Durr Dental Tyscor V 4 User manual

EN
Tyscor V 4
Installation and operating instructions
0297
7188100023L02
*7188100023L02*
2109V004

Contents
Important information
1About this document .. . . . . . . . . . . . . 3
1.1 Warnings and symbols .. . . . . . . 3
1.2 Copyright information .. . . . . . . . 4
2 Safety .. . . . . . . . . . . . . . . . . . . . . . . . . 4
2.1 Intended purpose .. . . . . . . . . . . 4
2.2 Intended use .. . . . . . . . . . . . . . . 4
2.3 Improper use .. . . . . . . . . . . . . . . 4
2.4 General safety information .. . . . . 5
2.5 Combining devices safely .. . . . . 5
2.6 Specialist personnel .. . . . . . . . . 5
2.7 Notification requirement of seri-
ous incidents .. . . . . . . . . . . . . . . 5
2.8 Electrical safety .. . . . . . . . . . . . . 5
2.9 Only use original parts .. . . . . . . . 5
2.10 Transport .. . . . . . . . . . . . . . . . . . 6
2.11 Disposal .. . . . . . . . . . . . . . . . . . 6
Product description
3Overview .. . . . . . . . . . . . . . . . . . . . . . . 7
3.1 Scope of delivery .. . . . . . . . . . . . 8
3.2 Optional items .. . . . . . . . . . . . . . 8
3.3 Consumables .. . . . . . . . . . . . . . 8
3.4 Wear parts and replacement
parts .. . . . . . . . . . . . . . . . . . . . . 8
4Technical data .. . . . . . . . . . . . . . . . . . . 9
4.1 Characteristic curves .. . . . . . . . . 10
4.2 Type plate .. . . . . . . . . . . . . . . . . 12
4.3 Evaluation of conformity .. . . . . . 12
5 Operation .. . . . . . . . . . . . . . . . . . . . . . 13
5.1 Condensate separator .. . . . . . . . 14
5.2 Radial blower .. . . . . . . . . . . . . . 14
5.3 LEDs .. . . . . . . . . . . . . . . . . . . . . 14
5.4 Operating modes .. . . . . . . . . . . 14
5.5 Quick Start .. . . . . . . . . . . . . . . . 14
5.6 Lag time .. . . . . . . . . . . . . . . . . . 14
5.7 Eco Stop .. . . . . . . . . . . . . . . . . . 14
5.8 Grouping of multiple devices .. . . 14
5.9 Overview of the touch screen
user interface .. . . . . . . . . . . . . . 15
Assembly
6 Requirements .. . . . . . . . . . . . . . . . . . . 16
6.1 Installation/setup room .. . . . . . . 16
6.2 Setup options .. . . . . . . . . . . . . . 16
6.3 Pipe materials .. . . . . . . . . . . . . . 16
6.4 Hose materials .. . . . . . . . . . . . . 16
6.5 Information about electrical con-
nections .. . . . . . . . . . . . . . . . . . 16
6.6 Information about connecting
cables .. . . . . . . . . . . . . . . . . . . . 16
7 System components .. . . . . . . . . . . . . . 17
7.1 Exhaust air filter / bacteria filter .. 17
7.2 Noise reduction .. . . . . . . . . . . . . 17
8 Installation .. . . . . . . . . . . . . . . . . . . . . . 18
8.1 Mounting the condensate sepa-
rator .. . . . . . . . . . . . . . . . . . . . . 18
8.2 Installation and routeing of hoses
and pipes .. . . . . . . . . . . . . . . . . 19
8.3 Installing the group of devices .. . 20
8.4 Network connection .. . . . . . . . . 20
8.5 CAN bus .. . . . . . . . . . . . . . . . . . 20
8.6 Electrical connections .. . . . . . . . 20
8.7 PCB (main board) electrical con-
nections .. . . . . . . . . . . . . . . . . . 21
8.8 Testing suction power after
installation .. . . . . . . . . . . . . . . . . 23
9 Commissioning .. . . . . . . . . . . . . . . . . . 23
9.1 Setup wizard .. . . . . . . . . . . . . . . 23
9.2 Settings on the touch screen .. . . 23
9.3 Monitoring the unit via the net-
work .. . . . . . . . . . . . . . . . . . . . . 25
Usage
10 LEDs .. . . . . . . . . . . . . . . . . . . . . . . . . . 26
10.1 Ready for operation .. . . . . . . . . . 26
10.2 Eco Stop .. . . . . . . . . . . . . . . . . . 26
Contents
7188100023L02 2109V004 1
EN

