Edge II Service Manual Oct 2018

Manufacturer FUJIFILM 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 EC Authorized Representative FujiFilm SonoSite B.V. Joop Geesinkweg 140 1114 AB Amsterdam, The Netherlands Australia Sponsor FUJIFILM SonoSite Australasia Pty Ltd 114 Old Pittwater Rd Brookvale, New South Wales 2100, Australia Caution:

Federal (United States) law restricts this device to sale by or on the order of a physician.

Edge, SiteLink, SonoCalc, SonoHD2, SonoMB, SonoMBe, SonoSite, and the SonoSite logo are registered (in some jurisdictions) and unregistered trademarks owned by FUJIFILM 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. The SonoSite ultrasound system(s) referenced in this document may be covered by one or more of the following U.S. patents: Patents: US 8,439,840; US 8,398,408; US 8,355,554; US 8,216,146; US 8,213,467; US 8,147,408; US 8,137,278; US 8,088,071; US 8,066,642; US 8,052,606; US 7,819,807; US 7,804,970; US 7,740,586; US 7,686,766; US 7,604,596; US 7,591,786; US 7,588,541; US 7,534,211; US 7,449,640; US 7,169,108; US 6,962,566; US 6,648,826; US 6,575,908; US 6,569,101; US 6,471,651; US 6,416,475; US 6,383,139; US 6,364,839; US 6,203,498; US 6,135,961; US 5,893,363 ; US 5,817,024; US 5,782,769; US 5,722,412; US 8,805,047; US 8,527,033; US 8,858,436; US 8,861,822; US 8,956,296; AU: 730822; AU: 727381; CA 2,372,152; CA: 2,371,711; CN 98108973.9; CN 98106133.8; CN 97113678.5; DE 69831698.3; DE 69830539.6; DE 69730563.5; DE 602004027882.3; DE 602004023816.3; DE: 60034670.6; DE 60029777.2; EP 1589878; EP 1552792; EP 1180971; EP 0875203; EP 0815793; EP 1180970; EP 0881492; ES 2229318; ES 159878; ES 1552792; ES 0881492; FR 158978; FR 1552792; FR 1180970; FR 0881492; FR 0875203; FR 0815793; GB 158978; GB 1552792; GB 1180971; GB 1180970; GB 0881492; GB 0875203; GB 0815793; IT 1589878; IT 1552792; IT 0881492; IT 0815793; JP 4696150; KR 532359; KR 528102; NO 326814; NO 326202 and pending.

P21828-02 10/2018 Copyright © 2018 FUJIFILM SonoSite, Inc. All rights reserved.

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Introduction...1 Audience ...1 Contact Information ...1 Conventions, symbols, and terms ...2 Labeling symbols...2

Specifications ...7 Specifications ...7 Dimensions...7 System ...7 Display...7 Environmental limits ...7 Operating (system, battery, and transducer)...7 Shipping and storage (system and transducer)...7 Shipping and storage (battery) ...7 Electrical specifications ...7 Battery specifications ...8 Compatible accessories and peripherals ...8

Safety...11 Electrical safety ...11 Electrical safety classification...13 Equipment safety...13 Battery safety ...14 Clinical safety ...15 Hazardous materials ...15 Electromagnetic compatibility...16 Electrostatic discharge ...16 Separation distance...17 Guidance and manufacturer’s declaration...18 Immunity testing requirements ...21 Standards ...21 Electrical safety standards ...21 EMC standards classification ...21 Acoustic standards ...21 Biocompatibility standards...21 Airborne equipment standards ...22 DICOM standard ...22 HIPAA standard...22

System Overview...23 About the System ...23 Theory of Operation ...24 Description of Operating Modes...25 Additional System Feature Performances...27 Front End Overview...28 PW Doppler Processing ...30 CW Doppler Processing ...31 Back End Overview ...32 Control Subsystem ...33 Power Supply and Control...34

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ECG Module...36 DICOM ...37

Troubleshooting ...39 System and Subsystem Diagnosis...39 System Repair...40 Test Equipment ...40 Failure (Assert) Codes ...40 Verifying a System Assert Code...40 DICOM ...42 Display...43 Battery ...43 Control Panel...43

