting bracket kits will
be listed is Sales Cat.

See Downloads Section Z-2 Interface for equipment center of gravity weight and locations where available.

8.3 CEILING
Finished ceiling height must not restrict service access, air flow and user’s appliances with the CT equipment.
See 8.1.2 for exam room ceiling height requirements.

8.4 WALL
N/A

9 ELECTRICAL DATA
9.1 MAINS SUPPLY & QUALITYMAINS SUPPLY
Supply configurations : 3 phase delta, 4 wires (L1, L2, L3, PE) to Teal LM unit
3 phase wye, 5 wires (L1, L2, L3, N, PE) to Power Filter Box
3 phase wye, 5 wires (L1, L2, L3, N, PE) from Teal or Power
Filter Box to Gantry
Mains resistance : 75 mOhm line to line, max. (voltage dependant)
Mains fuse (standards) : Connect to Teal unit
150 Amp Type-D class mini circuit breaker (200 to 240 VAC)
100 Amp Type-D class mini circuit breaker (380 to 480 VAC)
Connect to Power Filter Box
100 Amp Type-D class mini circuit breaker (380/220 VAC)
Measured current (standby, : MX 6000 Dual
steady state, maximum) Standby 3.42 Amps
Steady state 10 Amps
Maximum 80 Amps (50 KW scan @ 380 VAC)
MX 4000 Dual
Standby3.31 Amps
Steady state 10 Amps
Maximum 58 Amps (36 KW scan @ 380 VAC)
Voltage variation : +/-10 % total (absolute) limits for 50 Hz
+/-10 % total (absolute) limits for 60 Hz
Voltage impulse : +/- 2KV per IEC 61000-4-4
Voltage surge : Line to GND 2KV Line to Line 1KV volts (peak) max. less than
100ns
Voltage sag : 95%, 1 cycle, 5 sec.
Static frequency variation : +/- 1 Hz

Harmonic voltage distortion : 5 % max. THDv

(single, total)

16 CSIP Level 1 4598 002 32911

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(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

Branch power recommended : Capacity determined by input rating

Maximum power required : 38 kVA for MX 4000
53 kVA for MX 6000
Nominal input power : Connect to Teal unit
380 VAC,+/-10% total (absolute) limits
480 VAC,+/-10% total (absolute) limits
Connect to Power Filter Box
380/220 VAC, +/-10% total (absolute) limits
Line frequency range : 50 +/- 1 Hz
60 +/- 1 Hz
Room disconnect/ circuit breaker : Connect to Teal unit
100 Amps Type-D class mini circuit breaker @ 380 to 480 VAC
150 Amps Type-D class mini circuit breaker @ 200 to 240 VAC
Connect to Power Filter Box
100 Amps Type-D class mini circuit breaker @ 380 VAC
Phase to phase imbalance : 5%
Load voltage regulation : +/- 5% not to exceed absolute limits
Voltage drop allowed in feeders : 2% when supply source and other line impedance contributors
(copper) do not exceed an additional 3%, which equates to 5% total
regulation limit.
Conductor impedance : Ohms/ 1000 Ft. (305 M), .85 PF, copper wires in steel conduit
Power factor : 0.85 min. PF

Equipment Isolation
The CT system equipment components shall be insulated from building steel, such as; raceways, trough
ducts, junction boxes, floor rebar, etc. Apply 454110065793 isolation kit with supplied tools. See
Downloads Section Z-4 Templates for isolation template alignment. Only isolated ground wires from the
facility power source or power conditioner shall provide proper grounding to the CT system, assuring
safety and ground quality in compliance with country and local codes. See Protective Earth Ground
paragraph below.

Supply Device
For 380/220 VAC sites, it is possible not having to provide the Philips/Teal LM Isolation Transformer.
However, the facility transformer supply source shall provide isolation between its input mains and
output. The source shall be configured as a wye. Floating delta or corner/split leg ground is forbidden.
The neutral of the wye shall be bonded to protective earth. When stepping up voltage to meet Philips
requirements, reverse orientation and wiring of the supply transformer is forbidden. Philips shall approve
the type and use of any power protection and conditioning equipment.

For non 380 volt sites, or where a 4 wire with neutral is not present (any voltage between 200-480), the
Philips/Teal LM Isolation Transformer option must be ordered and provided with the CT system. The LM
will provide isolation between its delta input and wye output as a separately derived source.

