Air Techniques SensorX User manual

EN-
US
SensorX
Installation and Operating Instructions
2121100020L29
*2121100020L29*
G95012101V007

Contents
Important information
1About this document .. . . . . . . . . . . . . 3
1.1 Warnings and symbols .. . . . . . . 3
1.2 Copyright information .. . . . . . . . 4
2 Safety .. . . . . . . . . . . . . . . . . . . . . . . . . 5
2.1 Intended use (FDA) .. . . . . . . . . . 5
2.2 General safety information .. . . . . 5
2.3 Specialist personnel .. . . . . . . . . 5
2.4 Protection from electric shock .. . 5
2.5 Essential performance charac-
teristics .. . . . . . . . . . . . . . . . . . . 6
2.6 Notification requirement of seri-
ous incidents .. . . . . . . . . . . . . . . 6
2.7 Only use genuine parts .. . . . . . . 6
2.8 Transport .. . . . . . . . . . . . . . . . . . 7
2.9 Disposal .. . . . . . . . . . . . . . . . . . 7
2.10 Protection from cybersecurity
threats .. . . . . . . . . . . . . . . . . . . . 7
Product description
3Overview .. . . . . . . . . . . . . . . . . . . . . . . 8
3.1 Scope of delivery .. . . . . . . . . . . . 8
3.2 Accessories .. . . . . . . . . . . . . . . . 8
3.3 Optional items .. . . . . . . . . . . . . . 8
3.4 Consumables .. . . . . . . . . . . . . . 9
4Technical data .. . . . . . . . . . . . . . . . . . . 10
4.1 SensorX Size #1 .. . . . . . . . . . . . 10
4.2 SensorX Size #2 .. . . . . . . . . . . . 11
4.3 Electromagnetic compatibility
(EMC) .. . . . . . . . . . . . . . . . . . . . 11
4.4 Ambient conditions .. . . . . . . . . . 13
4.5 Model identification plate .. . . . . . 14
5 Function .. . . . . . . . . . . . . . . . . . . . . . . 14
Installation
6Requirements .. . . . . . . . . . . . . . . . . . . 15
6.1 Installation/setup room .. . . . . . . 15
6.2 Monitor .. . . . . . . . . . . . . . . . . . . 15
6.3 System requirements .. . . . . . . . . 16
7 Installation .. . . . . . . . . . . . . . . . . . . . . . 17
7.1 Fitting the sensor holder .. . . . . . 17
7.2 Electrical connection .. . . . . . . . . 17
7.3 Installation with VisionX .. . . . . . . 18
7.4 Installation with DBSWIN .. . . . . . 18
8Commissioning and first start-up .. . . 19
8.1 Configuring the unit in VisionX .. . 19
8.2 Configuring the unit in DBSWIN .. 20
8.3 Commissioning tests .. . . . . . . . . 22
Usage
9Operation .. . . . . . . . . . . . . . . . . . . . . . 24
9.1 Taking an X-ray image .. . . . . . . . 24
10 Cleaning and disinfection .. . . . . . . . . . 25
10.1 Clean and disinfect the accesso-
ries .. . . . . . . . . . . . . . . . . . . . . . 26
11 Reprocessing .. . . . . . . . . . . . . . . . . . . 26
11.1 Risk analysis and classification .. 26
11.2 Reprocessing procedures .. . . . . 26
11.3 General information .. . . . . . . . . . 27
11.4 Preparation at the operating
location .. . . . . . . . . . . . . . . . . . . 27
11.5 Manual cleaning, disinfection
and drying .. . . . . . . . . . . . . . . . . 28
12 Maintenance .. . . . . . . . . . . . . . . . . . . . 29
Troubleshooting
13 Tips for operators and service techni-
cians .. . . . . . . . . . . . . . . . . . . . . . . . . . 30
13.1 Poor X-ray image .. . . . . . . . . . . 30
13.2 Software error .. . . . . . . . . . . . . . 30
Contents
2121100020L29 2101V007 1
EN-
US

Appendix
14 Recommended exposure times .. . . . . 32
15 Handover record .. . . . . . . . . . . . . . . . . 33
Contents
2 2121100020L29 2101V007
EN-
US

