FSN FS-Y1901D User manual

Before connecting, operating or adjusting this product, please
read this instruction booklet carefully and completely.
English
FHD Monitor
Instructions for Use
FS-Y1901D
FS-E2101D
FS-E2101DT
FS-L2403D
FS-P2404D
FS-P2603D
FS-P2604D
FS-L2702D
FS-L2702DT
FS-L3202D

28/2021
eIFU indicator
Table of Contents
Product Description / Intended Use . . . . . . . . . . . . . . . . . . 3
Symbol Denitions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Safety Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Warnings and Precautions . . . . . . . . . . . . . . . . . . . . . . . . 7
Electromagnetic Compatibility . . . . . . . . . . . . . . . . . . . . 10
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15, 16
Connections and Mechanical Drawings . . . . . . . . . . . . . 17-20
Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
On Screen Display (OSD) . . . . . . . . . . . . . . . . . . . . . . 22-26
Standard Signal Tables. . . . . . . . . . . . . . . . . . . . . . . . 27-30
General Specications . . . . . . . . . . . . . . . . . . . . . . . . 31-41
Cleaning Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . 42
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/

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8/2021
Product Description / Intended Use
This product from FSN Medical Technologies is a high-end surgical display monitor designed for
advanced digital OR applications. This medical display is uniquely equipped to handle tasks in
the demanding operating room environment. Performance characteristics include:
• Rapid signal detection, robust mode tables
• Artifact-free images
• Fanless - sterile eld compatible
• Calibrated to clinical color
• Image pan, zoom, freeze, picture-in-picture
Intended Purpose
This device is intended to be connected to other medical equipment, and to display images or
videos from endoscopic cameras, room cameras, and patient information such as ultrasound,
cardiology, and anesthesiology. This device is not intended for diagnosis. This device is intended
to be compatible with other highly specialized surgical and diagnostic equipment used in surgi-
cal suites, operating rooms, emergency rooms, and procedural 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 to display images from procedures,
such as endoscopy, ultrasound, cardiology, and anesthesiology. This device connects to medical
imaging equipment to display images, videos or patient information during surgical procedures.
This device is not intended for diagnosis.

48/2021
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
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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8/2021
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 medical LCD monitor is U.L. Classied WITH RESPECT TO ELECTRIC SHOCK, FIRE AND ME-
CHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1/CAN/CSA C22.2 NO. 601.1
EU Conformity and EMC Compliance:
This medical LCD monitor unit 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 acces-
sory.
This medical LCD monitor complies to the above standards only when used with the supplied
medical grade power supply. Use 120V rating 5-15P type plug only in the U.S.
JMW190KB1200F04 ATM065T-P120 ATM090-P240 BM120S24F02 BPM150S24F10 ATM160T-P240
FS-Y1901D FS-E2101D
FS-E2101DT
FS-L2403D FS-P2404D FS-P2603D
FS-L3202D
FS-P2604D
FS-L2702D
FS-L2702DT
Caution: Make sure the power cord is the correct type that is required in your geographic area.
This medical LCD monitor has a universal power supply that allows operation in either 100-120V
AC or 200-240V AC voltage areas (no user adjustment is required).

68/2021
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.
A ground post, located on the back of the display, may be used for the purpose of grounding
the display’s chassis. Any such ground must be installed in accordance with applicable electrical
codes. The ground post is shown on the mechanical drawing found in this instructions for use.
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 medi-
cal LCD monitor, 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.

7
8/2021
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 medical LCD monitor. 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 medical LCD monitor.
4. Never use your medical LCD monitor 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 medical LCD monitor power
cord from an electric socket.
6. Unplug your medical LCD monitor power cord when it is going to be left unused for an ex-
tended period of time.
7. Unplug your medical LCD monitor power cord from the AC outlet before any service.
8.
If your medical LCD monitor does not operate normally, in particular, if there are any unusual sounds
or smells coming 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 medical LCD monitor 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 re-
quirements 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 equipment must only be connected to a supply
mains with protective earth. Power supply (AC/DC Adapter) is specied as a part of the LCD Color
Display. 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.

