Air Techniques ScanX Swift User manual

EN-
US
ES
FR
ScanX Swift View
Installation and Operating Instructions
Instrucciones para montaje y uso
Notice de montage et d'utilisation
2142100008L41
*2142100008L41*
G85052202V007

EN-
US
ScanX Swift View
Installation and Operating Instructions
2142100008L41
*2142100008L41*
G85052202V007

Contents
Important information
1About this document .. . . . . . . . . . . . . 3
1.1 Warnings and symbols .. . . . . . . 3
1.2 Copyright information .. . . . . . . . 4
2 Safety .. . . . . . . . . . . . . . . . . . . . . . . . . 5
2.1 Unauthorized modification .. . . . . 5
2.2 Intended use (FDA) .. . . . . . . . . . 5
2.3 General safety information .. . . . . 5
2.4 Specialist personnel .. . . . . . . . . 5
2.5 Protection from electric shock .. . 5
2.6 FCC note .. . . . . . . . . . . . . . . . . 6
2.7 Notification requirement of seri-
ous incidents .. . . . . . . . . . . . . . . 6
2.8 Only use genuine parts .. . . . . . . 6
2.9 Transport .. . . . . . . . . . . . . . . . . . 6
2.10 Disposal .. . . . . . . . . . . . . . . . . . 7
2.11 Protection from cybersecurity
threats .. . . . . . . . . . . . . . . . . . . . 7
Product description
3Overview .. . . . . . . . . . . . . . . . . . . . . . . 8
3.1 Scope of delivery .. . . . . . . . . . . . 9
3.2 Accessories .. . . . . . . . . . . . . . . . 9
3.3 Optional items .. . . . . . . . . . . . . . 9
3.4 Consumables .. . . . . . . . . . . . . . 9
3.5 Wear parts and spare parts .. . . . 9
4Technical data .. . . . . . . . . . . . . . . . . . . 10
4.1 Phophor storage plate scanner .. 10
4.2 Phosphor storage plate .. . . . . . . 12
4.3 Barrier envelope .. . . . . . . . . . . . 12
4.4 Model identification plate .. . . . . . 13
4.5 Conformity assessment .. . . . . . . 13
5 Function .. . . . . . . . . . . . . . . . . . . . . . . 13
5.1 Phophor storage plate scanner .. 13
5.2 Phosphor storage plate .. . . . . . . 14
5.3 Barrier envelope .. . . . . . . . . . . . 15
5.4 Stylus .. . . . . . . . . . . . . . . . . . . . 15
5.5 Protective cover (optional) .. . . . . 15
Installation
6 Requirements .. . . . . . . . . . . . . . . . . . . 16
6.1 Installation/setup room .. . . . . . . 16
6.2 System requirements .. . . . . . . . . 17
6.3 Monitor .. . . . . . . . . . . . . . . . . . . 17
7 Installation .. . . . . . . . . . . . . . . . . . . . . . 18
7.1 Setting up the unit .. . . . . . . . . . . 18
7.2 Removing the protective film
from the touch screen .. . . . . . . . 18
7.3 Attaching the Stylus .. . . . . . . . . 18
7.4 Checking the memory card .. . . . 18
7.5 Electrical connection .. . . . . . . . . 19
7.6 Connecting the unit to the net-
work .. . . . . . . . . . . . . . . . . . . . . 19
8Commissioning and first start-up .. . . 21
8.1 Configuring the network .. . . . . . 21
8.2 Configuring the unit in VisionX .. . 21
8.3 Configuring the unit in DBSWIN .. 22
8.4 X-ray unit settings .. . . . . . . . . . . 24
8.5 Commissioning tests .. . . . . . . . . 25
Usage
9Operating the touch screen .. . . . . . . . 26
9.1 Navigating .. . . . . . . . . . . . . . . . . 26
9.2 Using menus .. . . . . . . . . . . . . . . 26
9.3 Entering text in a field .. . . . . . . . 27
9.4 Calling up messages on the
touch screen .. . . . . . . . . . . . . . . 27
10 Correct use of phosphor storage
plates .. . . . . . . . . . . . . . . . . . . . . . . . . . 28
11 Operation .. . . . . . . . . . . . . . . . . . . . . . 29
11.1 X-ray .. . . . . . . . . . . . . . . . . . . . . 29
11.2 Scanning the image data via a
computer .. . . . . . . . . . . . . . . . . . 31
11.3 Scanning image data via the
touch screen on the unit .. . . . . . 32
Contents
2142100008L41 2202V007 1
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11.4 Erasing the imaging plate .. . . . . 34
11.5 Switching the unit off .. . . . . . . . . 34
12 Cleaning and disinfection .. . . . . . . . . . 35
12.1 Phophor storage plate scanner .. 35
12.2 Barrier envelope .. . . . . . . . . . . . 36
12.3 Phosphor storage plate .. . . . . . . 36
