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Magnerisuser guide
Dear Customer,
We would like to thank you for choosing Astar’s device.
We believe the proper work on it will bring you satisfaction and your
patients a quick recovery.
All our products are made from high quality materials using the modern
technology according to all safety rules.
We recommend to read this manual, especially the maintenace part
for perfect satisfation of our device.
Astar.physiotechnology
Astar’s devices
and their dedicated physiotherapy
Electrotherapy
Laser therapy
Ultrasound
Magnetotherapy
Du
ote
r P
lus
Ari
es
Po
lari
s 2
So
no
ter
Plu
s
So
na
ris
Ma
gn
er
Plu
s
Ma
gn
eri
s
Lu
min
a
Basic function
Additional function
Magneris user guide
ISSUE DATE 05.11.2010
page 4 MAGNERIS – USER GUIDE
0 INTRODUCTION AND DECLARATION OF CONFORMITY 6
1 INTENDED USE 8
2 WARRANTY AND MANUFACTURER’S RESPONSIBILITY 9
3 OPERATIONAL SAFETY 10
3.1 MAINS SUPPLY AND MODE OF OPERATION 10
3.2 STORAGE, OPERATION AND TRANSPORT CONDITIONS 10
3.3 WARNINGS AND SAFETY NOTICES 10
3.4 EXPLOSION PROOF ENVIRONMENT 11
3.5 PROTECTION AGAINST IMPACT OF ELECTROMAGNETIC FIELD 11
3.6 TECHNICAL SUPERVISION 12
3.7 DISPOSAL 12
4 UNIT DESCRIPTION 13
4.1 GENERAL CHARACTERISTICS 13
4.2 KEYBOARD 15
4.2.1 START key 15
4.2.2 STOP key 15
4.2.3 Confi rmation key 15
4.2.4 Escape key 15
4.2.5 Information key 16
4.2.6 Operation mode change key 16
4.2.7 Save key 16
4.2.8 Edit keys 16
4.3 REAR AND SIDE PANELS 16
4.4 NAME PLATE 16
4.5 TREATMENT PARAMETERS 17
4.6 MAGNETIC FIELD APPLICATORS 19
5 DEVICE INSTALLATION AND START-UP 20
5.1 UNIT INSTALLATION 20
5.1.1 Attaching the device to the shelf of the stand 20
5.1.2 Connecting applicators 20
5.1.3 Stand height adjustment 21
5.1.4 Plate applicator position adjustment 21
5.1.5 First start-up 22
5.2 SETUP MODE 23
5.2.1 Sounds 23
5.2.2 Contrast 24
5.2.3 Dose unit 24
5.2.4 Removal of user programs 24
5.2.5 Language 24
5.2.6 Start-up menu 24
Content
ISSUE DATE 05.11.2010 page 5
6 UNIT OPERATION 25
6.1 OPERATION WITH PRESET TREATMENT PROGRAMS 25
6.2 OPERATION IN THE MANUAL MODE 28
6.3 USER DEFINED PROGRAMS 28
7 INDICATIONS AND CONTRAINDICATIONS 30
7.1 INDICATIONS 30
7.2 CONTRAINDICATIONS 30
8 MAINTENANCE, CLEANING, DISINFECTION 31
8.1 CLEANING, DISINFECTION 31
8.2 FUSE REPLACEMENT 31
9 SPECIFICATION AND ACCESSORIES 32
9.1 TECHNICAL SPECIFICATION 32
9.2 EMC PARAMETERS 34
9.3 ACCESSORIES 38
APPENDIX
APPENDIX A
LIST OF PRESET TREATMENT PROGRAMS 39
APPENDIX B
DESCRIPTION OF THE SYMBOLS, WHICH ARE PLACED ON THE UNIT CASING 42
NOTES 43
This manual includes 44 pages.
page 6 MAGNERIS – USER GUIDE
0 INTRODUCTION AND DECLARATION OF CONFORMITY
0 Introduction and Declaration of Conformity
Read this Guide carefully before starting the operation of Magneris!
Follow the recommendations presented in this Guide!
The Magneris unit may only be operated by qualifi ed personnel
or under supervision of such personnel!
Descriptions of symbols used in this manual:
Read appropriate passage of this user guide, warnings or important information.
Failure to observe warnings can lead to injuries.
