KaVo ESTETICA E70 Vision User manual

Instructions for use
ESTETICA E70 Vision / E80 Vision

Distributed by:
KaVo Dental Technologies, LLC
11727 Fruehauf Drive
Charlotte, NC 28273 USA
Tel. [phone]
Fax [phone]
Manufacturer:
Kaltenbach & Voigt GmbH
Bismarckring 39
88400 Biberach
Germany
www.kavo.com

Table of contents
1 User instructions ................................................................................................................ 7
1.1 User guide .................................................................................................................... 7
1.1.1 Abbreviations ..................................................................................................... 7
1.1.2 Symbols ............................................................................................................ 7
1.1.3 Target group ...................................................................................................... 7
1.2 Service ......................................................................................................................... 8
1.3 Terms and conditions of warranty.................................................................................... 8
1.4 Transportation and storage............................................................................................. 8
1.4.1 Currently valid packaging regulations.................................................................... 8
1.4.2 Damage in transit ............................................................................................... 9
1.4.3 Information on the packaging: Storage and transportation...................................... 10
2 Safety.................................................................................................................................. 11
2.1 Description of safety instructions ..................................................................................... 11
2.1.1 Warning symbol ................................................................................................. 11
2.1.2 Structure ........................................................................................................... 11
2.1.3 Description of hazard levels ................................................................................. 11
2.2 Intended use................................................................................................................. 11
2.2.1 Indications for use .............................................................................................. 11
2.2.2 General ............................................................................................................. 13
2.3 Safety instructions ......................................................................................................... 15
2.3.1 General information ............................................................................................ 15
2.3.2 Product-specific .................................................................................................. 16
3 Product description ............................................................................................................ 20
3.1 Treatment centre........................................................................................................... 20
3.1.1 KaVo ESTETICA E70 Vision / E80 Vision T ............................................................. 20
3.1.2 KaVo ESTETICA E70 Vision S ............................................................................... 21
3.1.3 KaVo ESTETICA E70 Vision / E80 Vision Cart ......................................................... 22
3.2 Versions of the dentist element ....................................................................................... 23
3.2.1 T table............................................................................................................... 23
3.2.2 S-Table (ESTETICA E70 Vision only) ..................................................................... 24
3.2.3 Cart .................................................................................................................. 25
3.3 Assistant unit ................................................................................................................ 26
3.4 Three-function handpiece (3F handpiece)......................................................................... 26
3.5 Multifunctional handpiece (MF handpiece)......................................................................... 27
3.6 X-ray viewer 1440 ......................................................................................................... 27
3.7 Control elements ........................................................................................................... 28
3.7.1 Dentist element T-table and cart .......................................................................... 28
3.7.2 Dentist's unit S table........................................................................................... 29
3.7.3 Assistant element ............................................................................................... 30
3.7.4 Groups of keys ................................................................................................... 30
3.8 Foot control................................................................................................................... 32
3.9 Signs on the product...................................................................................................... 32
3.9.1 Warning signs and safety signs ............................................................................ 32
3.9.2 Rating plate and name plate ................................................................................ 33
3.10Technical data ............................................................................................................... 38
3.11KaVo Service table 1568 (optional accessory)................................................................... 44
Instructions for use ESTETICA E70 Vision / E80 Vision
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4 Operation............................................................................................................................ 45
4.1 Switching on the device.................................................................................................. 45
4.2 Move the dentist's unit ................................................................................................... 45
4.2.1 Moving the T table .............................................................................................. 45
4.2.2 Moving the S table.............................................................................................. 46
4.2.3 Move the cart ..................................................................................................... 47
4.2.4 Moving the tray .................................................................................................. 47
4.3 Moving the assistant element.......................................................................................... 48
4.3.1 Attaching the tray holder (optional assembly kit) ................................................... 49
4.4 Move patient chair ......................................................................................................... 49
4.5 Adjusting the patient chair.............................................................................................. 50
4.5.1 Swivelling the arm rest........................................................................................ 50