The Philips/Teal LM will accommodate and/or correct the following conditions:

a. Provides isolated earth (IG or PE) and neutral (N) conductors as a separately derived
source with Neutral / Ground X0 reference point.
b. The run length of feeders exceeds 61 meters (200 ft).
c. It is necessary to improve power factors and reduce fault current.
d. It is necessary to adjust voltages to meet CT system input ranges.
e. It is necessary to reduce harmonic currents induced in the supply.

Protective Earth Ground

A dedicated protective earth conductor shall be supplied by the facility. Preferably, the earth conductor
will have its origin at the electric utility’s power entrance to the facility or a newly derived supply source.
This conductor shall be sized equal to and routed with the output conductors between the supply device
and input of the Philips/Teal LM ground (X0) reference point at N/G. From here, an isolated ground (IG)
shall be routed with the power conductors and neutral wire from the output of the LM to the CT gantry
4598 002 32911 CSIP Level 1 17
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copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

incoming connections. If an LM is not provided, than the facility supply must be configured as described
above. Resistance between CT gantry ground and the facility earth ground must not exceed 0.1 Ohm.

Over-current Protection
Over-current protection shall be provided from the facility power supply to the Teal LM unit, or Power
filter Box, as specified by local and national codes. Where external protective devices are applied, such
as circuit breaker or line fuses, the recommended branch circuit protection level shall be 100 Amp rated
at 380 to 480 VAC and 150 Amp rated at 200 to 240 VAC. Apply Type - D class mini circuit breakers.
Note: The Power Filter Box requires 380/200 VAC input.

Remote Emergency Off (EPO)

As a minimum, there shall be a means for remotely turning OFF the power at the supply device or power
protection unit on the supply side of the Teal LM unit. These switches are to be installed in the control
room near the operator’s console or as determined by local or national codes. Other remote means of
disconnecting power at the supply device or power conditioner may be required by code. The Teal unit
has built-in provisions to accommodate a remote EPO switch.

Room Safety Disconnect

A means shall be provided to lockout power to the Teal LM unit or Power Filter Box as may be required
by local or national codes. This passive 3 phase room disconnect switch is to be located within visual
inspection of the Power Filter Box or Teal LM unit and CT scanner gantry such that service personnel
can lockout the power source, and easily view its state of operation.

Filters, Surge Suppressor & Phase Protection

Line filters and surge protection devices may be provided within Philips approved power conditioning
equipment.

Ground Fault Detectors

Provide ground fault detection equipment according to local or national codes.

Cable Containment
All system cables shall be contained in raceways or metallic conduit pipes as approved by local codes.
The CT system cables are not plenum rated.

Minimal Allowed Cable Bending

The fiber optics in this system must be handled carefully. The minimum bend radius is 5 cm (2 inches).
All other cables have a minimum bending radius of 10x the cable diameter.

9.1.1 Power Conditioning & UPS (Uninterruptible Power Supply)

A wall mounted Power Filter Box is provided by Philips when no other power protection options are ordered.

Nominal input voltage to the Power Filter Box or Factory approved voltage regulator (China option only)
requires 380 Vac, 50 Hz. Use of Teal isolation transformer has input range of 200-480 Vac, 50/60 Hz.
Special output circuits on all these Philips approved devices will accommodate the CT gantry scanner (380V)
and operator console (220V). Note: Teal option will NOT require use of standard Power Filter Box (PFB)
between Teal and CT gantry, even though the standard PFB may be provided with the Teal option.

Other commercial brands may not be compatible. Philips must approve substituting or adding other power
protection equipment. See Sale Catalog listings for all Factory approved power conditioners from Philips.

9.2 FACILITY WIRING

Run distances and cable/ conductor sizes from Facility Supply (through room disconnect) to Teal LM or
Power Filter Box units are all based on 380 VAC input.