Important notices and information.
Following texts marked with this symbol facilitates device operation.
REMARK
The outlook of screens shown in this manual may slightly diff er from their
actual outlook during device operation. These diff erences may concern size
and type of fonts and size of symbols. There are no diff erences in the content
of shown information.
No modifi cation of this equipment is allowed!
ISSUE DATE 05.11.2010 page 7
0 INTRODUCTION AND DECLARATION OF CONFORMITY
Version 1.1 date of issue 03.12.2010
DECLARATION OF CONFORMITY no 01/10/EN
Manufacturer: ASTAR ABR A.J DRZEJOWSKI, R.DZIENDZIEL S.J.
Address: Ul. STRA ACKA 81, 43-382, BIELSKO-BIAŁA, POLAND
Product name:
LOW FREQUENCY MAGNETIC FIELD THERAPY UNIT
Magneris Classification:
• class IIa rule 9 – for low frequency magnetic field therapy function
Declaration: Manufacturer declares under his own responsibility that the product described above complies with the requirements of Council Directive 93/42/EEC for medical devices.
Conformity assessment procedure: Annex II article 3 of EC Directive 93/42/EEC
Documentation of releasing a product to sell: „Final tests card” form MM-KBK, version 1.0, updated on 20.05.2010, as a part of the Technical File of the device, considered together with this Declaration of Conformity.
EC certificate: HD 60027842 0001 QMS certificate: SX 60027845 0001
Bielsko-Biała, Poland, 03.12.2010 signature:
(Robert Dziendziel)
page 8 MAGNERIS – USER GUIDE
1 Intended use
Magneris, the low-frequency magnetic fi eld treatment unit, is designed to carry out
treatments using magnetic fi eld generated by dedicated applicators. The unit can
be connected to a coupled CP-type plate applicator or to a CSL60-type solenoid
applicator with a diameter of 60 cm. (The latter was used previously in Magner LT
and Magner Plus units.) The medical product comprises the Magneris device,
applicator stand and CP-type applicator.
The Magneris unit can be used to treat the following disorders:
• orthopaedic:
fractures
dislocations, sprains, bruises
ligament and sinew injuries
traumas, arthroses
complex regional pain syndromes
• neurological:
neuralgias
neuromas
phantom pains
• circulatory system:
peripheral arterial bloodstream disorders
• dermatological:
ulcerations
The unit has a built-in database of pre-programmed treatment procedures, but it also
allows the user to program custom procedures.
The Magneris magnetotherapy unit is a fully mobile device that has the following
features:
• the ability to move the stand owing to the installed wheels
• the ability to adjust the height of the plate applicator by means of the servo
arm with tilt regulation
• the ability to adjust the angle of the plate applicator
• the ability to adjust the relative position of the plate applicator coils – from
parallel to perpendicular
The treatments can be conducted anywhere in the consulting room or the hospital
room. No dedicated workplace is necessary.
The treatments using the Magneris unit are conducted locally. The magnetic fi eld
aff ects only the part of the body that is to undergo the therapy. Unlike in the clas-
sical method of magnetic fi eld application that employs solenoid applicators,
plate applicators allow to reduce the eff ect of magnetic fi eld on other parts
of the patient’s body as well as on the device’s environment, including the operating
personnel.
1 INTENDED USE
ISSUE DATE 05.11.2010 page 9
2 WARRANTY AND MANUFACTURER’S RESPONSIBILITY
2 Warranty and manufacturer’s responsibility
The manufacturer warrants the device, stand and applicators to be free of faults
for two years and ensures after warranty service during 10 years from date of device
introduction in the market. The warranty includes all material and workmanship
faults.
The manufacturer undertakes to observe the warranty agreement, if the following
conditions are met:
• all repairs, changes, extensions and calibrations of equipment are performed
by manufacturer or authorized service personnel
• the mains supply system in the treatment room meets requirements of stan-
dards in force
• the unit is operated by qualifi ed personnel, in compliance with instructions
presented in this manual
• the unit is operated in compliance with its intended use
The warranty does not include consumables, such as connection cables, mains
cables, holders and fuses.
The manufacturer is not liable in case of transmission of infection by equipment
components.
The expected “life time” of the device is 10 years.
