Estetica E30

Instructions for use
ESTETICA E30
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Manufacturer: Distributed by:
Kaltenbach & Voigt GmbH KaVo Dental GmbH
Bismarckring 39 Bismarckring 39
D-88400 Biberach D-88400 Biberach
www.kavo.com Phone +49 (0) 7351 56-0
Fax +49 (0) 7351 56-1488

Instructions for use ESTETICA E30
Table of contents
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
3 / 134

Table of contents
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
4 / 134

Table of contents
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
5 / 134

1 User instructions | 1.1 User guide
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- Explanation
brevi-
ation
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.
6 / 134

1 User instructions | 1.2 Service
1.2 Service
KaVo Customer Service:
+49 (0) 7351 56-1000
Service.Einrichtungen@kavo.com
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.
7 / 134

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.
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.
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.
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).
8 / 134

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
9 / 134

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:
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.
10 / 134

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).
11 / 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:
2 10 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:
12 / 134

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 +49 (0)3304 3919 590 to enretec GmbH.
The following contact options are also available for questions and for initiat-
ing a disposal order:
Phone: +49 (0) 3304 3919-500
Email: eom@enretec.de 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 1.011.2130
ERGOcam One 160 1.011.2129
Caries diagnostic DIAGNOcam 2170 1.011.0400
device U
13 / 134

2 Safety | 2.3 Safety instructions
Accessories Use Name Material number

Cables between USB extension USB extension 1.004.6953
unit, accessories cord - 5 metres cord 5m with 1:1
and PC hub
USB extension USB extension 1.011.3745
cord - 10 metres cord 2x5m with
1:1 hub
Display port cable LTG Display port 1.011.3583
- 5 metres 5m Standard
Display port cable LTG Display port 1.011.0298
- 10 metres 10m Standard
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.
14 / 134

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.
15 / 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.
16 / 134

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.
17 / 134

3 Product description | 3.1 Treatment unit versions
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
18 / 134

3 Product description | 3.2 Patient chair
3.2 Patient chair
① Headrest ② Backrest
③ Kickplate (base plate) ④ Seat
⑤ Armrest (optional)
19 / 134

3 Product description | 3.3 Unit with patient element
3.3 Unit with patient element
① Patient element ② Spittoon bowl

③ Tumbler filler ④ Unit body
⑤ Pressurised water bottle ⑥ Supply element
Customer-provided connection of
central control, electrical power,
water, compressed air, wastewater,
and suction air
⑦ Intensive germ reduction bottle ⑧ Foot 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.
20 / 134

3 Product description | 3.4 Dentist unit versions
① Handle ② Triple function handpiece

③ Turbine (multiflex coupling) ④ INTRA LUX Motor KL 701 / KL 703
⑤ Scaler PIEZOsoft/PiezoLED ⑥ Tray support
⑦ Knob for locking brake of spring ⑧ Control element
arm
3.4.2 S table
Note
The holder assignment and arrangement of the instruments can be changed
as needed and does not have to follow the picture.
21 / 134

3 Product description | 3.4 Dentist unit versions
1 1
2 2
3 3
4 4
4 4
5 5
6 7 9 8 7
S table with handle trough | S table with handle trough left/right (optional)
① Control element ② Triple function handpiece

③ Turbine (multiflex coupling) ④ INTRAlux Motor KL 701 / KL 703
⑤ Scaler PIEZOsoft/PiezoLED ⑥ Handle trough with pushbutton for
locking brake of spring arm
⑦ Tray support ⑧ Removable handle left/right (op-
tional)
⑨ Knob for locking brake of spring
arm
22 / 134

3 Product description | 3.5 Assistant unit
3.5 Assistant unit
① Triple function handpiece ② High volume aspirator

③ Control element ④ Saliva ejector
⑤ KaVo Poly One / Satelec Mini LED ⑥ Tray holder for assistant
23 / 134

3 Product description | 3.6 Triple-function handpieces
3.6 Triple-function handpieces

1
2
3
Triple function handpiece One
① Cannula ② Water button (green ring)

③ Air button (blue ring) ④ Handpiece and hose
Triple-function handpiece
① Air button (A) ② Cannula

③ Gripping sleeve ④ Water button (W)
⑤ Ring blue
24 / 134

3 Product description | 3.7 X-ray viewer 1440
3.7 X-ray viewer 1440
X-ray viewer 1440
Note
The KaVo X-ray viewer 1440 is a type 1 radiological viewing device in accord-
ance as defined in DIN 6856-3.
3.8 Controls
3.8.1 Dentist's unit TM table

A B C D E F
A Group of keys for the dental chair B Group of keys for illumination
C Group of keys for the handpieces D Group of keys for the menu
E Group of keys for hygiene F Group of keys for the timer
25 / 134

3 Product description | 3.8 Controls
3.8.2 Dentist's unit S table
B C
D E
A Group of keys for the menu B Group of keys for illumination

C Group of keys for hygiene D Group of keys for the handpieces
E Group of keys for the timer F Group of keys for the dental chair
3.8.3 Assistant unit
A Group of keys for hygiene B Group of keys for illumination

C Group of keys for the timer D Group of keys for the dental chair
3.8.4 Groups of keys
Group of keys for the dental chair
The keys of the assistant unit each have two functions and show two symbols.
Assistant element key Dentist element key Name

"Chair up" key
26 / 134

Assistant element key Dentist element key Name

"AP 0" key
(automatic position 0)
"Chair down" key
"SP" key
(rinsing position)
"LP" key
(last position)
"AP" key
(activate automatic posi-
tion)
"Backrest down" key
"AP 1" key

"Backrest up" key
"AP 2" key

"Collapsed position" key
Group of keys for illumination/handpieces

Key Name Control element
Key Dentist element and as-
"Operating light" sistant element
"Operating light dimming" Dentist element

key
Key Dentist element

"X-ray viewer"
"Direction of motor rota- Dentist element

tion" button
"Preselected spray" but- Dentist element

ton
27 / 134


"Cold light" button Dentist element
Group of keys for hygiene

"Tumbler filler" key Dentist element and
assistant element
"Bowl rinsing" key Dentist element and

assistant element
"Bell" key Dentist element
"Intensive disinfection" Assistant element (unas-

key signed key)
"HYDROclean" key Assistant element (unas-

signed key)
Group of keys for the menu
Group of keys for the menu
① Menu function selection keys ② Display
Group of keys for the timer

Key Description Control element
"Remote Control" (CON- unassigned key
EXIO) key
"Additional motor drives" Dentist element

key
"Timer 1" key Dentist element and

assistant element
28 / 134

3 Product description | 3.9 Rating plate and serial number plates
3.8.5 Foot control
The footswitches of the foot control have two functions. The functions of the
footswitches depend on if an instrument is mounted or removed.
Item Name with mounted with removed

Handpiece Handpiece
① "LP/preselected spray" Drives dental chair to Optional. Sets the
footswitch previous position. spray pre-selection.
② U-shaped switch Switches the foot-
switches to the "Chair
motion" function.
③ "SP/blown air" foot- Drives dental chair to Optional. Sets the pre-
switch rinsing position. set blown air
(Chipblower) at the
handpiece (does not
apply to PiezoLED).
④ "Chair position/direc- Changes the position Selects the direction of
tion of motor rotation" of the dental chair. motor rotation (for KL
4-way switch 701 / KL 703 motor).
⑤ "Preselection of level/ Preselection of level Starts the handpieces
handpieces" foot-pedal and controls the
speed/intensity of the
handpieces.
3.9 Rating plate and serial number plates
ESTETICA E30 and chair nameplate
29 / 134

Site for affixing the rating plate and serial number plate
① Serial number plate of the chair ② Rating plate
SN Serial number
Read and take note of the content of accompanying documents
Type B applied part
Type BF applied part
Operating mode:
Operating time for the patient chair: 2 minutes
2 min
ED 10% Pause time of the patient chair: 18 minutes
18 min (The permissible operating times correspond to common dental pro-
cedure.)
Fuse ratings:
100/110/115/120/127/220/230/240 V AC = T6.3 A 250 V
For disposal information, see also: Purpose - Intended use
CE mark according to Medical Devices Directive EC 93/42
VDE mark
30 / 134

DVGW ID
(Deutscher Verein des Gas- und Wasserfaches e.V.)
(Equipment-dependent DVGW mark with certification number)
See also:
2 Technical Data
HIBC Code
eLabeling ID
Serial number plate and dentist element ID
Nameplate dentist element (e.g. table TM) / marking of the applied parts of type BF
Site of attachment of rating plate and type BF applied parts ID on dentist element
Type Device type

SN Year of manufacture - serial number
REF Material number
31 / 134

Marks and labels of triple-function handpieces
SN YY-???????
X.XXX.XXXX
3FH-One XXXX YYYY-MM
Marks and labels of triple-function handpiece One
① Company logo of the manufacturer ② Can be sterilised at up to 135°C

③ Serial number ④ CE mark according to 93/42/EEC
medical devices
⑤ Material number, name, production
date
5
2 3
4 3
Marks and labels of the triple-function handpiece
① Company logo of the manufacturer ② Please note the instructions for use
③ Can be sterilised at up to 135°C ④ CE mark according to 93/42/EEC
medical devices
⑤ Serial number
32 / 134

Nameplate of water bottle and intensive germ reduction

bottle
1 1
2 2
3 3
4 4
5 6 7 8 5 6 7 8
Nameplate of water bottle / intensive germ reduction bottle
① Manufacturer ② Concentration
③ Use-by date ④ Material number
⑤ Month manufactured ⑥ Expiration date (year)
⑦ Storage temperature ⑧ Please comply with accompanying
documents
Note
The specified concentration of KaVo OXYGENAL 6 must not be exceeded.
3.9.1 Rating plate 1440
1
7
3
9
2
4 8
5 6
Rating plate X-ray viewer 1440
① Device type ② SN: Year and month manufactured

- Serial number
③ Material number ④ Supply voltage, frequency
⑤ Power ⑥ Disposal instructions
⑦ CE mark ⑧ Serial number
⑨ Year and month manufactured
33 / 134

3 Product description | 3.10 Technical data
3.10 Technical data
Drilling template and setup plan

Layout plan (Mat. no. 1.009.2781)
Electrical system
Electrical lead 3 x 1.5 mm2 (customer-provided
fuse protection 10 A) 3 x 2.5 mm2
(customer-provided fuse protection
16 A)
Free end above the floor 1 000 mm
Input voltages 100/110/115/120/127/220/230/240
V AC
Frequency 50/60 Hz
Factory-set mains input voltage See nameplate
Power consumption 100 to 900 VA
Customer-provided fuse protection Auto-mat C16 or screw-plug fuse 10
A
Protective conductor above floor See DIN VDE 0100-710, 1000 mm
Heat emission 360 to 3240 kJ/h
Heat emission Ø 900 kJ/h
Degree of soiling 2
Installation category II
Mark of approval CE / DVGW / VDE
Foot control IPX1: Protection against water drips

Flush the water and air passages for 20 to 30 seconds before working at the
beginning of the day.
Water pressure 1.5 ± 0.3 bar; flow pressure; probe

tip (1.009.6634)
Water flow 90 ± 15 ml/min
Air pressure 1.5 ± 0.2 bar; flow pressure; probe
tip (1.009.6634)
Air flow 15 ± 3 Nl/min
Triple function handpiece

Flush the water and air passages for 20 to 30 seconds before working at the
beginning of the day.
34 / 134

Water pressure 1.5 ± 0.3 bar; Flow pressure; 4 x

manometer
Max. static pressure water 2.5 ± 0.3 bar
Water flow 80 ± 10 ml/min
Air pressure 3.3 ± 0.1 bar; Flow pressure; 4 x
manometer
Max. static pressure air 4 + 0.5 bar
Air flow at least 16 Nl/min
Water supply
CAUTION
The ESTETICA E30 treatment centre, as delivered, is not equipped
with an amalgam separator.
Contamination of wastewater.
▶ Disposing wastewater, it is imperative to comply with the national regula-
tions, in particular with regard to amalgam loads.
Note
KaVo recommends to connect an external amalgam separator to the ESTET-
ICA E30 treatment centre in compliance with the specifications of the manu-
facturer of the device.
Note
If the water is very hard (above 12 °dH), a water softening device must be
fitted in the ion-exchange process.
Insufficient water hardness (below 8.4 °dH) can promote the formation of al-
gae.
Note
The "water inlet block" assembly kit does not include a separation between
the treatment water and water supplied by the local mains. The operator
must observe and comply with relevant national directives concerning the
prevention of backflow. Upon failure to comply with these rules, the manu-
facturer accepts no liability for the quality of the treatment water and the mi-
crobial re-contamination of the public drinking water network.
WARNING
There is a risk of infection if you fail to comply with national regula-
tions.
Contamination of the treatment water and/or drinking water supply with
germs.
▶ Note and comply with national regulations concerning the quality of water
for human use (drinking water) - if applicable.
▶ Note and comply with national regulations concerning the prevention of
backflow (flow from the treatment centre back to the public water supply) -
if applicable.
35 / 134

