Durr Dental Vector Paro User manual

EN
Vector Paro / Vector Paro Pro
Installation and operating instructions
0297
9000-615-28/02
*9000-615-28/02*
1903V004

Contents
Important information
1About this document .. . . . . . . . . . . . . 3
1.1 Warnings and symbols .. . . . . . . 3
1.2 Copyright information .. . . . . . . . 4
2 Safety .. . . . . . . . . . . . . . . . . . . . . . . . . 5
2.1 Intended purpose .. . . . . . . . . . . 5
2.2 Intended use .. . . . . . . . . . . . . . . 5
2.3 Improper use .. . . . . . . . . . . . . . . 5
2.4 General safety information .. . . . . 5
2.5 Specialist personnel .. . . . . . . . . 5
2.6 Electrical safety .. . . . . . . . . . . . . 6
2.7 Only use original parts .. . . . . . . . 6
2.8 Transport .. . . . . . . . . . . . . . . . . . 6
2.9 Disposal .. . . . . . . . . . . . . . . . . . 7
Product description
3Overview .. . . . . . . . . . . . . . . . . . . . . . . 8
3.1 Vector Paro / Vector Paro Pro .. . 8
3.2 Scope of delivery .. . . . . . . . . . . . 10
3.3 Accessories .. . . . . . . . . . . . . . . . 10
3.4 Consumables .. . . . . . . . . . . . . . 10
3.5 Wear parts and replacement
parts .. . . . . . . . . . . . . . . . . . . . . 11
4Technical data .. . . . . . . . . . . . . . . . . . . 12
4.1 Type plate .. . . . . . . . . . . . . . . . . 14
4.2 Order number and serial number
for the handpieces .. . . . . . . . . . 14
4.3 ID number for tool kits .. . . . . . . . 14
4.4 Evaluation of conformity .. . . . . . 15
5 Operation .. . . . . . . . . . . . . . . . . . . . . . 15
5.1 Handpieces .. . . . . . . . . . . . . . . . 15
5.2 Fluid container .. . . . . . . . . . . . . . 15
5.3 Instrument change .. . . . . . . . . . 16
Assembly
6 Requirements .. . . . . . . . . . . . . . . . . . . 17
7 Installation .. . . . . . . . . . . . . . . . . . . . . . 17
7.1 Establishing the electrical con-
nections .. . . . . . . . . . . . . . . . . . 17
7.2 Connecting the flexible foot
switch .. . . . . . . . . . . . . . . . . . . . 18
8 Commissioning .. . . . . . . . . . . . . . . . . . 19
8.1 Function check .. . . . . . . . . . . . . 19
Usage
9 Components .. . . . . . . . . . . . . . . . . . . . 20
9.1 Paro handpiece .. . . . . . . . . . . . . 20
9.2 Scaler handpiece .. . . . . . . . . . . . 23
9.3 Instruments and tool kits .. . . . . . 24
9.4 Steri-box .. . . . . . . . . . . . . . . . . . 27
9.5 Flexible foot switch .. . . . . . . . . . 27
9.6 Service kit .. . . . . . . . . . . . . . . . . 28
9.7 Fluid container .. . . . . . . . . . . . . . 28
9.8 Vector Fluid Polish .. . . . . . . . . . . 28
9.9 Cleaning components .. . . . . . . . 29
9.10 Vector toolcard .. . . . . . . . . . . . . 29
10 Operation .. . . . . . . . . . . . . . . . . . . . . . 30
10.1 Display/handling .. . . . . . . . . . . . 30
10.2 Adjustment options .. . . . . . . . . . 31
10.3 Preparing the device for treat-
ment .. . . . . . . . . . . . . . . . . . . . . 32
11 Treatment .. . . . . . . . . . . . . . . . . . . . . . 36
11.1 Preparation .. . . . . . . . . . . . . . . . 36
11.2 Treatment using the Paro hand-
piece .. . . . . . . . . . . . . . . . . . . . . 36
11.3 Treatment with a Scaler hand-
piece .. . . . . . . . . . . . . . . . . . . . . 38
11.4 Use of the Scaler instruments .. . 39
11.5 After every treatment .. . . . . . . . . 40
12 Cleaning .. . . . . . . . . . . . . . . . . . . . . . . 40
12.1 Cleaning of the outside surfaces .. 40
Contents
