Arthrex AR-3200-0021, AR-3210-0022, AR-3210-0018, AR-3210-0021, AR-3210-0023 Service Manual
...
950-0073-00, Rev. B English
Synergy
UHD4
System
Service Manual
AR-3200-0020
AR-3200-0021
AR-3210-0018
AR-3210-0021
AR-3210-0022
AR-3210-0023
AR-3210-0025
AR-3210-0026
AR-3210-0028
AR-3210-0029
AR-3210-0030
The Arthrex Synergy
UHD4
System Camera Control Unit and
Camera Head Service Manual provides important information
for the safe operation and service of all components of the
Synergy
UHD4
Camera System, including accessories. Read
this Service Manual thoroughly prior to using this system and
keep it in an easily accessible place for use by all operating
personnel. Read and follow all safety warnings, cautions and
precautions.
Arthrex, Inc.
1370 Creekside Blvd.
Naples, FL 34108, USA
+1 (800) 934-4404
Technical Support
1-888-420-9393
EC
REP
Arthrex GmbH
Erwin-Hielscher-Strasse 9
81249 München, Germany
+49 89 909005-0
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 1 of 74
This is not a warranty document. For all warranty information, including disclaimers,
exclusions, terms, conditions and related provisions, refer to the "Arthrex U.S. Product
Warranty" section of the Arthrex, Inc. website, found at www.arthrex.com whose
provisions are incorporated herein by reference.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 2 of 74
Table of Contents
1.0 Introduction 5
1.1 Intended Use ................................................................................................................................. 5
1.2 Contraindications .......................................................................................................................... 5
1.3 Warnings and Precautions ............................................................................................................ 5
1.4 Symbol Definitions ...................................................................................................................... 11
1.5 End of Life, Environmental Directives ......................................................................................... 13
1.6 Initial Use of the Device .............................................................................................................. 13
1.7 Unpacking and Inspecting the Device ......................................................................................... 14
1.8 Returning the Device .................................................................................................................. 14
1.9 System Indicators ........................................................................................................................ 15
2.0 System Installation and Operation with Data Input Device 20
2.1 Installation .................................................................................................................................. 20
2.2 Accessories for Intended Use ...................................................................................................... 22
2.3 System Setup Facility and Surgeon Settings ............................................................................... 24
2.4 Scheduling and Starting Cases .................................................................................................... 33
2.5 System Operation without Tablet Data Input Device ................................................................. 40
3.0 Theory of Operation 42
3.1 SCOPE .......................................................................................................................................... 43
3.2 GENERAL DESIGN GOALS ............................................................................................................ 43
3.3 CAMERA CONTROL UNIT ............................................................................................................. 44
3.4 MOTHERBOARD .......................................................................................................................... 46
3.5 ISOLATION BOARD ...................................................................................................................... 46
3.6 CAMERA HEAD ............................................................................................................................ 47
3.7 PROGRAMMING .......................................................................................................................... 49
4.0 Maintenance 50
4.1 Life Expectancy............................................................................................................................ 50
4.2 Periodic Maintenance ................................................................................................................. 50
4.3 Cleaning and Sterilizing ............................................................................................................... 50
4.4 Troubleshooting .......................................................................................................................... 54
4.5 Recommended Annual Camera Control Unit Maintenance Requirements ............................... 56
4.6 Replacement of the Lithium Battery ........................................................................................... 56
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 3 of 74
5.0 Troubleshooting (Tests) 57
5.1 Procedure .................................................................................................................................... 57
6.0 Technical Information 61
7.0 APPENDIX [Radio Module Information] 66
8.0 APPENDIX [Detailed EMC Information] 67
9.0 APPENDIX [SW Version access] 72
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 4 of 74
1.0 Introduction
WARNING: The safety and/or health of
the patient, user, or a third party are at
risk. Comply with this warning to avoid
injury to the patient, user, or third party.
PRECAUTION: This contains
information concerning the intended
use of the device or accessory.
Damage to the equipment is possible if
these instructions are not followed.
