Mindray Zonare ZS3 User manual

ZS3 Diagnostic Ultrasound System
Service Manual

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©2019 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved.
ZONARE, the ZONARE logo, ZS3 and z.onepro are all trademarks of Shenzhen Mindray Bio-Medical Electronics Co.,
Ltd.. All other trademarks are the property of their respective holders.
The ZS3 Ultrasound Platform and products derived there from (for example, but not limited to, the ZS3 and the
z.onepro with and without the SP UI option) is covered by one or more of the following patents:
6,251,073; 6,569,102; 6,618,206; 6,663,567; 6,685,645; 6,733,455; 6,773,399; 6,866,631; 6,866,632; 6,896,658;
6,936,008; 6,980,419; 6,997,876; 7,022,075; 7,087,020; 7,226,416; 7,238,157; 7,352,570; 7,361,145; 7,510,529;
7,627,386; 7,382,309; 7,699,781; 8,002,705; 8,226,561; D461,814; D462,446; D467,002; D469,539; D469,877
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD.
Mindray Building, Keji 12th Road South, High-Tech Industrial Park, Nanshan,
Shenzhen, 518057, P.R.China
Shanghai international Holding Corp. GmbH(Europe)
Eiffestraβe 80, 20537 Hamburg, Germany
CAUTION: United States Federal Law restricts this device to sale by or on the order of a licensed physician or
licensed veterinarian.

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TABLE OF CONTENTS
1Introduction......................................................................................................................................... 7
Purpose.................................................................................................................................................... 8
Definitions/Acronyms ............................................................................................................................. 8
Documentation Conventions............................................................................................................... 10
Symbols.................................................................................................................................................. 10
2Safety.................................................................................................................................................. 12
Facility Needs........................................................................................................................................ 12
Notes When Returning or Transporting the System, Probes, and Repair Parts ........................ 13
Warning & Cautions............................................................................................................................. 13
3System Specifications.................................................................................................................... 24
General System Specifications........................................................................................................... 24
Display.................................................................................................................................................... 26
Battery Pack Specifications................................................................................................................. 27
Standards and Compliance................................................................................................................. 32
4System Overview............................................................................................................................. 34
Major System Assemblies................................................................................................................... 34
User Interface Overview...................................................................................................................... 35
Keyboard Functions............................................................................................................................. 38
On-Screen “Dashboard” System Status ICONs .............................................................................. 41
Accessory Components....................................................................................................................... 43
Rear I/O Panel ...................................................................................................................................... 44
5System Uncrating & Installation Procedures........................................................................... 45
Product Shipment................................................................................................................................. 45
Electrical Requirements....................................................................................................................... 45
Environmental and Space Requirements......................................................................................... 45
Uncrating................................................................................................................................................ 45
Mechanical Inspection......................................................................................................................... 49
System Installation............................................................................................................................... 49
ZS3 System Verification...................................................................................................................... 51
6Setup................................................................................................................................................... 54
System.................................................................................................................................................... 54
Preset Mgmt.......................................................................................................................................... 55
Calc......................................................................................................................................................... 56
Annotation.............................................................................................................................................. 56

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Body Pattern.......................................................................................................................................... 56
Protocols................................................................................................................................................ 56
Stress Echo........................................................................................................................................... 56
DICOM.................................................................................................................................................... 57
Network.................................................................................................................................................. 57
Keys........................................................................................................................................................ 58
Peripherals............................................................................................................................................. 58
Backup/Restore .................................................................................................................................... 58
7Security.............................................................................................................................................. 59
Access Control...................................................................................................................................... 59
Enabling Location Access Control..................................................................................................... 60
Enabling Account Access Control...................................................................................................... 61
System Login......................................................................................................................................... 61
Local Privilege Management............................................................................................................... 62
LDAP Privilege Management.............................................................................................................. 68
User Field Name................................................................................................................................... 70
Enable Barcode Login.......................................................................................................................... 70
Enable Encryption ................................................................................................................................ 71
8Patient Information Management................................................................................................ 72
Patient Information ............................................................................................................................... 72
New Patient Information...................................................................................................................... 73
Retrieve Patient Information ............................................................................................................... 78
9DICOM/HL7........................................................................................................................................ 84
DICOM Preset....................................................................................................................................... 85
Service Preset....................................................................................................................................... 87
DICOM Verifying................................................................................................................................. 101
DICOM Services................................................................................................................................. 102
DICOM Media Storage....................................................................................................................... 108
10 Peripheral ........................................................................................................................................ 110
Print Service........................................................................................................................................ 110
Barcode Reader Configuration......................................................................................................... 111
Power Save ......................................................................................................................................... 113
11 Network............................................................................................................................................ 115
Network Setup..................................................................................................................................... 115
FTP Setup............................................................................................................................................ 120

