Durr Dental V 600, V 900 S, V 1200 S, V 300 S Installation And Operating Instructions Manual

Download

Suction units

V 900 S, V 1200 S

V 600

Installation and Operating Instructions

V 300 S

0297

9000-606-89/30



1711V001

Contents

Important information

1 About this document � � � � � � � � � � � � � � � 3

1�1 Warnings and symbols � � � � � � � � � � 3 1�2 Copyright information � � � � � � � � � � � 3

2 Safety � � � � � � � � � � � � � � � � � � � � � � � � � � � 4

2�1 Intended purpose � � � � � � � � � � � � � � 4 2�2 Intended use � � � � � � � � � � � � � � � � � � 4 2�3 Improper use � � � � � � � � � � � � � � � � � 4 2�4 General safety information � � � � � � � � 4 2�5 Combining devices safely � � � � � � � � 4 2�6 Qualified personnel � � � � � � � � � � � � � 5 2�7 Protection from electric shock � � � � � 5 2�8 Only use genuine parts � � � � � � � � � � 5 2�9 Transport � � � � � � � � � � � � � � � � � � � � 5 2�10 Disposal � � � � � � � � � � � � � � � � � � � � � 5

Product description

3 Overview� � � � � � � � � � � � � � � � � � � � � � � � � 6

3�1 Scope of delivery � � � � � � � � � � � � � � 7 3�2 Special accessories � � � � � � � � � � � � 7 3�3 Disposable materials � � � � � � � � � � � � 7 3�4 Wear parts and spare parts � � � � � � � 7

4 Technical data � � � � � � � � � � � � � � � � � � � � 8

4�1 V 300 S � � � � � � � � � � � � � � � � � � � � � 8 4�2 V 600 � � � � � � � � � � � � � � � � � � � � � � 10 4�3 V 600 � � � � � � � � � � � � � � � � � � � � � � 11 4�4 V 900 S � � � � � � � � � � � � � � � � � � � � 12 4�5 V 1200 S � � � � � � � � � � � � � � � � � � � 13 4�6 Type plate � � � � � � � � � � � � � � � � � � � 14 4�7 Conformity assessment � � � � � � � � � 14

5 Operation � � � � � � � � � � � � � � � � � � � � � � � 15

Installation

6 Requirements� � � � � � � � � � � � � � � � � � � � 17

6�1 Installation/setup room � � � � � � � � � 17 6�2 Setup options � � � � � � � � � � � � � � � � 17 6�3 Pipe materials � � � � � � � � � � � � � � � � 17 6�4 Hose materials � � � � � � � � � � � � � � � 17 6�5 Information about electrical

connections � � � � � � � � � � � � � � � � � 17

6�6 Information about connecting

cables � � � � � � � � � � � � � � � � � � � � � � 17

7 System components � � � � � � � � � � � � � � 18

7�1 Control box � � � � � � � � � � � � � � � � � � 18 7�2 Bacteria filter � � � � � � � � � � � � � � � � � 18 7�3 Noise reduction � � � � � � � � � � � � � � � 18

8 Installation � � � � � � � � � � � � � � � � � � � � � � 19

8�1 Installation and routeing of hoses

and pipes � � � � � � � � � � � � � � � � � � � 19

9 Electrical connections � � � � � � � � � � � � � 21

9�1 Unit with integrated control

electronics � � � � � � � � � � � � � � � � � � 21

10 Commissioning and first start-up� � � � � 22

Operation

11 Disinfection and cleaning� � � � � � � � � � � 23

11�1 After every treatment � � � � � � � � � � � 23 11�2 Daily after the end of treatment � � � 23 11�3 Once or twice a week before the

midday break � � � � � � � � � � � � � � � � 23

12 Maintenance� � � � � � � � � � � � � � � � � � � � � 24

12�1 V 300 S � � � � � � � � � � � � � � � � � � � � 24 12�2 V 600, V 900 S, V 1200 S � � � � � � � 24

Troubleshooting

13 Tips for operators and service

technicians � � � � � � � � � � � � � � � � � � � � � � 25

14 Transporting the unit � � � � � � � � � � � � � � 27

9000-606-89/30 1711V001 1

Contents

Appendix

15 Information about EMC in

accordance with EN 60601-1-2 � � � � � � 28

15�1 General information � � � � � � � � � � � � 28 15�2 Abbreviations � � � � � � � � � � � � � � � � 28 15�3 Guidelines and manufacturer's

information � � � � � � � � � � � � � � � � � � 28

2 9000-606-89/30 1711V001

Important information

1 About this document

These installation and operating instructions form 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 liability for the safe operation and the safe functioning of the unit�

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 – hot surfaces

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 consequences of ignoring the warning

i 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�

Comply with the Operating Instructions�

Wear hand protection�

Wear protective goggles�

Switch off and de-energise the unit (e�g�unplug from mains)�

Protective ground connection

CE labelling with the number of the notiﬁed body

Order number

Serial number

Manufacturer

1.2 Copyright information

All names of circuits, processes, names, software programs and units used 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 Dental�

