S Series - Service Manual
S Series - Service Manual
S Series - Service Manual
Ultrasound System
Service Manual
SonoSite, Inc.
21919 30th Drive SE
Bothell, WA 98021-3904
USA
Telephone: 1-888-482-9449 or 1-425-951-1200
Fax: 1-425-951-1201
SonoSite Ltd
Alexander House
40A Wilbury Way
Hitchin, Herts
SG4 OAP UK
T: +44-1462-444800
F: +44-1462-444801
Caution: Federal (United States) law restricts this device to sale by or on the order of a physician.
S Series, SiteLink, SonoCalc, SonoHD, SonoMB, and SonoSite are registered trademarks or trademarks of SonoSite, Inc.
DICOM is the registered trademark of the National Electrical Manufacturers Association for its standards publications relating to digital communications
of medical information.
Non-SonoSite product names may be trademarks or registered trademarks of their respective owners.
Protected by U.S. patents: 5722412, 5817024, 5893363, 6135961, 6364839, 6371918, 6383139, 6416475, 6471651, 6569101, 6648826, 6962566, 7169108,
D456509, D538432. Patents pending.
P08386-01 3/2008
Copyright 2008 by SonoSite, Inc.
All rights reserved.
ii
Contents
Chapter 1: Introduction
Audience ........................................................................................................................... 1
Conventions .................................................................................................................... 1
Contact Information ..................................................................................................... 1
Chapter 3: Troubleshooting
Periodic Maintenance ................................................................................................11
Technical Bulletins .......................................................................................................11
System and Subsystem Diagnosis .........................................................................11
System Repair ...............................................................................................................11
Test Equipment ............................................................................................................11
Failure (Assert) Codes .................................................................................................12
iii
Ordering Replacement Parts ...................................................................................54
Index ........................................................................................................................ 59
iv
Chapter 1: Introduction
Before servicing the S Series ultrasound system, please read this manual. The information applies only to
the SonoSite S Series ultrasound system product manufactured after December 7, 2007.
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 depend on your system configuration,
transducer, and exam type.
Refer to the S Series Ultrasound System User Guide for additional information regarding safety, system
controls, operation, capabilities, and specifications.
Audience
The intended audience of this manual is properly trained field and in‐house service personnel.
Conventions
These conventions are used in this service manual:
• A WARNING describes precautions necessary to prevent injury or loss of life.
• A Caution describes precautions necessary to protect the products.
• Numbered steps must be performed in a specific order.
• Bulleted lists present information in list format but do not imply a sequence.
Labeling symbols are in the user guide.
Contact Information
Questions and comments are encouraged. SonoSite is interested in your feedback regarding the service
manual. If you encounter difficulty with the system, use the information in this manual to help correct the
problem. If the problem is not covered here, contact SonoSite Technical Support as follows:
Chapter 1: Introduction 1
2 Chapter 1: Introduction
Chapter 2: System Overview
Theory of Operation
The S Series ultrasound system has seven (7) major functional groups:
• Transducer
• Acquisition Subsystem
• Processing Subsystem
• Display Subsystem
• Control Subsystem
• User Interface Subsystem
• Power Subsystem
Figure 2.1 shows the relationship of the functional groups.
Power
subsystem
Battery
Display power pack
assembly
Transducer
Logic power
Pulser voltage
Power
adapter
External power
The Transducer elements convert the pulser voltage to acoustic energy during the transmit portion of the
ultrasound acquisition cycle. The elements convert the acoustic echo to voltage in the receive portion of the
acquisition. The voltage developed on the transducer elements is sensed by the acquisition subsystem. The
system transducers have 64 to 192 elements.
The Acquisition Subsystem consists of the beamformer and interface to the transducer. The beamformer
controls the timing of the transmit pulses to focus the acoustic beam. The beamformer amplifies the
low‐level received echoes and controls the receive focusing. The system beamformer transmits on up to 128
elements and receives on 64 elements.
The Processing Subsystem includes capabilities for interfacing with the beamformer and performing high
speed processing. The processing subsystem demodulates, filters, detects, and compresses the signal
supplied by the beamformer into display information.
The Display Subsystem converts the detected ultrasound data into picture elements (pixels). The software
user interface graphics are combined with the ultrasound information and converted to a video stream. The
external video port supports NTSC and PAL format.