4.5.2 Adjusting the Comfort backrest ............................................................................ 51
4.5.3 Automatically positioning the patient chair............................................................. 51
4.5.4 Manually positioning the patient chair ................................................................... 53
4.6 Moving the patient chair ................................................................................................. 55
4.7 Adjust the motorised headrest ........................................................................................ 55
4.7.1 Adjusting the motorised headrest with the joystick................................................. 56
4.7.2 Automatically position the motorised headrest ....................................................... 58
4.8 Adjusting double-jointed headrests.................................................................................. 58
4.9 Safety shut-off .............................................................................................................. 60
4.10Using functions through the touchscreen.......................................................................... 62
4.10.1 Selecting the dentist ........................................................................................... 64
4.10.2 Status message.................................................................................................. 64
4.10.3 Treatment menu................................................................................................. 64
4.10.4 Timer menu ....................................................................................................... 76
4.10.5 CONEXIO menu.................................................................................................. 77
4.10.6 Hygiene functions ............................................................................................... 85
4.10.7 Cleaning menu ................................................................................................... 86
4.10.8 Using other functions. ......................................................................................... 87
4.10.9 Settings menu.................................................................................................... 87
4.11Using the functions through the assistant unit controls ...................................................... 95
4.11.1 Using the chair functions ..................................................................................... 95
4.11.2 Using the hygiene functions ................................................................................. 95
4.11.3 Using the light functions ...................................................................................... 96
4.11.4 Using the timer................................................................................................... 96
4.12Using the foot control..................................................................................................... 97
4.12.1 General functions................................................................................................ 97
4.12.2 Special functions of the wireless foot control.......................................................... 97
4.12.3 Create a connection between the wireless foot control and treatment unit ................ 99
4.12.4 Position the patient chair with the foot control........................................................101
4.12.5 Pre-selecting the type of treatment.......................................................................102
4.12.6 Preselect dentist .................................................................................................103
4.12.7 Start and regulate instruments.............................................................................103
4.12.8 Setting the cooling condition ................................................................................104
4.12.9 Actuate blown air................................................................................................104
4.12.1
0
Preselect counterclockwise motor rotation .............................................................
104
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4.12.1
1
Adjusting the instrument light ..............................................................................
104
4.12.1
2
Use physiological saline solution (optional accessory) .............................................
105
4.12.1
3
Chargethe wireless foot control ...........................................................................
105
4.13Using instruments..........................................................................................................106
4.13.1 Holder logic........................................................................................................106
4.13.2 Using suction hoses ............................................................................................106
4.13.3 Using the three-function handpiece.......................................................................108
4.13.4 Using the multifunctional handpiece......................................................................109
4.13.5 Using the PiezoLED .............................................................................................112
4.14Using the KL 703 LED in ENDO mode (optional accessory) .................................................113
4.14.1 General information ............................................................................................113
4.14.2 Setting the storage position of the endo-motor ......................................................115
4.14.3 Open ENDO mode...............................................................................................116
4.14.4 Set parameters ..................................................................................................116
4.14.5 File database......................................................................................................117
4.14.6 Editing/defining/modifying file profiles...................................................................117
4.14.7 Exiting from the type of treatment "Endodontics" ...................................................123
4.15Using the SL600 surgical motor (optional accessory) .........................................................123
4.15.1 General .............................................................................................................123
4.15.2 Connecting and operating the pump for physiological saline ....................................124
4.15.3 Connecting the SL 600 surgery motor...................................................................124
4.15.4 Calling-up the surgery mode................................................................................125
4.15.5 Mount or pull off the handpiece or contra-angle handpiece......................................125
4.15.6 Start-up the motor..............................................................................................126
4.15.7 Using the surgical motor with programme steps.....................................................126
4.15.8 Using the surgical motor with "Free application" activity..........................................130
4.15.9 Setting the operating light (LUX) ..........................................................................132
4.15.1
0
One-touch calibration..........................................................................................
132
4.15.1
1
Exit surgery mode ..............................................................................................
