KaVo ESTETICA E30 User manual

Instructions for use
ESTETICA E30

Manufacturer:
Kaltenbach & Voigt GmbH
Bismarckring 39
D-88400 Biberach
www.kavo.com
Distributed by:
KaVo Dental GmbH
Bismarckring 39
D-88400 Biberach
Phone [phone]
Fax [phone]

Table of contents
1 User instructions ................................................................................................................ 6
1.1 User guide .................................................................................................................... 6
1.1.1 Abbreviations ..................................................................................................... 6
1.1.2 Symbols ............................................................................................................ 6
1.1.3 Target group ...................................................................................................... 6
1.2 Service ......................................................................................................................... 7
1.3 Terms and conditions of warranty.................................................................................... 7
1.4 Transportation and storage............................................................................................. 7
1.4.1 Currently valid packaging regulations.................................................................... 7
1.4.2 Damage in transit ............................................................................................... 8
1.4.3 Information on the packaging: Storage and transportation...................................... 9
2 Safety.................................................................................................................................. 10
2.1 Description of safety instructions ..................................................................................... 10
2.1.1 Warning symbol ................................................................................................. 10
2.1.2 Structure ........................................................................................................... 10
2.1.3 Description of hazard levels ................................................................................. 10
2.2 Purpose – Proper use ..................................................................................................... 10
2.2.1 General ............................................................................................................. 10
2.2.2 Product-specific .................................................................................................. 13
2.3 Safety instructions ......................................................................................................... 14
2.3.1 General information ............................................................................................ 14
2.3.2 Product-specific .................................................................................................. 16
3 Product description ............................................................................................................ 18
3.1 Treatment unit versions.................................................................................................. 18
3.1.1 KaVo ESTETICA E30 S......................................................................................... 18
3.1.2 KaVo ESTETICA E30 TM ...................................................................................... 18
3.2 Patient chair.................................................................................................................. 19
3.3 Unit with patient element ............................................................................................... 20
3.4 Dentist unit versions ...................................................................................................... 20
3.4.1 TM table ............................................................................................................ 20
3.4.2 S table............................................................................................................... 21
3.5 Assistant unit ................................................................................................................ 23
3.6 Triple-function handpieces .............................................................................................. 24
3.7 X-ray viewer 1440 ......................................................................................................... 25
3.8 Controls........................................................................................................................ 25
3.8.1 Dentist's unit TM table......................................................................................... 25
3.8.2 Dentist's unit S table........................................................................................... 26
3.8.3 Assistant unit ..................................................................................................... 26
3.8.4 Groups of keys ................................................................................................... 26
3.8.5 Foot control........................................................................................................ 29
3.9 Rating plate and serial number plates .............................................................................. 29
3.9.1 Rating plate 1440 ............................................................................................... 33
3.10Technical data ............................................................................................................... 34
4 Operation............................................................................................................................ 40
4.1 Switching the device on and off....................................................................................... 40
4.2 Converting from right handed to left handed..................................................................... 40
Instructions for use ESTETICA E30
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4.3 Adjusting the dental chair............................................................................................... 44
4.3.1 Adjusting the armrest (optional)........................................................................... 44
4.3.2 Adjust head rest ................................................................................................. 45
4.3.3 Positioning the dental chair manually .................................................................... 46
4.3.4 Automatic positioning of dental chair .................................................................... 48
4.3.5 Safety shut-off ................................................................................................... 52
4.4 Moving the patient chair ................................................................................................. 54
4.5 Moving the dentist unit................................................................................................... 54
4.5.1 Moving the dentist unit TM................................................................................... 55
4.5.2 Moving the dentist unit S..................................................................................... 56
4.6 Moving the patient unit................................................................................................... 56
4.6.1 Moving the patient element (optional)................................................................... 57
4.7 Attaching the tray holder (optional) ................................................................................. 58
4.8 Using functions through the menu................................................................................... 58
4.8.1 General menu navigation..................................................................................... 58
4.8.2 Using the user menu........................................................................................... 58
4.8.3 Standby menu.................................................................................................... 64
4.8.4 Selecting the dentist ........................................................................................... 65