10.3 Hose manifold start signal .. . . . . 26
10.4 Network .. . . . . . . . . . . . . . . . . . 26
10.5 Fault .. . . . . . . . . . . . . . . . . . . . . 26
11 Overview on the touch screen .. . . . . . 27
11.1 "Home" screen .. . . . . . . . . . . . . 27
11.2 "Settings" display .. . . . . . . . . . . 27
11.3 "Messages" screen .. . . . . . . . . . 27
12 Disinfection and cleaning .. . . . . . . . . . 28
12.1 After every treatment .. . . . . . . . . 28
12.2 Daily after the end of treatment .. 28
12.3 Once or twice a week before the
midday break .. . . . . . . . . . . . . . 29
13 Maintenance .. . . . . . . . . . . . . . . . . . . . 30
13.1 Cleaning the protective strainer .. 31
Troubleshooting
14 Tips for operators and service techni-
cians .. . . . . . . . . . . . . . . . . . . . . . . . . . 32
14.1 General faults .. . . . . . . . . . . . . . 32
14.2 Error messages .. . . . . . . . . . . . . 34
15 Transporting the unit .. . . . . . . . . . . . . 37
Appendix
16 Menu structure .. . . . . . . . . . . . . . . . . . 38
17 Handover record .. . . . . . . . . . . . . . . . . 40
Contents
2 7188100023L02 2109V004
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Important information
1 About this document
These installation and operating instructions rep-
resent part of the unit.
If the instructions and information in these
installation and operating instructions are
not followed, Dürr Dental will not be able
to offer any warranty or assume any liabil-
ity for the safe operation and the safe
functioning of the unit.
The German version of the installation and oper-
ating instructions is the original manual. All other
languages are translation of the original manual.
These installation and operating instructions
apply to:
Tyscor V 4
Order number: 7188100200; 7188200200
1.1 Warnings and symbols
Warnings
The warnings in this document are intended to
draw your attention to possible injury to persons
or damage to machinery.
The following warning symbols are used:
General warning symbol
Warning – dangerous high voltage
Warning - automatic start-up of the unit
Biohazard warning
The warnings are structured as follows:
SIGNAL WORD
Description of the type and source of
danger
Here you will find the possible conse-
quences of ignoring the warning
❯Follow these measures to avoid the
danger.
The signal word differentiates between four levels
of danger:
–DANGER
Immediate danger of severe injury or death
–WARNING
Possible danger of severe injury or death
–CAUTION
Risk of minor injuries
–NOTICE
Risk of extensive material/property damage
Other symbols
These symbols are used in the document and on
or in the unit:
Note, e.g. specific instructions regarding
efficient and cost-effective use of the unit.
Wear protective gloves.
Disconnect all power from the unit.
Refer to the accompanying electronic
documents.
XX
YY
Comply with the lower and upper temper-
ature limits
xx %
xx %
Comply with the lower and upper humid-
ity limits
CE labelling with the number of the noti-
fied body
Order number
Serial number
Medical device
Health Industry Bar Code (HIBC)
Manufacturer
Fragile, handle with care
This way up / store and transport in an
upright position
Important information
7188100023L02 2109V004 3
EN

