KaVo ESTETICA E30 User manual

Instructions for use
ESTETICA E30

Distributed by:
KaVo Dental GmbH
Bismarckring 39
88400 Biberach
Germany
Phone [phone]
Fax [phone]
Manufacturer:
KaVo Dental GmbH
Bismarckring 39
88400 Biberach
Germany
www.kavo.com

Instructions for use ESTETICA E30
Table of contents
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Table of contents
1 User instructions ............................................................................................................... 6
1.1 Terms and conditions of warranty.................................................................................... 8
2 Safety................................................................................................................................. 9
2.1 Explosion hazard ........................................................................................................... 9
2.2 Infection hazard ............................................................................................................ 9
2.3 Electrical shock.............................................................................................................. 10
2.4 Technical condition ........................................................................................................ 10
2.5 Electromagnetic fields .................................................................................................... 10
2.6 Use .............................................................................................................................. 11
2.7 Accessories and combination with other equipment........................................................... 11
2.8 Qualification of personnel ............................................................................................... 12
2.9 Service and repair ......................................................................................................... 12
2.10 Internet security (Cybersecurity)..................................................................................... 12
2.11 Intended use................................................................................................................. 13
3 Description of the product................................................................................................. 16
3.1 Treatment centre versions.............................................................................................. 16
3.1.1 KaVo ESTETICA E30 S ...................................................................................... 16
3.1.2 KaVo ESTETICA E30 TM .................................................................................... 16
3.2 Patient chair.................................................................................................................. 17
3.3 Unit with patient element ............................................................................................... 18
3.4 Versions of the dentist element ....................................................................................... 18
3.4.1 TM table .......................................................................................................... 18
3.4.2 S-Table ........................................................................................................... 20
3.5 Assistant element .......................................................................................................... 21
3.6 Triple function handpieces .............................................................................................. 22
3.7 Control elements ........................................................................................................... 23
3.7.1 Dentist element TM table .................................................................................. 23
3.7.2 Dentist element S-table .................................................................................... 23
3.7.3 Assistant element............................................................................................. 24
3.7.4 Groups of keys................................................................................................. 24
3.7.5 Foot control .................................................................................................... 26
3.8 Rating plate and serial number plates .............................................................................. 27
3.9 Technical Specifications.................................................................................................. 30
4 Operation........................................................................................................................... 36
4.1 Switching the device on and off....................................................................................... 37
4.2 Converting from right handed to left handed .................................................................... 37
4.3 Adjusting the dental chair............................................................................................... 42
4.3.1 Adjusting the armrest (optional) ........................................................................ 42
4.3.2 Adjusting the headrest...................................................................................... 43
4.3.3 Positioning the patient chair manually................................................................. 44
4.3.4 Automatic positioning of patient chair ................................................................. 45
4.3.5 Safety shutdown .............................................................................................. 49
4.4 Moving the patient chair................................................................................................. 51
4.5 Moving the dentist element............................................................................................. 51
4.5.1 Moving the dentist unit TM ................................................................................ 52
4.5.2 Moving the dentist unit S................................................................................... 53
4.6 Moving the patient unit .................................................................................................. 53
4.6.1 Moving the patient element (optional) ................................................................ 54

