FSN IPS4000 User manual

Before connecting, operating or adjusting this product, please
read this instruction booklet carefully and completely.
English
Image Processing System
Instructions for Use
IPS4000
UHD Modular Video Matrix Switcher and Converter.

211/2022
eIFU indicator
The specications and information in this document are subject to change without notice.
Instructions for Use for this product are also available in electronic form (eIFU). Choose
from several languages. Use Adobe Acrobat software to view eIFUs. Access the eIFUs
online at: fsnmed.com/support/eifu/
Table of Contents
Product Description / Intended Use . . . . . . . . . . . . . . . . . . 3
Symbol Denitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Warnings, Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . 5, 6
Safety Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-9
Electromagnetic Compatibility . . . . . . . . . . . . . . . . . . 10-14
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Sample Conguration . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17, 18
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19-28
Specication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Timing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 30, 31
Mechanical Drawing . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
Cleaning Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . 33

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Product Description / Intended Use
Intended Purpose
This device is intended to be connected to other medical equipment. This device is not intended
for diagnosis. This device is intended to be compatible with other highly specialized surgical and
diagnostic equipment used in surgical suites, operating rooms, emergency rooms, and proce-
dural facilities.
Intended Use Environment
This device is intended to be used by a trained medical professional in a healthcare facility set-
ting where contact with a patient is unlikely (no applied part).
This device is designed to meet the medical safety requirements for a patient vicinity device.
Warning: This device may not be used in connection with life support equipment.
Indications for Use
This device is to be used by a trained medical professional. This device connects to medical imag-
ing equipment to display images, videos or patient information during surgical procedures. This
device is not intended for diagnosis.
The next generation of medical image processing and control is here with IPS4000. FSN has
developed a powerful, yet compact, digital video integration solution that oers compatibility
for today, and tomorrow.
Congurable up to 16 inputs, 32 outputs, IPS4000 features 4096 x 2160 max resolution, signal
options for DisplayPort, HDMI, 12G-SDI, and analog. Users can save and recall custom presets,
choose from multi window layouts including dual (9 types) and quad (6 types). Dashboard inter-
face control can be accessed on the built-in 7 inch diagonal touch screen, or an external screen
via web, tablet or PC.

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eIFU indicator
Symbol Denitions
The following symbols appear on the product, its labeling, or the product packing. Each symbol
carries a special denition, as dened below:
Dangerous : High
Voltage Power adapter Consult accompanying documents
Direct current lndicates equipotential
earth ground Unique Device Identier
Indicates protective
earth ground
Indicates top-bottom
direction Korea Certication
DC Power control
switch Fragile Approved according to the CCC regulations
Do not get wet Maximum Stacking China RoHS labels
Consult the operating
instructions
Indicates the
manufacturer Catalog Number
Indicates the
manufacturing date
Authorized representative in
the European community
Medical Device
Serial Number Humidity limitation Consult the operating
instructions - electronic
Temperature limitation Atmospheric pressure
limitation Importer Entity
UK Conformity Assessed UK Responsible Person
Indicates proof of conformity to EU 2017/745 Medical Devices Regulation and applicable
standards.
Medical Equipment is in accordance with ANSI/AAMI ES60601‐1 (2005) + AMD 1 (2012) and CAN/
CSA‐C22.2 No. 60601‐1 (2014) in regards to electric shock, re hazards, and mechanical hazard.
Tested to comply with FCC Class B standard (USA).
Waste electrical and electronic equipment (WEEE Directive 2012/19/EU). This symbol indicates
that the waste of electronic equipment must not be disposed as unsorted municipal waste and
must be collected separately. Please contact the manufacturer or other authorized disposal
company to decommission your equipment.
Note: A printed copy of the manual in English is provided with the product. Users within EU member states,
please contact local distributor for other languages. This applies to EU member states where the product has
been purchased through authorized channels.