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QPath/QView....................................................................................................................................... 121
VPN....................................................................................................................................................... 123
12 Functional Descriptions............................................................................................................... 126
System Capabilities............................................................................................................................ 126
Major FRUs.......................................................................................................................................... 126
13 System Diagrams .......................................................................................................................... 131
Power Block Diagram......................................................................................................................... 132
Cabling Diagram................................................................................................................................. 133
System Block Diagram....................................................................................................................... 134
14 Peripherals & Accessories.......................................................................................................... 135
Black & White Printer......................................................................................................................... 135
Color Printer ........................................................................................................................................ 142
Pedal Footswitch ................................................................................................................................ 144
Ultrasound Gel Warmer..................................................................................................................... 144
15 Software Procedures.................................................................................................................... 151
Backup Operations............................................................................................................................. 151
Restore Operations............................................................................................................................ 152
Software Upgrade& Installation........................................................................................................ 155
Installing System Software................................................................................................................ 156
Clean Software Install Procedure..................................................................................................... 159
Mindray/Zonare FTP Site.................................................................................................................. 160
Diagnostic Panel Operations............................................................................................................ 161
16 Care and Maintenance.................................................................................................................. 170
Overview.............................................................................................................................................. 170
Basic System Care............................................................................................................................. 171
Transducer Maintenance................................................................................................................... 174
Check.................................................................................................................................................... 174
17 Preventative Maintenance Forms.............................................................................................. 185
18 System Troubleshooting............................................................................................................. 189
Diagnostics.......................................................................................................................................... 190
Troubleshooting.................................................................................................................................. 193
System Status LED & Error Code Definitions................................................................................ 203
Battery Performance –Charge Times - Reconditioning............................................................... 213
How to Obtain MAC Address............................................................................................................ 214
19 Replacement Procedures............................................................................................................ 218

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Recommended Tools......................................................................................................................... 218
ZS3 Module –Removal/Replacement............................................................................................. 219
Casters –Removal/Replacement.................................................................................................... 223
19” Display – Removal/Replacement.............................................................................................. 224
Display Arm w/Cables –Removal/Replacement........................................................................... 229
Cart Battery –Removal/Replacement............................................................................................. 235
Power Module –Removal/Replacement......................................................................................... 239
User Interface –Removal/Replacement......................................................................................... 244
OLED Assembly (UI Assy) –Removal/Replacement ................................................................... 250
Dock Module - Removal/Replacement............................................................................................ 255
Gas Spring –Removal/Replacement.............................................................................................. 259
20 Parts Catalog.................................................................................................................................. 263
System.................................................................................................................................................. 264
Display.................................................................................................................................................. 264
Accessories......................................................................................................................................... 266
User Interface...................................................................................................................................... 269
Module & Cart Electronics................................................................................................................. 270
Internal Cabling................................................................................................................................... 271
Power Module ..................................................................................................................................... 272
Miscellaneous Cart Items.................................................................................................................. 273
Peripherals........................................................................................................................................... 273
Options and Upgrading Package..................................................................................................... 274
Revision History.................................................................................................................................. 294

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1 Introduction
Mindray/Zonare Contact Information
Asia, Europe and ROW
Address
Mindray Building, Keji 12th Road South, High-tech
industrial park, Nanshan, Shenzhen 518057, P.R.China
E-mail Address
Web site
www.mindray.com
Tel
+86 755 81888998
Fax
+86 755 26582680
United States and Canada
Toll-free live voice support
1-877-913-9663
Live technical support (not toll free)
1-650-316-3199
Technical support by email
Sales support live voice
1-877-966-2731 ext 3
Sales support by email
Web site
www.mindraynorthamerica.com