9000-615-28L02 1903V004 1
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12.2 Activating the cleaning process
of the device .. . . . . . . . . . . . . . . 41
12.3 Cleaning the fluid container .. . . . 43
12.4 Cleaning the sleeve part and
adapter of the handpiece hose .. 43
13 Reprocessing .. . . . . . . . . . . . . . . . . . . 44
13.1 Risk analysis and categorisation .. 44
13.2 Reprocessing procedure in
accordance with EN ISO 17664 .. 44
13.3 Preparation at the operating
location .. . . . . . . . . . . . . . . . . . . 46
13.4 Dismantling the handpiece .. . . . 47
13.5 Manual cleaning, intermediate
rinsing, disinfection, final rinsing,
drying in the cleaning and disin-
fection bath .. . . . . . . . . . . . . . . . 47
13.6 Manual cleaning, intermediate
rinsing, disinfection, final rinse,
drying in ultrasonic bath .. . . . . . 50
13.7 Automatic cleaning, intermediate
rinsing, disinfection, final rinse,
drying .. . . . . . . . . . . . . . . . . . . . 53
13.8 Check for function .. . . . . . . . . . . 53
13.9 Packing .. . . . . . . . . . . . . . . . . . . 54
13.10 Steam sterilising .. . . . . . . . . . . . 54
13.11 Issue clearance for the parts for
sterilisation .. . . . . . . . . . . . . . . . 54
13.12 Storing parts for sterilisation .. . . 55
14 Treatment breaks for more than 24
hours .. . . . . . . . . . . . . . . . . . . . . . . . . . 56
14.1 Cleaning and disinfecting the
hose system .. . . . . . . . . . . . . . . 56
14.2 Initial start-up after a break in
treatment for more than 24
hours .. . . . . . . . . . . . . . . . . . . . . 57
15 Maintenance .. . . . . . . . . . . . . . . . . . . . 58
15.1 Service kit .. . . . . . . . . . . . . . . . . 58
15.2 Changing the seal .. . . . . . . . . . . 58
15.3 Changing the valve in the fluid
container .. . . . . . . . . . . . . . . . . . 59
15.4 Checking instrument wear .. . . . . 59
15.5 Replacing the light conductor in
the Scaler handpiece .. . . . . . . . . 60
15.6 Replacing the sealing screw .. . . 60
15.7 Inserting or changing the battery
in the flexible foot switch .. . . . . . 61
15.8 Changing the nozzle in the Paro
handpiece .. . . . . . . . . . . . . . . . . 63
15.9 Changing the support seal .. . . . 64
15.10 Checking the function of the tool
kit cover .. . . . . . . . . . . . . . . . . . 65
15.11 Changing the sealing ring of the
resonant ring .. . . . . . . . . . . . . . . 66
15.12 Changing the resonant ring .. . . . 67
15.13 Changing the interchangeable
bushing with union nut .. . . . . . . 67
Troubleshooting
16 Tips for operators and service techni-
cians .. . . . . . . . . . . . . . . . . . . . . . . . . . 70
Contents
2 9000-615-28L02 1903V004
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.
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
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.
Comply with the Operating Instructions.
Protection class II
CE labelling with the number of the noti-
fied body
Manufacturer
Health Industry Bar Code (HIBC)
Serial number
Order number
Lot designation
Dispose of correctly in accordance with
EU Directive 2012/19/EU (WEEE).
Type BF application part
Steam sterilise at 134 °C
Steam sterilise at 135°C
Not sterile
Recycling
The device contains a battery.
Use suitable tools.
The seal must only be removed by a qual-
ified expert.
On/off switch
Amplitude reduction
Important information
9000-615-28L02 1903V004 3
EN