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Warnings and Precautions
Caution Information
CAUTION
RISK OF ELECTRICAL SHOCK
DO NOT OPEN
This symbol alerts the user that important literature concerning the operation of this unit
has been included. Therefore, it should be read carefully in order to avoid potential problems.
This symbol warns users that un-insulated voltage within the unit may have sucient
magnitude to cause electrical shock. Therefore, it is dangerous to make contact with any part
inside the unit. To reduce the risk of electrical shock, DO NOT remove cover (or back). There are
no user-serviceable parts inside. Refer servicing to qualied service personnel.
To prevent re or shock hazards, do not expose this unit to rain or moisture. Do not use this unit’s
polarized plug with an extension cord receptacle or other outlets unless the prongs can be fully
inserted.
Underwriters Laboratories (UL) Classication:
UL safety Compliance:
This device is U.L. Classied WITH RESPECT TO ELECTRIC SHOCK, FIRE AND MECHANICAL
HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1/CAN/CSA C22.2 NO. 601.1
EU Conformity and EMC Compliance:
This device meets the requirements of EN60601-1 and EN60601-1-2 so as to conform to the EU
Medical Devices Regulation (MDR 2017/745). CE class I medical device accessory.
Use 120V rating 5-15P type plug only in the U.S.
Caution: Make sure the power cord is the correct type that is required in your geographic area.
This device has a universal power supply that allows operation in either 100-120V AC or 200-240V
AC voltage areas (no user adjustment is required).

611/2022
Use the proper power cord with correct attachment plug type. If the power source is 120 V AC,
use a power cord which is a Hospital Grade Power Cord with NEMA 5-15 style plug, labeled for
125 volts AC with UL and C-UL approvals. If the power source is a 240 V AC supply, use the tan-
dem (T blade) type attachment plug with ground conductor power cord that meets the respec-
tive European country’s safety regulations.
Recycling (WEEE Directive 2012/19/EU)
Follow local governing ordinances and recycling plans regarding the recycling or disposal of this
equipment.
Warning: Use of this equipment adjacent to or stacked with other equipment should be avoided
because it could result in improper operation. If such use is necessary, this equipment and the
other equipment should be observed to verify that they are operating normally.
Warning: Use of accessories, transducers and cables other than those specied or provided
by the manufacturer of this equipment could result in increased electromagnetic emissions or
decreased electromagnetic immunity of this equipment and result in improper operation.
Warning: Portable RF communications equipment (including peripherals such as antenna cables
and external antennas) should be used no closer than 30 cm (12 inches) to any part of this device,
including cables specied by the manufacturer. Otherwise, degradation of the performance of
this equipment could result.
Warning: Using this equipment in the X-ray or magnetic resonance environment could result in
degradation of the performance of this equipment, interference with other equipment or inter-
ference with radio services.
Warning: The use of cables and/or other accessories with this device, other than those specied,
may result in increased emissions or decreased immunity of this device.
Warning: This product is not considered physically to connect to HF (High Frequency) electrosur-
gical equipment.
Warning: Not suitable for use in the presence of a ammable anesthetics mixture with oxygen or
with nitrous oxide.

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Safety Instructions
On Safety
1. Before connecting the AC power cord to the DC adapter outlet make sure the voltage desig-
nation of the DC adapter corresponds to the local electrical supply.
2. Never insert anything metallic into the cabinet openings of the device. Doing so may create
the danger of electric shock.
3. To reduce the risk of electric shock, do not remove cover. No user-serviceable parts inside.
Only a qualied technician should open the case of the device.
4. Never use the device if the power cord has been damaged. Do not allow anything to rest on the
power cord, and keep the cord away from areas where people can trip over it.
5. Be sure to hold the plug, not the cord,when disconnecting the device power cord from an
electric socket.
6. Unplug the device power cord when it is going to be left unused for an extended period of
time.
7. Unplug the device power cord from the AC outlet before any service.
8. If the device does not operate normally, in particular, if there are any unusual sounds or smells com-
ing from it, unplug it immediately and contact an authorized dealer or service center.
9. Please contact the manufacturer if the set should be installed in an inaccessible area.
Warning: Do not touch input or output connectors and the patient simultaneously.
Warning: This device is intended for connection to input/output signals and other connectors
that comply with relevant IEC standard (e.g.,IEC60950 for IT equipment and IEC60601 series for
medical electrical equipment). In addition, all such combination-system shall comply with the
standard IEC 60601-1-1 or clause 16 of the 3 Ed. of IEC 60601-1, respectively, safety requirements
for medical electrical systems. Any person who has formed a combination-system is responsible
for the system to comply with the requirements of IEC 60601-1-1 or clause 16 of the 3 Ed. of IEC
60601-1, respectively. If in doubt, contact qualied technician or your local representative.
Warning: To avoid risk of electric shock, this device must only be connected to a supply mains
with protective earth. Power supply (AC/DC Adapter) is specied as a part of the device. Do not
position equipment in such a way that it is dicult to disconnect the power cord plug from the
appliance inlet.
Warning: Do not modify this equipment without authorization of the manufacturer.
Product fuse has a lower breaking capacity. Do not install at the building power system, prospec-
tive short-circuit current exceeding 35 A.

