DKL CHAIRS D2-SAE User manual

D2-SAE
Form no. GEN-D2SAE
Rev. 03 / 21.01.2022
Subject to change without
notice.
Manufacturer:
DKL CHAIRS GmbH
An der Ziegelei 3
D-37124 Rosdorf
[phone]
[email protected]
www.dkl.de
Operating Instructions

2
Symbols in the Operating Instructions 3
Symbols inside the Unit 4
Introduction 5
Electromagnetic Compatibility (EMC) 6
Safety Instructions - General 7
Safety Notes – Cuspidor with Assistant’s Device 8
Technical Specifi cations 9
Media Requirements 10
Product Description 13
Moving the Treatment Chair 15
Putting the Treatment Unit into Operation 17
Function Syringe 18
LED.light Operating Lamp 20
LED.light EVA Operating Lamp 22
Traytablett 24
Cuspidor 25
Suction System 26
Cleaning and Disinfection of the Suction Handpieces 28
Cleaning and Disinfection of the Suction System 30
Cleaning and Disinfection of the Surfaces 32
Cleaning and Disinfection of the Instrument Holders 35
Bottle Care System 36
Flushing Function with the Bottle Care System 37
Intensive Flushing with the Bottle Care System 37
Water Separation Unit (WSU) 38
Flushing Function with the Water Separation Unit 40
Intensive Flushing with the Water Separation Unit 40
Filling DK-DOX 150 into the Water Separation Unit 41
Maintenance and Inspection 42
Safety Inspections 42
Waste Disposal 43
EMC - Manufacturer‘s Declaration 44
Annex
> Operating Instructions DÜRR Dental Spittoon valve 3
> Operating Instructions DÜRR Dental CAS 1 Combi-Separator
> Operating Instructions DÜRR Dental CS 1 Combi-Sepamatic
> INSTRUCTION MANUAL FARO DENTAL SYRINGE SYR3
> Use Manual Luzzani Syringe Minilight
> USER MANUAL FARO EVA
Contents

3
Symbols in the Operating Instructions
WARNING!
(risk of injury)
General explanations,
without risk to
persons or objects
Thermodisinfectable Sterilisable up to the
specifi ed temperature Call customer service!
CAUTION!
(to prevent
damage occurring)
Symbols on the unit
Observe the operating
instructions!
ON / OFF Do not dispose of with
household waste.
CE-marking with iden-
tifi cation number of the
notifi ed body
Type B application part
Manufacturing date Model (designation) Serial number
VElectrical voltage VA
AC
AHz
Electrical power con-
sumption
Current intensity Frequency of alter-
nating current
Electrical fuse
Alternating current
Foot controller
Manufacturer Medical device UDI - Product
Identifi cation

4
Symbols inside the Unit
Earth conductor
connection - Protective
earth
Functional
earth
Symbols on the packaging
Transport upright; top
Permissible temperature range
Air humidity, limitation
Protect from moisture!
Do not stack!
Fragile
N
Connection point for neutral
conductor

5
Introduction
For your safety and the safety of your patients
These operating instructions are intended to explain how to use your product. However,
we must also warn of possible dangerous situations. Your safety, the safety of your team
and, of course, the safety of your patients are very important to us.
Please observe the safety instructions!
Intended purpose
This treatment unit is used for the diagnosis and therapy of children and adults in the fi eld of dentistry.
Improper use can damage the treatment unit and thus pose risks and
hazards to the patient, user and third parties.
Qualifi cation of the user
The DKL treatment unit may only be used after medically, professionally and practically trained
personnel have been instructed. The development and design of the treatment unit were geared
towards the target group of dentists, dental hygienists, qualifi ed dental employees (prophylaxis) and
dental assistants.
Production according to EU directive
The medical device complies with the provisions of Directive 93/42/EEC.
0123
Responsibility of the manufacturer
The manufacturer can only be held responsible for the impact on the safety,
reliability and performance of the treatment unit if the following instructions
are observed:
> The dental unit must be used in accordance with these operating
instructions.
> If assembly, additions, new settings, changes or repair work is carried out
by DKL or trained technicians authorised by DKL or personnel of authorized
dealers trained by DKL.
> The electrical installation of the room must comply with the regulations of
the IEC 60364-7-710 standard („Erection of electrical installations in rooms
used for medical purposes“) or comply with the regulations applicable in
your country.
> The recommended annual maintenance is carried out and any repair work
in this context meets the requirements of EN 62353.
„Repeat tests and pre-commissioning tests of medical electrical equipment
and systems – general regulations“are fully complied with.
> The national legal regulations are observed when using the device, in
particular the applicable health and safety regulations and accident
prevention measures.

6
Electromagnetic Compatibility (EMC)
Medical electrical equipment is subject to special precautions with regard to EMC and
must be installed and commissioned in accordance with the EMC instructions. DKL
guarantees that the dental unit complies with the EMC guidelines only if original DKL
accessories and spare parts are used. The use of accessories and spare parts not
approved by DKL may lead to an increased emission of electromagnetic interference or
to a reduced resistance to electromagnetic interference.
The EMC manufacturer declaration can be found on page 44.
HF communication equipment
Do not use portable and mobile HF-communication equipment (such as mobile
telephones) during operation. These can aff ect medical electrical devices.
Risks due to electromagnetic fi elds
The functionality of implantable systems, such as cardiac pacemakers and
implantable cardioverter defi brillators (ICD), can be infl uenced by electric, magnetic and
electromagnetic fi elds.
> Before using the product, ask the patient and user about implanted systems and
check the use.
> Perform a risk-benefi t analysis.
> Do not place the product near implanted systems.
> Do not place the instruments on the patient‘s body.
> Take appropriate emergency precautions and respond immediately to health changes.
> Symptoms such as increased heart rate, irregular pulse, and dizziness may be signs
of problems with a pacemaker or ICD.

7
Safety Instructions - General
> Before being put into initial operation, the treatment unit must be kept at room
temperature for 24 hours.
> Before each application, check the treatment unit and the instruments with cables for
damage and loose parts.
> Do not operate the treatment unit if it is damaged.
> Check the set parameters each time you restart the unit.
> Carry out a test run before each application.
> The application and timely shutdown of the system is the user’s responsibility.
> Make sure that in the event of a device or instrument failure, the treatment can be
completed safely.
> Use only original DKL fuses.
> Never touch the patient and the electrical connection at the treatment unit at the same
time.
> Do not lean on the doctor‘s device, the assistant‘s device, the tray or the operating
lamp.
> When moving the treatment chair, the doctor‘s device, the assistant‘s device, the tray or
the operating lamp, pay attention to the patient and the practice personnel.
> Always switch off the treatment unit before leaving the practice.
Hygiene and care before using the device
> Clean and disinfect the device immediately before or after each treatment!
> Wear protective clothing.
The treatment unit is classifi ed as an „ordinary device“ (closed device without protection
against water ingress).
The treatment unit is not suitable for use in an explosive atmosphere or in explosive
mixtures of anaesthetics with oxygen or nitrous oxide.
The treatment unit is not suitable for use in rooms with an oxygen enriched atmosphere.
Safety notes – Patient chair
> Not suitable for patients who cannot remain in a resting position due to mental or
physical disabilities.
> The patient‘s arms and legs must rest on the upholstered parts of the chair.
> Do not exceed the maximum patient weight of 150 kg.
> Do not sit on the head or foot rest of the horizontally aligned patient chair.
> Position changes must always be carried out under the surveillance of the person
giving treatment.
> Watch patients while moving the treatment chair.
> Make sure that there are no objects under the treatment chair.
Observe your country-specifi c guidelines, standards and specifi cations for
cleaning, disinfection and sterilisation.

8
> Do not exceed the maximum permissible load of 2 kg on the assistant’s
device
Safety Notes – Cuspidor with Assistant’s Device
>Before putting the device into initial operation and after downtimes (weekends,
(public) holidays etc.), fl ush the water lines intensively.
> Flush all instrument connections for 2 minutes before starting work.
> Press the cup fi ll button several times before starting work.
> Rinse used instruments for 20 seconds after each treatment.
Risk of injury or infection caused by instruments that are not in use:
The arrangement of the instruments may cause injury or infection to the hand and
forearm when accessing the tray or the display.
Therefore, when accessing the tray or the display, pay attention to the arrangement of
the instruments.
Highly immunosuppressed patients or patients with specifi c lung diseases should not
get into contact with the water of the treatment unit.
It is recommended to use sterile solutions.

Weight
D2-SAE max. 225 kg
9
Transport and storage conditions
Ambient temperature 30 to +70 °C
Relative humidity 10 to 80 %
Atmospheric pressure 500 hPA to 1060 hPa
Operating conditions
Quality and load-bearing capacity of the fl oor The fl oor must be level and horizontal according to
EN18202. Unevenness of the fl oor along the total length
of the chair base up to 2 mm is acceptable. The mini-
mum load-bearing capacity of the fl oor must be 0.5 N/
cm2 (equivalent to approx. 500 kg/m2).
Ambient temperature 10 to 35 °C
Relative humidity 15 to 80 %
Atmospheric pressure 700 hPA to 1060 hPa
Installation site ≤ 3,000 m above sea level
The treatment unit is not suitable for operation in
hazardous areas.
Permanently connected device. In order to avoid the risk of electric shock, this device may only be
connected to a power supply with an earth conductor.
Technical Specifi cations
The motors of the treatment unit are designed for intermittent operation in accordance with the dental
treatment method.
Driving motors for patient chair and backrest: duty cycle (max. 25 s „ON“ / 400 s „OFF“)
Supply voltage 230V AC
Nominal voltage max. 3 A
Frequency 50/60 Hz
Fuse T 6.3 A H 250 V primary/ time-delay
Maximum power consumption 625 VA
Device class according to the 93/42/EEC Directive IIa
Protection class Device of protection class I
Contamination level 2
Over voltage category II
Power cable 3x1,5 mm2
Suction control lines to the suction device 5x1,5 mm2
Potential equalisation 1x 4 mm2
Relay control line optional special function 3x1,5 mm2
Free end electrical cables above fl oor 500 mm
Fuse for domestic installation Circuit breaker: 16 A medium-lag
Recommendation: circuit breaker type C
Degree of protection against ingress of water Ordinary device (without protection against water ingress)

10
Media water
Water hardness 1.5 to 2.14 mmol/l
ph-value 6,5 to 8,5
Water fi ltration on site ≤ 100 µm
Water infl ow Pipe 10x1mm, angle valve outlet 3/8“
Water connection above fl oor min. 40 mm, max. 60 mm
Water inlet pressure 2.0 to max. 6.0 bars
Water quality Cold water in accordance with local and national drinking
water regulations.
Minimum fl ow rate 3 l/min
Media air
Air inlet pressure max. 7 bars
Air consumption 80 Nl/min
On-site air fi ltration ≤ 100 particles size 1 - 5 μm referred to one m3 of air
Oil content ≤ 0.5mg/m3,oil-free compressors; the compressor must suck
in hygienically perfect air.
Humidity Pressure dew point ≤ -20 °C at atmospheric pressure
Compressed air supply Pipe 10x1 mm, angle valve outlet 3/8“
Air connection above the fl oor min. 40 mm, max. 60 mm
Media Requirements
• Perform the installation according to the national installation requirements (e.g. EN 1717).
• For the reduction of microorganisms in the water supply pipe, please observe the following when laying this pipe to the
treatment unit:
- Avoid long stub lines to the treatment unit.
- Select the installation in such a way that other essential consumers (e.g. washbasin) are as far as possible
behind the connection of the treatment unit can be supplied from the same pipe.
- Avoid laying the hot water supply pipes in parallel.
• Recommendation: For the water supply of the treatment unit, install an angle valve with 2 outlets and 2 stop cocks. The
second outlet allows easy sampling of water for microbiological analysis.
Connection to the public drinking water supply
The treatment unit with a water separation unit complies with the requirements of EN 1717 (free outlet with separation
distance ≥ 20 mm) and the DVGW (German Technical and Scientifi c Association for Gas and Water). It is intrinsically safe
in accordance with worksheet W540 and therefore also meets the requirements of W270 and KTW (guideline for hygienic
assessment of organic materials in contact with drinking water).
When the treatment unit is equipped with a cuspidor, the bowl rinser ensures the free outlet with a separation distance ≥
20 mm.
Clean air and water pipes before installing the unit.
Chips and other foreign substances could be fl ushed or blown into the treatment unit.
Metal chips can interfere with the function of pneumatic components. Filters are clogged by foreign substances.
- When assembling, make sure that there are no chips or other foreign substances in the pipes.
- Flush the water pipes.
- Blow out the air ducts.
- Make sure that no further foreign substances get into the pipes and ducts after rinsing or blowing out.
Before the treatment unit is installed, the microbiologically perfect water quality of the domestic water supply
should be ensured and documented in the form of a microbial count.
Sampling and microbial count should be carried out by a competent laboratory.

11
Requirements for the suction system
Vacuum at supply connection min. 0,12 bar, max. 0,18 bar
Minimum suction power at supply connection ≥750Nl/min
Suction system Type 1: high fl ow rate
wet or dry suction
Diameter of suction handpieces: small suction handpiece: 6 mm
large suction handpiece: 16 mm
Suction pipe DN40 HT-PP (polypropylene, inside diameter approx. 36.5 mm)
Water drain DN40 HT-PP (polypropylene, inside diameter approx. 36.5 mm)
Gradient Min. 10 mm per metre
Wastewater volume 3 l/min
Filter in the treatment unit maintenance interval Article number
Particle fi lter water inlet 50 μm Replace annually 210623-WBG
Particle fi lter compressed air inlet 50 μm Replace annually 210623-LBG
Solid particle fi lter for the suction
system
Mesh size 1 mm In case of damage,
replace at least annually.
514100
1Air: pipe min. 10x1 mm, angle valve outlet 3/8“
2Water drain DN40 HT-PP
3Suction line DN40 HT-PP
4Power cable 3x1.5 mm2
4Equipotential bonding 1x 4 mm2
4Control line to suction device 5x1.5 mm2
5Water: pipe min. 10x1 mm, angle valve outlet 3/8“ (2
outlets with 2 stopcocks)
Requirements for Supply Connections
Typical pressure in the suction system
Spray mist suction Vacuum / mbar
90 NL/min 22,6
150 NL/min 38,2
200 NL/min 60,0
250 NL/min 88,8
300 NL/min 124
316 NL/min 137
Saliva ejector
50 NL/min 100,0
55 NL/min 120,0
60 NL/min 135,2
67 NL/min 162
80 NL/min 200

12
Dimensions in Millimetres
Treatment chair:
lowest position 395 mm
highest position 730 mm

13
1Treatment chair,seat
2Treatment chair, back rest
3Treatment chair, double-jointed head rest
4Treatment chair, joystick
5Treatment chair, arm rest
6Assistant’s device
7Cuspidor
8Operating lamp LED.light
Tray
1
6
2
3
4
5
8
7
9
9
Product Description
Identifi cation label

14
Product Description
1Spray mist suction
2Saliva ejector
3Syringe
1
2
3
Marking Type of holder
GS Spray mist suction
KS Saliva ejector
S Syringe
Connecting the instrument hoses and suction tubes.
The instrument hoses can be connected or disconnected via a plug connection under the
assistant’s device. Depending on the equipment of the model, the assistant’s device is
equipped with the following instruments (from the left): the syringe, Spray mist suction
and fi nally the Saliva ejector. The instrument holders are marked on the back. Do not
connect the tubes crosswise.

15
Moving the Treatment Chair
Move the joystick downwards
>Treatment chair moves downwards.
Move the joystick upwards
>Treatment chair moves upwards.
Move the joystick to the left
>Back rest tilts backwards.
Move the joystick to the right
>Back rest moves to an upright position.
Tap the JoystickTwice
>Treatment chair moves to the entry / exit position.
Tap the joystick twice downwards
>Treatment chair moves to the treatment positionp2.
Tap the JoystickTwice to the Left
>Treatment chair moves to the rinsing position and back to the last position when tapping twice again.
Tap theJoystickTwice to the Right
>Treatment chair moves to the treatment position p1.
Press “p0“
>Treatment chair moves to the position for getting on/off .
Press “p1“
>Treatment chair moves to treatment position p1.
Press “p2“
>Treatment chair moves to treatment position p2.
Press “p3“
>Treatment chair moves to treatment position p3.
Briefl y press “lp“
>Treatment chair moves to the rinsing position and after
renewed pressing back to the “last position”.
For programming the keys, move to the desired programme position manually and then keep the
respective programme key pressed for about 3 seconds until you hear a signal tone. Now you
have successfully saved your individual treatment position.
Saving programme key P0-P3
Press the ”lp“ key to move the chair to the rinsing position. By pressing the key “Ip” once again,
the chair moves back to the previous programme position or to the manually set position. In
order to programme the chair, move it manually to the desired rinsing position and then keep the
key “Ip” pressed for about 3 seconds until you hear a signal tone. Now you have successfully
saved your rinsing position.
Saving programme key LP
Emergency-Stop System
Briefl y tap the joystick or any programme key at the back rest to stop the active programme
immediately. For this purpose, you can also press the start button for the instruments at the foot
controller.
Programme keys at the back rest
Joystick at the chair base
Programme run
Press the programme keys “0” and “lp” simultaneously for about 3 seconds until you hear a
signaltone. The treatment chair then moves the seat and the back rest into the lowest position.
The motion sequence has been reset now.
Joystick

16
Moving theTreatment Chair
To facilitate getting on or off the chair, the right
arm rest (optional) can be swivelled by 90°.
Manually Extractable Double-Jointed
Head Rest
Pull the release lever up to freely adjust the doub-
le-jointed head rest. Press the lever down to fi x
the position of the double-jointed head rest. The
release lever must always be pulled up completely
to move the head rest.
When moving the back rest, there is a risk of injury
or crush. The patient’s hands and arms must
always rest on the chair upholstery
You can fi nd an application fi lm at www.youtube DKL Germany.
Video: DKL CHAIRS D2 SERIES FUNKTIONEN UPHOLSTERY POSITIONS
LINK: https://youtu.be/o307-rWGp5A

17
1
2
T 6,3A H 250V
The treatment unit is equipped with a power switch 1 on the chair base. The
power switch connects the treatment unit with the power supply. In the event of
longer downtimes, the treatment unit should be disconnected from the
power supply. The treatment unit contains a device fuse 2. Switch on the
treatment unit at the power switch.The power switch lights up green.
Putting the Unit into Operation
Before putting your treatment unit into initial operation, an intensive fl ushing
must be carried out [→page 37 or page 40].
Putting the Treatment Unit into Operation
Activating /
Deactivating the
Treatment Unit

18
Function FARO Syringe SYR3
To remove the sleeve, press button
„A“.
Pull out the sleeve in the direction of
the arrow.
To remove the nozzle, screw off
ring „B“ and pull out the
nozzle in the direction of the
arrow.
Press the green button to release water.
Press the light blue button to release air.
Press both buttons simultaneously to release spray.
Before reassembling the syringe, lubricate the 2 seals on the inner body and the metal tube of
the nozzle with Vaseline grease.
Cleaning the syringe
Clean the sleeve and nozzle under running water or using alcohol-based solutions.
Sterilisation
- Remove the sleeve including the nozzle from the syringe body.
- Clean the sleeve and the nozzle.
- Sterilize the sleeve including the nozzle in the autoclave.
Cleaning the spouts
If the nozzle from which the water and the air come is clogged, clean it with the supplied
probe.
Sleeve and spout sterilizable
See also operating instructions of the FARO
company for their SYR3 dental syringe!

19
Function Luzzani Syringe Minilight
See also operating instructions of the Luzzani company for their Minilight
syringe!
Symbol: Air
Symbol: Water Handpiece
Nozzle
Nozzle retainer Water Air
After each use on a patient, the handpiece and tip of the syringe MUST be cleaned and
sterilised to guarantee maximum hygiene.
To blow water into the operating
fi eld, just press the left button on
the handpiece, symbol: water.To
insuffl ate air into the operating
fi eld, just press the right button
on the handpiece, symbol: air.
To blow a combination of air and
water (spray), press both buttons
on the handpiece at the same
time.
Unscrew the
nozzle retainer.
Withdraw the
nozzle retainer.
Withdraw the
nozzle. Press the pawl to release
the handpiece.
Withdraw handpiece.
You will fi nd the
sterilisation procedure
on the handpiece.

20
LED.light Operating Lamp
When swivelling and moving the operating lamp, always make sure that no
objects or persons are in the swivelling range of the arm system. Otherwise,
personal injury or property damage may occur. In order to move the operating
lamp only touch its handles!
Switching the Lamp on and off
The operating lamp is switched on or off by
moving the microswitch to the left / right.
The intensity of the operating lamp can be
adjusted from 8,000 to 50,000 LUX. Press and
hold the switch to the left or right to adjust the
light intensity.
If the switch is pressed backwards or forwards,
the operating lamp dims to 8,000 LUX. When
the switch is pressed again, the light intensity
set last is selected.
Optical Properties:
Light fi eld : 170 mm x 85 mm
Lux : 8,000 to 50,000 lux at a distance of 700 mm
Colour temperature : 5,000 K
CRI (colour rendering index) : > 85
Mirror
Loosen the plastic cover at the front of the
protective cap by lightly pressing on its upper
end. On the back of the cover there is a mirror.
Attach the mirror to the plastic cover.
Refl ectors
Switch
Handles
You can fi nd an application fi lm at www.youtube DKL Germany.
Video: DKL CHAIRS L2-D2 SERIES FUNCTIONS LED.LIGHT OPERATING LAMP
LINK: https://youtu.be/OXSchFNIFXM