It is recommended that personnel study this
manual before attempting to operate, clean,
troubleshoot and/or sterilize the Arthrex
Synergy
safe and effective use of this equipment
requires the understanding of and
UHD4
System and accessories. The
This system is designed for use by
physicians and surgeons and is intended for
endoscopic camera use in a variety of
endoscopic surgical procedures, including
but not limited to, orthopedic, laparoscopic,
urologic, sinuscopic and plastic surgical
procedures. It is also intended to be used as
an accessory for microscopic surgery.
compliance with all warnings, precautionary
notices, and instructions marked on the
product, and included in this manual.
The Arthrex Synergy
UHD4
System is
comprised of:
AR-3200-0020 [Synergy
with Matrix]
AR-3200-0021 [Synergy
UHD4
UHD4
Console
Console]
1.2 Contraindications
Do not use the device if endoscopic surgery
is contraindicated.
Do not use the device if the environmental
conditions for use do not meet the standards
or regulations defined in the accompanying
documents.
1.3 Warnings and Precautions
AR-3210-0018 [HD, SynergyUHD4
Camera Head, autoclavable]
AR-3210-0021 [HD SynergyUHD4 C-
Mount Camera Head, autoclavable]
AR-3210-0022 [HD SynergyUHD4 C-
Mount Camera Head, 0 Degree,
autoclavable]
The words WARNING, PRECAUTION, and
NOTE carry special meanings and they should
be read carefully.
AR-3210-0023 [4K SynergyUHD4
Camera Head, autoclavable]
AR-3210-0025 [4K SynergyUHD4 C-
Mount Camera Head, autoclavable]
AR-3210-0026 [4K SynergyUHD4 C-
Mount Camera Head, 0 Degree,
autoclavable]
AR-3210-0028 [4K SynergyUHD4 C-
Mount w/20 foot cable, autoclavable]
AR-3210-0029 [4K SynergyUHD4
Broadband Camera Head, Autoclavable]
AR-3210-0030 [4K SynergyUHD4 C-
mount Broadband Camera Head,
Autoclavable]
NOTE: the AR-3200-0020 Synergy
Console is identical to the AR-3200-0021
except that the AR-3200-0020 Synergy
incorporates the Matrix PWA for transmission
of UHD4 data by fiber optic.
1.1 Intended Use
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 5 of 74
UHD4
UHD4
NOTE: A note is added to provide additional,
focused, information.
1.3.1 WARNINGS
This equipment is designed for use
by medical professionals completely
familiar with the required techniques
and instructions for use of the
equipment. Prior to using the device,
read and follow all warning and
precautionary notices and
instructions marked on the product
and included in this manual. Become
familiar with the operation and
function of this device and
associated accessories. Failure to
follow these instructions can lead to:
Life-threatening injuries to the patient
Severe injuries to the surgical team,
nursing or service personnel, or
Damage or malfunction of the device
or accessories.
1. Do not open or attempt to service this
system, as this may void your warranty.
There are no user-serviceable parts inside.
Removing the cover may introduce an
electric shock hazard by exposing you
to dangerous high voltages or other
risks. If the system malfunctions,
return it for service immediately.
2. For the protection of the patient it is
recommended that a back-up camera
system for the Arthrex Synergy
system be maintained, sterilized, and ready
to be implemented.
3. For the protection of the patient it is essential
that the endoscopic video system
interconnection is complete and produces a
viable color picture on the surgical monitor
PRIOR to administration of patient
anesthesia.
4. Disconnect camera head and endoscope
from the patient prior to applying cardiac
defibrillation to patient.
5. Only the physician can evaluate the clinical
factors involved with each patient and
determine if the use of this device is
indicated. The physician must determine the
specific technique and procedure that will
accomplish the desired clinical effect.
UHD4
video
6. This device and its accessories are to be
used only by physicians and medical
assistants under the direction of a physician
with appropriate technical qualifications.
7. This device shall only be used with original
and manufacturer’s accessories and
replacement parts. Use of other parts or
materials may degrade safety.
8. Do not use in the presence of
flammable anesthetics, gases,
disinfecting agents, cleaning
solutions, or any material susceptible to
ignition due to electrical sparking.
9. Equipment grounding is vital for safe
operation. Plug the power cord into a properly
earthed mains supply outlet whose voltage
and frequency characteristics are compatible
with those listed on the unit or in this manual.