The Control Subsystem consists of the central processing unit, program and video memory, permanent
image storage and retrieval memory, external communication interface ports, and connection to the user
interface keys. The control software includes the acoustic power and intensity software subsystem, power
group monitors, and a beamformer monitor. This software guarantees a level of patient safety by ensuring
the system is operating within acoustic power and intensity limits.
The User Interface Subsystem represents the software interface and form factor. The software interface is
the interaction between the user and the screen layout components. The form factor is the type of physical
buttons, location, and grouping of the buttons and the device size, shape, and weight. Dedicated controls
are for high usage activities and grouped according to the user workflow.
2D Mode 2D mode is a two dimensional image of the amplitude of the echo signal. It is used for
location and measurement of anatomical structures and for spatial orientation during
operation of other modes. In 2D, a two-dimensional cross-section of a 3-dimensional soft
tissue structure such as the heart is displayed in real time. Ultrasound echoes of different
intensities are mapped to different gray scale or color values in the display. The outline of
the 2D cross-section may be a rectangle, parallelogram, trapezoid, sector, or a full circle,
depending on the particular transducer used. 2D mode can be used in combination with
any other modes.
Color In color Doppler, a real-time, two-dimensional cross-section of blood flow is displayed. The
Doppler 2D cross-section may be presented as a rectangle, parallelogram, trapezoid, sector, or a full
(Color) circle, depending on the particular transducer used.
The 2D cross-section is presented as a full color display, with various colors being used to
represent the velocity, both positive and negative, of the blood flow echoes. Often, to
provide spatial orientation, the full color blood flow cross-section is overlaid on top of the
gray scale cross-section of soft tissue structure (2D echo). For each pixel in the overlay, the
decision of whether to display VCD, gray scale (echo) information or a blended combination
is based on the relative strength of echoes from the soft-tissue structures and from the red
blood cells.
A high pass filter (wall filter) is used to remove the signals from stationary or slowly moving
structures. Tissue motion is discriminated from blood flow by assuming that blood is
moving faster than the surrounding tissue, although additional parameters may also be
used to enhance the discrimination. The remaining signal after wall filtering may be
averaged over time (persistence) to present a steady state image of blood flow distribution.
Variance information may also be displayed to provide information when large variance is
observed in the velocity information.
Color Power In CPD, a real-time two-dimensional cross-section of blood flow is displayed. The 2D
Doppler cross-section may be presented as a rectangle, parallelogram, trapezoid, sector, or a full
(CPD) circle, depending on the particular transducer used.
The 2D cross-section is presented as a full color display, with various colors being used to
represent the power in blood flow echoes. Often, to provide spatial orientation, the full color
blood flow cross-section is overlaid on top of the gray scale cross-section of soft tissue
structure (2D echo). For each pixel in the overlay, the decision of whether to display CPD,
gray scale (echo) information or a blended combination is based on the relative strength of
echoes from the soft-tissue structures and from the red blood cells.
A high pass filter (wall filter) is used to remove the signals from stationary or slowly moving
structures. Tissue motion is discriminated from blood flow by assuming that blood is
moving faster than the surrounding tissue, although additional parameters may also be
used to enhance the discrimination. The power in the remaining signal after wall filtering
may be averaged over time (persistence) to present a steady state image of blood flow
distribution.
Broadband This ultrasound acquisition system uses high resolution broadband technology in the
Imaging transmit pulsers, transducer, and receivers. The receive path can capture and process
signals over a wide spectrum, from below 2.0 MHz to beyond 10 MHz. For each
application, the transmit pulse is designed to produce an appropriate bandwidth. For
example, in 2D grayscale imaging, a wide band pulse is used to support good axial
resolution. For Doppler modes, a narrower band pulse is used, which improves the
spectral resolution of the detected Doppler signal.
In addition to transmit pulse control, programmable digital signal processing is used in
the receive path to further refine the bandwidth used to produce the final image. Digital
filters are applied to the digitized received signal to limit and shape the spectral
bandwidth used to generate the displayed output.
Biopsy The system can display a pair of biopsy guidelines that represent the anticipated path of
Guidance the biopsy needle. The image of an anatomical target, biopsy guidelines, a scan plane
marker, and a biopsy needle are displayed to assist in guiding the biopsy needle to the
target. The system also provides needle guidance for vascular access procedures. For
additional information, see the biopsy user guides.
Measurement The system offers a variety of measurements and calculations, specific to exam type and
and transducer. A list of them, and author references, are in the system user guide.
Calculation Measurement accuracy is also discussed.