133
4.16Use pump for physiological saline solution (optional accessory) ..........................................133
4.16.1 General information ............................................................................................134
4.16.2 Connecting the coolant........................................................................................135
4.16.3 Connect coolant to instrument (general) ...............................................................136
4.16.4 Connecting the coolant container and hose set.......................................................136
4.16.5 Turn on pump and regulate .................................................................................138
4.16.6 Changing the coolant container ............................................................................138
4.16.7 After treatment: disposal.....................................................................................139
4.17Using the COMFORTdrive 200 XD/COMFORTbase (optional accessory) ................................140
4.17.1 General use........................................................................................................140
4.17.2 Fitting the motor hose on the dentist's element......................................................140
4.17.3 Replace O-rings ..................................................................................................140
4.17.4 Replacing the high-pressure bulb of the COMFORTbase ..........................................141
4.17.5 Replacing the KaVo MULTI LED lamp ....................................................................141
4.18Use USB interface..........................................................................................................141
4.19Using the camera...........................................................................................................142
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4.20Service table 1568 (optional accessory) ...........................................................................142
4.20.1 Moving the service table......................................................................................143
5 Preparation methods DIN EN ISO 17664...........................................................................145
6 Additional equipment and kits ...........................................................................................146
6.1 Device ..........................................................................................................................146
6.2 Assistant unit ................................................................................................................146
6.3 Dentist unit...................................................................................................................146
7 Safety check - Test instructions .........................................................................................148
7.1 Introduction ..................................................................................................................148
7.1.1 General instructions ............................................................................................148
7.1.2 Notes concerning medical electrical systems..........................................................149
7.1.3 Components of the safety check...........................................................................150
7.1.4 Test intervals .....................................................................................................150
7.1.5 Notes on test procedure in accordance with IEC 62353...........................................150
7.1.6 Notes on repeat tests ..........................................................................................151
7.2 Instructions for the safety check......................................................................................151
7.2.1 Preparatory measures on the device .....................................................................151
7.2.2 Visual inspection.................................................................................................152
7.2.3 Measurements....................................................................................................154
7.2.4 Functional tests ..................................................................................................163
7.2.5 Assessment and documentation ..........................................................................165
7.3 Test protocol for the safety check ....................................................................................166
8 Appendix - Additional measuring sites...............................................................................167
8.1 Additional scanning sites SL X in the protective conductor measurement .............................167
8.2 Additional measuring sites AP X for EUL/EPL measurement ................................................168
9 Eliminating disturbances ....................................................................................................169
10Information concerning the electromagnetic compatibility according to EN IEC
60601-1-2...........................................................................................................................173
10.1Electromagnetic Transmissions........................................................................................173
10.2Resistance to electromagnetic interference .......................................................................173
10.3Immunity to electromagnetic interference ........................................................................174
10.4Recommended safe distances between portable and mobile HF telecommunications
equipment and this product ............................................................................................176
Instructions for use ESTETICA E70 Vision / E80 Vision
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Instructions for use ESTETICA E70 Vision / E80 Vision
1 User instructions | 1.1 User guide
1 User instructions
1.1 User guide
Requirement
Read these instructions prior to first startup to avoid misuse and prevent dam-
age.
1.1.1 Abbreviations
Ab-
brevi-
ation
Explanation
IFU Instructions for use
CI Care instructions
KA Short instructions for use
AI Assembly instructions
TI Technician's instructions
IEC International Electrotechnical Commission
RI Repair instructions
RK Retrofitting kit
AS Assembly kit
CK Conversion kit
EP Enclosed parts
EMC Electromagnetic compatibility
PI Processing instructions
1.1.2 Symbols
See the Safety/Warning Symbols section
Important information for users and technicians
CE mark according to Medical Devices Directive EC 93/42
Action required
eLabeling ID
1.1.3 Target group
This document is for dentists and dental office staff.
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Instructions for use ESTETICA E70 Vision / E80 Vision
1 User instructions | 1.2 Service
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1.2 Service
KaVo Customer Service:
[phone]
[e-mail] or [e-mail]
Please refer to the serial number of the product in all inquiries!