Replacement Procedures ...45 Display Replacement ...45 Required Parts ...45 Required Tools ...45 Display Removal ...45 Display Replacement ...49 Test the Display...49 Control Panel Subassembly Replacement...49 Required Parts ...50 Required Tools ...50 Control Panel Removal ...51 Control Panel Replacement ...51 TGC Assembly Removal ...51 Main System Disassembly for Repair and/or Replacement ...52 Required Parts ...52 Required Tools ...52 System Disassembly ...53 Speaker Replacement...53 Required Part ...53 Power Supply PCBA Replacement ...55 Required Part ...55 SD Card Replacement ...56 USB Extension PCB Assembly Replacement ...56 Required Part ...56 Main PCBA Replacement...56 Required Parts ...56 Midframe Replacement ...59 Required Parts ...59 Bottom Enclosure Replacement...60 Required Parts ...60

Maintenance...61 Periodic Maintenance...61

Performance Testing...63 Overview ...63 Recommend Test Equipment...63 Setting Up Performance Tests ...63

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Basic Operational Tests ...64 2D Performance Tests ...64 2D Performance / Image Quality ...64 Axial Measurement Accuracy...65 Lateral Measurement Accuracy...65 Penetration ...66 Additional Performance Tests ...66 Color Doppler (Color) ...66 Color Power Doppler (CPD) ...67 M Mode Imaging...67 Tissue Harmonic Imaging...67 Image Quality Verification Test/Livescan ...67 Printer...68 Battery Charging ...68 Video Output ...68

Replacement Parts ...69 Replacement Parts...69 Display...69 Control Panel...70 Main PCBA...71 Miscellaneous Parts ...73 Transducer Nest Frame Assembly...77 Ordering Replacement Parts...78

Service Event Reporting ...79 Service Event Report Form ...80 Service Event Report Instructions ...81 Returning Products to SonoSite ...82 Shipping Instructions ...82

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Chapter 1: Introduction Before servicing the SonoSite Edge II Ultrasound System, please read this manual. 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 SonoSite Edge II Ultrasound System User Guide for additional information regarding safety, system controls, operation, capabilities, and specifications. This chapter also defines labeling symbols, specifications, and standards.

Audience The intended audience of this manual is properly trained field and in-house service personnel.

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: Technical Support (USA, Canada)

1-877-657-8118

Technical Support fax:

1-425-951-6700

Technical Support e-mail:

[email protected]

SonoSite website:

www.sonosite.com

International Technical Support:

Contact your local representative or call (USA) +425-951-1330

European Service Center

United Kingdom Tel: 0044 01462341151 e-mail: [email protected] France Tel: 0033 01/82880702 e-mail: [email protected] Germany Tel: 0049 069/80884030 e-mail: [email protected] Spain Tel: 0034 911238451 e-mail: [email protected] Italy Tel 0039 02 94753655 e-mail: [email protected]

Asia/Pacific

Tel: (+65) 63805581 e-mail: [email protected]

Chapter 1: Introduction

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Conventions, symbols, and terms The user guide follows these conventions: •

A WARNING describes precautions necessary to prevent injury or loss of life.

•

A Caution describes precautions necessary to protect the products.

•

Numbered steps in procedures must be performed in order.

•

Items in bulleted lists do not require performance in sequence.

Labeling symbols The following symbols are used on the products, packaging, and containers. Table 1: Labeling Symbols Symbol

Definition Alternating Current (AC) Class 1 device indicating manufacturer’s declaration of conformance with Annex VII of 93/42/EEC Class 1 device requiring verification by the Notified Body of sterilization or measurement features, or to a Class IIa, IIb, or III device requiring verification or auditing by the Notified Body to applicable Annex(es) of 93/42/EEC Attention, see the user guide Follow instructions for use.

Device complies with relevant Australian regulations for electronic devices.

LOT

Batch code, date code, or lot code type of control number Biological risk

Device complies with relevant Brazilian regulations for electro-medical devices. Canadian Standards Association. The “C” and “US” indicators next to this mark signify that the product has been evaluated to the applicable CSA and ANSI/UL Standards, for use in Canada and the US, respectively.

