KaVo Kerr elements e-motion User manual

Instructions for use
elements e-motion
Dental Motor

Table of contents
1 User instructions ................................................................................................................ 5
1.1 User guide .................................................................................................................... 5
1.1.1 Abbreviations..................................................................................................... 5
1.1.2 General marks and symbols ................................................................................ 5
1.2 Target group................................................................................................................. 6
1.3 Service......................................................................................................................... 6
1.4 Terms and conditions of warranty.................................................................................... 6
1.5 Transport and storage.................................................................................................... 7
1.5.1 Damage in transit .............................................................................................. 7
1.5.2 Information on the packaging: Storage and transportation ..................................... 7
1.6 Disposal........................................................................................................................ 9
1.7 Disposal of electronic and electrical devices ...................................................................... 9
2 Safety.................................................................................................................................. 10
2.1 Infection hazard ........................................................................................................... 10
2.2 Explosion hazard area ....................................................................................................10
2.3 Technical condition ........................................................................................................ 10
2.4 Ingress of liquids ........................................................................................................... 11
2.5 Accessories and combination with other equipment........................................................... 11
2.6 Qualification of personnel ............................................................................................... 12
2.7 Service and repair .........................................................................................................12
2.8 Electromagnetic fields ....................................................................................................13
3 Product description ............................................................................................................14
3.1 Intended use.................................................................................................................14
3.2 Scope of delivery...........................................................................................................15
3.3 Overview of elements e-motion.......................................................................................16
3.4 Motor cord ....................................................................................................................16
3.5 Control panel ................................................................................................................16
3.6 Technical specifications of the elements e-motion ............................................................. 19
3.7 Symbols on product and rating plate ............................................................................... 20
3.8 Power supply ................................................................................................................ 22
3.9 Technical specifications of the power supply 1.013.4796.................................................... 22
3.10 Symbols on the nameplate of the power supply ................................................................23
4 Installation ......................................................................................................................... 24
4.1 Location........................................................................................................................ 24
4.2 Installing the instrument tray.......................................................................................... 24
5 Startup................................................................................................................................ 26
5.1 Connector..................................................................................................................... 26
5.1.1 Connecting the foot control ................................................................................. 26
5.1.2 Connecting the motor......................................................................................... 26
5.1.3 Connect the motor cord ...................................................................................... 27
5.1.4 Connect the power supply................................................................................... 27
5.2 Changing the device settings ..........................................................................................28
6 Operation............................................................................................................................ 30
6.1 Switching the elements e-motion on/off........................................................................... 30
Instructions for use elements e-motion Dental Motor
Table of contents
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6.2 Stand-by mode .............................................................................................................30
6.3 Starting-up the motor ....................................................................................................31
6.4 Operating the elements e-motion.................................................................................... 31
6.4.1 Setting the speed............................................................................................... 32
6.4.2 Setting the torque.............................................................................................. 32
6.4.3 Selecting torque mode........................................................................................ 33
6.4.4 File database ..................................................................................................... 35
6.4.5 Selecting a file sequence..................................................................................... 36
6.4.6 Selecting files .................................................................................................... 36
6.4.7 Defining/changing file sequences in the file editor.................................................. 36
6.4.8 Deleting a file sequence ...................................................................................... 42
7 Decommissioning ............................................................................................................... 44
7.1 Disconnecting the electrical connection ............................................................................ 44
7.2 Disconnecting the foot control......................................................................................... 44
7.3 Unplugging the motor .................................................................................................... 44
8 Reprocessing steps in accordance with ISO 17664 ...........................................................45
8.1 Cleaning ....................................................................................................................... 45
8.1.1 Preparations at the site of use ............................................................................. 45
8.1.2 Manual external cleaning .................................................................................... 45
8.1.3 Manual internal cleaning ..................................................................................... 45
8.1.4 Automated external and internal cleaning ............................................................. 45
8.2 Disinfection................................................................................................................... 46
8.2.1 Manual external disinfection ................................................................................ 46
8.2.2 Automated external and internal disinfection......................................................... 46
8.3 Packaging ..................................................................................................................... 46
8.4 Sterilisation................................................................................................................... 46
8.5 Storage ........................................................................................................................ 47
8.6 Service, inspection and testing after preparation............................................................... 47
9 Servicing............................................................................................................................. 48
9.1 Replacing the LED lamp of the KL 703 motor....................................................................48
9.2 Replacing the motor cord ...............................................................................................49
10Troubleshooting ................................................................................................................. 50
11Accessories and consumables ............................................................................................52
12Information about electromagnetic compatibility .............................................................53
12.1 Guidelines and manufacturer's declaration - electromagnetic emission ................................ 53
12.2 Guidelines and manufacturer's statement - Electromagnetic immunity ................................ 53
12.3 Guidelines and manufacturer's statement - Electromagnetic immunity ................................ 54
12.4 Recommended safe distance between portable and mobile HF telecommunications
equipment and the elements e-motion............................................................................. 56
Instructions for use elements e-motion Dental Motor
Table of contents
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Instructions for use elements e-motion Dental Motor
1 User instructions | 1.1 User guide
1 User instructions
1.1 User guide
Requirement
Read these instructions prior to first startup to avoid misuse and prevent dam-
age.