Do not use plug adapters or extension cords;
such devices defeat the safety ground and
could cause injury.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 6 of 74
10. This equipment should not share an
electrical outlet or grounding with life
supporting or life sustaining equipment.
11. If one or more mains powered units are
connected simultaneously to one socket
by the means of a distribution box, the
sum of the individual leakage currents
may exceed the tolerated limits.
12. Before each use, the outer surface of
the portions of the Endoscope and any
Endoscopically Used Accessory, which
are intended to be inserted into the
patient, should be checked to ensure
there are no unintended rough edges,
sharp edges or protrusions which may
cause a safety hazard.
13. Safety hazards to patients may result
from gas embolism caused by, for
example, over-insufflation of air or inert
gas prior to high frequency surgery or
laser assist gas.
14. The leakage current through the patient
could increase using endoscopes with
powered accessories.
15. When Endoscopes are used with
Energized Endoscopically Used
Accessories, the Patient Leakage
Currents may be additive. This is
particularly true if a CF Applied Part is
used, in which case a Type CF
Endoscopically Used Accessory should
be used to minimize total Patient
Leakage Current.
16. Explosive gas concentrations inside the
patient can cause hazards while using
High-Frequency Endoscopically Used
Accessories.
17. For the protection of service personnel,
and for safety during transportation, all
devices and accessories that are
returned for repair must be prepared for
shipment as described in “Returning
the Device” of this manual. The
manufacturer has the right to refuse to
carry out repairs if the product is
contaminated.
18. This equipment/system is intended for
use by healthcare professionals only.
This equipment/system may cause radio
interference or may disrupt the
operation of nearby equipment. It may
be necessary to take mitigation
measures, such as re-orienting or
relocating the Synergy
UHD4
Video
System or shielding the location.
19. NOT for use in an Oxygen Rich
Environment.
20. Applied Parts of other ME Equipment
used within the configuration for
Endoscopic Application shall be type BF
or CF Applied Parts.
21. NO Modifications of this equipment is
allowed.
22. Connecting any equipment that has not
been supplied as part of this ME System
to Multiple Socket Outlets may result in
increased leakage currents. Use an IEC
Approved Isolation Transformer to
isolate any such interconnections from
the ME System.
23. Before each use or after changing
viewing modes/settings the Operator
should check to ensure that the view
observed through the Endoscope
provides a live image (rather than a
stored one) and has the correct image
orientation.
24. Risk of burns!
Light sources emit large amounts of light
energy and thermal energy. As a result:
The scope light guide tip can get
extremely hot as result of high intensity
light, giving rise to high temperatures in
front of the light emission window which
may cause severe burns. Always keep
the light source in the STANDBY mode
when not in use.
Surface temperatures of the insertion
portion of the endoscope as well as light
guide connectors on the Camera
Control Unit (CCU) and the endoscope
rise during use. This can cause the
temperature of the body tissue to rise to
106 °F (41°C).
Potential Thermal injury to the patient’s
tissue (e.g. from prolonged exposure to
the intense illumination in small cavities,
or if the endoscope’s distal end is
placed in close proximity with the tissue)
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 7 of 74
may result, as well as burns to the
patient’s or user’s skin. Burns or thermal
damage to surgical equipment may also
result.
Avoid prolonged exposure to intense
illumination.
Use the minimum level of illumination
necessary to satisfactorily illuminate the
target area.
Do not place the endoscope’s distal end
or light guide connector on the patient’s
skin, on flammable materials or on heat
sensitive materials.
Turn the light source off when detaching
the endoscope from the light guide
cable.
Allow the endoscope and light guide
cable to cool down after use.
25. High Frequency [HF] electrical surgical
instruments may lead to severe patient
injuries and/or damage to the endoscope.
Please take caution to insure that the working
element is kept within field of view to prevent
accidental burns. A sufficient distance from
the tip of the endoscope to other conductive
accessories and instruments should be
maintained (10 mm) before activating the HF
output to prevent burns and damage to the
endoscope. Refer to the HF Surgical Device
Instructions for proper and safe use.
26. HF surgical Instruments may interfere with
video images. To prevent such interference,
HF equipment and video imaging equipment
should be connected to different power
supply circuits.