18 CSIP Level 1 4598 002 32911

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copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

Connect to Teal LM unit:

2
0 – 50 Ft. (15.2 M) : 4 #2 (35 MM ) power and earth
2
51 – 100 Ft. (30.5M) : 4 #1 (42 MM ) power and earth
2
101 – 200 Ft. (61M) : 4 #00 (70 MM ) power and earth

Connect to Power Filter Box:

2
0 – 50 Ft. (15.2 M) see Note 1 : 5 #4 (16 MM ) power, neutral and earth
2
51 – 100 Ft. (30.5M) see Note 1 : 5#3 (25 MM ) power, neutral and earth

Connect from Teal LM or Power Filter Box to Scanner Gantry:

2
0 – 50 Ft. (15 M) see Note 1 : 5 #6 (10 MM ) power, neutral and earth

Note 1: Size neutral wire according to local codes. Philips recommends the neutral wire be oversized by at
least 2X.

Note 2: Licensed electrical contractor shall supply and install all copper cable/ conductor wiring described
above and is responsible for connecting to Philips supplied voltage regulator, isolation transformer or power
filter equipment. Philips FSE will make final connections to scanner gantry and consoles, as required.

9.3 SYSTEM CABLES

Cable Containment
All system cables shall be contained in metallic raceways, troughs, junction boxes or conduit pipes as
approved by local codes. The CT system cables are not plenum rated. Usable system cable lengths
from trough or junction box exit point to exit point should not exceed 19.2 M (63 feet).

Minimal Allowed Cable Bending

The fiber optics in this system must be handled carefully. The minimum bend radius is 5 cm (2 inches).
All other cables have a minimum bending radius of 10x the cable diameter.

See Downloads Section Z-14 Cable Data for cable chart defining specific lengths, routings, diameters and
connector sizes.

9.4 CABLE DUCTS & RACEWAYS

Full access to removable trough or raceway covers along the entire lengths is required. Do not route under or
behind heavy equipment that cannot be moved during cable installation or for cable replacement.
See Downloads Section Z-14 Cable Data for cable duct/trough and raceway sizes, routings and details.

9.5 CONDUIT PIPES

N/A

9.6 LIGHTING
9.6.1 Examination Room
 Light levels for operation of imaging equipment to be specified by customer.
 Light levels for servicing equipment to be a minimum of 500 lux

9.6.2 Technical Room

 Light levels for servicing equipment to be a minimum of 500 lux

9.6.3 Control Room

 Light levels for operation of imaging equipment to be specified by customer.
4598 002 32911 CSIP Level 1 19
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copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

 Light levels for servicing equipment to be a minimum of 500 lux

 Lights with adjustable dimmers are recommended to control illumination levels.

9.7 POWER OUTLETS / SOCKETS

9.7.1 Examination Room
 Quantity of wall sockets is customer and code dependent.
 A minimum of one socket within close proximity to gantry is required for servicing.

9.7.2 Technical Room

 A minimum of one socket within close proximity to Philips equipment is required for servicing.

9.7.3 Control Room

 Quantity of wall sockets is customer and code dependent. Specific requirements will depend on Hard
Copy units, other options and customer’s own equipment.
 A minimum of one socket within close proximity to CT Console is required for servicing.

10 NETWORK DATA
10.1 SYSTEM REQUIREMENTS
The following specifies the minimum network requirements for MX 6000/4000 installation:
 10/100/1000 Mbit connections

The following applies when connecting to the hospital’s network:

 The local system administrator must assign IP address, subnet masks and gateways.
 It is strongly advised to connect the CT system to the hospital network through a router of an
intelligent switch.

Pre-installation
Delivered : N/A
To be ordered : N/A
To be arranged locally : Network connections (RJ 45) at:
 Host Computer Rack
: Ethernet Connection must be 10/100/1000 Mbit

Installation
Delivered : N/A
To be ordered : N/A
To be arranged locally : CAT 6 cable (not longer than 6 meter)

Remote Service Network (RSN) connectivity is also required for Web-based applications to assist the Field
Service Engineer in troubleshooting equipment problems. Access to the hospital’s network via their remote
access server is needed with RJ45 network connection and IP address. The same network drop located at the
CT system Host computer may be utilized for RSN (See 10.2).

10.2 RSN (REMOTE SERVICE NETWORK)

Remote Service Network (RSN) connectivity is required for providing remote access to customer equipment.
Applications such as remote monitoring/alerts, software distribution, system status reports, and remote service
diagnostic tools use the RSN. These applications are used by the Remote Service Centers in
troubleshooting equipment problems.