For further information, please visit: www.kavo.com
1.3 Terms and conditions of warranty
KaVo provides the final customer with a warranty that the product cited in the
handover certificate will function properly and guarantees zero defects in the
material or processing for a period of 12 months from data of purchase, subject
to the following conditions:
Upon justified complaints of flaws or a short delivery, KaVo will make good its
warranty by replacing the product free of cost or repairing it according to the
customer's wishes. Other claims of any nature whatsoever, in particular with
respect to compensation, are excluded. In the event of default and gross negli-
gence or intent, this shall only apply in the absence of mandatory legal regula-
tions to the contrary.
KaVo cannot be held liable for defects and their consequences due to natural
wear, improper cleaning or servicing, non-compliance with operating, servicing
or connection instructions, calcification or corrosion, contaminated air or water
supplies or chemical or electrical factors deemed abnormal or impermissible in
accordance with factory specifications.
The warranty does not usually cover bulbs, glassware, rubber parts and the col-
ourfastness of plastics.
Defects or their consequences that can be attributed to interventions on or
changes made to the product by the customer or a third party are excluded
from the warranty.
Claims from this warranty can only be asserted when the transfer form (copy)
belonging to the product has been sent to KaVo, and the original can be
presented by the operator or user.
1.4 Transportation and storage
1.4.1 Currently valid packaging regulations
Note
Only valid for the Federal Republic of Germany.
Dispose of and recycle the sales packaging appropriately in accordance with
current packaging regulations, employing waste management or recycling com-
panies. Comply with the comprehensive return system. KaVo has had its sales
packaging licensed for this purpose. Please comply with the regional public
waste-disposal system.

Instructions for use ESTETICA E70 Vision / E80 Vision
1 User instructions | 1.4 Transportation and storage
1.4.2 Damage in transit
In Germany
If the packaging is visibly damaged on delivery, please proceed as follows:
1. The recipient of the package must record the loss or damage on the delivery
receipt. The recipient and the representative of the shipping company must
sign this delivery receipt.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use the product.
4. Report the damage to the shipping company.
5. Report the damage to KaVo.
6. Consult with KaVo first, before returning a damaged product.
7. Send the signed delivery receipt to KaVo.
If the product is damaged but there was no discernable damage to the pack-
aging on delivery, proceed as follows:
1. Report the damage to the shipping company immediately and no later than
7 days after delivery.
2. Report the damage to KaVo.
3. Leave the product and packaging in the condition in which you received it.
4. Do not use a damaged product.
Note
Failure on the part of the recipient to comply with any of the above-men-
tioned obligations will mean that the damage will be considered to have
arisen following delivery (in accordance with the General German Freight For-
warders' Terms and Conditions, Art. 28).
Outside Germany
Note
KaVo shall not be held liable for damage arising from transportation.
The shipment must be checked on arrival.
If the packaging is visibly damaged on delivery, please proceed as follows:
1. The recipient of the package must record the loss or damage on the delivery
receipt. The recipient and the representative of the shipping company must
sign this delivery receipt.
Without this evidence, the recipient will not be able to assert a claim for
damages against the shipping company.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use the product.
If the product is damaged but there was no discernable damage to the pack-
aging on delivery, proceed as follows:
1. Report any damage to the shipping company immediately and no later than
7 days after delivery.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use a damaged product.
Note
If the recipient fails to comply with any of the above-mentioned obligations,
the damage will be considered to have arisen following delivery
(in accordance with CMR law, Chapter 5, Art. 30).
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Instructions for use ESTETICA E70 Vision / E80 Vision
1 User instructions | 1.4 Transportation and storage
10 / 178
1.4.3 Information on the packaging: Storage and
transportation
Note
Please keep the packaging in case you need to return the product for servi-
cing or repair.
The symbols printed on the outside are for transportation and storage, and
have the following meaning:
Transport upright with the arrows pointing upwards!
Fragile - protect against impact!