27. Use of Lasers in surgery may result in Eye
Damage or damage to the endoscope from
reflected laser energy. Refer to the Laser
Device Instructions for proper and safe use.
When using a laser always wear
protective glasses designed for the
laser’s wavelength.
Cover the patient’s eyes, or use
protective glasses designed for the
laser’s wavelength.
To prevent damage to the
Endoscope, the Laser should be
activated only after the tip of the laser
can be seen thought the endoscope.
28. To ensure FCC RF Exposure limits for base
station transmissions devices is met, a
distance of 20 cm or more shall be
maintained between the Camera Control Unit
(which contains the antennas), and persons
during operation. To ensure compliance, an
operator closer than 20cm to Camera Control
Unit is not recommended.
1.3.2 PRECAUTIONS
1. United States Federal law restricts sale of
this device to or on the order of a physician.
2. Do not use the camera with incompatible
equipment or accessories that are not
authorized by Arthrex. Doing so may void
certifications and/or warranties.
3. The warranty becomes void and the
manufacturer is not liable for direct or
resulting damage if:
The device or the accessories are
improperly used, prepared or
maintained;
The instructions in the manual are not
adhered to;
Non-authorized persons perform
repairs, adjustments or alterations to the
device
Non-authorized persons open the
device.
NOTE: Receipt of technical documentation
from the manufacturer does not authorize
individuals to perform repairs, adjustments,
or alterations to the device or accessories.
Only authorized service personnel may
perform repairs, adjustments or alterations
on the device and accessories. Any violation
will void the manufacturer’s warranty.
Authorized service technicians are trained
and certified only by the manufacturer. The
Manufacturer will make available on request
circuit diagrams, component part lists,
descriptions, calibration instructions and
other information required for service to any
Arthrex Authorized Service Center.
4. This device should only be used in
compliance with its intended use.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 8 of 74
5. Prior to each use, the CCU and all
associated equipment must be inspected for
proper operation. Visually inspect lenses to
assure there are no scratches, chips or
cracks.
6. To carry out safe operation, it is absolutely
necessary to carry out proper care and
maintenance of the device and accessories.
See “Maintenance” section of this manual.
7. Ensure that the available mains voltage
matches the mains voltage data on the rear
of the device which is located near the
appliance inlet module.
8. This device may only be connected to
endoscopes which, in their intended use and
technical specifications, are appropriate for
use with the device for the intended medical
procedure. The endoscopes must comply
with the latest version of DIN EN 60601-2-18
and ISO 8600.
9. This equipment has been tested and found
to comply with Class A limits of EN 60601-12:2002. These limits are designed to provide
reasonable protection against harmful
interference in a typical medical installation.
However, if interference does occur with
other equipment, it may be corrected by one
or more of the following measures;
Reorient or relocate this equipment,
the other equipment, or both;
Increase the distance between the
different pieces of equipment;
Consult a biomedical engineer.
10. Do not expose the Camera Control Unit
[CCU] to moisture, or operate it in a wet
area, or store liquids above the CCU.
11. Do not excessively bend or kink instrument
power cord or camera head cable.
12. Handle all equipment carefully. If the CCU or
camera head is dropped or damaged in any
way, return it immediately for service.
13. If the camera head or camera head cable
are damaged in any way, or cable or
connector jacket are cut, do not autoclave
camera head, or immerse camera head in
liquid (water, chemical disinfectants or
sterilants, etc.). Notify your Arthrex Sales
Representative. If it is necessary to return
the camera head to Arthrex for service,
disinfect the camera head before shipping
and reference “Returning the Device”.
14. Store camera head and all accessories in a
protective container to prevent damage
during storage. Do not store CCU where it
will be exposed to temperatures in excess of
140°F (+ 60°C).
15. Additional equipment connected to medical
electrical equipment must comply with the
respective IEC or ISO standards (e.g. 60950
for data processing equipment).
Furthermore all configurations shall comply
with the requirements for medical electrical
systems (see IEC 60601-1 or clause 16 or
the 3rd edition of IEC 60601-1, respectively).
Anybody connecting additional equipment to
medical electrical equipment configures a
medical system and is therefore responsible
that the system complies with the
requirements for medical electrical systems.