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Purpose
This manual provides information to assist service personnel in performing
maintenance, and repair procedures that may be required to support ZS3 Ultrasound
System.
The Mindray/Zonare ZS3 Ultrasound System is used for ultrasound evaluation of the
following applications: Opthalmic; Fetal; Abdominal (renal, GYN/Pelvic); Intra-operative
(abdominal, thoracic(cardiac), and vascular); Intraoperative (Neuro); Pediatric; Small
organ (thyroid, breast, testes, etc); Neonatal cephalic; Adult Cephalic/Transcranial; Trans-
rectal; Trans-vaginal; Trans-esoph.(non-Card); Musculoskeletal (Conventional);
Musculoskeletal (Superficial); Cardiac Adult; Cardiac Pediatric; Trans-esoph. (Cardiac);
Intra-cardiac; Peripheral vessel. Users include ultrasound imaging technicians
(sonographers) and physicians. Mindray/Zonare Ultrasound Imaging Systems may be
used in a hospital (e.g., imaging laboratory, emergency room, patient bedside, and
operating room), medical clinic, physician’s office or a mobile imaging center. Please
refer to the ZS3 Instructions For Use for more information.
The ZS3 Ultrasound System consists of two major components: 1) Cart; and, 2)
Transducer(s). The Cart contains the software driven imaging electronics and user
interfaces (keyboard, monitor, handles, etc.). It houses the microprocessor, memory,
amplifiers and power supplies for the microprocessor. It sends electrical currents to and
receives electrical pulses from the compatible transducers. The Cart performs the
calculations involved in processing the data to produce the displayed ultrasound
images. The ZS3 Cart is available in two options: with or without Echocardiography. The
Echocardiography option allows users to perform advanced cardiac and intracardiac
imaging and related functions beyond what is available without the echocardiography
option.
Included with the system are one or more Mindray/Zonare Curvilinear, Endocavity,
Linear, or Phased array transducers allowing for many clinical applications. Accessories
include, but are not limited to the Mindray/Zonare ZPAK Battery and off-the-shelf
components: bar code reader, foot pedal, printers, biopsy guides, ECG cables and a
wireless Ethernet interface. Case studies can be stored to USB memory stick, and other
industry standard archiving devices.
Note: The availability of options may be limited based on country or region of use.
Definitions/Acronyms
2D:................Two dimensional (B-Mode, Color mode)
BMP:.............Bit MaP
C-Mode: .......Color Flow Mode (Doppler)
D-Mode: .......Doppler (Pulsed Wave) Mode
DICOM:.........Digital Imaging and COmmunication in Medicine

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DSP:.............Digital Signal Processing
ESD:.............Electro Static Discharge
EV:................Endo Vaginal
FPGA:...........Field Programmable Gate Array
FRU:.............Field Replaceable Unit
LCD:.............Liquid Crystal Display
LED: .............Light Emitting Diode
M:..................M-Mode (Motion Mode - Tissue)
NTSC:...........National Television Standards Committee (video standard)
PAL: .............Phase Alternation by Line (video standard)
PRF: .............Pulse Repetition Frequency
PW:...............Pulsed Wave Mode (Doppler)
Retrospective:Post-processing performed on frozen images from memory
DGC:.............Depth Gain Compensation
USB:.............Universal Serial Bus

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Documentation Conventions
The following alert conventions are used in this manual:
Symbols
The following symbols may be used in this manual or elsewhere in product labeling.
Symbol
Description
Information that may relate to safety of the patient, the operator, or the equipment
A type BF patient-applied part (B= body, F= floating applied part)
A type CF patient-applied part (C= cardiac, F= floating applied part)
Alternating current (AC)
Direct current (DC)
Date of manufacture
Manufacturer
Caution: ESD sensitive
Recyclable material
V
Voltage
Hz
Cycles per second
Waste Electrical & Electronic Equipment Standard
Applies to EU Member States only: this system should not be treated as household waste.
Mindray meets the WEEE Standard. For more information on returning or recycling this system, please
contact Shenzhen Mindray Bio-Medical Electronics Co. or the distributor from whom you purchased
the system.
Consult the Instructions for Use
Serial number