9000-606-89/30 1711V001 3

Important information

2 Safety

Dürr Dental has designed and constructed this device so that when used properly and for the intended purpose there is no danger to people or property� Nevertheless, residual risks can remain� You should therefore observe the following notes�

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 permitted if the exhaust air is transported from the unit to the outside of the building�

2.3 Improper use

Any other usage or usage beyond this scope is deemed to be improper� The manufacturer accepts no liability for damages resulting from this� In these cases the user/operator will bear the sole risk�

i Do not use this device to aspirate ﬂammable

or explosive mixtures�

i The unit must not be used as a vacuum

cleaner�

i Do not use chemicals containing chlorine or

foaming chemicals�

i Operation in operating theatres of explosive

areas is not permissible�

i The following suction units must not be set up

in the patient environment (within a radius of 1�5m): V600, V900S and V1200S�

2.4 General safety information

i When operating this device always observe all

guidelines, laws, and other rules and regulations that are applicable at the site of operation�

i Prior to each use, check condition of the de-

vice and make sure it is in perfect working or-

der�

i Do not convert or modify the units� i Observe the Installation and Operating In-

structions�

i Make the Installation and Operating Instruc-

tions available to the person operating the de-

vice 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 element of risk (e�g� due to leakage currents)�

i Only connect units when there can be no

question of danger to operator or to patient�

i Only connect units when it is safe to do so

and there is no risk of damage or harm to the

surroundings�

i 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�

i Where this device is installed within other

medical supply equipment, the requirements

set out in Directive 93/42EEC and the rele-

vant standards must be complied with�

A copy of the system manufacturer‘s declaration in accordance with Article 12 of Directive 93/42/EEC can be found in our download section at www�duerrdental�com (document no� 9000-461-264)�

4 9000-606-89/30 1711V001

Important information

2.6 Qualified personnel

Operation

Persons who operate the units must ensure safe and correct handling based on their training and knowledge�

i Instruct or have every user instructed in han-

dling the unit�

Installation and repairs

i Installation, readjustments, alterations, up-

grades and repairs must be carried out by Dürr Dental or by qualiﬁed personnel speciﬁcally approved and authorized by Dürr Dental�

2.7 Protection from electric shock

i When working on the units observe all the rel-

evant electrical safety regulations�

i Never touch the patient and unshielded plug

connections on the device at the same time�

i Immediately replace any damaged lines and

connections�

Observe the EMC rules concerning medical devices

i Observe speciﬁc precautionary measures re-

lating to electromagnetic compatibility (EMC) for medical devices, see "15 Information about EMC in accordance with EN 60601-12"�

2.10 Disposal

The unit may be contaminated� Instruct the company disposing of the waste to take the relevant safety precautions�

i Decontaminate potentially contaminated parts

before disposing of them�

i Uncontaminated parts (e�g� electronics, plastic

and metal parts etc�) should be disposed of in accordance with the local waste disposal regulations�

i If you have any questions about the correct

disposal of parts, please contact your dental trade supplier�

2.8 Only use genuine parts

i Only use Dürr Dental parts or accessories and

special accessories speciﬁcally approved by Dürr Dental�

i Only use only genuine working parts and

spare parts�

2.9 Transport

The original packaging provides optimum protection for the device during transport�

If required, original packaging for the unit can be ordered from Dürr Dental�

Dürr Dental does not accept any responsibility or liability for damage occurring during transport due to the use of incorrect packaging, even where the unit is still under guarantee�

i Only transport the device in its original pack-

aging�

i Keep the packing materials out of the reach of

children�

9000-606-89/30 1711V001 5

Product description

3 Overview

1 Suction unit 2 Control box 3 Set of connection ﬁttings 4 Suction hose 5 Exhaust air hose 6 Auxiliary air valve 7 Condensation separator 8 Connection pipes 9 Waste hose LW 20

6 9000-606-89/30 1711V001

Product description

3.1 Scope of delivery

The following items are included in the scope of delivery (possible variations due to country-speciﬁc requirements and/or import regulations):

V 300 S, 230 V, 1~, 50 Hz . . . . . .7119-01/002

V 300 S, 230 V, 1~, 50/60 Hz . . . .7119-02/002

– Set of connection ﬁttings – Suction hose LW 30, grey – Exhaust air hose LW 30, aluminium – Waste hose LW 20 – Condensation separator

V 600, 230 V, 1~, 50 Hz . . . . . . . .7127-01/002

V 600, 400 V, 3~, 50/60 Hz . . . . .7127-02/002

V 600, 230 V, 3~, 50/60 Hz . . . . .7127-02/003

– Control box

0700-500-50 for model 7127-01/002 0732-100-52 for model 7127-02/002

0732-100-53 for model 7127-02/003 – Set of connection ﬁttings – Suction hose LW 50 – Exhaust air hose LW 50 (aluminium) – Condensation separator

V 900 S, 230 V, 1~, 50 Hz . . . . . .7131-01/002

V 900 S, 400 V, 3~, 50 Hz . . . . . .7131-02/002

V 900 S, 230 V, 3~, 50 Hz . . . . . .7131-02/003

– Control box

0732-100-50 for model 7131-01/002

0732-100-52 for model 7131-02/002

0732-100-58 for model 7131-02/003 – Set of connection ﬁttings – Suction hose LW 50 – Exhaust air hose LW 50 (aluminium) – Condensation separator

