Dentsply Sirona inEos X5 User manual

New as of: 07.2018
inEos X5
Operating Instructions
English

Table of contents Dentsply Sirona
Operating Instructions inEos X5
264 17 096 D3586
D3586.201.01.11.0207.2018
Table of contents
1Dear Customer,....................................................................................................... 5
2General data ........................................................................................................... 6
2.1 Structure of the document............................................................................ 6
2.1.1 Identification of the danger levels .................................................. 6
2.1.2 Formats and symbols used............................................................ 7
2.2 Legend ......................................................................................................... 7
3Safety...................................................................................................................... 9
3.1 Basic safety information............................................................................... 9
3.1.1 Prerequisites.................................................................................. 9
3.1.2 Connecting the unit........................................................................ 9
3.1.3 Connection of external equipment ................................................. 9
3.1.4 Maintenance and repair ................................................................. 9
3.1.5 Modifications to the product........................................................... 9
3.1.6 Accessories.................................................................................... 10
3.1.7 In case of damage ......................................................................... 10
3.2 Blue light radiation (UV) ............................................................................... 11
3.3 To be taken into account during automatic operation .................................. 12
3.4 Intended use ................................................................................................ 12
3.5 Certification .................................................................................................. 13
4Technical description .............................................................................................. 14
4.1 Design and function ..................................................................................... 14
4.2 System components .................................................................................... 14
4.2.1 Components of the inEos X5 ......................................................... 14
4.3 Technical data.............................................................................................. 16
4.4 System requirements ................................................................................... 17
4.5 Electromagnetic compatibility ...................................................................... 17
4.5.1 Electromagnetic emission.............................................................. 17
4.5.2 Interference immunity .................................................................... 18
4.5.3 Working clearances ....................................................................... 20
5Transport to the installation site.............................................................................. 21
5.1 Transport and unpacking ............................................................................. 21
5.2 Installation site ............................................................................................. 22

Dentsply Sirona
Operating Instructions inEos X5
Table of contents
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6Initial startup ........................................................................................................... 23
6.1 Putting the inLab 4 PC into operation .......................................................... 23
6.1.1 Startup prerequisites...................................................................... 23
6.1.1.1 Required accessories................................................... 23
6.1.1.2 Making connections...................................................... 25
6.1.2 Safety............................................................................................. 26
6.1.3 Possible sources of error ............................................................... 26
6.2 Installing the software .................................................................................. 27
6.3 Connecting the unit ...................................................................................... 28
6.3.1 Connecting the unit to the PC........................................................ 28
6.3.2 Connecting the unit to the power supply........................................ 28
6.3.3 Connecting the foot switch (optional)............................................. 28
6.3.4 Switching the unit on and starting the software ............................. 29
6.4 Calibrating the motor arm ............................................................................ 29
6.5 Calibrating the inEos X5 camera ................................................................. 30
6.6 Updating the firmware.................................................................................. 31
7Controls and displays ............................................................................................. 32
7.1 Controls on the inEos X5 ............................................................................. 32
7.2 Operating state LED .................................................................................... 33
8Switching the system on ......................................................................................... 34
9Performing 3D acquisition....................................................................................... 35
9.1 General ........................................................................................................ 35
9.1.1 Acquisition methods....................................................................... 35
9.1.2 Scan modes................................................................................... 36
9.1.3 Scan options .................................................................................. 36
9.1.4 Model options................................................................................. 37
9.1.5 Scan models and impressions....................................................... 38
9.1.6 Autofocus....................................................................................... 39
9.1.7 Deleting images ............................................................................. 39
9.1.8 Operation via foot switch................................................................ 39
9.2 Starting the unit/standby mode .................................................................... 39
9.3 Automatic jaw scan ...................................................................................... 39
9.3.1 Preparing the optical impression.................................................... 40
9.3.2 Taking the scan.............................................................................. 41
9.3.3 Guideline editor.............................................................................. 41
9.3.4 Starting the automatic detail scan.................................................. 42