Capabilities
System Specifications
This section contains system and accessory specifications and agency approvals. The specifications for
recommended peripherals can be found in the manufacturers’ instructions. See the applicable SonoSite
accessory user guide for information on the accessories.
System Dimensions
Height: 15.1 in. (38.4 cm)
Width: 11.6 in. (29.5 cm)
Depth: 6.1 in. (15.5 cm)
Weight: 8.35 lbs. (3.79 kg)
Display Dimensions
Length: 8.4 in. (21.34 cm)
Height: 6.3 in. (16 cm)
Diagonal: 10.4 in. (26.4 cm)
Transducers
Note: Each of the S Series system types (S‐ICU, S‐Nerve, etc.) supports a unique combination of transducers.
C11x/5‐2 MHz 11 mm curved array (6 ft./1.8 m)
C60x/5‐2 MHz 60 mm curved array (5.5 ft./1.7 m)
HFL38x/13‐6 MHz 25 mm linear array (5.6 ft./1.7 m)
ICTx/8‐5 MHz 11 mm intracavitary array (5.5 ft./1.7 m)
L25x/13‐6 MHz 25 mm linear array (7.5 ft./2.3 m)
Imaging Modes
2D (256 gray shades)
Color power Doppler (CPD) (256 colors)
Color Doppler (Color) (256 colors)
Accessories
Hardware, Software, and Documentation
Battery
Biopsy Guide
Kensington Security Cable
Needle Guides
Power supply
SiteLink Image Manager 4.0
S Series Stand
System User Guide
System AC PowerCcord (10 ft / 3.1 m)
USB Keyboard
VESA Compliant Mounting
Video and printer cables
Cables
See the S Series Ultrasound System User Guide or the S Series Stand User Guide for information on cables.
Peripherals
Peripherals include the following medical grade (conforming to the requirements of EN60601‐1) and
non‐medical grade (commercial) products. Manufacturer’s instructions accompany each peripheral.
System setup instructions are in the S Series Ultrasound System User Guide. Instructions for using peripherals
with the system are in the applicable SonoSite accessory user guide.
Medical Grade
Black‐and‐white printer
DVD recorder
Barcode Scanner
Non-Medical Grade
USB Memory Stick
Electrical
Power Supply Input: 100‐240 VAC, 50/60 Hz, 2.0 A Max @ 100 VAC.
Power Supply Output 1: 15 VDC, 5.0A Max (system)
Power Supply Output 2: 12 VDC, 2.3A Max (battery)
Combined output not exceeding 75W.
Battery
6‐cell, 11.2 VDC, 5.2 amp‐hours, rechargeable lithium ion battery pack.
Run time is up to 2 hours, depending on imaging mode and display brightness.
DICOM Standard
NEMA PS 3.15: 2000, Digital Imaging and Communications in Medicine (DICOM)‐Part 15: Security
Profiles.
HIPAA Standard
The Health Insurance and Portability and Accountability Act, Pub.L. No. 104‐191 (1996).
45 CFR 160, General Administrative Requirements.
45 CFR 164, Security and Privacy.
Periodic Maintenance
There is no recommended periodic or preventive maintenance required for the system, transducers, or
accessories. There are no internal adjustments or alignments required. There are no functions that require
periodic testing or calibration. Performance tests are described in Chapter 5, “Performance Testing,” of this
manual. Performing maintenance activities not described in this manual may void the product warranty.
Local regulations may require electrical safety testing.
Contact SonoSite Technical Support for any maintenance questions.
Technical Bulletins
Product Technical Bulletins describing known system issues are periodically placed on SonoSite.com. Select
Resources > Support & Service, and then follow the links to S Series support documents.
Display TBA
Battery TBA
System Repair
The system is repairable through subassembly replacement or through replacement of parts as
recommended by SonoSite in Chapter 4, “Replacement Procedures.” Component level repair of Printed
Circuit Board Assemblies is performed only at the SonoSite repair facility. Replacement of board level
components by unauthorized service facilities voids the SonoSite warranty.
Test Equipment
Test equipment is not required for this troubleshooting section. Troubleshooting test aids include an
external monitor and a spare battery.
Chapter 3: Troubleshooting 11
Failure (Assert) Codes
ʺAssertʺ or ʺAssert Codeʺ are software error codes that are generated by all Sonosite products when certain
hardware or software fault conditions exist. Providing the Assert Code to the Technical Support Group may
assist in quicker and more accurate fault diagnosis.
Hardware Assert Codes typically cannot be reset and will usually require Main PCBA replacement. Many
software Assert Codes can be reset and the system may recover and operate normally.