V 1200 S, 400 V, 3~, 50 Hz . . . . . 7136-02/002

V 1200 S, 230 V, 3~, 50 Hz . . . . . 7136-02/003

V 1200 S, 400 V, 3~, 60 Hz . . . . . 7136-03/002

V 1200 S, 230 V, 3~, 60 Hz . . . . . 7136-03/003

– Control box

0732-100-54 for model 7136-02/002 0732-100-53 for model 7136-02/003 0732-100-54 for model 7136-03/002

0732-100-58 for model 7136-03/003 – Set of connection ﬁttings – Suction hose LW 50 – Exhaust air hose LW 50 (aluminium) – Condensation separator

3.2 Special accessories

The following optional items can be used with the device:

V 300 S

Wall bracket � � � � � � � � � � � � � � � � � 7130-190-00 Noise reduction hood � � � � � � � � � � 7122200000 Condensation separator kit for hous-

ing � � � � � � � � � � � � � � � � � � � � � � � � 7119-701-20 Bacteria ﬁlter with accessories � � �7120-143-00 Ventilation kit for cabinet

installation � � � � � � � � � � � � � � � � � � �7122-981-51

V 600, V 900 S, V 1200 S

Wall bracket � � � � � � � � � � � � � � � � � 7130-190-00 Console for ﬂoor-mounted

installation � � � � � � � � � � � � � � � � � � �7130-191-00 Noise reduction hood � � � � � � � � � � 7131-991-00 Bacteria ﬁlter � � � � � � � � � � � � � � � � � 0705-991-50 Noise reduction for exhaust air � � � 0730-991-00 Ventilation kit for cabinet

installation � � � � � � � � � � � � � � � � � � �7122-981-50

3.3 Disposable materials

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 spare parts

The following working parts need to be changed at regular intervals (refer to the "Maintenance" section):

Information on spare parts can be found on the website portal for authorised specialist dealers under: www�duerrdental�net�

9000-606-89/30 1711V001 7

Product description

4 Technical data

4.1 V 300 S

Electrical data 7119-01 7119-02

Nominal voltage V 230, 1~ 230, 1~ Mains frequency Hz 50 50 60 Nominal current A 2�9 2�9 3�7 Starting current A 8�2 8�2 9�1 Motor protection Motor winding overheat protector 160 °C

Rated power W 580 580 800

Type of protection IP 24 Protection class I Protective low voltage V 24 ~ Output VA 4

Connections

Vacuum connection DürrConnect Special mm ∅ 30 Exhaust air connection (external) mm ∅ 30

Media

Max� unimpeded ﬂow rate l/min 670 670 800 Max� suction system pressure * mbar/hPa -200

* Depending on unit type

(±5 °C)

General data

Speed rpm 2750 2750 3200 Duty cycle % 100 Dimensions (H x W x D) * cm 37 x 31 x 31 Weight, approx� without housing with housing Noise level ** approx� without housing with housing

* Values without accessories and add-on parts ** Noise levels in acc� with EN ISO 1680 "airborne noise emissions"; measured in a sound-proofed

room� The levels are average values with a tolerance of ±3dB(A)� Higher values may be obtained in rooms with reverberating sound characteristics�

8 9000-606-89/30 1711V001

kg kg

dB(A) dB(A)

63 54

12�5

63 54

65 56

Product description

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 Devices Directive (93/42/EU) Class IIa

9000-606-89/30 1711V001 9

Product description

4.2 V 600

Electrical data 7127-01

Nominal voltage V 230, 1~ Mains frequency Hz 50 Nominal current A 5�0 Starting current A 22 Motor protection * A Rated power W 1100 Type of protection IP 24 Protection class I

* Recommended setting values� As the motor protection switch is subject to tolerances, current

levels should be measured during installation and the motor protection setting adjusted accordingly�

Connections

Vacuum connection (external) mm ∅ 50 Exhaust air connection (external) mm ∅ 50

Media

Max� unimpeded ﬂow rate l/min 1500 Max� suction system pressure * mbar/hPa -160

* The pressure in the suction system is limited by the supplied auxiliary air valve� The suction unit is

capable of generating greater pressure� The auxiliary air valve is adjusted to the suction unit and must not be altered�

General data

Speed rpm 2850 Duty cycle % 100 Dimensions (H x W x D) cm 50 x 42 x 41 Weight, approx� kg 25 Noise level* c� without housing with housing

* Noise levels in acc� with EN ISO 1680 "airborne noise emissions"; measured in a sound-proofed

room� The levels are average values with a tolerance of ±3dB(A)� Higher values may be obtained in rooms with reverberating sound characteristics�

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 Devices Directive (93/42/EU) Class IIa

10 9000-606-89/30 1711V001

dB(A) dB(A)