Keep dry
Keep away from sunlight
n
Stacking limits
1.2 Copyright information
All circuits, processes, names, software pro-
grams and units mentioned in this document are
protected by copyright.
The Installation and Operating Instructions must
not be copied or reprinted, neither in full nor in
part, without written authorisation from Dürr Den-
tal.
2 Safety
Dürr Dental has designed and constructed this
unit so that when used properly and for the inten-
ded purpose it does not pose any danger to
people or property.
Despite this, the following residual risks can
remain:
– 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 suction unit provides the dental treatment
unit with vacuum and volume flow.
2.2 Intended use
Working in combination with the suction unit with
treatment unit, suction handpiece and cannula,
the media used in dental treatment (e.g. water,
saliva, dentine and amalgam) are removed by
suction for disposal.
This unit is technically suitable for the aspiration
of nitrous oxide (laughing gas). However, when
assembling a system for aspiration of nitrous
oxide, it is important to ensure that the other
components in the system are also suitable for
this purpose. Those responsible for setting up
the system must assess this and approve and
release the system for the aspiration of nitrous
oxide.
Operation with nitrous oxide is only per-
mitted if the exhaust air is transported
from the unit to the outside of the build-
ing.
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.
❯Do not use this device to aspirate flammable or
explosive mixtures.
Important information
4 7188100023L02 2109V004
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❯The unit must not be used as a vacuum
cleaner.
❯Do not use chemicals containing chlorine or
foaming chemicals.
❯Operation in operating theatres of explosive
areas is not permissible.
❯The suction unit must not be set up in the
patient environment (with a radius of 1.5 m).
2.4 General safety information
❯Always comply with the specifications of all
guidelines, laws, and other rules and regula-
tions applicable at the site of operation for the
operation of this unit.
❯Check the function and condition of the unit
prior to every use.
❯Do not convert or modify the unit.
❯Comply with the specifications of the Installa-
tion and Operating Instructions.
❯The Installation and Operating Instructions
must be accessible to all operators of the unit
at all times.
2.5 Combining devices safely
Take care when connecting units together or to
parts of other systems as there is always an ele-
ment of risk (e.g. due to leakage currents).
❯Only connect units when there can be no
question of danger to operator or to patient.
❯Only connect units when it is safe to do so and
when there is no risk of damage or harm to the
surroundings.
❯If it is not 100% clear from the unit data sheet
that such connections can be safely made or if
you are in any doubt, always get a suitably
qualified person (e.g. the manufacturer) to ver-
ify that the setup is safe.
Where applicable, the requirements for medical
products have been taken into account in the
development and construction of the device. As
a result, this device is suitable for installation
within medical supply equipment.
❯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.
2.6 Specialist personnel
Operation
Unit operating personnel must ensure safe and
correct handling based on their training and
knowledge.
❯Instruct or have every user instructed in han-
dling the unit.
The following groups are not permitted to
operate or use a commercially operated unit:
– People without the necessary experience and
knowledge
– People with reduced physical, sensory or men-
tal capabilities
– Children
Installation and repairs
❯Installation, readjustments, alterations,
upgrades and repairs must be carried out by
Dürr Dental or by qualified personnel specifi-
cally approved and authorized by Dürr Dental.
2.7 Notification requirement of
serious incidents
The operator/patient is required to report any
serious incident that occurs in connection with
the device to the manufacturer and to the com-
petent authority of the Member State in which
the operator and/or patient is established/resi-
dent.
2.8 Electrical safety
❯Comply with all the relevant electrical safety
regulations when working on the unit.
❯Never touch the patient and unshielded plug
connections on the device at the same time.
❯Replace any damaged cables or plugs immedi-
ately.
2.9 Only use original parts
❯Only use accessories and optional items that
have been recommended or specifically
approved by Dürr Dental.
❯Only use only original wear parts and replace-
ment parts.
Important information
7188100023L02 2109V004 5
EN

