Operator Manual
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PROGRAM-X Operator Manual 2103514–100 Revision 2
Copyright 1994, 1996, by General Electric Co. Operator Manual
WARNING X–RAY EQUIPMENT IS DANGEROUS TO BOTH PATIENT AND OPERATOR UNLESS MEASURES OF PROTECTION ARE STRICTLY OBSERVED Though this equipment is built to the highest standards of electrical and mechanical safety, the useful x–ray beam becomes a source of danger in the hands of the unauthorized or unqualified operator. Excessive exposure to x–radiation causes damage to human tissue. Therefore, adequate precautions must be taken to prevent unauthorized or unqualified persons from operating this equipment or exposing themselves or others to its radiation. Before operation, persons qualified and authorized to operate this equipment should be familiar with the Recommendations of the International Commission on Radiological Protection, contained in Annals Number 26 of the ICRP, and with applicable national standards.
Regulatory Requirements This product complies with the regulatory requirements of the following: -
Green QSD 1990 Standard issued by MDD (Medical Devices Directorate, Department of Health, UK).
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Medical Device Good Manufacturing Practice Manual issued by the FDA (Food and Drug Administration, Department of Health, USA).
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Underwriters’ Laboratories, Inc. (UL), independent testing laboratory.
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Canadian Standards Association (CSA).
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International Electrotechnical Commission (IEC), international standards organization, when applicable.
General Electric Medical Systems is ISO 9001 certified.
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Regulatory Requirements
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Services Offices For service issues, contact the Service Office in your country. USA
ASIA
AUSTRIA
GE Medical Systems Headquarters 3000 North Grandview Blvd. Waukeska, WI 53188 Mail: P.O. Box 414 Milwaukee, WI 53201 TEL: 414–544–3011
GEMSA Headquarters GE Medical Systems Asia 4–7–127 Asahigaoka, Hino–shi TOKYO, JAPAN 191 TEL: (81) 426 560007
GE GesmbH Medical Systems Austria Prinz Eugen Strasse 8/8 A–1140 WIEN TEL: 0660 8651 (gebÜhrenfrei) FAX: +43 1 505 38 74 TLX: 136314
USA GE Medical SYstems LATIN AMERICA HEADQUARTERS 5101 NW 21st Avenue, Suite 350 Ft. LAUDERDALE, FL 33309 TEL: 305–497–1200
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ASIA GE Pacific Pte. Ltd (GEMS Asia) South East Asia Pacific Operations (SEAPO) 298 Tiong Bahru Road #15–01/06 Tiong Bahru Plaza SINGAPORE 0316 TEL: (65) 291–8528 [8*548–8528] Fax : (65) 291–7006 [8*548–7006]
BELGIUM GE Medical Systems Benelux NV/SA Manhattan Center Bolwerklaan 21 b 9 Av. du Boulevard B–1210 BRUSSEL/BRUXELLES TEL: (NL)+32 2 644 09 38 TEL: (F) +32 2 644 08 42 TEL: (LUX) 0800 2973 FAX: +32 2 207 73 33
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SPAIN
SWITZERLAND
UNITED KINGDOM
GE Medical Systems Espana Avda. de Europa 22 Parque Empresarial la Moraleja E–28100 ALCOBENDAS TEL: +34 1 663 25 00 FAX: +34 1 663 25 01
GE Medical Systems (Schweiz) AG Sternmattweg 1 CH–6010 KRIENS TEL: +41 41 425577 FAX: +41 41 421859
SWEDEN
GE Medical Systems Turkiye A.S. Mevluk Pehliran Sodak Yilmaz Han, No 24 Kat 1 Gayretteppe ISTANBUL TEL: +90 212 75 5552 FAX: +90 212 211 2571
IGE Medical Systems Coolidge House 352 Buckingham Avenue SLOUGH Berkshire SL1 4ER TEL: +44 753 874000 FAX: +44 753 696067
GE Medical Systems Sverige AB Box 6768 St. Eriksgatan 117 S–113 85 STOCKHOLM TEL: +46 8 457 95 20 FAX: +46 8 457 95 47
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TURKEY
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Revision History REV
DATE
REASON FOR CHANGE
0
04/94
V2.0 software. New Doc No. assigned: 2103514 (Old Doc No.: 45560097).