Amplitude increase
Switch off and de-energise the unit
(e.g. unplug from mains).
Wear protective gloves.
Wear protective goggles.
Use a face mask.
Use protective clothing.
Rinse with water.
Rinse with instrument cleaner.
Rinse with instrument disinfectant.
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.
Important information
4 9000-615-28L02 1903V004
EN

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. Nevertheless, residual risks
can remain. You should therefore observe the fol-
lowing notes.
2.1 Intended purpose
This device is a piezo-operated ultrasonic device
for use in dental applications. It is mainly used for
the treatment of periodontal defects. In addition,
the device is used in the area of prophylaxis, peri-
implantitis treatment as well as dental hygiene.
2.2 Intended use
The ultrasonic device is designed for use in peri-
odontology, for the removal of plaque and for the
cleaning of tooth surfaces. This is done via cavi-
tation, polishing, grinding and scraping. Further
assistance for the treatment can be provided by
using hydroxyl and/or fluorapatite as a polishing
agent in periodontology. Only agents approved
by the manufacturer may be used. The treatment
is gentle on the teeth and almost painless.
Paro handpiece applications
– Periodontal treatment
Thorough removal of biofilm and concrement,
and smoothing of the root surface
– Recall
Removal of biofilm and gentle treatment of root
surfaces even with frequent instrument usage
– Peri-implantitis treatment
Cleaning of implant surfaces using fibrous
composite materials and special plastic instru-
ments. Avoids damaging the implant surfaces
Scaler handpiece applications
– Subgingival and supragingival removal of
dental calculus and concrement
The piezo-ceramic drive of the Vector Scaler
allows efficient removal of deposits while provid-
ing the best and gentlest possible protection of
sensitive tissue structures. The ergonomic design
of the handpiece offers six long-lasting high per-
formance LEDs to provide the best possible illu-
mination even into areas that are difficult to see.
2.3 Improper use
WARNING
Risk of explosion due to ignition of
combustible materials
❯Do not operate the unit in any rooms in
which inflammable mixtures may be
present, e.g. in operating theatres.
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.
2.4 General safety information
WARNING
Contraindication
Ultrasound vibrations can interfere with
the function of heart pacemakers and
defibrillators.
❯Patients with heart pacemakers or
defibrillators should not be treated with
these instruments.
❯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 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.
Important information
9000-615-28L02 1903V004 5
EN

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.
2.6 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.
❯Keep a minimum distance of 30 cm between
the unit and mobile radio devices.
❯Note that cable lengths and cable extensions
have effects on electromagnetic compatibility.
The following accessories can have an effect on
the electromagnetic compatibility:
Mains cable .. . . . . . . . . . . . . . . . . . 9000100846
Flexible foot switch cable .. . . . . 9000-119-130E
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.
2.7 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.
Dürr Dental accepts no liability for dam-
ages 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
cable) can have a negative effect in terms
of electrical safety and EMC.
2.8 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.
Important information
6 9000-615-28L02 1903V004
EN

2.9 Disposal
Unit
The unit must be disposed of properly.
Within the European Union, the unit must
be disposed of in accordance with EU
Directive 2012/19/EU (WEEE).
❯If you have any questions about the correct
disposal of parts, please contact your dental
trade supplier.
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.
Important information
9000-615-28L02 1903V004 7
EN

Product description
3 Overview
3.1 Vector Paro / Vector Paro Pro
5
P1
P2
P3
P4
346
7
8
10
9
1
2
4
5
16b
16a 16
7
18
17
14
12
13
6
11
5a
15
19
20
Product description
8 9000-615-28L02 1903V004
EN

8
8b 8a
12
13
13a
8c
9a9b9c
14
P1 - P4
P1 P2 P3 P4
9
15
1 Piercing mechanism for the fluid bag
2 Fluid-bag "Vector Fluid Polish"
3 Cover for fluid bag
4 Cover for fluid container
5 Fluid container
5a Valve
6 Power supply unit
7 Flexible foot switch cable
8 Paro handpiece
8a Handpiece
8b Ring cover
8c Rotary adaptor
9 Scaler handpiece
9a Handpiece
9b Light conductor
9c Cover
10 Handpiece hose
11 Vector toolcard
12 Paro tool kit (blue ring)
13 Recall/Implant tool kit (black ring)
13a Instruments for peri-implantitis treatment,
peri-implant soft and peri-implant hard
14 Scaler tool kit torque wrench with integrated
PREMIUMLINE instrument P1 - P4
15 Torque wrench for PREMIUMLINE instru-
ments (P1 - P4)
16 Steri-box
16a Paro steri-box
16b Scaler steri-box
17 Service kit
18 Flexible foot switch
19 Rinsing adapter for scaler instruments
20 Rinsing adapter for handpieces (yellow)
Product description
9000-615-28L02 1903V004 9
EN

