Documente Academic
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Manual de Instalación
Optima XR200amx Manual del Operador (Ingles)
Optima XR220amx Manual del Operador (Ingles)
Manual de Esquemáticos Optima XR200amx Actualización Digital OM (Ingles)
Optima XR200amx Conformidad DICOM
Manual con partes ilustradas Optima XR220amx Conformidad DICOM
EMC Estatuto de Conformidad
Estatuto IHE
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR
SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X
représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement
X entraîne des dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les
personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour elles-
mêmes. Avant chaque manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se
renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique,
Annales 26: Recommandations de la Commission Internationale sure la Protection Radiologique et les normes
nationales en vigueur.
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 (ICRP), contained in Annals Number 26
of the ICRP, and with applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS
NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro
al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede
causar daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o
no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán
informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales
No 26: Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE
GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den
Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte
Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden
Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen
Kommission für Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für
Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336112-1EN, REVISION 3 PRE-INSTALLATION MANUAL
Important information
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2
are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of
their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written
permission of General Electric Company, Inc.
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation
“damage in shipment” written on all copies of the freight or express bill before delivery is accepted
or “signed for” by a General Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event,
within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this
14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and
MIS.” Contact your local service coordinator for more information on this process.
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 (NCRP) 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.
Revision history
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert
symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation
mark within it. It Is always used next to the signal word to indicate the severity of the hazard.
Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert
symbol and signal word are placed immediately before any paragraph they affect. Safety
information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such
as Purpose, Example, Comment or Note) are used to identify important but non-safety related
information. Text styles are also applied to text within each paragraph modified by the specific
prefix.
Page Layout
Publication Part Number & Revision Number Publication Title
The current section and its title The current chapter and its title
are always shown in the footer of are always shown in the footer of
the left (even) page. the right (odd) page.
An exclamation point in a triangle is used Paragraphs preceeded by a symbol
to indicate important information to the user. (e.g. bullets) contain information that
Paragraphs preceeded by Alphanumeric has no specific order.
characters (e.g. numbers) contain infor-
mation that must be followed in a specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appears in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even page
footers show the current section and its title, as well as the current page number.
Table of contents
Chapter 1 General requirements .................................................................... 17
Section 1.1 Objectives and overview............................................................ 17
1.1.1 Pre-installation tasks ................................................................................................. 17
Section 1.2 System components and options ............................................. 18
Section 1.3 Customer responsibilities.......................................................... 19
1.3.1 Contract changes ...................................................................................................... 19
1.3.2 Responsibilities of the customer................................................................................ 19
Section 1.4 Delivery requirements ................................................................ 20
1.4.1 Product dimensions and weights............................................................................... 20
1.4.2 Shipping dimensions and weights ............................................................................. 22
1.4.2.1 United States shipments .................................................................................. 22
1.4.2.2 International shipments .................................................................................... 23
1.4.3 Door size requirements ............................................................................................. 23
1.4.3.1 System in crate ................................................................................................ 23
1.4.3.2 System in normal use (not in crate) ................................................................. 23
1.4.4 Minimum elevator depth requirements ...................................................................... 24
Section 1.5 Product storage and handling requirements ........................... 24
Section 1.6 Pre-installation results ............................................................... 24
Site data
Chapter 2 Special Radiation
collected from
construction requirements consultant
field
Chapter 3 Environmental
(HVAC) requirements
Site planning
Chapter 4 Electrical
requirements
Chapter 5 Communication
requirements
No
Chapter 6 Network / Pre-installation Planning and
workflow information site work site work
complete?
Yes
Delivery and
installation
Available components of the Optima XR200amx/Optima XR220amx system are listed below.
Shipped with the Optima XR200amx/Optima XR220amx system:
• Optima XR200amx/Optima XR220amx
• Backup tether for digital detector (Optima XR220amx only)
• Service keyboard
• Software CD
• External CD/DVD-ROM drive
• Operating System firmware USB drive
• Tablet holder assembly (optional, Optima XR220amx and Optima XR200amx)
Shipped separately:
• DAP meter (standard with Optima XR220amx, optional for Optima XR200amx)
• Digital detector (Optima XR220amx only)
• Detector batteries (Optima XR220amx only)
• Detector battery charger (Optima XR220amx only)
• 6:1 grid (Optima XR220amx only)
• Barcode reader (optional, Optima XR220amx only)
• Wireless Hand Switch (optional, Optima XR220amx and Optima XR200amx)
Product or
Length Width Height Weight Ref.
component
194.0 cm (76.4 in)
standard column
Optima XR200amx /
119.3 cm (47 in) 55.2 cm (21.7 in) or 404 kg (891 lb) Figure 1-2
Optima XR220amx
178.8 cm (70.4 in)
short column
FlashPadTM detector
(Optima XR220amx
or Optima 58 cm (22.8 in) 45.2 cm (17.8 in) 2.7 cm (1.1 in) 4.5 kg (10 lb) Figure 1-3
XR200amx with
digital upgrade)
DAP (Optima
XR220amx or
146 mm (5.75 in) 198 mm (7.8 in) 45 mm (1.8 in) 0.5 kg (1.1 lb) Figure 1-4
Optima XR200amx
with digital upgrade)
Barcode Reader
(option, for Optima
XR220amx or 42 mm (1.66 in) 19 mm (0.75 in) 125 mm (4.9 in) 85 g (3 oz) Figure 1-5
Optima XR200amx
with digital upgrade)
552
114.8 cm
(45.2 in)
105 cm
(42 in)
2
55.9 cm
(22 in)
91.5 cm
(36 in)
ITEM DESCRIPTION
1 Power cord, maximum extended length is 2.75 m (9 ft)
2 Ethernet cable
Ensure that the in-use and storage location conditions do not fluctuate more than the maximum
rates of change given in Table 3-2.
Table 3-2 Maximum rates of change for relative humidity and temperature
In-use Storage
Temperature change < 10° C (50° F)/hour < 20° C (68° F)/hour
Humidity change < 30%/hour < 30%/hour
In-use Storage
Min. Max. Min. Max.
-30 m 3,000 m -30 m 3,000 m
(-98.4 ft) (9843 ft) (-98.4 ft) (9843 ft)
In-use Storage
Min. Max. Min. Max.
70.1 kPa 106 kPa 70.1 kPa 106 kPa
Ensure that the in-use and storage location conditions do not fluctuate more than the maximum
rates of change given in Table 3-5.
In-use Storage
< 1.8 kPa/hour < 76 kPa/hour
For reference, a tightly closed room of 3 m x 3 m (10 ft x 10 ft) with a 2.4 m (8 ft) ceiling would require
2100 BTU/hour to raise the temperature by 12.2°C (10°F).
In-use Idle
Upper limit: 55 dBA Upper limit: 50 dBA
The system is equipped with Ethernet hardware for facilities connectivity of HIS/RIS, service
diagnostics, and (for Optima XR220amx only) to transfer digital images.
It is the customer’s responsibility to provide the Ethernet connection in a location convenient for
image transfer (Optima XR220amx only) and remote InSite connectivity. A minimum data rate of
54Mb/s is required to prevent delays when transferring images. A data rate of 100Mb/sec provides
optimal performance.
The network connection must be 802.3-compliant 10/100/1000 Base-T Ethernet, and there must be
at least one RJ45 jack dedicated (for Static IP) to connect the new equipment on the LAN.
Network infrastructure
What wired networks and/or wireless uplinks does this facility use?
Has 100/1000 Base-T installed
Will have 100/1000 Base-T installed by this date:___________
Has 10 Base-T installed
Will have 10 Base-T installed by this date: ___________
Has a different network installed: _____________________
If FIPS is enabled: _____________________
Does not have a network installed
Wireless security
What security protocol does the wireless network use?
WEP 64 bit or 128 bit WPATM-PSK (TKIP) WPA2TM-PSK (AES)
Management Frame Protection (MFP)
LEAP LEAP + WEP LEAP + WPATM
EAP-PEAP/MSCHAPv2) EAP-TLS EAP-TTLS/MSCHAPv2
EAP-FAST EAP-SIM PEAP-GTC
Other: _____________________
What is the wireless network key type?
Hexadecimal ASCII N/A
For WEP security wireless networks, what is the key or key number? _____________________
For PSK security wireless networks, what is the pass phrase? _____________________
For EAP/PEAP security wireless networks:
What is the domain/user name? _____________________
What is the password? _____________________
What is CA certificate? (if required) _____________________
What is Client certificate? (if required) _____________________
What is Private key file? (if required) _____________________
What is Private key password? (if required) _____________________
IMPORTANT: If keys/passwords are not provided here, the holder of those keys/passwords must
be available at installation to provide the information.
What type of access control (filtering) does the facility use? _____________________________
Subnets
Is the network segmented using subnets?
Yes No
If the facility will place the Optima XR200amx/Optima XR220amx system on a subnet, list the
subnet mask and router IP:
Subnet mask: _ _ _ . _ _ _ . _ _ _ . _ _ _
Router IP: _ _ _ . _ _ _ . _ _ _ . _ _ _
If the Optima XR220amx system will be on a subnet, is the wireless network routed to a different
network for image viewing?