4.8.5 Instruments menu .............................................................................................. 65
4.8.6 ENDO menu (optional) ........................................................................................ 68
4.8.7 Using the CONEXIOcom (optional)........................................................................ 73
4.9 Using function through the dentist or assistant unit ........................................................... 76
4.9.1 Using the hygiene functions ................................................................................. 76
4.9.2 Using the illumination functions for KaVoLUX 540 LED T ......................................... 77
4.9.3 Using the illumination functions for EDI and MAIA .................................................. 83
4.9.4 Using the X-ray viewer ........................................................................................ 83
4.9.5 Using the bell ..................................................................................................... 84
4.9.6 Using the timer................................................................................................... 84
4.10Operating the foot switch................................................................................................ 85
4.10.1 General functions................................................................................................ 85
4.10.2 Positioning the patient chair with the foot control ................................................... 85
4.10.3 Preselect dentist ................................................................................................. 85
4.10.4 Start and regulate instruments............................................................................. 85
4.10.5 Setting the cooling condition ................................................................................ 86
4.10.6 Activating blown air (optional).............................................................................. 86
4.10.7 Preselect counterclockwise motor rotation ............................................................. 86
4.10.8 Adjusting the instrument light .............................................................................. 86
4.10.9 Using CONEXIOcom (fee-based additional option).................................................. 87
4.11Using instruments.......................................................................................................... 88
4.11.1 Setting spray air and spray water......................................................................... 88
4.11.2 Using suction hoses ............................................................................................ 89
4.11.3 Using triple-function handpieces........................................................................... 90
4.11.4 Using the PIEZOsoft/PiezoLED.............................................................................. 92
4.12Using the KL 703 LED in ENDO mode (optional accessory) ................................................. 93
4.12.1 General information ............................................................................................ 93
4.12.2 Open ENDO mode............................................................................................... 94
4.12.3 Set torque mode................................................................................................. 95
4.12.4 Changing settings in the menu............................................................................. 96
4.12.5 Leaving ENDO Mode............................................................................................ 96
4.13Use USB interface.......................................................................................................... 97
Instructions for use ESTETICA E30
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4.14Using the camera........................................................................................................... 98
4.15Using the screen............................................................................................................ 98
5 Preparation methods DIN EN ISO 17664...........................................................................99
6 Accessories and kits ...........................................................................................................100
6.1 Device ..........................................................................................................................100
6.2 Dental chair ..................................................................................................................100
6.3 Assistant unit ................................................................................................................100
6.4 Dentist element.............................................................................................................100
7 Safety checks - testing instructions ...................................................................................102
7.1 Introduction ..................................................................................................................102
7.1.1 General instructions ............................................................................................102
7.1.2 Notes for medical electrical systems......................................................................103
7.1.3 Essential parts of the safety check........................................................................104
7.1.4 Testing intervals .................................................................................................104
7.1.5 Notes on the test method in accordance with IEC 62353.........................................104
7.1.6 Notes on repeat testing .......................................................................................105
7.2 Instructions for safety checks..........................................................................................105
7.2.1 Preparatory measures to be undertaken on the device............................................105
7.2.2 Visual inspection (inspection by examination) ........................................................106
7.2.3 Measurements....................................................................................................109
7.2.4 Functional test....................................................................................................118
7.2.5 Assessment and documentation ..........................................................................120
8 Appendix - Additional measuring sites...............................................................................122
8.1 Additional scanning sites SL X in the protective conductor measurement .............................122
8.2 Additional measuring sites AP X for EUL/EPL measurement ................................................124
9 Troubleshooting .................................................................................................................125
10Information about electromagnetic compatibility in accordance with EN60601-1-2........128
10.1Electromagnetic Transmissions........................................................................................128
10.2Resistance to electromagnetic interference .......................................................................128
10.3Recommended safe distance between portable and mobile HF telecommunications
equipment and the treatment unit ...................................................................................129
10.4Immunity to electromagnetic interference ........................................................................130
Instructions for use ESTETICA E30
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Instructions for use ESTETICA E30
1 User instructions | 1.1 User guide
6 / 134
1 User instructions
1.1 User guide
Requirement
Read these instructions prior to first use to avoid misuse and prevent damage.
1.1.1 Abbreviations
Ab-
brevi-
ation
Explanation
IfU Instructions for use
CI Care instructions
AI Assembly instructions
TI Technician's instructions
SC Safety checks
IEC International Electrotechnical Commission
RI Repair instructions
RK Retrofitting kit
AS Assembly set
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.

Instructions for use ESTETICA E30
1 User instructions | 1.2 Service
1.2 Service
KaVo Customer Service:
[phone]
[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.
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Instructions for use ESTETICA E30
1 User instructions | 1.4 Transportation and storage
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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).

Instructions for use ESTETICA E30
1 User instructions | 1.4 Transportation and storage
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
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Instructions for use ESTETICA E30
2 Safety | 2.1 Description of safety instructions
10 / 134
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:
NOTICE
In cases which – if not prevented – could lead to material damage.
CAUTION
CAUTION
indicates a hazardous situation that can cause damage to property or mild to
moderate injuries.
WARNING
WARNING
indicates a hazardous situation that can lead to serious or fatal injury.
DANGER
DANGER
indicates a maximal hazard due to a situation that can directly cause death or
fatal injury.
2.2 Purpose – Proper use
2.2.1 General
The user must ensure that the unit works properly and is in satisfactory condi-
tion before each use.

Instructions for use ESTETICA E30
2 Safety | 2.2 Purpose – Proper use
The KaVo ESTETICA E30 equipment system is a dental treatment centre in ac-
cordance with ISO 7494 equipped with a patient 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 these instruction for use for hardware and software, and they are
installed and set up according to the descriptions of these components.
▪ in the case of repairs, the requirements of IEC 62353 (DIN VDE 0751-1)
"Repeat tests and tests before start-up of electrical items of medical equip-
ment 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 start-up of medical
devices.
▪ Current occupational safety regulations.
▪ Current accident prevention regulations.
Regular performance of maintenance and safety checks is essential for the per-
manent assurance of the operating and functional safety of the KaVo product
and for the prevention of damage and hazards.
Testing and maintenance intervals: Maintenance must be performed once a
year, the safety check (STK) at intervals of 2 years. Shorter intervals for the
safety check may be specified by the tester if necessary.
The following persons are authorised to repair and service the KaVo product:
▪ Technicians of KaVo branch offices after appropriate product training.
▪ Specifically KaVo-trained technicians of KaVo franchised dealers.
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).
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Instructions for use ESTETICA E30
2 Safety | 2.2 Purpose – Proper use
12 / 134
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!
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.
See also:
210 Information about electromagnetic compatibility in accordance with
EN60601-1-2, Page 128
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.
Disposal of electronic and electrical devices
Note
According to EC directive 2012/19 concerning waste electrical and electronic
equipment, this product is subject to the cited directive and must be disposed
of accordingly within Europe.
For more information, please visit www.kavo.com or contact your specialised
dental supplier.
For final disposal:

Instructions for use ESTETICA E30
2 Safety | 2.2 Purpose – Proper use
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.
The following contact options are also available for questions and for initiat-
ing a disposal order:
Phone: [phone]
Email: [e-mail] and
Postal address: enretec GmbH, Geschäftsbereich eomRECYCLING®
Kanalstraße 17
D-16727 Velten
3. A unit that is not permanently installed will be picked up at the office.
A permanently 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.
International
For country-specific information on disposal, contact your dental supplier.
2.2.2 Product-specific
Designated use and target group
KaVo ESTETICA E30 is designed for dental treatment of children and adults.
The KaVo ESTETICA E30 equipment system is a dental treatment centre in ac-
cordance with ISO 7494 equipped with a patient chair in accordance with ISO
6875. 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. The KaVo X-ray viewer 1440 is designed for radiograph
viewing in dentistry and meets the requirements of DIN 6856-3. These KaVo
products are designed for use in dentistry only and must be used by trained
medical personnel only.
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
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Instructions for use ESTETICA E30
2 Safety | 2.3 Safety instructions
14 / 134
Accessories Use Name Material number
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.
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.

Instructions for use ESTETICA E30
2 Safety | 2.3 Safety instructions
WARNING
Injury or damage from damaged functional parts.
Damage to functional parts can cause further damage or personal injury.
▶Check the device, electrical cables and any accessories for possible damage
to the insulation and replace if necessary.
▶If functional parts are damaged: discontinue your work and
repair the damage or notify a service technician!
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!
CAUTION
Damage by liquids.
Faults on electric components.
▶Protect openings of the product from any ingress of liquids.
▶Have a service technician remove liquids from the interior of the device.
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.
NOTICE
Premature wear and malfunctions from improper servicing and care.
Reduced product life.
▶Perform regular proper care and servicing!
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.
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Instructions for use ESTETICA E30
2 Safety | 2.3 Safety instructions
16 / 134
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.
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.

Instructions for use ESTETICA E30
2 Safety | 2.3 Safety instructions
CAUTION
Electrical power.
Electrical shock.
▶Set up the external PC outside of the patient environment keeping a min-
imal distance of 1.5 m.
▶Connect the PC and equipment connected to the PC in accordance with IEC
60601-1 / 60950.
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
Health damage due to germ formation.
Infection hazard.
▶Before start-up and after downtimes (weekends, holidays, vacations, etc.),
rinse or purge the air and water lines with air.
▶Actuate the tumbler filler several times.
▶Carry out a manual intensive germ reduction.
CAUTION
Long stay in the patient chair.
Decubitus formation.
▶Take precautions against the formation of decubitus in long treatments.
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.
NOTICE
Damage to the instrument hoses from stickers.
Instrument hoses can burst.
▶Do not affix stickers or adhesive tape.
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.
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Instructions for use ESTETICA E30
3 Product description | 3.1 Treatment unit versions
18 / 134
3 Product description
3.1 Treatment unit versions
3.1.1 KaVo ESTETICA E30 S
ESTETICA E30 S
3.1.2 KaVo ESTETICA E30 TM
ESTETICA E30 TM

Instructions for use ESTETICA E30
3 Product description | 3.2 Patient chair
3.2 Patient chair
5
①Headrest ②Backrest
③Kickplate (base plate) ④Seat
⑤Armrest (optional)
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Instructions for use ESTETICA E30
3 Product description | 3.3 Unit with patient element
20 / 134
3.3 Unit with patient element
8
①Patient element ②Spittoon bowl
③Tumbler filler ④Unit body
⑤Pressurised water bottle ⑥Supply element
Customer-provided connection of
central control, electrical power,
water, compressed air, wastewater,
and suction air
⑦Intensive germ reduction bottle ⑧Foot control
Note
The tumbler filler ③ of the pivotable spittoon bowl (optional) can be taken
off.
3.4 Dentist unit versions
3.4.1 TM table
Note
The holder assignment and arrangement of the instruments can be changed
as needed and does not have to follow the picture.