After elapse of 10 years from date of introduction of device and accessories
in the market the manufacturer is not liable for device and accessories’ faults or its
consequences.
The manufacturer bears no responsibility for results of faulty installation, wrong
diagnosis, wrong use of the device and equipment, failure to observe user’s
manual and performance of repairs by unauthorised persons.
Inside the device there are no user serviceable components, except for fuses.
On demand, the producer makes available technical diagrams, parts lists, descrip-
tions, instructions for calibration or other helpful information to appropriately
qualifi ed user’s technical staff to repair these parts of unit, which are described
by the producer as a reparable.
page 10 MAGNERIS – USER GUIDE
3 Operational safety
3.1 Mains supply and mode of operationThe Magneris unit belongs to mobile devices. It is designed for supply from AC
mains with rating 230 V ±10 %, 50 Hz. It is a medical device under safety class I,
type BF. The unit features very high value insulation resistance and very small
leakage currents. The unit may be used only in rooms, where the electric system
is executed in compliance with standards in force.
3.2 Storage, operation and transport conditionsThe Magneris unit must be stored in closed rooms, where the atmosphere is free
from vapours and caustic substances and:
• the temperature is maintained between + 5°C and +45°C
• relative humidity does not exceed 75 %
• atmospheric pressure value is between 700 – 1060 hPa
The unit is intended for operation under the following conditions:
• ambient temperature between +10°C and +30°C
• relative humidity between 30 % and 75 %
• atmospheric pressure between 700 and 1060 hPa
In case further transport is necessary use the original package, in which the device
was delivered to the customer. The transport must be performed with covered
transport means.
Recommended transport conditions:
• ambient temperature between -10°C and +45°C
• humidity between 20 and 95 %
• atmospheric pressure between 700 and 1060 hPa
3.3 Warnings and safety notices• The Magneris unit may only be operated by qualifi ed personnel in compli-
ance with instructions presented further in this manual.
• To avoid the risk of electric shock, this equipment must only be connected
to supply mains with protective earth.
• No modifi cation of this equipment is allowed.
• The treatment station (bed, couch) shall be located away from other electric
devices and water supply/sewerage installation/central heating system,
so that it is impossible for the patient to touch any of them during treatment
procedure.
• Do not remove warning signs and labels put by the manufacturer on unit
casing and casings of magnetic fi eld applicators.
• Patient must wear protective glasses during treatment in a head area.
• Avoid exposing the unit and applicators to impact of high temperatures
and atmospheric conditions.
• Treatment of persons with implanted electronic devices (e.g. cardiac pace-
maker) shall be consulted with patient’s physician.
3 OPERATIONAL SAFETY
ISSUE DATE 05.11.2010 page 11
• The unit is intended for continuous operation. It is not necessary to switch it off
from the mains between particular treatment procedures.
• The unit and CP applicator are equipped with fans ensuring appropriate air
circulation. It is inadmissible to cover ventilation holes in any way whatsoever.
• Only one CSL60 type applicator may be placed on the single rehabilitation
table.
• Only personnel may change position of the CSL60 type applicator placed
on the rehabilitation table.
• Damaged cables must be replaced immediately.
• The unit must be operated exclusively together with accessories, spare
parts, consumables, which are known to be safe and appropriate inspection
authorities did not make any reservations about them.
• It is recommended to use original accessories, spare parts and equipment
of Astar ABR Company. Use of accessories other than recommended
by the manufacturer may result in reduction of resilience and raise in unit
emissions in regard with electromagnetic interference.
• Avoid penetrating of any liquid inside the unit and applicators. In case of liquid
penetrating inside unit switch the unit off immediately, separate from
the mains and contact the service for inspection.
• It is recommended to keep minimal distance 1 m between two optional
applicators.
• During magnetotherapy treatment session personnel and bystanders shall
not be closer than 1 m to the magnetic fi eld applicator.
• A long-lasting exposure of personnel and bystanders on magnetic fi eld
could cause irritation, headache and insomnia.
• It is necessary to be careful during carrying the applicators due to their
weight.