811/2022
Environmental Conditions for Operation and Storage
Temperature range within 0°C to 40°C(operation), -20°C to 60°C (storage)
Relative humidity range 10% to 85%
Atmospheric pressure range within 500 to 1060hPa.
On Installation
1. Openings in the device cabinet are provided for ventilation. To prevent overheating, these
openings should not be blocked or covered. If you put the device in a bookcase or some
other enclosed space, be sure to provide adequate ventilation.
2. Do not expose the device to rain or use it near water. If the device accidentally gets wet, un-
plug it and contact an authorized dealer immediately. You can clean the device with a damp
cloth if necessary, but be sure to unplug the device rst.
3. Place your device near an easily accessible AC outlet.
4. High temperature can cause problems. Max operating temperature is 40°C. Don’t use your
device in direct sunlight and keep it away from heaters, stoves, replaces, and sources of
heat.
5. Always use only the original cables and accessories with the device.
Repair
Do not attempt to service the device yourself, as opening or removing covers may expose you
to dangerous voltages or other hazards, and will void the warranty. Refer all servicing to qualied
service personnel. Unplug the device from its power source and refer servicing to qualied
personnel under the following conditions:
- If the power cord or plug is damaged or frayed.
- If liquid has been spilled into the device.
- If objects have fallen into the device.
- If the device has been exposed to rain or moisture.
- If the device has been subjected to excessive shock by being dropped.
- If the cabinet has been damaged.
- If the device seems to be overheated.
- If the device emits smoke or abnormal odor.
- If the device fails to operate in accordance with the operating instructions.

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Biohazards
To prevent spreading of infections, this device should only be used in environments where
biological decontamination can be successfully performed.
Returned Product
After troubleshooting, if problems persist, disinfect the device and return it to FSN using the
original packaging. Include the accessories that came with the device in the return shipment.
Please enclose a brief explanation of the malfunction.
Contact FSN Medical Technologies for a Return Authorization Number and instructions, prior to
returning the device.
Accessories
Use only accessories specied by the manufacturer, or sold with the device.
Classication for Safety Compliance
- Protection against electric shock : Class I including AC/DC adapter. This medical equipment is in
accordance with ANSI/AAMI ES60601‐1 (2005) + AMD 1 (2012) and CAN/CSA‐C22.2 No. 60601‐1
(2014) in regards to electric shock, re hazards, and mechanical hazard.
- Applied Parts : No Applied Parts.
- Degree of safety in the presence of ammable anesthetics mixture with air or with oxygen or
with nitrous oxide. Not suitable for use in the presence of a ammable anesthetics mixture with
oxygen or with nitrous oxide.
- For critical applications, it is recommended to have a replacement device available.
- Mode of operation : Continuous.
Notice to the user:
Any serious incident that has occurred in relation to the device should be reported to the manu-
facturer and the competent authority of the Member State in which the user and/or patient is
established. Contact your local FSN Medical Technologies sales representative for information on
changes and new products.

