Durr Dental V 300 S User manual

EN
V 300 S / VS 300 S
Installation and operating instructions
0297
7119100007L02
*7119100007L02*
1909V001

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 Systems, connection with other
devices .. . . . . . . . . . . . . . . . . . . 5
2.5 General safety information .. . . . . 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 .. . . . . . . . 6
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 V 300 S .. . . . . . . . . . . . . . . . . . . 9
4.2 VS 300 S .. . . . . . . . . . . . . . . . . 13
4.3 VS 300 S .. . . . . . . . . . . . . . . . . 17
4.4 Type plate .. . . . . . . . . . . . . . . . . 21
4.5 Evaluation of conformity .. . . . . . 21
5 Operation .. . . . . . . . . . . . . . . . . . . . . . 22
5.1 V 300 S .. . . . . . . . . . . . . . . . . . . 22
5.2 VS 300 S .. . . . . . . . . . . . . . . . . 24
Assembly
6 Requirements .. . . . . . . . . . . . . . . . . . . 26
6.1 Installation/setup room .. . . . . . . 26
6.2 Setup options .. . . . . . . . . . . . . . 26
6.3 Pipe materials .. . . . . . . . . . . . . . 26
6.4 Hose materials .. . . . . . . . . . . . . 26
6.5 Information about electrical con-
nections .. . . . . . . . . . . . . . . . . . 26
6.6 Information about connecting
cables .. . . . . . . . . . . . . . . . . . . . 26
7 System components .. . . . . . . . . . . . . . 27
7.1 Rinsing unit .. . . . . . . . . . . . . . . . 27
7.2 Flow accelerator .. . . . . . . . . . . . 27
7.3 Amalgam separator .. . . . . . . . . . 27
7.4 Surge tank .. . . . . . . . . . . . . . . . 27
7.5 Bacteria filter .. . . . . . . . . . . . . . . 28
7.6 Noise reduction .. . . . . . . . . . . . . 28
8 Installation .. . . . . . . . . . . . . . . . . . . . . . 29
8.1 Installation and routeing of hoses
and pipes .. . . . . . . . . . . . . . . . . 29
9 Electrical connections .. . . . . . . . . . . . 31
10 Commissioning .. . . . . . . . . . . . . . . . . . 31
Usage
11 Disinfection and cleaning .. . . . . . . . . . 32
11.1 After every treatment .. . . . . . . . . 32
11.2 Daily after the end of treatment .. 32
11.3 Once or twice a week before the
midday break .. . . . . . . . . . . . . . 32
12 VS 300 S .. . . . . . . . . . . . . . . . . . . . . . . 33
12.1 Cleaning the protective strainer .. 33
13 Maintenance .. . . . . . . . . . . . . . . . . . . . 34
13.1 V 300 S .. . . . . . . . . . . . . . . . . . . 34
13.2 VS 300 S .. . . . . . . . . . . . . . . . . 34
Contents
7119100007L02 1909V001 1
EN

Troubleshooting
14 Tips for operators and service techni-
cians .. . . . . . . . . . . . . . . . . . . . . . . . . . 35
15 Transporting the unit .. . . . . . . . . . . . . 37
Appendix
16 Handover record .. . . . . . . . . . . . . . . . . 38
Contents
2 7119100007L02 1909V001
EN

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:
V 300 S
Order number: 7119-01; 7119-01/002; 7119-02;
7119-02/002
VS 300 S
Order number: 7122-01; 7122-01/002;
7122-01/021; 7122-02; 7122-02/002; 7122-03;
7122-03/002; 7122-04; 7122-04/002;
7122-05/003
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 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.
Refer to Operating Instructions.
Wear protective gloves.
Disconnect all power from the unit.
Refer to the accompanying electronic
documents.
XX
YY
Lower and upper temperature limits
xx %
xx %
Lower and upper humidity limits
Protective ground connection
CE labelling with the number of the noti-
fied body
Serial number
Important information
7119100007L02 1909V001 3
EN