Assert Code
2 Press and release the Power button to power the system down.
3 Press the Power button again to power the system up.
• If the system powers up normally, it has recovered from the fault (software assert) and you may use
the system.
• If the Assert Code remains, corrective action must be taken; usually replacement of the main PCBA is
required. Contact SonoSite Technical Support for assistance and to obtain repair parts.
If the Power button is not functional, all sources of power must be removed to allow the system to
power down. I.e., disconnect AC power and remove the battery.
12 Chapter 3: Troubleshooting
Chapter 4: Replacement Procedures
Caution: Always use correct ESD procedures. ESD damage is cumulative and may not be noticeable at first.
Initial ESD symptoms may be slightly degraded performance or image quality.
Required Tools
• #1 Phillips screwdriver
• #1 Flat Blade screwdriver
• 2mm Allen Key
• Torque screwdriver, 2.0–10.0 inch pounds (0.23–1.1 Newton‐meter)
• Scissors
• Cotton swabs (Q Tips)
• Anti‐static mat
• Wrist grounding strap
Mini-dock Assembly
SD Card
Daughter
Card
(Shown
without
Copper
Tape)
Power Supply
Frame
Caution: Improper removal of the cable connectors could damage components on the Main PCBA. Use
extreme caution when removing the connectors.
1 Remove the Rear Cover as described in “Rear Cover Removal” on page 13.
2 Disconnect the five cable connectors as shown in Figure 4.3.
Remove 9 Superplug
Assembly screws.
4 Disconnect the Display Wire Harness from the bottom of the Superplug Assembly as shown in Figure 4.5.
5 Remove the Superplug Assembly from the system.
Figure 4.5 Display Wire Harness between LCD and Superplug Assembly
1 Carefully reconnect the Display Wire Harness between the bottom of the Superplug Assembly and the
LCD as shown in Figure 4.6.
2 Insert the Superplug Assembly into the system enclosure.
3 Reinstall the nine screws as shown in “Superplug Assembly Screw Removal” on page 16, and torque to
5.5 inch/pounds (.622 Newton‐meters).
4 Reconnect the cables as shown in Figure 4.3 on page 15.
5 Reinstall the Rear Cover as described in “Rear Cover Installation” on page 14.
Required Parts
• P08850 Service Assembly, Power Supply, M‐Turbo / S Series
Screws (7x)
Caution: Inspect the Power Supply Shield to ensure that none of the contacts are bent. Improper
contact between the shield and the Power Supply Frame can cause image noise problems.
Caution: The connector for the Mini-dock Assembly ribbon cable is fragile and will require replacement of
the Mini-dock Assembly if broken.
3 Disconnect the mini‐dock ribbon cable by gently lifting up on the connector latch as shown in Figure 4.8.
Ribbon Cable
Main PCBA Connector
P2
P1
6 Carefully separate the Mini‐dock Assembly from the Main PCBA as shown in Figure 4.10.
Required Parts
• P07442 SD Card Daughter‐Card
• P09216 Copper Tape (1” x 3.5mil), approximately 15” is required
• P00870 Kapton Tape (1” x 1mil), approximately 6” is required ‐ Kapton tape is a plastic tape used for
electrical isolation.
• Cotton swabs (Q Tips)
• Scissors
Power Supply
Frame Screw
SD Card Daughter-card
Long Screw Screws (4x)
4 Gently lift the SD Card Daughter‐card straight up and away from the Main PCBA.
Caution: Failure to reinstall the SD Cards in the same location from which they were removed will result in
loss of patient information and may prevent the operation of any transducer. Record the location
of any SD Cards removed and ensure that they are reinstalled in the same location.
Caution: Failure to reinstall the SD Cards in the same location from which they were removed will result in
loss of patient information and may prevent the operation of any transducer. Record the location
of any SD Cards removed and ensure that they are reinstalled in the same location.
1 Remove the SD Cards from the old daughter‐card, and install into the SD Card holders on the bottom of
the replacement Daughter‐card as shown in Figure 4.13.
2 Secure the SD Cards to the holders using Kapton tape as shown in Figure 4.13.
3 Rub the Kapton Tape with a cotton swab (Q‐Tip) to ensure that the tape is in contact with the SD Cards.
Kapton Tape
4 Install a strip of Kapton tape on the top of the SD Card Daughter‐card as shown in Chapter 4.14. This
protects the components underneath from the copper tape.