3.2 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):
Vector Paro .. . . . . . . . . . . . . . . . . . . . . 2031-50
– Paro handpiece
– Power supply unit
– Flexible foot switch (including cable)
– 3 V lithium CR 2032 battery
– Paro tool kit with integrated instruments
– Recall/Implant tool kit with integrated instru-
ments
– Paro steri-box
– Combination wrench
– Vector toolcard
– Service kit
– Vector fluid polish MORE EFFECTIVE
– Vector cleaner, special cleaner
– Vector/RinsEndo disinfection, first application,
120 ml
– Vector Paro/Vector Paro Pro installation and
operating instructions
– Quick start instructions
– Vector DVD: "Clinical Application" and "Tips
and Tricks"
or
Vector Paro Pro .. . . . . . . . . . . . . . . . . . 2031-51
like Vector Paro, 2031-50 plus additionally
– Scaler handpiece
– Scaler instrument P1
– Scaler steri-box
3.3 Accessories
The following items are required for operation of
the device, depending on the application:
Paro handpiece .. . . . . . . . . . . . . . . 2031-700-00
Scaler handpiece .. . . . . . . . . . . . . 2032-200-00
Flexible foot switch .. . . . . . . . . . . . 2031-600-00
Paro steri-box (cover: silver) .. . . . . 2031-330-00
Scaler steri-box (cover: blue) .. . . . . 2032-330-00
Service kit .. . . . . . . . . . . . . . . . . . . 2031-340-00
Vector toolcard .. . . . . . . . . . . . . . . 2031-400-01
Scaler instrument torque wrench
. . . . . . . . . . . . . . . . . . . . . . . . . . . 2032100004
Cover, Paro or Recall/Implant tool
kit .. . . . . . . . . . . . . . . . . . . . . . . . 2030-150-06E
Combination wrench .. . . . . . . . . . 2030-137-01E
Rinsing adapter set
(rinsing adapter for scaler instru-
ments and
rinsing adapter for handpieces (yel-
low)) .. . . . . . . . . . . . . . . . . . . . . . . . 2032100008
Instruments for Paro handpiece
Paro tool kit
Paro tool kit, complete .. . . . . . . . . 2031-450-00
Paro curette (3 pcs.) .. . . . . . . . . . 2030-151-04E
Paro lancet (3 pcs.) .. . . . . . . . . . . 2030-151-02E
Paro probe plus (3 pcs.) .. . . . . . . 2031-400-06E
Paro probe straight (3 pcs.) .. . . . 2030-151-01E
Paro probe curved (3 pcs.) .. . . . . 2030-151-03E
Recall/Implant tool kit
Recall/Implant tool kit, complete .. . 2031-460-00
Recall probe straight CFRP .. . . . . 2030-153-02E
Recall curette CFRP (3 pcs.) .. . . . 2030-153-05E
Supra probe flexible (3 pcs.) .. . . . 2030-152-01E
Instruments for peri-implantitis treatment
Periimplant soft (3 pcs.) .. . . . . . . 2031-474-01E
Periimplant hard (3 pcs.) .. . . . . . . 2031-473-01E
Instruments for Scaler handpiece
PREMIUMLINE
Tool-Kit Scaler P1, straight .. . . . . . 2032-411-00
Tool-Kit Scaler P2, right curved .. . . 2032-412-00
Tool-Kit Scaler P3, left curved .. . . . 2032-413-00
Tool-Kit Scaler P4, supra .. . . . . . . 2032-414-00
3.4 Consumables
The following materials are consumed during
operation of the device and must be ordered
separately:
Vector Fluid Polish MORE
EFFECTIVE, 200 ml .. . . . . . . . . . CWZ510C2350
Vector/RinsEndo Disinfection .. . . CDZ501C6150
Vector cleaner, special cleaner
for hose system, 4 x 2.5 l .. . . . . CCA531A6150
ID 213
Instrument disinfection .. . . . . . . . CDI213C6150
FD 322
rapid surface disinfection .. . . . . . CDF322C6150
FD 350 Classic
disinfection wipes .. . . . . . . . . . . CDF35CA0140
FD 370 cleaner - for medical
practices .. . . . . . . . . . . . . . . . . . CCF370C6150
FD 366 quick-acting disinfectant
for sensitive surfaces .. . . . . . . . . CDF366C6150
Product description
10 9000-615-28L02 1903V004
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3.5 Wear parts and replacement
parts
The following working parts need to be changed
at regular intervals (refer to the "Maintenance"
section):
Instruments for Paro handpiece and Scaler hand-
piece, see "3.3 Accessories"
Service kit .. . . . . . . . . . . . . . . . . . . 2031-340-00
Light conductor for Scaler hand-
piece (4 pcs.) .. . . . . . . . . . . . . . . 2032-200-03E
Information about replacement parts is
available from the portal for authorised
specialist dealers at:
www.duerrdental.net.
Product description
9000-615-28L02 1903V004 11
EN