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Symbol
Description
Authorized representative in the European Community
Catalog number
Shipping & Storage: Fragile
Shipping & Storage: Keep dry
Shipping & Storage: Temperature limits
Shipping & Storage: This side UP
Shipping& Storage: Do not stack above this container
Shipping & Storage: Humidity limits
Shipping & Storage: Pressure limits
Federal law restricts this device to sale by or on the order of a licensed healthcare practitioner (USA).
Protected against water immersion - Immersion for 30 minutes at a depth of 1 meter.

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2 Safety
Facility Needs
Users should prepare for the materials needed in the site, so as to avoid confusion and complete the task
in time without any waste of manpower. Follow the checklist in pre-installation to ensure that the required
steps are performed.
Action
Yes
No
Spare enough time before installing the system
Ensure that the operating environment meets the requirements.
Ensure that the system is fully cooled.
Ensure that you have adjusted the lighting environment to adapt to the
condition of the system.
Ensure that the electrical facilities conform to the standard
requirements.
Ensure that the EMI precautions are performed and all the sources
that might possibly cause unwanted interference are removed.
The system is put in a site according to the requirements.
Ensure that the network condition is set for the system.
Before installation, the users should:
Acquire the needed material.
Prepare for the delivery of the system.
Pay costs incurred for the modifications that are excluded from the sales list.
Note:
This equipment must be operated by skilled/trained clinical professionals.
Before delivering the system, ensure that the operating site is clean. Do not put the
system on a carpet that might attract dust and create static. In addition, the EMI
should also be taken into account during investigation.
It is important for the hospital or organization that employs this equipment to carry
out a reasonable service/maintenance plan. Neglect of this may result in machine
breakdown or personal injury.
Mindray's obligation or liability under this warranty does not include any
transportation or other charges or liability for direct, indirect or consequential
damages or delay resulting from the improper use or application of the product or
the use of parts or accessories not approved by Mindray or repairs by people other
than Mindray authorized personnel.

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Notes When Returning or Transporting the
System, Probes, and Repair Parts
When returning or transporting the ultrasound system in the original packaging, ensure
that:
The ultrasound system should be adjusted to its lowest height and the monitor
should be folded in the down position.
The control panel should be placed in the center and locked.
Note:
When you return the system, ensure that the system is fully decontaminated, and
human fluids or blood are removed from the system, parts or probes. This is to protect
those who transports, receives or opens this package.
The US Department of Transportation (DOT) has ruled that “items that were saturated
and/or dripping with human blood that are now caked with dried blood; or which were
used or intended for use in patient care” are “regulated medical waste” for transportation
purpose and must be transported as a hazardous material.
Warning & Cautions
It is extremely important to read the following definitions of WARNING information, prior
to beginning any service on any sub-system within the system. As you see applicability
of each of these noted WARNINGs, during the course of the servicing process, be
prepared to avoid harm to persons and equipment by proper adherence.
It is not possible to anticipate every condition and situation in which ultrasound system
will be used. The following warnings and cautions represent typical situations that
require special attention. User knowledge and experience with a specific application and
environment must also be taken into consideration in order to help ensure the safety of
personnel and equipment.
Safety Standards
All Mindray instruments, cables, and diagnostic ultrasound imaging transducers have
been designed to meet the essential requirements contained in 93/42/EEC (Medical
Device Directive), and all appropriate requirements contained within IEC 60601 -1,
AAMI STD ES 60601-1, CSA STD C22.2 NO. 60601-1 (Medical electrical equipment -
Part 1: General requirements for basic safety and essential performance), IEC 60601-2-
37 (Medical electrical equipment - Part 2-37: Particular requirements for the safety of
ultrasonic medical diagnostic and monitoring equipment), IEC 60601-1-2 (Medical
electrical equipment - Part 1-2: General requirements for basic safety and essential
performance Collateral Standard: Electromagnetic Compatibility), including limits for