DÜRR MEDICAL accepts no liability for
damages or injury resulting from the use
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.
2.10 Transport
The original packaging provides optimum protec-
tion for the unit during transport.
If required, original packaging for the unit can be
ordered from Dürr Dental.
Dürr Dental will not accept any responsi-
bility or liability for damage occurring dur-
ing transport due to the use of incorrect
packaging, even where the unit is still
under guarantee.
❯Only transport the unit in its original packaging.
❯Keep the packing materials out of the reach of
children.
2.11 Disposal
The unit may be contaminated. Instruct
the company disposing of the waste to
take the relevant safety precautions.
❯Decontaminate potentially contaminated parts
before disposing of them.
❯Uncontaminated parts (e.g. electronics, plastic
and metal parts etc.) should be disposed of in
accordance with the local waste disposal regu-
lations.
❯If you have any questions about the correct
disposal of parts, please contact your dental
trade supplier.
An overview of the waste keys for Dürr
Dental products can be found in the
download area at:
www.duerrdental.com
Document no.: P007100155
Important information
6 7188100023L02 2109V004
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Product description
3 Overview
2
1
7
3
4
5
6
1 Tyscor V 4 suction unit
2 Condensation separator
3 Mains cable with local mains plug
4 Hose LW 50, 1.5 m
5 Hose LW 50, 0.6 m
6 Waste water hose LW 20
7 Set of connection fittings
Product description
7188100023L02 2109V004 7
EN

3.1 Scope of delivery
The following items are included in the scope of
delivery (possible variations due to country-spe-
cific requirements and/or import regulations):
Tyscor V 4 .. . . . . . . . . . . . . . . . . . . 7188100200
Tyscor V 4 .. . . . . . . . . . . . . . . . . . . 7188200200
– Suction unit
– Condensation separator
– Mains cable
– Hose LW 50 (0.6 m)
– Hose LW 50 (1.5 m)
– Waste water hose LW 20
– Set of connection fittings
– Short description
3.2 Optional items
The following optional items can be used with the
device:
Wall bracket .. . . . . . . . . . . . . . . . . . 7188100015
Bacteria filter .. . . . . . . . . . . . . . . . . 0705-991-50
Noise reduction for exhaust air .. . . 0730-991-00
Bracket for floor-mounted installa-
tion .. . . . . . . . . . . . . . . . . . . . . . . . 7188100017
Radial blower .. . . . . . . . . . . . . . . . . 7188100060
Upgrade kit .. . . . . . . . . . . . . . . . . . 7188100075
Installation set for Tyscor V/VS Tan-
dem .. . . . . . . . . . . . . . . . . . . . . . . . 7188100300
3.3 Consumables
The following materials are consumed during
operation of the device and must be ordered
separately:
Orotol plus (2.5 litre bottle) .. . . . . CDS110P6150
MD 555 cleaner (2.5 litre bottle) .. CCS555C6150
3.4 Wear parts and replacement
parts
Information about replacement parts is
available from the portal for authorised
specialist dealers at:
www.duerrdental.net
If the mains cable of this unit is damaged
it must only be replaced by an original
mains cable from the manufacturer.
Product description
8 7188100023L02 2109V004
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4 Technical data
Electrical data 7188100200 7188200200
Rated voltage V 230, 1~ 230, 1~
Mains frequency Hz 50 / 60 50 / 60
Nominal current A 5.8
Rated power kW 1.3
Fuses 2x T 10.0 AH / 250 V~
(IEC 60127-2)
Type of protection IP 21
Protection class I
Control connection electrical data
Output:
Voltage
Max. current
V DC
mA
24
160
Input impedance kW6.9
Hi level V 10-30
Lo level V 0-2.5
Connections
Vacuum connection (external) mm Æ50
Exhaust air connection (external) mm Æ50
Condensation drain (DürrConnect) mm Æ20
Classification in accordance with EN ISO 10637
Classification based on separation of sol-
ids and liquids Dry suction system
Classification based on flow rate Type 1
General data
Max. number of users 4 2
Radial blower speed (nv) max. rpm 24000
Duty cycle % 100
Rate of heat generation kW 1.3
Dimensions (H x W x D) cm 54 x 45 x 62
Weight kg 19 19
Noise level * ca. dB(A) 62 / 62 62 / 62
* Noise level in accordance with ISO 3746
Network connection
LAN technology Ethernet
Product description
7188100023L02 2109V004 9
EN