Protect from moisture!
Permissible stacking load
Temperature range
Humidity
Air pressure

Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.1 Description of safety instructions
2 Safety
2.1 Description of safety instructions
2.1.1 Warning symbol
Warning symbol
2.1.2 Structure
DANGER
The introduction describes the type and source of the hazard.
This section describes potential consequences of non-compliance.
▶The optional step includes necessary measures for hazard prevention.
2.1.3 Description of hazard levels
The warning and safety notes in this document must be observed to prevent
personal injury and material damage. The warning notes are designated as
shown below:
DANGER
In cases which – if not prevented – directly lead to death or severe in-
jury.
WARNING
In cases which – if not prevented – can lead to death or severe injury.
CAUTION
In cases which – if not prevented – can lead to minor or moderate in-
jury.
NOTICE
In cases which – if not prevented – can lead to material damage.
2.2 Intended use
2.2.1 Indications for use
The ESTETICA Dental Treatment Unit and Accessories are intended to supply
power to and serve as a base for other dental devices and accessories by
providing air, water, vacuum and low voltage electrical power to dental instru-
ments and dental handpieces. The ESTETICA Dental Treatment Unit and Ac-
cessories are designed for use by a trained professional in the field of general
dentistry.
11 / 178

Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.2 Intended use
12 / 178
CAUTION
US Federal law restricts this device to sale by or on the order of a
health care professional / dentist.
For dental use only.
The KaVo service table 1568 is an accessory of KaVo treatment centres that do
not feature a dentist element mounted to the unit. The KaVo Service table 1568
serves as a support surface for the dentist during the treatment. The service
table 1568 can be used as a support for trays and for attachment of the X-ray
viewer 1440. The mobile support system allows the KaVo Service table 1568 to
be moved to the proper position.
Connecting devices
KaVo-approved accessories for patient communication. These accessories must
be used exclusively.
Accessories Use Name Material number
Monitors Monitor 22“ KaVo Screen HD 1.011.0302
Monitor 19“ KaVo Screen One 1.011.0300
Cameras Intraoral camera ERGOcam One 130
ERGOcam One 160
1.011.2130
1.011.2129
Caries diagnostic
device
DIAGNOcam 2170
U
1.011.0400
Cables between
unit, accessories
and PC
USB extension
cord - 5 metres
USB extension
cord 5m with 1:1
hub
1.004.6953
USB extension
cord - 10 metres
USB extension
cord 2x5m with
1:1 hub
1.011.3745
Display port cable
- 5 metres
LTG Display port
5m Standard
1.011.3583
Display port cable
- 10 metres
LTG Display port
10m Standard
1.011.0298
Note
The USB interfaces of the system may only be connected to IT devices ap-
proved by KaVo.
Note
When connecting IT equipment to the the medial electrical system, observe
EN 60601-1.
Note
Charge the wireless foot control with the charger supplied by KaVo only.
Note
The wireless foot control charger may only be used indoors and must be pro-
tected from moisture.

Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.2 Intended use
2.2.2 General
The functional safety and proper condition of the device must be checked be-
fore each use of the device.
The ESTETICA E70 Vision / E80 Vision equipment system is a dental treatment
centre in accordance with ISO 7494 featuring a dental chair in accordance with
ISO 6875. This KaVo product is designed for use in dentistry only and may only
be used by trained medical personnel. Any other type of use is not permitted.
"Proper use" includes compliance with all information in the Instructions for Use
and ensuring that all inspections and service tasks are performed.
The overarching guidelines and/or national laws, national regulations and the
rules of technology applicable to medical devices for start-up and use of the
KaVo product for the intended purpose must be applied and followed.
KaVo accepts liability for the safety, reliability, and performance of components
supplied by KaVo, provided:
▪ installation, instructions, expansions, adjustments, changes or repairs were
carried out by technicians trained by KaVo or third parties authorised by
KaVo, or by the personnel of authorised distributors.
▪ the unit was operated in accordance with the instructions for use, care and
installation.