20 CSIP Level 1 4598 002 32911

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copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

For all installation preparation guidelines, checklists and procedures refer to the following Philips Remote
Service (PRS) website for connection requirements and RSN Lead representatives:

Philips Remote Service (PRS) Homepage

GS&S North America RSN Lead Contacts:

GSSI RSN Lead Contacts:

10.2.1 Remote Service Network Configuration

For new system installations it is recommended to use the Philips SSL-based connection (iSSL Link). The
SSL-based connection is easier to configure and is “firewall friendly” in that it only requires one outbound port
443 to be opened. The RSN IPSec connection is also required to be configured. This will involve several
hospital firewall inbound ports that need to be opened. Refer to the product’s Remote Service User Guide on
InCenter for the network configuration details. There is also a list of RSN applications and ports for each
product available at the PRS Docs and Files section of the PRS website.

The RSN IPSec connection must also have the hospital firewall configured for outbound access to the RSN
servers in the IP range 192.68.48.0/255.255.252.0. Note that some sites use Source NAT IP addressing for
RSN servers and these IP addresses will need to be conveyed to the FSE doing the configuration of the CT
product. Source NAT IP addressing is used to translate the IP addresses at the healthcare facility to the IP
addresses at the Philips Remote Service (PRS) Data Center. The RSN coordinator must contact the Hospital
Network Administrator so that the necessary network configurations are done. Use the Philips CT – Site
Inspection/Pre-Installation Checklist and record the information obtained from the Network Administrator.
The checklist will be used by the FSE to do the remote configuration of the CT product.

The following web links provide more detailed information about Philips Remove Service

Philips Remote Service (PRS) Homepage

M2M User Guide and Troubleshooting Steps

iSSL Link FAQ

Source NAT Description

11 DOWNLOADS AND DRAWINGS

[will update this section later]

Z- # Description View Downloads

Section (PDF)
u-Station AutoCad Other Formats
All download sheets of this 459800232911 N/A N/A N/A
PRD document _all_sheets.pdf
Text file of this PRD 459800232911
document .doc

Z-1 Dimensions of Product

Z-1.1.1 Gantry & Table Couch Z_1_1_1.pdf Z_1_1_1.dgn Z_1_1_1.dwg
Plan/Side/Front Views for
drawing templates
Z-1.1.2 Gantry/ Table Couch Plan Z_1_1_2.pdf Z_1_1_2.dgn Z_1_1_2.dwg
View

4598 002 32911 CSIP Level 1 21

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
MX 6000/4000 CT System Requirements
Author: J. Credico

Z-1.2 Gantry/ Table Couch Side Z_1_2.pdf Z_1_2.dgn Z_1_2.dwg

View
Z-1.3 Gantry/ Table Couch Side Z_1_3.pdf Z_1_3.dgn Z_1_3.dwg
View
(+30 deg tilt)
Z-1.4 Gantry/ table Couch Side Z_1_4.pdf Z_1_4.dgn Z_1_4.dwg
View
(-30 deg tilt)
Z-1.5 Gantry/ Table Couch Side Z_1_5.pdf Z_1_5.dgn Z_1_5.dwg
View
(Lowest service position)
Z-1.6 Gantry Front/ Side View Z_1_6.pdf Z_1_6.dgn Z_1_6.dwg

Z-2 Interface
Z-2.1 Cable Access Locations to See Z-3.1
rear of Gantry
Z-2.2 Floor Level under Gantry/ Z_2_2.pdf Z_2_2.dgn Z_2_2.dwg
Table Couch
Z-2.3 Gantry/ Table Couch Floor Z_2_3.pdf Z_2_3.dgn Z_2_3.dwg
Anchor Detail
Z-2.4 Centre of Gravity Z_2_4.pdf Z_2_4.dgn Z_2_4.dwg
Z-2.5 Gantry Air Flow Z_2_5.pdf Z_2_5.dgn Z_2_5.dwg
Z-2.6 Floor Vibration Amplitude Z_2_6.pdf Z_2_6.doc
Limits

Z-3 Floor Plate

Z-3.1 Gantry/ Table Couch Base Z_3_1.pdf Z_3_1.dgn Z_3_1.dwg
Structure at Floor

Z-4 Template
Z-4.1 Gantry/ Table Couch Floor Z_4_1.pdf Z_4_1.dgn Z_4_1.dwg
Alignment Template
Z-4.2 Gantry Isolation Drill Z_4_2.pdf Z_4_2.dgn Z_4_2.dwg
Template
Z-4.3 Table Couch Isolation Drill Z_4_3.pdf Z_4_3.dgn Z_4_3.dwg
Template