Network connection
Standard IEEE 802.3u
Data rate Mbit/s 100
Connector RJ45
Type of connection Auto MDI-X
Cable type ³CAT5
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
Altitude above mean sea level m < 2000
Classification
Medical Device Class IIa
4.1 Characteristic curves
Fig. 1: Characteristic curves for: 7188100200
Nl Normal litres in accordance with ISO 10637
Product description
10 7188100023L02 2109V004
EN

Fig. 2: Characteristic curves for: 7188200200
Nl Normal litres in accordance with ISO 10637
Product description
7188100023L02 2109V004 11
EN

4.2 Type plate
The type plate can be found on the housing
lower part.
1
1 Type plate
4.3 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.
Product description
12 7188100023L02 2109V004
EN

5 Operation
18
3
4
1
6
7
5
2
9
10
11
12
13
14
16
15
19
1 Suction connection on condensation separator
2 Network connection
3 Mains connection (power plug)
4 Connection to amalgam separator (appliance power inlet)
5 CAN bus
6 Condensation drain
7 Exhaust air connection
9 Yellow LED – Ethernet
10 Red LED – fault
11 Green LED – ready for operation
12 Blue LED – start signal
13 Manual start button
14 SD card slot (Micro SD)
15 Control connection
16 Voltage supply for the rinsing unit
18 Touch screen
19 Protective strainer
The V suction unit is used in "dry" suction systems. The unit includes two centrifugal blowers and an
external condensation separator.
Product description
7188100023L02 2109V004 13
EN

5.1 Condensate separator
The condensate separator collects any condensate that occurs in the pipe system and directs it to the
outside.
5.2 Radial blower
The air that has been separated from the fluids is sucked into the radial blowers. The motors in the
radial blowers are regulated on a demand-driven basis by the unit electronics. Afterwards, the aspirated
air is passed through the exhaust air connections and out of the device.
5.3 LEDs
– The yellow LED lights up when the unit is connected to the network.
– The red LED lights up when there is a fault.
– The green LED lights up continuously when the unit is ready for operation.
– The blue LED lights up when a "start" signal is present from the treatment unit.
EcoStop:
– Green LED flashes. The unit has been switched off by the EcoStop function. To switch it on, lift a suc-
tion hose up out of the hose manifold or briefly disconnect the power supply from the unit.
5.4 Operating modes
Three different operating modes are available for Tyscor V/VS 4. These can be set up on the touch
screen. If you are using monitoring software then you can also change the settings there.
The operating modes are "Balanced", "Boost" and "Eco". The different operating modes can be used to
adjust the available power to the suction system (routeing of lines, line lengths, layout of treatment unit
etc.).
5.5 Quick Start
The Quick Start function is used to hold the unit in standby mode for a certain length of time, which
ensures fast availability of the suction flow when required. Since the motor remains switched on at a
very low speed when the unit is in standby mode, this option consumes slightly more energy.
5.6 Lag time
The device will continue to run for a few seconds after the suction hose has been hung back in the
manifold. The lag time ensures that the remaining fluid in the suction system can be processed.
Depending on the installation, the lag time can be adjusted accordingly.
5.7 Eco Stop
The Eco Stop function is used to protect the unit if it is operated inadvertently with no flow rate or with a
flow rate that is too low. If the unit is operated under these conditions without the manifold signal being
actuated in the mean time, the unit will switch off automatically after a pre-defined period of time (it is
possible to set this up so that it can be adjusted via the monitoring software). To switch it on, lift a suc-
tion hose up out of the hose manifold or briefly disconnect the power supply from the unit.
5.8 Grouping of multiple devices
Up to three devices can be operated together as a group. Here, one device takes on the role of the
main unit (main unit), which can control up to two further devices (auxiliary units). By combining multiple
devices together in this way, the available flow rate can be increased – which in turn means that more
therapists can use the system.
Product description
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When grouped together, mutual controlling and exchange of information takes place via the CAN
bus. Only one device is permitted to be configured as the main unit; additional devices must be
configured as auxiliary units.
5.9 Overview of the touch screen user interface
Display window
1
2
3
1 Context range (e.g. date, time)
2 Content area
3 Navigation buttons
Menu window
1
2
3
4
5
4
1 Title bar / submenus
2 Content area
3 Navigation buttons
4 Scroll button
5 Page indicator
Product description
7188100023L02 2109V004 15
EN