Requirement
If other language versions are required, they can be requested from the cor-
responding Kerr branch. Prior approval from Kerr must be obtained before
copying and passing on the Instructions for Use.
1.1.1 Abbreviations
Ab-
brevi-
ation
Explanation
IFU Instructions for use
CI Care instructions
AI Assembly instructions
TI Technician's instructions
IEC International Electrotechnical Commission
RI Repair instructions
RK Retrofitting kit
AS Assembly kit
CK Conversion kit
EP Enclosed parts
EMC Electromagnetic compatibility
PI Processing instructions
1.1.2 General marks and symbols
General Warning
Important information for users and technicians
CE mark (European Conformity mark)
Action required
Hazard levels
The warning and safety notes in this document must be observed to prevent
personal injury and material damage. The warning notes are designated as
shown below:
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Instructions for use elements e-motion Dental Motor
1 User instructions | 1.2 Target group
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DANGER
In cases which – if not prevented – directly lead to death or severe in-
jury.
WARNING
In cases which – if not prevented – can lead to death or severe injury.
CAUTION
In cases which – if not prevented – can lead to minor or moderate in-
jury.
NOTICE
In cases which – if not prevented – can lead to material damage.
1.2 Target group
This document is for dental professionals, dental office staff and service staff.
1.3 Service
Note
Send the product in for a service check every two years.
In this service check, the safety checks are performed according to IEC 62353 -
VDE 0751-1.
Kerr Customer Care
For repairs, please contact your local dealer or Kerr Customer Care directly:
Toll-free: +1-800-KERR-123
Homepage: www.kerrdental.com
Email: [e-mail]
1.4 Terms and conditions of warranty
Within the scope of the applicable Kerr delivery and payment conditions, Kerr
guarantees proper function, absence of defects in material and workmanship
for the following periods:
Control Unit and all not specified parts: 12 months
KL 703 LED motor: 36 months
from the date of purchase as confirmed by the salesperson.
In case of justified complaints, Kerr will honour its warranty with a free replace-
ment or repair.
The warranty does not cover defects and their consequences that arose or may
have arisen due to natural wear, improper handling, cleaning or maintenance,
non-compliance with operating, maintenance or connection instructions, corro-
sion or chemical or electrical influences deemed abnormal or impermissible in
accordance with factory specifications.
The warranty does not usually cover lamps, optical fibres made of glass and
glass fibres, glassware, rubber parts and the colourfastness of plastic parts.

Instructions for use elements e-motion Dental Motor
1 User instructions | 1.5 Transport and storage
The warranty expires if defects or their consequences could possibly have
arisen because the product has been modified or changed. Warranty claims can
only be asserted when they are immediately reported to Kerr in writing.
This notification must be accompanied by a copy of the invoice or delivery note
on which the manufacturing number is clearly visible. In addition to the guar-
anty, the statutory warranty claims of the purchaser also apply with a warranty
period of 12 months.
1.5 Transport and storage
1.5.1 Damage in transit
Note
Kerr shall not be held liable for damage arising from transportation.
The shipment must be checked on arrival.
If the packaging is visibly damaged on delivery, please proceed as follows:
1. The recipient of the package must record the loss or damage on the delivery
receipt. The recipient and the representative of the shipping company must
sign this delivery receipt.
Without this evidence, the recipient will not be able to assert a claim for
damages against the shipping company.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use the product.