REF

Catalog number Collect separately from other household waste (see European Commission Directive 93/86/EEC). Refer to local regulations for disposal.

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Chapter 1: Introduction

Table 1: Labeling Symbols (Continued) Symbol

Definition Corrugated recycle

Dangerous voltage Date of manufacture

Manufacturer

Direct Current (DC) Do not get wet.

Do not stack over 2 high.

Do not stack over 5 high.

Do not stack over 10 high.

Electrostatic sensitive devices

Device complies with relevant FCC regulations for electronic devices. Fragile

GEL

STERILE R STERILE EO

Gel Sterilized using irradiation Sterilized using ethylene oxide Hot

Chapter 1: Introduction

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Table 1: Labeling Symbols (Continued) Symbol

Definition Device emits a static (DC) magnetic field.

Non-ionizing radiation

Paper recycle

SN

Serial number type of control number Temperature limitation

Atmospheric pressure limitation

Humidity limitation

Submersible. Protected against the effects of temporary immersion. Water-Tight Equipment. Protected against the effects of extended immersion. Handle transducer with care.

Follow manufacturer’s instructions for disinfecting time.

Disinfect transducer.

Type BF patient applied part (B = body, F = floating applied part) Defibrillator proof type CF patient applied part Underwriter’s Laboratories labeling

Pollution Control Logo. (Applies to all parts/products listed in the China RoHS disclosure table. May not appear on the exterior of some parts/products because of space limitations.) China Compulsory Certificate mark (“CCC Mark”). A compulsory safety mark for compliance to Chinese national standards for many products sold in the People’s Republic of China.

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Chapter 1: Introduction

Table 1: Labeling Symbols (Continued) Symbol

Definition

WARNING: Connect Only

WARNING: Connect Only Accessories and Peripherals Recommended by FujiFilm SonoSite

Accessories and Peripherals Recommended by FujiFilm SonoSite

Chapter 1: Introduction

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Chapter 1: Introduction

Chapter 2: Specifications This chapter contains information regarding system specifications and accessory compatibility. The information applies to the ultrasound system, transducers, accessories, and peripherals.

Specifications Dimensions System •

Length: 13 in. (33 cm)

•

Width: 12.4 in. (31.5 cm)

•

Height: 2.5 in. (6.3 cm)

Display •

Length: 9.7 in. (24.6 cm)

•

Height: 7.3 in. (18.5 cm)

•

Diagonal: 12.1 in. (30.7 cm)

Environmental limits Note: The temperature, pressure, and humidity limits apply only to the ultrasound system, transducers, and battery.

Operating (system, battery, and transducer) 10–40°C (50–104°F), 15–95% R.H. 700 to 1060hPa (0.7 to 1.05 ATM) Mode of Operation: Continuous 35°C or below Non-Continuous above 35°C (30 minutes on /30 minutes off)

Shipping and storage (system and transducer) -35–65°C (-31–149°F), 15–95% R.H. 500 to 1060hPa (0.5 to 1.05 ATM)

Shipping and storage (battery) -20–60°C (-4–140°F), 15–95% R.H. (For storage longer than 30 days, store at or below room temperature.) 500 to 1060hPa (0.5 to 1.05 ATM)

Electrical specifications Power Supply Input: 100-240 VAC, 50/60 Hz, 2.0 A Max @ 100 VAC Power Supply Output #1: 15 VDC, 5.0 A Max Power Supply Output #2: 12 VDC, 2.3 A Max Combined output not exceeding 75 watts.

Chapter 2: Specifications

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Battery specifications The battery is comprised of six lithium-ion cells plus electronics, a temperature sensor, and battery contacts. Run time is up to two hours, depending on imaging mode and display brightness.

Compatible accessories and peripherals SonoSite has tested the SonoSite Edge II ultrasound system with the following accessories and peripherals and has demonstrated compliance to the requirements of IEC60601-1-2:2007. You may use these SonoSite accessories and third-party peripherals with the SonoSite Edge II ultrasound system. WARNING:

Use of the accessories with medical systems other than the SonoSite Edge II ultrasound system may result in increased emissions or decreased immunity of the medical system.