Order number
Medical device
Health Industry Bar Code (HIBC)
Manufacturer
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
Dental.
2 Safety
Dürr Dental has designed and constructed this
unit so that when used properly and for the
intended 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 7119100007L02 1909V001
EN

❯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.
2.4 Systems, connection with
other devices
Additional devices connected with medical elec-
trical devices must be proven to conform with
their corresponding IEC or ISO standards. All
configurations must continue to comply with the
standard requirements for medical systems (see
IEC 60601-1).
Whoever connects additional devices to medical
electrical devices automatically becomes the sys-
tem configurator and is responsible for ensuring
that the system corresponds with the standard
requirements for systems. Local laws take priority
over the requirements outlined above.
2.5 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.
2.6 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.
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.
Observe the EMC rules concerning medical
devices
❯The unit is intended for use in professional
healthcare facilities (in accordance with IEC
60601-1-2). If the appliance is operated in
another environment, potential effects on elec-
tromagnetic compatibility must be taken into
account.
❯Do not operate the unit in the vicinity of HF sur-
gical instruments or MRT equipment.
❯Maintain a minimum distance of at least 30 cm
between the unit and other electronic devices.
❯Note that cable lengths and cable extensions
have effects on electromagnetic compatibility.
❯No maintenance measures are required to
maintain the EMV basic safety.
NOTICE
Negative effects on the EMC due to
non-authorised accessories
❯Use only Dürr Dental parts or acces-
sories specifically approved by Dürr
Dental.
❯Using any other accessories may result
in increased electromagnetic interfer-
ence emissions or the unit having
reduced electromagnetic immunity,
leading to an erroneous operation
mode.
Important information
7119100007L02 1909V001 5
EN

NOTICE
Erroneous operation mode due to use
immediately adjacent to other devices
or with other stacked devices
❯Do not stack the unit together with
other devices.
❯If this is unavoidable, the unit and other
devices should be monitored in order
to ensure that they are working cor-
rectly.
NOTICE
Reduced performance characteristics
due to insufficient distance between
unit and portable HF communication
devices
❯Keep a distance of at least 30 cm
between the unit (including parts and
cables of the unit) and portable HF
communication devices (wireless units)
(including their accessories such as
antenna cables and external anten-
nas).
2.9 Only use original parts
❯Only use Dürr Dental parts or accessories and
special accessories specifically approved by
Dürr Dental.
❯Only use only original wear parts and replace-
ment parts.
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 7119100007L02 1909V001
EN

Product description
3 Overview
3
4
5
1
2
6
Fig. 1: V 300 S
1 Suction unit
2 Condensation separator
3 Suction hose
4 Exhaust air hose (aluminium)
5 Waste hose LW 20
6 Set of connection fittings
2
3
4
1
5
Fig. 2: VS 300 S
1 Combination suction unit
2 Suction hose
3 Exhaust air hose (aluminium)
4 Waste hose LW 20
5 Set of connection fittings
Product description
7119100007L02 1909V001 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):
V 300 S, 230 V, 1~, 50 Hz .. . . . . . . . . . 7119-01
V 300 S, 230 V, 1~, 50/60 Hz .. . . . . . . 7119-02
– Connector set
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
VS 300 S, 230 V, 1~, 50 Hz .. . . . . . . . . 7122-01
VS 300 S, 230 V, 1~, 50/60 Hz .. . . . . . 7122-02
VS 300 S, 230 V, 1~, 60 Hz .. . . . . . . . . 7122-03
VS 300 S, 230 V, 1~, 50 Hz, with rins-
ing unit .. . . . . . . . . . . . . . . . . . . . . . . . 7122-04
– Connector set
VS 300 S, 230 V, 1~, 50 Hz .. . . . . 7122-01/002
VS 300 S, 230 V, 1~, 50/60 Hz .. . 7122-02/002
VS 300 S, 230 V, 1~, 60 Hz .. . . . . 7122-03/002
VS 300 S, 230 V, 1~, 50 Hz, with
rinsing unit .. . . . . . . . . . . . . . . . . . 7122-04/002
VS 300 S, 100 V, 1~, 50/60 Hz .. . 7122-05/003
– Set of connection fittings
– Suction hose LW 30, grey
– Exhaust air hose LW 30, aluminium
– Waste hose LW 20
– OroCup
3.2 Optional items
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
housing .. . . . . . . . . . . . . . . . . . . . . 7119-701-20
Bacteria filter with accessories .. . . 7120-143-00
Ventilation kit for cabinet installa-
tion .. . . . . . . . . . . . . . . . . . . . . . . . 7122-981-51
Console for floor-mounted installa-
tion .. . . . . . . . . . . . . . . . . . . . . . . . 7130-191-00
VS 300 S
Wall bracket .. . . . . . . . . . . . . . . . . 7130-190-00
Noise reduction hood .. . . . . . . . . . 7122200000
Bacteria filter with accessories .. . . 7120-143-00
Rinsing unit .. . . . . . . . . . . . . . . . . . 7100-120-54
Rinsing unit II .. . . . . . . . . . . . . . . . 7100-250-50
Ventilation kit for cabinet installa-
tion .. . . . . . . . . . . . . . . . . . . . . . . . 7122-981-51
Secretion filter .. . . . . . . . . . . . . . . . 7123-120-00
Console for floor-mounted installa-
tion .. . . . . . . . . . . . . . . . . . . . . . . . 7130-191-00
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
The following working parts need to be changed
at regular intervals (refer to the "Maintenance"
section):
Nonreturn valve (pack of 3) .. . . . . 7128-100-03E
Information about replacement parts is
available from the portal for authorised
specialist dealers at:
www.duerrdental.net.
Product description
8 7119100007L02 1909V001
EN