If the product is damaged but there was no discernable damage to the pack-
aging on delivery, proceed as follows:
1. Report any damage to the shipping company immediately and no later than
7 days after delivery.
2. Leave the product and packaging in the condition in which you received it.
3. Do not use a damaged product.
Note
If the recipient fails to comply with any of the above-mentioned obligations,
the damage will be considered to have arisen following delivery
(in accordance with CMR law, Chapter 5, Art. 30).
1.5.2 Information on the packaging: Storage and
transportation
Note
Please keep the packaging in case you need to return the product for servi-
cing or repair.
The symbols printed on the outside are for transportation and storage, and
have the following meaning:
Follow instructions for use
Please note the instructions for use
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Instructions for use elements e-motion Dental Motor
1 User instructions | 1.5 Transport and storage
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Caution
Temperature limitation
Atmospheric pressure limitation
Humidity limitation
Rx
only
Caution: Federal (USA) law restricts device to sale by or on the order
of a dental professional.
MET mark
VDE mark
CE mark (European Conformity mark)
Medical device, labelling of medical devices
Importer
Transport upright with the arrows pointing upwards!
Fragile, handle with care!
Stacking limit by number
Keep dry!
Do not dispose this product into the ordinary municipal waste or
garbage system
Properly dispose of non-corrugated fiberboard (paperboard)
Properly dispose of low-density polyethylene
Properly dispose of all other plastics such as Polycarbonate (PC), poly-
amide (PA), styrene acrylonitrile (SAN), acrylic plastics/polyacrylonitrile
(PAN), bioplastics

Instructions for use elements e-motion Dental Motor
1 User instructions | 1.6 Disposal
1.6 Disposal
Note
Any waste which is generated must be recycled or disposed of in strict com-
pliance with all applicable national regulations in a manner which is safe both
for people and the environment.
If you have any questions regarding proper disposal of the Kerr product,
please contact the Kerr branch.
1.7 Disposal of electronic and electrical devices
Note
According to the general WEEE Directive (Waste Electrical and Electronic
Equipment) and EU Directive 2012/19 concerning waste electrical and elec-
tronic equipment, we wish to point out that this product is subject to the
aforementioned Directive and must be subjected to special disposal within
Europe.
For more information, please visit www.kavo.com or contact your specialised
dental dealers.
For final disposal:
In Germany
To return an electrical device, you need to proceed as follows:
1. On the homepage www.enretec.de of enretec GmbH, you can download a
form for a disposal order under the menu item, eom. Download the disposal
order or complete it as an online order.
2. Enter the corresponding information to complete the order, and submit it as
an online order or by fax [phone] to enretec GmbH.
The following contact options are also available for questions and for initiat-
ing a disposal order:
Phone: [phone]
Email: [e-mail] and
Postal address: enretec GmbH, Geschäftsbereich eomRECYCLING®
Kanalstraße 17
D-16727 Velten
3. A unit that is not permanently installed will be picked up at the office.
A permanently installed unit will be picked up at the curb at your address on
the agreed date.
The owner or user of the device will have to bear the cost of disassembly,
transportation and packaging.
International
For country-specific information on disposal, contact your specialised dealers.
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Instructions for use elements e-motion Dental Motor
2 Safety | 2.1 Infection hazard
10 / 58
2 Safety
Note
All serious events occurring in relation to the product must be reported to the
manufacturer and the competent authority of the member state, in which the
user and/or patient resides.
The instructions for use are a component of the product and must be read care-
fully prior to use and be accessible at all times.
The device may only be used in accordance with the intended use, any other
type of use is not permitted.
2.1 Infection hazard
Patients, users or third parties could be infected by contaminated medical
devices.
▶Take suitable personal protective measures.
▶Follow the instructions for use of the components.
▶Before initial startup and after each use, reprocess the product and ac-
cessories appropriately.
▶Carry out the reprocessing as described in the instructions for use. The pro-
cedure has been validated by the manufacturer.
▶If you deviate from this procedure, it is essential to make sure that the re-
processing is effective.
▶Reprocess the product and accessories appropriately before disposal.
2.2 Explosion hazard area
Electrical sparks in the product can lead to explosion or fire.
▶Do not use product in explosion hazard areas.
▶Do not operate the product in an oxygen-enriched atmosphere.
▶Do not use the product in the vicinity of flammable gases.
2.3 Technical condition
A damaged device or components could injure patients, users and third parties.