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Operating Instructions inEos X5
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9.4 Free scans ................................................................................................... 43
9.4.1 Preparing the optical impression.................................................... 43
9.4.2 Automatic and manual release in the "free scan" mode ................ 44
9.4.3 Taking a free scan (without previous automatic scans)................. 45
9.4.4 Taking a free detail scan................................................................ 45
9.5 Rotational scans .......................................................................................... 46
9.5.1 Preparing the optical impression.................................................... 47
9.5.2 Taking a rotational scan................................................................. 47
9.6 Acquiring a buccal registration..................................................................... 48
9.7 Scanbody scans for scanning with inPost and ATLANTIS-FLO-S
scanbodies................................................................................................... 48
10 Regular function test of the light barrier and the Start key...................................... 49
11 Cleaning and care................................................................................................... 51
11.1 Cleaning the outer surface........................................................................... 51
11.2 Protection against medicaments.................................................................. 51
11.3 Cleaning the optics ...................................................................................... 51
12 Accessories............................................................................................................. 52
12.1 Using the articulator plate ............................................................................ 53
13 Disposal .................................................................................................................. 54

Dentsply Sirona
Operating Instructions inEos X5
1 Dear Customer,
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1Dear Customer,
Thank you for purchasing your inEos X5® from Sirona.
Improper use and handling can create hazards and cause damage.
Please read and follow these operating instructions carefully and
Always keep them within easy reach.
To prevent personal injury or material damage, it is important to observe
all safety information.
Your
inEos X5 team,

2 General data
2.1 Structure of the document
Dentsply Sirona
Operating Instructions inEos X5
664 17 096 D3586
D3586.201.01.11.0207.2018
2General data
Please read this document completely and follow the instructions
exactly. You should always keep it within reach.
Original language of the present document: German.
2.1 Structure of the document
2.1.1 Identification of the danger levels
To prevent personal injury and material damage, please observe the
warning and safety information provided in these operating instructions.
Such information is highlighted as follows:
DANGER
An imminent danger that could result in serious bodily injury or death.
WARNING
A possibly dangerous situation that could result in serious bodily
injury or death.
CAUTION
A possibly dangerous situation that could result in slight bodily injury.
NOTE
A possibly harmful situation which could lead to damage of the
product or an object in its environment.
IMPORTANT
Application instructions and other important information.
Tip: Information for simplifying work.

Dentsply Sirona
Operating Instructions inEos X5
2 General data
2.2 Legend
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2.1.2 Formats and symbols used
The formats and symbols used in this document have the following
meaning:
Prerequisite
1. First action step
2. Second action step
or
➢ Alternative action
Result
➢ Individual action step
Prompts you to do something.
See "Formats and symbols used
[→7]"
Identifies a reference to another
text passage and specifies its
page number.
● List Designates a list.
“Command / menu item” Indicates commands / menu
items or quotations.
2.2 Legend
Year of manufacture
Safety symbols
"Warning of optical radiation" symbol
Warning of injuries to eyes and skin in the vicinity of optical radiation.
"Warning of hand injuries" symbol
Warning of hand injuries in the vicinity of devices with closing me-
chanical parts.

2 General data
2.2 Legend
Dentsply Sirona
Operating Instructions inEos X5
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Symbols on the packaging
Take note of the following symbols on the packaging:
Top
Protect from moisture
Fragile; handle with care
Do not stack
-40
+70
Temperature during storage and transport
95
10
Relative humidity during storage and transport
1060
500
Air pressure during storage and transport

Dentsply Sirona
Operating Instructions inEos X5
3 Safety
3.1 Basic safety information
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3Safety
3.1 Basic safety information
3.1.1 Prerequisites
NOTE
Important information on building installation
The building installation must be performed by a qualified expert in
compliance with the national regulations. DIN VDE 0100-710 applies
in Germany.
NOTE
Restrictions regarding installation site
The system is not intended for operation in areas subject to explosion
hazards.
NOTE
Do not damage the unit!
The unit can be damaged if opened improperly.
It is expressly prohibited to open the unit with tools!
3.1.2 Connecting the unit
Perform connection by following the directions given in the present
operating instructions.
3.1.3 Connection of external equipment
If any equipment not approved by Sirona is connected, it must comply
with the applicable standards:
● EN 60 950 for information technology equipment, and
● EN 61 010-1 for laboratory equipment.
3.1.4 Maintenance and repair
● The maintenance and repair of this unit may be performed only by
Dentsply Sirona or by agencies authorized by Dentsply Sirona.
● Components which have failed and influence the safety of the unit
must be replaced with original (OEM) spare parts.
Please request a certificate whenever you have such work performed. It
should include:
● The type and scope of work.
● Any changes made in the rated parameters or working range.
● Date, name of company and signature.
3.1.5 Modifications to the product
Modifications to this product which may affect the safety of the operator,
patients or third parties are prohibited by law!