10 11/2022
This unit has been designed and tested to comply with IEC 60601-1-2:2014/AMD1:2020 require-
ments for EMC with other devices. To ensure electromagnetic compatibility (EMC), the device
must be installed and operated according to the EMC information provided in this Instructions
for Use.
This unit has been tested and found to comply with the limits of a Class B digital device, pursuant
to Part 15 of the FCC rules. These limits are designed to provide reasonable protection against
interference. This device can radiate radio frequency energy and, if not installed and used in
accordance with the instructions, it may interfere with other radio communications equipment.
There is no guarantee that interference will not occur in a particular installation. If this equipment
is found to cause harmful interference to radio or television reception, the user is encouraged to
try to correct the interference by carrying out one or more of the following measures:
1. Reorient or relocate the receiving antenna.
2. Increase the distance between the device and the subject of interference.
3. Plug the device into an outlet on a dierent electrical circuit than that to which the subject of
interference is connected.
4. Consult the dealer or an experienced radio/TV technician for help.
NOTICES TO USER
This device complies with part 15 of the FCC Rules. Operation is subject to the following two
conditions: (1) this device may not cause harmful interference, and (2) this device must accept
any interference received, including interference that may cause undesired operation.
FCC WARNING
This device generates or uses radio frequency energy. Changes or modications to this device
may cause harmful interference unless the modications are expressly approved in the instruc-
tion manual. The user could lose authority to operate this equipment if an unauthorized change
or modication is made.
PRODUCT LIFETIME
The performance of this device may deteriorate over long periods of time. Periodically check that
this device is operating correctly. The expected service life of the device is four years. Keep the
clean clean to prolong its operational lifetime.
Electromagnetic Compatibility

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1. Guidance and manufacturer’s declaration - electromagnetic emission
The device is intended for use in the electromagnetic environment specied below. The user of the device
should make sure that the device is operated in such an environment.
Interference emission measurements Conformity level Electromagnetic environment -guidance
RF emissions acc. to CISPR 11 Complies with Group 1 The characteristics of this device determined
by broadcasting permit its industrial and
hospital use (CISPR 11, Class A). When used in a
living area (for which CISPR 11 usually requires
Class B), this device may not provide adequate
protection of radio services. The user must, if
necessary, take remedial action such as imple-
mentation or reorientation of the device.
RF emissions acc. to CISPR 11 Complies with Class B
Emission of harmonic oscilla-
tions acc. to IEC 61000-3-2 Complies with Class A
Voltage uctuations/icker
emissions acc. to IEC 61000-3-3 Complies
2. For the use of ME devices in professional healthcare facilities.
Guidance and manufacturer’s declaration - electromagnetic immunity
The device is intended for use in the electromagnetic environment specied below.
The user of the device should make sure that it is used in such an environment.
Interference
immunity test
IEC 60601-1-2:2014 con-
formity level
Electromagnetic environment-guidance
Electrostatic
discharge (ESD)
acc. to
IEC 61000-4-2
Complies ±2 kV, ±4 kV, ±6
kV, ± 8 kV contact discharge
±2 kV, ±4 kV, ±8 kV,
± 15 kV air discharge
Floors should be made of wood, concrete or ceramic tile.
If oors are covered with synthetic material, the relative
humidity must be at least 30%
Rapid transient elec-
tric interferences/
bursts acc. to
IEC 61000-4-4
Complies
± 2 kV for mains lines
± 1 kV for input/output lines
The quality of the supply voltage should correspond to
that of a typical business or hospital environment.
Surge acc. to
IEC 61000-4-5
Complies
± 1 kV push-pull voltage
± 2 kV common-mode
voltage
The quality of the supply voltage should correspond to
that of a typical business or hospital environment.
Voltage dips, short
interruptions and
uctuations of the
supply acc. to
IEC 61000-4-11
0 % UT*; 0.5 cycle
At 0°, 45°, 90°, 135°, 180°,
225°, 270°, 315°
0% UT; 1 cycle and
70% UT; 25/30 cycles
Single phase: at 0°
0% UT; 250/300 cycle
Mains power quality should be that of a typical commer-
cial or hospital environment.
If the user of the device requests continued functioning
even when interruptions of the power supply occur, it is
recommended that the device be supplied from a power
supply that is free of interruptions.
*Note: UTis the mains alternating voltage before applying the test levels.