Yes No
IP addresses/names
At the facility, equipment IP addresses are:
Static Acquired via DHCP Combination of both methods
Indicate the IP address that will be assigned to the Optima XR200amx/XR220amx system, if static
addresses are used at the site. (Some DICOM-compliant devices require a fixed IP for
authentication. If dynamic addresses are assigned, authentication may not be possible.)
Optima XR200amx/XR220amx IP address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The host name is the network's name for the Optima XR200amx/XR220amx system.
Optima XR200amx/XR220amx host name: _________________________
The Scheduled Station AE Title (Application Entity Title) is the name the HIS/RIS will use to send
worklist information to the Optima XR200amx/XR220amx system.
Scheduled Station AE Title: _________________________
Bandwidth/capacity
On average, images from the Optima XR220amx require 8.5 Mb per image. Be sure the network
bandwidth is sufficient.
Patient data
When the patient arrives in the system room for the exam, how is the patient data entered into the
system?
Manually typed
Entered via barcode reader
Barcode format:______________
Downloaded from HIS/RIS
How is the query structured? Check all that apply:
By date
By modality
By patient information
Other method - Please explain:
Patient schedule
In retrieving patient schedule information, how often is the query sent?:
Once at the start of a shift
Several times during a shift
Before each patient
After the diagnostic images are acquired, what is the facility’s default workflow? Pick one:
Manually send Automatically push
Send/push to (pick all that apply):
Review station(s) Archive system(s) Printer(s)
When images are configured for automatic push, what images should be sent to PACS/archive/
review stations?
Raw Processed Raw and Processed
When images are printed, on what device is the print command originated? Pick all that apply:
The system A review workstation A PACS system
How soon after the images are acquired is the first image quality check done?
Before next image is shot Before patient leaves After patient leaves
When it comes to image quality, would the site prefer to:
Consider all images good unless marked bad
Consider all images bad unless marked good
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
Image types supported: DX CR
Supports multi-framing: Yes No
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server? Yes No
If yes, provide: AE title: __________________________ Port number: ___________
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
Query/retrieve? Yes No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by: Study Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment? Yes No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
MPPS server Yes No
If yes, provide: AE title: _________________________ Port number:___________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
Image types supported: DX CR
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server? Yes No
If yes, provide: AE title: __________________________ Port number: ___________
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
Query/retrieve? Yes No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by: Study Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment? Yes No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
MPPS server Yes No
If yes, provide: AE title: _________________________ Port number:___________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
Image types supported: DX CR
Supports multi-framing: Yes No
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server? Yes No
If yes, provide: AE title: __________________________ Port number: ___________
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
Query/retrieve? Yes No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by: Study Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment? Yes No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
MPPS server Yes No
If yes, provide: AE title: _________________________ Port number:___________
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
DICOM supports a number of image types. Indicate if this device supports the DX and/or the CR
image types.
Image types supported: DX CR
Supports multi-framing: Yes No
The next four sections address the four services that remote host devices may offer. Each of the
services will have its own AE (application entity) title and port number. The AE title is the name given
to a service or application provided by a DICOM device. The port number is a logical designation
within the device. These pieces of information are available in the device's DICOM Conformance
Statement.
Being a remote host server allows the Optima XR220amx or Optima XR200amx with digital
upgrade system to push images to other devices.
Does the site plan to use this device as a remote host server? Yes No
If yes, provide: AE title: __________________________ Port number: ___________
Being a query/retrieve service class provider allows the Optima XR220amx or Optima XR200amx
with digital upgrade system to query this device and retrieve images stored there.
Query/retrieve? Yes No
If yes, provide: Query/retrieve AE title:________________________ Port number:__________
The query/retrieve by study or patient controls how much the user is able to retrieve at one time.
For study, the user may retrieve studies, series, images. For patient, the user may retrieve all of the
study attributes plus a patient's entire image collection.
Query/retrieve by: Study Patient
A storage commitment provider confirms that images sent by the Optima XR220amx or Optima
XR200amx with digital upgrade system to an archival system were received and stored. This option
is available only when the Optima XR220amx or Optima XR200amx with digital upgrade system is
sending DX type images.
Storage commitment? Yes No
If yes, provide: Storage commitment AE title: ______________________ Port number:________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
The MPPS server receives the messages sent by the Optima XR200amx or Optima XR200amx
with digital upgrade system. These messages consist of information such as when the exam started
and closed, how many images were acquired, dose information, etc. This information is then
updated on the facility’s scheduling system.
MPPS server Yes No
If yes, provide: AE title: _________________________ Port number:___________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Printer data
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler: Yes No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler: Yes No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler: Yes No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
Printer #___
Manufacturer/model: _________________________
Software/firmware version: _________________________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Prints via spooler: Yes No
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Look in the DICOM compliance statement for the printer's AE title and port number.
Printer AE title:_________________________
Port number:_________________________
HIS/RIS data
Manufacturer/model: _______________________ Software/firmware version: ______________
Network (IP) address: _ _ _ . _ _ _ . _ _ _ . _ _ _
Indicate the highest level of DICOM conformance for this device. If the device does have some level
of DICOM conformance, return a copy of the DICOM Conformance Statement with this completed
form. DICOM compatibility does not guarantee that all functions will work properly.
DICOM compliance level: 1.0 2.0 3.0 Not DICOM compliant
Look in the DICOM Compliance Statement for the AE title and port number.
HIS/RIS AE title: _________________________ Port number: __________________
DX and/or CR image type support should also be in the device's DICOM Conformance Statement.
Image types supported: DX CR
Modality used for scheduling: ________________________
www.gehealthcare.com
46
Front cover
GE Healthcare
Optima XR200amx/XR220amx
Installation Manual
Direction 5336113-1EN
Revision 10
GE HEALTHCARE
Warning OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN REVISION 10 INSTALLATION MANUAL
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR
SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X
représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement
X entraîne des dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les
personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour elles-
mêmes. Avant chaque manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se
renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique,
Annales 26: Recommandations de la Commission Internationale sure la Protection Radiologique et les normes
nationales en vigueur.
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 (ICRP), contained in Annals Number 26
of the ICRP, and with applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS
NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro
al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede
causar daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o
no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán
informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales
No 26: Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE
GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den
Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte
Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden
Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen
Kommission für Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für
Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Important information
Preface Page 3
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Page 4 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Preface Page 5
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Page 6 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2
are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of
their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material
presented and contained herein may not be reproduced in any form or manner, without the written
permission of General Electric Company, Inc.
Preface Page 7
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation
“damage in shipment” written on all copies of the freight or express bill before delivery is accepted
or “signed for” by a General Electric representative or a hospital receiving agent. Whether noted or
concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event,
within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this
14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and
MIS.” Contact your local service coordinator for more information on this process.
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 (NCRP) 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.
Page 8 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Preface Page 9
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Revision history
Page 10 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Preface Page 11
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Page 12 Preface
Preface - Publica-
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert
symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation
mark within it. It Is always used next to the signal word to indicate the severity of the hazard.
Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert
symbol and signal word are placed immediately before any paragraph they affect. Safety
information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Preface Page 13
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Page 14 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such
as Purpose, Example, Comment or Note) are used to identify important but non-safety related
information. Text styles are also applied to text within each paragraph modified by the specific
prefix.
Page Layout
Publication Part Number & Revision Number Publication Title
The current section and its title The current chapter and its title
are always shown in the footer of are always shown in the footer of
the left (even) page. the right (odd) page.
An exclamation point in a triangle is used Paragraphs preceeded by a symbol
to indicate important information to the user. (e.g. bullets) contain information that
Paragraphs preceeded by Alphanumeric has no specific order.
characters (e.g. numbers) contain infor-
mation that must be followed in a specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location.
The document part number and revision number appears in every header on every page. Odd
numbered page footers indicate the current chapter, its title and current page number. Even page
footers show the current section and its title, as well as the current page number.