63 55

Product description

4.3 V 600

Electrical data 7127-02

Nominal voltage V 400, 3~ 230, 3~ Mains frequency Hz 50 60 50 60 Nominal current A 1�8 2�3 3�1 4�1 Starting current A 8 9 Motor protection * A 2�5 4�0 3�5 4�5 Rated power W 1000 1420 Type of protection IP 24 Protection class I

* Recommended setting values� As the motor protection switch is subject to tolerances, current

levels should be measured during installation and the motor protection setting adjusted accordingly�

Connections

Vacuum connection (external) mm ∅ 50 Exhaust air connection (external) mm ∅ 50

Media

Max� unimpeded ﬂow rate l/min 1500 1700 1500 1700 Max� suction system pressure * mbar/hPa -160

* The pressure in the suction system is limited by the supplied auxiliary air valve� The suction unit is

capable of generating greater pressure� The auxiliary air valve is adjusted to the suction unit and must not be altered�

General data

Speed rpm 2850 3300 2850 3300 Duty cycle % 100 Dimensions (H x W x D) cm 50 x 42 x 41 Weight, approx� kg 25 Noise level* c� without housing with housing

* Noise levels in acc� with EN ISO 1680 "airborne noise emissions"; measured in a sound-proofed

room� The levels are average values with a tolerance of ±3dB(A)� Higher values may be obtained in rooms with reverberating sound characteristics�

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 Devices Directive (93/42/EU) Class IIa

9000-606-89/30 1711V001 11

dB(A) dB(A)

63 55

68 58

63 55

68 58

Product description

4.4 V 900 S

Electrical data 7131-01 7131-02

Nominal voltage V 230, 1~ 230, 3~ 400, 3~ Mains frequency Hz 50 50 Nominal current A 7�4 6�3 3�6 Starting current A 32 42 25 Motor protection * A 10 6�3 4�0 Rated power W 1680 1970 Type of protection IP 24 Protection class I

* Recommended setting values� As the motor protection switch is subject to tolerances, current

levels should be measured during installation and the motor protection setting adjusted accordingly�

Connections

Vacuum connection (external) mm ∅ 50 Exhaust air connection (external) mm ∅ 50

Media

Max� unimpeded ﬂow rate l/min 2300 Max� suction system pressure * mbar/hPa -170 -170

* The pressure in the suction system is limited by the supplied auxiliary air valve� The suction unit is

capable of generating greater pressure� The auxiliary air valve is adjusted to the suction unit and must not be altered�

General data

Speed rpm 2780 2870 Duty cycle % 100 Dimensions (H x W x D) cm 55 x 42 x 41 Weight, approx� kg 32 Noise level* c� without housing with housing

* Noise levels in acc� with EN ISO 1680 "airborne noise emissions"; measured in a sound-proofed

room� The levels are average values with a tolerance of ±3dB(A)� Higher values may be obtained in rooms with reverberating sound characteristics�

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 Devices Directive (93/42/EU) Class IIa

12 9000-606-89/30 1711V001

dB(A) dB(A)

65 60

Product description

4.5 V 1200 S

Electrical data 7136-02 7136-03

Nominal voltage V 230, 3~ 400, 3~ 230, 3~ 400, 3~ Mains frequency Hz 50 60 Nominal current A 6�5 3�8 6�8 3�9 Starting current A 43 25 - 26 Motor protection * A 6�3 4�0 7�0 4�0 Rated power W 2000 2400 Type of protection IP 24 Protection class I

* Recommended setting values� As the motor protection switch is subject to tolerances, current

levels should be measured during installation and the motor protection setting adjusted accordingly�

Connections

Vacuum connection (external) mm ∅ 50 Exhaust air connection (external) mm ∅ 50

Media

Max� unimpeded ﬂow rate l/min 2400 2900 Max� suction system pressure * mbar/hPa -170 -160

* The pressure in the suction system is limited by the supplied auxiliary air valve� The suction unit is

capable of generating greater pressure� The auxiliary air valve is adjusted to the suction unit and must not be altered�

General data

Speed rpm 2860 3180 Duty cycle % 100 Dimensions (H x W x D) cm 55 x 42 x 41 Weight, approx� kg 32 Noise level* c� without housing with housing

* Noise levels in acc� with EN ISO 1680 "airborne noise emissions"; measured in a sound-proofed

room� The levels are average values with a tolerance of ±3dB(A)� Higher values may be obtained in rooms with reverberating sound characteristics�

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 Devices Directive (93/42/EU) Class IIa

9000-606-89/30 1711V001 13

dB(A) dB(A)

65 60

68 63

Product description

4.6 Type plate

V 300 S

The type plate is is located on the noise reduction hood�

1 Type plate

V 600

The type plate is located on the top part of the turbine housing�

V 900 S, V 1200 S

The type plate is located on the top part of the turbine housing�

1 Type plate

4.7 Conformity assessment

This device has been subjected to conformity acceptance testing in accordance with the current relevant European Union guidelines� This equipment conforms to all relevant requirements�

1 Type plate

14 9000-606-89/30 1711V001

5 Operation

Product description

1 Motor 2 Turbine wheel 3 Intake nozzle 4 Exhaust air mufﬂer 5 Exhaust air connection

Functional description using example of V900S

The V-suction unit is suitable for use in dry air suction systems� The advantage of this system is that the suction unit, regardless of the actual connection layout, can be installed in any available and suitable room (including upper ﬂoors or basements)� The necessary air ﬂow and vacuum are generated according to the side channel compressor principle�

On the vacuum side the V-suction unit is equipped with a condensate separator that collects any condensation arising within the pipe system and transports it away to the outside� An auxiliary air valve in the condensate separator (V 600, V 900 S, V 1200 S models only) protects the suction unit from overheating, and also ensures smooth and even suction power�

9000-606-89/30 1711V001 15

Product description

When an appropriate vacuum for the machine is applied, approx� 300 l air/min� is sucked in through the suction cannula�

The exhaust air from the suction unit should be guided out of the building (via the roof where possible)� We recommended the installation of a bacteria ﬁlter in the exhaust air line� In addition, it is possible to install a noise-reducing mufﬂer in the exhaust air line in order to reduce the amount of noise generated by the unit and by the air ﬂow�

16 9000-606-89/30 1711V001

Installation

6 Requirements

The unit can be installed either on the same level as the surgery or on a ﬂoor below�

Further information can be found in our suction planning information leaﬂet� Order number 9000-617-03/��

6.1 Installation/setup room

The room chosen for set up must fulﬁl the following requirements:

– Closed, dry, well-ventilated room – Should not be a room made for another pur-

pose (e�g� boiler room or wet cell)

Ambient and environmental conditions must be taken into account� Do not operate the unit in damp or wet conditions�

– When installing in a cabinet the inlet and outlet

ventilation slots must be present; minimum free cross-section at least 120cm

– 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m

– Do not cover cooling slots or openings

with housing installations; ensure sufﬁcient clearance to the openings to permit sufﬁcient cooling�

6.2 Setup options

The following options for setting up the unit are available:

– Wall installation using a Dürr Dental wall

mounting – In a ventilated cabinet – In a Dürr Dental noise reducing housing

6.3 Pipe materials

Only use vacuum-sealed HT-waste pipes manufactured from the following materials:

– Polypropylene (PP), – Chlorinated polyvinyl chloride (PVC-C), – Unplasticized polyvinyl chloride (PVC-U), – Polyethylene (PE)�

The following materials must not be used:

– Acrylonitrile-butadiene-styrene (ABS), – Styrene copolymer blends (e�g� SAN + PVC)�

�

/min�

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 necessary�

The following types of hoses must not be used:

– Rubber hoses – Completely PVC hoses – Hoses that are not sufﬁciently ﬂexible

6.5 Information about electrical connections

i 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�

i Install an all-pole disconnect switch with a

contact opening width of at least 3mm in the electrical connection to the mains power supply�

i Observe the current consumption of the de-

vices that are to be connected�

Electrical fusing

LS switch 16A, characteristic B, C and D in accordance with60898�

6.6 Information about connecting cables

The diameter of the connections depends on the current consumption, length of line and the ambient temperature of the unit� Information concerning the current consumption can be found in the Technical Data supplied with the particular unit to be connected�

9000-606-89/30 1711V001 17

Installation

The following table lists the minimum diameters of the connections in relation to the current consumption:

Current consumption of

unit [A]

> 10 and < 16 1�5 > 16 and < 25 2�5 > 25 and < 32 4 > 32 and < 40 6 > 40 and < 50 10 > 50 and < 63 16

Cross-section

Mains supply cable

Installation type Line layout (minimum

Fixed installation – Plastic sheathed cable

Flexible – PVC ﬂexible line

Control cable

24 V protective low voltage for:

– Hose manifold – Place selection valve – Spittoon valve

Installation type Line layout (minimum

Fixed installation – Shielded sheathed cable

Flexible – PVC data cable

requirements)

(e�g� typeNYM-J)

(e�g�H05VV-F)

– Rubber connection

(e�g�H05RN-F or H05RR-F)

requirements)

(e�g� (N)YM (St)-J)

with shielded cable sheathing, as used for telecommunications and IT processing systems (e�g� type LiYCY)

– Lightweight PVC control

cable with shielded cable sheathing

[mm

7 System components

The system components listed below are required or recommended for various procedures

]

or for installation�

7.1 Control box

The unit is connected via a control box� The control box is either included in the scope of delivery or must be ordered separately� In some units, the control system is built in�

7.2 Bacteria filter

For hygienic reasons, we recommend the installation of a bacteria ﬁlter in the exhaust air line�

If the unit is installed in the surgery and the exhaust air cannot be discharged to the outdoors, it is essential to install a bacteria ﬁlter�

Depending on the type and condition of the bacteria ﬁlter, it will need to be replaced every 1-2 years at the latest�

The separation integrated in the system does not retain bacteria; this is why we recommend installing a suitable ﬁlter in the exhaust air system�

7.3 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�

18 9000-606-89/30 1711V001

Installation

8 Installation

The actual connection can vary depending on the chosen installation option� The connection shown is only an example�

8.1 Installation and routeing of hoses and pipes

i Establish connections between the pipe system and the unit using the ﬂexible hoses supplied� This

will prevent vibrations from being transmitted to the pipe system�

i The connection between the pipe line and unit suction connection should be kept as short as pos-

sible and straight, without bends�

i Waste water connections must be implemented in accordance with applicable local and national

regulations�

V 300 S

1 Hose clamp 25-40 mm 2 Suction hose ∅ 30 mm (internal) 3 Waste air pipe (aluminium)∅ 30 mm inside 4 Hose clip ∅ 28 mm 5 Hose sleeve 6 Waste water hose ∅ 20 mm (internal)

9000-606-89/30 1711V001 19

V 900 S, V 1200 S

Installation

1 Hose clamp 40-60 mm 2 Suction hose ∅ 50 mm 3 Elbow DN 50 / 87 4 Waste air pipe (aluminium)∅ 50 mm inside 5 Hose sleeve 6 Hose clip ∅ 28 mm 7 Waste water hose ∅ 20 mm (internal)

20 9000-606-89/30 1711V001

400 V 3/N/PE 230 V 3/N/PE

9 Electrical connections

230 V 1/N/PE

NOTICE Short circuit due to defective lead

i Do not route wires near hot surfaces�

i Before connecting, check that the power sup-

ply voltage matches the voltage speciﬁcations on the type plate�

i The connection of the unit to the mains power

supply must be done by means of a permanent connection�

i Only connect the unit to an original control

box�

i Connect the power supply line from the con-

trol box to the appropriate terminals in the motor terminal box�

Installation

U2 V2 W2

Figure 2: Terminal assignment for 3-phase units

9.1 Unit with integrated control electronics

i Connect control line to control connection� i Connect mains cable to mains connection�

i Insert screwdriver into terminal strip to open

spring clamp�

i Insert stranded wire into spring clamp� i Remove screwdriver�

4123

Figure 1: Terminal assignment for 1-phase units

9000-606-89/30 1711V001 21

X1 Mains connection X2 Motor connection X3 Control connection 24V AC / max� 80mA X4 Control signal output

24V AC / max� 20mA

Installation

10 Commissioning and first

start-up

i Turn on the unit power switch or the main sur-

gery switch�

i Carry out a function check of the system� i Check all connections for leak tightness� i Carry out an electrical safety check in accord-

ance with applicable regulations (e�g� regula-

tions concerning set up, operation and appli-

cation of medical devices) and record the re-

sults as appropriate, e�g� in the technical log

book�

In many countries technical medical products and electrical devices are subject to regular checks at set intervals� The owner must be instructed accordingly�

22 9000-606-89/30 1711V001

Operation

11 Disinfection and cleaning

NOTICE Device malfunctions or damage due to use of incorrect media

Guarantee claims may become invalid as a result�

i Do not use any foaming agents, e�g�

household cleaning agents or instru-

ment disinfection agents�

i Do not use abrasive cleaners� i Do not use agents containing chlo-

rine�

i Do not use any solvents like acetone�

11.1 After every treatment

i 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�

11.3 Once or twice a week before the midday break

Under harsher conditions (e�g� hard water or frequent use of prophylaxis powders) 1x daily before the midday break

The following are required for cleaning:

– Material-compatible, non-foaming special

cleaning agents that have been approved by

Dürr Dental, e�g� MD 555 Cleaner – Unit care system, e�g� OroCup

i To pre-clean, suck up 2 litres of water with the

care system�

i Aspirate the cleaning agent with the care sys-

tem�

i Rinse with ca� 2 l water after the application

time�

11.2 Daily after the end of treatment

After higher workloads before the midday break and in the evening

The following are required for disinfection/cleaning:

– Material-compatible, non-foaming disin-

fection/cleaning agents with Dürr Dental

approval, e�g� Orotol plus� – Unit care system, e�g� OroCup

i To pre-clean, suck up 2 litres of water with the

care system�

i Aspirate the disinfection/cleaning agent with

the care system�

9000-606-89/30 1711V001 23

Operation

12 Maintenance

All maintenance work must be performed by a qualiﬁed expert or by one of our Service Technicians�

Prior to working on the device or in case of danger, disconnect it from the mains (e�g� pull the mains plug)�

WARNING Infection due to contaminated unit

i Clean and disinfect the suction before working on the unit� i Wear protective equipment when working (e�g� impermeable gloves, protective goggles

12.1 V 300 S

Every 1-2 years i Replace bacteria ﬁlter (where ﬁtted)� Every 2 years i Check waste valve on condensation separator and replace it if neces-

* Only by customer services service technicians�

12.2 V 600, V 900 S, V 1200 S

Every 1-2 years i Replace bacteria ﬁlter (where ﬁtted)� * Every 2 years i Check auxiliary air valve function and clean or replace it if necessary� *

* Only by customer services service technicians�

and mouth and nose protection)�

Maintenance interval Maintenance work

sary� *

Maintenance interval Maintenance work

i Check waste valve on condensation separator and replace it if neces-

sary� *

24 9000-606-89/30 1711V001

Troubleshooting

13 Tips for operators and service technicians

Any repairs above and beyond routine maintenance must only be carried out by suitably qualiﬁed personnel or by one of our service technicians�

WARNING Infection due to contaminated unit

i Clean and disinfect the suction before working on the unit� i Wear protective equipment when working (e�g� impermeable gloves, protective goggles

and mouth and nose protection)�

Prior to working on the device or in case of danger, disconnect it from the mains (e�g� pull the mains plug)�

Fault Probable cause Solution Device does not start No mains voltage i Check the mains supply voltage�

Undervoltage i Measure the supply voltage; call

Motor protection switch set too low

Motor protection switch defective i Check the motor protection

Capacitor defective i Measure capacitance and

Turbine is blocked by solid particles or sticky soiling

The unit generates unusual noises

Water leaking from the exhaust air connection

Solid particles in the turbine chamber

Foam in turbine due to use of incorrect cleaning and disinfectant agents

Build-up of condensate in the exhaust air line

i Check the fuses and replace if

necessary� *

an electrician if necessary� *

i Measure current, set the motor

protection switch to the measured value plus safety margin� *

switch; replace if defective� *

replace if necessary� *

i Disassemble the unit and clean

the turbine� *

i Disassemble the unit and clean

the turbine and housing� *

i Use non-foaming cleaning and

disinfectant agents�

i Check the pipe system; avoid

over-cooling� *

9000-606-89/30 1711V001 25

Troubleshooting

Fault Probable cause Solution Suction performance too

low

* Only by customer services service technicians�

Coarse ﬁlters in system clogged (e�g� at separator devices)

Leak in the suction line i Check and if necessary establish

Mechanical sluggishness of turbine caused by soiling

i Clean coarse ﬁlters�

leak-tightness of suction system and connections� *

i Disassemble the unit and clean

the turbine� *

26 9000-606-89/30 1711V001

14 Transporting the unit

WARNING Infection due to contaminated unit

i Disinfect the unit before transport� i Close all media connections�

Wear protective equipment to avoid any risk of infection (e�g� liquid-tight protective gloves, protective goggles, face mask)�

i Before disassembly, clean and disinfect the

suction unit and the unit using a suitable disinfectant approved by Dürr Dental�

i Disinfect a defective unit using a suitable sur-

face disinfection agent�

i Seal all connections with sealing caps� i Pack the unit securely in preparation for trans-

port�

Troubleshooting

Figure 3: V 900 S, V 1200 S

1 Sealing cap

9000-606-89/30 1711V001 27

Appendix

The following information only applies to the V300S�

15 Information about EMC in accordance with EN 60601-1-2

15.1 General information

The information in this leaﬂet includes excerpts from the relevant European standards for electrical, medical devices� It must be observed when installing Dürr Dental devices or combining them with products of other manufacturers� If you are uncertain about anything, please refer to the complete standard�

15.2 Abbreviations

EMC Electromagnetic compatibility HF High frequency U V

P Rated power of the transmitter in Watts (W) in accordance with the speciﬁcations of the

d Recommended safety distance in metres (m)

15.3 Guidelines and manufacturer's information

Electromagnetic emissions for all devices and systems

The device is designed for operation in an electromagnetic environment as speciﬁed below� The customer or operator of the device should ensure that the device is operated in such an environment�

Interference emission measurements

HF emissions in accordance with CISPR11

Harmonics in acc� with IEC61000-3-2

Voltage ﬂuctuations/ﬂickers in acc� with IEC61000-3-3

Rated voltage of the device (supply voltage)

, V2Compliance level for the test in acc� with IEC61000-4-6

Compliance level for the test in acc� with IEC61000-4-3

transmitter manufacturer

Compliance

Group 1 The suction unit uses HF energy exclusively for internal

Class B The suction unit is suitable for use in all facilities includ-

Class A

Compliant

Electromagnetic environment - guidelines

functions� For this reason, HF emissions are very low and it is unlikely that any interference will be caused to neighbouring electronic devices�

ing those in living areas and areas that are directly connected to the public mains electricity supply that also supplies buildings used for residential purposes�

28 9000-606-89/30 1711V001

Appendix

Resistance to electromagnetic interference (immunity) for all devices and systems

The device is designed for use in electromagnetic environments speciﬁed below� The customer or operator of the device should ensure that the device is operated such an environment�

Interference immunity tests

Electrostatic discharge (ESD) in acc� with IEC61000-4-2

IEC 60601 - test level

±6kV contact discharge

±8kV air discharge

Compliance level Electromagnetic environment

- guidelines

±9kV contact discharge

±9kV air discharge

Floors should be made of wood or cement, or covered with ceramic tiles� If the ﬂoor is covered by synthetic material, then the relative humidity must be at least 30%�

Electrical fast transient/burst immunity test in accordance with IEC61000-4-4

Voltage surge in accordance with IEC61000-4-5

±2kV for mains cables

±1kV for input and output cables

±1kV voltage outer conductor/outer conductor

±2kV voltage outer

±2�5kV for mains

cables ±2�5kV for input

and output cables ±1kV push-pull volt-

age ±2kV common

mode voltage

The quality of the supply voltage should correspond to a typical commercial or hospital environment�

conductor/earth

Voltage drops, short-term interruptions and ﬂuctuations of the supply voltage in accordance with IEC61000-4-11