12 11/2022
3. For the use of ME devices in professional healthcare facilities.
Test specication for ENCLOSURE PORT IMMUNITY to RF wireless communica-
tions equipment (according to IEC 60601-1-2:2014)
The device is intended for use in the electromagnetic environment specied below.
The user of the device should make sure that it is used in such an environment.
Test fre-
quency
MHz
Band
MHz Service
Modulation
Maximum
power
W
Distance
m
IMMUNITY
TEST LEVEL
V/m
385 380 to 390 TETRA 400 Pulse modulation
18 Hz 1.8 1.0 27
450 430 to 470 GMRS 460,
FRS 460
FM
± 5 kHz stroke
± 1 kHz sine wave
2 1.0 28
710
704 to 787 Band 13, 17 Pulse modulation
217 Hz 0.2 1.0 9745
780
810
800 to 960
GSM 800/900
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
Pulse modulation
18 Hz 2 1.0 28870
930
1720
1700 to
1990
GSM 1800,
CDMA 1900,
GSM 1900,
DECT,
LTE Band 1,3,
4, 25 UMTS
Pulse modulation
217 Hz 2 1.0 281845
1970
2450 2400 to
2570
Bluetooth,
WLAN 802.11
b/g/n,
RFID 2450,
LTE Band 7
Pulse modulation
217 Hz 2 1.0 28
5240
5100 to
5800
WLAN 802.11
a/n
Pulse modulation
217 Hz 0.2 1.0 95500
5785
*Note: If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting antenna
and the device may be reduced to 1 m. The 1 m test distance is permitted by IEC 61000-4-3.

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4. Guidance and manufacturer’s declaration – electromagnetic immunity – for
equipment and systems that are not life-supporting
The device is intended for use in the electromagnetic environment specied below.
The user of the device should make sure that it is used in such an environment.
Interference
immunity tests
IEC 60601-1-
2:2014 test level
Conformity
level
Electromagnetic environment – guidelines
Conducted RF
disturbances
acc. to
IEC 61000-4-6
Radiated RF
disturbances
according to
IEC 61 000·4·3
3 V rms
150 kHz to
< 80 MHz
3 V/m
80 MHz to
2.5 GHz
3 V e
3 V/m
Portable and mobile RF communications equip-
ment should be used no closer to any part of the
device, including cables, than the recommended
separation distance calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance:
d = 1.2 P
Where P is the nominal power of the transmitter in
watts [W] according to the information provided
by the manufacturer of the transmitter and d is the
recommended separation distance in meters [m].
The eld strength of stationary transmitters at all
frequencies on site a should be, according to a
study, less than the conformity level b.
d = 1.2 P
80 MHz to < 800 MHz
d = 2.3 P
800 MHz to 2.5 GHz
Interference may occur in the vicinity of equipment
marked with the following symbol:
Note: These guidelines may not apply in all situations. The propagation of electromagnetic quantities is
aected by absorptions and reections of buildings, objects, and persons.
aField strengths from xed transmitters, such as base stations for radio [cellular/cordless] telephones and
land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theoretically with accuracy. To assess the electromagnetic environment of the stationary transmitters, a
site survey should be considered. If the measured eld strength in the location at which the device is used
exceeds the above conformity levels, the device should be observed to verify normal operation. If unusual
performance characteristics are observed, additional measures may be necessary, such as a modied
orientation or a dierent location for the device.
bOver the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3 V/m.

14 11/2022
5. Recommended separation distances between portable and mobile RF
communications equipment and the device
The device is intended for use in the electromagnetic environment in which the RF disturbances are con-
trolled. The user of the device can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the device – as a
function of the output power of the communication device, as shown below.
Nominal power of
transmitter [W]
Separation distanced [m] according to frequency of transmitter
150kHz to< 80 MHz
d = 1.2 P
80 MHz to< 800 MHz
d = 1.2 P
800 MHz to 2.5 GHz
d = 2.3 P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation dis-
tance din meters (m) can be estimated using the equation applicable to the frequency of the transmitter,
where Pis the maximum output power rating of the transmitter in watts (W) according to the transmitter
manufacturer.

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1
3
2
7
5
4
6
Accessories IPS4000
Item Description Pack Qty
1 Carton Box 1
2 Cushion
3
3 IPS4000 Unit 1
4 HDMI Cable 1
5 AC power Cord (6ft, Medical Grade) 1
6 Instructions For Use 1
7 Rack Mount Brackets 2

16 11/2022
IPS4000 Sample System Conguration
HDMI 2.0
DP 1.2
12G SDI
Analog (option)
Input
Up to 4096 x 2160 resolution.
Up to 16 inputs, 32 outputs.
Output
Multi window layouts.
Streaming.
IPS4000
Multi window layout options.
Interface Control
Dashboard is accessed on the built-
in 7 inch diagonal touchscreen, or
an external touchscreen or tablet.