Preface Page 15
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Page 16 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Table of contents
Chapter 1 Safety............................................................................................... 21
Section 1.1 Energy sources........................................................................... 21
Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power ..... 22
1.2.1 Preparing for LOTO................................................................................................... 22
1.2.2 Performing LOTO ...................................................................................................... 24
1.2.3 Returning system to service ...................................................................................... 27
Section 1.3 Electrostatic discharge (ESD) ................................................... 28
1.3.1 Important ESD considerations when working on a mobile system............................ 28
1.3.2 Generating static ....................................................................................................... 28
1.3.3 Personal grounding methods and equipment ........................................................... 29
1.3.3.1 Static shielding protection levels ...................................................................... 29
1.3.4 Grounding the work area........................................................................................... 29
1.3.5 Recommended materials and equipment ................................................................. 30
Chapter 3 Installation....................................................................................... 33
Section 3.1 Installation process.................................................................... 33
Section 3.2 Unpacking the system ............................................................... 34
Section 3.3 Replacing the electrical plug..................................................... 35
Section 3.4 Turning on the system ............................................................... 35
Section 3.5 Ground and leakage testing ...................................................... 37
3.5.1 Performing ground resistance testing ....................................................................... 37
3.5.1.1 Gathering test equipment................................................................................. 37
3.5.1.2 Attaching test cables ........................................................................................ 38
3.5.1.3 Setting test parameters .................................................................................... 40
3.5.1.4 Performing zero adjustment ............................................................................. 41
3.5.1.5 Taking ground measurements ......................................................................... 43
3.5.2 Performing leakage current testing ........................................................................... 47
3.5.2.1 Condition 1: Power off, normal outlet, X-ray off ............................................... 48
3.5.2.2 Condition 2: Power off, reversed outlet, X-ray off ............................................ 49
3.5.2.3 Condition 3: Power on, normal outlet, X-ray off ............................................... 50
3.5.2.4 Condition 4: Power on, reversed outlet, X-ray off ............................................ 50
3.5.2.5 Condition 5: Power on, normal outlet, X-ray on ............................................... 50
Section 3.6 Installing the digital detector..................................................... 50
3.6.1 Unpacking the detector ............................................................................................. 51
3.6.2 Inspecting the detector .............................................................................................. 52
3.6.3 Charging the detector battery.................................................................................... 52
3.6.4 Connecting the backup tether ................................................................................... 53
3.6.5 Download detector firmware ..................................................................................... 54
Chapter 4 Configuration.................................................................................. 57
Section 4.1 When should I configure the system? ...................................... 57
Section 4.2 Using the System Configuration Tool (SUIF) ........................... 57
4.2.1 Site configuration ...................................................................................................... 58
4.2.2 Networking configuration .......................................................................................... 59
4.2.3 General configuration ............................................................................................... 59
4.2.4 Hardware configuration............................................................................................. 60
4.2.5 Generator configuration ............................................................................................ 60
4.2.6 Wireless configuration .............................................................................................. 61
4.2.6.1 Adding certificates ........................................................................................... 61
4.2.6.2 Configuring broadcast SSID networks............................................................. 61
4.2.6.3 Configuring non-broadcast SSID networks ..................................................... 62
4.2.6.4 Troubleshooting connections........................................................................... 63
4.2.7 Options configuration................................................................................................ 64
4.2.8 InSite configuration ................................................................................................... 64
4.2.9 PNF configuration ..................................................................................................... 64
4.2.9.1 PNF GUI Control area ..................................................................................... 64
4.2.9.2 PNF tabs and parameters ............................................................................... 65
4.2.10 Time Server configuration......................................................................................... 66
4.2.11 Secure Login configuration ....................................................................................... 66
Section 4.3 Changing Auto Protocol Assist settings .................................. 67
Section 4.4 DICOM connectivity configuration ............................................ 67
4.4.1 Network host configuration ....................................................................................... 67
4.4.1.1 Adding network hosts ...................................................................................... 67
4.4.1.2 Performing a C-Echo test ................................................................................ 69
4.4.1.3 Removing network hosts ................................................................................. 70
4.4.2 Printer configuration.................................................................................................. 70
4.4.2.1 Adding printers ................................................................................................ 70
4.4.2.2 Removing printers ........................................................................................... 72
Section 4.5 Image management..................................................................... 72
Section 4.6 Image processing........................................................................ 72
4.6.1 Enabling EMI reduction............................................................................................. 72
Section 4.7 Loading demo images ................................................................ 73
4.7.1 Loading images from CD .......................................................................................... 73
Section 4.8 Installing the Operator Manual .................................................. 73
Section 4.9 Login and user management ..................................................... 74
Chapter 1 Safety
Table 1-1
Page 22 Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
2. Locate the AC power plug (E1), system circuit breaker (E2), and battery connectors (E3). See
Figure 1-2.
E2
E1
E3
Page 24 Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
8. Disconnect the two green battery power connectors J3 and J4 and the two sense connectors
J13 and J14 from the Cricket board. Apply a locking device, then apply your personal red lock
and tag. See Figure 1-5.
1
2
Item Description
1 Battery power connectors (J3, J4)
2 Battery sense connectors (J13, J14)
Item Description
1 Battery power connectors (J1, J2)
2 Battery sense connectors (J11, J12)
10. Press the power button and verify that the system does not turn on.
11. Verify that the voltage meter is working properly by testing it on a known live voltage source
(such as a wall outlet).
Page 26 Section 1.2 Lock Out/Tag Out (LOTO) procedure for electrical power
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
12. See Figure 1-7. Verify that electrical power has been removed from the system by applying
the DC voltmeter (+) lead to connector J5 pin 1 (Item 1, left-side screw terminal) on the Cricket
board and the meter (-) lead to chassis ground (Item 2).
Item Description
1 Connect DC voltmeter (+) to J5 pin 1 (left-side screw terminal)
2 Connect DC voltmeter (-) to chassis ground
Table 1-2
Relative humidity
Event
55% 40% 10%
Walking across carpet 7,500 V 15,000 V 35,000 V
Walking across vinyl floor 3,000 V 5,000 V 12,000 V
Motions of bench worker 400 V 800 V 6,000 V
Removing bubble pack from PCB 7,000 V 20,000 V 26,500 V
Packing PCBs in foam-lined box 5,000 V 11,000 V 21,000 V
Many electronic components are sensitive to ESD. Circuitry design and structure determine the
degree of sensitivity. The following packaging and grounding precautions are necessary to prevent
damage to electric components and accessories.
• Transport products in static-safe containers to avoid hand contact.
Table 1-3
Method Voltage
Antistatic plastic 1,500
Carbon-loaded plastic 7,500
Metalized laminate 15,000
Materials and equipment that are recommended for use in preventing static electricity include:
• Anti-static tape, smocks, aprons, or sleeve protectors
• Conductive bins, foam, tabletop workstations with ground cord of one-megohm +/-10%
resistance, and other assembly or soldering aids
• Static-dissipative table or floor mats with hard tie to ground
• ESD field service kits
• Static awareness labels
• Wrist straps and footwear straps providing one-megohm +/-10% resistance
• Material handling packages:
- Conductive plastic bags, plastic tubes and tote boxes
- Opaque shielding bags
- Transparent metalized shielding bags and shielding tubes
Available components of the Optima XR200amx/Optima XR220amx system are listed below.
Shipped with the Optima XR200amx/Optima XR220amx system:
• Optima XR200amx/Optima XR220amx
• Backup tether for digital detector (Optima XR220amx only)
• Service keyboard
• Software CD
• External CD/DVD-ROM drive
• Operating System firmware USB drive
• Tablet holder assembly (optional, Optima XR220amx and Optima XR200amx)
Shipped separately:
• DAP meter (standard with Optima XR220amx, optional for Optima XR200amx)
• Digital detector (Optima XR220amx only)
• Detector batteries (Optima XR220amx only)
• Detector battery charger (Optima XR220amx only)
• 6:1 grid (Optima XR220amx only)
• Barcode reader (optional, Optima XR220amx only)
• Wireless Hand Switch (optional, Optima XR220amx and Optima XR200amx)
Chapter 3 Installation
Yes
Perform
ground and
leakage
testing
Is the
Plug in and system an
turn on Install the
Optima detector
system power XR220amx? Yes
No
Install
optional
hardware
Ready for
configuration
and
calibration
Item Description
1 ON position
2 OFF position
3 Trip lever
2. Press and release the power button to turn on the Optima XR200amx/XR220amx system.
3. Check the battery level, indicated by the battery symbol on the interface.
In the figure below, the battery shows 25% capacity and discharging status.
Perform ground resistance testing & leakage testing only in the cases outlined in Table 3-1.
If it does not, perform the following steps to change the parameters as needed (the system will
save the settings even after system power is turned off). See Figure 3-8.
A. While in the ready state, press the or button until the output current display
begins flashing.
B. Press the or button to change the output current. The value changes in
0.1-A increments. To change the value by 1.0-A increments, press + or
button.
C. Press the button again to move to each of the other settings (Maximum Test
Value, Timer, and Frequency).
D. Use the or + buttons as needed to adjust the values.
E. Press .
3. While in the ready state, press the + buttons to display the Optional function
setting screen.
The Output Current Frequency is the first digit displayed, where the value is 0 for 50 Hz or 1
for 60 Hz. The Pass/Fail hold function is represented by the second digit.
Measured
Component Measurement point
resistance
Tube endcap screws or HV cable nuts
Tube
See Figure 3-12
Skin guards
Collimator
See Figure 3-13
Scroll support rivets
Column
See Figure 3-14
Screw used for mounting strain relief of wired handswitch cable
Bin
See Figure 3-15
Tube latch on top cover
Tube latch
See Figure 3-16
Perform leakage testing under the five specific conditions outlined in Table 3-4:
Test meter
Condition Power X-ray on Section reference
outlet
3.5.2.1 Condition 1: Power off, normal outlet,
1 Off Normal No
X-ray off
3.5.2.2 Condition 2: Power off, reversed
2 Off Reversed No
outlet, X-ray off
3.5.2.3 Condition 3: Power on, normal outlet,
3 On Normal No
X-ray off
3.5.2.4 Condition 4: Power on, reversed
4 On Reversed No
outlet, X-ray off
3.5.2.5 Condition 5: Power on, normal outlet,
5 On Normal Yes
X-ray on
Potential test equipment damage. Always pause in the OFF position when moving the OUTLET
switch from NORMAL to REVERSED or REVERSED to NORMAL. Failure to do so can result in the
internal test meter failure and tripping of facilities circuit breakers.
2. Insert the black coil cord with clamp into the CHASSIS connection located on the top of the
test meter (Figure 3-18).
