CS 1 Combi-Sepamatic 24 V AC

EN

Installation and operating instructions

2103V007

9000-606-39/30

*9000-606-39/30*
 Contents

Contents
6.2 Hose materials . . . . . . . . . . . . . 13
EN
6.3 Installation and routeing of hoses
and pipes . . . . . . . . . . . . . . . . . 13
Important information 6.4 Information about electrical con-
1 About this document . . . . . . . . . . . . . 2 nections . . . . . . . . . . . . . . . . . . 13
1.1 Warnings and symbols . . . . . . . 2 6.5 Information about connecting
1.2 Copyright information . . . . . . . . 3 cables . . . . . . . . . . . . . . . . . . . . 13
2 Safety . . . . . . . . . . . . . . . . . . . . . . . . . 3 7 Installation . . . . . . . . . . . . . . . . . . . . . . 14
2.1 Intended purpose . . . . . . . . . . . 3 7.1 Installation of the CS 1 in treat-
2.2 Intended use . . . . . . . . . . . . . . . 3 ment units . . . . . . . . . . . . . . . . . 14
2.3 Improper use . . . . . . . . . . . . . . . 3 7.2 Power supply . . . . . . . . . . . . . . 15
2.4 General safety information . . . . . 4 7.3 Electrical connections, controller . 15
2.5 Combining devices safely . . . . . 4 7.4 Electrical connections . . . . . . . . 15
2.6 Specialist personnel . . . . . . . . . 4 8 Commissioning . . . . . . . . . . . . . . . . . . 16
2.7 Notification requirement of seri-
ous incidents . . . . . . . . . . . . . . . 4
2.8 Electrical safety . . . . . . . . . . . . . 4
2.9 Only use original parts . . . . . . . . 5 Usage
2.10 Transport . . . . . . . . . . . . . . . . . . 5 9 Disinfection and cleaning . . . . . . . . . . 17
2.11 Disposal . . . . . . . . . . . . . . . . . . 5 9.1 After every treatment . . . . . . . . . 17
9.2 Daily after the end of treatment . 17
9.3 Once or twice a week before the
midday break . . . . . . . . . . . . . . 17
Product description
10 Maintenance . . . . . . . . . . . . . . . . . . . . 18
3 Overview . . . . . . . . . . . . . . . . . . . . . . . 6
3.1 Scope of delivery . . . . . . . . . . . . 6
3.2 Optional items . . . . . . . . . . . . . . 6
3.3 Consumables . . . . . . . . . . . . . . 6 Troubleshooting
3.4 Wear parts and replacement
11 Tips for operators and service techni-
parts . . . . . . . . . . . . . . . . . . . . . 6
cians . . . . . . . . . . . . . . . . . . . . . . . . . . 19
4 Technical data . . . . . . . . . . . . . . . . . . . 7 11.1 Replacing the fuse . . . . . . . . . . . 20
4.1 Type plate . . . . . . . . . . . . . . . . . 11
12 Transporting the unit . . . . . . . . . . . . . 20
4.2 Evaluation of conformity . . . . . . 11
12.1 Close the CS 1 . . . . . . . . . . . . . 20
5 Operation . . . . . . . . . . . . . . . . . . . . . . 12
5.1 Separation . . . . . . . . . . . . . . . . . 12
5.2 Station selection valve . . . . . . . . 12
Appendix
13 Handover record . . . . . . . . . . . . . . . . . 21

Assembly
6 Requirements . . . . . . . . . . . . . . . . . . . 13
6.1 Setup options . . . . . . . . . . . . . . 13