88/2021
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 medical LCD monitor cabinet are provided for ventilation. To prevent over-
heating, these openings should not be blocked or covered. If you put the medical LCD moni-
tor in a bookcase or some other enclosed space, be sure to provide adequate ventilation.
2. Do not expose the medical LCD monitor to rain or use it near water. If the medical LCD moni-
tor accidentally gets wet, unplug it and contact an authorized dealer immediately. You can
clean the medical LCD monitor with a damp cloth if necessary, but be sure to unplug the
medical LCD monitor rst.
3. Place your medical LCD monitor near an easily accessible AC outlet.
4. High temperature can cause problems. Max operating temperature is 40°C. Don’t use your
medical LCD monitor in direct sunlight and keep it away from heaters, stoves, replaces,and
sources of heat.
5. Don’t place your medical LCD Monitor on an unstable stand, Medical LCD monitor may mal-
function or fall.
6. This medical LCD monitor should not topple over when tilted at a 5° angle, in any position,
during NORMAL USE, excluding transport.
7. In the position specied for transport, medical LCD monitor shall not overbalance when tilted
at a 10 degree angle.
8. When carrying this product, please use both handles (if included) on the left and right side of
the product, and carry using two people. If you want the product to be installed in another
place, please call your service center.
9. Always use only the original cables and accessories with the device.
10. Do not lay this monitor on other equipment.

9
8/2021
Repair
Do not attempt to service the medical LCD monitor 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 medical LCD monitor 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 medical LCD monitor.
- If objects have fallen into the medical LCD monitor.
- If the medical LCD monitor has been exposed to rain or moisture.
- If the medical LCD monitor has been subjected to excessive shock by being dropped.
- If the cabinet has been damaged.
- If the medical LCD monitor seems to be overheated.
- If the medical LCD monitor emits smoke or abnormal odor.
- If the medical LCD monitor fails to operate in accordance with the operating instructions.
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 monitor and return it to FSN using the
original packaging. Include the accessories that came with the monitor 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 medical LCD monitor.
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 monitor 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 8/2021
This medical monitor unit has been designed and tested to comply with IEC 60601-1-2:2014/
AMD1:2020 requirements for EMC with other devices. To ensure electromagnetic compatibility
(EMC), the monitor must be installed and operated according to the EMC information provided in
this Instructions for Use.
This medical monitor 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 pro-
tection against interference. This monitor 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 medical LCD monitor and the subject of interference.
3. Plug the monitor 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 medical LCD monitor generates or uses radio frequency energy. Changes or modications
to this medical LCD monitor may cause harmful interference unless the modications are ex-
pressly approved in the instruction manual. The user could lose authority to operate this equip-
ment if an unauthorized change or modication is made.
PRODUCT LIFETIME
The performance of LCD panels may deteriorate over long periods of time. Periodically check that
this monitor is operating correctly. The expected service life of the device is four years. Keep the
monitor clean to prolong its operational lifetime.
Electromagnetic Compatibility

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1. Guidance and manufacturer’s declaration - electromagnetic emission
The medical LCD monitor is intended for use in the electromagnetic environment specied below. The user
of the device should make sure that the medical LCD monitor 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 medical LCD monitor is intended for use in the electromagnetic environment specied below.
The user of the medical LCD monitor 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 8/2021
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 medical LCD monitor is intended for use in the electromagnetic environment specied below.
The user of the medical LCD monitor 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 medical LCD monitor may be reduced to 1 m. The 1 m test distance is permitted by IEC 61000-4-3.

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8/2021
4. Guidance and manufacturer’s declaration – electromagnetic immunity – for
equipment and systems that are not life-supporting
The medical LCD monitor is intended for use in the electromagnetic environment specied below.
The user of the medical LCD monitor 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
medical LCD monitor, 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 8/2021
5. Recommended separation distances between portable and mobile RF
communications equipment and the medical LCD monitor
The medical LCD monitor is intended for use in the electromagnetic environment in which the RF distur-
bances are controlled. The user of the device can help prevent electromagnetic interference by maintai-
ning 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.
Monitor Maximum DC Extension Cable Length* (feet)
FS-P2404D, FS-P2603D, FS-P2604D, FS-L2702D,
FS-L2702DT, FS-L3202D 75
FS-L2403D 33
FS-Y1901D, FS-E2101D, FS-E2101DT 25
* If longer extension is used, there is a risk of abnormal operation of the product.
Connecting the Power Supply
Power input on
back of monitor.
AC-DC
adaptor.
AC power.