EXPOSURE TO RADIATION
Wear a lead vest to protect yourself from radiation.
The detector also has a backup tether that can be attached, if needed, to provide input power and
wired communication. The backup tether must be attached to the detector to register the detector
with the system, and can then be removed and stored.
2. Inspect the box for physical or water damage. If present, document the damage.
3. Remove all four clips and lift top of outer box from bottom. Instructions are printed on the
outside of the box.
4. Lift the plastic bag and inner box out of the outer box. See Figure 3-20. More instructions are
printed on the outside of the inner box.
For all customers that do not support the USA style wall plugs, locally obtain and install a computer
style power cord with a CE approved, IEC 60320-1 C13 style connector on one end and the locally
appropriate wall plug connector on the other. The cord must meet or exceed the following electrical
specification, AC 120-240V 50/60 Hz 130VA - 168VA 1.4 Amps. Do not modify the shipped US style
cord as this can present a shock hazard to the user.
The detector is delivered with two batteries and a desktop charger, which can be used to charge
the batteries when disconnected from the detector. The battery can also be charged by inserting it
into the detector, then docking the detector in the bin.
It can take up to eight hours to charge the detector battery, depending on remaining charge. The
battery LEDs (labeled with 1 in Figure 3-22) on the detector indicate remaining power.
Note: The first time a new detector is used with an Optima XR220amx or Optima XR200amx with digital
upgrade system, detector firmware must downloaded because the existing firmware present on the
detector may not be compatible with the system. If you attempt to use a detector that does not have
the correct firmware, an error message will be displayed stating The detector is not
compatible with this system. or Digital cassette firmware is incorrect.
• To remove, use a small flat-blade screwdriver. Insert the screwdriver tip under the slot in the
side of the tag, and pry until the tag pops out.
For more information about detector identification shapes,see the Optima XR220amx Operator
Manual, Chapter 14 Set Preferences (Detector Registration).
Item Description
1 Grid (6:1 grid is a standard component, 8:1 grid is a purchasable option)
2 Detector
Sensitive Device
The grid is manufactured with a delicate mechanical structure of thin lead strips, inter-spaced with
strips of aluminum. Do not subject it to drops, impacts or crushing conditions.
Pinch Hazard
Attach the grid holder according to Figure 3-24, being careful not to pinch fingers or clothing.
1. The grid clips onto the detector. Make sure you attach it to the imaging side of the detector.
2. With the system switched ON, verify that the grid detection operates correctly.
Each time the grid is attached, removed, or attached improperly the system alerts the user with
a double beep and displays a message on the status bar.
If the system is located at a site where the primary language is not English, follow these steps.
1. In the installation kit, locate the X-ray warning label for the local language.
2. Clean the surface of the English label with alcohol.
3. Allow at least two minutes for the area to dry.
4. Apply the local language label on top of the English label.
Chapter 4 Configuration
Table 4-1
Configuration Comments
SUIF (Site parameters, Generator See Section 4.2 Using the System Configuration Tool (SUIF)
parameters, etc.) on page 57
DICOM See Section 4.4 DICOM connectivity configuration on
page 67
Demo images See Section 4.7 Loading demo images on page 73
Operator manual See Section 4.8 Installing the Operator Manual on page 73
Hardware options such as the See Section 4.10 Installing hardware options on page 74
barcode reader
System login See Section 4.9 Login and user management on page 74
• If system backups are lost or missing. If the software is re-installed but system configuration
files are not restored, configure the system again. GE service may need to be contacted to
enable purchased options. A software install resets all configuration data. If the system
configuration files are restored, you do not need to re-configure the system.
• After adding purchased options. Installation of purchased options can only be performed by
an authorized GE Healthcare service representative. If you add purchased options to the
system, update the system configuration files immediately and create and save a new backup.
Purchased option configurations are described in 4.2.7 Options configuration on page 64.
Parameter Definition
Site Name Name of specific site where system is installed.
Street Address 1 Street address of site where system is installed.
Street Address 2 Street address, continued, of site where system is installed.
City City where system is installed.
State/Province State or province where system is installed.
Postal Code Postal or ZIP code where system is installed.
Department name (for example, Radiology) responsible for system
Department Name
maintenance.
Telephone Phone number of department responsible for system.
Fax Fax number of department responsible for system.
Contact Person Name Person responsible for system maintenance.
Contact Person Phone Phone number of person responsible for system maintenance.
Editable by GE Healthcare personnel only.
System identifier assigned by GE Healthcare following system
installation and prior to customer turnover.
System ID This field is a GE proprietary field and cannot be used for any purpose
other than the System ID. Violation of this mandate will result in Insite
and/or other features not working. Customer IT personnel need to use
other means for DICOM filtering on their DICOM machines.
Editable by GE Healthcare personnel only.
Installation Date
Date system installation is completed, created by GE Healthcare.
Editable by GE Healthcare personnel only.
Service Contract Number
Customer’s Service Contract number, created by GE Healthcare.
Editable by GE Healthcare personnel only.
Contract Expiration Customer’s Service Contract expiration date, created by GE
Healthcare.
Parameter Definition
Options: DHCP or Static.
DHCP Configuration Determines whether the IP address is assigned, or acquired
dynamically. If Static is selected, enter associated information in IP
Address, Subnet Mask, and DNS fields.
System IP address.
IP Address Fixed Only
Enabled only if Wired IP Settings is set to Static.
System subnet mask.
Subnet Mask Fixed Only
Enabled only if Wired IP Settings is set to Static.
Default gateway.
Default Gateway Fixed Only
Enabled only if Wired IP Settings is set to Static.
Site domain name server.
Static DNS Server 1
Enabled only if Wired IP Settings is set to Static.
Site domain name server.
Static DNS Server 2
Enabled only if Wired IP Settings is set to Static.
Application Entity Title for DICOM.
AE Title Fixed Only
Fixed value.
Software port used for network communications.
Port Number Fixed Only
Fixed value.
Parameter Definition
Timezone Time zone of site where system is installed.
System Clock System time in YYYYMMDD HH:MM:SS format.
Date Display Format MM-DD-YYYY or DD-MM-YYYY.
Time Display Format Military (24-hour) or AM/PM (12-hour).
Country Code Country where system is installed.
A list of selectable countries. The system auto configures to the
correct regulatory approved formats and frequencies for all wireless
Wireless Regulatory Code communications. If a country does not allow a specific wireless
communication technology then the feature is disabled, Flashpad
wireless for example.
Measurement System English or Metric.
Parameter Definition
Application Language Language used for application screens.
QAP Timeout (Optima
Interval between QAP tests, in days. When time-out is reached,
XR220amx or Optima
system users see a warning flag indicating that a QAP test should be
XR200amx with digital
performed.
upgrade)
Editable by GE Healthcare personnel only.
VA Site Applies to USA Veterans Affairs facilities.
Yes or No.
Period of inactivity (no user input or processing activity) after which
Screen Blank Timeout
the screen will go blank, in minutes.
Image Mask Adjustment
(Optima XR220amx or Adjust the mask that is applied to the acquired image from the
Optima XR200amx with detector. Options: 3mm, 2mm, 1mm, 0, -1mm, -2mm, -3mm.
digital upgrade)
Parameter Definition
Collimator Light Maximum
Time, in seconds, that the collimator light will remain on.
On Time
Collimator Lamp Install
Date the collimator lamp was installed. YYYY-MM-DD format.
Date
Parameter Definition
Percentage of the tube thermal capacity limit, from 0 to 100. When this
Tube HUR Alarm
limit is reached, X-ray exposure is inhibited and an alarm sounds.
Tube ID Tube ID. Not editable.
Serial number of the tube. Confirm the serial number matches that of
Tube Serial
the attached tube.
Tube Install Date and Date and time the tube was installed. YYYYMMDD HH:MM:SS
Time format.
1. Ensure that the restoration of all configuration parameters has been completed and the system
has been reset.
2. Launch the SUIF and navigate to CONFIGURATION > WIRELESS.
3. Launch the wireless configuration utility as instructed on the screen.
4. Connect the USB flashdrive containing the site-specific certificates to a left-side USB port.
5. Click on the Certificates tab.
a. Observe the USB flashdrive-resident certificates in the pull-down list next to the ADD
button.
b. If there is more than one certificate, you will need to select each certificate individually.
c. Click ADD to install the displayed certificate from the drop-down list.
6. Continue with the site-specific configurations as defined by the IT administrator.
7. Exit the Configuration utility.
8. Remove the USB flashdrive.
9. Reset the system.
Note: Some customers may have their network access in a non-broadcast mode. This may
result in strange naming conventions for the scan results. Confirm with your IT contact.
4. In the Scan Results window, double-click the network to which you want to connect.
5. In the Network Config window, some fields are auto-populated. Depending on the type of
authentication used by the network, complete the other required information, as described in
the table below:
Table 4-7
Table 4-7
6. Click ADD.
7. Select the Current Status tab, and click CONNECT. Verify successful connection message.
8. To verify connectivity:
a. Select FILE menu > TOOLS.
b. Enter the IP of the machine you want to ping.
c. Press START PING and check for messages verifying connectivity.
d. Press STOP PING.