Assembly
6 Requirements
The unit can be installed on the same level as the
surgery room or in a floor below.
Further information can be found in our
suction planning information leaflet.
Order number9000-617-03/..
6.1 Installation/setup room
The room chosen for set up must fulfil the follow-
ing requirements:
– Closed, dry, well-ventilated room
– Should not be a room made for another pur-
pose (e. g. boiler room or wet cell)
– When installing in a cabinet the inlet and outlet
ventilation slots must be present; minimum
free cross-section at least 120 cm2.
– Forced ventilation (fan) must be provided if
there is a risk that the recommended room air
temperature could be exceeded. The air flow
performance must be at least 2 m3/min.
– Do not cover cooling slots or openings with
housing installations; ensure sufficient clear-
ance to the openings to permit sufficient cool-
ing.
– Mains cable plug connections must be freely
accessible so they can be quickly disconnec-
ted if there is any danger.
6.2 Setup options
The following options for setting up the unit are
available:
– On the floor with a console for floor-mounted
installation
– Wall installation using a Dürr Dental wall
mounting
– In a ventilated cabinet
6.3 Pipe materials
Only use vacuum-sealed HT-waste pipes
manufactured from the following materials:
– Polypropylene (PP),
– Chlorinated polyvinyl chloride (PVC-C),
– Plasticizer-free polyvinyl chloride (PVC-U),
– Polyethylene (PE).
The following materials must not be used:
– Acrylonitrile-butadiene-styrene (ABS),
– Styrene copolymer blends (e.g. SAN + PVC).
6.4 Hose materials
For waste connections and suction lines only
use the following hose types:
– Flexible spiral hoses made of PVC with inte-
grated spiral or equivalent hoses
– Hoses that are resistant to dental disinfectants
and chemicals
Plastic hoses will display signs of ageing
over time. Therefore, they should be
inspected regularly and replaced as nec-
essary.
The following types of hoses must not be
used:
– Rubber hoses
– Hoses made completely of PVC
– Hoses that are not sufficiently flexible
6.5 Information about electrical
connections
❯Ensure that electrical connections to the mains
power supply are carried out in accordance
with current valid national and local regulations
and standards governing the installation of low
voltage units in medical facilities.
❯Observe the current consumption of the devi-
ces that are to be connected.
6.6 Information about connecting
cables
Mains supply cable
Only use the supplied mains cable to connect the
device.
Control cable
Installation type Line layout (minimum
requirements)
Fixed installation – Shielded sheathed cable
(e.g. (N)YM (St)-J)
Assembly
16 7188100023L02 2109V004
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Installation type Line layout (minimum
requirements)
Flexible – PVC data cable with
shielded cable sheath-
ing, as used for tele-
communications and IT
processing systems
(e.g. type LiYCY)
or
– Lightweight PVC control
cable with shielded
cable sheathing
Connect the shielding of the cables in
accordance with the regulations.
7 System components
The system components listed below are
required or recommended for various procedures
or for installation.
7.1 Exhaust air filter / bacteria fil-
ter
For reasons of hygiene, we recommend the
installation of an exhaust air filter in the exhaust
air line.
If the suction unit is installed in the surgery and
the exhaust air cannot be directed to the outside,
it is essential to install an exhaust air filter.
Depending on the design and condition of the
exhaust air filter, it will need to be replaced after
1‑2 years at the latest.
7.2 Noise reduction
If the noise level from the exhaust air vent or the
flow noise generated is too high, noise reduction
can be installed in the exhaust air line.
Assembly
7188100023L02 2109V004 17
EN

8 Installation
The actual connection can vary depend-
ing on the chosen installation option. The
connection shown is only an example.
8.1 Mounting the condensate
separator
❯Attach the condensation separator to the
holder with two screws.
❯Fit the double sleeve with integrated protective
coarse filter and elbow to the inlet.
❯Attach the condensation separator with the
holder to the unit and secure.
Assembly
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