Important information
1 About this document
These installation and operating instructions are
an integral part of the unit.
Air Techniques shall not be held liable and
offers no guarantees of the safe and
smooth operation of this unit if you fail to
comply with notes and instructions con-
tained in these Installation and Operating
Instructions.
The German version of the installation and oper-
ating instructions is the original manual. All other
languages are translations of the original manual.
These operating instructions are valid for the fol-
lowing SensorX versions:
Item number:
– G9510A (2121100021)
– G9520A (2121100022)
1.1 Warnings and symbols
Warnings
The warning notes in this document highlight
possible injury to persons or damage to machi-
nery.
They are marked with the following warning sym-
bols:
General warning symbol
The warnings are structured as follows:
SIGNAL WORD
Description of type and source of
danger
Here you will find the possible conse-
quences of ignoring the warning
❯Follow these measures to avoid the
danger.
The signal word differentiates between different
levels of danger:
–DANGER
Direct danger of severe injury or death
–WARNING
Possible danger of severe injury or death
–CAUTION
Risk of minor injuries
–NOTICE
Risk of extensive material/property damage
Important information
2121100020L29 2101V007 3
EN-
US

Miscellaneous symbols
These symbols are used in the document and on
or in the unit:
Note, e.g. specific instructions regarding
the efficient use of the unit.
Part number
Serial number
Medical device
Health Industry Bar Code (HIBC)
EC REP
Authorized EU representative
Manufacturer
Date of manufacture
Dispose of correctly in accordance with
EU Directive 2012/19/EU (WEEE).
Take note of the accompanying electronic
documents.
Refer to Operating Instructions.
Wear hand protection.
Use a mask.
Wear eye protection.
Wear protective clothing.
Do not reuse
Protection class II
Type BF applied part
XX
YY
Lower and upper temperature limits
XX
YY
Lower and upper atmospheric pressure
limits
no condensation
XX
YY
Lower and upper humidity limits
1.2 Copyright information
All electronic drawings, processes, names, soft-
ware, and appliances mentioned here are pro-
tected under copyright.
Printing or copying these Installation and Operat-
ing Instructions, including excerpts thereof, may
only be carried out with the written approval of
Air Techniques.
Important information
4 2121100020L29 2101V007
EN-
US

2 Safety
The unit has been developed and designed
appropriately such that hazards are largely
excluded if the unit is used in accordance with its
Intended use.
Therefore, please note the following.
Despite this, the following residual risks can
remain:
– Personal injury due to incorrect use/misuse
– Personal injury due to mechanical effects
– Personal injury due to electric shock
– Personal injury due to radiation
– Personal injury due to fire
– Personal injury due to thermal effects on the
skin
– Personal injury due to lack of hygiene, e.g.
infection
2.1 Intended use (FDA)
Indications for use
The intraoral sensor is intended to convert X-ray
photons into electronic impulses that may be
stored, viewed and manipulated for diagnostic
use by dentists.
Intended use (FDA)
The intraoral sensor is used to generate intraoral
X-ray images in conjunction with an intraoral X-
ray unit. Hygienic protective covers must be
used.
Only those accessories or parts specifically men-
tioned in the Installation and Operating Instruc-
tions may be used with the device.
The device must only be cleaned and disinfected
using the disinfectants and cleaning agents that
are listed in the Installation an Operating Instruc-
tions.
Improper use
Any other usage or usage beyond this scope is
deemed to be improper. The manufacturer
accepts no liability for damage resulting from
improper usage. In such cases, the user/operator
will bear the sole risk.
The intraoral sensor is not suitable for monitoring
patients over a long-term period.
2.2 General safety information
The sale or prescription of this device by a
medical practitioner is subject to the restrictions
of the applicable Federal Acts. The device may
be used only under permanent supervision by a
dentist or licensed medical practitioner.
Caution: Federal law restricts this device
to sale by or on the order of a Doctor.
❯Comply with the guidelines, laws, rules and
regulations applicable at the site of operation
when you use this unit.
❯Prior to each use, check the function and
proper condition of the device.
❯Do not convert or modify the unit.
❯Comply with the Installation and Operating
Instructions.
❯Make the Installation and Operating Instruc-
tions always available to the operator in the
vicinity of the device.
2.3 Specialist personnel
Operation
Persons operating the unit must ensure safe and
correct handling based on their training and
knowledge.
❯Instruct or have every user instructed in han-
dling the unit.
Units for commercial use may not be oper-
ated or used by:
– People lacking the necessary experience and
knowledge
– People with reduced physical, sensory or men-
tal capabilities
– Children
Installation and repairs
❯All installation, resetting, alteration, expansion,
and repair work must be carried out either by
Air Techniques personnel or by a suitably quali-
fied person approved by Air Techniques.
2.4 Protection from electric
shock
❯Working on the unit, comply with all the rele-
vant electrical safety regulations.
❯Never touch the patient and unshielded plug
connections or metallic parts of the device at
the same time.
Important information
2121100020L29 2101V007 5
EN-
US