▪ the IT components supplied by the operator meet the technical require-
ments in the present instruction for use for hardware and software, and are
installed and set up according to the descriptions of these components.
▪ in the case of repairs, the requirements of IEC 62353 "Recurrent tests and
tests before start-up of electrical items of medical electrical equipment and
systems - general regulations" are met in full.
It is a responsibility of the user:
▪ to only use equipment that is operating correctly,
▪ to protect him or herself, the patient and third parties from hazards, and
▪ to prevent contamination from the product
The applicable national legal regulations must be observed during the use of the
device, in particular the following:
▪ Applicable regulations governing the connection and startup of medical
devices.
▪ Current occupational safety regulations.
▪ Current accident prevention regulations.
Regular servicing and safety checks are essential for the permanent assurance
of the operating and functional safety of the KaVo product and for the preven-
tion of damage and hazards.
Testing and maintenance intervals: Maintenance must be performed once a
year, the safety checks at intervals of 2 years. Shorter intervals for the safety
checks may be specified by the tester if necessary.
The following persons are authorised to conduct repairs and servicing and the
safety check on the KaVo product:
▪ Technicians of KaVo branch offices after appropriate product training.
▪ Specifically KaVo-trained technicians of KaVo franchised dealers.
13 / 178

Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.2 Intended use
14 / 178
In Germany, operators, equipment managers and users are obliged to operate
their equipment in accordance with the MPG regulations.
The services encompass all the test tasks required in accordance with § 6 of the
medical devices operator ordinance (Medizinprodukte-Betreiberverordnung, MP-
BetreibV).
Note
The product must be cleaned and serviced according to instructions if it is not
to be used for an extended period of time.
Note
The MULTIflex couplings, the current K/KL motors, and the ultrasonic scaler
hoses of KaVo are equipped as standard with a protective device to prevent
treatment water from being drawn back into the treatment centre via the
handpieces. If products from other manufacturers are used at the standard-
ised interfaces, it must be ensured that they are equipped with an appropri-
ate protective device! If this is not the case, they may not be used!
The product includes open source licences to a certain extent. The exact licens-
ing conditions, liability disclaimers, concessions and instructions will be provided
to you in the device software. KaVo offers to provide the source code on a CD
ROM; efforts and costs incurred (e. g. costs for auxiliaries, transport and pro-
cessing) will be invoiced in terms of an expense allowance. You can address a
corresponding inquiry to KaVo Dental GmbH in written form.
Information about electromagnetic compatibility
Note
Based on IEC 60601-1-2 (DIN EN 60601-1-2) concerning the electromag-
netic compatibility of electrical medical devices, we must draw your attention
to the following points:
• Medical electrical devices are subject to special precautions concerning the
electromagnetic compatibility and must be installed and operated in accord-
ance with the KaVo assembly instructions.
• High-frequency communications devices may interfere with electrical med-
ical devices.
Note
KaVo cannot guarantee the compliance of accessories, cables, and other
components not supplied by KaVo with the EMC requirements of IEC
60601-1-2 (DIN EN 60601-1-2).
Disposal
Note
Any waste which is generated must be recycled or disposed of in strict com-
pliance with all applicable national regulations in a manner which is safe both
for people and the environment.
If you have any questions regarding proper disposal of the KaVo product,
please contact the KaVo branch.

Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.3 Safety instructions
2.3 Safety instructions
2.3.1 General information
Note
The safety and reliability of the system can only be ensured when the de-
scribed procedure is followed.
DANGER
Explosion hazard.
Risk of fatal injury.
▶Do not use KaVo product in areas subject an explosion hazard.
WARNING
Inappropriate operating conditions.
Impairment of the electrical safety of the device.
▶It is essential to comply with the operating conditions specified in the
"Technical Specifications" chapter.
WARNING
Application of un-authorised accessories or un-authorised modifica-
tions of the product.
Accessories that have not been approved and/or inadmissible modifications of
the product could lead to hazards and/or personal injury or property damage.