4 Technical data
Electrical data – power supply unit
Rated voltage V AC 100 - 240
Mains frequency Hz 50 - 60
Rated power W 30
Current consumption A 1 - 0.5
Protection class II
Type of protection IP 20
Electrical data – basic unit and handpieces
Voltage V DC 24
Electrical power ON W 4.8
Electrical power Active W 9.6
Electrical power Standby W 1.2
Type of protection IP 20
Classification
Medical Devices Directive (93/42/EEC) Class IIa
General technical data – basic unit and handpieces
Operating frequency, Paro handpiece kHz approx. 23
Operating frequency, Scaler handpiece kHz approx. 27–32
Duty cycle % 100
Fluid Polish bag contents ml 200
Fluid container fill capacity ml 600
Paro handpiece water consumption ml/min approx. 3.3
Scaler handpiece water consumption ml/min approx. 30–45
Max. surface temperature of instruments °C 58
Weight
Paro basic unit kg 1.5
Scaler basic unit kg 1.43
Paro handpiece g approx. 59
Scaler handpiece g approx. 56
Dimensions (W x H x D)
Paro basic unit cm 21.5 x 25.2 x 16
Scaler basic unit cm 15.3 x 25.2 x 16
Paro handpiece cm Ø 1.9 x 14.8
Scaler handpiece cm Ø 2.0 x 9.4
Product description
12 9000-615-28L02 1903V004
EN

Battery for flexible foot switch
Voltage V 3
Type Lithium CR2032
Ambient conditions during transport and storage
Temperature °C -15 to +60
Relative humidity % Max. 95
Ambient conditions during operation
Temperature °C +10 to +40
Relative humidity % Max. 80
Electromagnetic compatibility (EMC)
Interference emission measurements
High-frequency emissions in accordance
with CISPR 11
Group 1
Class B
Harmonics in acc. with IEC 61000-3-2 Not applicable
Voltage fluctuations/flickers in acc. with
IEC 61000-3-3
Not applicable
Electromagnetic compatibility (EMC)
Interference immunity tests
Static electricity discharge in accordance with
IEC 61000-4-2
Compliant
Magnetic field for a supply frequency (50/60 Hz) in accor-
dance with IEC 61000-4-8
Compliant
Emitted HF disturbance variables in accordance with
IEC 61000-4-3
Compliant
Product description
9000-615-28L02 1903V004 13
EN

4.1 Type plate
The type plate is located on the rear of the
device.
The seal is located on the base of the device.
Incorrectly performed work can endanger
the correct operation and safety of the
device.
The seal must only be removed by a qual-
ified expert.
The device must only be opened by a
qualified expert.
4.2 Order number and serial num-
ber for the handpieces
The serial number of the handpieces is
located in the area marked in grey.
1
2
1 Paro handpiece
2 Scaler handpiece
4.3 ID number for tool kits
There is an ID number on the Paro and Recall/
Implant tool kit covers and on the Scaler tool kits.
The ID number serves to document the repro-
cessing.
These parts may no longer be used after a cer-
tain number of reprocessing cycles, or after the
end of the service life.
The ID number is made up of the following mark-
ing: MMXXXX
MM Date of manufacture: year and
month
XXXX Consecutive alphanumerical ID
number
Paro and Recall/Implant tool kit cover
Scaler tool kit
Product description
14 9000-615-28L02 1903V004
EN