12.4 Stylus .. . . . . . . . . . . . . . . . . . . . 37
13 Maintenance .. . . . . . . . . . . . . . . . . . . . 38
13.1 Recommended maintenance
schedule .. . . . . . . . . . . . . . . . . . 38
13.2 Check image quality .. . . . . . . . . 38
Troubleshooting
14 Tips for operators and service techni-
cians .. . . . . . . . . . . . . . . . . . . . . . . . . . 40
14.1 Poor X-ray image .. . . . . . . . . . . 40
14.2 Software error .. . . . . . . . . . . . . . 44
14.3 Fault on the unit .. . . . . . . . . . . . 45
14.4 Error messages on the touch
screen .. . . . . . . . . . . . . . . . . . . . 46
Appendix
15 Menu structure Settings .. . . . . . . . . . . 49
16 Scanning times .. . . . . . . . . . . . . . . . . . 52
17 File sizes (uncompressed) .. . . . . . . . . 53
18 Handover record .. . . . . . . . . . . . . . . . . 54
Contents
2 2142100008L41 2202V007
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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 ScanX
Swift View, order number: G8500 (2142100510).
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
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)
Batch name
CE mark
CE labeling with the number of the noti-
fied body
Manufacturer
Date of manufacture
Distributor
Dispose of correctly in accordance with
EU Directive 2012/19/EU (WEEE).
Take note of the accompanying electronic
documents.
Please note the operating instructions.
Wear hand protection.
Disconnect all power from the unit.
Do not reuse
DC current
Important information
2142100008L41 2202V007 3
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Warning – risk of dangerous electric vol-
tages
Warning - laser beams
This way up / store and transport in an
upright position
Keep dry
n
Stacking limits
no condensation
XX
YY
Lower and upper humidity limits
XX
YY
Lower and upper temperature limits
XX
Upper temperature limit
Fragile, handle with care
Keep away from sunlight during storage
Adhesive label
Fig. 1: Laser class 3B
Fig. 2: Warning - laser beams
Fig. 3: Specification of laser source
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 2142100008L41 2202V007
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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 Unauthorized modification
Pursuant to Part 15.21 of the FCC rules, any
changes or modifications to this equipment not
expressly approved by the manufacturer may
cause, harmful interference and void the FCC
authorization to operate this equipment.
2.2 Intended use (FDA)
ScanX Swift View
Indications for use
The ScanX Swift View is intended to be used for
scanning and processing digital images exposed
on Phosphor Storage Plates (PSPs) in dental
applications.
Contraindications
Any other usage or usage beyond this scope is
deemed to be improper. The manufacturer
accepts no liability for damage resulting from
improper usage. The user bears the sole risk.
This unit is not suitable for monitoring patients
over extended periods of time. This unit must not
be used in operating rooms or similar rooms, in
which hazards may arise from the combustion of
flammable materials. The touch screen only
shows a preview as an initial impression of the X-
ray image. For purposes of diagnosis, the X-ray
image must be viewed on a diagnostic monitor.
The preview of the X-ray image on the touch
screen is not suitable for the purposes of diagno-
sis.
Barrier envelope
Indication for use
Disposable Barrier Envelopes are intended to be
used as a disposable barrier for Air Techniques
Phosphor Storage Plates. This device is non-
sterile and intended for single patient use only.
Contraindication
This Device has no contraindications.
2.3 General safety information
The sale or prescription of this device by a medi-
cal 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: By virtue of Federal Law, the
device may only be sold to dentists or
bought on behalf of a dentist.
❯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.
2.4 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.