Some fields are auto-populated. Depending on the type of authentication, complete the other
required information, as described in the table below:
Table 4-8
5. Click ADD.
6. Select the Networks tab, and verify that the network is listed.
7. Select the Current Status tab, and click CONNECT. Verify successful connection message.
8. To verify connectivity:
a. Select FILE > TOOLS.
b. Enter the IP of the machine you want to ping.
c. Press START PING and check for messages verifying connectivity.
d. Press STOP PING.
Option Action
Configure filter settings that allow access through the firewall by
Filter Settings
adding allowed services and IP addresses, and removing filters.
Options:
BACKUP CURRENT FILTERS: Create a backup of the current filters.
RESTORE FROM BACKUP FILTERS: Restore the filters to a
Backup/Restore previously backed up set.
RESTORE TO FACTORY DEFAULTS: Reset all filter settings to
those originally installed.
REMOVE BACKUP FILTERS:
Show the firewall rules that are currently in effect on this system.
Network Tools
Select REFRESH to refresh the list of rules.
Select which red interfaces the filter settings should be applied to.
Configure PNF
Select UPDATE RED INTERFACES to apply the changes.
Option Description
Named Services tab
Used to set up filters to allow traffic to common network services (such as telnet or ftp) by
name, without needing to know the port and protocol.
Services/Allowed IPs Lists current filters by name and IP.
Select the Delete box checkbox next to the filter to delete, then
Remove Existing Filters
select DELETE EXISTING FILTERS.
From the Service Name drop-down list, select the service to be
allowed (such as telnet, ssh, ftp).
Add New Filter In the Allowed IPs field, specify a particular IP address, a range
of IP addresses, or a masked subnet.
Select ADD FILTER to apply your changes.
Allowed Nodes tab
Used to set up filters to allow all traffic from specified nodes. You can specify a particular IP
address, a range of IP addresses, or a masked subnet.
Allowed IPs Lists current filters by IP.
Select the Delete box checkbox next to the filter to delete, then
Remove Existing Filters
select DELETE EXISTING FILTERS.
In the Allowed IPs field, specify a particular IP address, a range
Add New Filter of IP addresses, or a masked subnet.
Select ADD FILTER to apply your changes.
DICOM tab
Used to add DICOM port numbers (all IP addresses are allowed DICOM access; the DICOM
application may limit access by IP). You can add multiple DICOM ports.
Allowed DICOM Ports Lists current DICOM ports by number.
Select the Delete box checkbox next to the port to delete, then
Remove Existing Filters
select DELETE EXISTING FILTERS.
In the Allowed Port field, specify a particular DICOM port.
Add New Filter
Select ADD FILTER to apply your changes.
Expert tab
Used to set up detailed filters by port, protocol, and node-lock (source).
Used only by advanced IT users.
Name/Port/Protocol Lists current filters by name, port number, protocol, and IP.
Select the Delete box checkbox next to the filter to delete, then
Remove Existing Filters
select DELETE EXISTING FILTERS.
Option Description
In the Name field, specify the filter name.
In the Allowed IPs field, specify a particular IP address, a range
of IP addresses, or a masked subnet.
Add New Filter In the Allowed Port field, specify a particular port.
From the Protocol drop-down list, select the protocol to be
allowed (TCP, UDP, Any).
Select ADD FILTER to apply your changes.
NAT tab
Used to define NAT (Network Address Translation) rules.
Lists current filters by name, source IP, destination IP,
Name/Source IP/Dest. IP
destination port, and protocol.
Select the Delete box checkbox next to the filter to delete, then
Remove Existing Filters
select DELETE EXISTING FILTERS.
In the Name field, specify the filter name.
In the Source IP field, specify the source IP.
In the Destination IP field, specify the destination IP.
Add New Filter In the Destination Port field, specify the destination port.
From the Protocol drop-down list, select the protocol to be
allowed (TCP, UDP, Any).
Select ADD FILTER to apply your changes.
GE Service tab
Used to set IIP node-lock IP address and DICOM port. This page is limited to GE service
personnel.
Option Description
Audit Message Settings tab
Audit Source ID IP address of audit message source.
Patient Name
On or Off.
Anonymized
Enterprise Repository tab
Enterprise Repository 1 On or Off.
Host Name/IP Primary audit server name or IP.
Option Description
Port Number Port number used to communicate with primary audit server.
Protocol used to communicate with primary audit server (TCP,
Protocol
UDP).
Send Test Message Test connection with primary audit server.
Enterprise Repository 2 On or Off.
Host Name/IP Secondary audit server name or IP.
Port Number Port number used to communicate with secondary audit server.
Protocol Protocol used to communicate with secondary audit server.
Send Test Message Test connection with secondary audit server.
Local Repository tab
On/Off Radio buttons.
Refresh Button to refresh the list.
Event ID / Time / Event
Headers for list of messages.
Outcome
Display Raw XML Display the raw data file to the user.
5. On the Add Network Host window, on the Host tab, enter the appropriate values in the fields
listed below. Some fields are available only on the Optima XR220amx or Optima XR200amx
with digital upgrade system.
Function Description
Name of the host that appears in the Network Hosts lists and
Host Label on the Image Management screen. Host labels cannot
contain spaces; use underscores ( _ ) to separate words.
Application Entry Title DICOM application title.
IP/Network Address IP address of the network host.
Port Number Port number for the network host.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Query Retrieve
Type of information the host will provide upon query from
another host. Options are No provider, Study, and Patient.
Available only on the Optima XR220amx or Optima
Storage Commitment XR200amx with digital upgrade system.
Designates whether the host will store image data.
Storage Commitment - Available only on the Optima XR220amx or Optima
Application Entry Title (if XR200amx with digital upgrade system.
Storage Commitment is
Yes) DICOM application title.
6. Press SAVE.
7. Select the PREFERENCES tab.
8. On the Add Network Host window, on the Preferences tab, select the appropriate options as
described below. All options except "Make this network host the HIS/RIS source" are available
only on the Optima XR220amx or Optima XR200amx with digital upgrade system.
Function Description
Available only on the Optima XR220amx or Optima
Allow this network host to query the XR200amx with digital upgrade system.
(system name)
Allows this host to search and filter the system.
Available only on the Optima XR220amx or Optima
Allow this network host to retrieve from XR200amx with digital upgrade system.
the (system name) Allows this host to open and display exams from the
system.
Function Description
Available only on the Optima XR220amx or Optima
Allow this network host to send images XR200amx with digital upgrade system.
to the (system name)
Allows the host to send images to the system.
Available only on the Optima XR220amx or Optima
This network host accepts multiple XR200amx with digital upgrade system.
frame image. Allows multiple frame images to be sent to this
network host.
Available only on the Optima XR220amx or Optima
Perform de-identification (anonymous XR200amx with digital upgrade system.
patient images) when sending to this
network host. Automatically de-identifies (anonymizes) any
images that the system sends to this host.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
Burns the VOI LUT (Look-Up Tables) into the
Apply “Burn-On-Send” to images when DICOM header to be displayed by PACS. Leaving
sending to this network host. this option unselected sends all available VOI LUTs
to the DICOM header for PACS to query and apply.
Note: PACS should be configured to read the first
VOI LUT for proper display of images on the
Acquisition workstation.
Available only on the Optima XR220amx or Optima
XR200amx with digital upgrade system.
This node acts as the Destination for receiving the
Send MPPS N-Create and N-Set MPPS NCreate & N-Set Notification. When
notification to this network host. configured for MPPS, the System sends information
like which exam is in progress, when a Study is
completed, how many images were acquired, and
what was the radiation dose to which the patient
was exposed during that session, etc.
Designates the host as the DICOM Worklist
provider. Defining the Radiology Information
System (RIS) and Hospital Information System
Make this network host the HIS/RIS (HIS) host allows patient worklists to be downloaded
source. (Only one host can be from those networks to the system.
designated as the HIS/RIS source.)
Note: Only one HIS/RIS source may be designated
on the system. Selecting this option will de-select
any other hosts as the HIS/RIS source.
Available only on the Optima XR220amx or Optima
DR Images sent as CR Modality XR200amx with digital upgrade system.
Options are Yes or No.
9. Press SAVE.
10. Repeat this process for each network host device the site wants to add.
For suggested parameter values for specific printer brands and models, refer to the System
Manual, Appendix A Printer configuration.
Attribute Value
Printer tab
Name of the printer that appears in the DICOM Printers list
and on the print setup screens. DICOM printer labels
DICOM Printer Label
cannot contain spaces in the name. Use underscores ( _ )
to separate words.
DICOM application title, provided by the site’s network
Application Entry Title
administrator.
IP address of the printer, provided by the site’s network
Network Address
administrator.
Port number of the printer. May be site-specific; check with
Port Number
site.
Pixel Depth Resolution of the printer. Options are 10 or 12.
Designates the pixel size the printer uses. This is specified
Printer Pixel Size (micron)
by the printer manufacturer.
Configuration Information Area for notes about the printer or configuration.
Density Min Minimum density range.
Density Max Maximum density range.
Magnification Type Options are Replicate, Bilinear, Cubic, None.
Smooth Factor Image smoothing factor.
Trim Designates whether there is to be trim. Yes or No.
Polarity Options are Normal, Reverse.
Border Density Color of the image border. Options are Black, White.
Color of areas that have no image printed. Options are
Empty Image Density
Black, White.