3 Safety
3.1 Basic safety information
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3.1.6 Accessories
In order to ensure product safety, this device may be operated only with
original Dentsply Sirona accessories or third-party accessories
expressly approved by Dentsply Sirona. In particular, only the power
cable also supplied or the corresponding original spare part may be
used with the unit. The user is responsible for any damage resulting
from the use of non-approved accessories.
3.1.7 In case of damage
In case of noticeable malfunctions or damage, stop using the instrument
immediately and notify your authorized dealer or the manufacturer.

Dentsply Sirona
Operating Instructions inEos X5
3 Safety
3.2 Blue light radiation (UV)
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3.2 Blue light radiation (UV)
A Lamp
WARNING
Potentially hazardous optical radiation
Do not look directly at the lamp during operation, as eye damage can
result.
NOTE
No reflective objects in the working area
Do not bring any reflective objects into the working area of the lamp.
WARNING
Risk of injury for those diagnosed with epilepsy
For persons who have been diagnosed with epilepsy, there is a risk of
epileptic shock through the flashing light of the inEos X5.
➢ Patients who have been diagnosed with epilepsy must not work
with the inEos X5.

3 Safety
3.3 To be taken into account during automatic operation
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3.3 To be taken into account during automatic
operation
CAUTION
Risk of injury! / collision hazard!
During automatic operation there is a risk of injury/collision hazard as
a result of the swiveling movement of the articulated arm.
➢ Ensure that there are no objects and/or body parts on the work
plate (shaded area) during automatic operation.
3.4 Intended use
This system is used for 3D digitization of single tooth or complete jaw
models and impressions.
This unit must not be used for any other purpose. If the unit is used for
any purpose other than the one mentioned above, it may be damaged.
Intended use also includes compliance with these Operating
Instructions and the relevant maintenance instructions.
CAUTION
Follow the instructions
If the instructions for operating the unit described in this document are
not observed, the intended protection of the user may be impaired.

Dentsply Sirona
Operating Instructions inEos X5
3 Safety
3.5 Certification
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3.5 Certification
CE mark
This product bears the CE mark in accordance with the provisions of
Council Directive 2006/42/EC (machinery directive). As such, the
following standards apply: DIN EN ISO 12100:2011-03, DIN EN
61010-1:2011-07 and DIN EN 61326-1:2013-07.
CAUTION
CE mark for connected products
Further products which are connected to this unit must also bear the
CE mark. These products must be tested according to the applicable
standards.
Examples of CE mark for connected products:
● EN 60950:1992 + A1:1993 + A2:1993 + A3:1995 + A4:1997 based
on IEC 60950
● CAN/CSA-C22.2 No.61010-1-04.
CSA mark
C US
VDE mark
EAC certification
Mark of conformity of the Eurasian Economic Community
RoHS compliance
This symbol indicates that this product does not contain any toxic or
hazardous substances or components above the maximum concen-
tration value set out in the Chinese standard SJ / T 11364-2014, and
can be recycled following disposal and should not be carelessly dis-
carded.

4 Technical description
4.1 Design and function
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Operating Instructions inEos X5
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4Technical description
4.1 Design and function
The inEos X5 is designed as a desktop unit and consists of several
components (see Chapter "System components [→14]“). It is powered
from the standard local power network via an external power supply
unit.
The unit is connected to a PC via a USB port. The PC must fulfill the
minimum requirements (see Chapter on "System requirements").
The PC serves both for controlling the inEos X5 and for displaying the
captured images by means of the user software.
4.2 System components
"inEos X5" consists of a base plate, a vertical unit and an articulated
arm. In addition, various accessories are included in the scope of supply
of the unit.
4.2.1 Components of the inEos X5
Front side
AVertical unit DReady LED
BArticulated arm EStart button
CBase plate FScan element opening,
scan element

Dentsply Sirona
Operating Instructions inEos X5
4 Technical description
4.2 System components
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Rear side
M
24 V USB
2.0
M6324649
Model-No. D3586
Merial-No. 00106
REF 6324649
Sirona Dental Systems GmbH
Fabrikstr. 31 D-64625 Bensheim
Made in Germany
2013
S00106
24 V / 120 W
A B C
AMain switch
BSupply voltage input (external power supply unit)
CUSB port