3.4 Explosion proof environmentMagneris is not adapted to operation in rooms, where combustible gases
or their vapours occur. It is recommended to avoid anaesthetic or oxygen
derivate gases, such as nitrous oxide (N2O) and oxygen. Some materials (e.g.
cotton, wool) may after saturation with oxygen become combustible at high
temperatures generated with normal operation of equipment. It is recom-
mended that solutions of adhesive and combustible solvents be vaporised before
equipment is operated. It is also recommended to pay attention to the danger
of ignition of endogenous gases. The unit must be separated from the mains
before approaching the disinfection of the room, where it is installed.
3.5 Protection against impact of electromagnetic fi eldSimultaneous operation of the device and equipment generating strong elec-
tromagnetic fi eld, such as short wave and micro wave diathermies, may disturb
unit operation. For that reason keep appropriately big distance between them
or switching off the generator of strong fi elds during therapy with Magneris unit.
Mobile communication equipment operated with radio frequencies RF may infl u-
ence operation of Magneris unit.
3 OPERATIONAL SAFETY
page 12 MAGNERIS – USER GUIDE
The unit meets requirements of standards in regard with electromagnetic inter-
ference and resistivity against such interference and shall not pose threat for correct
operation of other devices.
Sockets of magnetic fi eld applicators, marked with symbol shown to the left, are sen-
sitive to electrostatic discharges. Attention must be paid not to touch with fi ngers
sockets of the unit, especially in rooms with low air humidity. At the moment, when
applicators are being connected, the unit must be separated from the mains, and
the user must remove electrostatic charges from his fi ngers by touching earthed
metal component (e.g. earthed pin in mains socket or metal casing of earthed device).
Magnetic fi eld applicators are marked with non-ionizing radiation symbol.
3.6 Technical supervisionThe User of Magneris unit must perform technical inspection of the unit at year’s
intervals. The inspection must be performed by a unit authorized by manufac-
turer. The inspection is performed at the user’s expense.
The inspection should include:
• evaluation of keyboard function and operation
• control of correctness of the performed auto-test
• safety test
• cable test
• magnetic fi eld applicators operation test
The inspection must also include checking the quality of applied accessories
and treatment materials. The inspection results must be recorded with periodical
inspection register delivered with the unit.
3.7 DisposalIn case, when the liquidation of the unit will become necessary (e.g. after elapse
of its life time), please contact the manufacturer or manufacturer representative,
which must react in an appropriate way, i.e. collecting the unit from the user.
The user may also contact companies busy in the business of disposal of electrical
devices or computer equipment.
3 OPERATIONAL SAFETY
ISSUE DATE 05.11.2010 page 13
4 Unit description
4.1 General characteristicsGeneral view of the unit, stand and plate applicator is presented in fi gure 4.1.
Figure 4.1 General view
Figure 4.1. View of rear side panel.
Construction of the stand allow to height adjustment (application of industrial
gas spring – further called servo) of the plate applicator, angle of rotation and
defl ection adjustment also.
4 UNIT DESCRIPTION
page 14 MAGNERIS – USER GUIDE
Available methods of adjustments are presented in fi gure 4.3.
Figure 4.3. Adjustments of the plate applicator.
The stand has four wheels with brakes. Wheel with brake and servo are presented
in fi gures 4.4 and 4.5.
Figure 4.4 Wheel with brake.
Figure 4.5 Servo.
4 UNIT DESCRIPTION
ISSUE DATE 05.11.2010 page 15
4 UNIT DESCRIPTION
4.2 Keyboard Arrangement of keyboard components is shown in fi gure 4.6.
Figure 4.6 Arrangement of keyboard components.
4.2.1 START keyPressing START button after:
• selection of treatment program or user-defi ned program in program mode
• edition of parameters in manual mode
causes the start of the treatment procedure.
Pressing START button after interruption of a treatment procedure (pause) makes
it possible to continue the procedure.
4.2.2 STOP keyPressing STOP button while performing treatment procedure causes the interrup-
tion of procedure. The unit enters the waiting state (pause). The timer will stop
then.
4.2.3 Confi rmation keyIt is used to confi rm:
• selection of function in program mode
• saving of user-defi ned program
• changes in the unit settings
4.2.4 Escape keyIts pressing causes abolition of action and going over on an early menu level.
Pressing the key during treatment procedure results in immediate interruption
of the procedure.
LCD
Indicator of selectedapplicator
Edit keys
Save key
Information key
Escape key
Confirmation key
Operation modechange key
page 16 MAGNERIS – USER GUIDE
4 UNIT DESCRIPTION
4.2.5 Information keyPressing of this key causes displaying of more information with full name
and parameters of:
• treatment program
• user defi ned program
Escape from information menu follows after pressing of or key.
4.2.6 Operation mode change key Pressing of this key results in change from program operation mode to manual
mode (and vice versa).
4.2.7 Save key Pressing of this key enables saving of parameters of treatment procedure edited
in manual mode in the shape of user defi ned program.
4.2.8 Edit keysMenu item change keys:
Pressing of them results in change of menu item or change of arrow position with
introduction of access codes and name during edition of user defi ned programs.
Parameter change keys:
Pressing of them results in change of value of edited parameter and selection
of sign with introduction of access codes and name during edition of user defi ned
programs.
4.3 Rear and side panelsOn the right side wall of the unit the name plate is located.
On rear side wall are located:
• mains socket
• fuse socket
• mains on/off button
4.4 Name plateThe name plate is located on the rear wall of unit casing. On the name plate are
shown data as follows:
• unit version
• serial number
• rated voltage and operation frequency
• max. power consumption
• protection degree provided by casing
• appropriate graphic symbols
• types of applied fuses
• manufacturer’s data (address, phone and fax numbers)
ISSUE DATE 05.11.2010 page 17
REMARKS:
• Magneris features two modes of generating magnetic fi eld: continuous and
interrupted. In the continuous mode magnetic fi eld is generated with
constant amplitude during the whole treatment procedure period. This mode
is selected by setting the pause time to cont. In the interrupted mode the mag-
netic fi eld is generated for 1 second, which is followed by a pause. The pause
length can be set between 0,5 s and 8 s. The drawing beneath shows operation
principle in interrupted mode.
Figure 4.7. Field shape in interrupted mode.
• Magnetic fi eld induction – is measured in militeslas (mT) or gausses (Gs).
The maximum value that can be set is 2.5 mT (25 Gs). This value is set in relation
to the geometric centre of the CSL60 applicator or the coils of the CP applicator
4 UNIT DESCRIPTION
4.5 Treatment parametersParameters description:
Rectangular
Triangular
Sinusoidal
Half-rectangular
Half-triangular
Półsinusoidalny
Symbol Defi nition
Applicator type
Magnetic fi eld shape
Frequency of magnetic fi eld
Pause time in operation mode with modulation
Magnetic fi eld induction
Timer
Available settings
2 – 60 Hz
cont – continuous operation 0,5 – 8 s
0 – 2,5 mT0 – 25 Gs
1 – 30 minutes, step 1 minute
CP type – plate applicator
CSL60 type – sollenoid applicator
pulse
1 s
break
0,5–8 s
page 18 MAGNERIS – USER GUIDE
turned towards each other. At the edges of the applicator, the magnetic induction
can even be four times as high as the original value. The distribution of the magnetic
-fi eld induction of the CP applicator, depending on the relative position of the coils,
is shown below.
Figure 4.8. The distribution of the magnetic-fi eld induction and the relative position of CP applicator coils.
4 UNIT DESCRIPTION
9mT 9m
T6mT 6m
T4mT 4m
T3mT 3m
T
2,5mT
2,5mT
2mT
1,5mT
1mT
2mT
1,5mT
1mT
0 5 10 1551015 [cm]
0
5
10
5
10
[cm]
9mT
6mT
4mT
3mT
2,5mT9mT6mT4mT3mT
2mT
1,5mT
1mT
0 5 10 15 20510
0
5
10
5
10
1520[cm]
[cm]
1mT
1,5mT
2mT
2 mT,5
3mT
4mT
6mT
8mT
3mT
4mT
6mT
8mT
0
5
5
10
15
[cm]
0 5 10 15 20 25510152025[cm]
ISSUE DATE 05.11.2010 page 19
4 UNIT DESCRIPTION
4.6 Magnetic fi eld applicatorsTwo types of magnetic fi eld applicators can be used with the Magneris unit:
• CSL60 – used previously in the Magner Plus and Magner LT units, solenoid
-type, can be attached to a treatment couch, diameter of 60 cm, maximum
induction of 2.5 mT
• CP – coupled plate applicator comprising two elements (labelled CP-ID1
and CP-ID2), mounted on a stand, allows for height and angle adjustment,
treatment fi eld illumination by means of LEDs, which also indicate the presence
of the magnetic fi eld (glow in continuous operation, pulse in intermittent
operation)
While adjusting the position of the CP applicator elements, care should be
taken not to excessively twist the connection cables.