Attention is drawn to the fact that local laws
take priority over the above mentioned
requirements. If in doubt, consult your local
representative, or the technical department.
16. Any person who connects external
equipment to signal input and signal output
ports or other connectors has formed a
system and is therefore responsible for the
system to comply with the requirements of
IEC 60601-1-1. If in doubt, contact a
qualified Biomedical technician or your local
representative.
17. This equipment has been tested and found
to comply with the Class A limits for medical
devices to the EN 60601-1 and EN60601-12:2002. These limits are designed to provide
reasonable protection against harmful
interference in a typical medical installation.
This equipment generates and can radiate
radio frequency energy and, if not installed
and used in accordance with the
instructions, may cause harmful interference
to other device(s) in the vicinity. However,
there is no guarantee that interference will
not occur in a particular installation. If this
equipment does cause harmful interference
to other devices, which can be determined
by turning the equipment off and on, the
user is encouraged to try to correct the
interference by one or more of the following
measures:
(a) Reorient or relocate the receiving
device.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 9 of 74
(b) Increase the separation between the
equipment.
(c) Connect the equipment into an outlet on
a circuit different from that to which the
other devices are connected.
(d) Consult the manufacturer or field service
technician for help.
This unit was not evaluated for use with
electrosurgical devices which access the
site via the same endoscope as the light
source and camera. The unit must be reevaluated prior to use with electrosurgical
devices when they will operate through the
same endoscope as the light source and
camera.
18. After each use, thoroughly clean unit and
accessories (See “Cleaning and
Sterilizing”).
NOTES:
1. Observe all national waste management
regulations.
2. Do not dispose of WEEE as unsorted
municipal waste.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 10 of 74
1.4 Symbol Definitions
Safety Sign
Follow Operating
Instructions
Caution: Federal
Law Restricts
this device to
sale by or on the
order of a
Physician.
Power Standby/On
Not for use in the
Presence of
Flammable
Anesthetics.
ON-OFF
Push-Push
USB Tablet
Computer
Connection
Attention, Consult
Accompanying
Documents
Fragile
Precaution of
Warning Notice
This Side Up
Defibrillation Proof
Type CF Equipment
Keep Dry
Electrical Hazard,
Dangerous Voltages
are Present. Never
attempt to repair the
equipment. Only
Trained Service
Personnel may
remove the cover, or
obtain access to
system
components.
Temperature
Limits for
Storage and
Transport
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 11 of 74
Alternating Current
Pressure Limits
for Storage and
Transport
Protective Earth
[Ground]
Humidity Limits
for Storage and
Transport
Equipotential
[Equipment
Potential]
Universal Serial
Bus
WEEE [Waste
Electronics and
Electrical
Equipment] Symbol.
Regarding European
Union End-of-Life of
Product.
RF Symbol. Non-
ionizing
Electromagnetic
Radiation
White Balance
Symbol
Color Video
Camera
LED Light
Do Not Use if
Damaged
MFi
Made for iPad
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 12 of 74
1.5 End of Life, Environmental
Directives
WEEE Directive [2002/96/EC] on Waste
Electrical and Electronic Equipment
The Directive on Waste Electrical and Electronic
Equipment obliges manufacturers, importers,
and/or distributors of electronic equipment to
provide for recycling of the electronic equipment
at the end of its useful life.
Do not dispose of WEEE in unsorted municipal
waste.
The WEEE symbol on the product or its
packaging indicates that this product must not
be disposed of with other waste. Instead, it is
your responsibility to dispose of your waste
equipment by handing it over to a designated
collection point for the recycling of Waste
Electrical and Electronic Equipment. The
separate collection and recycling of your waste
equipment at the time of disposal will help
conserve natural resources and ensure that it is
recycled in a manner that protects human health
and the environment. For more information
about where you can drop off your medical
endoscopic video equipment at the end of its
useful life for recycling, please contact Arthrex
Customer Service Department.
The Camera Control Unit (CCU)
contains a Lithium Coin BATTERY. The
BATTERY must be recycled or disposed
of properly.