▶Only use accessories that have been approved for combination with the
product by the manufacturer or are equipped with standardised interfaces
(e. g. MULTIflex couplings, INTRAmatic).
▶Do not make any modifications to the device unless these have been ap-
proved by the manufacturer of the product.
WARNING
Injury or damage from damaged functional parts.
If functional parts are damaged, it can cause additional damage or personal in-
jury.
▶Check the device, electrical cables and any accessories regularly for pos-
sible damage to the insulation and replace them according to need.
▶If functional parts are damaged: discontinue your work and
repair the damage or notify a service technician!
WARNING
Dispose of the product in appropriate manner.
Infection hazard.
▶Before disposal, reprocess and sterilise the product and accessories appro-
priately.
CAUTION
Health hazard and property damage due to non-compliance with servi-
cing schedule.
Infection hazard to users and patients.
Product damage.
▶Comply with servicing schedule.
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Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.3 Safety instructions
16 / 178
CAUTION
Risks from electromagnetic fields.
Electromagnetic fields might interfere with the functions of implanted systems
(such as pacemakers).
▶Ask patients if they have a cardiac pacemaker or other system implanted
before you start the treatment!
CAUTION
Malfunctions due to electromagnetic fields.
The product meets the applicable requirements regarding electromagnetic
fields. Given the complex interactions between equipment and cell phones, the
product may be influenced by a cell phone that is in use.
▶Do not use cell phones in medical offices, hospitals or laboratories!
▶Put electronic devices such as e.g. computer storage media, hearing aids
etc. down during operation!
NOTICE
Damage from liquids.
Residual liquids of any type can cause stains on or damage to cushions and
parts of the housing.
▶Remove any residual liquids without delay.
NOTICE
Premature wear and malfunctions from improper servicing and care.
Reduced product life.
▶Perform regular proper care and servicing!
Note
The operator may only carry out repair work if the device is switched off and
no patient is being treated.
2.3.2 Product-specific
WARNING
Injury or infection hazard from laid down instruments.
Given the arrangement of the instruments, injury or infections in the hand and
underarm may occur when reaching for the tray holder or operating device. In-
creased risk of infection from ill patients.
▶Be aware of the arrangement of the instruments when you reach for the
tray holder or operating device.
WARNING
Health damage due to back-suction on the instruments.
Infection hazard.
It is feasible to use, on standardised interfaces, products from other manufac-
turers, which are not equipped with a protective device preventing back-suc-
tion of treatment water via the instruments into the dental treatment centre.
▶If products from other manufacturers are used at the standardised inter-
faces, you must make sure that the products are equipped with an appro-
priate protective device!
▶Do not use products with no protective device.

Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.3 Safety instructions
CAUTION
Electrical power.
Electrical shock from incorrectly connecting a non-medical system to the USB
interfaces of the device.
▶Connect any IT device to the medical system in accordance with IEC
60601-1.
▶Use USB devices with no additional power supply (USB-powered) only.
▶Applied parts connected to the USB interface of the dentist element must
comply with the requisite insulation.
▶USB-powered devices failing to meet the requisite insulation for applied
parts must be placed appropriately such that direct contact of the USB
device and the patient is excluded.
▶It is not permissible to touch USB-powered devices failing to meet the re-
quisite insulation for applied parts and the patient at the same time.
CAUTION
Sitting down on a dental chair that is in horizontal orientation is asso-
ciated with a risk of injury.
▶Do not sit on the head or foot end of the patient chair when it is in a hori-
zontal position.
CAUTION
Risk of injury if you support yourself on the swivel arm.
Exposing the swivel arm to an overload may damage the swivel arm and cause
injury to the patient or user.
▶Never strain the swivel arm, spring arm, assistant element and dentist ele-
ment by using it as a support!
CAUTION
Risk of injury by suspended instruments (S table).
Patients may get injured by sharp instrument tips.
▶When you move the dentist's unit, make sure that nobody is injured.
▶Alert patients and care providers to the risk of injury.
CAUTION
Risk of injury during cleaning of the treatment unit.