❯Immediately replace any damaged cables or
plugs.
Comply with the EMC rules concerning
medical devices
❯The unit is intended for use in professional
healthcare facilities (in accordance with IEC
60601-1-2). If the unit is operated in any other
environment, potential effects on the electro-
magnetic compatibility must be taken into
account.
❯Do not use the device near HF surgical devices
and MRI equipment.
❯Keep a minimum distance of 30 cm between
the device and other electronical devices.
❯Note that cable lengths and cable extensions
have effects on electromagnetic compatibility.
❯No maintenance measures are required to
maintain the basic EMC safety.
NOTICE
Negative effects on the EMC due to
non-authorized accessories
❯Use only Air Techniques accessories or
accessories approved by Air
Techniques.
❯Using any other accessories may result
in increased electromagnetic interfer-
ence emissions or the unit having
reduced electromagnetic immunity,
leading to an erroneous operation
mode.
NOTICE
Erroneous operation mode due to use
immediately adjacent to other devices
or with other stacked devices
❯Do not stack the unit together with
other devices.
❯If this is unavoidable, the unit and other
devices should be monitored in order
to ensure that they are working cor-
rectly.
NOTICE
Reduced performance features due to
insufficient distance between unit and
mobile HF communication devices
❯Keep at least 30 cm distance between
the unit (including parts and cables of
the unit) and mobile HF communica-
tion devices (wireless units) (including
their accessories such as antenna
cables and external antennas).
2.5 Essential performance char-
acteristics
The unit does not have any essential perform-
ance characteristics as set out in IEC 60601-1
section 4.3.
The unit meets the requirements according to
IEC 60601-1-2:2014.
2.6 Notification requirement of
serious incidents
The operator/patient has to report any serious
incident related the product to the manufacturer
and the competent authority of the Member
State, in which the operator and/or patient is
established/resident.
2.7 Only use genuine parts
❯Only use accessories and optional items speci-
fied or approved by Air Techniques.
❯Only use original working parts and spare
parts.
Air Techniques accepts no liability for
damage resulting from the use of non-
approved accessories, optional items or
any parts other than original spare and
wear parts.
The use of non-approved accessories,
optional items or non-genuine wear
parts / replacement parts (e. g. mains
cable) can adversely affect the electrical
safety and EMC.
Important information
6 2121100020L29 2101V007
EN-
US

2.8 Transport
Only the original packaging ensures optimum
protection for the unit during transport.
If necessary, the original packaging for this unit
can be ordered from Air Techniques.
Air Techniques cannot be held responsi-
ble for any damage resulting from trans-
port in unsuitable packaging, even during
the warranty period.
❯Only transport the unit in its original packaging.
❯Keep all packaging away from children.
2.9 Disposal
Disposal of the units, electronic circuitry and
PSPs must be accomplished only at the appro-
priate facilities for recovery and recycling. Make
sure to dispose of such items in accordance with
current federal, national, state and local govern-
ment rules and regulations.
2.10 Protection from cybersecurity
threats
The unit is to be connected to a computer that
can be connected to the Internet. Therefore, the
system needs to be protected from threats from
the Internet.
❯Use antivirus software and update it regularly.
Look for evidence of possible virus infection
and, if applicable, check with the antivirus soft-
ware and remove the virus.
❯Perform regular data backups.
❯Provide access to units only to trustworthy
users, e.g. by means of user name and pass-
word.
❯Make sure that only trustworthy contents are
downloaded. Install manufacturer-authenti-
cated software and firmware updates only.
Important information
2121100020L29 2101V007 7
EN-
US