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8/2021
FS-Y1901D 1, 2

FS-E2101D 7
 
FS-E2101DT 6, 7
 
FS-L2403D 2, 3

FS-P2404D 1, 4

* US,UK,EU, China. Hospital grade.
1 D-SUB cable available for purchase.
2S-Video cable available for purchase.
3RS-232C cable available for purchase.
4
DC cable terminal male/female available for purchase.
5Remote control.
6USB cable, 8.2ft/2.5m.
7DVI to HDMI cable.
Accessories
Item IFU
AC-DC
Adaptor
6.23ft/1.9m
AC Power
Cord
6ft/1.8m*
DVI-D Cable
6ft/1.8m
BNC Cable
6ft/1.8m
Mounting
Screws

16 8/2021
FS-P2604D 1, 4

FS-P2603D 4

FS-L2702D 4

FS-L2702DT 4, 6

FS-L3202D 4, 5

Accessories
Item IFU
AC-DC
Adaptor
6.23ft/1.9m
AC Power
Cord
6ft/1.8m
DVI-D Cable
6ft/1.8m
BNC Cable
6ft/1.8m
Mounting
Screws
* US,UK,EU, China. Hospital grade.
1 D-SUB cable available for purchase.
2S-Video cable available for purchase.
3RS-232C cable available for purchase.
4
DC cable terminal male/female available for purchase.
5Remote control.
6USB cable, 8.2ft/2.5m.
7DVI to HDMI cable.

17
8/2021
395 mm / 15.55 in.
423 / 16.65
76.5 / 3.0
31 / 1.22
100
3.94
4-M4
VESA MOUNT
HOLES
351.5
13.84
203
8.0
88.5
3.48
60
2.36
GROUND DC IN RS-232C GPIO VGA IN
USB
(Touchscreen) DVI IN
SDI
IN
SDI
OUT
GROUND DC IN RS-232C GPIO VGA IN DVI IN
SDI
IN
SDI
OUT
FS-E2101D, FS-E2101DT
FS-E2101D
FS-E2101DT
125
4.92
100
3.94
4-M4
VESA MOUNT
HOLES
100 / 3.94
527.9 mm / 20.78 in.
57.9 / 2.28
334.5
13.17
29.9
1.18
FS-Y1901D

18 8/2021
FS-P2404D
FS-L2403D
565.9 mm / 22.28 in.
85 / 3.35
520.4 / 20.49
326
12.83
378.4
14.90
100 / 3.94
100
3.94
GROUND S-VIDEO
3G SDI
IN
VGA
IN
DVI
IN
3G SDI
OUT
DC IN C-VIDEO RS-232C
DVI 2 IN
(fiber optional)
575.4 mm / 22.66 in.
82 / 3.23
392
15.43
171.5
6.75
35.7
1.41
100
3.94
4-M4
VESA MOUNT
HOLES
100 / 3.94

19
8/2021
FS-P2604D
FS-P2603D
DVI 2 IN
(fiber optional)
640 mm / 25.20 in.
78 / 3.07
402
15.83
31.7
1.25
171.2
6.74
100
3.94
100 / 3.94
8-M4
VESA MOUNT
HOLES 200 / 7.87
668 mm / 26.3 in.
421
16.57
88.8 / 3.5
100 / 3.94
39.5
1.56

20 8/2021
FS-L3202D
FS-L2702D, FS-L2702DT
770 mm / 30.31 in.
702 mm / 27.64 in.
80.5 / 3.17
141.5
5.57
35.5
1.40
100
3.94
12-M4
VESA MOUNT HOLES
4-M6
VESA MOUNT
HOLES
200
7.87
100 / 3.94
200 / 7.87
300 / 11.81
400 / 15.75
471.5
18.56
396.4
15.60
ON/OFF RS232C GPIO
DVI 2
IN
DVI 1
IN
DVI 1
OUT
5V
OUT 2
DC IN R/Pr
G/Y
B/Pb
C/S VGA 5V
OUT 1
IN OUT
SDI
GROUND USB (touch) GPIO
R/Pr
G/Y
B/Pb
C/S IN OUT
SDI
425
16.73
673 mm / 26.5 in.
75.2
2.96
44.6
1.76
100
3.94
8-M4
VESA MOUNT
HOLES
100
3.94
200 7.87
187.3
7.37
FS-L2702D FS-L2702DT