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.
2.5 Protection from electric
shock
❯Comply with all relevant electrical safety regula-
tions when you work with this unit.
Important information
2142100008L41 2202V007 5
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❯Never touch the patient and unshielded plug
connections of the device at the same time.
❯Replace any damaged cables or plugs immedi-
ately.
Comply with the EMC rules concerning medi-
cal devices
The device is designed for use in a basic electro-
magnetic environment in accordance with
IEC 61326‑1.
NOTICE
Negative effects on the EMC due to
non-authorized accessories
❯Use only Air Techniques accessories or
accessories approved by Air Techni-
ques.
❯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.
2.6 FCC note
This device has been tested and complies with
the limits for a class B digital device as set out in
part 15 of the FCC regulations. These limits are
designed to provide adequate protection against
harmful interference in residential environments.
This device generates, uses, and can emit high-
frequency energy, and it can cause harmful inter-
ference to wireless communication systems if it is
not installed and used in accordance with the
instructions. However, this statement does not
offer a guarantee that no interference will occur in
a certain installation. If this device causes harmful
interference to radio or TV reception (this can be
tested by switching the device off and back on
again), users are recommended to attempt to
eliminate the interference by taking one or more
of the following measures:
❯Realign or reposition the reception aerial.
❯Increase the distance between the device and
the receiver.
❯To meet FCC requirements on HF exposure
compliance, a safety distance of at least 20 cm
must be maintained between the device's inter-
nal aerial and all persons.
❯Connect the device to a power outlet on a dif-
ferent circuit to the one the receiver is con-
nected to.
❯Consult a dealer or experienced radio/TV tech-
nician.
2.7 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.
2.8 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.
2.9 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.
Important information
6 2142100008L41 2202V007
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❯Keep all packaging away from children.
❯Do not expose the unit to any strong vibrations
or shocks.
2.10 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.
2.11 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
2142100008L41 2202V007 7
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Product description
3 Overview
2
Opposite side
towards tube.
2142
a
D4847587
1
3
4
8
2
5
6
7
1 ScanX Swift View PSP scanner
2 Stylus
3 Intraoral phosphor storage plate (PSP)
4 Barrier envelope intraoral
5 SDHC memory card (installed in the unit)
6 Network cable
7 WLAN stick
8 Power supply unit with country-specific adapter
Product description
8 2142100008L41 2202V007
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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):
ScanX Swift View
PSP scanner .. . . . . . . . . . . . . . . . . . . . G8500A
– ScanX Swift View basic unit
– Power supply unit
– Network cable
– SDHC memory card
– Stylus
– VisionX Imaging software data carrier/down-
load
– DBSWIN Imaging software data carrier/down-
load
– ScanX View third-party software instructions
data carrier/download
– WLAN stick (pre-installed depending on ver-
sion)
– Phosphor storage plates:
– Size 0
– Size 2
– Barrier envelopes:
– Size 0
– Size 2
– PSP cleaning wipes
– Installation and Operating Instructions
– Quick Reference Guide
3.2 Accessories
The following items are required for operation of
the device, depending on the application:
SDHC memory card .. . . . . . . . . . . . . . . . G8590
Phosphor storage plates (PSPs)
Intraoral phosphor storage plate size 0
(2 pcs.) .. . . . . . . . . . . . . . . . . . . . . . . . . 73445-0
Intraoral phosphor storage plate size 1
(2 pcs.) .. . . . . . . . . . . . . . . . . . . . . . . . . 73445-1