4.4 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.
5 Operation
5.1 Handpieces
During treatment using the Paro or Scaler hand-
pieces, they can be operated using just water or
using water and Vector Fluid Polish as required.
Vector Fluid Polish can be switched on or off
using the operating panel.
Paro handpiece
On the Paro handpiece, the Vector basic unit
produces a largely linear vibration of the instru-
ment (perpendicular to the longitudinal axis of the
handpiece) with an adjustable amplitude of
approx. 15–40 mm and a frequency of approx.
23 kHz.
During treatment using the Paro handpiece fluid
is applied as a pulsating jet. Once the flexible foot
switch is released a small amount of fluid will still
drip out. The amount of water that comes out is
pre-defined automatically and cannot be
changed.
Scaler handpiece
On the Scaler LED handpiece, the Vector basic
unit generates a spatial vibration of the instru-
ment tip (transverse to the instrument axis) with
an amplitude of approx. 20–120 mm.
During treatment using the Scaler handpiece,
fluid is applied as a constant stream. The amount
of water that comes out can be adjusted via the
operating panel.
6 LEDs are integrated into the front section of the
handpiece. As soon as the flexible foot switch is
switched on and "Power" is selected on the
operating panel, the LEDs light up.
The LEDs go out approx. 4 seconds after the
flexible foot switch is released.
Handpiece detection
The last used settings in the operating panel are
saved by the relevant handpiece.
After the device is switched off and back on
again the handpiece detection is maintained.
Unplugging the mains plug of the device will
cause the last used settings to be lost.
5.2 Fluid container
The fluid level is monitored via a sensor. When
the level drops to a minimum level, the LEDs in
the area of the fluid container flash and a warning
signal sounds (3x).
Product description
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5.3 Instrument change
A torque wrench is required for inserting/chang-
ing the instruments. This is integrated in the tool
kit cover for the instruments of the Paro hand-
piece. For the instruments of the Scaler hand-
piece there is a separate torque wrench.
Product description
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Assembly
6 Requirements
The room chosen for installation must satisfy the
following requirements:
– Closed, dry room
– Clean, level and sufficiently stable subsurface
– There should be no large interference fields
present (e.g. strong magnetic fields) that could
interfere with correct operation of the unit.
– The required ambient conditions are satisfied
(refer to the "Technical Data").
7 Installation
7.1 Establishing the electrical
connections
The connection ports are located in the recess
on the rear of the unit.
Requirements:
üCorrectly installed power outlet in the vicinity of
the unit (max. length of mains cable 3 m)
üThe plug connection of the power supply is
freely accessible so that it can be quickly dis-
connected in the event of danger.
üMains voltage must match the information
shown on the type plate of the power supply
unit
üThe supply voltage of the power supply unit
matches the data on the type plate.
❯Plug in the connecting plug of the connecting
cable into the connecting socket of the unit.
❯Fit the correct country-specific adapter.
❯Plug the mains plug into the power outlet.
Assembly
9000-615-28L02 1903V004 17
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7.2 Connecting the flexible foot
switch
The flexible foot switch can be operated
using a foot switch cable or wirelessly.
LED PEDAL flashes in orange after the unit is
switched on:
– No cable connection between the unit and the
foot switch.
– Pairing not performed for wireless operation.
The LED will keep flashing until a cable connec-
tion is established or pairing is performed.
Operation with a cable
❯Plug the connector of the foot switch cable into
the connecting socket on the flexible foot
switch.
Click !
❯Plug the connector of the foot switch cable into
the connecting socket on the unit.
Wireless operation
If the flexible foot switch is to be operated wire-
lessly, pairing (synchronization/coupling) of the
flexible foot switch and the unit needs to be per-
formed during initial start-up.
In order to avoid interference in wireless
operation, we recommend that a maxi-
mum of 4 flexible foot switches is used
wirelessly within a single surgery.
If interference does occur during wireless
operation, we recommend using the flexi-
ble foot switch with foot switch cables.
Wireless operation is not possible if the
foot switch cable is connected to either
the unit or the flexible foot switch.
CAUTION
Risk of injury
Mixing up flexible foot switches can
cause malfunctions such as the acci-
dental operation of a different hand-
piece. This can cause injuries.
❯If multiple devices are used simultane-
ously in wireless operation, make sure
that the flexible foot switch that is
paired with the relevant device is
always used.
❯Make sure they are stored together as
well.
Performing pairing
üPlace the flexible foot switch ready.
üInsert a battery in the flexible foot switch,
"15.7 Inserting or changing the battery in the
flexible foot switch".
üDisconnect the foot pedal cable from the unit
and foot switch (if previously connected).
Before carrying out the pairing process,
make sure that no other Vector device
with a flexible foot switch is running dur-
ing the process within a range of around
10 m. Otherwise the connection may be
established incorrectly.
Assembly
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