WARNING
Risk of infection if the "Water inlet block" is used without additional
safeguards.
Contamination of the treatment water and/or drinking water supply with
germs.
▶ Regarding the use of the "Water inlet block" assembly kit, please note that
no disinfection facility is installed in the unit, and take appropriate safe-
guards.
▶ If the Water bottle assembly kit is used with the enclosed dosing attach-
ment (Mat. no. 10020287), add the proper amount of KaVo OXYGENAL 6
(Mat. no. 04893451) with each filling. For the correct amount, please
refer to the instructions of the dosing attachment for water germ reduction.
Water germ reduction is integrated in combination with the water bottle with
manual Oxygenal 6 dosing through the dosing attachment and the intensive
germ reduction bottle.
According to DIN EN 1717, each unit that is not listed by DVGW must be
provided with an upstream type AA, AB or AD safety device. (The DVGW water
bottle kit is certified; see the following list.)
When establishing a water connection, make sure that there are no sections of
brackish water with standing water (also in the house plumbing).
For further information, please refer to www.dvgw.de
Free drainage according to DIN EN Water bottle DVGW, reg. no.:

1717 - DVGW certified AS-0630BT0111
Water quality Tap water, cold water connection
Water hardness 1.5 to 2.14 mmol/l ≙ 8.4 to 12 °dH
pH 7.2 to 7.8
Customer-site water filtering 80 microns
Water connection Shut-off valve with brass cone com-
pression screw connection 3/8" to Ø
10 mm provided
Above-floor water connection min. 50 mm, max. 105 mm with
valve opened
Water inlet pressure 2.0 to 6.0 bar
Water inflow 4 l/min
Diameter of the drain connection 40 mm
Above-floor drain connection 20 mm
Outflow quantity max. 4 l/min
Slope of water drain pipe downstream from device: at least 10
mm per metre
36 / 134

Air supply
WARNING
Non-adherence to national guidelines regarding the quality of the
dental air.
Infection hazard.
▶ Observe and adhere to the national guidelines regarding the quality of the
dental air - if any.
▶ Blow through the air line prior to commissioning.
Air inlet pressure 5.5 to 7 bar

Minimum air flow rate min. 60 Nl/min
Air consumption with 1 Venturi suc- max. 105 Nl/min.
tion unit
Air consumption with 2 Venturi suc- max. 150 Nl/min
tion units
Pressure dew point < -30 ºC (compressor with
dry air system)
Oil content < 0.1 mg/m3 (oil-free compressor)
Contamination < 100 particles/m3 at particle sizes
of 1 to 5 µm
Customer-site air filtration 50 microns
Air connection Shut-off valve with brass cone com-
pression screw connection 3/8" to Ø
10 mm provided
Air connection above floor level min. 50 mm, max. 105 mm with
valve opened
Suction
Pressure drop at the connecting point with semi-dry and wet suction
Note
If the negative static pressure is > 180 mbar, the unit must be equipped with
the negative pressure regulating valve assembly kit.
37 / 134

Cannula connecting pieces according to DIN EN ISO 7494 - 2

Diameter of cannula of saliva ejector 7 mm
and surgical suction
Diameter of cannula of spray mist 15 mm
suction
Suction air quantity at spray mist minimum 250Nl/min (suction system
cannula with high flow rate), recommended
300Nl/min
Diameter of the suction connection 40 mm

Suction connection above floor 20 mm
Operating environment
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.
Floor quality The quality of the flooring must meet

the load bearing ability for buildings
DIN 1055 page 3 and have a pres-
sure resistance in accordance with
DIN 18560 T 1.
Ambient temperature +10 to +40 oC
Relative humidity 30 to 75%
Air pressure 700 hPa - 1,060 hPa
Max. elevation for operation up to 3000 m
Maximum loads
Max. patient weight load 180 kg
Tray holder of the dentist element - 2 kg
loadable up to
Assistant element standard tray - 1 kg
loadable up to
Dentist element - loadable up to 2 kg
Transportation and storage conditions

Ambient temperature -20 to +55 oC
Relative Humidity 5% to 95% non-condensing
Air pressure 700 hPa to 1,060 hPa
38 / 134

Weight
Treatment centre with 305 kg gross, 243 kg net
patient chair Standard
For more information about the packages, please refer to Assembly Instructions
X-ray viewer 1440

Input voltage 24 V AC
Frequency 50/60 Hertz
Power consumption max. 35 VA
ON-time 100 %
Lights 2x Osram Lumilux de Luxe G5 Day-
light L8W/954
Light field dimensions 300 mm x 150 mm in accordance
with DIN 6856-3
Case dimensions 340x216x48 in accordance with DIN
6856-3
Operating light KaVoLUX 540 LED
See also:
2 Instructions for Use KaVoLUX 540 LED
39 / 134

4 Operation | 4.1 Switching the device on and off
4 Operation
4.1 Switching the device on and off
Note
Always switch the machine off before leaving the office.
▶ Switch on the device using the main switch.

ð The display of the dentist element ① shows the preselected basic menu.
ð The green LED "Device turned on" lights up on the assistant element ②.
4.2 Converting from right handed to left handed

NOTICE
Collision and damage to the unit.
▶ Make sure there is sufficient clearance for swivelling.

▶ Switch the device off before you convert it.
40 / 134

4 Operation | 4.2 Converting from right handed to left handed
NOTICE
Instrument hoses getting caught on the patient chair or other objects.
▶ When you swivel the dentist element or rotate the hinge body make sure
that the instrument hoses do not get caught anywhere.
① Right handed model ② Left handed model
▶ Remove the seat.
▶ Undo the screw.
41 / 134

▶ Swivel the dentist and assistant element to the other chair side and re-
tighten the screw.
42 / 134

▶ Undo the locking and swivel the patient unit by 180° until the locking
snaps-in again. patient element
43 / 134

4 Operation | 4.3 Adjusting the dental chair
▶ Fasten the seat again proceeding in reverse order.
4.3 Adjusting the dental chair
4.3.1 Adjusting the armrest (optional)
To make it easier for the patient to sit in the chair, the armrest can be swung
up.
44 / 134

CAUTION
The patient's hands are in a bad position when the chair is rising
Danger of crushing fingers between the backrest and armrest.
▶ Make sure that the patient is sitting in the right position (especially chil-
dren).
4.3.2 Adjust head rest
Setting locking dial of 2-joint headrest
CAUTION
Adjusting the headrest.
Injury of neck muscles.
▶ Make sure that the patient is aware of the headrest setting.
▶ Patients need to raise their head slightly during adjustment.
45 / 134

▶ Push in or pull out the headrest depending on the patient's size.
▶ To swing the headrest, turn the locking dial to the left, move the headrest
into position, and turn the dial to the right to lock it.
▶ To remove the headrest cushion, remove the screw ②, pull the cushion ①
up slightly, and remove it to the front.
4.3.3 Positioning the dental chair manually
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.
CAUTION
Motorised movement of the chair
The patient or treatment personnel can be clamped or crushed.
▶ Monitor the patient and treatment personnel when changing the patient's
position.
46 / 134

Positioning the chair and backrest manually using the

dentist or assistant unit
Use the following buttons to adjust the chair height and position of the back-
rest:
Key Function
The chair moves up.
The chair moves down.
The backrest moves upward.
The backrest moves downward.
▶ Press the related key.

ð The chair or backrest moves in the desired direction.
Positioning the chair and backrest manually using the
foot control
The 4-way switch of the foot control assumes the function of the button wheel
on the dentist unit when manually positioning the dental chair.
See also:
2 Positioning the dental chair manually
Requirement
All instruments are in their holder.
▶ Chair up: Move the cross switch on the foot control in direction ①.
▶ Chair down : Move the cross switch on the foot control in direction ③.
▶ Backrest up: Move the cross switch on the foot control in direction ②.
47 / 134

▶ Backrest down: Move the cross switch on the foot control in direction ④.
4.3.4 Automatic positioning of dental chair
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.
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.
The chair position can be adjusted continuously.

Automatic positions can be saved, and the saved positions can be recalled by
the push of a button.
Recalling automatic positions with the dentist unit
The following keys can be used to recall saved chair positions.
Key Operation
Move to the rinsing position.
The last position before actuating the SP is assumed.
Move to automatic position 0.
Move to the collapsed position.
▶ Briefly press the desired button.

ð Chair automatically moves to the stored position.
ð Upon arrival at the stored position, the display diode on the button is turned
on.
Saving automatic positions with the dentist unit

Recommended assignment of buttons:
"SP" button: rinsing position
"AP 0" button: entry and exit position
48 / 134

"AP 1" button: treatment position, e.g. for lower jaw treatment
"AP 2" button: treatment position, e.g. for upper jaw treatment
"Collape position" button: collapse position
▶ Move the chair to the desired position.
▶ To save the chair position, press "AP 0", "AP 1", "AP 2", "SP" or "Collapsed
position" button until you hear a signal.
ð The display diode of the pressed button is turned on. The chair position is
saved.
See also:
2 Manual positioning of the patient chair using the MEMOdent control element
Last position
After the "LP" button is pressed, the chair moves into its position before the
"SP" button was pressed.
Note
The memory is erased when you turn off the device. After turning on the
device again (for example in the morning or after lunch), the chair does not
execute a specific movement when you press the "LP" button.
Recalling automatic positions with the assistant unit
▶ Briefly press the "AP" key.
ð The LEDs of the "AP 0", " AP 1", " AP 2", "SP", and "LP" keys flash for ap-
proximately four seconds.
▶ During these four seconds, briefly press the "AP 0", " AP 1", " AP 2", "SP" or
"LP" key.
ð The chair moves into the selected automatic position.

Saving automatic positions with the assistant unit
Note
The automatic position "Last position" is saved on the "LP" button. Press the
"LP" button for the chair to automatically move to the last position before the
rinsing position. The "LP" button cannot be assigned to another automatic
position.
▶ Move the chair to the desired position.
▶ Briefly press the "AP" key.
ð The LEDs of the "AP 0", " AP 1", " AP 2", "SP", and "LP" keys flash for ap-
proximately four seconds.
49 / 134

▶ During these four seconds, press the "AP 0", "AP 1", "AP 2", "SP" or "LP"
button, until a signal sound is transmitted.
ð LED of the pressed button lights up. The chair position is saved.
Recalling automatic positions with the foot control
Note
If an instrument is removed, the chair functions of the foot control are
blocked. The blocking can be removed by briefly pressing the stirrup switch.
The functions are then available.
① Spray preselection/AP footswitch ② Footswitch blowing air/AP (optional)

③ Foot pedal
The chair positions can be recalled with two foot switches; the standard setting
is as follows:
▪ "Spray selection" foot switch: automatic position "LP" (last position)
▪ "Blown air" foot switch: automatic position "SP" (rinsing position)
Move the chair when the instrument is mounted
▶ Press the "SP" foot-operated button.
or
▶ Press the "LP" foot-operated button.
50 / 134

Move the chair when the instrument is removed
Note
If an instrument is removed, the chair functions of the foot control are
blocked. The blocking can be removed by briefly pressing the stirrup switch.
The functions are then available.
▶ Press the stirrup switch and then the "Preselected spray" or "Blown air" foot
switch.

Saving an automatic position with the foot control
① Spray preselection/AP footswitch ② Footswitch blowing air/AP (optional)

③ Foot pedal
The chair positions can be saved on two footswitches; the standard setting is as
follows:
▪ "Spray default" footswitch: "LP" automatic position (last position)
▪ "Blown air" footswitch: "SP" automatic position (rinsing position)
▶ Hold down the foot pedal and foot-operated button "SP", and simultan-
eously press any button for an automatic position ("AP 0", "AP 1", "AP 2" or
"SP") on the dentist or assistant unit until you hear a beep.
ð The automatic position is saved to the foot-operated button.

or
▶ Hold down the foot pedal and foot-operated button "LP", and simultan-
eously press any button for an automatic position ("AP 0", "AP 1", "AP 2" or
"SP") on the dentist or assistant unit until you hear a beep.
ð The automatic position is saved to the foot-operated button.
51 / 134

4.3.5 Safety shut-off
To prevent collisions arising from the movement of the patient chair, safety
shutoff switches are installed to protect the patient and practice personnel from
injury and the treatment centre from damage.
NOTICE
Damage to the assistant element and dental chair.
Despite some safety shut-downs being present, certain positions of the
assistant element may collide with the dental chair.
▶ Keep the assistant element out of the motion range of the patient chair.
▶ Always monitor the chair movement.
CAUTION
Pinching from the treatment chair.
The safety shutoff of the treatment chair is activated by lifting the respective
component. Depending on the patient's body weight and the leverage, more
force can be exerted on the object to be triggered than is necessary to trigger
the switching function.
▶ The treatment personnel must move outside of the chair's swivelling range
whenever the chair moves.
CAUTION
Risk of injury when moving the patient or patient chair.
The patient or treatment personnel can be pinched or crushed.
▶ Position all moving parts, such as dentist element, assistant element, oper-
ating light, screens, etc., outside the collision range when you move the pa-
tient or patient chair.
The safety cut-offs can be found at the following places on the treatment unit.
52 / 134

Pos. Safety switch-off ac- LED on assistant LED on dentist ele-

no. tuated element ment
① Bracket on the foot
control
② Assistant element
③ Backrest
④ Kickplate
⑤ Seat
For right/left conver-
sion with bench re-
moved
The safety shutoff occurs if a movement angle has been exceeded or if a part of
the treatment centre collides with an object.
If a person or object actuates a safety shutoff, the chair immediately stops
moving.
The fact that the safety shutoff has been activated is displayed by the corres-
ponding display flashing on the dentist or assistant element.
Note
The chair's position cannot be changed with the key wheels when a safety
shutoff is activated.
▶ To deactivate an activated safety shutoff, remove the triggers from the mo-
tion range of the chair.
CAUTION
Changing the chair's position when the safety circuit is on.
Personal injury.
Damage to the device.
▶ Changing the chair position while a safety shutoff is active, do not move the
chair against the active safety circuit.
CAUTION
Pinching from the treatment chair.
The safety shutoff of the treatment chair is activated by lifting the respective
component. Depending on the patient's body weight and the leverage, more
force can be exerted on the object to be triggered than is necessary to trigger
the switching function.
▶ The treatment personnel must move outside of the chair's swivelling range
whenever the chair moves.
To allow the chair to move freely, it can also be moved when the safety circuit
is on. Use this function for repair purposes only.
▶ Press and hold down both the "SP" and "LP" keys on the dentist element.
or
53 / 134

4 Operation | 4.4 Moving the patient chair
▶ Press and hold down the "LP/AP" key on the assistant element.
▶ Move the chair using the button wheel buttons of the chair.
4.4 Moving the patient chair

245
45°
45° 245
+5° / - 5°
70°
825 mm
765 mm
360 mm
305 mm
4.5 Moving the dentist unit

NOTICE
Damage from overloading the dentist element.
Exceeding the maximum weight of more than 2 kg by adding handpieces, ac-
cessories, etc., can cause damage.
▶ Do not overload the dentist element!
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.
The swinging range of the dentist unit is limited by stops.
Note
Do not pull the dentist unit by the instrument hose.
54 / 134

4 Operation | 4.5 Moving the dentist unit
① Knob for locking brake of spring

arm
▶ To adjust the height of the dentist unit, release the brake ① adjust the
height, and lock the brake again.
4.5.1 Moving the dentist unit TM
CAUTION
Excessive load on the support system
The patient or treatment personnel may be injured.
The support system may be damaged.
▶ Do not exceed the permissible maximum weight (generated e.g. by instru-
ments and accessories).
▶ Do not use the swinging arm for a support!
25° 25°
°
120
12
0°
160°
80°
160°
80°
55 / 134

4 Operation | 4.6 Moving the patient unit
4.5.2 Moving the dentist unit S
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.
25° 25°
°
120
12
0°
160°
80°
160°
80°
4.6 Moving the patient unit
The device body can be swivelled away from the patient chair by 60o.
The spittoon bowl can be removed.
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4 Operation | 4.6 Moving the patient unit
4.6.1 Moving the patient element (optional)
CAUTION
The left armrest can collide with the manually adjusted patient's unit
when the chair moves.
Injury hazard.
▶ Each time before the chair is adjusted (automatic and manual), swing the
manually adjusted patient's unit into resting position.
Note
No liquids may be emptied into the mouth rising basin when the devices is
turned off. Mechanical and electronic damage could occur as a result of over-
flowing liquid.
The spittoon bowl of the swivelling patient element (optional) can be swivelled
by approx. 180o: 90o each to the left and right.
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4 Operation | 4.7 Attaching the tray holder (optional)
4.7 Attaching the tray holder (optional)
① Tray holder ② Holder
The support ② for the tray holder ①is an optional accessory.
4.8 Using functions through the menu
4.8.1 General menu navigation
The functions in the menu are used through the selections keys (S1 to S4) on
the display
① Selection keys (S1 to S4) for menu ② Display

functions
4.8.2 Using the user menu
The following options can be opened in the user menu:
Op- Feature Description

tion
1 Users Set number of users.
2 Tumbler Set tumbler filling time.
3 Bowl Set bowl rinsing time.
4 Handpiece light Set cold light afterglow period.
5 ENDO Set ENDO holder.
Available only with an ENDO li-
cense.
6 Time of day Set time of day.
7 Date Set date.
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4 Operation | 4.8 Using functions through the menu
Op- Feature Description

tion
8 Time/date display mode Set display mode for time of day
and date:
▪ Time of day only
▪ Time of day without seconds
▪ Time of day and date
▪ Date only
9 LCD Set contrast of LCD display.
10 Language Set menu language:
▪ Deutsch
▪ English
▪ Italiano
▪ Français
▪ Castellano
13 License Display of activated licenses:
▪ ENDO: Endo function
▪ PLED: PiezoLED function
▪ FCR: (foot control) control of
CONEXIO by foot control
14 Firmware Display current firmware version.
① Selection keys (S1 to S4) for menu ② Display

functions
▶ Press the "Next" key (S4) to start-up the user menu.

ð The user menu displays options and parameters that can be set and
changed by the user.
▶ Press the "Save" (S1) key to save the selection made.
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Option 1: Set number of users
S1 S2 S3 S4
S1 S2 S3 S4
▶ Press the "S1", "S2", "S3" key to select user 1, 2, and 3, respectively.
▶ Press the "S4" button to call up the second level.
Option 2: Set tumbler filling time
2. Becherfüllzeit
Einstellung: 7.0s
S1 S2 S3 S4
▶ Press the "reduce value" or "increase value" key to select a tumbler filling
time from 0 - 51 seconds.
Option 3: Set bowl rinsing time
S1 S2 S3 S4
▶ Press the "reduce value" or "increase value" key to select a bowl rinsing
time from 1.0 - 50.0 seconds. Interval: 0.2 seconds.
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Option 4: Set LUX afterglow period
S1 S2 S3 S4
▶ Press the "reduce value" or "increase value" key to set the afterglow period
between 0 to 10 seconds. The default value is 3 seconds.
Option 5: Set ENDO holder
S1 S2 S3 S4
▶ Press the "increase value" or "reduce value" keys to set the selected holder.
Option 6: Set the time of day
S1 S2 S3 S4
▶ Press the "SET" (S2) key to change the values of minutes and hours.
ð The value to be changed flashes.
S1 S2 S3 S4
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▶ Press the "reduce value" or "increase value" key to set the marked time of
day.
▶ Press the "SS:MM" (S1) key to switch between hours and minutes.
▶ Press the "Save" (S4) key to save the values and switch to the SET display.
Option 7: Set the date
S1 S2 S3 S4
▶ Press the "SET" (S2) key to change the values of day, month, and year.
ð The value to be changed flashes.
S1 S2 S3 S4
▶ Press the "reduce value" or "increase value" key to set the marked value.
▶ Press the "SS:MM" (S1) key to switch between day, month, and year.
▶ Press the "Save" (S4) key to save the values and switch to the SET display.
Option 8: Set display mode for time of day and date
S1 S2 S3 S4
▶ Press the "reduce value" or "increase value" key to set the display mode of
date/time.
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▶ The following displays can be selected: time of day only, time of day<no
seconds> only, time of day and date, date only, day of the week, no display
Option 9: Setting the display contrast
S1 S2 S3 S4
▶ Press the "reduce value" or "increase value" key to set the contrast of the
LCD display.
Option 10: Setting the menu language
S1 S2 S3 S4
▶ Press the "reduce value" or "increase value" key to select the menu lan-
guage.
▶ The following languages can be selected: Deutsch, English, Italiano, Fran-
cais, Castellano.
Option 13: Displaying the activated licenses
13
Lizenz
ENDO PLED FCR
S1 S2 S3 S4
Displays the activated licenses:

▪ ENDO: Endo function
▪ PLED: PiezoLED function
▪ FCR: (foot control) control of CONEXIO by foot control
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Option 14: Displaying the firmware version
14
S1 S2 S3 S4
The firmware version is displayed
4.8.3 Standby menu
The stand-by menu is used to start the device.

The device switches to the stand-by menu upon closing of the handpiece and
endo menus.
S1 S2 S3 S4
▶ Press the "Next" key (S4) to start-up the user menu.
Service and error messages in the stand-by menu

Service and error messages are displayed in the stand-by menu through the "!"
symbol.
S1 S2 S3 S4
▶ Press the "S2" button to display messages.
S1 S2 S3 S4
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▶ Press the function keys to navigate between the messages.
Key Settings
S2 Previous message
S3 Next message
S4 Switch to stand-by menu
Error messages in the status display
See also:
2 Troubleshooting
4.8.4 Selecting the dentist
The first symbol in the stand-by menu displays the current user.
S1 S2 S3 S4
▶ Press the "S1" key to start the user selection menu.
User selection (max. 6 users)

The user selection menu displays the available users.
S1 S2 S3 S4
S1 S2 S3 S4
▶ Press the "S4" button to call up the second level.
4.8.5 Instruments menu
handpiece-specific values are displayed and adjusted in the menu.
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The display depends on which instrument was withdrawn.
Changing motor settings in the menu
Note
Following instructions for use, service instructions and installation instructions
in the instrument packaging.
Motor status
The status of a handpiece is displayed on the display or control keys once a
handpiece is taken out.
S1 S2 S3 S4
Setting Actuation Pane

Motor speed Foot control Display
Light intensity Foot control, control keys Display
Direction of motor rota- Foot control, control keys LED control keys
tion
Spray status Foot control, control keys LED control keys
Adjusting the motor

▶ Settings can be changed using the corresponding keys on the control panel
or on the foot control.
Motor speed is set with the foot control only.
The direction of motor rotation, cooling status and light intensity are set
with the foot control or the control keys.
ð The current settings are saved and activated the next time the handpiece is
taken out.
PIEZOsoft/PiezoLED
Note
The setting of the mode is only available in combination with a PiezoLED Ul-
trasonic Scaler. The PiezoLED menu and all PiezoLED functions are only avail-
able if a PiezoLED license is existent.
Setting the PIEZOsoft
The status of the handpiece is shown on the display when the PIEZOsoft is be-
ing taken out:
▪ Intensity
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The light intensity is set with the foot control only.
Modus, spray, is set with the foot control or the control keys.
taken out.
S1 S2 S3 S4
Setting the PiezoLED
The status of the handpiece is shown on the display when the PiezoLED is being
taken out.
▪ Intensity
▪ Mode
▪ Light intensity
The light intensity is set with the foot control only.
Modus, spray, light on/off are set with the foot control or the control keys.
taken out.
S1 S2 S3 S4
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Power output as a function of operating mode and tip load
Power output as a function of device pre-setting (foot control) and tip load (shown using modes P3
and E as examples)
Note
If you stay in the range of dynamic response, the treatment is ensured to be
gentle. The output is adjusted according to load.
4.8.6 ENDO menu (optional)
Note
The functions of the ENDO menu are available only if an ENDO license is ex-
istent.
Start-up ENDO menu
The ENDO menu is started-up through:

▪ taking the ENDO motor out of the dentist element (setting in user menu,
option 5)
▪ activating the (M) "Additional motor drives" key afterwards
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ENDO status menu
S1 S2 S3 S4
The status of the ENDO motor is displayed in the ENDO menu:
Parameters Values
Transmission factor 1:1, 3:1
Parameter memory P1,P2,P3,P4,P5,P6
Torque mode TQ-Ctrl, Autoreverse, AutoRev/Forw.
Direction of motor rotation R, L
Speed 100 to 6,000 rpm
Torque Transmission ratio 1:1: 0.15 to 2.50
Ncm
Transmission ratio 3:1: 0.4 to 8.0 Ncm
Using the ENDO menu
Displaying parameters
▶ Press the respective keys on the display to navigate between parameters.
S1 S2 S3 S4
Key Settings
S1 (short) Displays the next set of parameters
(Briefly) press the "SP/ 1,2,3,4,5,6,1,..(ring counter)
Blown air" foot-operated
button
S4 Selects the ENDO options menu
Setting the ENDO menu

▶ Press the "S1" key for an extended time to select the ENDO settings menu.
The individual parameters can be set and changed in this menu.
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S1 S2 S3 S4
Key Settings
S1 Saves the parameters.
Selects the ENDO menu.
S2 Changes the value.
S4 Moves the flashing cursor:
Torque mode, speed, torque, torque mode, ... (ring counter).
Set torque mode

▶ The torque mode parameter can be changed after selecting it in the settings
menu.
ð The selected parameter is marked by a flashing cursor on the display.
S1 S2 S3 S4
Key Settings
S1 Saves the parameters
Selects the ENDO menu
S2 Changes the torque mode
Autoreverse, Torque Control only, Autorev. / Forward, Autoreverse,..
(ring counter)
S3 Changes the torque mode
Autoreverse, Autorev. / Forward, Torque Control only, Autoreverse,..
(ring counter)
S4 Moves the flashing cursor
Setting the speed

▶ The speed parameter can be changed after selecting it in the settings
menu.
ð The selected parameter is marked by a black triangle on the display.
S1 S2 S3 S4
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Key Settings
S2 Changes the speed
Range: 100 rpm to 500 rpm: in 10 rpm increments
Range: 500 rpm to 1,000 rpm: in 50 rpm increments
Range: 1,000 rpm to 6,000 rpm: in 100 rpm increments
S3 Changes the speed
Range: 100 rpm to 500 rpm: in 10 rpm increments
Range: 500 rpm to 1,000 rpm: in 50 rpm increments
Range: 1,000 rpm to 6,000 rpm: in 100 rpm increments
Setting the torque

▶ The torque parameter can be changed after selecting it in the settings
menu.
ð The selected parameter is marked by a black triangle on the display.
▶ Sets the maximum torque.
ð The torque is limited to the set maximal value.
ð The ENDO warning signal is issued when 90% of the pre-set maximal value
are reached.
S1 S2 S3 S4
Key Settings
Selects the ENDO settings menu
S2 Changes the torque
1:1 transmission ratio
Range: 0.15 Ncm to 2.5 Ncm: in 0.05 Ncm increments
Range: 1% to 100%: in 2% increments
S3 Changes the torque
ENDO options menu

▶ Press the "S4" key to select the ENDO options menu.
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S1 S2 S3 S4
Option 1: Transmission ratio

▶ Press the "S2" or "S3" key to set the transmission factor.
S1 S2 S3 S4
Key Settings
S1 Saves the option
S2 Changes the transmission factor
1:1 or 3:1
S3 Changes the transmission factor
1:1 or 3:1
S4 Selects the next option
Option 2: Torque
▶ Press the "S2" or "S3" key to change the torque setting display.
S1 S2 S3 S4
Key Settings
S1 Saves the option
S2 Changes the torque setting display
Unit: % or Ncm
Transmission ratio 1:1: 100% = 2.5 Ncm
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Key Settings
S3 Changes the torque setting display
Unit: % or Ncm
Option 3: AutoRev. / Fwd

▶ Press the "S2" or "S3" key to set the period of time after which the motor
rotates clockwise automatically. This dispenses with having to stop it using
the foot control.
S1 S2 S3 S4
Key Settings
S1 Saves the option
S2 Sets the time
1 second to 10 seconds
S3 Sets the time
1 second to 10 seconds
4.8.7 Using the CONEXIOcom (optional)
Note
To start the CONEXIOcom menu, no handpiece may be removed.
Note
For all CONEXIOcom functions, the dental unit must be connected to an in-
stallation of the KaVo "CONEXIO" software.
The function of the CONEXIOcom menu is to control the display of previously

recorded and saved images and videos. In order to use the function, the unit
must have access to the data of the KaVo Software "CONEXIO" software. For
details on the configuration, please refer to the "CONEXIO" installation instruc-
tions.
Opening the CONEXIOcom menu
In order to display extant images, open the menu with the "Remote Control"
button. Select the proper patient on the corresponding PC for this purpose. It is
also feasible to automatically transfer the patient from your invoicing pro-
gramme to CONEXIO. For details on the configuration, please refer to the
"CONEXIO" installation instructions.
73 / 134

If no patient is selected, images from the clipboard are displayed. If the clip-
board is empty, no image is displayed. The clipboard is deleted automatically
when the patient is logged off the corresponding PC.
The CONEXIOcom menu is opened automatically for recording of images or
videos as soon as a device (DIAGNOcam U, ERGOcam One) is taken out.
To close CONEXIOcom: Replace the active device to its holder or close the
CONEXIOcom menu with the "Remote Control" button.
No Icon Setting
1 - Info line
This line displays the active patient name (if selected
in CONEXIO) under which the acquired data are
stored.
If no patient is selected, images and videos are
stored temporarily in the clipboard under "unas-
signed patient".
2 - If a device is active, the device type is shown. The
following is implemented at this time:
DIAGNOcam U
ERGOcam One
3 Next image/video
To be able to communicate efficiently with the pa-
tient, individual images can be selected and dis-
played directly. This uses a rolling system that ad-
vances from left to right and from top to bottom.
4 Screen display:
This button changes the display on the monitor. The
following settings can be made:
1/2/4/6 – number of images displayed.
The live image is always shown as the last image in
split view.
Note
CONEXIO can show only those patients who have been entered in the CON-
EXIO database.
Patient files can be transferred to the treatment centre by one of 2 ways:

▪ Transfer patient via VDDS media or Slida interface to CONEXIO in the re-
spective treatment room. The patient is now automatically activated on the
treatment centre. This might be an option of your patient management sys-
tem that is subject to a charge; please contact your IT specialist.
74 / 134

▪ Opening the patient file of the patient on the PC workstation in the treat-
ment room. The patient is now automatically activated on the treatment
centre.
75 / 134

4 Operation | 4.9 Using function through the dentist or assistant unit
4.9 Using function through the dentist or assistant unit
4.9.1 Using the hygiene functions
The following buttons are available for the hygiene functions:

"Tumbler filler" key Dentist element and
assistant element
"Bowl rinsing" key Dentist element and

assistant element
"Bell" key Dentist element
"Intensive disinfection" Assistant element (unas-

key signed key)
"HYDROclean" key Assistant element (unas-

signed key)
Note
The preparation methods can be found in the care instructions.
The following settings can be changed:

▪ Tumbler filling time
▪ Bowl rinsing time
Using the tumbler filling
▶ Press the "Tumbler" button briefly to start filling the tumbler.
ð Tumbler filling is started and then stopped after the saved period of time.
ð Default = 7 s.
ð An on/off operation is not supported.
▶ Press the "Tumbler filling" key for more than 4 seconds to start the pro-
gramming mode.
Set the period of time in 200 ms increments. Minimum: 0.4 s.
ð If the key stays depressed, the elapsed time is counted in 200 ms steps and
an acoustical signal is issued each second.
ð Once the key is released, the current value is saved.
Using the bowl flush
▶ Press the "Bowl flush" key briefly to start the bowl flush.
ð The bowl flush is started and then stopped after the saved period of time.
ð Default = 7 s. An on/off operation is not supported.
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▶ Press the "Bowl flush" key for more than 4 seconds to start the program-
ming mode.
Set the period of time in 200 ms increments. Minimum: 0.4 s.
ð If the key stays depressed, the elapsed time is counted in 200 ms steps and
an acoustical signal is issued each second.
ð Once the key is released, the current value is saved.
4.9.2 Using the illumination functions for KaVoLUX 540

LED T
WARNING
Unintentional activation of the KaVo KEY Laser III and KEY Laser 3+.
Simultaneous application of the operating light KaVoLUX 540 LED and the
KaVo KEY Laser III or KEY Laser 3+ can lead to the unintentional activation of
the KaVo KEY Laser III and KEY Laser 3+.
▶ When using the KaVo KEY Laser III or the KEY Laser 3+, switch the operat-
ing light to laser mode.
▶ Or switch off the operating light, do not use the KaVo KEY Laser III or KEY
Laser 3+ and the KaVoLUX 540 LED operating light simultaneously.
WARNING
Wrong handling.
Reversible blinding (temporary sight impairment).
▶ Do not direct the light field at patients, users or/and third parties while you
switch on the light.
▶ Do not direct the light field at the patient´s eyes when you move the light
head.
▶ Maintain a clearance of ca. 700 mm between the light and the mouth of the
patient.
CAUTION
Stroboscopic effect of the rotating instrument.
A stroboscopic effect could arise in instruments rotating at a certain speed dur-
ing application of the KaVoLUX 540 LED. This is an optical illusion, where the
instrument appears to be standing still or rotating extremely slowly.
Injury hazard.
▶ If the stroboscopic effect appears, change the speed fractionally and con-
tinue operating in the usual manner.
CAUTION
Faulty measurement in connection with KaVo DIAGNOdent.
Simultaneous application of the operating light KaVoLUX 540 LED and the
KaVo DIAGNOdent can lead to faulty measurements.
▶ Switch the operating light to laser mode when using the KaVo DIAGNO-
dent.
▶ Or switch off the operating light, do not use KaVo DIAGNOdent and operat-
ing light KaVoLUX 540 LED simultaneously.
CAUTION
Premature hardening of composite fillings.
A light intensity that is too high can have a negative impact on the durability of
the treatment.
▶ Select the appropriate dimming level according to the processing time.
77 / 134

Note
The KaVoLUX 540 LED T cannot be operated through the control functions of
the treatment centre. The operating light an only be switched on and off.
The KaVoLUX 540 LED operating light can be used in the following modes:
▪ Normal light: preset at 5,500 Kelvin and 30,000 Lux corresponding to day-
light quality
▪ COMPOsave mode: Enables longer working times for composites by filtering
the blue components of the light (compatible mode for light-activatable res-
toration materials).
▪ Dimmed light: approx. 4,000 Kelvin; equivalent to the light of a halogen op-
erating light
▪ Laser mode: Light mode with no detrimental effect on the KaVo KEY Laser
III, the KEY Laser 3+ or the KaVo DIAGNOdent
When operated In dimmed mode, the LED lamp functions according to a

dimmed halogen lamp. The colour temperature is approx. 4,000 K and the
composite can harden prematurely. This can have a negative impact on the
durability of the treatment.
The COMPOsave modes prevents the composite from hardening prematurely.
As opposed to the dimmed light, the blue components of the light are filtered in
the process. Therefore the composite can be processed longer in COMPOsave
mode.
Control panel KaVoLUX 540 LED T
① "Treatment lamp" key ② "Treatment lamp dimming" key

③ "Mode/ colour temperature" button
Turning the operating light On and Off

light quality
▪ COMPOsave-Modus: enables longer processing periods for composites by fil-
tering the blue components of the light
erating lamp
▪ Laser mode: Light mode, which has no negative influence on the KaVo KEY
Laser III, the KEY Laser 3+ or the KaVo DIAGNOdent.
78 / 134

▶ Press the "Operating light" button on the dentist or assistant element.
ð The operating light is switched on in its most recent active state: operating
light on, COMPOsave mode on or dimmed light.
▶ Press the "operating light" button once again.
ð Operating light is switched off.

A sensor can be used to switch the operating light on or off as follows:
Sensor KaVoLUX 540 LED
▶ Put your hand just in front of the sensor of the operating light.
ð Operating light is switched on.
▶ Again put your hand just in front of the sensor of the operating light.
ð Operating light is switched off.
Setting the brightness
Note
The maximum possible brightness of the light is set in five steps using the
"Treatment light" key.
▶ Press and hold down the "operating light" button.
ð Brightness varies between five stages.

▶ When the desired brightness is reached, release the "Treatment light" key.
Changing between COMPOsave mode res. dimmed light

and normal light
light quality
▪ COMPOsave-Modus: enables longer processing periods for composites by fil-
tering the blue components of the light
79 / 134

erating lamp
▪ Laser mode: Light mode, which has no negative influence on the KaVo KEY
Laser III, the KEY Laser 3+ or the KaVo DIAGNOdent.

mode.
▶ Press the "Mode/colour temperature" button
ð The treatment light switches from COMPOsave mode to dimmed normal

light.
▶ Press the "Mode/colour temperature" button once again.
ð The treatment light switches back to COMPOsave mode.
ð The COMPOsave mode can be recognised by the yellow light.
Switch on COMPOsave mode

mode.
Note
The COMPOsave mode switches on. when the "Dim operating light" button is
activated. The light can be dimmed in COMPOsave mode.
80 / 134

▶ Press the "operating light" button.
or
▶ Hold your hand in front of the sensor for 2 sec.
ð The COMPOsave mode or dimmed light switches on.
ð The COMPOsave mode can be recognised by the yellow light.
▶ Press the "Dim operating light" button once again.
or
ð The treatment light switches back to normal light mode.
Setting the brightness of the dimmer
Note
The brightness of the light is set in five stages using the "Dim treatment
light" key.
Note
The time it takes for composites to harden is dependent on the brightness or
the effective radiation intensity of the light: The processing time is reduced
with increasing brightness / effective radiation intensity. The processing time
for composites is prolonged with reducing brightness / effective radiation in-
tensity.
▶ Press and hold down the "Dim operating light" button.
ð Brightness is increased in five stages.

▶ Release the "Dim operating light" button when the desired brightness is
achieved.
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Set colour temperature
Note
The colour temperature of the treatment light KaVoLUX 540 LED T can be is
set between five stages with the "Mode/Colour temperature" button. The
visual perception of the teeth can be adapted or enhanced by changing the
colour temperature.
4.000 to 4.500 Kelvin: similarity to halogen light
5.500 Kelvin: daylight quality
▶ Press and hold down the "Mode/colour temperature" button
ð Colour temperature changes in five steps.

▶ Release the button when the desired colour temperature is achieved.
Turning the laser mode On and Off
Note
The "laser mode" function is available only from the following version:
- Operating light V1.2.1
Older versions must be updated prior to download.
Note
Falsified colour reproduction: the laser mode only possesses a restricted

spectrum output. Therefore a colour comparison should not be carried out in
laser mode.
In laser mode, another light mode is generated, which has no negative influ-
ence on the KaVo KEY Laser III, the KEY Laser 3+ or the KaVo DIAGNOdent.
▶ Press the „operating light“ button and the "operating light dimming" button
on the operating light simultaneously.
ð The laser mode switches on.
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ð Laser mode is activated: the operating light shines for 1 second in green
and then changes to a white light.
or
ð The laser mode switches on.
ð Laser mode is activated: the operating light switches initially in COMPOsave
mode and then shines for 1 second in green and then changes to a white
light.
Operation of the 3D joint
▶ Turn the switching ring to the left until it snaps into place.
ð Treatment light can be rotated 45° to the left or 45° to the right.
▶ Turn the switching ring to the right and it will spring back to its original pos-
ition.
ð If the treatment light is turned to the centre position (zero position), it will
automatically lock into place in the centre position.
4.9.3 Using the illumination functions for EDI and MAIA
▶ Press the "operating light" key briefly to turn the operating light on or off.
4.9.4 Using the X-ray viewer
▶ Press the "X-ray viewer" key to turn the X-ray viewer on or off.
83 / 134

4.9.5 Using the bell
▶ Press the "Bell" key to activate the bell relay.
ð The bell relay is activated for as long as the key is being pressed.
4.9.6 Using the timer
▶ Press the "Timer" key briefly to start or stop the timer.
ð LED flashes while the timer counts down.
Setting the timer

▶ Press the "Timer" key for an extended period of time to start the timer pro-
gramming mode. The programming mode can be started in the stand-by
menu only.
S1 S2 S3 S4
Key Settings
S1 Saves the parameters.
Quits the programming mode.
S4 Switches counter/timer function.
84 / 134

4 Operation | 4.10 Operating the foot switch
4.10 Operating the foot switch
4.10.1 General functions
The footswitches of the foot control have two functions. The function of the con-
trol depends on whether an instrument is in its holder or whether it has been
removed.
See also:
2 Foot control
4.10.2 Positioning the patient chair with the foot control
See also:
2 Automatic positioning of patient chair
2 Position the dental chair using the button cross or 4-way switch
4.10.3 Preselect dentist

Requirement
All instruments are in their holder.
▶ Hold down the foot pedal and press the stirrup switch.
ð Each time the stirrup switch is pressed, the selection advances to the next
dentist (dentist 1 to 6).
The number of dentists can be set in the user menu.

Two dentists are set as the default.
4.10.4 Start and regulate instruments

▶ Remove the handpiece (such as turbine, motor) from the holder.
ð The handpiece is active.
▶ Press the foot pedal.
ð The removed handpiece runs at the set speed or intensity.
▶ Changing speed or intensity with the foot pedal.
ð The left stop corresponds to the minimum speed/intensity.
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ð The right stop corresponds to the maximum speed/intensity.
4.10.5 Setting the cooling condition

▶ Remove the handpiece (e.g., turbine, motor) from the holder.
▶ Press "Preselected spray" footswitch.
ð The cooling status is switched each time the foot switch is pressed: spray air
- spray.
ð The cooling status is displayed on the dentist and assistant element.
4.10.6 Activating blown air (optional)

▶ Remove the handpiece (such as turbine, motor) from the holder.
▶ Press the "Blown air" foot-operated button.
ð As long as the foot-operated button is pressed, blown air exits from the re-
moved handpiece (does not apply to PiezoLED).
4.10.7 Preselect counterclockwise motor rotation

▶ Take motor off the holder.
▶ Slide the cross switch upward.
ð The direction of motor rotation is reversed each time the cross-switch is ac-
tuated: counterclockwise rotation - clockwise rotation.
ð The direction of motor rotation is displayed on the dentist element.
4.10.8 Adjusting the instrument light
▶ Slide the cross switch to the right. (spotlight function)
86 / 134

ð Cold light "On" (even if Cold light "Off" is preselected).
▶ Slide the cross switch to the left.
ð Change the cold light status: "On/Off".
4.10.9 Using CONEXIOcom (fee-based additional option)
No Setting
① U-shaped switch
Discard image/video
Press briefly - deletes the selected image/video
Press long - all images/videos in the clipboard are deleted
② Previous image/video
Select previous image/video
③ Next image/video
Select next image/video
④ Screen display
The number of displayed images (Split View) is reduced:
The live image is always shown as the last image in split view.
⑤ Screen display
The number of displayed images (Split View) is increased:
The live image is always shown as the last image in split view
⑥ Capture Mode
Toggles between the recording modes, video recording and image recording
⑦ Screen display
Toggles between full screen and normal view
⑧ Save image/video
Press briefly - freezes the live image
Press long - saves the live image directly.
If no patient is selected, the images are stored directly under "unassigned patient".
87 / 134

4 Operation | 4.11 Using instruments
Note
If no patient is selected, the images stay in the "Swap Tray" and are not
saved permanently. As soon as a patient is selected, these temporary data in
the "Swap Drying" are deleted. When an active patient is logged off (or a
new patient is logged on) in CONEXIO, a query is shown asking whether the
images shall be deleted or saved. Data deleted at this point cannot be re-
stored subsequently.
4.11 Using instruments
Note
Consult the pertinent separate instructions for information regarding the in-
stallation, use and servicing of the individual handpieces (such as the turbine,
PIEZOsoft, Satelec Mini LED, etc.).
4.11.1 Setting spray air and spray water
The adjusting screws for spray air and spray water are situated on the under-
side of the table and correspond to the handpiece that is actually connected.
For KaVo Midwest handpieces, spray air and spray water are pre-set suitable at
the factory such that no re-adjustment is required.
2
1
▶ Use the short adjusting screw ② on the control valve to adjust the spray
air.
ð Counterclockwise rotation (seen from below) increases the flow rate.
▶ Use the long adjusting screw ① on the control valve to adjust the spray wa-
ter.
ð Counterclockwise rotation (seen from below) increases the flow rate.
88 / 134

Borden handpieces
Note
In the case of Borden handpieces, the drive air needs to be adjusted for each
handpiece by a Service Technician using adjusting screw ③. The adjustment
can be made using the measuring set Mat. no. 0.4179807 (Mat. no.
10039374) or the test manometer for Borden handpieces Mat. no.
04118531.
4.11.2 Using suction hoses

▶ Remove the spray mist suction device and/or saliva ejector from the holder.
ð The spray mist suction device and/or saliva ejector is turned on automatic-
ally and turned off when it is replaced in the holder.
The suction flow of the saliva ejector or spray mist suction device can be re-
duced or blocked with the slide valves integrated in the handpieces.
6 5
4
6 5
▶ Move the slide valve completely upward.

ð The slide valve is open: maximum suction.
▶ Move the slide valve down all the way.
ð The slide valve is closed: no suction.
Note
Connectors for the spray mist suction and the saliva ejector without slider as
well as reducing pieces for the spray mistsuction are available as accessories.
▪ Cannula holder, short, for spray mist ejector ② (Mat. no. 0.764.5783)
▪ Cannula holder, long, for spray mist ejector ② (Mat. no. 0.764.5853)
▪ Cannula holder, short, for saliva ejector ① (Mat. no. 0.764.5863)
89 / 134

▪ Cannula adapter, reducing handpiece to 7 mm ② (Mat. no. 0.764.5873)

▪ Cannula adapter, reducing handpiece to 11 mm ② (Mat. no. 0.764.5883)
Vacuum stop
CAUTION
Danger of backflow
Swallowing or choking hazard for the patient
▶ Only actuate the vacuum stop when the suction cannula is not in the pa-
tient's mouth.
Note
Vacu-Stop is available in combination with Venturi suction, external wet suc-

tion system, and suction valve.
When the base switch is actuated, the suction of the removed hose is stopped.
① Vacu-Stop
4.11.3 Using triple-function handpieces
CAUTION
Cannulas that are worn, not screwed in or not locked into place.
Injury from swallowing the cannula.
▶ Before each treatment, ensure that the cannula is properly locked or
screwed into place and firmly seated.
▶ Use original KaVo cannulas only.
CAUTION
Risk of injury from touching the cheek with the handpiece.
Irritation of the mucosa.
▶ Rotate the cannula of the handpiece into an operating position where there
is no contact of the mucosa.
90 / 134

① Cannula ② Water button (green ring)

③ Air button (blue ring) ④ Handpiece and hose
Triple-function handpiece
① Air button (A) ② Cannula

③ Gripping sleeve ④ Water button (W)
⑤ Ring blue
Note
The cannulas can be rotated 360o..
▶ Remove the turbine from the holder.
▶ Press the air button ① and continuously increase or decrease the exiting air
flow by applying more or less pressure on the air button ①.
or
▶ Press the water button ④ and continuously increase or decrease the exiting
water jet by applying more or less pressure on the water button ④.
or
▶ Simultaneously press the air button ① and water button ④ and continu-
ously increase or decrease the exiting spray by applying more or less pres-
sure on the two buttons.
91 / 134

Removing the cannulas

▶ Hold the valve body of the triple-function handpiece and screw off the can-
nula.
4.11.4 Using the PIEZOsoft/PiezoLED
CAUTION
Handpiece inserts can be damaged from long-term use, or when
dropped or bent.
They cannot be guaranteed to function properly.
Injury from insert breakage.
▶ Check the handpiece inserts before each use.
CAUTION
Sharp-edged tips.
Risk of injury.
▶ When not in use, always keep the supplied torque wrench attached to the
tip!
Note
Please comply with the enclosed "PIEZOsoft/PiezoLED" Instructions for Use.
Controlled through the menu
See also:
2 4.8.5.2 PIEZOsoft/PiezoLED, Page 66
Operation with the foot control
ð The PIEZOsoft/PiezoLED works at the pre-set intensity.
92 / 134

4 Operation | 4.12 Using the KL 703 LED in ENDO mode (optional accessory)
▶ To adjust the intensity, press the foot pedal and move it to the side.
4.12 Using the KL 703 LED in ENDO mode (optional

accessory)
4.12.1 General information
Note
The endo drive can only be operated with the INTRA LUX KL 703 LED.
INTRA LUX KL 703 LED
CAUTION
Use of impermissible filing systems.
Do not use impermissible filing systems which can damage the product or
cause personal injury.
▶ Only use approved NiTi filing system with a conicity >2% that are suitable
for rotary preparation.
▶ Only use files with shafts in conformance with DIN EN ISO 1797-1, DIN EN
ISO 1797-2, DIN EN ISO 3630-1 and DIN EN ISO 3630-2 having a shaft
diameter of 2.334 to 2.350 mm
▶ Follow manufacturer's instructions (mode of operation, speed, torque
levels, torsion resistance, etc.), and use the files according to their intended
use.
CAUTION
Use of damaged files.
Injury to the patient or damage to the medical device.
▶ Before preparing each root canal, insert a dental dam for safety reasons.
▶ Before each use, the files must be checked for possible signs of
material fatigue, deformation or excessive stress and if such signs appear,
they must be replaced.
CAUTION
Incorrect transmission ratio.
Damage from incorrect speed / incorrect torque.
▶ Only use KaVo 1:1 reducing shanks 20LH or 20LP or MASTERmatic LUX
M20 L with 1:1 INTRA LUX head L68 B (Mat. no. 1.008.1834) or 3:1 IN-
TRA head L66 B (Mat. no. 1.008.1831).
93 / 134

CAUTION
Excessive torque.
Injury or damage to instruments.
▶ Use root canal instruments in ENDO mode only.
Technical specifications for the KL 703 LED in ENDO

mode
Note
The technical specifications apply to the KL 703 LED in ENDO mode.LED
Speed range 200 to 3,200 min-1

Maximal torque 2.5 Ncm
Operating mode
Note
30 seconds operating time/9 minutes pause is the potential load threshold of
the motor (full load at maximum speed).
In practice, pulse loads lasting seconds or pause times lasting seconds or

minutes are realistic given that the maximum possible motor current is not nor-
mally reached. This equates to the dentist's normal way of working.
4.12.2 Open ENDO mode

▶ Remove the endomotor INTRA LUX KL 703 LED from the holder.
▶ Press the "Additional motor drives" key.
ð The display switches to the "ENDO" menu.
The device exits from Endo mode as soon as the INTRA LUX KL 703 LED endo-
motor is returned to the holder. The Endo mode is activated automatically once
the endomotor is removed, providing that the Endo mode was previously ended
by putting the endomotor back in place.
Note
The device does not automatically start when endo mode was left by pressing
the "Motorised auxiliary drives" button, or if endo mode has never been ac-
tivated since the last time the unit was turned on.
A service technician can deactivate the automated start.
Note
Before using the endomotor, always check the speed and transfer ratio.
94 / 134

S1 S2 S3 S4
Parameters Values
Transmission factor 1:1, 3:1
Parameter memory P1,P2,P3,P4,P5,P6
Torque mode TQ-Ctrl, Autoreverse, AutoRev/Forw.
Direction of motor rotation R, L
Speed 100 to 6,000 rpm
Torque Transmission ratio 1:1: 0.15 to 2.50
Ncm
Transmission ratio 3:1: 0.4 to 8.0 Ncm
CAUTION
Incorrectly set parameters.
Injury or property damage from incorrect input values.
▶ Check all input values before use.
4.12.3 Set torque mode

Three different torque modes are available:
▪ Autoreverse
▪ Torque Control only
▪ Autorev / Forward
▶ Press the "Up" or "Down" key to select the desired torque mode.
ð The torque mode is shown on the display and is effective immediately.

Torque mode Torque Control only
ð The motor starts by rotating clockwise (if not selected otherwise).

The torque is limited to the set threshold. The speed reduces until it stops de-
pending on the load.
The direction of rotation is always to the right.
A tone sounds when the set torque threshold is reached.
95 / 134

▶ Push 4-way button on the foot control upward in order to switch to counter-
clockwise rotation.
Torque mode Autorev / Forward
ð The motor starts by rotating clockwise (if not selected otherwise)

When the set torque is reached, a signal sound is emitted, and the motor
switches to counterclockwise rotation. After the set time, the motor automatic-
ally reverts to clockwise rotation. The time can be set in the option menu (Op-
tion 3).
See also:
2 4.8.6 ENDO menu (optional), Page 68
Note
The motor's rotational direction can be reversed with the cross-switch on the
footswitch in all torque modes.
▶ To stop this, release the foot pedal.
ð The motor rotates clockwise again.
4.12.4 Changing settings in the menu
See also:
2 ENDO menu (optional)
4.12.5 Leaving ENDO Mode
▶ Press the "Additional motor drives" key.
or
96 / 134

4 Operation | 4.13 Use USB interface
▶ Place the INTRA LUX KL 703 LED back in the holder.
Note
If the unit was switched to "Instant ENDO" mode, ENDO mode is only inter-
rupted when the ENDO motor is placed in the holder, and it is continued
when the ENDO motor is removed.
The function can be set by the service technician.
See also:
2 4.12.2 Call up ENDO mode, Page 94
4.13 Use USB interface
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.
The treatment unit may be fitted with up to three USB ports. Camera interfaces
are situated on the underside of the dentist element (T-table) or in the dentist
element (S-table). Only the cameras approved/enclosed in the delivery by KaVo
may be connected to these interfaces.
The USB port in the back is connected directly to the back-of-the-head PC (in
the presence of the corresponding wiring). USB devices meeting the specifica-
tions listed above can be connected to this interface. To use USB devices that
have been connected, it may be necessary to install a suitable driver software
on the back-of-the-head PC.
Getting the USB ports ready for use

▶ To run an USB device, connect the USB port in the terminal box of the
treatment centre to an external back-of-the-head PC. Use one or maximally
two USB extension cables 5 m (Mat. no. 1.004.6953) according to need.
▶ USB devices connected to the dentist element must meet the USB stand-
ards, USB 1.0, 1.1 or 2.0, and consume max. 500 mA of electrical power.
97 / 134

4 Operation | 4.14 Using the camera
4.14 Using the camera
See also:
2 Instructions for Use ERGOcam One
See also:
2 Instructions for Use DIAGNOcam 2170 U
4.15 Using the screen
See also:
2 Instructions for use Screen One
98 / 134

5 Preparation methods DIN EN ISO 17664
5 Preparation methods DIN EN ISO 17664
Note
The preparation methods can be found in the care instructions.
99 / 134

6 Accessories and kits | 6.1 Device
6 Accessories and kits
6.1 Device
Name Description
Water inlet block Without DVGW permit.
With water filter and pressure controller.
Water bottle For a water supply for tumbler and handpieces inde-
pendent of the public water supply.
External wet suction sys- Suction handpieces and bowl valve are suctioned
tem with bowl valve centrally.
External wet suction sys- Suction handpieces are suctioned centrally.
tem, direct discharge
with no bowl valve
Venturi suction system Compressed air-operated saliva ejector
Venturi suction system Compressed air-operated spray mist
Operating light KaVoLUX Operating light.
540 LED T / EDI / MAIA
Tray support For the small handpiece tray.
Warm water heater Heats the tumbler water.
Low-pressure regulator Regulator for suction air when the suction vacuum is
too high.
Intensive germ reduc- Intensive germ reduction with increased Oxygenal 6
tion, manual dosing
See also:
2 PA ESTETICA E30
Electrical water shut-off Water pressure shut-down during off-times
6.2 Dental chair

Name Description
Armrest The armrest can be swung up to make it easier for
the patient to get in and out.
Child’s seat For paediatric treatment.
Trendelenburg (optional) Bench movement synchronous to backrest
6.3 Assistant unit

Name Description
Satelec Mini LED and LED polymerisation light.
KaVo Poly One
Triple-function handpiece Handpiece featuring air, water, no heating, and no
One / triple-function cold light.
handpiece
6.4 Dentist element

Name Description
Air handpiece hose For connection of turbine and SONICflex and all
handpieces fitting on the multiflex coupling.
100 / 134

6 Accessories and kits | 6.4 Dentist element
Name Description
Borden hose For Borden (2-hole) handpieces.
Assembly kit INTRA LUX Brushless motor with light.
motor KL 703 LED
Assembly kit INTRA LUX Brushless motor with light.
motor KL 701
Triple-function handpiece Handpiece featuring air, water, no heating, and no
One / triple-function cold light.
handpiece
PiezoLED Handpiece with LED light for removal of dental cal-
culus with Scaler tip sets.
PIEZOsoft Handpiece without light for removal of dental calcu-
lus with tip sets, Scaler / Paro / Endo / Prep.
X-ray viewer 1440 For installation on the lamp mounting pole.
Tray holder for a stand- Standard tray, US tray, and/or 2x-standard trays
ard tray / US tray / 2x- (install on left or right side of dentist element).
standard tray
Torque control (Endo) Drive for endodontic treatment.
Chipblower (optional) Sets the preset blown air at the handpiece (does not
apply to PiezoLED and PIEZOsoft).
Patient communication: Controls the display of previously recorded and
saved images and videos.
▪ Screen One
▪ DIAGNOcam 2170 U
▪ ERGOcam One
101 / 134

7 Safety checks - testing instructions | 7.1 Introduction
7 Safety checks - testing instructions
7.1 Introduction
7.1.1 General instructions
Note
The safety checks may only be carried out by one or more electricians (as
defined in IEC 61140) who have received appropriate training for the device
to be inspected.
Note
The contents and specified tests in this document are based on the interna-
tional standard, IEC 62353 (DIN VDE 0751-1). This standard applies to the
testing and inspections of medical electrical equipment or medical electrical
systems complying with IEC 60601-1 (DIN EN 60601-1).
Note
In order to evaluate the safety of medical devices, systems or components of
medical devices or systems, the safety checks must be carried out at the
times specified below:
▶ Prior to startup
▶ during maintenance
▶ during inspections and servicing
▶ following repair
▶ on the occasion of recurrent tests
Note
With regard to devices that have not been manufactured in accordance with
IEC 60601-1 (DIN EN 60601-1), these requirements can be applied taking
the mandatory safety standards for the production of these devices into con-
sideration.
Note
If the unit comprises several electrical devices or electrical devices from sev-
eral manufacturers that are connected to a system in connection with the
KaVo dental unit, the manufacturer data contained in the instructions for use
for all products subject to safety controls must also be observed.
Note
Accessories to ME devices that could have an impact on the safety of the
device to be tested or the measured results must be included in the safety
checks.
Note
All tests concerning the included safety checks of accessories must be docu-
mented.
Note
Furthermore, the manufacturer data contained in the instructions for use
must be adhered to in all products to be tested and inspected.
102 / 134

Note
KaVo offers a medical device book for keeping an inventory and recording es-
sential master data on the medical device. The medical device book is only
available in German (Mat. no. 0.789.0480).
Note
The following tests and measurements must be documented, for example in
the medical device book. We recommend using the templates at the end of
the document.
Note
The tests must be performed in the order specified by the manufacturer!
7.1.2 Notes for medical electrical systems
Note
An ME System is the combination of individual devices (as defined by manu-

facturers) that must meet the following conditions:
▶ At least one of these devices must be a medical electrical device.
▶ The devices must be functionally connected or at least they should be
connected by the application of a multiple socket outlet.
Note
With ME systems, the person responsible for putting the system together
must define the necessary measuring parameters and measuring procedures
as required in IEC 60601-1 (DIN EN 60601-1).
Note
Each individual device in an ME system, which has a separate connection to

the power supply network or which can be connected to or separated from
the power supply network without the aid of a tool, must be checked indi-
vidually. Moreover, the ME system must be checked as one unit to avoid any
"aging" of individual devices leading to unacceptable values in sum.
Note
An ME system that is connected to the supply network by means of a mul-

tiple socket outlet must be treated as one device during checks and testing.
Note
If the ME system or part of the system is connected to the supply network by

means of an insulating transformer, the transformer must be included in the
measurements.
103 / 134

Note
In ME systems, in which more than one ME device are interconnected via

data lines or otherwise, e.g. via electrically conductive attachments or coolant
tubes, the earth wire resistance of every single device must be checked.
Note
If it should be impossible to check single ME devices that are functionally

connected to an ME system individually for technical reasons, the ME system
must be checked as a whole.
7.1.3 Essential parts of the safety check
Visual inspection
Optical appraisal of the safe and usable condition of the medical device and its
accessories.
Measurements
▪ Measurement of the protective earth resistance in accordance with IEC
62353 (DIN VDE 0751-1)
▪ Measurement of the leakage current of the device EUL in accordance with
IEC 62353
▪ Measurement of the leakage current of the user part EPL in accordance with
IEC 62353 (DIN VDE 0751-1)
Note
Measurement of the insulation resistance in accordance with IEC 62353 (DIN

VDE 0751-1) is not required. This check is covered by the measurement of
the leakage current provided a prescribed safety tester in accordance with
IEC 62353 (DIN VDE 0751-1) Annex C is used!
Functional test
Medical device function test as well as testing of all safety shutdowns with refer-
ence to accompanying documentation/instructions for use.
7.1.4 Testing intervals

▪ Check every 2 years in accordance with Type II
7.1.5 Notes on the test method in accordance with IEC

62353
▪ Protection class 1
▪ Type BF
▪ The device is firmly connected / threshold: SL < 0,3 Ω
▪ Measurement according to EUL / threshold: < 10mA*
▪ Measurement according to EGA / threshold: < 5 mA*
104 / 134

7 Safety checks - testing instructions | 7.2 Instructions for safety checks
*The EUL limit corresponds to the value defined in IEC 60601 (DIN EN 60601),
taking comment 2 from table 2 into consideration.
7.1.6 Notes on repeat testing
Note
The value determined in these tests must be documented and evaluated to-
gether with the measuring process. The measured values must not exceed
the specified values.
Note
Comparisons with previous measurements must be carried out if the meas-

ured values are lower than the threshold values by more than 10 %. The test
intervals should be reduced if a deterioration in values is determined!
7.2 Instructions for safety checks
7.2.1 Preparatory measures to be undertaken on the

device
WARNING
Electrical power.
Death or injury from electric shock.
▶ Before servicing, pull the mains plug out of the socket or completely discon-
nect the device from the power to de-energise it!
▶ After conversion, check the electrical safety in accordance with IEC 62353
(DIN VDE 0751-1).
▶ Turn off the main switch before any maintenance work.
▶ Lift the upholstery at the foot end ① and remove from the chair.
▶ Remove two screws ② from the cover of the junction box.
105 / 134

▶ Take the cover off proceeding in upward direction.
7.2.2 Visual inspection (inspection by examination)

Check the following items in advance:
▪ Has the equipment of the ME device or the ME system been changed since
the last inspection?
▪ Was the change documented and approved (test protocol, safety check
STK)?
▪ Are there any indications of insufficient safety?
Check the ratings of fuses that are accessible from

outside
▶ Verify whether the main fuse on the main switch ② of the unit complies
with the specified nominal data ①.
106 / 134

Visual inspection and appraisal of the medical device

and accessories
The following list is for exemplary purposes and makes no claim of being com-
plete.
Check the following items:

▪ Stability of the device
▪ No damage to the cladding or casing (cracks, breakage)
▪ Functioning of the carrier systems on dentist and assistant side, treatment
lamp, and display (brakes, height adjustment, etc.)
▪ Condition of the handpiece and suction hoses
▪ Condition of all installed application parts
▪ Condition of the control panels
▪ Condition of the threads for the fitting of tips to the ultrasound scaler hand-
piece
▪ Condition of the operating light
▪ Absence of leaks on the body of the device
▪ Condition of the power connection provided by the treatment centre
▪ Condition of air and water connections
▪ Any damage on the sight window and the casing of the camera ERGOcam
▪ Expiry date of the water bottle inserted in the BS water bottle not exceeded
Check of legibility and completeness of the safety-

related labels
▶ Check if all safety-related markings (plates and labels) are present and
legible.
▶ Check if the rating plate and serial number plates are present and legible.
ESTETICA E30 and chair nameplate
107 / 134

Site for affixing the rating plate and serial number plate
① Serial number plate of the chair ② Rating plate
E30 TM
E30 S
Attachment locations for serial number plate and BF labelling
Control of the availability of the necessary documents

▶ Check if the required instructions for use and care instructions are available
in the surgery.
108 / 134

Note
Any irregularities determined in the visual inspection must be recorded in the

test protocol. It is essential to determine whether defects and deficiencies
could have an adverse impact on the safe operation of the unit. If the de-
termined irregularities present a safety hazard and cannot be rectified dir-
ectly, the unit must be closed down until the safe operation is restored.
7.2.3 Measurements
WARNING
Danger to persons due to a lack of care exercised during the safety
checks and testing.
▶ Prior to connecting the treatment centre to the safety tester, disconnect it

from the mains supply network.
▶ Carry out all safety checks and tests in a manner that will ensure that there
will be no danger to the testing personnel, patients or other persons.
Note
The safety tester must comply with the requirements defined in IEC 62353
(DIN VDE 0751-1), Annex C.
Note
If no other specifications have been made, all values relating to voltage and
current are effective values of alternating voltage, direct voltage or pulsating
voltage res. alternating current, direct current or pulsating current.
Note
Cables and wires, e.g. power supply cords, measuring circuits and data lines,
must be arranged appropriately such that their influence on measurements is
minimised.
Note
Connection cables such as data cables and cables for the functional earth
could simulate protective conductor connections. These types of supplement-
ary but unintentional protective earth connections could lead to erroneous
measurements.
Note
The following measuring aids can be ordered: KaVo measuring cable (Mat.
no. 0.411.8811)
109 / 134

Using the measuring cable ① the unit is disconnected from the mains supply
and connection of the treatment centre to the safety tester is enabled. Hence,
the customer-provided mains supply L & N on the power input board need not
be disconnected. The adapter cable ② is included in the delivery of the KaVo
measuring cable and is required for older treatment centres that are not
equipped with an X2 connector.
Connecting the safety tester to KaVo measuring cables

on the treatment centre
▶ Disconnect plug X2 from the unit control and plug it into the matching con-
nector X2 of the KaVo measuring cable (Mat. no. 0.411.8811).
▶ Connect the second plug X2 of the KaVo measuring cable to the unit control
(X2).
▶ Insert the protective contact plug of the KaVo measuring cable into the
sight window.
110 / 134

Connecting the safety tester without the KaVo

measuring cable to the treatment centre.
① Protective earth conductor terminal

(PE)
▶ Switch L + N of the on-site power supply cord to be voltage-free.

▶ Disconnect L + N on terminals X8.L Mains (mains supply) and X8.N Mains
(mains supply).
▶ Connect the safety tester directly to terminals X8.L Mains (mains supply)
and X8.N Mains (mains supply) and protective earth conductor terminal
(PE).
Note
The main switch of the ME device / ME system must be turned on during the
measurement.
Connect the application parts [AP] to the safety tester:

▶ Connect ① to ③ to the safety tester.
▶ Connect the safety tester to additional measuring points AP X.
Note
Additional measuring points AP X must be taken into consideration in the

presence of accessories: e.g. accessories such as PIEZO ultrasonic scaler,
etc.
111 / 134

See also:
2 8 Annex - Additional measuring points, Page 122
Connect accessible conductive parts [ACP] with PE
ACP = accessible conductive parts
ACP
ACP
Note
Additional measuring points ACP X must be taken into consideration in the

presence of accessories.
See also:
ACPs on the treatment centre

No ACPs need to be connected to the protective conductor (PE) during the
measurement on the treatment centre ESTETICA E30, as all relevant parts are
connected to the PE at the factory and are included in the test.
ACPs on treatment lamps

No ACPs need to be connected to the operating lights during the measurement
with protective conductor (PE) because all relevant parts have already been
connected to the protective conductor (PE) at the factory and are included in
the test.
112 / 134

Measure protective conductor resistance
Limit < 0,3 Ω (maximum value!)
Note
The integrity of the power supply cable, in particular the protective earth wire
of the power cable must be ensured. As this is a fixed installation, the evalu-
ation can be conducted by means of a visual inspection. If damage is determ-
ined, the further procedure to be taken is specified in the general instruc-
tions.
Note
In this measurement the resistance of the protective earth connection of the

supply network can be taken into consideration.
Note
If applicable: all removable supply connection lines, which are kept handy for
possible use, should be taken into consideration and the respective PE meas-
ured.
Protective earth measurement
The protective conductor resistance must be measured at the following parts of

the device:
▪ Treatment centre
▪ Treatment lamp
▪ Accessories
Note
Additional measuring points SL X need to be taken into consideration in the

presence of accessories: e.g. if accessories are connected, connection to ex-
ternal devices, camera module of the multimedia system, etc.
See also:
113 / 134

Scan the treatment centre with the test tip
Measuring points on the device base
① Surroundings of the protective ② Main switch holding plate

earth conductor terminal
③ Stand cover base plate ④ Top part of the chair
⑤ Foot control floor plate
(bottom side)
▶ Slide cover ① in upward direction.
114 / 134

Standard dental chair measuring points
▶ Check firm seating of the PE headless screw ②.

▶ Scan headless screw ② with the measuring probe.
① Dentist element S: installation site ② Dentist element TM: installation site

of the tray holder of the tray holder
115 / 134

① Assistant element: Fastening screw

on the bottom of the assistant ele-
ment
Scan the treatment lamp with the test tip
Operating light KaVoLUX 540 LED U
① Fastening screw of the handle sup-

port when the gripping sleeve has
been removed
Operating light EDI/MAIA

No measuring points need to be scanned on the operating lights EDI and MAIA.
Measure protective conductor resistance of accessories
See also:
Measure equivalent unit leakage current
Limit < 10 mA (maximum value!)
116 / 134

ACP
Protection class 1
WARNING
Electrical power.
▶ Conduct test for leakage current in devices of Protection Class 1 only after
the protective earth test has been passed.
WARNING
Electrical power.
▶ Prior to connecting the treatment centre to the safety tester, disconnect the
treatment centre from the mains supply network.
Measure equivalent patient leakage current
Limit < 5 mA (maximum value!)
ACP
Protection class 1
WARNING
Electrical power.
▶ Conduct test for leakage current in devices of Protection Class 1 only after
the protective earth test has been passed.
WARNING
Electrical power.
▶ Prior to connecting the treatment centre to the safety tester, disconnect the
treatment centre from the mains supply network.
Note
In the testing of ME devices with several application parts, the parts must be
connected in succession. The measured results must be evaluated using the
threshold values. Application parts, which are not included in the measure-
ment, remain open.
117 / 134

Note
An additional measurement of the leakage current from type B applied parts

need only be carried out if this is specified by the manufacturer (see accom-
panying documents).
Note
A separate measurement is not usually required for type B applied parts. The
applied parts are connected to the casing (see diagram) and included in the
measurement of the leakage current of the casing, whereby the same per-
missible values are applicable.
7.2.4 Functional test

The following conditions must be met in all function tests:
▪ The basic function of the treatment centre must be guaranteed.
▪ The treatment centre must be fit for use.
▪ There must be no irregularities, noise or abrasion, etc., present.
The following list is for exemplary purposes and makes no claim of being com-
plete.
▪ Function test of the safety circuits (see diagram below)
▪ Functioning of the master switch of the device
▪ Functioning of the displays
▪ Function test of the holder switch of the dentist and assistant element
▪ Functional test of the 3F handpiece – seating of the cannula
▪ Functional test of operating light
▪ Function test of the suction hoses
▪ Function test of the foot control
▪ Function of the chair:
- Travel on all axes
- Testing of the limit switches
▪ Functional test ...
118 / 134

Pos. Safety switch-off ac- LED on assistant LED on dentist ele-

no. tuated element ment
① Bracket on the foot
control
② Assistant element
③ Backrest
④ Kickplate
⑤ Seat
For right/left conver-
sion with bench re-
moved
119 / 134

7.2.5 Assessment and documentation
Note
All tests conducted must be documented comprehensively. The doc-
uments must contain at least the following particulars:
▶ Name of the test centre

▶ Name of the test engineer
▶ Name of the tested device (e. g. type, serial number)
▶ Tests and measurements
▶ Data, type and measuring results of the visual inspections
▶ Data, type and measuring results of the measurements
▶ Data, type and measuring results of functional tests
▶ Measuring/test equipment including SN/test equipment number and cal-
ibration period
▶ Final evaluation
▶ Name, date and signature of test engineer
There is a copy of a test report template at the end of chapter STK. KaVo re-
commends the use of this template.
Note
Following testing, repair or adjustment, it must be verified whether the ME
equipment or ME system has been restored to the state that is required for
the intended usage before it is employed once again.
Note
If the safety of the tested ME equipment or ME system has not been
established, e.g. the tests have not been completed with positive
results, the equipment or system must be marked accordingly and
the potential hazard emanating from the equipment or system must
be communicated in writing to the RESPONSIBLE ORGANISATION
(to the operator, as a rule). This action is not required if the cause of
the malfunction could be determined and rectified. The defect must
be recorded in the protocol.
120 / 134

121 / 134

8 Appendix - Additional measuring sites | 8.1 Additional scanning sites SL X in the protective conductor measure-
ment
8 Appendix - Additional measuring sites
Note
With reference to accessories, which are not listed here, the specifications of
the relevant instructions for use must be observed. Example: ERGOcam 5.
8.1 Additional scanning sites SL X in the protective

conductor measurement
Connector for third-party equipment
▶ Position the test tip on the middle contact ①.
122 / 134

8 Appendix - Additional measuring sites | 8.1 Additional scanning sites SL X in the protective conductor measure-
ment
Ceiling adapter for operating light assembly kit
① Base plate for the ceiling adapter ② Surroundings of the protective con-
ductor connector
③ Surroundings of the protective con-
nector terminal
Touch monitor with test tip
▶ Scan the measuring point ① with the test tip.

or
123 / 134

8 Appendix - Additional measuring sites | 8.2 Additional measuring sites AP X for EUL/EPL measurement
▶ Scan the measuring point ② after removing the display cover.
8.2 Additional measuring sites AP X for EUL/EPL

measurement
Scan the PIEZO ultrasonic scaler with test probe
Exemplary presentation of the measuring point on the PiezoLEDultrasonic scaler
① Test probe on ultrasonic scaler tip

in ultrasonic scaler handpiece
124 / 134

9 Troubleshooting
9 Troubleshooting
Note
In case of malfunctions of the individual handpieces (e.g. turbine, motor,
camera, Satelec, Mini LED etc.), consult the separate instructions for the use
and care of the individual instruments.
Malfunction Cause Remedy

Nothing works. Main switch is off. ▶ Turn on the main switch.
Main service fuse inter- ▶ Unplug the unit from the mains.
rupted the electric cir- ▶ Check and replace, if required, the main ser-
vice fuse.
cuit.
The main service fuse is situated next to the
master switch.
▶ For this purpose, open the bayonet closure
with a screwdriver and replace the fine-wire
fuse (T 6.3 H Mat. no. 0.223.2783).
▶ The re-close the bayonet closure with the
screwdriver.
The patient chair does The safety shutoff is ▶ Check the safety shutoff and eliminate the
not move. activated. reason for the shutoff.
(LED on the control

panel flashes.)
Display without indic- Bus / hardware error. ▶ Turn the device off and on.
ator. ▶ Call the service technician to look into the
problem if it continues to exist.
Operating device no Bus / hardware error. ▶ Turn the device off and on.
function. ▶ Call the service technician to look into the
problem if it continues to exist.
Turbine making loud Turbine wheel faulty. ▶ Replace turbine wheels.
running noises. Follow the operating instructions for the tur-
bine.
Satelec Mini LED / Also refer to: Instruc-
KaVo Poly One does not tions for Use of the
work. Satelec Mini LED /
KaVo Poly One
No cold light on the Cold light not preselec- ▶ Preselect cold light.
handpieces. ted.
The high-pressure lamp ▶ Replace the high-pressure lamp or Multi LED.
or Multi LED on the Also refer to: Instructions for Use of the
handpiece
handpiece is defective.
See also:
2 Instructions for Use of the handpiece
125 / 134

9 Troubleshooting

No spray in the hand- No spray preselected. ▶ Preselect spray.
pieces. Check setting on butterfly valves of the dentist
element.
Close the ring for con- ▶ Open the ring for controlling the spray on the
trolling the spray on handpieces.
Check setting on butterfly valves of the dentist
the handpieces. element.
Spray throttle Ws20
connected to control
valve.
The main water valve ▶ Open main valve.
in the office is closed.
The compressor is not ▶ Turn on the compressor.
turned on.
No water in the tumbler Water bottle is empty. ▶ Fill the water bottle.
and spittoon bowl No air pressure in the ▶ Turn on the compressor.
unit.
Spray at the instru- The spray nozzles are ▶ Clean the spray nozzles according to the ac-
ments is insufficient. dirty/clogged. companying instrument operating instructions.
Leaks in instruments. O-rings at MULTIflex or ▶ Replace O-rings.

motor coupling, grip-
ping sleeve or cannula
of the triple-function
handpiece are dam-
aged.
PiezoLED or PIEZOsoft PiezoLED or PIEZOsoft ▶ Also refer to: Instructions for Use of the
without function. not pivoting. PIEZOsoft/PiezoLED
The suction hoses do Slides on the conical ▶ Open the slide valve.
not have any suction. sections are closed.
Sieves in suction con- ▶ Replace sieves.
nector are blocked.
Base plate for vacu- ▶ Relieve base plate.
stop has been activ-
ated.
Suction machine not ▶ Turn on the suction machine.
running. ▶ Check the suction machine fuse.
Water in the return air O-rings of the MUL- ▶ Replace all O-rings of the MULTIflex coupling.
filter. TIflex coupling are
damaged.
The operating light Switch on the lamp ▶ Turn on the switch.
cannot be switched on. head is switched off.
126 / 134

9 Troubleshooting

ERGOcam/DIAGNOcam PC is switched off. ▶ Turn on the computer.
does not work. USB cable too long. ▶ Make sure that the cable length does not ex-
ceed 10 m (2 x 5 m passive with repeater).
No data transmission to No or faulty ethernet ▶ Notify network administrator.
the multimedia menu connection between
of the unit. dental unit and office
network.
Camera images shows Electrical or electro- ▶ Restart the CONEXIO PC.
images only as black/ magnetic interference
white images. by other equipment.
Camera image freezes Electrical or electro- ▶ Replace the camera in the holder and then
without the release magnetic interference take it out again.
button or foot control by other equipment.

having been triggered.
Camera image fails to
return to live image
mode.
Camera image freezes Electrical or electro- ▶ Restart the software.
without the release magnetic interference
Taking the camera out
again did not solve the
problem.
Camera image freezes Electrical or electro- ▶ Restart the treatment unit and the CONEXIO
without the release magnetic interference PC.

The monitor turns itself
off.
An acoustic signal is is- Leaking water switch ▶ Remove water from the unit body. If neces-
sued every second. recognises leaking wa- sary, have a technician fixed the leak.
ter.
127 / 134

10 Information about electromagnetic compatibility in accordance with EN60601-1-2 | 10.1 Electromagnetic Trans-
missions
10 Information about electromagnetic compatibility in
accordance with EN60601-1-2
10.1 Electromagnetic Transmissions
The treatment unitESTETICA E30 is designed for operation in an environment

as specified below. The customer or user of the ESTETICA E30 should make
sure that the device is used in an environment of the specified type.
Measurements of emitted in- Conformance Electromagnetic environment

terference -
Guidelines
HF emissions according to CISPR Group 1 The ESTETICA E30 device uses
11 HF energy for its internal func-
tions exclusively. Therefore, the
HF emission of the device is very
low and interference with adja-
cent electronic devices is unlikely.
HF emissions according to CISPR Class B The ESTETICA E30 device is suit-
11 able for use in all facilities includ-
ing residential ones, and facilities
that are directly connected to a
public power supply that also
supplies residential buildings.
Emission of harmonics according Class A The ESTETICA E30 device is suit-
to EN 61000-3-2 able for use in all facilities includ-
Emission of voltage fluctuations/ Conforms The ESTETICA E30 device is suit-
flicker according to EN 61000-3-3 able for use in all facilities includ-
10.2 Resistance to electromagnetic interference

Interference im- EN 60601 test level Compliance level Electromagnetic en-

munity tests vironment -
Guidelines
Electrostatic discharge ± 6 kV contact discharge ± 2/4/6 kV contact dis- Floors should be made of
(ESD) according to EN ± 8 kV atmospheric discharge wood or concrete or be
61000-4-2 charge ± 2/4/8 kV atmospheric fitted with ceramic tiles.
discharge If the floor is fitted with
synthetic material, the
relative humidity must
be at least 30%.
128 / 134

10 Information about electromagnetic compatibility in accordance with EN60601-1-2 | 10.3 Recommended safe
distance between portable and mobile HF telecommunications equipment and the treatment unit
Interference im- EN 60601 test level Compliance level Electromagnetic en-
munity tests vironment -
Guidelines
Fast transient electrical ± 2 kV for power lines ± 2 kV for power lines The quality of the supply
interference / bursts ac- ± 1 kV for input and out- voltage should corres-
cording to EN 61000-4-4 put lines pond to that of a typical
business or
hospital environment.
Surges according to EN ± 1 kV push-pull voltage ± 1 kV push-pull voltage The quality of the supply
61000-4-5 ± 2 kV common mode ± 2 kV common mode voltage should corres-
voltage voltage pond to that of a typical
business or
Voltage interruptions, < 5% UT < 5% UT The quality of the supply
short-term interruptions (> 95% interruption) (> 95% interruption) voltage should corres-
and fluctuations of the for ½ period for ½ period pond to that of a typical
supply voltage according 40% UT 40% UT business or hospital en-
to EN 61000-4-11 (60% interruption) (60% interruption) vironment. If the user
for 5 periods for 5 periods needs the ESTETICA E30
70% UT 70% UT to work even if the
(30% interruption) (30% interruption) power supply is interrup-
for 25 periods for 25 periods ted, we recommend sup-
< 5% UT < 5% UT plying energy to the ES-
(> 95% interruption) (> 95% interruption) TETICA E30 from an un-
for 5 s for 5 s interruptible power sup-
(250 periods) (250 periods) ply or battery.
Magnetic field at a sup- 3 A/m 3 A/m Magnetic fields at the
ply frequency (50/60 Hz) mains frequency should
according to EN correspond to typical
61000-4-8 values in a business and
NOTE: V T is the alternating mains voltage before the test level is used.
10.3 Recommended safe distance between portable and

mobile HF telecommunications equipment and the
treatment unit
The ESTETICA E30 is intended for use in an electromagnetic environment in

which the HF interference parameters are controlled. The customer or user of
the ESTETICA E30 can help prevent electromagnetic interference by maintain-
ing the minimum clearance between portable and mobile HF telecommunication
devices (transmitters) and the ESTETICA E30 depending on the output of the
communication device as indicated below.
Safe distance depending on the transmission frequency:
Rated power of the 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
transmitter in W d=1.17 P m d=1.17 P m d=2.33 P m
0.01 0.1 0.1 0.2
0.1 0.4 0.4 0.7
1 1.2 1.2 2.3
10 3.7 3.7 7.4
100 11.7 11.7 23.3
129 / 134

10 Information about electromagnetic compatibility in accordance with EN60601-1-2 | 10.4 Immunity to electro-
magnetic interference
For transmitters whose maximum rated power is not in the above table, the re-
commended safe distance d in meters (m) can be calculated using the equation
for the respective gap, where P is the maximum rated power of the transmitter
in Watts (W) according to the manufacturer's information.
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not be applicable in every case. The spread of
electromagnetic waves is absorbed and reflected by buildings, objects and
people.
10.4 Immunity to electromagnetic interference

Interference im- EN 60601 test level Compliance level Electromagnetic environment

munity tests - Guidelines
Wire-based HF inter- 3 Veff 3 Veff Handheld and mobile wireless
ference according to 150 kHz to 80 MHz 3 V/m devices should not be used at a
EN 61000-4-6 outside the ISM shorter distance from the ESTET-
Wireless HF interfer- bandsa ICA E30 including cables than the
ence according to EN 3 V/m recommended safe clearance cal-
61000-4-3 80 MHz to 2.5 GHz culated using the appropriate
equation for the emission fre-
quency.
Recommended safe distance:
d = 1.17 P
d= 1.17 P for 80 MHz to 800
MHz
d= 2.33 P for 800 MHz to 2.5
GHz
where P is the maximal nominal
power of the transmitter in watts
(W) as specified by the transmit-
ter manufacturer and d is the re-
commended safe clearance in
metres (m).
b
The field strength of stationary
wireless radio transmitters as
measured locallyc should be
lower than the conformance level
at all frequencies.
d
Interference is possible in the vi-
cinity of devices bearing the fol-
lowing icon.
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not be applicable in every case. The spread of
electromagnetic waves is absorbed and reflected by buildings, objects and
people.
a
The ISM frequency bands (for industrial, scientific, and medical applications)
between 150 kHZ and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz to
13.567 MHz; 26.957 MHz to 27.283 MHz, and 40.66 MHz to 40.70 MHz.
130 / 134

10 Information about electromagnetic compatibility in accordance with EN60601-1-2 | 10.4 Immunity to electro-
magnetic interference
b
The compliance levels in the ISM frequency bands between 150 kHz and 80
MHz and in the frequency range from 80 MHz to 2.5 GHz are intended to re-
duce the probability of mobile/handheld communications facilities causing inter-
ference when they are inadvertently introduced into the patient area. For this
reason, the additional factor of 10/3 is applied in the calculation of the recom-
mended safe clearances in these ranges of frequencies.
c
The field strength of stationary transmitters, such as, e.g. base stations of mo-
bile phones and mobile terrestrial radio devices, amateur radio stations, AM and
FM radio and television transmitters, cannot be determined exactly based on
theoretical considerations. A site study should be considered to determine the
electromagnetic environment in terms of stationary transmitters. If the meas-
ured field strength at the site, at which the ESTETICA E30 is used, exceeds the
compliance levels shown above, the ESTETICA E30 should be monitored to
demonstrate proper function. If any uncommon performance characteristics are
observed, additional measures may be required, such as, e.g., changing the
orientation or using a different location for the ESTETICA E30.
d
In the frequency range of 150 kHz to 80 MHz, the field strength should be less
than 3V eff V/m.
131 / 134

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Instructions for use

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3 Product description ............................................................................................................ 18

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4.3 Adjusting the dental chair ............................................................................................... 44

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4.14Using the camera........................................................................................................... 98

5 Preparation methods DIN EN ISO 17664 ........................................................................... 99

6 Accessories and kits ...........................................................................................................

7 Safety checks - testing instructions ...................................................................................

8 Appendix - Additional measuring sites...............................................................................

10Information about electromagnetic compatibility in accordance with EN60601-1-2........

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1.1 User guide

Important information for users and technicians

CE mark according to Medical Devices Directive EC 93/42

1.1.3 Target group

This document is for dentists and dental office staff.

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1.3 Terms and conditions of warranty

1.4 Transportation and storage

1.4.1 Currently valid packaging regulations

Dispose of and recycle the sales packaging appropriately in accordance with

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1.4.2 Damage in transit

If the packaging is visibly damaged on delivery, please proceed as follows:

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1.4.3 Information on the packaging: Storage and

Transport upright with the arrows pointing upwards!

Fragile - protect against impact!

Protect from moisture!

Permissible stacking load

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2.1 Description of safety instructions

2.1.1 Warning symbol

2.1.3 Description of hazard levels

2.2 Purpose – Proper use

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It is a responsibility of the user:

In Germany, operators, equipment managers and users are obliged to operate

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Information about electromagnetic compatibility

Disposal of electronic and electrical devices

For final disposal:

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To return an electrical device, you need to proceed as follows:

Designated use and target group

Accessories Use Name Material number

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Accessories Use Name Material number

2.3 Safety instructions

2.3.1 General information

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3.1 Treatment unit versions

3.1.1 KaVo ESTETICA E30 S