NOTE for State of California, USA:
State of California Requirement: Lithium
Batteries contain Perchlorate Material -special
handling may apply. See
www.dtsc.ca.gov/HazardousWaste/Perchlorate
In the US a list of recyclers in your area can be
found at www.eiae.org/
1.6 Initial Use of the Device
WARNINGS:
1. The device is only completely isolated
from the mains if the power plug is
disconnected from the device’s power
inlet module. Avoid positioning
equipment such that removal of plug is
difficult.
2. The electrical installation of the operating
room where the device is used must
comply with applicable national
requirements.
3. Loss of the Mains Voltage may result in
an unacceptable risk due to loss of
Clinical Function. An Uninterruptable
Power Supply [UPS] is recommended to
mitigate this risk.
4. The device is not intended for use in
areas of explosion hazards. If explosive
nitrous gases are used the Camera
Control Unit may not be operated in the
danger zone.
5. Do not simultaneously touch the Camera
Control Unit and the patient. Camera
Control Unit is intended to be used
outside the Patient Vicinity.
6. Additional peripheral equipment
connected as part of the Endoscopic
Video System must meet the
requirements of the following
specifications:
EN 60950 for Information Technology
Equipment.
EN 60601-2-18 for endoscopic
devices.
EN 60601-1 for electro medical
devices.
7. All final Endoscopic Video Systems must
meet the requirements of EN 60601-1-1.
8. Whoever connects additional equipment
to signal input or signal output is
obligated to meet the requirements of the
EN 60601-1-1 standard.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 13 of 74
CAUTION: Do not install the device
in a location near heat sources such
as air ducts or radiators and do not
expose the device to direct sunlight,
excessive dust, or mechanical vibration.
1.7 Unpacking and Inspecting the
Device
Upon receipt, carefully unpack the Synergy
Controller Unit (CCU) and accessories. Ensure
contents are complete and are free from
damage. If any damage is noted contact your
Arthrex Customer Service. Contact the
Manufacturer for Return Authorization PRIOR to
shipping your device for service. Save ALL
packaging materials; they may be needed to
verify any claims of damage by the shipper.
UHD4
1.8 Returning the Device
If it becomes necessary to return the device,
always use the original packaging. The
manufacturer does not take responsibility for
damage that has occurred during transportation
if the damage was caused by inadequate
transport packaging. Please make sure that all
required information has been supplied. Call
Arthrex for a RMA Number for the device return
for service.
Owner’s Name
Owner’s Address
Owner’s Daytime Telephone Number
Device type and model.
Serial Number
Detailed explanation of the damage.
NOTE:
1. The CCU shall be cleaned per section
Cleaning and Sterilization prior to returning
for service.
2. The Camera Head shall be cleaned and
Sterilized per Cleaning and Sterilization prior
to returning for service. Camera Head shall
be clearly labeled as “Sterile.”
Equipment will not be repaired unless
decontaminated as stated above prior to return
to the manufacturer.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 14 of 74
Figure 1 - Synergy
UHD4
Front Panel [AR-3200-002x]
1.9 System Indicators
1.9.1 Synergy
1. On/Standby Switch-The On/Standby switch
toggles the Camera Control Unit (CCU)
between ON [operational mode] and
STANDBY. The Green LED will illuminate
when the CCU is in the ON mode. Press
and HOLD the switch to toggle between ON
and STANDBY.
2. Light Guide Turret-Turret for Light Guide
input
UHD4
Front Panel
Wolf Input
Storz Input
ACMI Input
Olympus Input
NOTE: Rotate Light Guide Turret until the
appropriate port is aligned with LED
INDICATOR then Insert
Light Guide.
3. USB Port-Connect USB devices here.
4. iPad USB Port-Connect iPad to this port.
5. “WHITE BALANCE” Button-Press to
initiate camera white balance.
6. “CAMERA” Input Connection-Insert the
camera head connector here. The camera
head connector and receptacle are specially
keyed to prevent the camera head from
being improperly connected. Ensure that the
“UP” label on the camera head connector is
facing upwards when the camera head
connector is inserted.
PRECAUTION: Ensure camera head
contacts are clean and dry and cool 15
minutes prior to insertion.
7. Light Source On/Standby Switch-The
Light Source On/Standby Switch toggles the
Light Source between ON [Operational
Mode] and STANDBY.