4 Technical data
4.1 V 300 S
Electrical data 7119-01 7119-02
Rated voltage V 230, 1~ 230, 1~
Mains frequency Hz 50 50 60
Nominal current A 2.9 2.9 3.7
Starting current, approx. A 10.4 10.4 9.5
Motor protection Motor winding overheat protector 160 °C
(±5 °C)
Rated power W 580 580 800
Type of protection IP 24
Protection class I
Protective low voltage V 24 ~
Output VA 4
Connections
Suction connection, DürrConnect special mm Æ30
Exhaust air connection (external) mm Æ30
Media
Max. unimpeded flow rate l/min 700 700 800
Max. suction system pressure * mbar/hPa -200
* Depending on unit type
General data
Duty cycle % 100
Dimensions (H x W x D) * cm 38 x 31 x 32
Weight, approx.
without housing
with housing
kg
kg
13
21
Noise level ** approx.
without housing
with housing
dB(A)
dB(A)
63
51
63
51
65
54
* Values without accessories and add-on parts
** Noise level in accordance with ISO 3746
Ambient conditions during storage and transport
Temperature °C -10 to +60
Relative humidity % < 95
Product description
7119100007L02 1909V001 9
EN

Ambient conditions during operation
Temperature °C +10 to +40
Relative humidity % < 70
Classification
Medical devices class IIa
Electromagnetic compatibility (EMC)
Interference emission measurements
High-frequency emissions in accordance with CISPR 11 Group 1
Class B
Interference voltage at the power supply connection
CISPR 11:2009+A1:2010
Compliant
Electromagnetic interference radiation
CISPR 11:2009+A1:2010
Compliant
Emission of harmonics
IEC 61000-3-2:2005+A1:2008+A2:2009
Compliant
Voltage changes, voltage fluctuations and flicker emis-
sions
IEC 61000-3-3:2013
Compliant
Electromagnetic compatibility (EMC)
Interference immunity measurements
Immunity to electrostatic discharge
IEC 61000-4-2:2008
Compliant
Immunity to high-frequency electromagnetic fields
IEC 61000-4-3:2006+A1:2007+A2:2010
Compliant
Immunity to near fields of wireless HF communication
devices
IEC 61000-4-3:2006+A1:2007+A2:2010
Compliant
Immunity to fast electrical transients/bursts – AC mains
voltage
IEC 61000-4-4:2012
Compliant
Immunity to electrical fast transients/bursts – I/O,
SIP/SOP ports
IEC 61000-4-4:2012
Compliant
Immunity to interference, surges
IEC 61000-4-5:2005
Compliant
Immunity to conducted disturbances, induced by radio-
frequency fields – AC mains voltage
IEC 61000-4-6:2013
Compliant
Immunity to conducted disturbances, induced by radio-
frequency fields – SIP/SOP ports
IEC 61000-4-6:2013
Compliant
Immunity to power frequency magnetic fields
IEC 61000-4-8:2009
Compliant
Product description
10 7119100007L02 1909V001
EN

Electromagnetic compatibility (EMC)
Interference immunity measurements
Immunity to voltage dips, short interruptions and voltage
variations
IEC 61000-4-11:2004
Compliant
Immunity to interference table, near fields of wireless HF communication devices
Radio service Frequency band
MHz
Test level
V/m
TETRA 400 380 - 390 27
GMRS 460
FRS 460 430 - 470 28
LTE band 13, 17 704 - 787 9
GSM 800/900
TETRA 800
iDEN 820
CDMA 850
LTE band 5
800 - 960 28
GSM 1800
CDMA 1900
GSM 1900
DECT
LTE band 1, 3, 4, 25
UMTS
1700 - 1990 28
Bluetooth
WLAN 802.11 b/g/n
RFID 2450
LTE band 7
2400 - 2570 28
WLAN 802.11 a/n 5100 - 5800 9
Electromagnetic compatibility (EMC)
Interference immunity measurements on the supply input
Immunity to fast electrical transients/bursts – AC mains
voltage
IEC 61000-4-4:2012
± 2 kV
100 kHz repetition rate
Compliant
Immunity to surges, line-to-line
IEC 61000-4-5:2005
± 0.5 kV, ± 1 kV
Compliant
Immunity to surges, line-earth
IEC 61000-4-5:2005
± 0.5 kV, ± 1 kV, ± 2 kV
Compliant
Product description
7119100007L02 1909V001 11
EN

Electromagnetic compatibility (EMC)
Interference immunity measurements on the supply input
Immunity to conducted disturbances, induced by radio-
frequency fields – AC mains voltage
IEC 61000-4-6:2013
3 V
0.15–80 MHz
6 V
ISM frequency bands
0.15–80 MHz
80% AM at 1 kHz
Compliant
Immunity to voltage dips, short interruptions and voltage
variations
IEC 61000-4-11:2004
Compliant
Electromagnetic compatibility (EMC)
Interference immunity measurements SIP/SOP
Immunity to electrostatic discharge
IEC 61000-4-2:2008
± 8 kV contact
± 2kV, ± 4 kV, ± 8 kV, ± 15 kV air
Compliant
Immunity to electrical fast transients/bursts – I/O,
SIP/SOP ports
IEC 61000-4-4:2012
± 1 kV
100 kHz repetition rate
Compliant
Immunity to impulse voltages, conductor to earth
IEC 61000-4-5:2005
± 2 kV
Immunity to conducted disturbances, induced by radio-
frequency fields – SIP/SOP ports
IEC 61000-4-6:2013
3 V
0.15–80 MHz
6 V
ISM frequency bands
0.15–80 MHz
80% AM at 1 kHz
Compliant
Product description
12 7119100007L02 1909V001
EN

4.2 VS 300 S
Electrical data 7122-01
7122-04
7122-02 7122-03
Rated voltage V 230, 1~ 230, 1~ 230, 1~
Mains frequency Hz 50 50 60 60
Nominal current A 2.9 2.9 3.7 3.7
Starting current, approx. A 10.4 10.4 9.5 9.5
Motor protection Motor winding overheat protector 160 °C
(±5 °C)
Rated power W 580 580 800 800
Type of protection IP 24
Protection class I
Protective low voltage V 24 ~
Output VA 4
Connections
Suction connection, DürrConnect special mm Æ30
Exhaust air connection (external) mm Æ30
Drain connection, DürrConnect mm Æ20
Media
Max. unimpeded flow rate l/min 700 700 800 800
Max. suction system pressure * mbar/hPa -200
Max. rate of flow of fluids l/min 4
Max. suction height cm 50
* Depending on unit type
General data
Duty cycle % 100
Dimensions (H x W x D) * cm 38 x 31 x 32
Weight, approx.
without housing
with housing
kg
kg
13.5
21.5
Noise level ** approx.
without housing
with housing
dB(A)
dB(A)
63
51
63
51
65
54
65
54
* Values without accessories and add-on parts
** Noise level in accordance with ISO 3746
Ambient conditions during storage and transport
Temperature °C -10 to +60
Product description
7119100007L02 1909V001 13
EN

Ambient conditions during storage and transport
Relative humidity % < 95
Ambient conditions during operation
Temperature °C +10 to +40
Relative humidity % < 70
Classification
Medical devices class IIa
Electromagnetic compatibility (EMC)
Interference emission measurements
High-frequency emissions in accordance with CISPR 11 Group 1
Class B
Interference voltage at the power supply connection
CISPR 11:2009+A1:2010
Compliant
Electromagnetic interference radiation
CISPR 11:2009+A1:2010
Compliant
Emission of harmonics
IEC 61000-3-2:2005+A1:2008+A2:2009
Compliant
Voltage changes, voltage fluctuations and flicker emis-
sions
IEC 61000-3-3:2013
Compliant
Electromagnetic compatibility (EMC)
Interference immunity measurements
Immunity to electrostatic discharge
IEC 61000-4-2:2008
Compliant
Immunity to high-frequency electromagnetic fields
IEC 61000-4-3:2006+A1:2007+A2:2010
Compliant
Immunity to near fields of wireless HF communication
devices
IEC 61000-4-3:2006+A1:2007+A2:2010
Compliant
Immunity to fast electrical transients/bursts – AC mains
voltage
IEC 61000-4-4:2012
Compliant
Immunity to electrical fast transients/bursts – I/O,
SIP/SOP ports
IEC 61000-4-4:2012
Compliant
Immunity to interference, surges
IEC 61000-4-5:2005
Compliant
Immunity to conducted disturbances, induced by radio-
frequency fields – AC mains voltage
IEC 61000-4-6:2013
Compliant
Product description
14 7119100007L02 1909V001
EN

Electromagnetic compatibility (EMC)
Interference immunity measurements
Immunity to conducted disturbances, induced by radio-
frequency fields – SIP/SOP ports
IEC 61000-4-6:2013
Compliant
Immunity to power frequency magnetic fields
IEC 61000-4-8:2009
Compliant
Immunity to voltage dips, short interruptions and voltage
variations
IEC 61000-4-11:2004
Compliant
Immunity to interference table, near fields of wireless HF communication devices
Radio service Frequency band
MHz
Test level
V/m
TETRA 400 380 - 390 27
GMRS 460
FRS 460 430 - 470 28
LTE band 13, 17 704 - 787 9
GSM 800/900
TETRA 800
iDEN 820
CDMA 850
LTE band 5
800 - 960 28
GSM 1800
CDMA 1900
GSM 1900
DECT
LTE band 1, 3, 4, 25
UMTS
1700 - 1990 28
Bluetooth
WLAN 802.11 b/g/n
RFID 2450
LTE band 7
2400 - 2570 28
WLAN 802.11 a/n 5100 - 5800 9
Electromagnetic compatibility (EMC)
Interference immunity measurements on the supply input
Immunity to fast electrical transients/bursts – AC mains
voltage
IEC 61000-4-4:2012
± 2 kV
100 kHz repetition rate
Compliant
Immunity to surges, line-to-line
IEC 61000-4-5:2005
± 0.5 kV, ± 1 kV
Compliant
Immunity to surges, line-earth
IEC 61000-4-5:2005
± 0.5 kV, ± 1 kV, ± 2 kV
Compliant
Product description
7119100007L02 1909V001 15
EN