Kapton Tape
5 Remove the last Power Supply Frame screw as shown in Figure 4.12 on page 24.
6 Remove the Power Supply Frame from the Main PCBA.
7 Ensure all old copper tape has been removed before proceeding.
Ventilation Cut-outs
10Place the Power Supply Frame back onto the Main PCBA.
11Reinstall the Power Supply PCBA as described in “Power Supply PCBA Installation” on page 19.
12Install the SD Card Daughter‐card onto the Power Supply PCBA Frame using the alignment holes/pins
on the card and frame as shown in Figure 4.16.
Caution: Improper installation of the SD Card Daughter-card will cause all or part of the internal image
storage memory to be unrecognized by the system.
SD Card
Daughter-card
Alignment Pins
16Install a third strip of 1” x 5” self‐adhesive copper tape over the other two strips as shown in Figure 4.18.
Screws (7x)
Loosely install
two screws.
3 Observe the alignment features of the Main PCBA and the Nest Frame Assembly as shown in Figure 4.23.
The Nest Frame Assembly must be properly installed using the alignment pins to ensure proper
transducer operation.
6 Loosely reinstall the four 2.5mm cap screws as shown in Figure 4.25.
Caution: Failure to properly align the Main PCBA as indicated in the following steps will prevent
transducers and the battery from properly attaching to the system.
8 With all retaining screws loosely installed, move the Main PCBA on the Superplug Assembly to the
upper right corner as shown in Figure 4.26.
Loosely install
five screws
9 Tighten the Phillips head screws on the top of the Main PCBA, and torque to 5.5 inch/pounds (.622
Newton‐meters).
10Tighten the Cap Screws on the back of the Superplug Assembly and torque to 4.5 inch/pounds (.508
Newton‐meters).
11Reinstall the Power Supply PCBA as described in “Power Supply PCBA Installation” on page 19.
Caution: Failure to reinstall the SD Cards in the same location from which they were removed will result in
loss of patient information and may prevent the operation of any transducer. Record the location
of any SD Cards removed and ensure that they are reinstalled in the same location.
12Reinstall the SD Card Daughter‐card as described in “SD Card Daughter‐card Installation” on page 25.
13Reinstall the Mini‐dock Assembly as described in “Mini‐dock Assembly Installation” on page 22.
14Reinstall the Superplug Assembly as described in “Superplug Installation” on page 18.
15Reinstall the Rear Cover as described in “Rear Cover Installation” on page 14.
LCD Mounting
Frame Screws (4x)
Control Panel
PCBA
LCD Removal
1 Disconnect the wire harness connecting the LCD and the Display Backlight Inverter PCBA.
2 Remove the four LCD frame mounting screws shown in Figure 4.27.
3 Remove the LCD mounting frame from the enclosure.
4 Remove the four screws that mount the LCD to the mounting frame as shown in Figure 4.28.
LCD Mounting
Screws (4x)
Caution: Use extreme caution when installing the Display Wire Harness to prevent irreparable damage to
the LCD.
P08086
Control Panel
Snap Dome
Scotch Tape
3 Insert the replacement Control Panel PCBA into the system enclosure.
4 Reinstall the six mounting screws, and torque to 5.5 inch/pounds (.622 Newton‐meters).
5 Reconnect all cables.
To obtain 2D images, SonoSite recommends using the RMI 413A Soft Tissue Phantom or the RMI 403 GS
Multipurpose Phantom. A .7db/cm phantom is required for performing penetration measurements. Any
equivalent .7db/cm Phantom is acceptable.
When making penetration measurements on a phantom, apply the phantom reference value and tolerance
to the measurement.
Some features and capabilities are optional and therefore may be unavailable to test.
Test Equipment
• SonoSite ultrasound system under test
• Transducer compatible with the system under test
• RMI 413A Soft Tissue Phantom, RMI 403 GS Multipurpose Phantom, or equivalent. A referenced .7db/cm
phantom is required for performing penetration measurements.
• Video printer
• Acoustic gel
Measurements Tolerance
Penetration
Caution: A referenced .7db/cm phantom is required for performing penetration measurements
Test Penetration
1 Adjust the system controls to obtain a clear image that shows the limits of echo penetration as shown in
Table 2.
2 Set the system optimization mode settings to the values shown in Table 2.
3 Measure from the center of the skinline to the deepest vertical position—where the scatter echoes start to
break up and tissue definition is lost.
4 When making penetration measurements on a phantom, apply the phantom reference value and
tolerance to the measurement.