Designates the memory size of the printer, in Mbytes. This
Printer Memory Size
is specified by the printer manufacturer.
Layouts tab
Number and layout of images that may be printed on a
single sheet of film or paper.
Select the desired layouts
allowed for this printer Some selections control the orientation of the images on
the page. For example, two images per page may be side
by side, or one above the other.
Slide formats available for the printer, if any. Options are 35
Slide formats
or 40 mm.
Film Sizes tab
Select the sizes of film available for this printer, and enter the pixel width (W) and pixel height
(H). Pixel width and height values are provided by the printer manufacturer based on what
the printer supports.
Printer Settings tab
Attribute Value
# Of Copies
Print Mode
Magnification
Format
Orientation
Media Type
Destination
Media Size
6. Press SAVE.
7. Repeat this process for each printer the site wants to add.
Note: Except the login and user management account and password created specially to the system
administrator, GE field engineers also need to provide the related account and password
information to system administrator for the below configuration:
• Installing the Operator Manual.(Account:xruser/Password:4$xray)
• IP Address Change Procedure.(Account:su/Password:#superxr)
Note: If the position of the label makes the barcode unreadable, move the label so the barcode
can be read. A sample label similar to the one on the USB receiver is shown in Figure 4-1
below.
2. Remove the system side covers and the top cover. See the System manual, Replacement
Procedures, Top cover removal.
3. Remove the two screws from the inside of the left drive handle support, then remove the cover.
See Figure 4-2.
4. Route the USB cable through the opening in the bottom of the left drive handle support. See
Figure 4-3.
Note: You may need to loosen the detector bin mounting screws to provide clearance for
routing the cable.
Cable
access
hole
5. Attach the USB receiver to the plastic clip with the barcode facing out as shown in Figure 4-3.
6. Plug the USB cable into a USB port on the PC. See Figure 4-4.
Item Description
1 Host PC
2 Detector power supply (Optima XR220amx and Optima XR200amx with digital
upgrade only)
The Windows standard device driver will be installed automatically when you connect the
barcode reader receiver to the USB port and the system is powered up.
During initialization, the LED is orange. When the receiver LED turns green, the initialization
is complete and a connection has been made.
Color Description
Green Barcode was successfully read.
Red Blinking Data transmission error. The battery may need to be charged.
Red Solid Charging on the cradle. The LED changes from red to green when the battery
is fully charged.
Figure 4-5 OPI-4002 barcode reader charging cradle and power adapters
The following section provides instructions for the default configuration and two optional settings.
Have a printed copy of these pages on hand so you can scan the necessary barcodes. Refer to the
OPI-4002 User’s Guide for additional configuration options.
This configuration sets the barcode reader to add a Tab at the end of the scan instead of a Return.
Have a printed copy of these pages on hand so you can scan the necessary barcodes. If you make
a mistake during this configuration, start over at step 1.
1. Power up the system. Wait until the green LED on the receiver starts flashing.
2. Perform 4.10.2.1 Setting to default configuration on page 78.
3. Scan the barcodes shown in Figure 4-7, top to bottom.
After scanning each barcode you will hear one set of high-low-high beeps. The scanner will
beep at a one-second interval, and the LED will alternate green and red.
After scanning the last barcode, the scanner beam will turn off.
SET
RZ
TAB
END
This configuration sets the barcode reader to strip the first two and last four characters, and add a
Tab at the end of the scan. Have a printed copy of these pages on hand so you can scan the
necessary barcodes. If you make a mistake during this configuration, start over at step 1.
1. Power up the system. Wait until the green LED on the receiver starts flashing.
2. Perform 4.10.2.2 Verifying the default configuration on page 79.
3. Scan the barcode shown in Figure 4-8.
After scanning the barcode you will hear three sets of high-low-high beeps.
Figure 4-8 Strip first two and last four characters, and add a Tab suffix
5. For Optima XR220amx systems, the DAP meter option is a standard option and has already
been enabled. It can be turned on/off at the Applications level.
Notice: The system must be reset using the power button each time the DAP meter is
disconnected and then reconnected with system power on. The DAP meter does not support "Hot
Swapping". Failure to reset the system in this occurrence can result in an inaccurate dose value
reported by the DAP meter.
6. Perform DAP calibration. See the System Manual, Calibration Chapter, Hardware Calibration/
DAP Calibration section, for calibration procedure.
a. Connect the round cable connector to the DAP meter. See Figure 4-10.
b. Route the long DAP cable through the cable drape along the horizontal arm and vertical
column.
Loosely attach cable ties to hold the cable in position, but do not tighten them until range
of motion is confirmed.
Leave enough extra cable length at the DAP meter so that the tube/collimator assembly
can be moved through the normal range of motion without unplugging the cable.
c. Route the DAP cable through the cable access opening in the right-front cover. See
Figure 4-11.
d. Remove the HV cable clamp mounting screws. See Figure 4-11.
Item Description
1 HV cable clamp mounting screws (2)
e. Remove the clamp from the HV cable bundle. See Figure 4-12.
f. Plug the other end of the DAP cable into the J6 bulkhead connector. See Figure 4-13.
Install cable ties as necessary to secure cable within the bulkhead area.
J6
7. Confirm that there is sufficient slack in the DAP cable at the tube/collimator assembly:
a. Move the tube/collimator assembly through the full range of motion and verify that the
DAP cable remains connected to the DAP meter.
b. Once sufficient cable slack is confirmed, tighten down the cable ties to secure the DAP
cable to the existing cable drape.
8. Arrange the cable bundle as shown in Figure 4-14, use a cable tie to maintain cable positions.
9. Install the clamp onto the cable bundle. DO NOT TIGHTEN THE CLAMP YET.
10. Mount the clamp to the Thorax chassis. Slide the clamp to the rear of the mounting screw slots.
11. Tighten the clamp around the cable bundle, ensuring that the cables are not pinched by the
clamp.
C
1 2
4 3
Item Description
1 DAP cable (optional for Brivo XR285amxOptima XR200amx systems)
2 Wireless cable (only valid for Optima XR220amx systems)
3 Vertical brake cable
4 Horizontal arm lock cable
12. Install the front bin, top cover and side covers.
13. Re-install the cable cover on the vertical column cable bundle. See the System manual,
Replacement Procedures chapter, Cable Cover Installation section.
14. Configure the system to enable the DAP meter option. See 4.2.7 Options configuration on
page 64.
15. Once the DAP meter option has been enabled, it must be ’switched on’ at the Applications
level:
The system must be reset using the power button each time the DAP meter is disconnected and
then reconnected with system power on. The DAP meter does not support "Hot Swapping". Failure
to reset the system in this occurrence can result in an inaccurate dose value reported by the DAP
meter.
16. Perform DAP calibration. See the System Manual, Calibration Chapter, Hardware Calibration/
DAP Calibration section, for calibration procedure.
3. Remove the 4 screws on the lead apron hanger, and then remove the lead apron hanger from
the column.
4. Hang on the whole tablet holder assembly (item 2) on the column. Put the lead apron hanger
(item 3) on the tablet holder assembly in order to install the lead apron hanger and the tablet
holder assembly on the column.Apply thread locker (i.e. Loctite 243 ) to the 4 tablet holder
assembly mounting screws (new item 1), and tighten the screws. Torque to 3.2 N-m (2.36 lbft).
Item Description
1 Tablet holder assembly mounting screws (4)
2 Tablet holder assembly
3 Lead apron hanger
lock
7. Put the tablet on the tablet holder and make sure the tablet is clamped well.
After you turn the key to lock the clamp, please check the back of the tablet clamp assembly to make
sure the tablet is well fixed by the clamp without any possibility to fall down from the holder. (See
below figures)
Front
Back
8. Lock the tablet clamp assembly with the key and remove the key.
Lock
Tablet
c. Pull the handle on the tablet holder assembly to relax it from the column.
d. Rotate the tablet holder arm around the column from 0° to 180°.
1. Remove both side covers and the top cover. See System manual 5336122-1EN, Chapter 8,
Section 8.1.2 - Top cover removal.
2. Identify the components of the kit shown below (Table 4-16, Figure 4-16, Figure 4-17):
PCB Module
Remote Finder/Transmitter
Receiver
3. Remove the existing nut and washer located behind where the PCB Module is to be placed,
then attach the ground wire from the PCB Module to the system chassis stud and re-install the
washer and nut. See Figure 4-18.
4. Mount the PCB Module in the bottom of the Thorax as shown below (Figure 4-19) by removing
the adhesive liner and applying pressure to activate the adhesive.
5. Route the cable attached to the PCB Module up along the main cable bundle between the
Spyder and Locust boards. See Figure 4-20.
6. Disconnect the J5 plug from the Spyder board and plug into End C of the main cable from the
PCB Module.
Plug End B of the main cable into Spyder J5.
See Figure 4-21 to see how connections appear after re-wiring is complete.
End B
J5 Connector
J5 Plug
End C
Spyder Board
Figure 4-21 Cable connection to Spyder board
7. Remove the top-left mounting fastener on the Spyder board and mount the ground terminal,
End D, of the main cable underneath the head of the fastener. See Figure 4-22.
End D
Ground Fastener
8. Continue routing the main cable (twisted black and red wires) up through the Thorax (Figure 4-
23) to the LVLE2 and plug End A of the main cable into J6 on the LVLE2 (Figure 4-24).