Z-5 Transport Data

Z-5.1 Gantry in Wooden Crate Z_5_1.pdf Z_5_1.dgn Z_5_1.dwg
Z-5.2 Gantry with Dolly Wheels Z_5_2.pdf Z_5_2.dgn Z_5_2.dwg
Z-5.3 Table Couch in Wooden Z_5_3.pdf Z_5_3.dgn Z_5_3.dwg
Crate
Z-5.4 Table Couch with Dolly Z_5_4.pdf Z_5_4.dgn Z_5_4.dwg
Casters
Z-5.5 Gantry Overhead Lifting Z_5_5.pdf Z_5_5.dgn Z_5_5.dwg
from above
Z-5.6 Gantry Moving Path Z_5_6.pdf Z_5_6.dgn Z_5_6.dwg
Clearances

Z-6 Pre-installation Data

22 CSIP Level 1 4598 002 32911

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
System Requirements MX 6000/4000 CT
Author: J. Credico

Z-6.1 Site Inspection/ Pre-

installation Checklist
See 4550_193_09571

Z-7 Miscellaneous
Z-7.1 MX6000 Dual Gantry Z_7_1.pdf Z_7_1.dgn Z_7_1.dwg
Radiation Dose Map
Z-7.2 MX4000 Dual Gantry Z_7_2.pdf Z_7_2.dgn Z_7_2.dwg
Radiation Dose Map
Z-7.3 MX4000 CT Gantry Z_7_3.pdf Z_7_3.dgn Z_7_3.dwg
Radiation Dose Map

Z-11 Preferred & Minimum Room Layouts

Z-11.1 Preferred Room Layout Z_11_1.pdf Z_11_1.dgn Z_11_1.dwg
Z-11.2 Medium Room Layout Z_11_2.pdf Z_11_2.dgn Z_11_2.dwg
Z-11.3 Minimum Room Layout Z_11_3.pdf Z_11_3.dgn Z_11_3.dwg

Z-12 Room Size

Z-12.1 Equipment Space Z_12_1.pdf Z_12_1.dgn Z_12_1.dwg
Clearances
Z-12.2 Exam Room Side View Z_12_2.pdf Z_12_2.dgn Z_12_2.dwg
Z-12.3 Exam Room Front View Z_12_3.pdf Z_12_3.dgn Z_12_3.dwg

Z-13 Mechanical Relation Data

Z-14 Cable Data

Z-14.1.1 System Mains Connection Z_14_1_1.pdf Z_14_1_1.dgn Z_14_1_1.dwg
Power Filter Box only
380V, 50/60 Hz
Z-14.1.2 System Mains Connection Z_14_1_2.pdf Z_14_1_2.dgn Z_14_1_2.dwg
Teal Iso Unit with Power
Filter Box
200 – 480V, 50/60 Hz
Z-14.1.3 System Mains Connection Z_14_1_3.pdf Z_14_1_3.dgn Z_14_1_3.dwg
Teal Iso Unit only
200 – 480V, 50/60 Hz
Z-14.2 Preferred Raceway Layout Z_14_2.pdf Z_14_2.dgn Z_14_2.dwg
Z-14.3.1 Preferred Conduit/Jct. Box Z_14_3_1.pdf Z_14_3_1.dgn Z_14_3_1.dwg
Layout with Power Filter
Box
Z-14.3.2 Preferred Conduit/Jct. Box Z_14_3_2.pdf Z_14_3_2.dgn Z_14_3_2.dwg
Layout with Teal and
Power Filter Box
Z-14.3.3 Preferred Conduit/Jct. Box Z_14_3_3.pdf Z_14_3_3.dgn Z_14_3_3.dwg
Layout with Teal
Z-14.4 Interconnect System Z_14_4.pdf Z_14_4.dgn Z_14_4.dwg
Cable Diagram

4598 002 32911 CSIP Level 1 23

This document and the information contained in it is proprietary and confidential information of Philips Medical Systems ("Philips") and may not be reproduced,
copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Philips Legal Department.
(c) 2012 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED