3300 Service Manual

3300 G_W_C
Diagnostic Ultrasound System
Service Manual
Rev A
10391431
Revision History
Version Date Author Description
A 2020-10-9 Song Fengjiu First Release
II
About This Manual
This manual is the 3300 G_W_C Diagnostic Ultrasound System service

manual.
This manual describes the service safety relevant information of 3300

G_W_C Diagnostic Ultrasound System. FSE should read and make sure to
understand this manual. Please read this manual carefully before operat-
ing.
The Manufacturer will not bear any responsibility for unauthorized

contents.
Manual Name: 3300 G_W_C Diagnostic Ultrasound System Service Man-

ual
Manual Number: NPS-US-0521
Revision: Rev A
How to use this manual
The user must read the manual carefully to prevent potential losses and
damages.
Please read warnings, cautions, and notes carefully.
For daily operations, it is recommended to refer to the manual at any time.
Copyright
The copyright of the manual belongs to Philips Medical Systems Co.,

Ltd.
It is prohibited to copy or modify the contents of this manual without
authorization.
Customer Assistance
Various support locations around the world can provide customers

technical assistance with the ultrasound system. Customers should
contact the representative or sales office from which they purchased
the system or the nearest Philips Ultrasound office.
III
Philips Ultrasound, Inc.
22100 Bothell Everett Hwy
Bothell, WA 98021-8431 USA
425-487-7000 or 800-426-2670
www.healthcare.philips.com/ultrasound
IV
Symbol Descriptions
!!
WARNING Attention symbol
WARNING Electrical warning symbol
!!
CAUTION CAUTION SYMBOL
Note Note Description
V
3300 G_W_C Manual Name
Section 1 General Information . . . . . . . . . . . . . . . . . . . . . . . . . 1

1.1 System Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1.2 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
1.3 System Administration . . . . . . . . . . . . . . . . . . . . . . . . 6
1.4 CDs and DVDs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
1.5 USB Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Section 2 Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
2.1 Equipment Safety Classification . . . . . . . . . . . . . . . . . . 10
2.2 Acoustic Output Power . . . . . . . . . . . . . . . . . . . . . . . . 11
2.3 Acoustic Statement . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
2.4 AIUM/NEMA Output Display Standard . . . . . . . . . . . . . . 12
2.5 Automatic Index Selection . . . . . . . . . . . . . . . . . . . . . . 13
2.6 Exposure Risk . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
2.7 Eclectic Warning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
2.8 Connect Peripheral . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
2.9 Glutaraldehyde Exposure . . . . . . . . . . . . . . . . . . . . . . . 16
2.10 Move System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
2.11 EMC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
2.12 Symblos . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Section 3 Theory of Operation . . . . . . . . . . . . . . . . . . . . . . . . . 24
3.1 General Information . . . . . . . . . . . . . . . . . . . . . . . . . . 24
3.2 Functional Description . . . . . . . . . . . . . . . . . . . . . . . . . 25
3.3 Main Functional Segments . . . . . . . . . . . . . . . . . . . . . . 26
3.4 System Functional block diagram . . . . . . . . . . . . . . . . . 36
Section 4 Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
4.1 Preparing for Installation . . . . . . . . . . . . . . . . . . . . . . . 37
4.2 Environmental Requirements . . . . . . . . . . . . . . . . . . . . 37
4.3 Installing System . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
4.4 Power On/Off . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
4.5 Connecting/Disconnecting the transducer . . . . . . . . . . . 48
4.6 Configuring the System Settings . . . . . . . . . . . . . . . . . 50
4.7 Peripherals Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . 53
4.8 Optional Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . 55
4.9 Service Platform . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Section 5 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 65
5.1 Air Filter Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . 66
5.2 Control Panel Cleaning . . . . . . . . . . . . . . . . . . . . . . . . 67
5.3 Caster Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . 68
5.4 LED Movement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 69
5.5 Exterior Surfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . 70
5.6 Test and Paperwork . . . . . . . . . . . . . . . . . . . . . . . . . . 70
Section 6 Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
6.1 Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 71
6.2 System Software Installation . . . . . . . . . . . . . . . . . . . . 101
6.3 Finishing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 106
Section 7 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . 107
7.1 Clarifying Symptoms . . . . . . . . . . . . . . . . . . . . . . . . . . 107
7.2 Categorize/Localize the Problem . . . . . . . . . . . . . . . . . . 108
7.3 Re-creating a Problem . . . . . . . . . . . . . . . . . . . . . . . . . 108
7.4 Isolating Causes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 108
NPS-US-0521 i Rev C
Warning: This page contains copyrighted materials that are confidential and/or proprietary. Any
release or distribution of this material, without permission, is a violation of Law.
3300 G_W_C Manual Name
7.5 Known Symptoms, Causes, and Corrective Actions . . . . . 111

7.6 Checking for EMI and RFI . . . . . . . . . . . . . . . . . . . . . . 113
7.7 USB and Peripherals Failures . . . . . . . . . . . . . . . . . . . . 116
Section 8 Spare Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118
8.1 Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 118
8.2 E-BOX (PCBAS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 121
8.3 Power Supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125
8.4 Control Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 126
8.5 PC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 129
8.6 Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 131
8.7 Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 139
8.8 Transducer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 141
8.9 Peripherals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 143
NPS-US-0521 ii Rev C
3300 G_W_C Service Manul
General Information
Section 1 General Information
Introduction
This section describes the contents of the manual, and provides a general
overview and physical description of the 3300 G_W_C Diagnostic Ultra-
sound System and summarizes system application, feature, and regulatory
information.
1.1 System Overview
Figure1: 3300 G_W_C System with jiont arm
NPS-US-0521 1 REV A
System Overview
Figure2: 3300 G_W_C System with simple arm
1.1.1 Applications
The clinical options or applications, for each transducer available for the
system are listed here.
1) C6-2 Abdominal, GYN, OB, Fetal Cardiac, Abdominal Vascular, Urinary

2) C8-5 Abdominal, GYN/OB, Neonatal Head (Transcranial), Peripheral
Vascular
3) C9-4v GYN, OB
4) L12-4 Small Parts (except Transorbital), Superficial, Peripheral Vascular,
Musculoskeletal, Pediatric, Vascular
5) S4-2 Abdominal, Cardiac (Adult and Pediatric), Transcranial Doppler
(TCD), GYN/OB
6) S8-3 Abdominal, Adult and Pediatric Cardiac, Neonatal Head (Transcra-
nial), GYN/OB
7) V6-2 GYN, OB, Abdominal, Abdominal Vascular, Fetal Cardiac
1.1.2 Imaging modes
• 2D
• 3D/4D
• Anatomical M-mode
• Color mode
NPS-US-0521 2 REV A
System Overview
• CW Doppler
• Color Power Angio (CPA) imaging
• Doppler iSCAN Intelligent Optimization
• Duplex and Triplex
• Freehand 3D
• Frequency Compound Imaging
• Iscan Intelligent Optimization
• M-mode
• Panoramic Imaging
• PW Doppler
• Special Compound Imaging
• Tissue Harmonic Imaging
• Tissue Doppler Imaging (TDI)
1.1.3 Transducer
• C6-2
• C8-5
• C9-4v
• L12-4
• S4-2
• S8-3
• V6-2
1.1.4 Languages
• English
• Genman
• Spanish
1.1.5 Options: Software Options
The system ships from the factory with all of the software options option,
allowing those options to operate. The purchased options are enabled at
the factory. Options purchased later are enabled in the field. For more
information on the software options available, see the system user manu-
als.
NPS-US-0521 3 REV A
System Overview
1.1.6 System Reference Information
• A User Manual
• An Acoustic Output Tables document
• A Shared Roles for System and Data Security document
• An AIUM Medical Ultrasound Safety booklet
• Help
1.1.7 System Monitor
The system video monitor is a 21.5 inch widescreen LCD color display.
1.1.8 System Control Panel
Figure3: Control Panel
1.1.9 Supplies and Accessories
Customers can order transducer covers and biopsy guides from CIVCO
Medical Solutions:
NPS-US-0521 4 REV A
Specifications
1.2 Specifications
1.2.1 Physical Specifications
Dimensions
• 3300 G_W_C systems with jiont arm height (bottom of caster to top
of monitor):
Lowest position: 1320 ± 20mm
Highest position: 1600 ± 20mm
• 3300 G_W_C systems height with simple arm (bottom of caster to

top of monitor):
Lowest position: 1320 ± 20mm
Highest position: 1470 ± 20mm
• Width: 550 ± 20mm

• Depth: 650 ± 20mm
Weight
• 3300 G_W_C systems with jiont arm weight: 60 ± 5kg

• 3300 G_W_C systems with simple arm weight: 55 ± 5kg
NPS-US-0521 5 REV A
System Administration
1.2.2 Environmental Specifications
Operating Environment
Temperature Range 10°C to 40°C
Relative Humidity 20% to 85%, non-condensing
Atmospheric Pressure 700 hPa to 1,060 hPa
Storage Environment
Temperature Range -20°C to 60°C
Relative Humidity 15% to 95%, non-condensing
Atmospheric Pressure 500 hPa to 1,060 hPa
1.3 System Administration
1.3.1 Options Information
The system options information can be found on the system Options screen
(touch Setup, click the Options tab and then Options).
Information in the Status column in the Options window indicates the sta-
tus of each application:
• Not installed An application that is not yet installed

• Permanent An installed application
• Expires on [date]A trial application that expires on the specified
date
• Expired An expired trial application
• Removed A permanently deleted application
1.3.2 Installing, Removing, and Disabling System Options
When you receive your system, the options you purchased are installed
and enabled. At some points, however, you may need to install a new
option, remove an option, or disable an option.
NPS-US-0521 6 REV A
System Administration
To install an option, remove, or disable an option:
1) Touch Utilities.
2) Touch Setup.
3) Click the Options tab.
4) Click the Options button.
5) In the Options window, perform one of the following:
• To install an option with an access code, select an option, click
Install, and type the access number.
• To install an option from removable media, insert the media and
click Install from File.
• To permanently remove an option, click Remove. A password is
required to prevent accidental deletion of an option. Note the
confirmation number.
• To temporarily disable an option, clear the appropriate check box.
To re-enable an option, select the appropriate check box.
6) Click OK.
Information in the Status column in the Options window indicates the sta-
tus of each application.
1.3.3 Media Compatibility
You can use the following types of removable media with your system:
• CD-RW and CD-R

• DVD+R, DVD-R, DVD+RW, and DVD-RW
• USB storage devices
Removable media is most often used to back up and restore presets and
other system settings. You can also use removable media to store images,
studies, and reports, as well as save obstetric trending data.
Cautions:
• The systems may become vulnerable to security breaches when

they accept removable media. Removable storage devices may
contain viruses. Philips recommends that you use the system to
format USB storage devices before working with them.
• When there is a DVD in the DVD drive, system startup may halt at
the PHILIPS logo display and will not proceed to the imaging
NPS-US-0521 7 REV A
CDs and DVDs
display. To correct the problem, eject the DVD and restart the
system.
Note PHILIPS recommends that you do not use U3 Smart Drives

with the system
Note The system includes four USB ports for USB storage
devices. Two standard USB ports are conveniently located
on the left side of the touch screen. If your USB device
requires additional power (such as some USB external
hard drives), use one of the two USB ports on the rear
panel of the system.
Note The system only supports USB devices that have a sin-
glepartition hard drive.
1.4 CDs and DVDs
DVD and CD media are available in a number of types. Not all media types
are fully compatible with the system DVD drive.
CD media capacity is approximately 700 MB; DVD media capacity is

approximately 4.7 GB. DVD+RW media can be erased and used again, but
DVD+R and CD-R media cannot be erased.
Multiple studies can be written to a disc, up to the limit of its capacity. This
includes moving a single DVD or CD between different 3300 G_W_C Diag-
nostic Ultrasound Systems and writing studies from each system to the
disc. The DVD can be used to record studies among different 3300
G_W_C systems. The RW type DVD must be erased before using it.
Note For CDs, the system supports “multi-session writes” (you

can save some studies to a CD, and then add more studies
later).
Note For DVDs, the system suports “single-session writes” (you

must select all the studies to be written to the DVD, and
export them in one “batch”). After you write to a DVD, the
system will not allow additional exports to that same DVD
unless it is an RW-type DVD that has been erased.
PHILIPS recommends using no more than 95% of the capacity of any CD

or DVD.
The following disc types can be used in the system DVD drive:
• CD-RW and CD-R

• DVD+R, DVD-R, DVD+RW, and DVD-RW
NPS-US-0521 8 REV A
USB Devices
The DVD drive and the system accept both CD-R and CD-RW disc types,
but writing data to a CD-RW disc takes much longer and does not provide
the same quality recording, so it is not recommended.
1.5 USB Devices
The 3300 G_W_C Diagnostic Ultrasound Systems provide USB ports. The
system USB ports can be used to connect USB storage devices. Such
devices include USB memory devices and USB hard disk drives. Read the
following information before using USB storage devices.
Note There are differences between the USB ports, some USB
devices may work in one port and not in another. If you
enconter a problem in one port, try one or each of the oth-
ers;
Note You should not use more than two USB devices at a time;
Note The system supports the following USB devices;
Note Single-partition USB flash memory drives;
Note USB flash memory drives that do not use or contain any
antivirus or other executable software;
Note USB hard disk devices that require 500 mA or less per USB
port;
Note USB 2.0 compliant devices;
!!
WARNING Connecting externally powered USB hard
disk drives to the system involves electrical
safety risks. If you connect disk drives to
the system, you must observe the electrical
safety warnings in the “Safety” section of
the User Manual. PHILIPS recommends that
you use only USB hard disk drives powered
from the USB connector, or use USB memory
devices.
NPS-US-0521 9 REV A
Safety
Section 2 Safety
Introduction
This section summarizes the safety information for the 3300 G_W_C
Diagnostic Ultrasound System. These safety concerns apply to patients,
operators and service engineers.
About Safety Information
Please read this and related information before using or servicing a PHIL-
IPS ultrasound system. It applies to the ultrasound system, transducers,
recording devices, and any optional equipment.
This system is intended for use by, or by the order of, and under the super-
vision of a licensed physician qualified to direct the use of the device.
In this manual, WARNING is used to indicate the presence of a hazard

that can cause personal injury, death, or substantial property damage if
the warning is ignored.
In this manual, NOTICE is used when additional comment or explanation

is required about installation, operation, or maintenance information that is
important but not necessarily hazard-related.
2.1 Equipment Safety Classification
The safety classification of the 3300 G_W_C Diagnostic Ultrasound Sys-

tem is as shown below:
According to the type of protection against electric shock:
CLASS I EQUIPMENT
According to the degree of protection against electric shock:
When connect to the ECG and L12-4, C6-2, C8- type BF

4ec, VC6-2 transducers
When connect to the S4-2C transducers type CF
NPS-US-0521 10 REV A
Acoustic Output Power
According to the degree of protection against ingress of water:
IPX0 System for non-protective liquid into the equipment

IPX1 Footswitch
IPX7 Transducers
According to the degree of safety of application in the presence of a flam-

mable anesthetic mixture with air or with oxygen or nitrous oxide:
Equipment not suitable use in the presence of a flammable anesthetic mix-

ture with air or with oxygen or nitrous oxide.
According to the mode of operation:
Continuous operation
!!
WARNING Do not modify this equipment without
authorization of the manufacturer.
2.2 Acoustic Output Power
Acoustic output is shown on screen by index.
The best diagnostic image is obtained under the minimum power output.
Use the following four power points to represent the index's display crite-
ria:
• Mechanical index (MI)

• Soft tissue thermal index (TIS)
• Bone thermal index (TIB)
• Cranial bones thermal index (TIC)
Using the power index in the System Setup menu Display index is based
on local system setup, Preset configuration, and Image model.
NOTICE
The System Setup selects any index of the four power indexes on the
menu of the system Setup menu at any time.
Acoustic Statement
For additional information on acoustic power settings and the power index,
see the acoustic output information provided with the system.
2.3 Acoustic Statement
Although there is no harm caused by ultrasonic frequency intensity and

exposure time in ultrasonic application, it is advisable to consider the fol-
lowing information and use the lowest ultrasonic exposure for diagnosis:
Ultrasound diagnostic equipment should be used only if necessary medical

examination reasons.
Reset before examination.
Do not increase examination time because of low acoustic output index.
Collect clinical data as soon as possible and complete the examination.
Choose the transducer component that is suitable for the focus depth to be
checked. Then use the image control to adjust the image precision.
2.4 AIUM/NEMA Output Display Standard
For 3300 G_W_C Diagnostic Ultrasound System the potential correlation

power output index of bioelectricity is shown in accordance with the output
display standard (ODS) jointly developed by AIUM and NEMA.
Power output related real-time information is shown on screen, Displays

the index type and the current sound output value.
EX:
1) Output a mechanical index of 0.8.is shown as: MI: 0.8.

2) Soft tissue thermal index TIS Used for heart, fetuses and
abdominal scans.
3) Bone thermal index TIB Used for phase ii or phase iii fetal and
neonatal head (via fontanels) scan.
4) Cranial bones thermal index TIC Used for skull imaging.
These ultrasound abbreviations are all followed on AIUM/NEMA Output dis-

play standard.
Automatic Index Selection
Please see Specific sound output value and accuracy: 3300 G_W_C Diag-
nostic Ultrasound System Acoustic output table.
Note The power index displayed on the screen depends on the

preset type, Active transducer component type, Image
mode and selected Power index.
Note The system Setup selects any index of the four setting
Power index in real-time.
2.5 Automatic Index Selection
Automatic selection of a power index is based on system mode. The user

sets the power index in the system Setup menu. The system automatically
selects an index based on the currently active preset image mode.
When the mechanical index is displayed with Normal

Settings.
The mechanical index will be displayed if any of the following conditions is

satisfied.
• Only 2D is the active image mode

• The active image mode is the monochrome M mode preview mode.
• The active image mode is the monochrome Doppler preview mode.
• When the soft tissue thermal index is displayed with Normal
Settings.
If no mechanical index is used to set the conditions for display, and transc-
ranial presupposition is activated, and satisfy any of the following condi-
tions, the soft tissue heat index will be displayed:
I) The color mode is open.
II) The energy mode is open.
III) The activated image mode is described in M mode.
IV) The activated image mode is the Doppler spectrum mode (the
2D activity mode is closed).
When the bone thermal index is displayed with Normal
Settings.
Exposure Risk
If no mechanical index is used to set the conditions for display, and transc-
ranial presupposition is activated, and satisfy any of the following condi-
tions, the soft tissue heat index will be displayed:
I) The color mode is open.
II) The energy mode is open.
III) The activated image mode is described in M mode.
IV) The activated image mode (the 2D activity mode is closed) is

the Doppler spectrum mode.
If the user selects ODS instead of Normal Settings display, the selected
index type is displayed in the form of sound power and is not related to the
image mode, the transducer component and preset Settings.
The value of the index is not the exact value of the patient's potential bio-
electricity, but potential bioelectricity is proportional to the display value.
Use it as much as possible to reduce the value of the index.
Select the appropriate transducer component and make the appropriate

adjustments, to reduce the potential bioelectricity. And reduction of diag-
nosis time can also play a role in reducing bioelectricity.
!!
WARNING The ODS power index formula is defined in
terms of the least ideal conditions for
patients. For some patients, the actual con-
dition is better than the index indicated if
the operator may reduce the exposure as
appropriate.
2.6 Exposure Risk
Follow these principles to avoid exposure:
Do not operate in an environment with flammable gases and anesthetics.
When using the imaging system in the operating room, do not switch the
system power switch; make sure the system is powered on before opera-
tion until the operation is over.
Eclectic Warning
!!
WARNING Do not use foot switch in the operating
room.
2.7 Eclectic Warning
Observe the following rules to prevent electric shocks:
Only qualified service engineers can remove the system hood. (Trim the
shell and control panel) the circuit in the accidental contact system can
cause serious damage.
Only use the power cord with the machine. Connect to the socket with pro-
tective grounding.
!!
WARNING Failure to comply with these warnings may
affect the personal safety of patients and
operators.
!!
WARNING No life-supporting equipment should be
connected to an ultrasonic diagnostic device
in the same circuit.
2.8 Connect Peripheral
Peripheral devices (Such as printers) in theory satisfy the general electrical

safety requirements. But it does not necessarily meet medical equipment
standards. So within 1.5 meters of the patient, do not use non-medical
peripherals, unless the peripheral equipment is powered by a transformer
that meets medical safety standard, and the power outlet is independently
powered.
Note If peripheral devices (such as printers) are powered by a

separate power supply rather than a system, the periph-
eral equipment cannot be used within 1.5m of the patient.
Otherwise it may cause harm to the patient.
Glutaraldehyde Exposure
2.9 Glutaraldehyde Exposure
The U.S. occupational safety and health administration (OSHA) has issued
regulations regarding the allowable exposure of glutaraldehyde in the
working environment. The products sold by our company do not include
agents based on glutaraldehyde. This kind of disinfectant is recommended
to be used for the sterilization of the Biopsy transducer components.
!!
WARNING Reduce the exposure of glutaraldehyde to
the minimum; maintain good ventilation;
and properly protect the eyes and skin.
2.10 Move System
When moving the instrument, please use the protective measures dscribed
in this section.
Ultrasound diagnostic system is designed to be lightweight and portable.

System weight (including the weight of the monitor printer) is about 65kg.
Because of the heavy weight, be careful when moving the system. The abi-
ity of the mobile device is directly related to the height and strength of the
mobile operator and some of the people who weigh less than 45.4kg may
complain about back injuries when moving similar systems. These cplaints
have nothing to do with the accident. Be careful when handling medical
devices such as ultrasonic diagnostic equipment.
2.10.1 Before Moving the System
When moving the instrument, please use the protective measures dscribed
in this section.
Ultrasound diagnostic system is designed to be lightweight and portable.

System weight (including the weight of the monitor printer) is about 65kg.
Because of the heavy weight, be careful when moving the system. The abi-
ity of the mobile device is directly related to the height and strength of the
mobile operator and some of the people who weigh less than 45.4kg may
complain about back injuries when moving similar systems. These cplaints
have nothing to do with the accident. Be careful when handling medical
devices such as ultrasonic diagnostic equipment.
Move System
2.10.2 Moving the System
!!
WARNING Make sure the straps are securely strapped
to the cart.
Note When moving the system from one place to another, fol-
low the steps below to take precautions
Moving the system
• Make sure the system plug has been pulled out.
• Release the wheel lock before moving the system.
• Move system.
• After the system is moved in place, the meshing wheel lock makes
the system fixed.
2.10.3 To Move on a Slope or Uneven Surface
If the floor at the elevator entrance is uneven, do not lift any part of the
equipment or equipment. If the length of the sloped road exceeds 6 meters
or if the inclination exceeds 5 degrees, move the unit by two persons. (The
wheelchair ramp is usually less than 5 degrees)
Avoid steep slopes above 10 degrees to prevent the instrument from tip-
ping over.
2.10.4 Tilt System
The stability of the system has been tested in accordance with the IEC
60601-1 test protocol. The protocol requires the device to move in any
drection on the slope of more than 10 degrees without tipping. Over 10
degrees, and the system is in danger of tipping over.
!!
WARNING Be careful when tilting the system on the
slope to prevent tipping, and the tilt should
not exceed 10 degrees. But when the diag-
nostic instrument pushes through the curb
Move System
or other small, steep slopes, the Angle can

be more than 10 degrees.
2.10.5 Transportation System
When using a vehicle to transport system, the wheel locks must always be
engaged and the straps should be used to secure the system.
Do not rely on wheel locks to secure the system on slopes with a slope of
more than 5 degrees.
Ensure that the transport can load the system plus the total weight of the
carrier.
Ensure that the loading capacity of the lift can meet the weight require-
ments of the ultrasonic system.
!!
WARNING Make sure the straps are securely strapped
to the instrument cart.
!!
WARNING When loading and unloading of diagnostic
instrument, the truck should be parked on
the ground. If the truck is parked on the
slopes, the system weight will easily lead to
fall over. The system may be easy to tilt
combined with the weight of the loader. It
may cause personal injury and system dam-
age
!!
WARNING Never share the lift with the system; and
the weight of the person plus the weight of
EMC
the diagnostic instrument may exceed the

carrying capacity of the lift.
!!
WARNING Ensure the ultrasonic diagnostic equipment
is fixed firmly when it is in the van.
Note If you use a color Doppler ultrasound diagnostic system in
a movingvehicle, follow the basic precautions outlined
above.
2.11 EMC
The electromagnetic compatibility (EMC) test of this system has been com-
pleted according to EMC International standard of medical equipment (IEC
60601-1-2).
2.11.1 Avoid electromagnetic interference
Medical equipment may produce or receive electromagnetic interference

(EMI). EMC standard describes the test method of transmitting and receiv-
ing interference. Emission test processing equipment to be tested .Accord-
ing to the test described in the reference standard The Company’s
ultrasound system in IEC60601-1-2 does not cause interference within the
limits.
Color Doppler Diagnostic Ultrasound system receives the RF signal, so sus-

ceptible to RF radiation generated interference. Interference sources
including medical equipment and information technology products and
radio communications equipment and television towers.
Only doctors can determine whether the pseudo image caused by radiation
interference has negative effects on image quality and subsequent diagno-
sis.
2.11.2 Use Restrictive
The use of the 3300 G_W_C Diagnostic Ultrasound System is described

below.
2.11.3 Interference Level Test Results
EMC Standard requirements: The equipment manufacturer must specify

the anti-interference level of its instrument. People recognized that such
Symblos
equipment is designed for interference with the same bandwidth in receiv-

ing and amplification in the low level signals. In a standard anti-interfer-
ence is defined as the presence of electromagnetic interference,
Instrument performance does not downgrade. Image quality degradation is
a subjective qualitative assessment. The easiest way to evaluate down-
grades is to be aware of when you see the first sign of artifacts in the
image. This method has the advantage of avoiding subjective judgment
and providing the most rigorous test results. So you should be cautious
when comparing the anti-EMC interference levels of different ultrasound
systems. The criteria used for demotion are not specified in the standard,
and may vary with the manufacturer. Each of these 3300 G_W_C Diag-
nostic Ultrasound System transducer assemblies has been tested for each
mode of operation over a wide frequency range.
2.11.4 ESDs
Electrostatic discharge (ESDs) The ECG heart rate may increase by 10% to
15% within seconds of the discharge, but ECG heart rate will return to nor-
mal within 4 seconds.
2.11.5 Electrical Surgical Instruments
Electrical surgical instruments (ESUs) may interfere with other equipment

intended to patients with the introduction of radio frequency electromag-
netic fields and current. Because of the frequency of the ultrasonic imaging
and radio frequency range overlap, ultrasonic transducer component circuit
is easily affected by radio frequency interference when using ESUs, serious
noise interference to black and white images, and even complete annihila-
tion color images.
Note High frequency electrosurgical instruments are not associ-

ated with ultrasonography and high frequency electrosur-
gical instruments themselves are in danger of burns.
2.12 Symblos
The International Electro-technical Commission (IEC) has established a set

of symbols for medical electronic equipment that classify a connection or
warn of potential hazards. The classifications and symbols are shown here.
Symblos
Type of BF applied part
Type of CF applied part
Type of B applied part
Safety warning. Understand its meaning before

use. See the documentation provided with your
device.
IPX0 Non-protected
IPX1 Prevent dripping in vertical direction
IPX7 Anti-short time immersion effect
Means compliance with Waste Electrical and

Electronic Equipment (WEEE) directives requir-
ing electrical and electronic equipment to col-
lect classified.
Indicates that the equipment components may
contain lead or mercury, respectively, must be
pressed recycle or dispose of the equipment
according to local, state, or federal law. The
LCD system monitor backlight may contain
mercury
Do not throw away. Dispose of in accordance

with
local, state, or federal laws.
Symblos
RoHS: the restriction of the use of certain haz-

ardous substances in electrical and electronic
equipment
No pushing warning
Foot switch connection
DVI output port
S-Video connection
Universal Serial Bus (USB) connection
Ethernet connection
Identifies the On/Standby switch.
Equipotential grounding terminal
The following symbols are used in the internal system:
Symblos
Identifies high-voltage components.
Identifies the point where the safety system

ground
Connect earth
Theory of Operation
Section 3 Theory of Operation
Introduction
This chapter provides a system’s block diagram, main functional segments,

and service platform to describe main components and functions.
• General Information
• Block Diagram
• Main Functional Segments
• Service Platform
Note All installation steps must be performed by PHILIPS

authorize service engineers.
3.1 General Information
3.1.1 System Modes
3300 G_W_C Diagnostic Ultrasound System is a medical ultrasound sys-

tem that is used for the following modes:
• 2D mode
• M mode
• Color Flow (CF) mode
• Tissue Doppler (TD) Mode
• Power Doppler mode
• Pulsed Wave (PW) Doppler mode with High PRF
• CW Doppler Mode (Cardiac Version Only)
• Color/Energy Doppler
• Color M mode
• Harmonic imaging
• 3D and 4D mode
• Different combination of the above modes
Functional Description
3.1.2 Software Options
The following options and features are available for the 3300 G_W_C
Diagnostic Ultrasound System . Some features are options that you must
purchase separately.
• Patient Case input, storage and load

• Transducer Automatic Identification
• B-Mode, M-Mode, Color Doppler, and Harmonic Imaging
• PW Doppler
• CW Doppler
• Duplex
• Triplex
• 3D/4D Imaging
• Real-time display, freeze, invert, update, storage, and zoom
• User-defined setup
• Color Invert
• Label and Measure
• Image Print
• Anatomical M-Mode
• Auto Freeze
• Contrast Harmonic Imaging
• Panoramic Imaging
• Tissue Doppler
• Adaptive Doppler setting in PW Doppler and CW Doppler modes
• Adaptive Flow frequency setting in Color Mode
• Eight focal zones rather than four for some transducers
• Up to five fusion settings rather than three
3.2 Functional Description
3300 G_W_C system Functional block diagram, the main functional seg-
ments of the 3300 G_W_C Diagnostic Ultrasound System platform are
listed and described as follows
• Cart
Main Functional Segments
• PC segment
• Monitor segment
• Control Panel segment
• E-box segment
• Power Supply Unit Segment
• Software Segment
• Peripherals
3.3 Main Functional Segments
3.3.1 Cart
The cart is made up of a base and framework that provides a chassis on

which the system components are installed and interconnected. A height
adjustment allows vertical and horizontal positioning of the system control
panel and monitor.
An input/output ( I/O) panel installed into the rear of the cart framing pro-
vides system connections for external devices. Swivel-casters at the four
corners of the cart provide system maneuverability and braking. All casters
can be set locked or unlocked, by foot-operated wheel locks to mobilize or
immobilize the system as needed.
3.3.2 PC Segment
3.3.2.1 Intel x86 architecture
The PC is Intel x86 architecture includes the following module:
1) Type6 COM-Express module

2) The component of the COM-Express module is Intel 6th CPU and PCH or
higher performance IC.
3) Carrier board and memory, the carrier board is compatible with the
basic type and compact type two sizes of type 6 modules.
4) Graphics card using CPU internal integration of the core graphics card,
while configuring the 2GB or 4GB DDR4 memory
5) Hard disk
6) BOX PC contains one 2.5 inch normal HDD hard disk, and the hard disk
can be removed.
3.3.2.2 User interface
PC box for user interface contains:
1) One DB9 foot switch;

2) One RJ45 network interface;
3) One S-Video interface;
4) One DVI interface;
5) Two USB2.0 interface
6) The corresponding power state and the system state indicator LED.
7) DVD ROM is 12.7mm notebook CD-ROM, support CD/DVD recording
function.
3.3.3 Monitor Segment
1) The LCD component comprises a 21.5 inch LCM and AD board and a
case assembly.
2) 21.5 inches LCD resolution is 1920x1080, the ratio of length and width
is 16:9.
3) The LCD includes two interfaces: a DVI interface for PC to transmit video
signal; a power interface used for connect to the power
3.3.4 Control Panel Segment
Control panel consists of:
1) One simple and pleasing body

2) Two loudspeakers
3) One touch screen
4) One key backlight
5) Two USB interfaces on the side edge of the touch screen
6) One heater of the coupling agent
7) One keyboard under the control panel
8) One 2 inch track ball.
Control panel can be rotated and lifted. Control panel swivel range is to
cart positive for the center. Upon completion of the lift or rotational adjust-
ment, you can lock the current position by releasing the knob or button.
3.3.5 E-box Segment
The E-box segment includes the following modules:
• SP board
• BF board
• Mother LE board
• DC-DC board
• probe LE board
• Probe interface boards
Figure4: SP board block diagram
3.3.5.1 SP Board
SP Board function:
• Provides interfaces between E-box and PC
• Communicates with PC
• Communicates with BF boards

• Sends control sets and receives RF stream data from BF boards
• Digital filters and mixers for demodulating RF data
• HV control and real-time monitoring
• Transducer recognition, control and status monitoring
• Monitoring main parts working status and temperature
Figure5: SP board block diagram
3.3.5.2 BF Board
BF Board function:
• 64 transmit and receive channels
• Transmit pulse generation
• TGC signals generation Received signal preamplifier and A/D con-
version
• Transmit and receive beamforming in one FPGA
• Summation of received channel data and transfers SP board
• CW function circuits
Figure6: BF board block diagram
3.3.5.3 Mother LE Board
Mother LE Board function:

• PCBAs are plugged onto mother board, including one BF board, one
SP board, one Probe board and one Power-supply board.
• Providing data paths between boards and distribution power for
boards.
• Providing data paths between boards and distribution power for
boards.
• For a 64-channel-system, only one BF board is plugged in mother
board.
3.3.5.4 Probe Base LE board and Probe Interface Boards
• Probe interface board: provides compact type transducer interface,

maxim to 4.
• Probe Base board:transmit and receive signals from the BF boards
to the active transducer
• 4 groups HV switches for probe selection
• 4D driver module
3.3.5.5 DC/DC PS Board
• DC module input
• Input voltage range: +12Vdc±0.6V200W
Table 1: DCDC Board output

DCDC Module 64/128 channel
Input Output
Out Voltage MAX Current Power
+3.7VD_SP 8A 29.6W
Digital Voltage
+3.7VD_BF 10A 37W
+5.5VA 3A 16.5W
-5.5VA 1A 5.5W
12VDC +3.3VA 8A 26.4W

Analogs Voltage
+2.2VA 6A 13.2W
0-±90 <1A 20W
±95V 0.02 3.8W
+12V_4D 1A 12W 4D
Total Power 165W
3.3.6 AC/DC power supply
• Input voltage range: 90Vac~264Vac

• Output voltage: DC 12V
• Frequency range: 47Hz~63Hz
• Input Transients: 318Vac for up to 500 msec
• Safety ground leakage current<300uA at 264Vac
• Remaining voltage<60V in 1s
• Power factor :> 0.99
3.3.7 Software
3.3.7.1 System UI applications program
Based on the X86 architecture of the windows operating system UI applica-

tions program
• AP process program
• UI application program
• Handling user's control input
• Conversion of user data into ultrasound system control collection
• Acquiring ultrasound imaging data
• Display each mode of ultrasound data
• User Information Management
• Case management
• Generate report
• Measurement calculation
Figure7: UI application component interaction diagram
3.3.8 AP Processor
• AP process program
• Acoustic data processing
• Scan conversion
Figure8: AP Processing Component Interaction Diagram
3.3.9 BP Processor
3.3.9.1 BP Processor Architecture
BP Processor Architecture
• PowerPC, 32-bit high performance RISC architecture processor. The
frequency of work is 300M Hz.
• Integrated DDR2 controller, the system uses 128Mbit two DDR2
memory.
• Integrated Flash controller. The system uses Nor Flash as the BP
boot program memory.
• Integrated PCIE interface and controller. Connect as a PC slave
interface and controller. Connect as a PC slave device with COM-E.
• A 16-bit PPC Local Bus is provided as a peripheral expansion inter-
face.
• BPX processing software for ThreadX real-time operating system

based on PowerPC architecture
3.3.9.2 ThreadX Operating System
• The system is an open source RTOS system. Suitable for medium-

sized real-time system control. Adopt Green Hill's compiler.
3.3.9.3 BP Initialization Program Loading Process
• The program is divided into several parts.

• The boot program is stored in Nor Flash.
• After booting, the system enters the boot state.
• The boot program in Flash is first transferred to DDR2.
• Complete the basic function configuration.
• PowerPC started working.
• The PCI-E interface is recognized and communicated by the PC.
• Load the APP program through the PCIE port into BP's DDR2 mem-
ory.
• Synchronize the entire system. Loading is complete. And work nor-
mally.
3.3.9.4 BP's Processor Features
• Receives CS information from the PC and converts it to configurable

parameters required by the hardware acquisition and processing
circuitry.
• Through the local bus and according to the ultrasound line trans-
ceiver timing, Load these configuration parameters.
• Checking the working status of the circuit board and Feedback sta-
tus information to the PC.
Figure9: BP application component interaction diagram
System Functional block diagram
3.4 System Functional block diagram
Figure10: system Functional block diagram
Installation
Section 4 Installation
Introduction
This chapter describes necessary requirements to prepare for installing a

new system. Before installing the system, you should consider all of the
following requirements:
The 3300 G_W_C Diagnostic Ultrasound System is designed to be

installed by qualified service personnel.
4.1 Preparing for Installation
4.1.1 Inspecting the Installation Site
Check that the installation site is physically acceptable as follows:
• customer, evaluate site access for delivery. Consider the availability

of a loading dock, elevators, ramps, and the width of passageways
and doors.
• Verify that there is adequate space available for system uncrating
and installation.
• At each location where the system will be operated, verify that
there is enough space for the system and any external peripherals.
• Check adjacent rooms for activity and types of equipment that
might negatively affect the ultrasound system.
• Environmental Requirements
• Electrical Requirements
• EMI Limitations
• Facility Requirements
• Networking Requirements
4.2 Environmental Requirements
In an ultrasound room, check the following environmental requirements

first to make the system work properly.
Environmental Requirements
Table 2: Environmental Requirements for System
Item Values
AC/DC power supply 90Vac~264Vac

Current rating 4.8A (100V-120V); 2.0A (220-240V)
Radiation shielding not required
Temperature 20 ~ 28 °C(68 ~79 °F)
Humidity 20 ~ 85%
Floor landing about 680 800 kg/m2 without
Floor condition Gradient within 10 degrees
Lighting Combination lighting (Dim and bright)
Environmental requirements for ultrasound room
Operation 10 ~ 40 °C
Storage -10 ~ 60 °C
Note Keep always your transducer in storage temperature.

When the transducer is exposed to large temperature dif-
ferences, store the transducer in storage temperature for
about 10 hours before using it.
4.2.1 Electrical Requirements
The ultrasound system has multiple configurations and feature sets.
All are described in this service manual but not every option may apply to
your system. System features are dependent on your system configura-
tion, transducer and exam type. Sites with a mains power system with
defined neutral and live.
The dedicated line shall consist of one phase, a neutral (not shared with
any other circuit), and a full size ground wire from the distribution panel to
the Ultrasound outlet. Sites with a mains power system without a defined
neutral.
The dedicated line shall consist of one phase (two lines), not shared with
any other circuit, and a full size ground wire from the distribution
panel to the ultrasound outlet.
Note Please note that image artifacts can occur, if at any time
within the facility, the ground from the main facility's
incoming power source to the ultrasound unit is only a
conduit.
4.2.2 Power Requirements
Before installing the system, you need to check the following power
requirements.
Table 3: Power Requirements
Parameter Specification
AC input voltage:100V-120V or 220-240Vacfrequency:50/60 Hz
input power Not less than 450W
4.2.2.1 Site Circuit Breaker
The branch circuit breaker is recommendable for the system.
!!
CAUTION To prevent the system from power outage or circuit
overload, do not do not
4.2.2.2 Site Power Outlets
The AC power outlet should exist within reach of the system. Also, periph-
eral devices and all other medical equipment should be placed within 1m
(3.2 feet) of the system. Avoid using extension cord to connect to the sys-
tem.
4.2.2.3 Unit Power Plug
When the system comes with the wrong plug, contact your local agent for
replacement.
Power stability requirements
4.2.2.4 Power Stability Requirements
• Voltage drop-out: Max 10 ms
• Power Transients (for all applications): Less than 25% of nominal

peak voltage for less than 1millisecond for any type of transient,
including line frequency, synchronous, asynchronous, or a periodic
transients
4.2.3 EMI Limitations
The ultrasound system is sensitive to Electromagnetic Interference (EMI)

from radio frequencies (RF), magnetic fields, and transient in the air wir-
ing. Before installing the system, consider possible EMI sources from elec-
trical and electronic machines nearby the ultrasound system. The possible
EMI sources are from: medical lasers, scanners, cauterizing guns, comput-
ers, monitors, fans, gel warmers, microwave ovens, light dimmers, mobile
phones. The following descriptions are tips to prevent your system from
unintentionally exposing EMI:
• Be aware of RF sources
• Ground the unit
• Replace all screws, RF gaskets, covers, and cores
• Replace broken RF gaskets
• Do not place labels where RF gaskets touch metal
• Use specified harnesses and peripheral machines
• Take care with mobile phones
• Properly dress peripheral cable
4.2.4 Facility Requirements
Feature Requirements
• Dedicated single branch power outlet of adequate amperage meet-
ing all local and national codes which is located less than 2.5 m (8
feet) from the unit’s proposed location
• Door opening is at least 76 cm (30 inch) wide
• Proposed location for unit is at least 0.3 m (1 foot) from the wall for
cooling
• Power outlet and place for any external peripheral are within 2 m
(6.5 feet) of each other with peripheral within 1 m of the unit to
connect cables.
Installing System
4.3 Installing System
This chapter introduces the basic install information and procedures when
the new equipment arrives at the site of a purchaser.
Performing installation includes safety considerations, unpacking and

installing the system, and verifying hardware/software specifications.
• Safety Information
• Average Installation Time
• Unpacking
• Verifying the Customer Order
• Powering On/Off
• Configuring the System Settings
• Specifications
4.3.1 Safety Information
The following note, CAUTIONs, and warnings describe safety information

before or while installing the system.
Note Read the user manual carefully before operating the sys-
tem. For quick reference, keep the manual nearby the
equipment.
!!
WARNING Do not touch the equipment while testing
the AC ground line with a test instrument.
!!
WARNING The equipment weighs approximately
89.5kg without any peripherals. To prevent
injury from transporting and unpacking the
equipment, two people are required.
!!
CAUTION Adapt the equipment to room temperature first after
transporting it. Turning on the system may cause dam-
age before adapting the equipment. The following
table shows the different adaptation time depending
on the actual temperature of the equipment after it is
Installing System
being transported. The maximum adaptation time is up

to 24 hours.
!!
CAUTION Connect the unit to a safely grounded power outlet to
prevent any electrical shock. Do not use a two to three
prong adapter for safety grounding.
!!
CAUTION Make sure that all board covers and frame panels are
securely in place before operating the equipment. This
may affect system performance and cooling.
!!
CAUTION Do not wear an ESD wrist strap while working on live
circuits. power cord. This unit requires a dedicated
20A circuit and can have a 15A plug if the on board
peripherals do not cause the unit to draw more than
14 amps.
!!
CAUTION Although the ultrasound energy transmitted from your
transducers is within safety limits, avoid unnecessary
exposure. Ultrasound energy may produce heat and
mechanical damage.
!!
WARNING Do not remove any covers or panels, to pre-
vent shock. If problems or malfunctions
occur, unplug the power cord from the out-
let.
4.3.2 Unpacking
When new equipment arrives, check all components are included in the
package and they are not damaged. If any component is damaged or
excluded, contact your local agent.
To unpack the equipment
Installing System
1) Cut it off and tied to the boxes

as the red box shows.
2) Peel the self-adhesive backing
off of the Shock Watch device
and adhere it to the crate
where shown.
3) Peel the self-adhesive backing
off of the Tilt Watch device and
adhere it to the crate where
shown
Figure11: Cutting the Plastic

Bands
4) Remove the lid from the top of

the crate as the picture shows.
Figure12: removing the top cover
Installing System
5) Remove top fixed cardboard;

6) Remove the top packaging
from the pallet.
Figure13: Removing packaging from the pallet
7) Remove all of the accessory

boxes from the pallet and set
them aside.
Figure14: removing the accessor
Installing System
8) Unscrew the two locklatches

that secure the ramp to the
pallet by turning the screw
handle counterclockwise, until
the latch is loose.
9) Rotate both latches away from
the metal plate on the ramp.
Figure15: unscrew the lock-latches
10) Put the ramp off the pallet.

11) Place the crate ramp in front
of the open end of the crate,
with the beveled edge of the
ramp positioned at the floor,
facing up.
12) Put the front hold-down
brace out of the crate.
Figure16: removing the front hold-down brace
Installing System
13) Remove the antistatic bag

from the system.
14) Carefully pull the system
down the ramp and onto the
floor.
Figure17: Removing the antistatic bag
!!
CAUTION Do not lift the equipment by holding the control panel
or any cover. The equipment may be damaged.
!!
CAUTION While moving the equipment, be very careful not to tilt
the unit over. To avoid injury from the tipping over,
keep the monitor at the lowest position.
!!
CAUTION Store all loose parts of the units in a separate place to
prevent damage before moving. For transducers, wrap
them in soft cloth or foam.
4.3.3 Verifying the Customer Order
When you are finished with unpacking the equipment, you need to verify
all items listed in the delivery sheet. If any component is missing or dam-
aged, contact your local agent.
Power On/Off
4.4 Power On/Off
4.4.1 Power on
1) Make sure that the power out-

let is proper type.
2) Plug the power cord into the
power outlet.
3) Make sure power LED light.
Figure18: Power LE
!!
CAUTION When connecting the AC power cable without its plug
to the wall outlet, protective earth should be taken.
!!
CAUTION Make sure that the system power is supplied from a
separate and properly rated power outlet.
4) Press the System On/Off key

on the control panel to turn on
the system power.
5) The start-up screen is shown
on the display and the system
is initialized.
Figure19: Power on
Note To reboot the system, wait for a few seconds before pow-
ering on the system.
Connecting/Disconnecting the transducer
4.4.2 Power-up Screen Sequence
1) The start-up screen will be shown on the monitor when the system is
powered on.
2) When the system boots, all keys on the control panel are lighted the
default 2D mode.
3) Verify that the system fans are operating.
4.4.3 Power Off
1) Press the Power On/Off key on

the control panel to turn the
power off.
2) When the shutdown dialog box
appears, wait for a few
seconds before power off the
system. Figure20: Shutdown dialog box
!!
CAUTION Do not unplug the power cord during the system oper-
ation. This may lead to data loss or system software
damage.
4.5 Connecting/Disconnecting the transducer
You can connect or disconnect the transducer to/from the transducer port
regardless of when the system is turned off or on. Make sure that you
press the Freeze key on the control panel before connecting or disconnect-
ing the transducer.
To connect the transducer to the system, follow these steps:
Connecting/Disconnecting the transducer
!!
CAUTION Do not touch the patient when connecting or discon-
necting a transducer.
1) Check if you press Freeze key

on the control panel.
2) Insert the transducer
connector into the transducer
port.
3) Push the connector locking
handle to right.
Figure21: Connecting the Transducer
!!
CAUTION Do not forcibly insert the transducer connecter to the
system. Improper connection may cause damage to
the system and transducer.
Note After connecting the transducer to the system, you need to
activate the desired transducer by selecting it from the
screen.
Note You can disconnect the transducer from the transducer

port when the system is powered off or on.
Note Make sure that you press the Freeze key on the control
panel before disconnecting the transducer.
To disconnect the transducer from the system, follow these
steps:
1. Check if you press the Freeze key on the control panel.
2. Push the connector locking handle to left.
3. Pull out the transducer connector from the transducer port
Configuring the System Settings
!!
CAUTION Do not touch the exposed surface of the transducer
connector when the transducer is removed.
4.6 Configuring the System Settings
Configure the system’s basic settings such as date, time, language, and
basic user information.
Reset the system time and date if the system has been stored near the low
end of the temperature range for prolonged periods (near - 34°C).
• Time and date

• System header information
• User interface language
• Video format
• configure the system’s network settings
• Peripherals setup
4.6.1 Setting the System Time and Date
Note Reset the system time and date if the system has been
stored near the low end of the temperature range for pro-
longed periods (near -34°C).
Note Customizing the date format to one that is longer than any
in thelist may cause dates in the display to be truncated.
4.6.2 To Set the System Time and Date
1) Click Setup on touch screen or Press Setup on the keyboard
Click Setup on touch screen or

Press Setup on the keyboard
Figure22: Connecting the Transducer
2) Click System tab

3) Click Date/Time.
4) Input the Instant Time Password and click OK.
5) On the Date & Time tab, set the month, day, and year
6) Also, on the Date & Time tab, click on the time information you wish to
change (hours, minutes, or seconds.)
7) Increment the time using the up and down arrows, or type the exact
time you wish to set.
8) Click Apply. The new time is set.
9) Click the Time Zone tab.
10) Select the appropriate time zone and daylight saving time settings for
your location.
Note Ensure automatically adjust clock for daylight savings

changes is deselected.
11) Click OK to exit the dialog box. The new time zone setting is set.
System Header Information
If properly configured, the system header contains the institution name,

patient name, institution logo, medical record number, date of birth, and
the name of the person performing the exam.
4.6.3 To Change the System Header Information

2) Click System.
3) Click Top Border.
4) Input the Institution Name.
5) Click OK.
6) Click Close to exit setups.
4.6.4 To Change the System User Interface Language

2) Click System
3) Click Local
4) In the Regional and Languages Options window, click the Languages tab
5) Select the desired language
6) Click Apply
7) Click OK
8) Restart the system
Note You must restart the system for the user interface lan-
guage to change Video Format
4.6.5 To Change the System Video Format (NTSC or PAL)

2) Click Peripherals.
3) Select NTSC or PAL.in Lower left corner of the screen
Configuring the System’s Network Settings
Before you can add a DICOM server, you need to configure the system’s
net work settings. Check with your system administrator for the specific
values that you need to enter.
Peripherals Setup
4.6.6 To Configure the Network Settings
1) Do not connect the LAN cable to the system. If it is already connected,

disconnect it.
2) Press the Setup key or touch Setup to open the Setup window.
3) Click the System tab.
4) In the Setup window, click DICOM.
5) In the DICOM Setup window, click Change Settings for current preset.
6) Either type the AE title that the network administrator assigned to the
3300 G_W_C system or click Derive the AE Title from PC’s name.
7) Set the Port number to the number assigned to the 3300 G_W_C
system by the network administrator.
8) Click Network Settings.
9) In the Network Settings window, click TCP/IP Properties.
10) In the Internet Protocol (TCP/IP) Properties window, perform one of
the following actions.
• To have an IP address automatically assigned, click Obtain an IP
address automatically.
• To use a pre-assigned IP address, click Use the following IP address
and enter the address you obtained from your system
administrator.
11) When finished, click OK.
12) Click Close.
4.7 Peripherals Setup
These types of installations will have their own installation instructions.
An external DVI-I monitor may be connected to the system and installed

externally as well B/W Printer Setup.
You may set up system operation so you can print with Print or Acquire on
the system control panel. You may also assign the print function to any of
the three footswitches.
Peripherals Setup
4.7.1 To Configure the Print Controls for the Printer
1) Press Setup.
2) Click Peripherals.
3) In the Peripheral Selection area, select the printer for the control (Print
or Acquire) you wish to use.
4) In the Footswitch Selection area, select the Print or acquire for
footswitch you wish to use.
5) Click Apply.
6) Click Close.
4.7.2 External Monitor
The system video characteristics are optimized for use with 5:3 aspect
ratio LCD panels. If an external digital monitor or other device is connected
to the AUX monitor output (DVI-I connector).
!!
CAUTION Avoid using U3 smart USB flash memory drives on the
system. If you do use a U3 smart drive on the system,
and it is in the USB port on boot-up, the system will
crash on going to Review or Report.
!!
CAUTION 3300 G_W_C Diagnostic Ultrasound System may
become vulnerable to security breaches when they
accept removable media. Removable USB storage
devices may contain viruses. Philips recommends that
you use the system to format USB storage devices
before working with them.
!!
CAUTION Use only Class-B compliant USB storage devices with
the system. Some plastic-cased unshielded USB
devices may cause RF emissions that exceed Class B
Optional Peripherals
limits. See the device's documentation to determine

whether it is Class-B compliant.
!!
CAUTION When the monitor is being rotated or laid down, take
care your fingers from hurt by the arm angle of the
LCD support.
4.8 Optional Peripherals
The following table shows the list of optional recording devices.
Refer to the each manufacturer’s manual for installation and connection

procedures.
4.8.1 Optional Peripherals
• B/W Printer SONY UP-X898MD Digital/Analog USB Interface

• 220V isolation transformer assembly
• 110V isolation transformer assembly
• Gel Warmer and Probe kit
• foot switch
4.9 Service Platform
The Service platform contains a set of software modules for the diagnostic
each modules.
4.9.1 Service Login
1) Click Setup on touch screen or Press

Setup on the keyboard;
2) Click Service on the Service tab;
3) The service login window for Service
Platform appears on the display.
4) Enter pass word or plug in FSE USB

Key.
Figure23: Service Login screen
Service Platform
4.9.2 Service Homepage
When the Service station starts, the service homepage appears. The
homepage contains the software revision along with the hardware inven-
tory and the results of the latest system information.
5) Enter pass word or plug in FSE USB

Key.
6) The Service homepage appears
Figure24: Service homepage
4.9.3 Resident Self-Test
The RST is a stand-alone application with a suite of on-system diagnostic

tests for system hardware and software, using no external instrumenta-
tion. You start the RST application while the ultrasound application is run-
ning or while the system is booting. Starting the application during the
power-up sequence is useful when the ultrasound application fails to start
and you want access to the tests and logs. If the ultra-sound application is
running, the RST application will close the ultrasound application.
To start RST while the service homepage appearing
Service Platform
1) Click “Run RST Reboot“ button;

2) Reboot system;
3) While system reboot the RST homep-
age appears;.
Figure25: RST Tests
1) If you want to run specific tests, click

the names of those tests;
2) To run the test a specific number of
times, enter the number in the Repeat
Test;
3) Click Run. Testing begins;
4) When the testing is done, click OK in
the message box running a Subsystem
or Sub module Test.
Figure26: RST Extended Tests
Each subsystem test consists of test modules, and each test module has
sub modules. You can select individual modules or sub modules to run sep-
arate from the other tests in its group by using the tree control in the left
side of the RST window.
Service Platform
The DP/AP subsystem test’s SP board test

module
Figure27: SP board test module
Note The two-digit codes that precedes the sub module test
reused in the Application Test Log display, in its Category
column, and in the Status window at the lower left of the
window
To run an interactive test
The interactive tests check the operation of the system’s controls.
They require you to make selections and operate controls as they execute.
To run an interactive test:
1) Start the RST application;

2) Click the Test tab in the main RST window;
3) Click Interactive Test in the tree view, to show the available interactive
tests;
4) Select the test you want to run.
Note Only one interactive test can run at a time.

5) Click Run. Testing begins.
Service Platform
1) Select display test;

2) Click Run. Testing begins;
3) To end a display test, press the ESC
key.
Figure28: display test
To end a keyboard test, right-click the test name, and click Stop on the
Shortcut menu.
4.9.4 Log
The Log window shows the system RST log information. The left pane
shows a directory of the available information. The Log tab displays errors
and test parameter data in the Event Viewer and displays service log
entries in the service log. The two main items are:
• Event Viewer displays errors and test parameter data.

• Service Log allows authorized personnel to record information
about the system. The right pane of the Log window shows the spe-
cific information for the selected item. This is useful when multiple
service personnel may be servicing the system (Such as for inter-
mittent problems).
To view details of the test results
1) Click the Log tab.

2) Select the information type from the Event Viewer directory. When the
tests are finished, a test complete message appears.
3) Click OK.
4.9.4.1 Service Log
You can enter notes in the Service Log section of the Event Viewer, to
record service procedures Viewing Error Logs.
Service Platform
The RST application records errors in logs during operation of the system
and when you run a test. The Event Viewer includes application logs, a
security log, and a system log.
4.9.4.2 To view error logs
Click Event Viewer on the Log tab of the RST window and select the log you
want to see.
The logs list errors in chronological order, with the most recent errors at
the top of the list. You can view more detail of an error by doubleclicking
the entry in the list view.
4.9.4.3 Application Log
This log includes run-time errors encountered by both the ultrasound appli-
cation and the RST application. The log lists the date and time the error
occurred, the name of the error, the applications and subsystems affected,
and other information.
4.9.4.4 Clearing the Application Log
To clear the Ultrasound Application Log
1) Right-click Ultrasound App Log;

2) Click Clear Log on the shortcut
menu;
3) Click Yes in the confirmation
dialog box.
Figure29: Ultrasound Application Log Display
RST Test Log
This log includes parameters of past RST tests and errors encountered
while running the tests the Event Viewer Application RST Test Log.
Service Platform
Figure30: Application RST Test Log Display
4.9.4.5 RST Log Codes
The right pane shows coded information that relates to the specific test
performed, in the Category column.
The code is in the following format: SSMMNN
Where:
• SS is the subsystem tested.
- BP is the beam processor subsystem.
- DP is the display processor subsystem.
• mm is the module number.

• NN is the sub module number.
For example, code DP0102 indicates:
DP:display processor subsystem
01:module 01
02:sub module 02
The example indicates that the A/D converter (sub module 02 of module
01) of the display processor was tested. To find the meaning of the
numeric codes.
4.9.4.6 Clearing the RST Test Log
To clear the RST Test log
1) Right-click RST Test Log in the tree view.

2) Click Clear Log on the shortcut menu.
3) Click yes in the confirmation dialog box.
Service Platform
Test Result Details
You can view test results in the Event Properties window. The details of the
test results may provide clues for diagnosing system problems.
Viewing Test Details

To view the test details:
1) In the right side of the Event Viewer window, double-click the event you
want detailed information on.
The Event Properties window opens
the string option provides the most useful

information.
Figure31: Event Properties Window
2) Click the appropriate Data: option button to change the data display
type. Typically, the string option provides the most useful information.
4.9.4.7 System Log
The Event Viewer system log includes hardware errors filtered from the
application run-time error log and the RST test log.
Figure32: System Log Display

Service Platform
Clearing the System Log

To clear the system log
1) Right-click System Log in the tree view.

2) Click Clear Log on the shortcut menu.
4.9.4.8 Making an Entry in the Service Log
You can enter information in the Service Log that is displayed on the Log
tab.
The Add Service Entry dialog box opens.
To make a new entry in the service log:
1) Start the RST application;

2) Right-click Service Log;
3) Click Add Service Entry;
4) Type your name in the top two fields,
and the service information in the
Comments field;
5) Click OK;
6) Your entry appears in the service log;
7) Right-click Service Log and click Save
Log to File to save the entry;
4.9.4.9 Modifying an Entry in the Service Log
You can change the information in an existing service log entry. You must
log on to the RST application by using a valid service name and password
to modify an entry in the service log.
Service Platform
To modify a service log entry
1) Start the RST application.

2) Click Service Log.
3) Double-click the log entry you want to modify.
4) The Change Service Entry window is displayed.
5) Click in the entry field and modify the text.
6) Click OK.
7) Right-click Service Log and click Save Log to file to save the modifica-
tion.
Maintenance
Section 5 Maintenance
This section identifies activities supporting the quality assurance audit

(QAA) concept that you should perform in accordance with Customer Field
Service policies and schedules. QAA activities include, but are not neces-
sarily limited to, the following types of concerns:
• System Performance
• Electrical and Mechanical Integrity
• Cleaning
Note For the Philips-recommended preventive maintenance

actions to be performed by the customer, see the system
user manuals.
!!
CAUTION Use adequate ESD safeguards when performing ser-
vice and maintenance procedures.
1) FSE Tool Kit

2) Vacuum
3) Microfiber or lint-free cloth
4) Liquid display cleaner specifically designed for LCDs
Remove system covers, turn on the system, and check the
following:
• Proper fan rotation. Note the amount of noise, rubbing, and air
flow;
• Air flow passages. Note the amount of dust collected in the air path
and vacuum.
Clean or as necessary.
• Cable condition. Note connector soundness, condition of insulation,
and whether the cables are properly secured.
• tion details. Note that hardware is in the correct locations, properly
• secured in place.
• Plastic cover condition. Note cracked fastener locations.
• Power cord condition. Note whether bracket is secure at the system
connector and condition of the cable itself.
Air Filter Maintenance
• Transducer condition. Note damaged cables and plastic covers, and

pin condition
5.1 Air Filter Maintenance
The system air filter is located beneath the cart. The recommended interval
for air filter Maintenance is every three months.
!!
CAUTION When you use a vacuum cleaner, be aware that the
hose and nozzle can produce an electrostatic dis-
charge. To avoid damaging system components, prac-
tice ESD-safe procedures.
To remove and clean the air filter
Rear up of system
Figure33: Air Filter Location
Control Panel Cleaning
Figure34: Remove and clean the air filter
1) Locate the air filter on the rear up of the cart base.

2) Remove rear up enclosure of the cart base
3) Slide the filter out the rear up enclosure and remove it.
4) Vacuum the filter and clean it with warm soapy water.
5) Thoroughly dry the air filter.
6) Re-install the dry filter.
5.2 Control Panel Cleaning
The recommended interval for cleaning the control panel is every six
months.
5.2.1 To Clean the Control Panel
1) Vacuum dust and lint from the keyboard and controls.

2) Use a rag with mild soap and water to clean the external surfaces,
including control panel surfaces and the actual controls.
3) Remove ink stains with rubbing alcohol on a soft cloth.
4) Follow up immediately with mild soap and water on a soft cloth.
!!
CAUTION When you clean the system keyboard and monitor,
take care not to get any solution inside the housings.
Caster Maintenance
Also, take care not to scratch the face of the monitor

while cleaning it.
!!
CAUTION Trackball Cleaning The recommended interval for
trackball cleaning maintenance is every six months.
5.2.2 To Clean the Trackball
1) Unscrew and remove the bezel that surrounds the trackball on the sys-
tem control panel.
2) Clean the trackball with an alcohol-dampened pad.
3) Clean the two encoder shafts and the bearing surface with an alcohol-
dampened pad.
4) Reinstall the trackball and bezel.
Figure35: Cleaning the Trackball
5.3 Caster Maintenance
The recommended interval for caster maintenance is every 12 months.
LED Movement
To check the casters
1) Check the casters for cut or damaged tires.

2) Move the system and check caster rotation.
3) Check the steering and brake lock operation.
4) Replace the casters if necessary.
5.4 LED Movement
The recommended interval for checking monitor movement is every 12

months.
5.4.1 To Check LED Movement
1) Check the monitor movement mechanism for smooth operation.

2) Check that the monitor does not droop (tilt). Order replacement parts as
needed.as needed.
3) Check the monitor swivel mechanism. Order replacement parts as
needed.
5.4.2 LED Maintenance
The LED has a plastic front surface. The surface is resistant to fluids nor-
mally found in clinical environments, such as ultrasound gel, alcohol, and
disinfectants, but fluids spilled on the display should be wiped off with a
soft cloth to avoid forming spots on the display surface the video monitor
should be cleaned as necessary. For routine cleaning, use only cleaners
specifically designated for LCD displays. Disinfectants may be used when
necessary, but they are not recommended for routine display cleaning.
!!
CAUTION To avoids damage to the display, do not touch it with
any sharp objects such as pencils, or calipers.
!!
CAUTION Repeated use of common cleaners such as glass
cleaner or products containing alcohol may damage
Exterior Surfaces
the monitor and should not be used. Use cleaners spe-

cifically designed for cleaning LCDs.
!!
CAUTION Do not use paper towels to clean LCD surfaces; they
may scratch the surface. Use only a microfiber cloth or
lint-free cloth.
To clean the LED
1) Clean dust from the display with a microfiber cloth or lint-free soft cloth.
(Philips recommends microfiber.)
2) Remove fingerprints or other marks from the display by using a liquid
display cleaner specifically designed for LCDs. Spray directly on the
cleaning cloth or apply sparingly to the display Premoistened wipes may
also be used.
3) Dry the surfaces using a microfiber or lint-free cloth.
5.5 Exterior Surfaces
Use a rag with mild soap and water to clean exterior surfaces, including
those on the system monitor, and peripherals. To prevent multiple nearly
simultaneous control activations, turn the system off before cleaning the
control panel. Remove ink or stubborn stains with rubbing alcohol or a
stronger detergent and immediately wash with mild surfaces as necessary
(spot-paint) soapy water. Exterior surfaces should be cleaned at least
every 12 months.
!!
CAUTION Does not use acetone, methyl ethyl ketone (MEK),
paint thinner, or other strong solvents to clean exte-
rior plastic covers. Doing so damages the covers.
Operational
5.6 Test and Paperwork
After completing the PM procedure, operationally test the system by initiat-

ing a System Confidence Test. Complete PM paperwork by filling out a
work order.
Replacement
Section 6 Replacement
Overview
This section provides specific information about system disassembly that

may be required for the removal and installation of fieldreplaceable parts.
If not covered by a detailed procedure, the means of removing a system
part can be discerned from the Illustrations in this section as well as in
(see Spare Parts )
This chapter provides the following procedures.
• Disassembly
• System Software installation
Warnings and Cautions
Before continuing, review (see Safety ). Also follow any additional warnings
and cautions contained in this section.
!!
WARNING Always turn off power, disconnect the main
power cord from the wall outlet, and wait at
least 30 seconds before removing or install-
ing any PCB, module, or component.
!!
CAUTION Always use correct ESD procedures. ESD damage is
cumulative and may not be noticeable at first. ESD
symptoms may be first exhibited as a slight degrada-
tion of performance or image quality.
Note The video monitor and batteries inside this product con
taint mercury and must be recycled or disposed of accord-
ing to local, state, and federal laws.
6.1 Disassembly
Disconnection the Power to the System
Disassembly
!!
WARNING Before performing any maintenance on this
ultrasound system, ensure that the system
is powered down and that the system power
cord is disconnected from the AC power
source.
Figure36: Disconnecting the System Power Cord
To disconnect the power to the system
1) Power-down the system.

2) Disconnect the system power cord from the main AC supply.
6.1.1 Removing the Enclosure
Figure37: Removing the Rear up Enclosure
To remove the system enclosures
1) Gently pull the enclosure approximately 2 cm (1 in) toward the back of

the system until the ball studs release from the back of the rear up
enclosure.
Disassembly
Figure38: Removing the Side Enclosures
2) Gently pull outside the enclosure;

3) Slide the side enclosure out from the ball studs;
4) Pull the top edge of the side enclosure down and then pull toward the
rear of the system to slide the side enclosure tabs out from the front
panel enclosure.
Figure39: Removing the Front Enclosure
1) Remove the three screws (on two sides) that secure the front enclosure
to the cart frame.
2) Pull the top edge of the side front enclosure down and then pull toward
the front of the system to slide the front enclosure tabs out from the
system.
Disassembly
Figure40: Removing Rear down Enclosure
1) Remove the four screws that secure the rear down enclosure to the cart
frame.
Figure41: Removing Control panel arm housing assembly
1) Hold the sides of the case with both hands and gently pull them to the
sides.
2) Gently pull the enclosure approximately 2 cm (1 inch) toward the two
side until the ball studs release from control arm
Disassembly
Figure42: Removing join arm housing assembly
1) Hold the sides of the case with both hands and gently pull them to the
sides.
2) Gently pull the enclosure approximately 2 cm (1 inch) toward the two
side until the ball studs release from control arm.
Figure43: Removing join arm housing assembly
1) Hold the top of the bottom case with hand and gently pull down.
2) Gently pull down the enclosure approximately 2 cm (1 inch) until the
ball studs release from join arm.
6.1.2 Removing the Monitor Assembly
To remove the monitor assembly
Disassembly
Figure44: Removing the Small Rear Enclosure
1) Remove the two screws that secure the small rear monitor enclosure.
2) Pull the small enclosure down about 6 mm (0.25 in) and lift it off the
back of the monitor.
Figure45: Disconnecting the Monitor Cables
3) Remove the two screws that secure the two cable clamps.
4) Disconnect the power cable.
5) Unscrew the two connector screws and disconnect the signal cable.
Disassembly
Figure46: Removing the Monitor Assembly
6) Remove the four screws that secure the monitor to the monitor mount
assembly.
7) Lift the monitor off the monitor mount bracket.
Figure47: Installing the Monitor Assembly
8) Place the monitor onto the monitor mount. Ensure that all two hanger
tabs on the Monitor are engaged into the monitor mount bracket.
Note There are three hanger tabs on the monitor that fit into the
two slots on the monitor mount bracket.
6.1.3 Removing the simple arm
1) Remove the monitor assembly
Disassembly
Figure48: Removing the simple arm cable cover
2) Remove the four screws (on the rear side) and take off simple arm cable
cover (on the front)
Figure49: Removing the arm bottom cover
3) Remove a screw (on the bottom) and take off arm bottom cover
Disassembly
Figure50: Removing the simple arm
4) Pull out the video cable, power cable

5) Remove the 4 screws with M4 Hexagon screwdriver
6) take off simple arm
6.1.4 Removing the join arm
1) Remove the monitor assembly

2) Removed join arm housing assembly
3) take off arm bottom cover
Figure51: Removing screws that fixed the arm ground wire
4) Remove the three screws that secure the arm ground wire to thejoin
arm frame.
Disassembly
5) Pull out the video cable, power cable and arm ground wire.
6) Remove the 4 screws with M4 Hexagon screwdriver
7) Remove the join arm
6.1.5 Removing the DVD Drive and Physio Assembly
To remove the DVD drive and physio Modules
Figure52: Removing the DVD Drive and Physio Assembly
1) Disconnect the USB cable from the DVD

2) Disconnect the DB9 cable from the Physio
3) Remove the four screws (on both side) that secure the DVD drive and
Physio Modules to the cart frame.
Disassembly
Figure53: Removing the Physio Modules
4) Remove the four screws that secure the Physio Modules to the frame.
Figure54: Removing the DVD Drive
5) Remove the TORX T-10 screw that secures the DVD drive to the drive
cover.
Disassembly
6.1.6 Removing Control Panel Assembly
To Remove the Control Panel Assembly
Figure55: Removing the Control Panel Screws
1) Remove the 9 screws securing the control panel assembly to the control
panel base enclosure.
2) Lift the front of the control panel and gently rotate it on its left side
.Continue supporting the assembly while removing the cable connection.
Disassembly
Figure56: Disconnecting the Control Panel Cables
3) Disconnect the control panel cable from the control panel PCB.
4) Take off the Control Panel Assembly
To Remove the Trackball
Figure57: Remove the Trackball
1) Disconnect the trackball cable from the control panel PCB.

2) Remove the four screws that secure the trackball assembly to thecontrol
panel.
To Remove the Touch Screen Modules
Disassembly
Figure58: Removing Cable metal shield
1) Remove the 4 screws that secure Cable metal shield in the middle
2) Disconnect the cables from the control panel PCB.
Figure59: Unlocking cable connector
3) Remove 12 screws that the metal shield in the top

4) Pull up the wire lock , disconnect touch screen video cable
Disassembly
Figure60: Removing the Touch Screen Modules
5) Remove the 6 screws that secure Touch Screen Module to thecontrol

panel.
6) Take off the Touch Screen Module from other side
To remove the QWERT keyboard assembly
1) Remove the 9 screws securing the control panel assembly to the control
panel base enclosure.
2) Lift the front of the control panel and gently rotate it on its left side
.Continue supporting the assembly while removing the two keyboard
cable connection
3) Disconnect the keyboard cable
Disassembly
Figure61: Removing the keyboard cable
4) Remove a screw and tablet withT-10 Disconnect the keyboard ground

wire
5) Pull down right is data cable lock then pull out the data cable
Figure62: Removing the keyboard bracket cover
6) Remove 9 screw and tablet with T-10 take off the Keypad bracket cover
Disassembly
Figure63: Removing the keyboard
7) Remove 4 screws and tablet withT-20 and take off the Keypad
6.1.7 Removing the control panel arm (600N /500N)
1) Removed control panel assembly and monitor assembly

2) Removing Control panel arm housing assembly
Figure64: Removing the Line buckle and screws
3) cut off the Line buckle and remove screws of the fixed cable
Disassembly
Figure65: Removing the Armrest cover
4) Remove the two screws securing the Armrest cover to the control panel
base frame.
5) ake off the Armrest cove
Figure66: Removing the Bourdon line
6) Remove the double-sided Bourdon line
Disassembly
Figure67: Removing the control panel base
7) Remove 6 nuts with the M10 ratchet socket wrench

8) Remove the control panel base
9) Remove Attachment placement shell or Printer mounting case
Figure68: Removing the control panel arm
Disassembly
Figure69: Removing the control panel arm
10) Remove the four screws that secure the control panel arm to the cart
frame.
Figure70: Removing the Rotating mechanism
11) Pull out all cables

12) Remove the six nuts that secure the Rotating flange to the control
panel base frame.
13) Remove the two screws that secure the Rotary locking device to the
control panel base frame
Note The control panel arm 500N is used for simple arm, the
control panel arm 600N is used for jiont arm
Disassembly
6.1.8 To remove the Lockable gas spring
Figure71: Removing the Lockable gas spring
1) Removing Control panel arm housing assembly

2) Remove the circlips at both ends
3) Remove the lock line
Disassembly
Figure72: Removing the gas spring
4) Pull outward (or forced open with a slotted screwdriver))

5) Take off gas spring
Note Lockable gas spring 500N is used for simple arm systems
Lockable gas spring 600N is used for jiont arm systems
Note The process of removing the Freestyle gas spring 500N/

600N is the same as the Lockable gas spring except that
the removing the lock line.
Disassembly
6.1.9 To Remove the E-box PCBs
Figure73: disconnecting the E-box Cables
To remove the E-box PCBs
1) Disconnect the two cables from the E-box.
Disassembly
Figure74: Removing the Cover of the E-box
2) Remove the four screws that secure the cover to the E-box.
Disassembly
Figure75: Removing the E-box PCB Assemblies
1) Remove the DC-DC board from the right of the E-box. Place it on an
antistatic mat;
2) Remove the SP board from the E-box. Place it on an antistaticmat;
3) Remove the BF boards from the left of the E-box. Place them on an
antistatic mat.
Figure76: Removing the Front Panel Cover
1) Remove the 7 screws that secure the front panel cover to the Ebox.
Disassembly
Figure77: Removing the Probe interface board
1) Remove the two screws that secure the Probe interface board to the
Probe base board;
2) Pull off Probe interface board from Probe Board;
Figure78: Removing the Probe Board
1) Remove the 17 screws that secure the Probe board to the frame;
2) Pull off Probe Board from frame.
Disassembly
6.1.10 Removing the PC Modules
Disconnecting the PC Cables
Figure79: Disconnecting the PC Cables
1) Unscrew the connector screws and disconnect the cables.
Figure80: Removing the PC Modules
2) Remove the 4 screws that secure the PC Modules to the frame.
Removing the Hard Disk
Disassembly
Figure81: Removing the Hard Disk panel
1) Remove the two screws that secure the panel to the PC Modules.
Figure82: Removing the Hard Disk
2) Pull out hard disk from PC module.
Disassembly
6.1.11 Removing the AC/DC Power Supply Module
Figure83: Removing the AC/DC Power Supply Module Mounting Screws
1) Remove the 2 screws that secure the power supply module to the cart
frame.
Figure84: Removing the Power Supply Module
2) Grasp the handle on the power supply module and pull the power supply
straight out of the cart housing.
Disassembly
6.1.12 Disassembly the Air Filter
Figure85: Removing the Air Filter
1) Gently pull the enclosure approximately 2 cm (1 in) toward the back of

the system until the ball studs release from the back of the rear up
enclosure.
2) Pull the air filter straight out from the rear up enclosure.
Note The air filter can only be removed from the rear up enclo-
sure
6.1.13 Disassembly the Fan
1) Locked the system wheels;

2) Tile the system on the wall or table ( use foam to protect the case);

System Software Installation
Figure86: Removing the Fan
3) Disconnect the fan cable;

4) Remove the 4 screws that secure the fan to the cart frame;
Figure87: Removing the Fan
5) Take the fan from frame.
6.2 System Software Installation
Overview
This section describes the procedures how to install and upgrade a Soft-
ware.

!!
CAUTION Before starting software installation, you shall make
backup of patient, system data if necessary.
Requirements
1) 3300 G_W_C Software (U-DISK);

2) Blank CD-R, DVD, USB, (for patient image or preset databackup);
Average installation time
The installation procedures may take about 25 min based on an experi-

enced service engineer.
6.2.1 Preparations
Retrieving Backup Data
Before software installation, you need to backup data in the System set
menu.
1) Press the System set key on the touch screen and go to USB device
menu;
2) Select USB device DVD or USB;
3) Click [Backup] to export in storage device.
6.2.2 Installing the Software
Installing the system software
This section describes the procedures about the software installation.
!!
WARNING This installation may result in user data loss
including patient and Application Data loss.
Please back up patient and application data
before performing the installation.
Note All digital peripherals, reporting systems connected via
the USB ports should be either power off or disconnected

network and remove all transducers prior to the software

installation.
1) Insert the 3300 G_W_C System Software U-Disk to the USB port.
2) Power the system on.
3) When the system asks for password, enter “go2install” andpress the
Enter key.
Figure88: Password screen
4) To start the installation, select one of the following options:

• This option recovers the system software including operation
systemand erases all the system completely.
!!
WARNING All patient and application data will be
removed permanently.
• This option recovers the system software including operation sys-
tem.

Figure89: loading system software
5) When the above dialog box appears. Type A then type Y
!!
WARNING When replacing a new hard disk, A option
shall be selected when the software is
installed for the first time for a full disk
installation. B option is only used for the

reinstallation of the hard disk that has been

divided into good zones - C drive.
Figure90: Ghost System Software
6) The system will be installing automatically;

7) When the installation is finished, the system will be shutting down.
8) After completing the system reboot, the screen appears “set or restore
system Hard ware Revision”message.
Figure91: set or restore system Hard ware Reversion
9) Press the System set key on the touch screen and go to servicemenu.
10) 6. Select “set hardware info”
11) 7. Set hardware reversion

Finishing
12) 8. Select “Switch Software Version”
Figure92: set hardware info and Switch Software Versions
13) Select right version( 3300 G\3300 W\3300 C)
6.3 Finishing
Restore backup data
1) Press the System setup key on the touch screen and go to USB device
menu.
2) Select USB device DVD or USB.
3) Click [restore] to restore backup data in system.
Reset the system settings

• Time and date
• System header information
• User interface language
• Video format
• configure the system’s network settings
• Peripherals setup
4) Verified once again by performing the functional checks.
5) Ensure that each peripheral operates properly and then inform the
customer.
6) Keep this documentation with this service manual for future reference.

Troubleshooting
Section 7 Troubleshooting
The troubleshooting information provided in this section will assist you in

determining if a system is failing, and, if so, can help you isolate the cause
and initiate a corrective action.
!!
WARNING Before continuing, please review (see Safety )
Also follow any additional warnings and
cautions contained in this section.
!!
WARNING Reviewing and applying the following basic
guidelines can produce effective trouble-
shooting and responsible call resolution.
Always make notes as you troubleshoot; if properly communicated, some
or all of the information you discover can help you or others in the future.
7.1 Clarifying Symptoms
These actions and considerations can help to clearly describe a symptom,

which is useful in isolating the cause and can also be useful later when doc-
umenting the problem and the solution. Make notes about the problem you
are investigating as you read through this section:
• Have the user restate problem and verify that you are checking the
correct system.
• Are there any other systems exhibiting this symptom or is it
exclusive to one system?
• Is this the symptom of a real problem, or possibly an unrealistic
7.1.1 System Features and Options Set?
the symptom: Is it a hang, a crash, a shutdown, an image artifact, an error

code, not booting, and so on? Write down a clear statement of what the
symptom is and how it manifests itself:
• How does it happen: What keystrokes, what modality, what preset,

what transducer?

Categorize/Localize the Problem
• When does it happen: Time of day, during boot-up, during scan,

image review, sending to a network, during a calculation, during a
measurement, printing, acquiring an image, annotating, and so on?
• How often does it happen: Intermittently, predictably, all of the
time?
7.2 Categorize/Localize the Problem
• Is it a printing problem, an image quality or viewing problem, a

data export or import problem, and so on?
• Consider if the symptom indicates an operating procedural error or
system failure; and if a system failure, whether it seems to be a
hardware or software problem; and if a software problem, if it is an
operating system or ultrasound problem.
• first and subsequent indications of the failure. Do this as soon as
possible to ensure this type of data is not lost. (Relevant data is
often lost when the system is rebooted.)
• What, if anything, does the user do to recover from the problem?
7.3 Re-creating a Problem
Successfully re-creating a problem that doesn’t damage the system can

produce information that is useful to troubleshooting and solution verifica-
tion.
But, before you try, be sure that you have noted all the useful information
you can. Before changing anything, consider if the attempt will cause the
loss of information or change a circumstance that is better than re-creating
the problem. If you decide to attempt to re-create the problem, try to do
so several times.
7.4 Isolating Causes
Remember that, sometimes, more than one cause can produce similar
symptoms. Try to identify as many causes for the given symptom as your
experience and research allows and then prioritize them in order of most
likely root cause of the problem. Attempt to eliminate them one-by-one,
starting with the most likely cause.

Isolating Causes
7.4.1 Checking for Obvious Causes
• Check for correct voltage at electrical outlets, “tripped” circuit

breakers, blown fuses, disconnected or damaged wires, and so on.
Always check that power cords are plugged in, and inspect them for
wear.
• Consider the situation: Was there a system option or hardware
change recently?
When the last time was the system was working correctly and
what, if any, influencing circumstances have occurred since?
• Check if the symptom and probable cause may already be listed for
quick reference and resolution.
7.4.2 Investigating and Testing
If you haven’t discovered the cause of the problem yet, more in-depth
analysis is necessary:
• Take a moment to review the data you°Øve collected about the prob-
lem so far. Hopefully you have been able to categorize the symptom
as hardware, software, an operator-induced, or an environmental fail-
ure.
I) Hardware failure: Cause usually determined through use of

troubleshooting tools (RST, Device Manager, Debug Info, Event
Logs, and so on). A fix is typically realized by replacing
suspect/candidate hardware until the problem is resolved.
Note Consider the value against the difficulties of swapping
(suspect) hardware components with good ones. Do not
cause additional problems or confuse your search. Never
swap parts if a known good item might be damaged.
II) Software failure or corruption: Even if a fix is realized by

reloading software, the case of the failure or corruption needs
to be investigated: Is there a system architecture failure, is the
user doing anything to cause the problem?
III) Operator-induced: Is the user expecting more than the system

is designed to deliver, exceeding the capability of the system,
or mis-operating it (overfilling the hard disk drive, pulling the
plug, pressing and holding the power button for longer than 5
seconds, and so on)? A solution can be more user training or a
work-around. Investigate to see if an option ought to be

Isolating Causes
enabled or if there is an enhancement scheduled in a future

release that might solve the problem.
IV) Environmental: Are there any electrical power, EMI/RFI, or net-

work connectivity difficulties external to the system affecting
its performance?
• Verify more easily checked factors first, such as system setup/config-
uration.
• been ready, verify that all system voltages are present and within tol-
erance.
7.4.3 Developing a Solution
When think you know what the problem is, decide what changes you need
to make to correct the problem and write down the steps you want to take
to make the repair, especially if the sequence of your actions is important.
Even if you don’t think you need to do this for yourself, it can be useful to
others when you properly document the problem and its resolution. You
may benefit from this yourself in the future.
7.4.4 Implementing a Solution
Implement your solution by performing the corrective actions you devel-

oped. Proceed cautiously and systematically.
Make only one change at a time, and verify that it is not unusual for
another problem to surface when you are applying changes to fix what you
thought was the problem.
Check if the changes achieve the result you expected or not consider
returning the system to the known condition it was in before your last
change and verify its condition before proceeding.
Review your solution and any “discovery” that your change produced.
Decide if you should proceed with your original solution or go back to
investigating and testing.
To avoid producing confusing and conflicting data, do not deviate too far
from the methodical approach that allows you to isolate the failure by elim-
inating possible causes along the way.
7.4.5 Verifying Corrective Actions
After the system fault has been identified and you have performed (autho-
rized) corrective actions to repair the failure, conduct whatever tests are

Known Symptoms, Causes, and Corrective Actions
necessary to ensure that the problem is fixed and that system meets its
optimum level of performance. Typically, it will be the same testing that
lead you to isolating the cause of the specific problem (refer to your notes)
and then additional tests that give you confidence that the system is gen-
erally performing as it should.
7.4.6 Returning the System to Service
After the reported problem is fixed and the system tests are successful,
return the system to the customer and close the call:
• Formally document the problem and the solution: Write down

exactly what problems you discovered and what corrections you
made.
• Provide feedback: Communicate to all affected parties what prob-
lems you discovered, how you arrived at that conclusion, and what
corrections you made. Include this information with parts that are
returned for repair and, if appropriate, send an e-mail message of
this information to ISS personnel who could find it useful.
7.5 Known Symptoms, Causes, and Corrective

Actions
Some problems that have been previously experienced and corrected are
documented here and are summarized for quick reference at below.
7.5.1 System Will Not Boot
If the system does not start proceed as follows:
1) Confirm that the system power cord is plugged in.

2) A green LED on the right side of the power supply indicates that the
power supply is energized by the AC source. If it is not lit, the power
supply or the source is suspect.
Note When the system is not on, that is a problem of system

power cord or power grid voltage is not correct.
3) Unplug the power cord from the top outlet on the power supply.
7.5.2 System Boots, but Monitor Is Blank
If the system starts, but the monitor stays blank, the monitor could be bad

Known Symptoms, Causes, and Corrective Actions
or other possibilities are that the monitor power cable may be bad or dis-
connected.
System Boots, but Ultrasound Application Fails to Start
If the ultrasound application now starts properly (there will be only noise in
the image area), the PC is okay and the problem is in one of the following:
• E-BOX
• SP Board
After checking the items in the preceding list, if the ultrasound application
still does not start; the problem is in the PC modules.
7.5.3 System Boots, but Peripherals Do Not Power On
If the system starts, and the monitor functions normally, but one or more
peripheral devices do not work, proceed as follows:
1) Check the device’s power cord connections.

• If the device turns on, the power supply is bad. Replace it.
• If the device does not turn on, try replacing its power cord. If the
device still does not power up, it is faulty. Replace the device.
7.5.4 System Starts, But Database Reset Message

Appears
This problem occurs when an invalid language is set for the user interface
language.
First reset the user interface language to a valid language.
Database errors can also occur when the database is corrupted. Use the
Database Repair feature on the Setup screen as described in the system
Help or the User Manual. It is important to tell your customers to back up
patient exams on a regular basis because these exams can be lost if data-
base corruption occurs.

Checking for EMI and RFI
7.5.5 Non-English User Interface
To change the system user interface language to English:
1) In the Setup window, click the Locale button.

2) In the Regional and Languages Options window, click the Languages
tab.
3) Choose English.
4) Click OK
5) Restart the system.
7.5.6 Input Language Is Non-English
If you are required to type in English on a non-English system, you can use
English if the system was set up with the English keyboard. Press left
Alt+Shift to cycle through the languages until you find English.
7.6 Checking for EMI and RFI
Electromagnetic interference (EMI) and radio frequency interference (RFI)

can degrade the performance of the 3300 G_W_C system. For example,
a tran ducer placed close to an ECG cable can increase interference. Mov-
ing the ECG cable or other medical equipment away from the transducer
can reduce interference. EMI and RFI can conceivably cause image noise or
monitor distortion if the system EMI shielding has been compromised. EMI
and RFI can be generated by a variety of electrical devices. The interfer-
ence can be transmitted over power lines or radiated through the air.
Answering the following questions can help locate the source of interfer-
ence and can help determine whether the problem is with the system or
with the scanning environment.
• Is the interference intermittent or constant?

• Does the interference appear with only one transducer or with
several transducers?
• Do two different transducers operating at the same frequency have
the same problem?
• Is the interference present if the system is moved to a different
location in the facility?
• Can the EMC coupling path be attenuated?
• tuned between stations around 1,600 Hz (thus using it as an EMI/
RFI source tester) identify interference,

• Considering and locating the source/cause is important, but

regardless of the source, since the system is shielded against EMI
and RFI, troubleshoot the system to determine if the EMI/RFI
shielding has been compromised.
7.6.1 System Hangs or Crashes
Often the terms “hang“ and “crash“ are used interchangeably to describe
the same symptom. However, with the HD8 system, these two terms
describe two different behaviors. It is important to understand the differ-
ence between these terms because the causes are different, the trouble-
shooting techniques are different, and the information available to the FSE
is different.
A “hang“ is when the system simply stops responding to the keyboard.

There is a normal image on the monitor and the system may continue to be
working (updated data in the image area, clock is correct and continues
changing), but the system does not respond to hard keys, soft keys, or the
trackball.
A “crash“ occurs when the system detects an abnormal condition in either

the hardware or the software. When this happens, the system starts the
saves various logs and memory dumps. The Crash Recorder displays a dia-
log box on the screen.
Figure93: System Crash Message (“Crash Box”)
• Check Event Viewer under Application for Ultrasound errors. Review

the Event Viewer information.
• Gray crash box shows up after the ultrasound application appears
• IF RST passes, try replacing the SP board.

7.6.2 RST Failures
3300 G_W_C Diagnostic Ultrasound Systems contain the stand-alone

Resident Self-Test (RST) application. The RST is a suite of onsystem diag-
nostic tests for system hardware and software, using no external instru-
mentation.
RST generates error results that can be viewed in the event viewer file. Go
to the Log tab in RST or the Windows event Viewer. In general, replace the
assembly that is showing the failure.
7.6.3 Using the Maintenance Tools
The system provides maintenance tools that you access through the Field
Service Options window. These tools are useful while troubleshooting.
The following describes the Field Service Window options. With the excep-
tion of Command Line, you must reboot the system after using the options.
Notepad Opens the Windows Notepad application. Allows you to create,

edit, or view text and log files.
Control Panel: Opens the Windows Control Panel that allows you to
access Windows settings and options.
Reedit Accesses the Windows registry for editing if you are instructed to
do so.
Command Accesses the DOS window, in which you can access PC files and
Line functions by using DOS commands.
Event Viewer Opens the Windows Event Viewer window where you can
view and manage logs of system, program, and security events on your
computer. Event Viewer gathers information about hardware and software
problems, and monitors Windows security events. You can export event
viewer data to external media.
Task Manager Opens the Windows Task Manager to allow you to view
system performance and applications and processes running on the PC.
Allows you to end programs or processes to start programs, and to view a
dynamic display of PC performance.
Explorer Opens the Windows Explorer, in which you can view the system
directories and files. You can copy, move, rename, and search for files and
folders.

USB and Peripherals Failures
Explorer Opens the Windows Explorer, in which you can view the system
directories and files. You can copy, move, rename, and search for files and
folders.
Disk Defrag Opens the Windows Disk Defragmenter, which allows you to
rearrange files and unused space on the hard disk, to make the software
run faster, and to increase the speed of access and retrieval.
Save Debug Allows you to export debug files to removable media.
7.6.4 Hardware Configuration
The hardware configuration does not normally require adjustment. The

software usually installs everything just fine. If there is a problem, it
appears in the Device Manager window in yellow with a question mark. The
Device Manager is accessed in the OS (right-click My Computer, then select
Properties and then Hardware). Right-clicking on the question item will tell
you the slot location in the computer. This will help to identify which board
is the problem. The slots are numbered from the top starting at 0.
7.6.5 Software Loading (Ghost)
The software should load with simple few steps than inserting a U-disk
• If any peripherals are attached, they must be turned off.

• At the end of the loading process the system will automatically boot
up into ultrasound. If there is a hardware problem the system may
crash, but this does not mean that the software did not install prop-
erly. If the install finished ok the software is probably ok.
7.7 USB and Peripherals Failures
7.7.1 USB Failures
There are differences between the USB ports on the system; some devices
may work in one port and not the other, so be sure to try both.
This problem is related to the amount of power consumed by the USB drive
(it likely requires more power than can be provided by that port).
7.7.2 Peripherals Failures
If a printer is installed, but it does not print, check that the printer is con-
nected correctly.

USB and Peripherals Failures
Each system is capable of NTSC or PAL configuration. The software default

is PAL. To change the video format, reinstall the video drivers from the
Peripherals tab of the setups. (Click Install Software Drivers, select Video,
and click OK.) During the driver installation, you can select NTSC or PAL.

Spare Parts
Section 8 Spare Parts
8.1 Covers
The following table shows a list of FRU (Field Replaceable Unit).
Item Part number Part name Q’ty Remark
1 453562034811 Upper shell _PH 1

2 453562034821 Attachment placement shell _PH 1
3 453562034831 Left side shell assembly_PH 1
4 453562034921 Front panel assembly _PH 1
5 453562034931 Rear panel assembly _PH 1
6 453562034941 Filter shell assembly _PH 1
7 453562034951 Right side shell assembly_PH 1

8 453562034971 Control panel arm housing assembly 1
9 453562035041 Foot cover _PH 4
10 453562035071 Monitor arm housing assembly 1
11 453562035091 Printer mounting case _PH 1
12 453562035101 Power shield cover assembly 1
Part number Part name Q’ty Picture
Upper shell
453562034811 1
_PH

Covers
Attachment
453562034821 placement 1
shell
_PH
Left side
453562034831 shell 1
assembly
PH
Front panel
453562034921 assembly 1
_PH

Covers
Rear panel
453562034931 assembly 1
_PH
Filter shell
453562034941 assembly 1
_PH
Right side
453562034951 shell 1
assembly
PH
Control
453562034971 panel arm 1
housing
assembly

E-BOX (PCBAS)
Foot cover
453562035041 4
_PH
Monitor
453562035071 arm 1
housing
assembly
Printer
453562035091 mounting 1
case _PH
HD8 Power
453562035101 shield 1
cover
assembly
8.2 E-BOX (PCBAS)

E-BOX (PCBAS)
1 453562035141 NeuEcho Physio Ass 1

2 453562055371 Physio Board 1
3 453562028821 DVD Assembly 1
4 453562028871 DC/DC Power Board 1
5 453562083411 HD8 SP board Assembly 1
Conditional com-
6 453562083431 HD8 BF Board PCBA 1
patibility
7 453562055691 Mother LE Board PCBA 1

8 453562055721 Probe Base LE Board 1
9.1 453562028841 Probe Interface PH Board PCBA 2
Two way compat-

9.2 453562083441 Probe Interface PH Board PCBA 2
ibility
10 453562055522 Heating Coupler Board 1
11 453562035111 Fan & Metal Mesh 1
12 453562035031 With brake casters 1
NeuEcho
453562035141 Physio 1
Ass

E-BOX (PCBAS)
Physio
453562055371 1
Board
DVD
453562028821 1
Assembly
DC/DC
453562028871 Power 1
Board
HD8 SP
453562083411 board 1
Assembly

E-BOX (PCBAS)
453562083431 HD8 BF 1
Board PCBA
Mot453562
055691Mot
453562055691 her LE 1
Board
PCBA
Probe Base
453562055721 LE 1
Board
Probe
453562028841 Interface 2
PH Board
PCBA

Power Supply
Probe
453562083441 Interface 2
PH Board
PCBA
Heating
453562055522 Coupler 1
Board
453562035111 Fan & Metal 1

Mesh
453562035031 With brake 4

casters
8.3 Power Supply

Control Panel
1 453562092981 Power Module 1
Power Mod-
453562092981 1
ule
8.4 Control Panel
The following table shows a list of FRU (Field Replaceable Unit)
1 453562080301 3300 Control Panel FRU Ass 1
2 453562080581 touch screen£®3300£© 1
3 453562035201 Trackball(HD8) 1
4 453562035211 QWERT keyboard assembly(HD8) 1

5 453562034961 600N control panel arm 1
6 453562034981 Lockable gas spring 600N 1
7 453562034991 Freestyle gas spring 600N 1

8 453562035001 500N control panel arm 1
9 453562035011 Lockable gas spring500N 1
10 453562035021 Freestyle gas spring500N 1
11 453562055401 Knob assembly 1

Control Panel
Control
453562080301 Panel 1
FRU Ass
touch
453562080581 1
screen
453562035201 Trackball 1
QWERT
453562035211 keyboard 1
assembly

Control Panel
600N con-
453562034961 trol 1
panel arm
Lockable
453562034981 gas 1
spring
600N
Freestyle
453562034991 gas 1
spring
600N
500N con-
453562035001 trol 1
panel arm

PC
Lockable
453562035011 gas 1
spring500N
Freestyle
453562035021 gas 1
spring500N
Knob
453562055401 1
assembly
8.5 PC
The following table shows a list of FRU (Field Replaceable Unit)
1 453562035121 PC Assembly 1
2 453562078081 Hard Disk Assembly 1

3 Backward com-
453562092721 3300 Installation Image 1.0.0.11 1
patible

PC
PC Assem-
453562035121 1
bly
453562078081 Hard Disk 1

Assembly
3300
Installation
453562092721 1
Image
1.0.0.11

Cables
8.6 Cables
1 453562028701 POWERCORD, CHINA 1

2 453562080161 Power Cable (UK) 1
3 453562080171 Power Cable (Australia and Australian 1

countries)
4 453562080181 Power Cable (Europe) 1
5 453562080251 Power Cable (USA, Canada, Japan) 1
6 453562080191 Power Cable (Switzerland) 1
7 453562080201 Power Cable (Denmark) 1

8 453562080211 Power Cable (South Africa and other Afri- 1
can countries)
9 453562080221 Power Cable (Israel) 1
20 453562080231 Power Cable (Argentina and other South 1

American countries)
11 453562080241 Power Cable (Brazil) 1
12 453562028291 CP to monitor power cable (joint arm) 1
13 453562028301 CP to monitor power cable (simple arm) 1

14 453562037991 CCC AC output cable 1
15 453562080261 UL AC output cable 1
16 453562028311 PC to monitor DVI cable (joint arm) 1

17 453562028681 PC to monitor DVI cable (simple arm) 1
18 453562037601 Printer USB cable 1
19 453562028321 PC to touch screen DVI cable 1
20 453562028711 Audio cable 1
21 453562028782 PC to control panel and Physio cable 1
22 453562028771 DVD power supply and data cable 1
23 453562028721 IPASS communication cable 1
24 453562037581 Coupling agent heating power cable 1
25 454110430361 Ground wire 1
26 453562028691 Arm ground wire 1

Cables
27 453562080271 PC board DC power supply cable 1
28 453562080281 DC board DC power supply cable 1
29 453562028791 Control panel DC power cable 1
30 453562055341 Fan power cable 1
POWER-
453562028701 CORD, 1
CHINA
453562080161 Power 1
Cable (UK)
Power
Cable (Aus-
453562080171 tralia and 1
Australian
countries)
Power
453562080181 Cable 1
(Europe)

Cables
Power
453562080251 Cable 1
(USA, Can-
ada, Japan)
Power
453562080191 Cable 1
(Switzer-
land)
Power
453562080201 Cable 1
(Denmark)
Power
Cable
(South
453562080211 Africa and 1
other Afri-
can coun-
tries)
Power
Cable
(Argentina
453562080221 and other 1
South
American
countries)

Cables
Power
453562080231 Cable 1
(Israel)
Power
453562080241 Cable (Bra- 1
zil)
CP to moni-
tor
453562028291 power cable 1
(joint
arm)
CP to moni-
tor
45356202830 1
1 power cable
(simple
arm)

Cables
CCC AC
453562037991 output 1
cable
UL AC out-
453562080261 put 1
cable
PC to moni-
tor
453562028311 DVI cable 1
(joint
arm)
PC to moni-
tor
453562028681 DVI cable 1
(simple
arm)

Cables
Printer USB
453562037601 1
cable
PC to touch
453562028321 screen DVI 1
cable
454110430351 Audio cable 1
PC to con-
trol
453562028782 panel and 1
Physio
cable

Cables
DVD power
454110430271 supply and 1
data
cable
IPASS
454110430281 communi- 1
cation
cable
Coupling
agent
454110430341 heating 1
power
cable
Ground
454110430361 1
wire

Cables
Arm
453562028691 ground 1
wire
PC board
DC
453562080271 power sup- 1
ply
cable
DC board
DC
453562080281 power 1
supply
cable
Control
454110430221 panel DC 1
power cable

Monitor
Fan power
453562055341 1
cable
8.7 Monitor
1 453562080291 3300 display assembly 1
2 453562035051 Joint arm _PH 1
3 453562035081 simple arm 1
4 453562035061 Gas spring 500N 1

Monitor
3300 dis-
453562080291 play 1
assembly
Joint arm
453562035081 1
_PH
453562035081 simple arm 1
Gas spring
453562035081 1
500N

Transducer
8.8 Transducer
1 453561962211 L12-4 transducer 1

2 453561636604 S4-2 transducer (HD8)
3 453561265614 S8-3 transducer (HD8)
4 453561652565 C6-2 probe (HD8)
5 453561411266 C8-5 probe (HD8)
6 453561652574 C9-4v probe (HD8)
7 453561806762 VC6-2 transducer (HD8)

8 453562037421 Coupling Heater Assembly-PH
9 453562037481 Probe cup assembly
L12-4
453561962211 1
transducer
S4-2 trans-
453561636604 1
ducer

Transducer
S8-3 trans-
453561265614 1
ducer
453561652565 C6-2 probe 1
453561411266 C8-5 probe 1
C9-4v
453561652574 1
probe

Peripherals
453561806762 VC6-2 1
transducer
Coupling
453562037421 Heater 1
Assembly-
PH
Coupling
Heater
453562037422 1
Assembly-
PH
453562037481 Probe cup 1

assembly
8.9 Peripherals

Peripherals
1 454110406091 DB9 Convertor(hole) 1

2 454110406081 USB to RS232 Cable 1
3 453561778122 Sony UP-898B&W Printer 1
4 454110432911 220V isolation transformer assembly 1
5 453562080361 Foot switch assembly 1
6 453562080351 DVI to HDMI adapter DVI-D plug 1
7 453562080331 USB WiFi Adapter 1

8 453562080341 WiFi-Blu USB Adapter 1
9 453562080331 110V isolation transformer
DB9
454110406091 Conver- 1
tor(hole)
USB to
454110406081 RS232 1
Cable

Peripherals
Sony UP-
453561778122 898B&W 1
Printer
220V isola-
454110432911 tion 1
transformer
assembly
453562080361 Foot switch 1

assembly
DVI to
453562080351 HDMI 1
adapter
DVI-D plug

Peripherals
453562080331 USB WiFi 1

Adapter
WiFi-Blu
453562080341 USB 1
Adapter
110V isola-
453562080331 tion trans- 1
former
assembly
DVI to S-
453562091561 Video 1
Adapter


3300 Service Manual

Uploaded by

Document Information

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

3300 Service Manual

Uploaded by

Copyright:

Available Formats

3300 G_W_C

Diagnostic Ultrasound System

Version Date Author Description

A 2020-10-9 Song Fengjiu First Release

This manual is the 3300 G_W_C Diagnostic Ultrasound System service

This manual describes the service safety relevant information of 3300

The Manufacturer will not bear any responsibility for unauthorized

Manual Name: 3300 G_W_C Diagnostic Ultrasound System Service Man-

Manual Number: NPS-US-0521

How to use this manual

The copyright of the manual belongs to Philips Medical Systems Co.,

Various support locations around the world can provide customers

WARNING Electrical warning symbol

Section 1 General Information . . . . . . . . . . . . . . . . . . . . . . . . . 1

7.5 Known Symptoms, Causes, and Corrective Actions . . . . . 111

Section 1 General Information

1.1 System Overview

Figure1: 3300 G_W_C System with jiont arm

Figure2: 3300 G_W_C System with simple arm

1) C6-2 Abdominal, GYN, OB, Fetal Cardiac, Abdominal Vascular, Urinary

1.1.2 Imaging modes

1.1.5 Options: Software Options

1.1.6 System Reference Information

1.1.7 System Monitor

1.1.8 System Control Panel

Figure3: Control Panel

1.1.9 Supplies and Accessories

1.2.1 Physical Specifications

Lowest position: 1320 ± 20mm

Highest position: 1600 ± 20mm

• 3300 G_W_C systems height with simple arm (bottom of caster to

Lowest position: 1320 ± 20mm

Highest position: 1470 ± 20mm

• Width: 550 ± 20mm

• 3300 G_W_C systems with jiont arm weight: 60 ± 5kg

1.2.2 Environmental Specifications

Temperature Range 10°C to 40°C

Relative Humidity 20% to 85%, non-condensing

Atmospheric Pressure 700 hPa to 1,060 hPa

Temperature Range -20°C to 60°C

Relative Humidity 15% to 95%, non-condensing

Atmospheric Pressure 500 hPa to 1,060 hPa

1.3 System Administration

1.3.1 Options Information

• Not installed An application that is not yet installed

1.3.2 Installing, Removing, and Disabling System Options

To install an option, remove, or disable an option:

1.3.3 Media Compatibility

• CD-RW and CD-R

• The systems may become vulnerable to security breaches when

Note PHILIPS recommends that you do not use U3 Smart Drives

1.4 CDs and DVDs

CD media capacity is approximately 700 MB; DVD media capacity is

Note For CDs, the system supports “multi-session writes” (you

Note For DVDs, the system suports “single-session writes” (you

PHILIPS recommends using no more than 95% of the capacity of any CD

• CD-RW and CD-R

1.5 USB Devices

Note The system supports the following USB devices;

Note Single-partition USB flash memory drives;

Note USB 2.0 compliant devices;

About Safety Information

In this manual, WARNING is used to indicate the presence of a hazard

In this manual, NOTICE is used when additional comment or explanation