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4.7 Attaching the tray holder (optional) ................................................................................. 55
4.8 Using functions through the menu................................................................................... 55
4.8.1 General menu navigation .................................................................................. 55
4.8.2 Using the user menu......................................................................................... 56
4.8.3 Standby menu ................................................................................................. 61
4.8.4 Selecting the dentist ......................................................................................... 62
4.8.5 Instruments menu............................................................................................ 62
4.8.6 ENDO menu (optional)...................................................................................... 65
4.8.7 Operating the CONEXIO menu (optional) ............................................................ 69
4.9 Using function through the dentist or assistant element..................................................... 71
4.9.1 Using the hygiene functions............................................................................... 71
4.9.2 Illumination functions for KaVoLUX 540 LED T ..................................................... 72
4.9.3 Using the illumination functions for EDI and MAIA................................................ 78
4.9.4 Using the X-ray viewer...................................................................................... 78
4.9.5 Using the bell................................................................................................... 78
4.9.6 Using the timer ................................................................................................ 78
4.10 Operating the foot control............................................................................................... 79
4.10.1 General functions ............................................................................................. 79
4.10.2 Positioning the patient chair with the foot control................................................. 79
4.10.3 Preselecting the dentist..................................................................................... 79
4.10.4 Starting and adjusting instruments..................................................................... 79
4.10.5 Setting the cooling status .................................................................................. 80
4.10.6 Activating blown air (optional) ........................................................................... 80
4.10.7 Preselecting counterclockwise motor rotation....................................................... 80
4.10.8 Setting the instrument light............................................................................... 80
4.10.9 CONEXIO operation (fee-based additional option) ................................................ 81
4.11 Using handpieces........................................................................................................... 82
4.11.1 Setting spray air and spray water....................................................................... 82
4.11.2 Using suction hoses .......................................................................................... 83
4.11.3 Using triple-function handpieces......................................................................... 84
4.11.4 PIEZOUsing the PIEZO SoftPiezoLED .................................................................. 86
4.12 Using the KL 703 LED in ENDO mode (optional accessory)................................................. 87
4.12.1 General ........................................................................................................... 87
4.12.2 Calling up ENDO mode...................................................................................... 89
4.12.3 Set torque mode .............................................................................................. 90
4.12.4 Changing settings in the menu........................................................................... 91
4.12.5 Exiting ENDO mode .......................................................................................... 91
4.13 Using the USB interface.................................................................................................. 91
4.14 Using the camera .......................................................................................................... 92
4.15 Using the screen............................................................................................................ 92
4.16 Connector for third-party equipment................................................................................ 92
5 Reprocessing methods DIN EN ISO 17664 ....................................................................... 94
6 Accessories and kits .......................................................................................................... 95
6.1 Equipment .................................................................................................................... 95
6.2 Patient chair.................................................................................................................. 96
6.3 Assistant element .......................................................................................................... 96
6.4 Dentist element ............................................................................................................ 96
7 Safety check - Test instructions ........................................................................................ 97
7.1 Introduction .................................................................................................................. 97
7.1.1 General notes .................................................................................................. 97

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7.1.2 Notes for medical electrical systems ................................................................... 98
7.1.3 Components of the safety check ........................................................................ 98
7.1.4 Testing intervals............................................................................................... 99
7.1.5 Notes on the test method in accordance with IEC 62353 ...................................... 99
7.1.6 Notes on recurrent testing................................................................................. 99
7.2 Instructions for the safety check .....................................................................................
100
7.2.1 Preparatory measures to be undertaken on the device .........................................100
7.2.2 Visual inspection (inspection by examination)......................................................100
7.2.3 Measurements .................................................................................................103
7.2.4 Functional tests................................................................................................111
7.2.5 Assessment and documentation.........................................................................112
7.3 Test protocol for the safety check....................................................................................
113
8 Annex - Additional measuring points ................................................................................114
8.1 Additional scan points SL X for the protective earth measurement ......................................
114
8.2 Additional measuring points AP X for the EUL/EPA measurement........................................
116
9 Troubleshooting ................................................................................................................117
10Information concerning the electromagnetic compatibility according to EN IEC
60601-1-2..........................................................................................................................
119
10.1 Operating environment and EMC warning notes................................................................
119
10.2 Results of the electromagnetic tests ................................................................................
119

Instructions for use ESTETICA E30
1 User instructions |
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1 User instructions
Dear user,
Congratulations on purchasing this KaVo quality product. By following the notes
below you will be able to work smoothly, economically and safely.
© Copyright by KaVo Dental GmbH
All other trademarks are property of their respective owners.
Target group
The instructions for use are intended for medical professionals, in particular
dentists and dental practice personnel.
General marks and symbols
See Chapter on User Instructions/Hazard Levels
Important information for users and service technicians
Action request
CE- mark (European Community). A product bearing this mark meets
the requirements of the applicable EC directives.
Sterilisation parameters
▪ Steriliser with Dynamic-Air-Removal (pre-vacuum) method:
– 3 minutes at 135oC (275 oF)
– Drying time: 16 min.
▪ Steriliser with gravity displacement method:
– 10 minutes at 135oC (275 oF)
– Drying time: 30 min.
Thermodisinfectable
Original language German
Information on the packaging
Material number
Serial number
Manufacturer
Note: Please note accompanying documents
Follow the electronic instructions for use