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IN OUT
1 2 3 4
1
MONITOR
OUTPUT
INPUT SLOT 1-4 OUTPUT SLOT 5-8 OUTPUT SLOT 9-12
RS-232 UART AS
2
3
4
5
6
7
8
9
10
11
12
AUDIO
1
2
3
4
I
O
Connections
Up to 4 input slots available. Up to 8 output slots available.
Input Output Output
* Scaled output. Adjustments available for resolu-
tion, window layout, zoom, pan functions.
IPS4000 is designed for modular conguration. Various combinations of input and output cards
can be assembled at the factory. Not all IPS4000 units will look the same.
Following are descriptions of IPS4000 input and output cards and their unique functions.
HDMI quad input
card.
Name: HDIN
HDMI 1 HDMI 2 HDMI 3 HDMI 4
HDIN
DisplayPort quad
input card.
Name: DPIN
DP 1 DP 2 DP 3 DP 4
DPIN
Dual HDMI, dual
DisplayPort input
card.
Name: DHIN
HDMI 1 HDMI 2 DP 1 DP 2
DHIN
Analog input
card.
Name: ANIN
CVBS 1 CVBS 2 VGA 1 VGA 2 ANIN
12G SDI input
card.
Name: SDIN INPUT OUTPUT INPUT OUTPUT
12G-SDI 1 12G-SDI 2
SDIN
HDMI quad
output card.
Name: HQOUT
HDMI 1 HDMI 2 HDMI 3 HDMI 4
HQOUT
DisplayPort quad
output card.
Name: DQOUT
DP 1 DP 2 DP 3 DP 4
DQOUT
HDMI (scalable)*
output card.
Name: HDOUT
HDMI
RS-232
HDOUT
DisplayPort
(scalable)*
output card.
Name: DPOUT
RS-232 DP
DPOUT
12G SDI
(scalable)*
output card.
Name: SDOUT
12G-SDI 2
RS-232
SDOUT

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IN OUT
1
1
MONITOR
OUTPUT
INPUT SLOT 1-4 O
RS-232 UART AS
2
3
4
5
6
7
8
AUDIO
1
2
3
4
I
O
IN OUT
1 2 3 4
1
MONITOR
OUTPUT
INPUT SLOT 1-4 OUTPUT SLOT 5-8 OUTPUT SLOT 9-12
RS-232 UART AS
2
3
4
5
6
7
8
9
10
11
12
AUDIO
1
2
3
4
I
O
Connections
Connect Power
Only use the specied plug and voltage. Power requirements are: AC 100~240V / 50~60Hz ,
2A(max). Use the supplied 6 ft. hospital grade AC power cord. Improper power may cause electric
shock or equipment damage. To avoid the risk of electric shock, this equipment must only be
connected to a power supply with protective grounding.
Earth terminal
AC Inlet
AC On/O Switch
USB (USB 3.0)
Service port (Mini USB, A/S)
UART (Mini USB, Console terminal)
RS-232 (Dsub9)
Ethernet Ports (RJ45)
Audio in / out (3.5Ø phone)
Monitor output (HDMI 1.4 1080p@60)
Item Description
Earth terminal A direct physical connection to ground or earth.
USB Connects a keyboard, mouse, or memory stick, or rmware updating.
Service port For factory use.
UART Use for serial communication with other devices.
RS-232 Use for serial communication with other devices.
Monitor output Connects an external web or PC screen for interface viewing and controlling.
Ethernet ports For network streaming.
Audio in / out Connects audio.

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1
INPUT SLOT 1-4
RS-232 UART AS
2
3
4
1
2
I
O
Starting IPS4000
Powering O IPS4000
1. Turn on power using the AC
switch on the back of IPS4000.
2. The power button on the front
will illuminate green.
Press the power button, and a dialog will appear.
Press Power O or Cancel. After powering
o, the green light will stay on unless power is
turned o on the back of IPS4000.
3. Press the power button to turn on IPS4000. The green light will
ash during initialization, then go dark when the system is ready.

20 11/2022
Dashboard
Input source list.
After IPS4000 has initalized, the interface control dashboard will appear on the built-in 7 inch
diagonal touch screen, or a connected external screen (tablet or PC).
Swipe up or down to show more
of any list on the dashboard.
Output destination list. Setup
Streaming on/o
indicator.
Active layout. Routed source.
User preset
control.
Routed sources for
multi-window layouts.