Lack of instructions to the cleaning staff and lack of preparation of the treat-
ment unit can lead to the cleaning personnel sustaining injuries.
▶Only trained professionals and instructed cleaning personnel may be
present in the treatment rooms.
▶Position the chair for cleaning and turn the device off.
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Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.3 Safety instructions
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CAUTION
Third-party device connection assembly kit (optional): Risk of reverse
contamination by stagnant water.
Infections.
If a water consumer is connected to the third-party device connection as-
sembly kit, always perform the following actions on the device:
▶Before starting, rinse all the water drain lines with no handpieces attached
(if applicable).
▶Before initial start-up and after downtimes (weekends, holidays, vacations,
etc.), rinse or purge the air and water lines with air.
▶Mind the H2O2 resistance of the water consumer since the water is doped
with OXYGENAL 6 cleaner (concentration up to 0.02 %).
CAUTION
Health damage due to germ formation.
Infection hazard.
▶Before starting, rinse all the water drain lines without instruments.
▶Before start-up and after the device has not been used for a while (week-
ends, holidays, vacations, etc.), rinse or purge with air the air and water
lines.
▶Carry out an intensive germ reduction.
▶Actuate the tumbler filler repeatedly.
CAUTION
Risk of injury and material damage from incorrect use of the charger
for the wireless foot control.
Personal injuries, damage to the wireless foot control or the charger.
▶Do not use the treatment unit during the charging process!
▶Do not use the wireless foot control charger supplied to charge non-re-
chargeable batteries.
▶Charge the wireless foot control with the charger supplied only.
CAUTION
Long stay in the patient chair.
Decubitus formation.
▶Take precautions against the formation of decubitus in long treatments.
CAUTION
Danger of injury from tipping the treatment unit.
Injury to the patient and user.
▶Do not support yourself on the swinging arm.
▶Do not sit on the head or foot end of the patient chair when it is in a hori-
zontal position.
CAUTION
Danger of injury from overload or dynamic load.
The patient chair might collapse.
▶Do not subject the patient chair to a load exceeding its limit (180 kg).
▶Do not subject the patient chair to dynamic loads.

Instructions for use ESTETICA E70 Vision / E80 Vision
2 Safety | 2.3 Safety instructions
CAUTION
Risk of injury when the dental chair or headrest is moved.
Hair of the patient or practice personnel may get caught when the headrest of
the dental chair is moved.
▶Mind the hair of the patient or practice personnel when moving the dental
chair or the headrest.
CAUTION
Risk of injury when the dentist or assistant element is moved.
The patient or office staff may be injured or bruised.
▶Monitor the patient and office staff when moving the dentist or assistant
element.
CAUTION
Danger of crushing during automatic chair movement.
The patient or treatment personnel can be clamped.
▶Monitor the patient and treatment personnel when changing the chair posi-
tion.
NOTICE
Damage to the instrument hoses from stickers.
Instrument hoses can burst.
▶Do not affix stickers or adhesive tape.
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Instructions for use ESTETICA E70 Vision / E80 Vision
3 Product description | 3.1 Treatment centre
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3 Product description
The ESTETICA Dental Treatment Unit and Accessories serves as a base that in-
cludes components to deliver air, water, electrical power, and vacuum to dental
handpieces, instruments, and accessories. The device includes a patient chair,
foot control, dentist element, assistant element and a water unit. The unit may
also include a dental operating light and a monitor. Various handpieces and ac-
cessories can be added to the ESTETICA Dental Treatment Unit and Accessor-
ies. These include, but not limited to, pneumatic handpieces, electric motors
with handpieces, scalers, intra-oral cameras, curing lights, air/water syringes
and SE and HVE vacuum instruments.
3.1 Treatment centre
3.1.1 KaVo ESTETICA E70 Vision / E80 Vision T
①Patient element ②Assistant element
③Headrest ④Backrest
⑤Operating light ⑥Dentist element
⑦Seat ⑧Arm rest
⑨Kick plate ⑩Foot control