A damaged power cable or missing protective conductor can lead to electrical
shock.
▶Only operate devices or components if they are undamaged on the outside.
▶Check the power cable before use.
▶Connect only to sockets with a protective contact that meet the respective
national regulations.
▶Check the proper working order and proper condition of product and ac-
cessories before each use.
▶Have parts with sites of breakage or surface changes checked by the Ser-
vice.
▶Safety checks may only be performed by trained service personnel.
▶Perform a test run with the handpiece before each use.
▶If any of the following defects on the product or accessories occurs, stop
working and have the service personnel carry out repair work:

Instructions for use elements e-motion Dental Motor
2 Safety | 2.4 Ingress of liquids
▪ Malfunctions
▪ Damage
▪ Irregular running noise
▪ Excessive vibration
▪ Overheating
▪ Endodontic files are not seated firmly in the handpiece
Careless setup/installation of the product or accessories can cause injury to pa-
tients, users and third parties. Power supplies and/or cords/hoses on the floor
can cause slipping or tripping.
▶Power supply and cord/hoses need to be set-up/routed appropriately such
that they are not on the floor.
2.4 Ingress of liquids
Use of the product in moist or electrically conductive environments can lead to
electrical shock and injury to patient, user and third parties.
▶Use the product in dry environments exclusively.
▶Use the product only in environments that are not electrically conductive.
▶Protect openings of the product from any ingress of liquids.
▶Do not place the product in a trough-like container.
▶If any liquid is detected on the device, disconnect the power cable from the
supply mains right away and do not touch the product.
▶Make sure that the surface of the product is absolutely dry before plugging
the power cable back in the socket.
▶After interventions on and repairs of the device and before re-use, have the
service personnel perform safety checks on the device.
2.5 Accessories and combination with other equipment
Use of un-authorised accessories or un-authorised modifications of the device
could lead to injury.
▶Only use accessories that have been approved for combination with the
product by the manufacturer.
▶Only use accessories that are equipped with standardised interfaces.
▶Do not make any modifications to the device unless these have been ap-
proved by the manufacturer of the product.
Improper use of handpieces can cause injuries.
You need to comply with the following guidelines to ensure the safe use of the
electrically-driven handpieces:
▶Follow the instructions for use of the respective handpiece.
▶Check the speed setting each time you turn on the device.
▶Comply with the permissible maximal speed and maximal contact pressure
of the tools as specified by the tool manufacturer.
▶Comply with the servicing instructions for handpieces as specified in the re-
spective instructions for use.
▶Never press the push-button during operation of the device.
▶Never use the push-button to lift the cheek or tongue.
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Instructions for use elements e-motion Dental Motor
2 Safety | 2.6 Qualification of personnel
12 / 58
If the transmission ratio selected on the device differs from the transmission ra-
tio of the dental instrument, the files may rotate too fast and cause injury.
▶Make sure that the handpiece you use and the setting of the transmission
ratio are consistent.
Improper use of tools, e.g. wrong files, can cause injuries.
▶Follow manufacturer's instructions (mode of operation, speed, torque levels,
torsion resistance, etc.), and use the files according to their intended use.
Some file systems are designed for use with certain contra-angle handpieces.
They must not be used with other contra-angle handpieces as this may lead to
injury.
▶Only use the Kerr TF Adaptive file system with the Kerr elements 8:1 or
KaVo SMARTmatic 8:1 handpiece.
▶Use hand files with the Kerr M4 contra-angle handpiece exclusively.
2.6 Qualification of personnel
Application of the product by users without the appropriate medical training
could injure the patients, the users or third parties.
▶Make sure that the user has read and understood the instructions for use.
▶Only employ the device if the user has the appropriate medical training.
▶Observe national and regional regulations.
The bluish LED light of the motors can damage the cornea or lens of the eye.
▶Do not gaze into the lamp when it is in operation.
▶Use adequate shielding for eye protection.
2.7 Service and repair
Servicing work that is described in the "Servicing" chapter of the present In-
structions for Use can be performed by the operator/user.
Repairs and safety checks may only be performed by trained service personnel.
The following persons are authorised to do this:
▪ Service technicians of Kerr branches after the appropriate product training
▪ Service technicians of Kerr authorised dealers after the appropriate product
training
▪ Independent service technicians after the appropriate product training
Observe all the following items during servicing work:
▶Have the service and testing tasks carried out according to the Medical
Device Operator Ordinance.