Intraoral phosphor storage plate size 2
(4 pcs.) .. . . . . . . . . . . . . . . . . . . . . . . . . 73445-2
Intraoral phosphor storage plate size 3
(2 pcs.) .. . . . . . . . . . . . . . . . . . . . . . . . . 73445-3
Intraoral phosphor storage plate, size 4
(1 pcs.) .. . . . . . . . . . . . . . . . . . . . . . . . . 73445-4
Barrier envelopes
Barrier envelope Size 0
2 x 3 cm (100 pcs.) .. . . . . . . . . . . . . . . G8511-0
Barrier envelope Size 1
2 x 4 cm (100 pcs.) .. . . . . . . . . . . . . . . G8511-1
Barrier envelope Size 2
3 x 4 cm (300 pcs.) .. . . . . . . . . . . . . . . G8511-2
Barrier envelope Size 2
3 x 4 cm (1000 pcs.) .. . . . . . . . . . . . . G8511-2k
Barrier envelope Size 3
2.7 x 5.4 cm (100 pcs.) .. . . . . . . . . . . . G8511-3
Barrier envelope Size 4
5.7 x 7.6 cm (50 pcs.) .. . . . . . . . . . . . . G8511-4
3.3 Optional items
The following optional items can be used with the
device:
Network cable (5 m) .. . . . . . . . . . . . . . . . G8595
Stylus .. . . . . . . . . . . . . . . . . . . . . . . . . . . G8585
Protective cover .. . . . . . . . . . . . . . . . . . . G8423
Commissioning and intraoral constancy tests
2D X-ray test phantom .. . . . . . . . . . . . . . G8795
3.4 Consumables
The following materials are consumed during
operation of the device and must be re-ordered:
Cleaning and disinfection
PSP cleaning wipes (50 pieces) .. . . . . . . . B8910
Barrier envelopes
refer to "3.2 Accessories"
3.5 Wear parts and spare parts
Phosphor storage plates (PSPs)
refer to "3.2 Accessories"
Product description
2142100008L41 2202V007 9
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4 Technical data
4.1 Phophor storage plate scanner
Electrical data of the device
Voltage V DC 24
Max. current consumption A 1.25
Output W < 30
Type of protection IP20
Electrical data of the power supply unit
Nominal Voltage V AC 100 - 240
Frequency Hz 50/60
General technical data
Dimensions (W x H x D) mm 226 X 275 X 243
in 8.90 X 10.83 X 9.57
Weight kg approx. 7
lbs approx. 15
Duty cycle S2 (in accordance with IEC
60034-1)
min 25
Duty cycle S6 (in accordance with IEC
60034-1)
% 25
Pixel size (selectable) μm 12.5 - 50
Max. theoretical resolution Line
pairs/mm
(Lp/mm)
approx. 40
Noise level
Ready to scan dB(A) approx. 37
During scanning dB(A) approx. 55
Network connection
LAN technology Ethernet
Standard IEEE 802.3u
Data rate Mbit/s 100
Connector RJ45
Type of connection Auto MDI-X
Type of cable ³CAT5
WiFi connection
WiFi technology IEEE 802.11b/g
Encryption WPA, WPA2
Product description
10 2142100008L41 2202V007
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Ambient conditions during operation
Temperature °C +10 to +35
°F +50 to +95
Relative humidity % 20 - 80
Air pressure hPa 750 - 1060
Ambient conditions during storage and transport
Temperature °C -20 to + 60
°F -4 to +140
Relative humidity % 10 - 95
Air pressure hPa 750 - 1060
Classification
Medical Device Class (MDR) I
FDA classification (CFR Title 21) II
Laser class (unit)
in accordance with IEC 60825-1:2014
1
Laser source
Laser class
In accordance with IEC 60825-1:2014
3B
Wavelength lnm 635
Output mW 10
Memory card
Type SDHC
Maximum memory capacity GB 32
File system FAT32
Performance class Class ³4
Product description
2142100008L41 2202V007 11
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4.2 Phosphor storage plate
Classification
Medical Device Class (MDR) IIa
FDA classification (CFR Title 21) I
Ambient conditions during operation
Temperature °C 18 - 45
°F 64 - 113
Relative humidity % < 80
Ambient conditions during storage and transport
Temperature °C < 45
°F < 113
Relative humidity % < 80
Dimensions of intraoral phosphor storage plates
Size 0 mm 22 x 35
in 0.87 x 1.38
Size 1 mm 24 x 40
in 0.94 x 1.57
Size 2 mm 31 x 41
in 1.22 x 1.61
Size 3 mm 27 x 54
in 1.06 x 2.13
Size 4 mm 57 x 76
in 2.24 x 2.99
4.3 Barrier envelope
Classification
Medical Device Class (MDR) I
FDA classification (CFR Title 21) Class II
Product description
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4.4 Model identification plate
The type plate is located on the rear of the
device.