Product description
3 Overview
1
2
4
5
6
3
1 Sensor
2 Sensor holder
3 Hygienic protective covers in box
4 Data carrier for imaging software
5 Calibration data carrier
6 USB extension cord
3.1 Scope of delivery
The following items are included in the scope of
delivery (possible variations due to country-spe-
cific requirements and/or import regulations):
SensorX Size #1 .. . . . . . . . . . . . . . . . . G9510A
– SensorX Size #1, Sensor
– Calibration data carrier
– Sensor holder
– Adhesive pad
– Velcro strip
– Cable holder
– USB extension cord, 1 m
– Hygienic protective covers (qty. 100)
– Imaging software VisionX
– Imaging software DBSWIN
– Installation and Operating Instructions
SensorX Size #2 .. . . . . . . . . . . . . . . . . G9520A
– SensorX Size #2, Sensor
– Calibration data carrier
– Sensor holder
– Adhesive pad
– Velcro strip
– Cable holder
– USB extension cord, 1 m
– Hygienic protective covers (qty. 100)
– Imaging software VisionX
– Imaging software DBSWIN
– Installation and Operating Instructions
3.2 Accessories
The following items are required for operation of
the device, depending on the application:
The hygienic protective covers are not
sterile at the time of delivery.
Hygienic protective covers Size #1
(qty. 100) .. . . . . . . . . . . . . . . . . . . . . . . . G9550
Hygienic protective covers Size #1
(qty. 500) .. . . . . . . . . . . . . . . . . . . . . . . . G9551
Hygienic protective covers Size #2
(qty. 100) .. . . . . . . . . . . . . . . . . . . . . . . . G9554
Hygienic protective covers Size #2
(qty. 500) .. . . . . . . . . . . . . . . . . . . . . . . . G9555
3.3 Optional items
The following optional items can be used with the
device:
2D X-ray test phantom .. . . . . . . . . . . . . . G8795
Product description
8 2121100020L29 2101V007
EN-
US

3.4 Consumables
The following materials are consumed during
operation of the unit and must be reordered sep-
arately:
Hygienic protective covers Size #1
(qty. 100) .. . . . . . . . . . . . . . . . . . . . . . . . G9550
Hygienic protective covers Size #1
(qty. 500) .. . . . . . . . . . . . . . . . . . . . . . . . G9551
Hygienic protective covers Size #2
(qty. 100) .. . . . . . . . . . . . . . . . . . . . . . . . G9554
Hygienic protective covers Size #2
(qty. 500) .. . . . . . . . . . . . . . . . . . . . . . . . G9555
Product description
2121100020L29 2101V007 9
EN-
US

4 Technical data
4.1 SensorX Size #1
Electrical data
Nominal voltage V DC 5
Nominal current mA 100
Classification
FDA classification (CFR Title 21) II
General technical data
Dimensions W x H x D mm
in
27.4 x 39.0 x 6.3
1.08 x 1.54 x 0.25
Cable length, sensor m
in
2.5
98.43
Max USB cable extension m
in
1
39.37
Computer connection USB 2.0
Compatible with USB 3.0
Sensor characteristics
Active sensor size W x H mm
in
20 x 30
0.79 x 1.18
Min. pixel size µm 19
Max. no. of pixels 1050 x 1580
Theoretical resolution LP/mm 26.3
Sensor type CMOS
Scintillator Structured CsJ scintillator on fibre-optics
Product description
10 2121100020L29 2101V007
EN-
US

4.2 SensorX Size #2
Electrical data
Nominal voltage V DC 5
Nominal current mA 100
Classification
FDA classification (CFR Title 21) II
General technical data
Dimensions W x H x D mm
in
33.1 x 44.7 x 6.3
1.30 x 1.76 x 0.25
Cable length, sensor m
in
2.5
98.43
Max USB cable extension m
in
1
39.37
Computer connection USB 2.0
Compatible with USB 3.0
Sensor characteristics
Active sensor size W x H mm 26 x 36
1.02 x 1.42
Min. pixel size µm 19
Max. no. of pixels 1368 x 1896
Theoretical resolution LP/mm 26.3
Sensor type CMOS
Scintillator Structured CsJ scintillator on fibre-optics
4.3 Electromagnetic compatibility (EMC)
The information on electromagnetic compatibility (EMC) applies to both SensorX Sensor Size #1
and Size #2.
Electromagnetic compatibility (EMC)
Interference emission measurements
Electromagnetic interference radiation
CISPR 11:2009+A1:2010
Group 1, Class B
Electromagnetic compatibility (EMC)
Interference immunity measurements on cover
Immunity to interference by discharge of static electricity
IEC 61000-4-2:2008
±8 kV contact
± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air
Compliant
Product description
2121100020L29 2101V007 11
EN-
US