Instructions for use ESTETICA E30
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HIBC Code
EAC conformity mark (Eurasian Conformity)
Transportation and storage conditions
(temperature range)
Transportation and storage conditions
(air pressure)
Transportation and storage conditions
(Humidity)
Protect from moisture (Keep dry)
Protect from impact
Transport upright
Permissible stacking load
Medical device, labelling of medical devices
CE mark for medical devices
UDI symbol
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:
HAZARD
In cases which – if not prevented – directly lead to death or severe injury.
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 injury.
CAUTION
In cases which – if not prevented – can lead to material damage.

Instructions for use ESTETICA E30
1 User instructions | 1.1 Terms and conditions of warranty
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KaVo Technical service
If you have any technical questions or complaints, please contact the KaVo
Technical service:
[phone]
[e-mail] or [e-mail]
Please refer to the serial number of the product in all inquiries! For further in-
formation, please visit: www.kavo.com
Currently applicable packaging law
Dispose of and recycle the packaging appropriately in accordance with current
packaging law, employing waste management / recycling companies. Comply
with the comprehensive return system. KaVo has had its packaging licensed for
this purpose. Please comply with the regional public waste-disposal system.
1.1 Terms and conditions of warranty
KaVo provides the final customer with a warranty that the product cited in the
transfer form will function properly and guarantees zero defects in the material
or processing for a period of 12 months from the date 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.

Instructions for use ESTETICA E30
2 Safety | 2.1 Explosion hazard
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2 Safety
The instructions for use are an integral part of the product and must be read
carefully prior to use and must be accessible at all times.
The device may only be used in accordance with the intended use, any other
type of use is not permitted.
NOTE
All serious events occurring in relation to the product must be reported to the
manufacturer and the competent authority of the member state, in which the
user and/or patient resides.
2.1 Explosion hazard
Electrical sparks in the product can lead to explosion or fire.
4 Do not set up or operate the product in areas where there is an explosion
hazard.
The use of medical gases can lead to explosion or fire.
4Do not used medical gases in the vicinity of the product.
2.2 Infection hazard
Patients, users or third parties could be infected by contaminated medical
devices.
4Take suitable personal protective measures.
4Follow the instructions for use of the components.
4Before initial startup and after each use, reprocess the product and ac-
cessories appropriately.
4Reprocess the product and accessories appropriately before disposal.
Given the arrangement of the instruments, injury or infections may occur when
reaching for the tray holder or control panel.
4Be aware of the arrangement of the instruments when you reach for the
tray holder or operating device.
Suspended instruments (S-table) can cause injury.
4When you move the dentist element, make sure that nobody gets injured.
It is feasible to use, on standardised interfaces, products from other manufac-
turers, which are not equipped with a protective device preventing back-suction
of treatment water via the instruments into the dental treatment centre. Infec-
tion may be caused by back-suction at the instruments.
4If 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.
4Do not use products with no protective device.
If a water consumer is connected to the third-party connector assembly kit (op-
tional), stagnant water may cause reverse contamination with germs.
4Before starting, rinse all water drain lines while no handpiece is attached (if
applicable).
4Before initial start-up and after downtimes (weekends, holidays, vacations,
etc.), rinse or purge the air and water lines with air.
4Mind the H2O2 resistance of the water consumer since the water is doped
with OXYGENAL 6 (concentration up to 0.02 %).
Germ formation can lead to infection.
4Carry out an intensive germ reduction.
4Actuate the tumbler filler several times.