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current leakage and isolation from a primary power line. Testing for compliance with the
essential requirements of the Medical Device Directive has been performed.
Warnings
Do not remove any of the System covers other than the module cover. Other
than the scan module there are no user-serviceable parts internal to the
system. Only trained Mindray/Zonare service personnel should access the
system’s internal electronics.
The ultrasound systems contain no operator-serviceable components within
the enclosures. To avoid electrical shock, do not remove covers. As with any
other electrical equipment, always observe care when operating this
instrument. For service issues, contact Mindray/Zonare Technical Support.
Failure to follow these restrictions may void your warranty or service contract
coverage.
To reduce the risk of electric shock, DO NOT connect the ZS3 system input
or output connections to equipment that is not properly connected to an Earth
ground.
To achieve proper grounding reliability, the ultrasound system power plug
must be fully inserted into a receptacle marked “hospital grade.” Do not
remove the grounding wire. If there is any question of power outlet or power
cord integrity, do not proceed. Obtain qualified assistance
To maintain proper grounding reliability, use only Mindray/Zonare-
recommended peripherals and accessories. Use of non-specified peripherals
and accessories could result in risk of electrical shock or injury.
The ultrasound systems represent a potential explosion hazard if used in the
presence of flammable anesthetics.
The system does not contain a user-serviceable lithium ion battery.
The optional ZPAK cart battery is not a user serviceable item. Contact
Mindray/Zonare’s Technical Support group for assistance with the ZPAK
battery.
Follow guidelines provided by relevant IEC standards) when connecting
peripherals.
The USB Memory Sticks supplied by Mindray/Zonare are the recommended
brand, type, and sizes for use in ZS3 Systems. They have been verified for
optimum reliability and performance.
No modification of the system is permitted. Modifying the system may subject
the operator or patient to hazardous conditions.
The ZS3 ultrasound system represents a potential explosion hazard if used in
the presence of flammable gases or oxygen rich environment.
Use only transducers that are specifically approved for the ultrasound system.
If the proper identification of a connected transducer is not displayed on
screen, do not proceed with its use.
Transducers covers may be contaminated and must be handled accordingly.

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Inspect the transducer and ZS3 System before each use. Inspect the
transducer face, housing, cable, connectors, and cases. Do not use the unit if
damage is detected.
Bent, broken, or missing pins on the transducer connector may cause poor
image quality, including possible mirror image artifact. Be sure to check pins
before connecting transducer to the Mindray/Zonare ultrasound system. If
pins are bent, broken, or missing, do not use the transducer and call
Mindray/Zonare Technical Support.
To avoid electrical shock, always unplug the ultrasound system AC power
cord from wall outlet before cleaning any part. Do not immerse the transducer
past the specified cleaning/disinfection level, as specified in Transducer
Cleaning and Disinfection. Do not immerse the transducer for longer than the
specified cleaning/disinfecting time. Do not use any transducer that has been
immersed beyond the maximum limit or has been soaked longer than the
maximum specified time.
Do not allow disinfectant to contact metal surfaces. Always use protective
eyewear and clothing when cleaning or disinfecting device.
Disinfectant wipes and topical spray products are not FDA cleared high-level
disinfectants and do not provide adequate protection should the transducer
become cross-contaminated.
The transducer must be removed from patient contact before application of a
high-voltage defibrillation.
The system is not intended for use in conjunction with high frequency (HF)
surgical equipment (tissue ablation devices). Do not use transducers
connected to the ultrasound system on patients while HF surgical devices are
in use.
If using relevant standards compliant equipment that was not provided by
Mindray/Zonare, it is required that total leakage currents be tested and
validated to be below the IEC 60601-1 chapter 16 limits.
This equipment must only be connected to a supply main with protective
earth.
Validate that measured and calculated results shown in Calc Package reports
reflect the clinical observations.
Auto-Dop Trace is intended to serve as an adjunct to the diagnostic process
in evaluating blood flow during PW Doppler examinations. When using the
Auto-Dop Trace feature, please evaluate the results to verify that you are in
agreement before committing the values to the Calc Report Package.
Always examine transducers for damage, such as cracks, splitting, holes, or
fluid leaks. If damage is evident, discontinue use of the transducer and
contact Mindray/Zonare.
Prior to initiating any disinfection process, disconnect the transducer from the
ultrasound system.
Ensure that any connected external equipment, such as external monitors,
printers and peripherals, comply with relevant standards such as IEC60601-1
and IEC60601-1-2.