Electromagnetic compatibility (EMC)
Interference immunity measurements on cover
Immunity to interference by high-frequency electromag-
netic fields
IEC 61000-4-3:2006+A1:2007+A2:2010
3 V/m
80 MHz - 2.7 GHz
80% AM at 1 kHz
Compliant
Immunity to interference by near fields of wireless HF
communication devices
IEC 61000-4-3:2006+A1:2007+A2:2010
See Table on immunity to interference table by near fields
of wireless HF communication devices.
Compliant
Immunity levels with respect to near fields of wireless HF communication devices
Radio service Frequency band
MHz
Test Level
V/m
TETRA 400 380 - 390 27
GMRS 460
FRS 460 430 - 470 28
LTE band 13, 17 704 - 787 9
GSM 800/900
TETRA 800
iDEN 820
CDMA 850
LTE band 5
800 - 960 28
GSM 1800
CDMA 1900
GSM 1900
DECT
LTE bands 1, 3, 4, 25
UMTS
1700 - 1990 28
Bluetooth
WLAN 802.11 b/g/n
RFID 2450
LTE band 7
2400 - 2570 28
WLAN 802.11 a/n 5100 - 5800 9
Electromagnetic compatibility (EMC)
Interference immunity measurements SIP/SOP
Immunity to interference by discharge of static electricity
IEC 61000-4-2:2008
±8 kV contact
± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air
Compliant
Product description
12 2121100020L29 2101V007
EN-
US

4.4 Ambient conditions
Ambient conditions during operation
Temperature °C
°F
10 - 35
+50 to +95
Humidity % < 80
Air pressure hPa 750 - 1160
Height above sea level m
ft
< 2000
< 6562
Ambient conditions during storage and transport
Temperature °C
°F
-20 to +60
-4 to +140
Humidity % 10 to 95
Air pressure hPa 750 - 1160
Height above sea level m
ft
< 16000
< 52493
Product description
2121100020L29 2101V007 13
EN-
US

4.5 Model identification plate
The model identification plate is located on the
sensor cable and on the case.
Fig. 1: Model identification plate on the sensor
cable
Fig. 2: Model identification plate on the case
REF Order number/type number
SN Serial number
5 Function
1
2
3
4
Fig. 3: SensorX
1 X-ray sensor
2 Sensor holder
3 Cable holder
4 USB extension cord
The X-ray sensor is connected to the computer
via the sensor cable, and if required, the USB
extension cable.
The sensor is to be fitted with a hygienic protec-
tive cover and to be placed in the mouth of the
patient. It is activated via an imaging software
(e. g. DBSWIN).
During the X-ray procedure, the X-rays are
received by the scintillator (luminescent material)
installed in the sensor and are converted into
beams of light. These light beams are recorded
by the sensor as image information, digitalized
and transmitted to the computer. If an error
occurs during the transmission, the image infor-
mation is sent again.
No further X-ray image can be recorded during
data transmission.
The application part BF in accordance with IEC
60601-1 is the X-ray sensor.
Product description
14 2121100020L29 2101V007
EN-
US

Installation
6 Requirements
6.1 Installation/setup room
❯The unit may only be used in a room that has
been set up specifically for this purpose (e. g.
an x-ray room). Do not use outdoors.
❯Do not expose the unit to direct sunlight or
heat.
❯The setup room may not contain any major
interference fields (e. g. strong magnetic fields).
They could cause malfunction in the unit.
6.2 Monitor
The monitor must meet the requirements for digi-
tal X-ray with a high light intensity and wide con-
trast range.
Strong ambient light, sunlight impinging directly
onto the monitor and reflections can make it
more difficult or even impossible to perform a
diagnosis based on the X-ray images.
Installation
2121100020L29 2101V007 15
EN-
US