Instructions for use ESTETICA E30
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2.3 Electrical shock
Improper connection of a non-medical system to the USB interfaces of the
device can lead to electrical shock and injury to patient, user and third parties.
4Connect any USB device to the medical system in accordance with IEC
60601-1 / IEC 62368-1.
4Set up the external PC outside of the patient environment keeping a min-
imum distance of 1.5 m.
4Connect the PC and equipment connected to the PC in accordance with IEC
60601-1 / 62368.
4Use USB devices with no additional power supply (USB-powered) only.
4Applied parts connected to the USB interface of the treatment centre must
comply with IEC 60601-1 type BF.
4USB-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.
4It 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.
2.4 Technical condition
If damaged, the device or components could injure patients, users and third
parties.
4Only operate devices or components if they show no signs of damage on the
outside.
4Check to make sure that the device is working properly and is in satisfactory
condition before each use.
4Have parts with sites of breakage or surface changes checked by the service
personnel.
4If the following defects occur, stop working and have the service personnel
carry out repair work:
▪ Malfunctions
▪ Damage
▪ Irregular running noise
▪ Excessive vibration
▪ Overheating
▪ Dental bur is not seated firmly in the handpiece
The electrical safety of the device may be affected by improper operating condi-
tions.
4Comply with the operating conditions specified in the "Technical Specifica-
tions" chapter.
Instrument hoses may burst due to stickers.
4Do not affix stickers or adhesive tape to instrument hoses.
2.5 Electromagnetic fields
Electromagnetic fields might interfere with the functions of implanted systems
(such as pacemakers).
4Ask patients if they have a cardiac pacemaker or other system implanted
and counsel them about the risks before you start the treatment.
High-frequency communications devices may interfere with medical electrical
devices.
4Do not use cell phones in medical offices, hospitals or laboratories.
4Remove electronic devices such as e.g. computer storage media, hearing
aids etc. during operation.

Instructions for use ESTETICA E30
2 Safety | 2.6 Use
11 / 124
4Comply with the tables of electromagnetic compatibility during installation
and commissioning.
4If the device needs to be used in the immediate vicinity of other equipment,
monitor the device or system for malfunctions.
2.6 Use
Sitting down on a dental chair that is in horizontal orientation may lead to in-
jury.
4Do not sit down or support yourself on the head or foot end or edges of the
upholstery of the patient chair when it is in a horizontal position.
4Do not support yourself or sit on the armrest.
Exposing the arm system to an overload may cause damage and ensuing in-
jury.
4Never strain the swivel arm, spring arm, assistant element and dentist ele-
ment by using it as a support.
Lack of instructions to the cleaning staff and improper preparation of the treat-
ment centre can lead to the cleaning staff sustaining injuries.
4Only trained professionals and instructed cleaning personnel may be present
in the treatment rooms.
4Position the chair for cleaning and turn the device off.
Long stay in the patient chair can lead to decubitus (pressure sores).
4Take precautions against the formation of decubitus in long treatments.
Overload or dynamic loads can lead to injury and material damage.
4Do not subject the patient chair to a load exceeding its limit (180 kg).
4Do not subject the patient chair to dynamic loads.
Hair of the patient or practice personnel may get caught when the headrest of
the dental chair is moved.
4Mind the hair of the patient or practice personnel when moving the dental
chair or the headrest.
Manual motions of components can lead to injury and material damage.
4Monitor the patient and treatment personnel when you move components.
While entering or exiting, the patient make get entangled in instrument hoses
of the dentist element.
4Position the dentist element outside the entry and exit area.
Automatic motions of the patient chair can lead to injury and material damage.
4Monitor the patient and treatment personnel when changing the chair posi-
tion.
Components of the product may be in the walking path and may lead to injury.
4In use, mind the walking path.
4Keep entry and exit positions unobstructed.
2.7 Accessories and combination with other equipment
Use of non-authorised accessories or non-authorised modifications of the device
could lead to injury.
4Only use accessories that have been approved for combination with the
product by the manufacturer.
4Do not make any modifications to the device unless these have been ap-
proved by the manufacturer of the product.