9000-606-39/30 2103V007 1
 Important information

The signal word differentiates between four levels

Important information of danger:
– DANGER
Immediate danger of severe injury or death
EN 1 About this document – WARNING
These installation and operating instructions rep- Possible danger of severe injury or death
resent part of the unit. – CAUTION
Risk of minor injuries
If the instructions and information in these
installation and operating instructions are – NOTICE
not followed, Dürr Dental will not be able Risk of extensive material/property damage
to offer any warranty or assume any liabil- Other symbols
ity for the safe operation and the safe
These symbols are used in the document and on
functioning of the unit.
or in the unit:
The German version of the installation and oper- Note, e.g. specific instructions regarding
ating instructions is the original manual. All other efficient and cost-effective use of the unit.
languages are translation of the original manual.
These installation and operating instructions
apply to: Refer to Operating Instructions.
CS 1
7117-100-70; 7117-100-70E; 7117-100-74;
7117-100-74E; 7117-100-76; 7117-100-77; Wear protective gloves.
7117-100-78; 7117-100-79; 7117-100-80;
7117-100-80E
Disconnect all power from the unit.
1.1 Warnings and symbols
Warnings
The warnings in this document are intended to Hose manifold connection
draw your attention to possible injury to persons
or damage to machinery.
The following warning symbols are used: Suction unit connection

General warning symbol

Drain connection

Biohazard warning
Order number
The warnings are structured as follows:
Serial number
SIGNAL WORD
Description of the type and source of
Medical device
danger
Here you will find the possible conse- Health Industry Bar Code (HIBC)
quences of ignoring the warning
❯ Follow these measures to avoid the CE labelling
danger.

Protection class II

Manufacturer

2 9000-606-39/30 2103V007
 Important information

1.2 Copyright information 2 Safety

All circuits, processes, names, software pro- Dürr Dental has designed and constructed this
grams and units mentioned in this document are unit so that when used properly and for the inten-
protected by copyright. ded purpose it does not pose any danger to
The Installation and Operating Instructions must people or property. EN
not be copied or reprinted, neither in full nor in Despite this, the following residual risks can
part, without written authorisation from Dürr Den- remain:
tal. – Personal injury due to incorrect use/misuse
– Personal injury due to mechanical effects
– Personal injury due to electric shock
– Personal injury due to radiation
– Personal injury due to fire
– Personal injury due to thermal effects on skin
– Personal injury due to lack of hygiene, e.g.
infection

2.1 Intended purpose

The separation system is designed for the contin-
uous separation of air and liquids in the suction
flow of dental treatment units.

2.2 Intended use

The separation system is intended for installation
in the suction line of a dry suction system after
the manifold.
Service, maintenance, recurring tests and clean-
ing must be performed in accordance with the
manufacturer's information.
The permissible flow rate must be observed.
A rinsing unit is required for surgical procedures
and for procedures using prophy powders.

2.3 Improper use

Any use of this appliance / these appliances
above and beyond that described in the Installa-
tion and Operating Instructions is deemed to be
incorrect usage. The manufacturer cannot be
held liable for any damage resulting from incor-
rect usage. The operator will be held liable and
bears all risks.
This includes:

9000-606-39/30 2103V007 3
 Important information

– Use for separation of dust, sludge, plaster or 2.6 Specialist personnel

similar.
– Use in conjunction with flammable or explosive Operation
mixtures. Unit operating personnel must ensure safe and
– Installation in a manner that does not comply correct handling based on their training and
EN knowledge.
with the installation instructions, in particular
installation in rooms containing a potentially ❯ Instruct or have every user instructed in han-
explosive atmosphere. dling the unit.
– Cleaning and disinfection with agents contain- Installation and repairs
ing sodium hypochlorite or potassium hypo- ❯ Installation, readjustments, alterations,
chlorite. upgrades and repairs must be carried out by
Dürr Dental or by qualified personnel specifi-
2.4 General safety information cally approved and authorized by Dürr Dental.
❯ Always comply with the specifications of all
guidelines, laws, and other rules and regula- 2.7 Notification requirement of
tions applicable at the site of operation for the serious incidents
operation of this unit.
The operator/patient is required to report any
❯ Check the function and condition of the unit serious incident that occurs in connection with
prior to every use. the device to the manufacturer and to the com-
❯ Do not convert or modify the unit. petent authority of the Member State in which
❯ Comply with the specifications of the Installa- the operator and/or patient is established/resi-
tion and Operating Instructions. dent.
❯ The Installation and Operating Instructions
must be accessible to all operators of the unit 2.8 Electrical safety
at all times. ❯ Comply with all the relevant electrical safety
regulations when working on the unit.
2.5 Combining devices safely ❯ Never touch the patient and unshielded plug
Take care when connecting units together or to connections on the device at the same time.
parts of other systems as there is always an ele- ❯ Replace any damaged cables or plugs immedi-
ment of risk (e.g. due to leakage currents). ately.
❯ Only connect units when there can be no
question of danger to operator or to patient. Observe the EMC rules concerning medical
❯ Only connect units when it is safe to do so and devices
when there is no risk of damage or harm to the ❯ The unit is intended for use in professional
surroundings. healthcare facilities (in accordance with IEC
❯ If it is not 100% clear from the unit data sheet 60601-1-2). If the appliance is operated in
that such connections can be safely made or if another environment, potential effects on elec-
you are in any doubt, always get a suitably tromagnetic compatibility must be taken into
qualified person (e.g. the manufacturer) to ver- account.
ify that the setup is safe. ❯ Do not operate the unit in the vicinity of HF sur-
Where applicable, the requirements for medical gical instruments or MRT equipment.
products have been taken into account in the ❯ Keep a minimum distance of 30 cm between
development and construction of the device. As the unit and mobile radio devices.
a result, this device is suitable for installation ❯ Note that cable lengths and cable extensions
within medical supply equipment. have effects on electromagnetic compatibility.
❯ Where this device is integrated in other medical
supply equipment, the requirements of Euro-
pean Union Medical Device Regula-
tion 2017/745 and the relevant standards must
be observed.

4 9000-606-39/30 2103V007
 Important information

2.10 Transport
NOTICE
The original packaging provides optimum protec-
Negative effects on the EMC due to tion for the unit during transport.
non-authorised accessories If required, original packaging for the unit can be
❯ Use only Dürr Dental parts or accesso- ordered from Dürr Dental. EN
ries specifically approved by Dürr Den-
Dürr Dental will not accept any responsi-
tal.
bility or liability for damage occurring dur-
❯ Using any other accessories may result
ing transport due to the use of incorrect
in increased electromagnetic interfer-
packaging, even where the unit is still
ence emissions or the unit having
under guarantee.
reduced electromagnetic immunity,
leading to an erroneous operation ❯ Only transport the unit in its original packaging.
mode. ❯ Keep the packing materials out of the reach of
children.
NOTICE
Erroneous operation mode due to use
2.11 Disposal
immediately adjacent to other devices The unit may be contaminated. Instruct
or with other stacked devices the company disposing of the waste to
❯ Do not stack the unit together with take the relevant safety precautions.
other devices. ❯ Decontaminate potentially contaminated parts
❯ If this is unavoidable, the unit and other before disposing of them.
devices should be monitored in order
❯ Uncontaminated parts (e.g. electronics, plastic
to ensure that they are working cor-
and metal parts etc.) should be disposed of in
rectly.
accordance with the local waste disposal regu-
lations.
2.9 Only use original parts ❯ If you have any questions about the correct
❯ Only use accessories and optional items that disposal of parts, please contact your dental
have been recommended or specifically trade supplier.
approved by Dürr Dental. An overview of the waste keys for Dürr
❯ Only use only original wear parts and replace- Dental products can be found in the
ment parts. download area at:
DÜRR MEDICAL accepts no liability for www.duerrdental.com
damages or injury resulting from the use Document no.: P007100155
of non-approved accessories or optional
accessories, or from the use of non-origi-
nal wear parts or replacement parts.
The use of non-approved accessories,
optional accessories or non-genuine wear
parts / replacement parts (e.g. mains
cables) can have a negative effect in
terms of electrical safety and EMC.

9000-606-39/30 2103V007 5
 Product description

3.2 Optional items

Product description The following optional items can be used with the
device:
Various installation sets are available on request
EN 3 Overview Safety transformer 24 V, 100 VA . . 9000-150-46
Station selection valve for CAS 1 /
CS 1 . . . . . . . . . . . . . . . . . . . . . . . 7560-500-80
Station selection valve . . . . . . . . . . 7560-500-60
Vario rinsing unit . . . . . . . . . . . . . . 7100-260-51
Rinsing unit II . . . . . . . . . . . . . . . . 7100-250-50
OroCup care system . . . . . . . . . . . 0780-350-00

3.3 Consumables
The following materials are consumed during
operation of the device and must be ordered
separately:
DürrConnect protective strainer,
5 pieces . . . . . . . . . . . . . . . . . . . 0700-700-18E
Orotol plus (2.5 litre bottle) . . . . . CDS110P6150
MD 550 spittoon bowl cleaner
(750 ml bottle) . . . . . . . . . . . . . . CCS550C4500
MD 555 cleaner (2.5 litre bottle) . CCS555C6150

1 3.4 Wear parts and replacement

1 CS 1 Combi-Sepamatic parts
The following working parts need to be changed
3.1 Scope of delivery at regular intervals (refer to the "Maintenance"
section):
The scope of delivery can vary slightly
– Protective strainer
depending on the version.
– Rubber grommets
The following items are included in the scope of – O-rings
delivery: Replacement parts set (3 years) . . 7117-980-33
CS 1 . . . . . . . . . . . . . . . . . . . . . . . 7117-100-7x O-ring set for CS 1 . . . . . . . . . . . . 7117-980-22
or
Information about replacement parts is
CS 1 . . . . . . . . . . . . . . . . . . . . . . . 7117-100-8x
available from the portal for authorised
– Combi-Sepamatic specialist dealers at:
– or Combi-Sepamatic inc. station selection www.duerrdental.net
valve
– Rinsing unit
– Installation and Operating Instructions

6 9000-606-39/30 2103V007
 Product description

4 Technical data
Electrical data – centrifuge motor 7117-100-7x
7117-100-8x
Rated voltage V 24 AC EN
Frequency Hz 50 / 60
Rated power VA 70
Nominal current in standby mA 80
Signal input from the hose manifold V 24 AC
Hz 50/60
Signal output V 24 DC
mA 300

Media
Fluid volume
min. l/min ³ 0.1
max. l/min £ 2.0
Air flow volume l/min £ 350
Flow rate high
The suction system must be suitable for a high flow rate in accordance with EN ISO 10637.
Max. pressure hPa/mbar -160

General data
Operating mode % 100 (S1)
Type of protection IP 20
Protection class II
Noise level, approx.* dB(A) 45
Dimensions (H x W x D) cm 15 x 16 x 12
Weight, approx. kg 1.4

* in accordance with EN ISO 3746

Ambient conditions during storage and transport

Temperature °C -10 to +60
Relative humidity % < 95

Ambient conditions during operation

Temperature °C +10 to +40
Relative humidity % < 70

Classification
Medical Device Class I

9000-606-39/30 2103V007 7
 Product description

Electromagnetic compatibility (EMC)

Interference emission measurements
High-frequency emissions in accordance with CISPR 11 Group 1
Class B
EN Interference voltage at the power supply connection
Compliant
CISPR 11:2009+A1:2010
Electromagnetic interference radiation
Compliant
CISPR 11:2009+A1:2010
Emission of harmonics
N/A
IEC 61000-3-2:2005+A1:2008+A2:2009
Voltage changes, voltage fluctuations and flicker emis-
sions N/A
IEC 61000-3-3:2013
N/A = not applicable

Electromagnetic compatibility (EMC)

Interference immunity measurements
Immunity to electrostatic discharge
Compliant
IEC 61000-4-2:2008
Immunity to high-frequency electromagnetic fields
Compliant
IEC 61000-4-3:2006+A1:2007+A2:2010
Immunity to near fields of wireless HF communication
devices Compliant
IEC 61000-4-3:2006+A1:2007+A2:2010
Immunity to fast electrical transients/bursts – AC mains
voltage Compliant
IEC 61000-4-4:2012
Immunity to electrical fast transients/bursts – I/O,
SIP/SOP ports Compliant
IEC 61000-4-4:2012
Immunity to interference, surges
Compliant
IEC 61000-4-5:2005
Immunity to conducted disturbances, induced by radio-
frequency fields – AC mains voltage Compliant
IEC 61000-4-6:2013
Immunity to conducted disturbances, induced by radio-
frequency fields – SIP/SOP ports Compliant
IEC 61000-4-6:2013
Immunity to power frequency magnetic fields
Compliant
IEC 61000-4-8:2009
Immunity to voltage dips, short interruptions and voltage
variations Compliant
IEC 61000-4-11:2004

8 9000-606-39/30 2103V007
 Product description

Electromagnetic compatibility (EMC)

Interference immunity measurements on the supply input
Immunity to fast electrical transients/bursts – AC mains
voltage
IEC 61000-4-4:2012 Compliant EN
± 2 kV
100 kHz repetition rate
Immunity to surges, line-to-line
IEC 61000-4-5:2005 Compliant
± 0.5 kV, ± 1 kV
Immunity to conducted disturbances, induced by radio-
frequency fields – AC mains voltage
IEC 61000-4-6:2013
3V
0.15–80 MHz Compliant
6V
ISM frequency bands
0.15–80 MHz
80% AM at 1 kHz
Immunity to voltage dips, short interruptions and voltage
variations Compliant
IEC 61000-4-11:2004

Electromagnetic compatibility (EMC)

Interference immunity measurements SIP/SOP
Immunity to electrical fast transients/bursts – I/O,
SIP/SOP ports
IEC 61000-4-4:2012 Compliant
± 1 kV
100 kHz repetition rate
Immunity to conducted disturbances, induced by radio-
frequency fields – SIP/SOP ports
IEC 61000-4-6:2013
3V
0.15–80 MHz Compliant
6V
ISM frequency bands
0.15–80 MHz
80% AM at 1 kHz

Immunity to interference table, near fields of wireless HF communication devices

Radio service Frequency band Test level
MHz V/m
TETRA 400 380 - 390 27
GMRS 460
430 - 470 28
FRS 460
LTE band 13, 17 704 - 787 9

9000-606-39/30 2103V007 9
 Product description

Immunity to interference table, near fields of wireless HF communication devices

Radio service Frequency band Test level
MHz V/m
GSM 800/900
EN TETRA 800
iDEN 820 800 - 960 28
CDMA 850
LTE band 5
GSM 1800
CDMA 1900
GSM 1900
1700 - 1990 28
DECT
LTE band 1, 3, 4, 25
UMTS
Bluetooth
WLAN 802.11 b/g/n
2400 - 2570 28
RFID 2450
LTE band 7
WLAN 802.11 a/n 5100 - 5800 9

10 9000-606-39/30 2103V007
 Product description

4.1 Type plate

The type plates are on the motor cover and on
the motor flange.
EN

1 Type plate

4.2 Evaluation of conformity

This device has been subjected to conformity
acceptance testing in accordance with the cur-
rent relevant European Union guidelines. This
equipment conforms to all relevant requirements.

9000-606-39/30 2103V007 11
 Product description

5 Operation
1
EN

2
3
9 4
8 5
6
7
1 Motor
2 Vacuum, to suction unit
3 Separation
4 Aspiration input
5 Pump wheel
6 Separation rotor
7 Fluid output
8 Waste valve
9 Relief valve

5.1 Separation
Every time the suction hose is taken out of the hose manifold, the CS 1 Combi-Sepamatic and the suc-
tion unit are started.
The mixture of liquid and air drawn up is accelerated in the intake connection and then set in spiral
motion in the separation. The resulting centrifugal forces sling the aspirated particles against the outer
wall. The air is continuously separated from the fluid and escapes to the suction unit via the spinning
separation rotor.
The aspirated air is subject to high centrifugal forces by the separation rotor, which ensures that no fluid
or blood foam can be carried into the suction unit.
The spiral motion serves to continuously transport the separated liquid to the pump wheel, this then
pumps the liquid into the central waste water drainage system via the waste water valve.
The air bleed is carried out via the relief valve. If fluid escapes upwards into the air bleed area following a
fault, the relief valve closes automatically.

5.2 Station selection valve

The station selection valve interrupts the suction flow between the hose manifold and the suction unit.
As soon as a suction hose has been removed from the hose manifold, the station selection valve is
opened and suction flow is enabled.
A station selection valve is already integrated in various versions of the CS 1. An external station selec-
tion valve can be electrically controlled via the CS 1.

12 9000-606-39/30 2103V007
 Assembly

❯ Install an all-pole disconnect switch with a con-

Assembly tact opening width of at least 3 mm in the elec-
trical connection to the mains power supply. It
must be possible to secure the disconnect
6 Requirements switch so that it cannot be inadvertently
EN
switched back on again.
6.1 Setup options ❯ Install electrical lines without mechanical ten-
CS 1 Combi-Sepamatic sion.
– Directly in the treatment unit. ❯ Make the electrical connection via the main
– In a special housing in an extension of the power switch of the treatment unit or via the
treatment unit. main power switch of the practice.

6.2 Hose materials 6.5 Information about connecting

For waste connections and suction lines only cables
use the following hose types:
Mains supply cable
– Flexible spiral hoses made of PVC with inte-
grated spiral or equivalent hoses Installation type Line layout (minimum
– Hoses that are resistant to dental disinfectants requirements)
and chemicals Fixed installation – Plastic sheathed cable
Plastic hoses will display signs of ageing (e.g. type NYM‑J)
over time. Therefore, they should be Flexible – PVC flexible line
inspected regularly and replaced as nec- (e.g. H05 VV‑F)
essary. or
The following types of hoses must not be – Rubber connection
used: (e.g. H05 RN‑F or
– Rubber hoses H05 RR‑F)
– Hoses made completely of PVC
– Hoses that are not sufficiently flexible Control cable
Installation type Line layout (minimum
6.3 Installation and routeing of requirements)
hoses and pipes Fixed installation – Shielded sheathed cable
❯ Execute the on-site pipe installation in accord- (e.g. (N)YM (St)-J)
ance with the applicable local regulations and Flexible – PVC data cable with
standards. shielded cable sheath-
❯ Lay the hose installation of the drains to or ing, as used for tele-
from the unit at a sufficient incline. communications and IT
If incorrectly laid, the hoses can processing systems
become blocked with sedimentation. (e.g. type LiYCY)
or
– Lightweight PVC control
6.4 Information about electrical cable with shielded
connections cable sheathing
❯ Ensure that the electrical connections to the
mains power supply are established in accord- Wire cross-section
ance with current valid national and local regu- Unit feed:
lations and standards governing the installation – 0.75 mm²
of low voltage units in medical facilities. Connection external valves / units:
– 0.5 mm²

9000-606-39/30 2103V007 13
 Assembly

7 Installation Inlet and outlet hoses

Connect and attach the inlet and outlet hoses
WARNING with DürrConnect connectors to the relevant
connections on the unit. Route the hoses at an
Infection due to contaminated unit
incline.
EN ❯ Clean and disinfect the suction before Recommended diameter of the connection
working on the unit. hoses: Æ 25 mm.
❯ Wear protective equipment when The minimum nominal width for the outlet hose is
working (e. g. impermeable gloves, 15 mm.
protective goggles and mouth and
nose protection). 1
2
Prior to working on the unit or in case of
danger, disconnect it from the mains.

7.1 Installation of the CS 1 in 3

treatment units 4
Attach the unit vertically at a suitable position in
the treatment unit. The unit is mounted on rubber
pads and suspended in a metal frame. This
mounting arrangement prevents the transmission
of any vibrations to the treatment unit while the
device is running. Vibrations may occur if the unit
is not positioned vertically. A minimum distance
of 3 mm must be maintained to the surround- 4
ings.
1 Hose manifold
2 Vent
3 Outlet
4 Suction unit

Rinsing unit
It is recommended that the suction system is
equipped with a rinsing unit, e.g. in the treatment
unit. The rinsing unit provides a small amount of
water during aspiration. This dilutes the aspirated
fluids (blood, saliva, rinsing water etc.), which can
then be transported more effectively.
Station selection valve
In various types, the place selection valve is Installation sets
directly mounted on the CS 1. The station selec- Installation sets and detailed documentation for
tion valve (for separate installation) should be fit- various installation situations are available from
ted in the suction pipe in the treatment unit, pref- the manufacturers.
erably near the end connection in the floor When installed in a housing, ventilation
socket. The electrical connection should then slits should be provided to avoid heat
also be carried out on the CS 1. build-up in the housing.
For further information, refer to the station selec-
tion valve installation and operating instructions

14 9000-606-39/30 2103V007
 Assembly

7.2 Power supply 7.4 Electrical connections

– Safety transformer order number:
9000‑150‑46
– Safety transformer 24 V AC with an isolator
consisting of two means of patient protection EN
(MOPP) between the mains circuit and secon-
dary circuit, min. 100 VA, secondary fuse X1
X2
T 4 AH (or IEC 60127‑2/V T 4 AH, 250 V)
X3
7.3 Electrical connections, con-
troller

X1 Power supply
X2 Hose manifold start signal
X3 Outgoing signal station selection valve
and/or rinsing unit
❯ Remove the motor cover of the CS 1.
❯ Attach the connector to the connection lines.
X1 Power supply in accordance with EN To open, lift the terminal lever upwards.
60601-1
X2 Signal input / start signal ❯ Plug the connector onto the control.
X3 Place selection valve and/or rinsing unit
❯ Put the motor cover on.
24 V DC (max. output: 8 W)
F1 T 4 AH, 250 V in accordance with
IEC 60127-2

9000-606-39/30 2103V007 15
 Assembly

8 Commissioning
In many countries technical medical prod-
ucts and electrical devices are subject to
regular checks at set intervals. The owner
EN must be instructed accordingly.
❯ Turn on the unit power switch or the main sur-
gery switch.
❯ Carry out an electrical safety check in accord-
ance with applicable local regulations (e.g. the
German Ordinance on the Installation, Opera-
tion and Use of Medical Devices / Medizinpro-
dukte-Betreiberverordnung) and record the
results as appropriate, e.g. in the technical log
book.
❯ Check the aspiration function.
❯ Check the connections, hoses and device for
leaks.

16 9000-606-39/30 2103V007
 Usage

The following are required for disinfection/clean-

Usage ing:
ü Non-foaming disinfectant/cleaning agent that
is compatible with the materials.
9 Disinfection and cleaning ü Unit care system, e.g. OroCup
EN
❯ To pre-clean, suck up 2 litres of water with the
NOTICE care system.
Device malfunctions or damage due ❯ Aspirate the disinfection/cleaning agent with
to use of incorrect media the care system.
Guarantee claims may become invalid
as a result.
9.3 Once or twice a week before
❯ Do not use any foaming agents such
the midday break
as household cleaning agents or Under harsher conditions (e.g. hard water
instrument disinfectants. or frequent use of prophy powders) 1x
❯ Do not use abrasive cleaners. daily before the midday break
❯ Do not use agents containing chlorine. The following are required for cleaning:
❯ Do not use any solvents like acetone. ü Special non-foaming detergent for suction
units that is compatible with the materials.
Dürr Dental recommends ü Unit care system, e.g. OroCup
– For disinfection and cleaning:
❯ To pre-clean, suck up 2 litres of water with the
Orotol plus or Orotol ultra
care system.
– For cleaning:
❯ Aspirate the cleaning agent with the care sys-
MD 555 cleaner
tem.
Only these products have been tested by Dürr
❯ Rinse with ca. 2 l water after the application
Dental.
time.
When using prophy powders, Dürr Dental recom-
mends the water-soluble Lunos prophy powders
in order to protect the Dürr Dental suction sys-
tems.

9.1 After every treatment

❯ Aspirate a glass of cold water through the large
and the small suction hoses. Do this even if
only the small suction hose was actually used
during treatment.

Suction through the large suction hose

causes a large amount of air to be drawn
up, thereby considerably increasing the
cleaning effect.

9.2 Daily after the end of treat-

ment
After higher workloads before the midday
break and in the evening

9000-606-39/30 2103V007 17
 Usage

10 Maintenance
All maintenance work must be performed by a qualified expert or by one of our Service Techni-
cians.
EN
WARNING
Infection due to contaminated unit
❯ Clean and disinfect the suction before working on the unit.
❯ Wear protective equipment when working (e. g. impermeable gloves, protective goggles and
mouth and nose protection).

Prior to working on the unit or in case of danger, disconnect it from the mains.

Maintenance interval Maintenance work

Dependent upon the ❯ Clean or replace the protective sieves at the aspiration inlet. At the latest,
level of usage of the however, when the suction power of the unit diminishes.
device

Annually ❯ Cleaning of the suction unit in accordance with the operating instructions.
❯ Clean or replace the protective sieves at the aspiration inlet.
❯ If a rinsing unit is present: clean the sieve in the water supply. *
❯ Perform a functional test. *
Every 3 years ❯ Replace the rubber grommets on the connections. *
Every 5 years ❯ Replace the rubber grommets on the connections. *
❯ Replace all o-rings in the device. *

* Only by customer services service technicians.

18 9000-606-39/30 2103V007
 Troubleshooting

Troubleshooting

11 Tips for operators and service technicians EN

Any repairs exceeding routine maintenance may only be carried out by qualified personnel or our
service.

WARNING
Infection due to contaminated unit
❯ Clean and disinfect the suction before working on the unit.
❯ Wear protective equipment when working (e. g. impermeable gloves, protective goggles and
mouth and nose protection).

Prior to working on the unit or in case of danger, disconnect it from the mains.

Error Possible cause Remedy

Device does not start No power supply ❯ Check power supply. *
❯ Check the fuses and replace if
necessary. *
No start signal ❯ Check the control voltage at
the signal input. *
Suction power too weak or Coarse sieve is blocked on the ❯ Clean the coarse sieve.
interrupted inlet of the aspiration
Place selection valve not or ❯ Check the control voltage. *
incompletely open ❯ Clean the place selection
valve. *

* Only to be done by service technicians.

9000-606-39/30 2103V007 19
 Troubleshooting

11.1 Replacing the fuse 12 Transporting the unit

Prior to working on the unit or in case of WARNING
danger, disconnect it from the mains. Infection due to contaminated unit
EN ❯ Disinfect the unit before transport.
Transformer
❯ Close all media connections.
❯ Unscrew and remove the safety cover.
❯ Replace the fuse. Wear protective equipment to avoid any
risk of infection (e.g. liquid-tight protective
gloves, protective goggles, face mask).
❯ Before disassembly, clean and disinfect the
suction unit and the unit using a suitable disin-
fectant approved by Dürr Dental.
❯ Disinfect a defective unit using a suitable sur-
face disinfection agent.
❯ Seal all connections with sealing caps.
❯ Pack the unit securely in preparation for trans-
port.
Fuse housing 12.1 Close the CS 1
❯ Turn the fuse housing to open it.
1
❯ Replace the fuse.
2

2
2
1
1
1 Dummy bushing
2 Ring clamp
1 Fuse housing
2 Fuses

20 9000-606-39/30 2103V007
 Appendix

Appendix

13 Handover record EN
This document confirms that a qualified handover of the medical device has taken place and that
appropriate instructions have been provided for it. This must be carried out by a qualified adviser for the
medical device, who will instruct you in the proper handling and operation of the medical device.
Product name Order number (REF) Serial number (SN)

o Visual inspection of the packaging for any damage

o Unpacking the medical device and checking for damage
o Confirmation of the completeness of the delivery
o Instruction in the proper handling and operation of the medical device based on the operating
instructions

Notes:

Name of person receiving instruction: Signature:

Name and address of the qualified adviser for the medical device:

Date of handover: Signature of the qualified adviser for the medi-

cal device:

9000-606-39/30 2103V007 21
 Appendix

EN

22 9000-606-39/30 2103V007
Hersteller / Manufacturer:
DÜRR DENTAL SE
Höpfigheimer Str. 17
74321 Bietigheim-Bissingen
Germany
Fon: +49 7142 705-0
www.duerrdental.com
info@duerrdental.com