6.3 System requirements
The system requirements of the software being used to operate the device must always be met during
its operation.
If third-party software is being used to operate the device, compliance with its system requirements
must be assured.
The following additional system requirements must also be met:
Drive: DVD ROM
Interface: USB 2.0
USB 3.0
Total maximum
cable length:
USB: 5 m
Software: VisionX from version 2.4.10 (order number: E7300)
DBSWIN from version 5.17 (order number: E7200A), VistaEasy, Image Bridge
For the system requirements of the computer systems, visit the download area at www.airtech-
niques.com (document no. E7201).
Installation
16 2121100020L29 2101V007
EN-
US

7 Installation
7.1 Fitting the sensor holder
The sensor holder and the cable holder can be
secured to the wall or treatment unit using either
the adhesive pad or screws and dowel.
The sensor holder can also be fitted to the lamp
stand using the Velcro strip.
Fastening the sensor holder with screws
Use screws and dowel which are suited
to the base surface.
❯Screw the screws into the wall with the same
spacing as between the slits. Insert the screw
only to the extent such that the screw head
can be hooked into the slits.
69 mm
❯Place the sensor holder on the screw heads
from above.
Fastening the sensor holder with the adhesive
pad
Fastening the sensor holder using the Velcro
strip
❯Thread the Velcro strip into the sensor holder.
❯Fasten the sensor holder with the Velcro strip.
7.2 Electrical connection
Combining devices safely
Take care when connecting units together or to
parts of other systems as there is always an ele-
ment of risk (e.g. due to leakage currents).
❯Only connect units when there can be no
question of danger to operator or to patient.
❯Only connect units when it is safe to do so and
when there is no risk of damage or harm to the
surroundings.
❯If it is not completely clear from the data sheet
of the unit that such connections can be safely
made or if you are in any doubt, always get a
suitably qualified person (e.g. the relevant man-
ufacturer) to verify that the setup is safe.
Installation
2121100020L29 2101V007 17
EN-
US

❯When connecting the unit to other devices,
e. g. a PC system, comply with the require-
ments set out in section 16 of IEC 60601-1
(EN 60601-1).
❯When setting up the PC system in the vicinity
of the patient:
Only connect components (e.g. computer,
monitor, printer) that comply with the standard
IEC 60601‑1 (EN 60601‑1).
❯When setting up the PC system outside of the
vicinity of the patient:
Connect components (e.g. computer, monitor,
printer) that comply at least with the
IEC 60950‑1 (EN 60950‑1) standard.
Connecting the device to a computer
NOTICE
Damage to the sensor
The interior parts of the sensor can be
damaged by mechanical forces.
❯Do not drop the sensor.
❯Do not subject the sensor to any pres-
sure.
❯Do not fold, clamp or crush the cable.
❯Do not carry the sensor by the cable.
❯Connect the USB plug of the sensor cable to a
free port on the computer.
❯If necessary, extend the cable by 1 m using the
enclosed USB extension cable.
Further extensions are not permitted.
The USB extension can also be used if
the device needs to be plugged in and
unplugged regularly and the USB port
on the computer is not easily accessi-
ble. This protects the USB connection
on the computer.
The unit has no main power switch.
Therefore, it is important that the USB
connection on the PC and, if necessary,
the socket outlet for the power supply,
are easily accessible and that the appli-
ance can be unplugged if necessary.
7.3 Installation with VisionX
Install the additional component
If the additional component of the unit was not
installed along with the installation of the imaging
software, it can be installed later on.
❯Place the data carrier of the imaging software
in the drive or run the installation file.
The Start menu opens.
❯If the Start menu does not open automatically,
run the file Start.exe.
❯Select the installation language you require.
❯Accept the License Agreement.
❯Select the required components.
❯Select the SensorX unit.
❯Follow the further instructions given by the
installation wizard.
Installing the calibration data
Every sensor requires the individual cali-
bration data stored on the enclosed data
carrier.
❯Insert or plug the enclosed data carrier in the
drive.
The data carrier starts automatically and the
calibration data are installed.
❯If the data carrier fails to start automatically, run
the setup.exe file.
7.4 Installation with DBSWIN
Installing the driver(s)
❯Close all programs.
❯Insert or plug the enclosed DBSWIN data car-
rier in the drive.
The start window opens.
❯If the data carrier fails to start automatically, run
the CD_Start.exe file.
❯Select the required language.
Installation
18 2121100020L29 2101V007
EN-
US