1
15–Sep–96
Updated. Document size changed from A4 (portrait) to A5 (landscape).
2
15–Oct–96
Updated. LIST OF EFFECTIVE PAGES
PAGE
REVISION
PAGE
REVISION
Title page
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i thru xvi
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1–1 thru 1–10
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3–1 thru 3–4
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2–1 thru 2–18
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4–1 thru 4–12
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NUMBER 2103514–100TPH
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SIZE A5
REVISION 2
Revision History
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Chapter Tabs
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Description
1
Operation
2
Glossary
3
Prerecorded Protocols
4
Chapter Tabs
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Chapter Tabs
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Table of Contents
Chapter 1
Regulatory Requirements...
i
Services Offices...
iii
Revision History...
vii
Chapter Tabs...
ix
Table of Contents...
xi
Foreword...
xv
Description...
1–1
S
1–1 1–1 1–2 1–3 1–3 1–5
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Overview... Purpose of Program-X... User-Friendly Program-X... Equipment Shipped... Program-X Console... Accessories...
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S
Chapter 2
Specifications... Generator Compatibility... Maximum Number of Protocols for a given X–Ray Room... Protocol Contents... Type of Keyboard... Languages Used... Computer Connection...
1–8 1–8 1–8 1–8 1–9 1–9 1–10
Operation...
2–1
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2–2 2–2 2–6 2–8 2–10 2–12 2–12 2–14 2–14 2–14 2–16 2–16 2–18 2–18 2–18 2–18
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S
xii
Table of Contents
Using the Recorded Protocols (Read Mode)... Powering Up... Category Screen... Anatomy Screen-Example: Digestive Tube and Specials 1/2 (8) . . . Protocol Screen... Warning Messages... Exposure... Customizing Program-X (Write Mode)... Write Mode Access Code... Customizing the Anatomy Names... Customizing the Protocols... Validating a Protocol... Backup and Transfer of Programs... Precautions to Take at Installation... Backup Operation... Transfer...
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Chapter 3
Glossary...
3–1
Chapter 4
Prerecorded protocols...
4–1
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Foreword This Operator Manual describes how to use Program-X configured with the MPG 65/ MPG 80/MPG 100 and MPH 50/MPH 65/MPH 80 generators. Prerecorded protocol floppy disks are included with the manual.
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Foreword
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Foreword
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CHAPTER 1
Description 1
Overview Purpose of Program-X Program-X is an anatomic programmer, compatible with the MPG or MPH Generators. It provides the operator with a means of storing expertise in the form of recorded exam protocols. These protocols contain optimized radiography and fluoroscopy parameters for given exams. -
Program-X increases the return on investment on the installation as follows: –
Number of manipulations required prior to each exposure is significantly reduced,
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Possibility of error is minimal,
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Results are much more consistent,
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Exams always run the same way, irrespective of a change of operator.
Terms in italics are defined in the Glossary-Chapter 3.
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Description
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Program-X is easy to learn: –
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Operator training courses are short and simple.
User-Friendly Program-X -
Program-X is operational once switched on. The Program-X memory contains prerecorded protocols for all standard exams. These protocols are re-classified by anatomy names which are divided into 10 Categories.
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Chapter 4 contains the list of the prerecorded protocols.
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The prerecorded protocols may be operator-modified in a simple and logical way. This modification may range from anatomy names to the rad parameters, to obtain a customized Program-X.
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It is always possible to provisionally modify the parameters with Program-X during an exam.
Terms in italics are defined in the Glossary-Chapter 3.
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Description
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Equipment Shipped Program-X Console
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See Illustration: Program–X Console. The Console comprises two parts: the screen and the Control Panel.
Screen An articulated arm supports the screen over the Generator Console. The screen displays the anatomy names, along with various messages and data. Display is in yellow characters on a gray field, or vice versa.
Control Panel The 300 x 120 mm Control Panel is incorporated into the upper part of the Generator Console. The Control Panel comprises three keypads (D1, D2 and D3). Keypad D1: READ/WRITE
R
45:
Accesses the Read Mode.
44:
Key with four-figure code protects access to Write Mode.
41, 42 and 43: Write Mode.
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Description
1–3