5 Press the Freeze key and then save the image. Press the Freeze key again to return to live imaging.
Table 2: Imaging Performance
Imaging
C11x C60x ICTx HFL38 L25x L38x P21x
Performance
Battery Charging
Test Battery Charging Operation
1 Insert a battery into the system.
2 Press the power key to turn the system on.
3 Allow the battery to discharge. The battery indicator icon on the display, below the Transducer Type
indicator, extinguishes from left to right as the battery discharges.
Note: The Power and Sleep delay settings in the Audio, Battery setup page should be selected to Off to properly
perform this test. The battery may take 1–2 hours to discharge.
4 Attach the AC power cord to the power connector.
5 Note that the battery indicator indicates that the battery is charging. The sections of the battery indicator
will light sequentially from left to right as the battery charges.
Video Output
Caution: Use only the recommended video monitor or printer when verifying the video output at the
video receptacle.
5 4 3 2
Table 1: Major System Components
11 3
10
4
5
6
8 7
5 4
4 3
2 3
7 2
3
6
5 4
The Service Event Report provides information about product failures to the manufacturer and to
authorized service facilities, which provide approved warranty services for SonoSite products. For all
repairs completed, complete the form and email a copy of it to [email protected] or mail to the
following address:
SonoSite, Inc.
Technical Support
21919 30th Drive SE
Bothell, Washington 98021
USA
Parts Status
x Check One.
Service Provider
x Name: the name of the technician performing the work.
x Provider Reference: a unique number used by the Provider to track Service Event Reports. Any format is acceptable.
x Company: the name of the Distributor or authorized repair facility.
x Address: the address replacement parts will be shipped to.
x Date Reported: the date the failure was reported to SonoSite.
x Phone Number: the phone number to contact the service technician.
x Fax Number: the fax number to contact the service technician.
x Email Address: the email address to contact the service technician.
Device Description:
x Name: the description of the failed product.
x Ref Number: the reference number from the part number label of the failed product.
x Serial Number: the serial number from the part number label of the failed product.
x Lot Number: if applicable, the Lot Number from the device identification label.
x ARM/SHDB Version: the software level of the failed device. Typically found on the system information screen.
x Configuration: for configurable devices, the optional features enabled.
Event Description
x A description of the problem in the words of the user. Typically what the user reports to the repair facility.
Diagnosis
x A description of what the repair technician found. Include a list of the suspect parts.
Service Performed
x A description of the work performed to repair the system. Typically only completed if it is repaired from stock repair parts.
Parts Removed
x Part Name: the name of the failed/suspect part to be replaced.
x Part Number: the part number of the failed/suspect part.
x Serial Number: the serial number from the failed/suspect part.
x Lot Number: the lot number if applicable.
x Rev: the revision of the failed/suspect part if available.
x Replaced By: the person replacing the part.
Parts Installed
x The same information as the Parts Removed except from the parts installed if work has already been performed. If you are
waiting for parts to be ordered, leave this section blank.
Tests Performed
x The results of any testing performed, if testing has already been performed.
Shipping Instructions
Please contact SonoSite to get a return material authorization number (RMA). Contact SonoSite before
returning any product.
The shipping address for all returned products is:
SonoSite, Inc.
Attn: Technical Support RMA ___________________
21919 30th Drive SE
Bothell, Washington 98021
USA
Numerics R
2D performance tests replacement parts
axial measurement accuracy 44 list 49
image quality 44 ordering 54
lateral measurement accuracy 45 replacement procedures 13
penetration 45 Backlight Inverter PCBA 38
control panel PCBA 39
LCD 36
A main PCBA 30
accessories 6 mini-dock assembly 20
assistance, customer 1 power supply PCBA 19
SD Card Daughter-card 23
TGC PCBA 28, 41
B return material authorization number (RMA) 58
battery
charging test 47
specifications 8 S
storage and shipping 8 service event report 55
shipping instructions 58
system
C dimensions 6
cable specifications 7 measurement accuracy 45
conventions used 1 overview 3
specifications 6, 8
I
image
T
quality verification test 46 theory of operation 3
review 46 transducer
specifications 6, 8
storage and shipping 8
M
main PCBA failures 12
monitor 6
V
video output tests 47
P
parts list 49
performance tests
2D 44
battery 47
CPD 46
overview 43
printer 46
Velocity Color 46
video output 47
periodic maintenance 11
peripherals 7
printer test 46
product failures, reporting 55
products, returning 58
Index 59
60 Index
P08386-01
*P08386-01*