Electromagnetic compatibility (EMC)
Interference immunity measurements on the supply input
Immunity to conducted disturbances, induced by radio-
frequency fields – AC mains voltage
IEC 61000-4-6:2013
3 V
0.15–80 MHz
6 V
ISM frequency bands
0.15–80 MHz
80% AM at 1 kHz
Compliant
Immunity to voltage dips, short interruptions and voltage
variations
IEC 61000-4-11:2004
Compliant
Electromagnetic compatibility (EMC)
Interference immunity measurements SIP/SOP
Immunity to electrostatic discharge
IEC 61000-4-2:2008
± 8 kV contact
± 2kV, ± 4 kV, ± 8 kV, ± 15 kV air
Compliant
Immunity to electrical fast transients/bursts – I/O,
SIP/SOP ports
IEC 61000-4-4:2012
± 1 kV
100 kHz repetition rate
Compliant
Immunity to impulse voltages, conductor to earth
IEC 61000-4-5:2005
± 2 kV
Immunity to conducted disturbances, induced by radio-
frequency fields – SIP/SOP ports
IEC 61000-4-6:2013
3 V
0.15–80 MHz
6 V
ISM frequency bands
0.15–80 MHz
80% AM at 1 kHz
Compliant
Product description
16 7119100007L02 1909V001
EN

4.3 VS 300 S
Electrical data 7122-05
Rated voltage V 100, 1~
Mains frequency Hz 50 60
Nominal current A 8 10
Starting current, approx. A 21 20.5
Motor protection Motor winding overheat protector 160 °C
(±5 °C)
Rated power W 650 850
Type of protection IP 24
Protection class I
Protective low voltage V 24 ~
Output VA 4
Connections
Suction connection, DürrConnect special mm Æ30
Exhaust air connection (external) mm Æ30
Drain connection, DürrConnect mm Æ20
Media
Max. unimpeded flow rate l/min 700 800
Max. suction system pressure * mbar/hPa -200
Max. rate of flow of fluids l/min 4
Max. suction height cm 50
* Depending on unit type
General data
Duty cycle % 100
Dimensions (H x W x D) * cm 38 x 31 x 32
Weight, approx.
without housing
with housing
kg
kg
13.5
21.5
Noise level ** approx.
without housing
with housing
dB(A)
dB(A)
63
51
65
54
* Values without accessories and add-on parts
** Noise level in accordance with ISO 3746
Ambient conditions during storage and transport
Temperature °C -10 to +60
Relative humidity % < 95
Product description
7119100007L02 1909V001 17
EN

Ambient conditions during operation
Temperature °C +10 to +40
Relative humidity % < 70
Classification
Medical devices class IIa
Electromagnetic compatibility (EMC)
Interference emission measurements
High-frequency emissions in accordance with CISPR 11 Group 1
Class B
Interference voltage at the power supply connection
CISPR 11:2009+A1:2010
Compliant
Electromagnetic interference radiation
CISPR 11:2009+A1:2010
Compliant
Emission of harmonics
IEC 61000-3-2:2005+A1:2008+A2:2009
Compliant
Voltage changes, voltage fluctuations and flicker emis-
sions
IEC 61000-3-3:2013
Compliant
Electromagnetic compatibility (EMC)
Interference immunity measurements
Immunity to electrostatic discharge
IEC 61000-4-2:2008
Compliant
Immunity to high-frequency electromagnetic fields
IEC 61000-4-3:2006+A1:2007+A2:2010
Compliant
Immunity to near fields of wireless HF communication
devices
IEC 61000-4-3:2006+A1:2007+A2:2010
Compliant
Immunity to fast electrical transients/bursts – AC mains
voltage
IEC 61000-4-4:2012
Compliant
Immunity to electrical fast transients/bursts – I/O,
SIP/SOP ports
IEC 61000-4-4:2012
Compliant
Immunity to interference, surges
IEC 61000-4-5:2005
Compliant
Immunity to conducted disturbances, induced by radio-
frequency fields – AC mains voltage
IEC 61000-4-6:2013
Compliant
Immunity to conducted disturbances, induced by radio-
frequency fields – SIP/SOP ports
IEC 61000-4-6:2013
Compliant
Immunity to power frequency magnetic fields
IEC 61000-4-8:2009
Compliant
Product description
18 7119100007L02 1909V001
EN