Instructions for use ESTETICA E30
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12 / 124
The use of non-approved accessories as well as non-approved modifications
made to the medical device cause the conformity of the medical device accord-
ing to MDR 2017/745 to be voided. Anybody using non-approved accessories or
making non-approved modifications is deemed, according to MDR 2017/745, to
be the sole liable manufacturer of the medical device and to assume full re-
sponsibility. The new manufacturer is obliged to provide a new declaration of
conformity for the new medical device.
2.8 Qualification of personnel
Application of the product by users without the appropriate medical training
could injure patients, users or third parties.
4Make sure that the user has read and fully comprehends the instructions for
use.
4Make sure that the user has read and comprehends the national and re-
gional regulations.
4The device may be used only if the user has completed the appropriate
medical training.
The operator is responsible for making sure that the product is not used by un-
authorised persons.
2.9 Service and repair
Repairs, servicing and safety checks may only be performed by trained service
personnel. The following persons are authorised to do this:
▪ Service technicians of KaVo branches after the appropriate product training
▪ Service technicians of KaVo authorised dealers after the appropriate product
training
Observe all the following items during servicing work:
4Have the service and testing tasks carried out according to the Medical
Device Operator Ordinance.
4After servicing, interventions on and repairs of the device and before re-use,
have the service personnel perform safety checks on the device.
Improper maintenance and care may lead to premature wear and malfunction.
4Service regularly with suitable agents.
Residual liquids of any type can cause stains on or damage to cushions and
parts of the housing.
4Remove any residual liquids without delay.
The operator may only carry out repair work if the device is switched off and no
patient is being treated.
2.10 Internet security (Cybersecurity)
Unauthorised access by malware can lead to data loss are unauthorised disclos-
ure of sensitive data.
4Always use a current virus scanner with firewall.
Hard disk defects can lead to data loss.
4Generate backup copies regularly.
4Keep backup copies in a safe location.
The user is responsible for backing up data.
For security reasons, the database and all document files should be backed up
regularly. A data backup schedule should be prepared.
KaVo recommends daily backup.

Instructions for use ESTETICA E30
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Backup copies must be stored in a safe place protected from access of third
parties. The detailed procedure should be defined in a data protection concept.
2.11 Intended use
Indications for use:
▪ The medical device is designed for dental treatment of children and adults.
▪ The KaVo equipment system is a dental treatment centre in accordance with
ISO 7494 equipped with a patient chair.
▪ The triple-function handpiece is a dental instrument in accordance with EN
1639. It aids the dental application in the mouth of the patient by supplying
air, water or spray.
▪ These KaVo products are designed for use in dentistry only and must be
used by trained medical personnel only. The installation is done exclusively
in a fixed place in premises used for medical purposes.
Connection of devices
KaVo-approved accessories for patient communication. Use these accessories
exclusively.
Accessories Use Name (material num-
ber)
Monitors Monitor 22“ KaVo Screen HD
(1.011.0302)
Monitor 19“ KaVo Screen One
(1.011.0300)
Cameras Intraoral camera ERGOcam One 130
(1.011.2130)
ERGOcam One 160
(1.011.2129)
Caries diagnostic device DIAGNOcam 2170 U
(1.011.0400)
Cables between unit, ac-
cessories and PC
USB extension cord USB extension cord 5m
with 1:1 hub
(1.004.6953)
USB extension cord 2x5m
with 1:1 hub
(1.011.3745)
HDMI cables HDMI cable 10 m
(1.014.7351)
HDMI cable 3 m
(1.014.7352)
Patient communication
systems
Patient communication KaVo CONEXIO
(1.010.2000;
1.010.1500)
NOTE
The USB interfaces of the system may only be connected to IT devices ap-
proved by KaVo.
NOTE
Connecting IT equipment to the medical electrical system make sure to com-
ply with EN 60601-1.

Instructions for use ESTETICA E30
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Proper use:
The general guidelines and/or national laws, national regulations and technical
rules for medical devices relating to the commissioning and use of the KaVo
product in accordance with the prescribed indications for use 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, servicing
and assembly.
▪ 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.
According to these regulations, the user is required:
▪ to only use equipment that is operating correctly
▪ to comply with the specified intended use
▪ to protect him or herself, the patient and third parties from hazards
▪ to prevent contamination from the product
According to these regulations, this product may only be used for the described
application by a properly trained user. You need to comply with the following:
▪ the applicable health and safety regulations
▪ the applicable accident prevention regulations
▪ these Instructions for use
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 neces-
sary.
Operators, equipment managers and users in Germany are obliged to operate
their equipment in compliance with the medical device law ("MPG"). The main-
tenance services encompass all the test tasks required in accordance with § 6
of the operator ordinance ("MPBetreiberV").
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 appropriate
protective device! They must not be used unless this is the case!