4 Technical description
4.3 Technical data
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Operating Instructions inEos X5
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4.3 Technical data
Model designation inEos X5
Power supply line via power supply unit:
INPUT: 100 - 240 VAC / 47- 63 Hz / 2.0 A max.
permissible line voltage fluctuations:
± 10% of nominal voltage
Overvoltage category II
OUTPUT: 24 V / 6.25 A max.
Power consumption 150 W
Ambient conditions For indoor use
Pollution degree 2
Temperature: 10°C – 35°C (50°F ~ 95°F)
Relative humidity: 30% – 75%
Air pressure: 700hPa–1060hPa
Operating altitude: ≤ 2,000m
Transport and
storage conditions
Temperature: -40°C – +70°C (-40°F ~ 158°F)
Relative humidity: 10% – 95%
Air pressure: 500hPa – 1060hPa
Dimensions (WxHxD)
in mm
in inches
475 x 740 x 460mm
18 ¾ x 29 ⅛ x 18 ⅛in.
Weight
● without power supply unit and
accessories
39.6 kg (87.3 lbs)
Protection class Class I device
Degree of protection against
ingress of water
Ordinary equipment (not protected)
Operating mode Continuous operation with intermittent loading corresponding to the
laboratory mode of working.
Desktop unit

Dentsply Sirona
Operating Instructions inEos X5
4 Technical description
4.4 System requirements
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Tests/approvals This unit complies with the following requirements:
DIN EN 61 010-1: 2011 (safety)
DIN EN 61 326-1: 2006 (EMC)
DIN EN ISO 12 100: 2011 (risk management)
4.4 System requirements
A 64-bit inLab 4 PC is required to run this software. The hardware
version must be PC hardware version 2.0.1 or higher.
4.5 Electromagnetic compatibility
Observance of the following information is necessary to ensure safe
operation regarding EMC aspects.
inEos X5 complies with the requirements for electromagnetic
compatibility (EMC) according to DIN EN 61326-1:2006-10.
inEos X5 is hereinafter referred to as "UNIT".
4.5.1 Electromagnetic emission
The UNIT is intended for operation in the electromagnetic environment
specified below.
The customer or user of the UNIT should make sure that it is used in
such an environment.
Emission measurement Conformity Electromagnetic environment - guidelines
RF emissions according to CISPR 11 Group 1 The UNIT uses RF energy only for its internal
function. Therefore, its RF emissions are very low
and are not likely to cause any interference in
nearby electronic equipment.
RF emissions according to CISPR 11 Class B The UNIT is intended for use in all facilities, in-
cluding residential areas and in any facilities con-
nected directly to a public power supply providing
electricity to buildings used for residential pur-
poses.
Harmonics
according to IEC 61000-3-2
Class A
Voltage fluctuations / flicker according
to IEC 61000-3-3
coincides

4 Technical description
4.5 Electromagnetic compatibility
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4.5.2 Interference immunity
The UNIT is intended for operation in the electromagnetic environment
specified below.
The customer or user of the UNIT should make sure that it is used in
such an environment.
Interference immu-
nity tests
DIN EN 61326-1 Test
level
Compliance level Electromagnetic environment –
guidelines
Electrostatic dis-
charge (ESD) ac-
cording to IEC
61000-4-2
± 6 kV contact
± 8 kV air
± 6 kV contact
± 8 kV air
Floors should be wood, concrete, or
ceramic tile. If floors are covered
with synthetic material, the relative
humidity should be at least 30%.
Electrical fast tran-
sient/burst accord-
ing to
IEC 61000-4-4
± 1 kV for input and out-
put lines
± 2 kV for power supply
lines
± 1 kV for input and
output lines
± 2 kV for power supply
lines
The quality of the line power supply
should be that of a typical commer-
cial or hospital environment.
Surge voltages
according to IEC
61000-4-5
± 1 kV differential mode
voltage
± 2 kV common mode
voltage
± 1 kV differential
mode voltage
± 2 kV common mode
voltage
The quality of the line power supply
should be that of a typical commer-
cial or hospital environment.
Voltage dips, short
interruptions and
variations of the
power supply
according to IEC
61000-4-11
<5% UT for ½ period
(>95% dip of UT)
40% UT for 5 periods
(60% dip of UT)
70% UT for 25 periods
(30% dip of UT)
<5% UT for 5sec. (>95%
dip of UT
<5% UT for ½ period
(>95% dip of UT)
40% UT for 5 periods
(60% dip of UT)
70% UT for 25 periods
(30% dip of UT)
<5% UT for 5sec.
(>95% dip of UT
The quality of the line power supply
should be that of a typical commer-
cial or hospital environment.
Continued operation of the UNIT is
possible following interruptions of
the power supply, since the UNIT is
powered by an uninterruptible power
supply backed up by a storage bat-
tery.
Magnetic field of
power frequencies
(50/60 Hz) accord-
ing to
IEC61000-4-8
3 A/m 3 A/m Power frequency magnetic fields
should be at levels characteristic of
a typical location in a typical com-
mercial or hospital environment.
Note: UT is the AC supply voltage prior to application of the test level.
Portable and mobile radio equip-
ment must not be used within the
recommended working clearance
from the UNIT and its cables, which
is calculated based on the equation
suitable for the relevant transmission
frequency.
Recommended working clearance:

Dentsply Sirona
Operating Instructions inEos X5
4 Technical description
4.5 Electromagnetic compatibility
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Interference immu-
nity tests
DIN EN 61326-1 Test
level
Compliance level Electromagnetic environment –
guidelines
Conducted RF in-
terference
IEC 61000-4-6
3 Veff
150 kHz to 80 MHz
3 Veff d= [1.2] √P
Radiated RF inter-
ference
IEC 61000-4-3
3 V/m
80 MHz to 800 MHz
3 V/m
800 MHz to 2.5 GHz
3 V/m
3 V/m
d= [1.2] √P
at 80 MHz to 800 MHz
d= [2.3] √P
at 800 MHz to 2.5 MHz
where P is the nominal transmitter
output in watts (W) specified by the
transmitter manufacturer and d is
the recommended working clear-
ance in meters (m).
Field strengths from fixed RF trans-
mitters, as determined by an electro-
magnetic site survey1 should be less
than the compliance level2 in each
frequency range.
Interference is possible in the vicinity
of equipment bearing the following
graphic symbol.
Remark 1
The higher frequency range applies at 80 MHz and 800 MHz.
Remark 2
These guidelines may not be applicable in all cases. The propagation of
electromagnetic waves is influenced by their absorption and reflection
by buildings, objects and persons.
1. Field strengths from fixed transmitters, such as base stations for
radio (cellular/cordless) telephones and land mobile radios, amateur
radio, AM/FM radio and TV broadcasts, cannot be predicted
theoretically with accuracy. An investigation of the location is
recommended to determine the electromagnetic environment
resulting from stationary RF transmitters. If the measured field
strength in the location in which the UNIT is used exceeds the
applicable RF compliance level specified above, the UNIT should
be observed to verify normal operation. If unusual performance
characteristics are observed, it may be necessary to take additional
measures such as reorientation or repositioning of the UNIT.
2. Over the frequency range 150kHz to 80 MHz, field strengths should
be less than 3 V/m.

4 Technical description
4.5 Electromagnetic compatibility
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4.5.3 Working clearances
Recommended working clearances
between portable and mobile RF
communication devices and the UNIT
The UNIT is intended for operation in an electromagnetic environment,
where radiated RF interference is checked. The customer or the user of
the UNIT can help prevent electromagnetic interference by duly
observing the minimum distances between portable and/or mobile RF
communication devices (transmitters) and the UNIT. These values may
vary according to the output power of the relevant communication
device as specified below.
Rated maximum output power
of transmitter
[W]
Working clearance according to transmission frequency [m]
150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
d= [1.2] √P d= [1.2] √P 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 whose maximum nominal output is not specified in the
above table, the recommended working clearance d in meters (m) can
be determined using the equation in the corresponding column, where P
is the maximum nominal output of the transmitter in watts (W) specified
by the transmitter manufacturer.
Remark 1
An additional factor of 10/3 is applied when calculating the
recommended working clearance between transmitters in the 80 MHz to
2.3 GHz frequency range in order to reduce the probability that a
mobile/portable communication device unintentionally brought into the
patient area could lead to interference.
Remark 2
These guidelines may not be applicable in all cases. The propagation of
electromagnetic waves is influenced by their absorption and reflection
by buildings, objects and persons.