REF Order number
SN Serial number
4.5 Conformity assessment
This device has been subjected to conformity
acceptance testing in accordance with the cur-
rent relevant guidelines of the European Union.
This equipment conforms to all relevant require-
ments.
5 Function
5.1 Phophor storage plate scan-
ner
1
2
3
5
4
6
1 Operating elements
2 Input unit
3 Stylus
4 Release key
5 Collection tray
6 Memory card slot
The phosphor storage plate scanner is used to
read image data stored on the phosphor storage
plate.
The unit can be used in two different ways: via
the imaging software (e. g. VisionX) on a PC or
directly via the touch screen on the unit.
The transport mechanism guides the phosphor
storage plate through the device. A laser in the
scanner unit scans the PSP. The scanned data is
converted into a digital image.
If a scanning job is started via the imaging soft-
ware, the image is automatically transmitted to
the computer.
Product description
2142100008L41 2202V007 13
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If a scanning job is started via the touch screen,
the image is saved to the memory card and
needs to be transferred to the computer later on.
After scanning, the phosphor storage plate runs
through the erasure unit. Image data still held on
the phosphor storage plate is erased with the aid
of bright light.
The phosphor storage plate is then ejected for
re-use.
Operating elements
1
2
1 Touch screen
2 On/off switch
The touch screen allows the unit to be operated
when it is not connected to a computer. Instruc-
tions can be entered on the touch screen either
with the tip of a finger or the stylus.
The Help button can be used to open a help
page for the respective page. The Messages
button can be used to call up current messages.
Connections
The connections are located on the rear of the
unit, underneath the cover.
1
2
6
4
5
3
1 Connection for power supply unit
2 Reset button
3 USB connection (for WLAN stick)
4 Network connection status LEDs
5 Network connection
6 AUX connection for diagnostic units
ScanManager
When the ScanManager is enabled, more than
one X-ray job can be transmitted simultaneously
to the unit from different computers. The unit
manages the X-ray jobs in a queue from which
the respective X-ray job can be selected using
the touch screen and then executed.
Without ScanManager, the unit processes one X-
ray job at a time and is blocked until this job has
been completed. During this time, no further X-
ray jobs can be transmitted to the unit from other
computers.
ScanManager can be enabled via Set-
tings > System Settings> Operating
Type.
5.2 Phosphor storage plate
The PSP stores X-ray energy, which is re-emitted
in the form of light after excitation by the laser.
This light is then converted into image informa-
tion in the phosphor storage plate scanner.
The PSP has an active side and an inactive side.
The PSP must always be exposed on the active
side.
When used properly, a PSP can be exposed,
read and erased several hundred times provided
there is no mechanical damage. The PSP must
be replaced if there are any signs of damage, e.g.
if the protective layer is damaged or there are
visible scratches that could interfere with the
diagnostics.
Product description
14 2142100008L41 2202V007
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2
Opposite side
towards tube.
2142
aD4847587
a
1
2
1 Inactive side Black, size and manufac-
turer information printed
on it
2 Active side Light blue, with position-
ing aid a
Positioning aid ais visible on the x-ray image and
makes orientation easier during diagnosis.
5.3 Barrier envelope
Disposable Barrier Envelopes are intended to be
used as a disposable barrier for Air Techniques
Phosphor Storage Plates. This device is non-
sterile and intended for single patient use only.
5.4 Stylus
The touch screen can be operated using the Sty-
lus as an alternative to the tip of a finger.
5.5 Protective cover (optional)
The protective cover protects the device against
dust and dirt, e. g. during extended periods, in
which it is not in use.
Product description
2142100008L41 2202V007 15
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Installation
Only qualified specialists or persons
trained by Air Techniques may install,
connect, and commission the unit.
6 Requirements
6.1 Installation/setup room
The room chosen for set up must meet the fol-
lowing requirements:
– Closed, dry, well-ventilated room
– It should not be a room made for another pur-
pose (e.g. boiler room or wet cell)
– Max. light intensity 1000 Lux, no direct sun-
light at the place of installation of the unit
– There should be no major fields of interference
(e.g. strong magnetic fields) present that can
interfere with the proper operation of the unit.
– Ambient conditions correspond to "4 Techni-
cal data".
Installation
16 2142100008L41 2202V007
EN-
US