Instructions for use ESTETICA E30
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Information about electromagnetic compatibility
NOTE
Based on IEC 60601-1-2 (DIN EN 60601-1-2) concerning the electro-
magnetic 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 medical electrical
devices.
KaVo does not 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 of electronic and electrical devices
NOTE
According to the general WEEE Directive (Waste Electrical and Electronic
Equipment) and EU Directive 2012/19 concerning waste electrical and elec-
tronic equipment, we wish to point out that this product is subject to the
aforementioned Directive and must be subjected to special disposal within
Europe. For more information, please visit www.kavo.com or contact your
specialised dental dealers.
Final disposal in Germany
To return an electrical device, you need to proceed as follows:
1. On the homepage www.enretec.de of enretec GmbH, you can download a
form for a disposal order under the menu item, eom. Download the disposal
order or complete it as an online order.
2. Enter the corresponding information to complete the order, and submit it as
an online order or by fax [phone] to enretec GmbH. Alternat-
ively, the following contact options are available to you to initiate a dispos-
able order or if you have any questions:
Phone: [phone]
Email: [e-mail]
and Postal address: enretec GmbH, eomRECYCLING® business unit
Kanalstraße 17
D-16727 Velten
3. A unit that is not permanently installed will be picked up at the office. A per-
manently installed unit will be picked up at the curb at your address on the
agreed date. The owner or user of the device will have to bear the cost of
disassembly, transportation and packaging.
Final disposal, international
For country-specific information on disposal, contact your specialised dealers.
Currently applicable packaging law
Dispose of and recycle the packaging appropriately in accordance with current
packaging law, employing waste management / recycling companies. Comply
with the comprehensive return system. KaVo has had its packaging licensed for
this purpose. Please comply with the regional public waste-disposal system.

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3 Description of the product | 3.1 Treatment centre versions
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3 Description of the product
3.1 Treatment centre versions
3.1.1 KaVo ESTETICA E30 S
ESTETICA E30 S
3.1.2 KaVo ESTETICA E30 TM
ESTETICA E30 TM

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3 Description of the product | 3.2 Patient chair
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3.2 Patient chair
5
①Headrest ②Backrest
③Kickplate (base plate) ④Bench
⑤Arm rest (optional)

Instructions for use ESTETICA E30
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18 / 124
3.3 Unit with patient element
8
①Patient element ②Spittoon bowl
③Tumbler filler ④Unit body
⑤Pressurized water bottle ⑥Supply element
customer connection of central
control, electricity, water, com-
pressed air, wastewater and suc-
tion air
⑦Intensive germ reduction bottle ⑧Foot control
NOTE
The tumbler filler ③ of the pivotable spittoon bowl (optional) can be taken off.
3.4 Versions of the dentist element
3.4.1 TM table
NOTE
The holder assignment and arrangement of the instruments can be changed
as needed and does not have to be as shown in the figure.

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3 Description of the product | 3.4 Versions of the dentist element
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①Handle ②Triple function handpiece
③Turbine handpiece (MULTIflex
coupling)
④INTRA LUX Motor KL 701 / KL 703
⑤Scaler PIEZOsoft/PiezoLED ⑥Tray support
⑦Knob for locking brake of spring
arm
⑧Control element

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3 Description of the product | 3.4 Versions of the dentist element
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3.4.2 S-Table
NOTE
The holder assignment and arrangement of the instruments can be changed
as needed and does not have to be as shown in the figure.
3
1
5
4
4
2
3
1
5
4
4
2
9
77
8
6
S table with handle trough | S table with handle trough left/right (optional)
①Control element ②Triple function handpiece
③Turbine handpiece (MULTIflex
coupling)
④INTRAlux Motor KL 701 / KL 703
⑤Scaler PIEZOsoft/PiezoLED ⑥Handle trough with pushbutton for
locking brake of spring arm
⑦Tray support ⑧Removable handle left/right (op-
tional)
⑨Knob for locking brake of spring
arm