PRECAUTION:
Use only FUSED Light Guides to ensure
proper operation of LED Engine.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 15 of 74
Figure 2 - Synergy
UHD4
Rear Panel
1.9.2 Rear Panel
1. “DVI” Video Output Connectors-Supplies a
digital video signal output in DVI-D format.
2. Display Ports (2X)-Supplies UHD Video
Signal output in either 1.1 [dual cable] or 1.2
[MST].
NOTE: Arthrex recommends connecting
Synergy
UHD4
to the primary surgical monitor
via multiple output types (e.g., display port
and DVI, Synergy Matrix and 3G-SDI) in the
event that one type of connection is lost.
3. Audio In / Audio Out-Audio In: Line Level
Audio input for Microphone. Audio Out: Line
Level Audio output to Medical Grade Devices.
4. RS-232 Connector-Isolated connection to
devices requiring Serial Control.
5. DVI Input-1080P/60 Input for Picture in
Picture [PIP].
6. USB 2.0 (2X)-USB 2.0 Connection.
7. USB 3.0 (2X)-USB 3.0 Connection.
8. Accessory Ports (Inputs/Outputs (2X) mini
Stereo-Phone Connectors)-Accessory ports
allow for control of the CCU with a footswitch
or external device or for the CCU to control
external devices via the camera head buttons.
9. Tablet Connection-Connection for Tablet
Data Input device. Provides for data
interchange and tablet charging
10. Synergy Matrix [Synergy Matrix Only]-Fiber
Optic output to Matrix Monitor (point to point
or managed) via Custom SFP+ Fiber
Transceivers. Use Output 1 and 2 for 4K
Video. Custom SFP+ Fiber Transceivers and
Matrix License may be obtained from Arthrex
Customer Service.
11. 3G-SDI Out-1080P/60 Output.
12. Ethernet Connector-Isolated 10/100 Mb/sec.
13. Potential Equalization Connector (POAG)Potential Equalization Connector per DIN
42801.
NOTE: The purpose of the Potential
Equalization Connector is to equalize the
potentials between different metal parts of the
various Medical Electrical [ME] equipment
which make up a Medical Electrical system, or
to reduce differences of potential which can
occur during operation between the bodies of
the Medical Electrical devices and conductive
parts of other objects. The Potential
Equalization Connector may be connected
directly between any ME Devices, or to a
common busbar of the electrical installation.
Reference IEC 60601-1 for ME Systems.
14. IEC 320 Power Inlet Module (100-240V~,
50/60 Hz)-The CCU is equipped with a
switching power supply that automatically
adjusts to the line voltage being used.
Accepts the supplied hospital grade power
cord.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 16 of 74
Figure 3 - AR-3210-0023 4K SynergyUHD4 Camera Head, autoclavable
Figure 4 - AR-3210-0029 HD, SynergyUHD4 Broadband Camera Head, autoclavable
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 17 of 74
Figure 5- AR-3210-0018 HD, SynergyUHD4 Camera Head, autoclavable
1.9.3 Camera Heads with Integrated Optics
1. Button 1 A programmable button that
can activate various functions of the
camera. See “Optional Tablet Data Input
Device” for programming information.
2. Button 2 A programmable button that
can activate various functions of the
camera. See “Optional Tablet Data Input
Device” for programming information.
3. Focus Ring Used to sharpen, or bring
into focus, the image detail.
4. Grasping Mechanism Accepts and
locks into place the compatible scope.
DIN 58105 compliant endoscope
interface.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 18 of 74
Figure 6 - AR-3210-0025 [4K SynergyUHD4 C-Mount Camera Head, autoclavable], AR-3210-0028 [4K
SynergyUHD4 C-Mount w/20 foot cable, autoclavable] and
Not Pictured AR-3210-0026 [4K SynergyUHD4 C-Mount Camera Head, 0 Degree, autoclavable]
Figure 7 - AR-3210-0021 [HD SynergyUHD4 C-Mount Camera Head, autoclavable], and Not Pictured AR-
3210-0022 [HD SynergyUHD4 C-Mount Camera Head, 0 Degree, autoclavable]
1.9.4 C-Mount Camera Heads
1. Button 1 A programmable button that
can activate various functions of the
camera. See “Optional Tablet Data Input
Device” for programming information.