Connect to J6
9. Position the Receiver Mount on the top cover. The mount is curved and will fit the contour of
the top cover when it is located in the proper position. See Figure 4-25 for approximate
location.
10. While holding the Receiver Mount securely in position, mark the locations for the 3 mounting
holes and the cable access hole. See Figure 4-26.
11. Drill the holes in the top cover using the drill bits provided in the kit. See Figure 4-27.
12. Temporarily remove the two nylon nuts from the standoffs on the Receiver. Run the cable of
the Receiver through the ½" diameter hole in the Receiver Mount, then place the Receiver onto
the Receiver Mount and reinstall the nylon nuts to secure it to the mount. Do not over-tighten
the plastic nuts. See Figure 4-28.
13. Use a pair of cutters to remove the excessive length of the standoffs so that they are flush with
the surface of the Receiver Mount. See Figure 4-29.
14. Run the cable of the Receiver through the ½" diameter hole in the top cover.
15. Attach the Receiver/Mount assembly to the top cover using the 3 self-tapping screws provided
in the kit. See Figure 4-30. Do not over-tighten the screws.
16. Route the cable along the power switch cable of the top cover. See Figure 4-31. Zip tie the
cables as necessary.
17. Continue routing the cable along the side of the PC and down through the hole in the sheet
metal of the Thorax and between the Locust and Spyder boards. Plug the cable into the
connector on the PCB Module. See Figure 4-32. Zip tie the cables as necessary.
a. Apply the rating plate label to front cover, next to the power cord area. See Figure 4-33.
instructions to change the default internal IP Address if an IP Address conflict occurs with the
hospital network.
Note: To change IP address or configure the snapshot tool, you need the Account and Password
information. Please consult your administrator for them.
1. Plug in the Service Keyboard.
2. Open a terminal window using CTRL+SHIFT+F5 and click on the terminal window icon.
3. Change users by entering the account and password at the prompt:
Note: Please consult your administrator for the Account and Password information.
su
#superxr
4. Run the Change IP script by entering the following text at the prompt:
/magichome/xruser/engg/changeIp.sh
5. Select 1 of the 5 options of subnet IP addresses. Write down the IP Address you select, you
will need this in a later step.
1. 172.16.x.x
2. 172.17.x.x
3. 172.18.x.x
4. 192.168.x.x (SW LFC default)
5. 192.169.x.x
6. The PC will reboot automatically, select SHUTDOWN when the system presents the Degraded
mode screen.
7. Login to system.
8. Open a terminal window and become root.
Note: Please consult your administrator for the Account and Password information.
xruser@magic: su
Password: #superxr
At prompt, type: ifconfig | more
Confirm the br0 IP Address is XXX.XXX.3.1 (where XXX.XXX equals the address range
selected above).
9. To test network connectivity, perform a C-Echo test to one or more of the Network Hosts.
10. This step applies to Optima XR220amx or Optima XR200amx with Digital Upgrade only.
Verify that all connected detectors boot successfully. Verify that you can take an exposure on
all available receptors.
11. This step applies to Optima XR220amx or Optima XR200amx with Digital Upgrade only.
Verify the Detector Wireless connection is active by acquiring an image.
12. Perform the Snapshot Tool Configuration.
#superxr
3. Open Firefox Browser by typing the following command :
firefox http://localhost/snapshot/Manual_Snapshot.html
4. Click on SNAPSHOT PREFERENCES. See Figure 4-34.
Figure 4-34 Snapshot Preferences
5. Repeat Steps 6 through 17 (below) for the following four Configurations (available under the
drop-down menu):
* Asnapshot_Lightning
* ASnapshot_BKP
* Snapshot_ResetTimeOut
* QuickSnapshot
7. In the IP Address data entry text box, change 192.168.3.1 to “xxx.xxx.3.1” (where
xxx.xxx.3.1 is the same IP Address range used in Section 4.13 IP Address Change
Procedure and 3.1 is the specific address assignment for the host pc port). See Figure 4-
37.
Figure 4-37 Change IP Address
10. In the IP Address data entry text box, change 192.168.3.1 to “xxx.xxx.3.1” (where
xxx.xxx.3.1 is the same IP Address range used in Section 4.13 IP Address Change
Procedure and 3.1 is the specific address assignment for the host pc port). See Figure 4-
40.
Figure 4-40 Edit Magic IP Address
12. Back on Snapshot Preferences main screen, click on Target Names – Table_IDC –
DELETE. See Figure 4-42.
Figure 4-42 Delete Target Name “Table_IDC”
13. You will get a popup like below, select OK. See Figure 4-43.
Figure 4-43 Table_IDC Popup Message
14. Under Target Names – WallStand_IDC click on DELETE. See Figure 4-44.
Figure 4-44 Delete Target Name “WallStand_IDC”
15. You will get a popup like below, select OK. See Figure 4-45.
Figure 4-45 WallStand_IDC Popup Message
16. Under Manage Preferences section, click on SAVE AS.... See Figure 4-46.
Figure 4-46 Save Changes
If everything is fine you should be able to see Auto Snapshots getting generated after
reset:
a. Perform a system reset.
b. After system is booted up, login and wait for 5 minutes.
(Snapshot is being created in a temp location)
c. While you are waiting, open a terminal window using CTRL+SHIFT+F5 and click
on the terminal window icon.
d. Run following command:
ls –ltr /enggdata/Snapshots/*3400017*.zip
e. Note the date/time stamp of the most recently created file.
f. After 5 minutes reset and reboot the system, login.
(Snapshot from temp location is written to Snapshots directory and a new
snapshot is being created in a temp location)
g. Open a terminal window using CTRL+SHIFT+F5 and click on the terminal
window icon.
h. Run following command:
ls –ltr /enggdata/Snapshots/*3400017*.zip
i. The output of (c) above should show a snapshot file, having the string 3400017
embedded in the snapshot filename, created after the most recent system boot
(in Step b above).
j. Type date to see the current system time.
The latest snapshot file should have been created a few minutes before the date
command output.
k. Verify the file size is greater than 400,000:
-rw–rw-r- - 1 xruser xruser file size date time /path/filename
20. Close all windows.
21. Complete all system configurations and customer settings.
22. Create a new System Backup on DVD media.
Note: Do not use backup media from any other system. The result will be that half of the
system is configured for 172.x.x.x and other half is configured for 192.x.x.x
The system will then boot into Degraded Mode only.
Also, when performing a Software Load, you must perform this procedure first before
doing a System Restore.
Chapter 5 Calibration
This chapter explains how to calibrate the printer and configure PACS features. No other
calibrations are required during system installation. The unit has been fully calibrated and tested
during the manufacturing process. If desired, please reference the System manual for instructions
of the various calibration processes.
6. In the Destination icon list, press the appropriate PACS network host.
- If PACS test images #1 and #6 appear visually identical (with an equal number of bright
and dark bands), the PACS supports VOI-LUT. Configure the PACS as No-Burn for this
host.
- If PACS Test Images #1 and #6 appear visually different (with a different number of bright
and dark bands), or if you can see saturation in the lung or abdomen of the chest region
(saturation appears as a completely flat dark or white area), the PACS does not support
VOI-LUT or applies it incorrectly. Configure the PACS as Burn-on-Send for this host.
5. Repeat sections 5.4.2.3 Sending no-burn images to the PACS and 5.4.2.4 Sending burn-on-
send images to the PACS for each PACS destination host.
In addition to the test results above, use Table 5-2 as a guideline to determine if a PACS should be
configured as Burn-on-Send. This table considers only whether a PACS supports VOI-LUT
No-Burn Burn-on-Send
GE Centricity RA1000 v1.0, v2.0, v2.1 GE Pathspeed v7.12, 8.0
GE Centricity RA600 v6.1, 7.0 GE AW v3.1, 4.0
GE Radworks v5.1 Kodak DirectView v4.3
GE Pathspeed v8.1 or later Kodak DirectView v5.1, 5.2
McKesson HRS v3.3, 3.3.2 Kodak Directview(CEMAX ICON), v4.3
Fuji Synapse v3.0, 3.1 Merge eFilm, v2.0
Agfa IMPAX v4.5, 5.2 Stentor iSite v3.0, v3.3.1
Philips Siemens Magic View 300
RealTime iPACS Viewer v5.0 VA Vista
- Picker
- Neusoft v3.0
- Thinking Systems
The loss of dynamic range is most common in the top dark band. If reduced dynamic range
occurs, the five squares will not be visible in the top dark band (band #1).
3. Record the results in Table 5-4.
Tests Results
WC = __________
DICOM header on PACS (image #1 No-Burn) WW = __________
VOI-LUT (Yes/No)
WC = __________
DICOM header on PACS (image #6 Burn-on-Send) WW = __________
VOI-LUT (Yes/No)
WC = __________
Values displayed on PACS viewer (image #1)
WW = __________
WC = __________
Values displayed on PACS viewer (image #6)
WW = __________
Saturation visible in lung or abdomen region
Able to see all five squares in top band of image #6
Able to see all five squares in top band of image #1
Images #1, 4, 5 appear visually identical
Images #6, 7, 8 appear visually identical
PACS able to select Normal/Harder/Softer
VOI-LUT not present;
DICOM header on PACS (image #9 CR-Fallback).
correct WW/WC
Perform QAP every time you calibrate the detector, and as the final step in calibrations during
installation.