Magnetic ﬁeld for a supply frequency (50/60Hz) in accordance with IEC61000-4-8

(> 95%

< 5% U

drop in UT) for 1/2 period

40% U

(60% drop

in UT) for 5 periods 70% U

(30% drop

in UT) for 25 periods < 5% U

(> 95%

drop in U

) for 5 s

< 5% U drop in UT) for 1/2

(> 95%

period 40% U

(60% drop

in UT) for 5 periods 70% U

(30% drop

in UT) for 25 periods < 5% U

drop in U

(> 95%

) for 5 s

3 A/m 30 A/m The magnetic ﬁelds at electrical

The quality of the supply voltage should correspond to a typical commercial or hospital environment� If the operator of the device needs the unit to continue working even if the mains power supply is interrupted, we recommend powering the device from an uninterruptible power supply (UPS) or from a battery�

frequency should be within the range of typical values encountered in a commercial or hospital environment�

Table 1: Resistance to electromagnetic interference (immunity) for all devices and systems

9000-606-89/30 1711V001 29

Appendix

Electromagnetic interference immunity for devices or systems that are not life-sustaining

Portable and mobile communication devices should not be used any closer to the unit (including cables) than the recommended safety distance, which is calculated based on the applicable formula for the transmission frequency�

Interference immunity tests

Conducted HF disturbance varia-

IEC 60601 - test level

3V

150kHz to

eff

80MHz

Compliance

Recommended safety distance

level

[V1] = 10 V d = 0�35 ⋅ √P

bles in accordance with IEC61000-4-6

Emitted HF distur-

bance variables in accordance with

10V/m 80MHz up to 2�7GHz

] = 10 V/m d = 0�35 ⋅ √P for 80 MHz to 1000 MHz

d = 0�7 ⋅ √P for 1000 MHz to 2�7 GHz

IEC61000-4-3

Table 2: Electromagnetic interference immunity for units or systems operated in healthcare facilities

P Rated power of the transmitter in Watts (W) in accordance with the speciﬁcations of the

transmitter manufacturer

d Recommended safety distance in metres (m)

The ﬁeld strength of stationary communication devices should be lower than the compliance level for all frequencies based on inspections on sitea�

Interference is possible in the environment of units that have the following symbols�

Comment 1 The higher frequency range applies for 80 MHz and 800 MHz� Comment 2 These guidelines may not apply in all cases� The propagation of electromagnetic

radiation is affected by absorption and reﬂection on the building, objects and people�

The ﬁeld strength of stationary transmitters, such as the base stations of mobile phones and land mobile radios, amateur radio stations, AM and FM radio and television broadcasters, for example, cannot be accurately predicted� In order to determine the electromagnetic environment with regard to stationary transmitters, a study of electromagnetic phenomena at the site should be considered� If the measured ﬁeld strength at the location where the unit is used exceeds the compliance levels stated above, the unit should be monitored to verify that it works as intended� If unusual performance characteristics are observed additional measures may be required, such as a changing the orientation of the unit or moving it to a different location�

Over the frequency range of 150 kHz to 80 MHz, the ﬁeld strength should be less than [V1] V/m�

30 9000-606-89/30 1711V001

Appendix

Recommended safety distance between portable and mobile HF communication devices and the unit

The device is designed for use in the electromagnetic environments speciﬁed below, in which the HF disturbance variables are controlled� The customer or the operator of the device can help to prevent electromagnetic interference by maintaining the minimum distances between mobile HF communication equipment (transmitters) and the device as recommended below in accordance with the maximum output line of the communication equipment�

Keep a minimum distance of 30 cm between the device and mobile communication devices�

Rated power of the transmitter (W)

0�1 0�11 0�11 0�22 1 0�35 0�35 0�7 10 1�11 1�11 2�21 100 3�5 3�5 7

Table 3: Recommended safety distance between portable and mobile HF communication devices and the unit

For transmitters whose maximum rated power is not speciﬁed in the table shown above, the recommended safety distance d in metres (m) can be determined from the formula that belongs to the respective column where P is the maximum rated power of the transmitter in watts (W) in accordance with the speciﬁcations of the transmitter manufacturer�

Comment 1 The higher frequency range applies for 80 MHz and 800 MHz� Comment 2 These guidelines may not apply in all cases� The propagation of electromagnetic

waves is affected by absorption and reﬂection on the building, objects and people�

Safety distance based on the transmission frequency (m)

150 kHz to 80 MHz d = 0.35 ⋅√P

80 MHz to 1000 MHz d = 0.35 ⋅√P

1000 MHz to 2.7 GHz d = 0.7 ⋅√P

9000-606-89/30 1711V001 31

Hersteller/Manufacturer:

DÜRR DENTAL SE

Höpfigheimer Str. 17

74321 Bietigheim-Bissingen

Germany

Fon: +49 7142 705-0

www.duerrdental.com info@duerrdental.com

Durr Dental V 600, V 900 S, V 1200 S, V 300 S Installation And Operating Instructions Manual

Specifications and Main Features

Frequently Asked Questions

User Manual