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If an external video monitor is connected to the ZS3 system, it is necessary to
ensure that an RF ferrite is clamped to the cable as close to the ZS3 system
as possible. Use a ferrite such as Fair-Rite Products Corp.
The potential equalization terminal, located by the AC Mains connection, is
connected to the system chassis. It can be connected to corresponding
terminals on other equipment to eliminate potential differences. Do NOT use it
for additional protective grounding.
Damage to the system may cause poor image quality, including possible
imaging artifacts sometimes referred to as ‘halo’ or ‘headlight’
artifacts. Regularly inspect the system for damage and know how to
recognize imaging artifacts.
There are many types of system use and system error messages that might
be displayed during the use of the ZS3 Ultrasound System. If a message is
encountered that is not self-explanatory, contact Mindray/Zonare service for
assistance.
Do not touch any of the connector contacts while performing a patient
examination to prevent the possibility of a hazardous current path.
Warnings - Ocular Imaging
To avoid injury to the patient, use only the Ocular Preset when imaging
through the eye. The FDA has established lower acoustic energy limits for
ophthalmic use. The system will not exceed these limits only if the Ocular
Preset is selected
Warnings –Battery
To avoid electrical shock, do not touch the battery contact.
To avoid risk of fire, explosion, or burns:
Do not disassemble or alter the battery.
Do not short-circuit the battery by directly connecting the positive and
negative terminals with metal objects.
Do not heat or discard the battery in a fire.
Do not expose the battery to temperatures above 60°C (150°F).
Do not charge the battery near a heat source.
Do not leave the battery in direct sunlight.
Do not use a damaged battery.
Charge the battery at room temperature.
Inspect the battery for damage before charging or placing the battery in the
ZS3 System.
Do not connect battery to an electrical power outlet.
Warnings –ECG
The ECG and the Respirometer functionality are not intended for ECG
diagnosis. It must not be used for intraoperative applications of the heart. Use
only the recommended patient cable supplied by Mindray/Zonare. Make sure

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that bare parts of the electrodes and the patient do not come in contact with
conductive parts, such as metal examination beds, trolleys, and similar items.
Before defibrillation, always disconnect the ECG cable connector from the
system and make sure the connector does not come in contact with other
persons or conductive surfaces, such as metal examination beds, trolleys,
and similar items.
Operating your system with ECG signals below 0.25 mV may cause
inaccurate results.
Warnings –TEE Transducer
The multiplane TEE transducer should be used only by a qualified physician
who has received appropriate training in proper operation of the probe and in
endoscopic techniques as dictated by current relevant medical practices.
Electrical Hazard: Any evidence of damage indicates the probe cannot be
used and should be returned to Mindray/Zonare for evaluation and repair.
Biological Hazard: Adequate cleaning and, if necessary, disinfection are
carried out to prevent disease transmission. It is the responsibility of the user
to verify and maintain the effectiveness of the procedure used. A single-use,
sterile disposable sheath for TEE purposes can be used.
Inspect the transducer connector pins for contamination or damaged pins that
might interrupt signal flow through the connection. Be sure to check pins
before connecting transducer to the Mindray/Zonare ultrasound system. If
pins are bent, broken, or missing, do not use the transducer and call
Mindray/Zonare Technical Support.
Immediately replace a transducer that exhibits any damage symptoms.
Before introducing the probe, do not rub or spray the tip of the probe with an
anesthetic agent.
Avoid forceful manipulations and excessive force in using the probe that could
result in patient injury.
Withdraw the probe only with the deflection control in the unlock mode and
with the distal end of the probe straight.
The use of a bite guard is mandatory. Failure to use the bite guard may result
in damage to the probe, which could result in a safety hazard. Damage to the
probe due to biting is not covered by the probe's warranty.
Check if the maximum deflection of the tip is 90°to 120°upward, 60°to 90°
downwards and 30°to 45°left/right. If the deflection shows an unwanted
amount of free play or exceeds the maximal deflection angles given above,
do not use the probe. Contact the service organization to re-adjust the
steering of the probe. In this way, the risk of "buckling" or "U-turning" of the
probe in the esophagus is minimized.
Avoid damage to the probe by allowing nothing to protrude beyond the case
when closing the lid.
Prior to cleaning any device, turn off the system and disconnect power cord
from AC power source to avoid electrical shock.
Always use protective eyewear and clothing when cleaning or disinfecting the
transducers.