▶After interventions on and repairs of the device and before re-use, have the
service personnel perform safety checks on the device.
▶The device should be serviced, cleaned, and stored in a dry location, and
should be disconnected from the mains, according to instructions, if it is not
to be used for extended periods.
Note
Kerr provides wiring diagrams, component lists, descriptions, calibration in-
structions or other information on request to support the service personnel
during repair work.

Instructions for use elements e-motion Dental Motor
2 Safety | 2.8 Electromagnetic fields
2.8 Electromagnetic fields
Electromagnetic fields might interfere with the functions of implanted systems
(such as pacemakers).
Medical electrical devices are subject to special precautions regarding electro-
magnetic compatibility and must be installed and operated in accordance with
the tables of electromagnetic compatibility.
See also:
212 Information about electromagnetic compatibility, Page 53
High-frequency communications devices may interfere with medical electrical
devices.
▶Ask patients if they have a cardiac pacemaker or other system implanted
before you start the treatment.
▶Comply with the tables of electromagnetic compatibility during installation
and commissioning.
▶If the device needs to be used in the immediate vicinity of other equipment,
monitor the device or system for malfunctions.
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Instructions for use elements e-motion Dental Motor
3 Product description | 3.1 Intended use
14 / 58
3 Product description
The elements e-motion is a dental treatment unit for endodontic treatments.
The elements e-motion consists of the control unit, power supply, power cable,
foot control, motor cord, motor, instrument tray, and the elements 8:1 hand-
piece.
See also:
23.2 Scope of delivery, Page 15
3.1 Intended use
Indications for use:
The medical device is intended to drive a dental motor for operation of
electrically-driven dental handpieces. This device is intended for use by a
trained professional in the field of general dentistry.
Proper use:
The overarching guidelines and/or national laws, national regulations and the
rules of technology applicable to medical devices for startup and use of the
KaVo product for the intended indications for use must be applied and followed.
Definition (indications for use) Explanation
Main function Dental treatment for endodontics
Application For dental treatment of humans -
root canal treatment
KaVo shall not be responsible for damage caused by:
▪ External factors or faulty installation
▪ The use of incorrect information
▪ Repair work carried out incorrectly
▪ If the 2-year service check have not been done

Instructions for use elements e-motion Dental Motor
3 Product description | 3.2 Scope of delivery
3.2 Scope of delivery
5
Scope of delivery of the elements e-motion:
①Control unit ⑦elements 8:1 handpiece
②Power supply ⑧Instrument tray, base plate
(preinstalled)
③Power cable (country-specific) ⑨Attachment for instrument tray
④Foot control ⑩Offset screwdriver Torx T20
⑤INTRA LUX Motor KL 703 LED ⑪Instructions for use
⑥Motor cord
Note
Use exclusively the power cables and mains plugs approved in the specific
country. Use exclusively the power cables and mains plugs with the electrical
nominal data as listed in the following table.
Power cable Power plug IEC coupler
▪ H05 VV F 3G C131.00
▪ 250 VAC
▪ 10 A
▪ black
▪ 250 VAC
▪ 16 A
▪ black
▪ EN 60320 / C13
▪ 10 A
▪ 250 VAC
▪ black
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Instructions for use elements e-motion Dental Motor
3 Product description | 3.3 Overview of elements e-motion
16 / 58
3.3 Overview of elements e-motion
Front and rear of the elements e-motion
①Control panel ⑤Power supply connector
②Control unit ⑥Motor cord connector
③Instrument tray ⑦Foot control connector
④Inspection window status LED
3.4 Motor cord
2
1
3
①Connector for elements e-motion ③Connector for motor
②Motor cord
3.5 Control panel
The device is operated by means of a touch display. The control elements on
the touch display are either toggle switches or show a selection list when
touched.
▪ Values/figures shown with a blue background are active
▪ Values/figures shown with a grey background are deactivated
▪ Speed/file shown with a white background is activated/selected

Instructions for use elements e-motion Dental Motor
3 Product description | 3.5 Control panel
Example, display information
3
2
4
4
1
12
13
76
8
10
11
5
*
9
Pos.
no.