15. Button 2 A programmable button that
can activate various functions of the
camera. See “Optional Tablet Data Input
Device” for programming information.
16. C-Mount Threads Accepts standard CMount Optical Couplers.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 19 of 74
2.0 System Installation
and Operation with
Data Input Device
2.1 Installation
NOTE:
1. Your Synergy
indicate which software configuration is
enabled at boot up on the Video Monitor’s
Splash screen.
2.1.1 Typical System Installation
NOTE: See Typical Interconnect Diagram,
Figure .
NOTE: Synergy
tower or on an equipment boom.
1. Place Synergy
(CCU) on tower shelf or installed on
equipment boom.
2. Attach monitor to the tower or equipment
boom and connect monitor DC power cable
to the rear panel of the monitor as shown.
3. Attach Synergy
secondary tower arm or equipment boom.
Connect the cable from the Data Input
Device to the connector labeled “tablet” on
the back of the Synergy
4. Connect a Display Port cable to a Display
Port output on the rear panel of the
Synergy
of the Display Port cable to the Display Port
input of the display monitor. (3G-SDI or DVI
UHD4
Camera Control Unit will
UHD4
may be installed in a
UHD4
Camera Control Unit
UHD4
Data Input Device to
UHD4
CCU.
UHD4
CCU. Connect the other end
cables may be used instead of Display Port
cables.) Note: Arthrex recommends
connecting Synergy
UHD4
CCU to the primary
surgical monitor via multiple output types
(e.g., Display Port and DVI, Display Port and
3G-SDI) in the event that one type of
connection is lost.
5. If using a printer, connect the printer cable to
the USB connector on the rear panel of the
Synergy
UHD4
CCU. Connect the other end
of printer cable to the printer.
6. Plug the AC power cord into the
Synergy
UHD4
power inlet module and a
standard grounded AC Mains outlet (100240 V˜, 50-60Hz).
7. Insert the card edge connector of the
Synergy
UHD4
camera head into the camera
receptacle on the front of the CCU.
NOTE: Ensure the camera head connector
contacts are clean and dry prior to
insertion.
8. Connect the Light Guide cable into the Light
Guide receptacle on the front panel of the
Synergy
UHD4
CCU. Attach the other end of
the Light Guide cable to the endoscope.
10. Insert the endoscope into the Synergy
UHD4
camera head grasping mechanism or into
the C-Mount Adapter for C-Mount Heads.
11. Press the Light Source On/Standby Switch
to activate the LED light engine.
NOTE: If there is no Light Guide cable
connected to the Synergy
UHD4
CCU,
pressing the On/Standby Switch will not
activate the LED light engine until one is
connected.
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 20 of 74
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 21 of 74
Figure 8 - Synergy
UHD4
Typical Interconnect Diagram With OPTIONAL Tablet Data Input Device
[Integrated Optics Heads]
Figure 9 - Synergy
UHD4
Typical Interconnect Diagram [C-MT Heads]
Arthrex Synergy
UHD4
System Accessories
Part Number
Description
AR-3250-XXXX
Arthrex Monitors
SONY UP-PR80MD
SONY UP-PR80MD with UP-
DR80MD/NKIT
Medical Grade Printers
AR-3350-XXXX
AR-3351-XXXX
AR-3355-XXXX
Arthrex Arthroscopes
Arthrex Laparoscopes
Arthrex C-Mount Arthroscopes
AR-3200-1006
Tablet Computer Data Input Device
AR-3200-1026, -1027
AR-3200-1020
AR-3200-1030, -1034
BioOptico Licenses
DICOM Licenses
Synergy.net Licenses
2.2 Accessories for Intended Use
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 22 of 74
Arthrex Synergy
UHD4
System Accessories
Part Number
Description
AR-3210-XXXX
AR-3200-1010, -1012
AR-3200-1040
AR-3370-0006
Arthrex C-mount couplers
Arthrex encrypted USB sticks
Arthrex Pump/Shaver Kit
Arthrex Starfish
AR-3201-1005
Video Input-Output 1080P Converter
AR-3240-XXXX
Arthrex Light Guides
950-0073-00 B SM, English, Arthrex Synergy UHD4 System 23 of 74
Loading...