WARNING:

Use of accessories other than those specified may result in increased emissions or decreased immunity of the ultrasound system.

Accessories and peripherals compatible with SonoSite Edge II ultrasound system

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Description

Part Number

Maximum Cable Length

C8x transducer

P08010

6.0 ft/1.8 m

C11x transducer

P07678

6.5 ft/2.0 m

C35x transducer

P21981

6.0 ft/1.8 m

rC60xi transducer

P21070

5.5 ft/1.7 m

rC60xi transducer armored

P21636

5.5 ft/1.7 m

rP19x transducer

P21015

6.0 ft/1.8 m

rP19x transducer armored

P21556

6.0 ft/1.8 m

HFL38xi transducer

P20311

5.5 ft/ 1.7 m

HFL38xi transducer armored

P20377

5.5 ft/1.7 m

HFL50x transducer

P07693

6.0 ft/1.8 m

HSL25x

P20679

7.5 ft/2.3 m

ICTx transducer

P07690

6.0 ft/1.8 m

L25x transducer

P07691

7.5 ft/2.3 m

L25x transducer armored

P22950

7.5 ft/2.3 m

L38xi transducer

P12742

6.0 ft/1.8 m

L38xi transducer armored

P19626

6.0 ft/1.8 m

L52x transducer (Vet)

V00033

7.5 ft/2.3 m

L52x transducer armored (Vet)

V20962

7.5 ft/2.3 m

P10x transducer

P07696

6.5 ft/2.0 m

TEExi transducer

P19825

7.5 ft/2.3 m

Chapter 2: Specifications

Accessories and peripherals compatible with SonoSite Edge II ultrasound system (Continued) Bar code scanner

P14166

4.8 ft/1.5 m

Kit, PowerPack

P13559

-

Black & white printer

P13745

-

Hybrid black & white printer

P20006

Black & white printer power cable

-

3.3 ft/1 m

Black & white printer USB cable

-

10.8 ft/3.3 m

Color printer

P13983

-

Color printer power cable

-

3.3 ft/1 m

Color printer video cable

-

6.0 ft/ 1.8 m

ECG lead wires

P14202

24 in/ 0.6 m

ECG module

P08501

5.8 ft/1.8 m

Edge Mini-Dock

P15078

-

Edge Stand

P15800

-

Dual USB Footswitch

P14689

9.8 ft/3.0 m

Power cord (system)

P00848 (USA)

10 ft/3 m

Power Supply/Battery Charger

P09823

6.8 ft/ 2 m

PowerPark

P12822

-

Storage bin kit, Universal/Edge stands

P22048

Triple Transducer Connect

P16535

-

USB wireless adapter

P17725

-

EU compliant wireless adapter

P22625

Edge Battery Pack

P15051

Wireless mounting kit

P17724

-

Chapter 2: Specifications

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Chapter 2: Specifications

Chapter 3: Safety This chapter contains electrical and clinical safety information required by regulatory agencies. The information applies to the ultrasound system, transducers, accessories, and peripherals.

Electrical safety This system meets EN60601-1, Class I/internally-powered equipment requirements and Type BF and Type CF isolated patient-applied parts safety requirements. This system complies with the applicable medical equipment requirements published in the Canadian Standards Association (CSA), European Norm Harmonized Standards, and Underwriters Laboratories (UL) safety standards. See “Standards” on page 21. For maximum safety observe the following warnings and cautions. WARNING:

To avoid the risk of injury, do not operate the system in the presence of flammable gasses or anesthetics. Explosion can result.

WARNING:

To avoid the risk of electrical shock or injury, do not open the system enclosures. All internal adjustments and replacements, except battery replacement, must be made by a qualified technician.

WARNING:

To avoid the risk of electrical shock: • This equipment must be connected only to a supply mains with protective earth. • Use only properly grounded equipment. Shock hazards exist if the power supply is not properly grounded. Grounding reliability can be achieved only when equipment is connected to a receptacle marked “Hospital Only” or “Hospital Grade” or equivalent. The grounding wire must not be removed or defeated. • When using the system in an environment where the integrity of the protective earth conductor arrangement is in doubt, operate the system on battery power only and disconnect the power supply. • Do not let the bar code scanner or external mouse touch the patient. • Do not touch any of the following: • The power supply and the patient at the same time • The ungrounded signal input/output connectors on the back of the ultrasound system • The system battery contacts (inside the battery compartment) • The system transducer connector when the transducer or Triple Transducer Connect (TTC) is disconnected • The system transducer connector on the TTC if no transducers are connected

Chapter 3: Safety

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• Do not connect the system power supply or docking system to a multiple portable socket outlet (MPSO) or extension cord. • Before using the transducer, inspect the transducer face, housing, and cable. Do not use the transducer if the transducer or cable is damaged. • Always disconnect the power supply from the system before cleaning the system. • Do not use any transducer that has been immersed beyond the specified cleaning or disinfection level. See Chapter 7, “Maintenance”. • Use only accessories and peripherals recommended by SonoSite, including the power supply. Connection of accessories and peripherals not recommended by SonoSite could result in electrical shock. Contact SonoSite or your local representative for a list of accessories and peripherals available from or recommended by SonoSite. WARNING:

To avoid the risk of electrical shock and fire hazard: • Inspect the power supply, AC power cords, cables, and plugs on a regular basis. Ensure that they are not damaged. • The power cord set that connects the power supply of the ultrasound system or the stand to mains power must only be used with the power supply or docking system, and cannot be used to connect other devices to mains power.

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WARNING:

To prevent injury to the operator/bystander, the transducer must be removed from patient contact before the application of a high-voltage defibrillation pulse.

WARNING:

To avoid possible electrical shock or electromagnetic interference, verify proper operation and compliance with relevant safety standards for all equipment before clinical use. Connecting additional equipment to the ultrasound system constitutes configuring a medical system. SonoSite recommends verifying that the system, all combinations of equipment, and accessories connected to the ultrasound system comply with JACHO installation requirements and/or safety standards such as AAMI-ES1, NFPA 99 OR IEC Standard 60601-1-1 and electromagnetic compatibility standard IEC 60601-1-2 (Electromagnetic compatibility), and are certified according to IEC Standard 60950 (Information Technology Equipment (ITE)).

Caution:

Do not use the system if an error message appears on the LCD display. Note the error code and call SonoSite Technical Support for further assistance.

Caution:

To avoid increasing the system and transducer connector temperature, do not block the airflow to the ventilation holes on the side of the system.

Chapter 3: Safety

Electrical safety classification Class I equipment

The ultrasound system is classified as Class I equipment when powered from the external power supply or mounted on the stand because the external power supply is a Class 1 protectively earthed power supply. The stand has no protective earth. Ground bond testing is not applicable to the ultrasound system or the stand. Note:AC powered peripherals that may be used with the system are Class I and are individually protectively earthed. Ground bond testing may be conducted on each AC powered peripheral.

Internally powered equipment

Ultrasound system not connected to the power supply (battery only)

Type BF applied parts

Ultrasound transducers

Type CF applied parts

ECG module/ECG leads

IPX-7 (watertight equipment)

Ultrasound transducers

IPX-8 (watertight equipment)

Footswitch

Non AP/APG

Ultrasound system power supply, docking system, and peripherals. Equipment is not suitable for use in the presence of flammable anaesthetics.

Equipment safety To protect your ultrasound system, transducers, and accessories, follow these precautions. Caution:

Excessive bending or twisting of cables can cause a failure or intermittent operation.

Caution:

Improper cleaning or disinfecting of any part of the system can cause permanent damage. For cleaning and disinfecting instructions, see Chapter 7, “Maintenance”.

Caution:

Do not submerge the transducer connector in solution. The cable is not liquid-tight beyond the transducer connector/cable interface.

Caution:

Do not use solvents such as thinner or benzene, or abrasive cleaners on any part of the system.

Caution:

Remove the battery from the system if the system is not likely to be used for a month or more.

Caution:

Do not spill liquid on the system.

Chapter 3: Safety

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