Description active/deactivated Presentation
①Display/toggle switch
"Speed"/"Torque"*
Torque is deactivated
= 3.00 Ncm
grey font color
②Selection list "File se-
quence"
KERR ROTARY FILES blue background
③Display/toggle switch
"Speed"/"Torque"*
Speed is active = 500
rpm (min-1)
blue font color
④Displays the selected
File System
File system “Twisted
Files” is selected
white background
④* Displays specific file
within a file system
(when applicable)
Specific file “TF” is se-
lected
white background
⑤Selection list
"Files" (up to 10 files
can be pre-set)
Selection list can be
shifted vertically by
touching it
File TF is selected white background =
file is selected
grey background = file
is not selected
dark grey = file is de-
activated
⑥Slider for speed/
torque*
Speed is active Slider shows the posi-
tion within the avail-
able range by the blue
bar.
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Instructions for use elements e-motion Dental Motor
3 Product description | 3.5 Control panel
18 / 58
Pos.
no.
Description active/deactivated Presentation
⑦Menu "Settings" deactivated Menu "Settings"
See also:
25.2 Changing the
device settings,
Page 28
⑧Toggle switch "Direc-
tion of motor rotation"
Clockwise rotation is
active
(is preset)
⑨Selection list "Torque
mode"
Autorev / Forward is
active
⑩Selection list "Instru-
ment transmission ra-
tio"
1:1 is active
⑪Toggle switch "Lock" Lock is locked
(is preset)
⑫Speed/torque are in-
consistent with the
data from the file data-
base (file manufac-
turer’s recommended
settings)
active
⑬File representation
Rotary files or hand
files (only shown for
"M4 Safety")
Rotary File is displayed

Instructions for use elements e-motion Dental Motor
3 Product description | 3.6 Technical specifications of the elements e-motion
3.6 Technical specifications of the elements e-motion
Dimensions of the package
Length 525 mm / 20.67"
Width 230 mm / 9.06"
Altitude 255 mm / 10.04"
Dimensions and weight of control unit including
instrument tray base plate
Width 168 mm / 6.61“
Depth 148 mm / 5.83“
Altitude 81 mm / 3.19“
Weight of the elements e-motion ca. 680 g / 23.99 ounces
Requirements
Protection class control unit IP 31
Protection class for the footswitch IP X8
Ambient conditions
Permissible installation sites Indoor use
Permissible ambient temperature
range
+10oC to +26oC / +50oF to +79oF
Maximum relative humidity 80 % at 31 oC / 88 oF
Maximum relative humidity linearly decreasing 50 % at 40 o /
104 oF
Pollution degree 2
Permissible up to 3,000 m / 9843 feet altitude
Atmospheric pressure limitation 700 to 1060 hPa
Transportation and storage conditions
Permissible ambient temperature
range
-20oC to +50oC / -4oF to +122oF
Permissible up to a maximum hu-
midity of
5% to 90% non-condensing
Atmospheric pressure limitation 700 to 1060 hPa
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Instructions for use elements e-motion Dental Motor
3 Product description | 3.7 Symbols on product and rating plate
20 / 58
Mode: intermittent operation
Operating time 0.5 minutes
Pause time 9 minutes
▶Do not exceed the threshold load of the motor of 0.5 minutes operating
time / 9 minutes pause.
Note
In practice, pulse loads lasting seconds or pause times lasting seconds or
minutes are realistic, usually without reaching the maximal possible motor
current. This corresponds to the common working procedure of a dental pro-
fessional.
Speed
Speed range of the Motor KL 703 100 - 20,000 rpm (min-1)
Motor torque
Maximum torque of the
Motor KL 703
2 Ncm
Torque of the Motor KL 703 min-
imum
0.1 Ncm
Electrical ratings
Input voltage 24 V DC
Power max. 65 W
Motor cords
Length of connection cord 2.00 m / 78.74"
3.7 Symbols on product and rating plate
The rating plates are affixed to the underside of the unit.
Accompanying documents
Caution
Follow instructions for use
Consult instructions for use
Please note the electronic instructions for use

Instructions for use elements e-motion Dental Motor
3 Product description | 3.7 Symbols on product and rating plate
Certification
CE mark (Communauté Européenne)
VDE mark
MET mark
Product characteristics
Manufacturer
Type Device type
SN Serial number
REF Material number
Type B applied part
Supply voltage
Operating mode: continuous operation with intermittent load
Class II equipment
Do not dispose this product into the ordinary municipal waste or
garbage system
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