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Do not allow the disinfectant to come in contact with metal surfaces
(transducer connector). Use a soft cloth and warm soapy water to remove any
disinfectant that remains on metal surfaces.
Keep the control handle and transducer connector out of any cleaning or
disinfection solutions. The control handle and cable may be cleaned with a
damp cloth, but only the distal end of the probe up to the 100cm marker on
the P8-3 TEE and 70cm marker on the P8-3m TEE shaft may be placed into
a disinfection solution.
Do not use other disinfection methods like Iodine, Steam, Heat or Ethylene
Oxide.
When servicing the ZS3 System, always be sure to turn the circuit breaker to
the OFF position.
Precautions
Transducers are individually licensed according to system configuration. Only
the following transducers are available without an advanced feature
configuration: P9-3ic E9-3, C4-1, C6-2, C6-1, C9-3, C9-3sp, C8-3 3D, C10-3,
C18-5, E9-3 3D, E9-4, L8-3, L10-5, L14-5w, L14-5sp, L20-5, P4-1c, P8-
3mTEE and P8-3TEE. The A2CW and A5CW transducers are enabled if the
system is configured with "CW Enabled", and can be used under either the
Echocardiology (optional) or the Advanced Vascular Imaging (mandate)
mode. Attempting to use any other transducers will result in an error
message.
Be aware of the potential hazards associated with the environment where the
ultrasound systems will be used. The systems and/or the external equipment
can be damaged if signal levels are not appropriate. If peripheral equipment
not specifically authorized by Mindray/Zonare is to be connected to the
system, it must meet all applicable electrical safety standards that apply to the
system in order to maintain Mindray/Zonare’s safety integrity. Any equipment
not supplied by Mindray/Zonare must be approved by Mindray/Zonare. Use of
non-Mindray/Zonare-approved equipment may result in an unsafe condition,
impair operation of the ultrasound system, impair diagnostic capabilities, and
void your warranty or service contract coverage.
Mindray/Zonare transducers have a specific range of acceptable application
use. Users are advised to restrict each transducer’s use to those applications.
Excessive bending, twisting, pulling, dragging, or compression of transducer
cables may cause failure or intermittent operation of the system. Avoid rolling
the cart wheels over cables. Use of cable hooks is recommended to minimize
chance of damage to cables.
If a transducer that has not been approved and licensed for use with the
ultrasound system to which it is connected, or if a licensed transducer is not
properly connected, the corresponding transducer identification data will not
display on the LCD Display. Imaging will be disabled. Resolve this issue
before continuing use.