For more information about performing QAP and viewing QAP results, see the Optima XR200amx
or Optima XR220amx Operator Manual, Quality Assurance and Maintenance.
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DIRECTION 5336113-1EN, REVISION 10 INSTALLATION MANUAL
Table 7-1
2 3
Table 7-1
Item Description
1 Primary rating plate location, located on cover above main circuit breaker. Consists of:
• System rating plate
• Generator rating plate
• X-ray tube rating plates
See Figure 7-2 on page 123, Figure 7-3 on page 123.
2 Generator rating plate, also located inside unit on generator module. See Figure 7-4
on page 124.
3 X-ray tube/casing rating plates, also located on bottom of X-ray tube casing. See
Figure 7-5 on page 124.
4 Collimator rating plate, located on side of collimator. See Figure 7-6 on page 125.
5555000-x
123456789
January 201x
Optima XR220amx
130
Front cover
GE Healthcare
Optima XR200amx/XR220amx
System Parts List
Direction 5336115-1EN
Revision 6
GE HEALTHCARE
Warning OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
ATTENTION
LES APPAREILS A RAYONS X SONT DANGEREUX A LA FOIS POUR LE PATIENT ET POUR LE MANIPULATEUR SI LES MESURES DE PROTECTION NE SONT PAS STRICTEMENT APPLIQUEES
Bien que cet appareil soit construit selon les normes de sécurité les plus severes, la source de rayonnement X représente un danger lorsque le manipulateur est non qualifié ou non averti. Une exposition excessive au rayonnement X entraîne des
dommages a l’organisme. Par conséquent, toutes les précautions doivent être prises pour éviter que les personnes non autorisées ou non qualifées utilisent cet appareil créant ainsi un danger pour les autres et pour elles-mêmes. Avant chaque
manipulation, les personnes qualifiées et autorisées à se servir de cet appareil doivent se renseigner sur les mesures de protection etablies par la Commission Internationale sur la Protection Radiologique, Annales 26: Recommandations de la
Commission Internationale sure la Protection Radiologique et les normes nationales en vigueur.
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 (ICRP), contained in Annals Number 26 of the ICRP, and with
applicable national standards.
ATENCION
LOS APARATOS DE RAYOS X SON PELIGROSOS PARA EL PACIENTE Y EL MANIPULADOR CUANDO LAS NORMAS DE PROTECCION NO ESTAN OBSERVADAS
Aunque este aparato está construido según las normas de seguridad más estrictas, la radiacion X constituye un peligro al ser manipulado por personas no autorizadas o incompetentes. Una explosicion excesiva a la radiación X puede causar
daños al organismo.
Por consiguiente, se deberán tomar todas las precauciones necesarias para evitar que las personas incompetentes o no autorizadas utilicen este aparato, lo que seria un peligro para los demás y para si mismas.
Antes de efectuar las manipulaciones, las personas habilitadas y competentes en el uso de este aparato, deberán informarse sobre las normas de protección fijadas por la Comisión Internacional de la Protección Radiológica, Anales No 26:
Recomendaciones de la Comisión Internacional sobre la Protección Radiológica y normas nacionales.
ACHTUNG
RÖNTGENAPPARATE SIND EINE GEFAHR FUR PATIENTEN SOWIE BEDIENUNGSPERSONAL, WENN DIE GELTENDEN SICHERHEITSVORKEHRUNGEN NICHT GENAU BEACHTET WERDEN
Dieser Apparat entspricht in seiner Bauweise strengsten elektrischen und mechanischen Sichereitsnormen, doch in den Händen unbefugter oder unqualifizierter Personen wird er zu einer Gefahrenquelle.
Übermäßige Röntgenbestrahlung ist für den menschlichen Organismus schädlish.
Deswegen sind hinreichende Vorsichtsmaßnahmen erforderlich, um zu verhindern, daßunbefugte oder unqualifizierte Personen solche Geräte bedienen oder sich selbst und andere Personen deren Bestrahlung aussetzen können.
Vor Inbetriebnahme dieses Apparats solite sich das qualifizierte und befugte Bedienungspersonal mit den geltenden Kriterien für den gefahrlosen Strahleneinsatz durch sorgfältiges Studium des Hefts Nr. 26 der Internationalen Kommission für
Strahlenschutz (ICRP) vertraut machen: Empfehlungen der Internationalen Kommission für Strahlenschutz und anderer nationaler Normenbehörden.
Page 2
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DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Important information
Preface Page 3
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Page 4 Preface
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DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Preface Page 5
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Page 6 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Legal notes
TRADEMARKS
Optima XR200amxTM and Optima XR220amxTM are trademarks of GE Healthcare. WPA and WPA2 are trademarks of the Wi-Fi Alliance. All other products and their name brands are trademarks of their respective holders.
COPYRIGHTS
All material copyright © 2011 by General Electric Company, Inc. All rights reserved. The material presented and contained herein may not be reproduced in any form or manner, without the written permission of General Electric Company, Inc.
Preface Page 7
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DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Important precautions
DAMAGE IN TRANSPORTATION
All packages should be closely examined at time of delivery. If damage is apparent, have notation “damage in shipment” written on all copies of the freight or express bill before delivery is accepted or “signed for” by a General Electric representative
or a hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A
transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period.
To file a report, call 1-800-548-3366. Select the option for “Install Support Services for FOA and MIS.” Contact your local service coordinator for more information on this process.
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 (NCRP) 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.
Page 8 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Revision history
Preface Page 9
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Page 10 Preface
GE HEALTHCARE Preface - Publica- OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6
tion conventions SYSTEM PARTS LIST
Hazard Messages
Any action that will, could or potentially cause personal injury will be preceded by the safety alert symbol and an appropriate signal word. The safety alert symbol is the triangle with an exclamation mark within it. It Is always used next to the signal
word to indicate the severity of the hazard. Together, they are used to indicate a hazard exists.
Signal words describe the severity of possible human injures that may be encountered. The alert symbol and signal word are placed immediately before any paragraph they affect. Safety information includes:
1.) Signal Word - The seriousness level of the hazard.
2.) Symbol or Pictorial - The consequence of interaction with the hazard.
3.) Word Message:
a.) The nature of the hazard (i.e. the type of hazard)
b.) How to avoid the hazard.
The safety alert symbol is not used when an action can only cause equipment damage.
Preface Page 11
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Page 12 Preface
GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Publication Conventions
General Paragraph and Character Styles
Prefixes are used to highlight important non-safety related information. Paragraph prefixes (such as Purpose, Example, Comment or Note) are used to identify important but non-safety related information. Text styles are also applied to text within
each paragraph modified by the specific prefix.
Page Layout
Publication Part Number & Revision Number Publication Title
The current section and its title The current chapter and its title
are always shown in the footer of are always shown in the footer of
the left (even) page. the right (odd) page.
An exclamation point in a triangle is used Paragraphs preceeded by a symbol
to indicate important information to the user. (e.g. bullets) contain information that
Paragraphs preceeded by Alphanumeric has no specific order.
characters (e.g. numbers) contain infor-
mation that must be followed in a specific order.
Headers and footers in this publication are designed to allow you to quickly identify your location. The document part number and revision number appears in every header on every page. Odd numbered page footers indicate the current chapter,
its title and current page number. Even page footers show the current section and its title, as well as the current page number.
Preface Page 13
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DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
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GE HEALTHCARE OPTIMA XR200AMX/XR220AMX
DIRECTION 5336115-1EN, REVISION 6 SYSTEM PARTS LIST
Table of contents
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Table 1-1 Optima XR200amx/XR220amx, US and International, 15kW (5555000-3, -5) & 30kW (5555000-4, -6)
Table 1-4 Software Collector and Firmware dongle for Optima XR220amx for VA
5391109 02
THIS DRAWING WAS MADE
BY DELTATECH CONTROLS Overlay Board Assembly
FOR GE HEALTHCARE.
[
Approved Document - 5555003ADW_r9.pdf Page 2 of 2
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Section 2.5 PC
2.5.1 Whip antenna for 802.11abgn wireless/SMA coaxial connector with swivel mount - 5367724
Figure 2-43 Whip antenna for 802.11abgn wireless/SMA coaxial connector with swivel mount - 5367724
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
5391109 02
THIS DRAWING WAS MADE
BY DELTATECH CONTROLS Overlay Board Assembly
FOR GE HEALTHCARE.
o
Figure 3-14 Hornet Display Module Board PWA - 5350004-2
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
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DIRECTION 5336115-1EN, REVISION 6
State: RELEASE - Document is released and under formal Change Control. Changes are subject to the ECR/ECO Process.
See the GEHC Myworkshop System to determine the status of this document.
Page 118
GE HEALTHCARE
DIRECTION 5336115-1EN, REVISION 6
Section 3.5 PC
3.5.1 Whip antenna/SMA coaxial connector
Figure 3-42 Whip antenna for 802.11abgn wireless/SMA coaxial connector with swivel mount - 5367724
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Section 5.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
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Table 5-2 2.1 Base, Column, Arm, Drive Handle, Thorax Assembly - 5509900-3
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