Planning Reference Data Product

Product Patient observation system

Contents

FRONT PAGE PRODUCT MAINS PATIENT OBSERVATION SYSTEM ................................................................................2

1 HISTORY OF THE DOCUMENT.............................................................................................................3

1.1 History file version 01.0 ...........................................................................................................................3
1.2 History file version 05.0 ...........................................................................................................................3

2 INTRODUCTION .....................................................................................................................................4
2.1 Scope.......................................................................................................................................................4
2.2 Attention points ........................................................................................................................................4

3 PRODUCT INFORMATION.....................................................................................................................5

4 MECHANICAL DATA..............................................................................................................................5
4.1 Cable length.............................................................................................................................................5
4.2 Dimensions, weigh and center of gravity .................................................................................................5

5 ENVIRONMENTAL DATA ......................................................................................................................5

5.1 Maximum allowed magnetic field.............................................................................................................5

6 ELECTRICAL DATA ...............................................................................................................................5

7 TOOLS / MATERIAL REQUIRED...........................................................................................................5

8 NETWORK DATA ...................................................................................................................................5

9 TRANSPORT DATA ...............................................................................................................................5

10 WATER DATA.........................................................................................................................................5

11 HELIUM DATA ........................................................................................................................................5

12 PRE-INSTALLATION DATA...................................................................................................................6

13 DRAWINGS AND DOWNLOADS ...........................................................................................................6

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(c) 2005 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
Planning Reference Data Product Planning Data

FRONT PAGE PRODUCT MAINS PATIENT OBSERVATION SYSTEM

PlanningReferenceData
MR

Section:
Product: Patient observation system

Document release: 2001December

Document revision: 05.0
PROPRIETARY NOTICE

This manual and the information contained therein is proprietary to Philips Medical Systems
Nederland B.V. and shall not be reproduced, copied in whole or part, adapted, modified, or
disseminated without the written permission of Philips.
Use of this manual and the information contained therein is strictly reserved for Philips
engineers or persons licensed by Philips. Use of the manual by unauthorized persons is strictly
prohibited.
This manual is not a contractual document. Specifications and features of Philips medical equipment are
subject to change and may differ from what is described herein.

Printed in Best, the Netherlands.

Copyright © 2005 Philips Medical Systems Nederland B.V.

ALL RIGHTS RESERVED

2 (05.0)
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ALL RIGHTS RESERVED
Planning Reference Data Product

1 HISTORY OF THE DOCUMENT

If the system or parts change and site planning is affected, an updated version with a new year and month will
be introduced.

Revision updates are given if administrative changes have been made in the document. However technical
specification of the System has not been changed. This means that a revision update is backward compatible
with already installed System (parts).

All site-planning differences in relation to previous versions are highlighted pink.

If a local PRD is in use please compare the complete text and all drawings for minor changes and rewritten
info.

1.1 HISTORY FILE VERSION 01.0

• No history file. This is a new document.

1.2 HISTORY FILE VERSION 05.0

• Text rewritten and updated
• Drawings better detailed.

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(c) 2005 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
Planning Reference Data Product Planning Data

2 INTRODUCTION
2.1 SCOPE
The information is written for Philips SSD and SSR Site Planning departments and Project Managers. The info
must be used together with local code and regulations for local use. The information is meant as guide for
design and construction professionals, clinical users and any other group that may be involved in each unique
project.

Information regarding individual system parts can be found in this section Product Planning Data.
The information needed to determine if a potential site and its surroundings are suitable for a MR system can
be found in System Planning Data.
Information regarding system parts in relation with individual rooms can be found in Room requirements.

Clinical specifications are applicable only if the requirements mentioned in the PRD are maintained. If the
environment is out of specification it may result in mis-performance or malfunction and shorten the lifetime of
system parts.

2.2 ATTENTION POINTS

• -

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Planning Reference Data Product

3 PRODUCT INFORMATION
The Patient Observation System is an option.

The Patient Observation System (POS) in general consists of the following parts:
• Wall mounted camera.
• Monitor Optional. To display images from optional extra cameras a manual switch is needed.

The camera and the monitor are separate options.

4 MECHANICAL DATA
4.1 CABLE LENGTH
Wall camera System Filter Box or FCC 15 m
System Filter Box or FCC Monitor 30 m

4.2 DIMENSIONS, WEIGH AND CENTER OF GRAVITY

See the drawings

5 ENVIRONMENTAL DATA
N.A.

5.1 MAXIMUM ALLOWED MAGNETIC FIELD

See the drawings

6 ELECTRICAL DATA
The Patient observation system camera is powered via the SFB or FCC.
The monitor is power via the Operator’s console.

7 TOOLS / MATERIAL REQUIRED

No special tools required

8 NETWORK DATA
N.A.

9 TRANSPORT DATA
N.A.

10 WATER DATA
N.A.

11 HELIUM DATA
N.A.

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(c) 2005 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED
Planning Reference Data Product Planning Data

12 PRE-INSTALLATION DATA
N.A.

13 DRAWINGS AND DOWNLOADS

Name View drawing Download Download text

CAD
Patient observation system 452298126351_z 452298126351 pro12_1_050.d
p12_1_030.pdf _zp12_1_030.z oc
ip
Monitor 452298126351_z 452298126351
p12_2_030.pdf _zp12_2_030.z
ip

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(c) 2005 Koninklijke Philips Electronics N.V.
ALL RIGHTS RESERVED