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The ultrasound system and/or the transducer could be damaged if a non-
approved transducer is connected.
Improper cleaning or disinfection of patient applied parts may cause
permanent damage. Carefully review the manufacturer’s directions for any
component used with Mindray/Zonare ultrasound systems. MINDRAY
assumes no liability with respect to single-use devices that are reused,
reprocessed, or resterilized and makes no warranties, expressed or implied
(including the warranties of merchantability or fitness for a particular use),
with respect to such devices.
Use of peripherals or other equipment not provided by Mindray/Zonare may
result in system damage or degraded performance. Carefully review the
labeling of any such equipment before connecting to the Mindray/Zonare
system.
Improper setting of imaging controls may obscure diagnostically valuable
information in the display. The factory default preset maps were preselected
as appropriate for most imaging circumstances. Improper user configuration
of custom presets may obscure diagnostically valuable information.
Mindray/Zonare ultrasound systems are manufactured in compliance with
existing electromagnetic immunity (EMI) and electromagnetic compatibility
(EMC) requirements. Use of the systems in the presence of an
electromagnetic field can cause degradation of the ultrasound image.
Electrostatic discharge (ESD), or static shock, is a naturally occurring
phenomenon. ESD is common in low humidity, which can be caused by
heating or air conditioning. ESD shock occurs when electrical energy is
discharged from one body, to a differently charged body. To lessen the
occurrence of ESD, use antistatic spray on carpets and flooring, and antistatic
mats.
To minimize potential ESD damage and electrical contact contamination,
avoid touching the metal contacts for the transducer connections, at both the
ZS3 port and the transducer connector.
If the ZS3 System has been moved between environments with extremes of
temperature and/or humidity, allow the ZS3 System to rest for at least 30
minutes in a controlled environment before using.
Do not use the ultrasound system if any error message displays on the
screen.
Do not block airflow to any ventilation holes on the system.
Do not submerge the transducer past the points indicated in ‘Mindray/Zonare
Transducers Cleaning and Disinfection’.
Do not spill liquid on the systems or transducers.
Using a non-recommended cleaning or disinfectant solution, incorrect solution
strength, or immersing the transducer deeper or longer than indicated can
damage the transducer. Damages linked to the use of disapproved chemicals
are not covered under product warranty or service contract.
The use of non-shielded cables may result in increased emissions and
decreased immunity to external signals
Operating the systems in the presence of external electromagnetic fields can
degrade the quality of the ultrasound image. High-frequency devices, such as

ZS3 Service Manual
Page 20 of 295
electro-surgical devices, can produce image artifacts. If required, a review of
the local electromagnetic environment may be required to minimize the
sources of external noise generators.
The use of non-Mindray/Zonare approved cables and accessories may result
in increased radiated emissions as well as decreased immunity to external
signal fields.
Before beginning to image a new patient, be sure to conclude any in-progress
patient exam by pressing the New Patient key. Failure to do so will result in
any subsequent storing of images being mistakenly written to the previous
patient exam directory.
Some components or devices such as transducer covers used with
Mindray/Zonare systems are for single-patient use only. Reuse, reprocessing,
or re-sterilization of these devices may compromise their structural integrity.
Any image sets stored on the system, which are not identified by patient
name and number, will be stored with a unique number based off of the
system ID.
Exercise care in adjusting all settings to avoid obscuring low-level signals that
may have diagnostic value. Improper settings can seriously degrade image
quality.
Do not touch exposed metal of transducer connector.
Validate all entries in the Measurement Summary.
Ultrasound imaging capabilities can vary from patient to patient. Ultrasound
should be used as one component in a comprehensive diagnostic plan.
Never leave a probe in the disinfection solution for more than the specific time
by the disinfection manufacturer. Please refer to the instructions for use that
came with the disinfectant for minimal required exposure times. Do not forget
to rinse the probe directly after disinfection.
Only use water-soluble acoustic coupling gel. Other coupling gels can cause
probe damage.
Long-term exposure to ultrasound should be minimized. Although there have
been no confirmed adverse effects produced by diagnostic levels of
ultrasound, unnecessary patient exposure to ultrasound energy should be
avoided, especially in the Doppler mode.
Use of a non-compatible USB Memory Stick may result in file corruption or
long file transfer times. Please confirm proper operation of any memory stick
prior to attempting to use for clinical data.
Make sure the ZS3 System has fully completed downloading upgrades,
importing/exporting, or collecting log data to the USB Memory Stick before
removing it from the ZS3 System. Failure to do so will result in loss of data.
Review the ZS3 DICOM conformance statement before integrating with any
PACS system.
Validate Structured Report export prior to clinical use.
Use-time from the optional ZS3 battery pack will vary depending on the
system usage and battery conditioning. Ensure the battery is adequately
charged before starting a procedure without AC main power.
Export patient studies in a timely manner. Do not use the system storage as
the sole location of patient studies for an extended period of time.
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