The CSL and CP applicators feature cooling systems that prevent overheating
of the applicators’ surfaces:
• CSL60 – a passive system installed between the coil and the outer casing
• CP – active system consisting of fans (one in each applicator coil)
Under no circumstances should the vents in CP applicator element casings
be covered!
Figure 4.9. View of the CP applicator.
page 20 MAGNERIS – USER GUIDE
5 DEVICE INSTALLATION AND START-UP
5 Device installation and start-up
5.1 Unit installationFirst installation of the unit should be done by qualifi ed distributor employee.
The instructions for the stand assembly are provided in a separate manual.
After removing the unit from carton, check if the complete unit has been deliv-
ered. In case of any inconsistencies contact the seller or manufacturer.
After removing the unit from transportation packaging wait approximately
two hours before proceeding to next installation steps. This is aimed at adap-
tation of the unit to conditions in operation room.
5.1.1 Attaching the device to the shelf of the standPlace the device on the shelf of the stand and secure it by means of the two screws
underneath the shelf, as shown in the fi gure 5.1.
Figure 5.1. Attaching the device to the shelf of the stand.
5.1.2 Connecting applicatorsOn the back of the unit, there are two dedicated applicator sockets. Plug
the applicator connector into the socket and turn clockwise 1/8 of a turn.
In order to disconnect the applicator, slide the metal latch on the connector
backwards, then turn the connector counterclockwise 1/8 of a turn. The sockets
are shown in the fi gure 5.2. The socket for the CSL60 applicator is labelled
as , while the socket for the CP applicator as . The meaning
of the ESD symbol is explained in section 3.5.
Figure 5.2. Applicator sockets.
ISSUE DATE 05.11.2010 page 21
5.1.3 Stand height adjustmentIn order to adjust the height of the stand, use one hand to unlock the servo arm
actuator by means of its lever, and the other hand to move the arm up or down.
Figure 5.3. Actuator release lever.
5.1.4 Plate applicator position adjustmenta) in order to adjust the tilt of the applicator, perform the following:
• approach the applicator from the push-button side (see fi gure 5.4)
• with your right hand, move the lever (forwards or backwards, depending
on the spring’s torsion) and hold it in its place
• with your left hand, push the button labelled PUSH and hold it – changing
the applicator position will be much easier
• adjust the applicator position accordingly
• release the push-button
Figure 5.4. Plate applicator position adjustment.
5 DEVICE INSTALLATION AND START-UP
Push-button
Lever
page 22 MAGNERIS – USER GUIDE
NOTE 1
If the push-button is loose, perform the following:
• pry the rubber cap labelled PUSH and take it off
• adjust the push-button in such a way that the gap between the stand arm
and the push-button is 1.5 – 2 mm wide
• using Allen wrench (supplied), tighten the setscrew in the centre of the push
-button
• install the rubber cap labelled PUSH
b) in order to adjust the angle of the applicator, rotate the bar that supports
the two applicator coils
c) in order to adjust the relative position of the applicator coils, rotate them
accordingly.
NOTE 2
If the thumbscrews fi xing the applicator coils to the bar or the bar to the arm
are too loose, tighten them.
NOTE 3
If the said thumbscrews are tightened too much, move the applicator coils
or the bar several times in order to loosen them.
While adjusting the position of the CP applicator elements, care should be
taken not to excessively twist the connection cables.
5.1.5 First start-upConnect the unit to the 230 V mains power supply using the supplied cable. After
switching the unit on, all functional blocks are tested. When the tests are fi nished,
a list of detected applicators is displayed. Screen examples are shown below:
If after the self-test procedure the screen displays an error message with an error
code, switch the unit off and contact technical support.z serwisem.
5 DEVICE INSTALLATION AND START-UP
ISSUE DATE 05.11.2010 page 23
5 DEVICE INSTALLATION AND START-UP
If after the self-test procedure the screen displays information regarding incor-
rectly connected applicators, replace the connectors in the correct sockets
and start the unit again.
5.2 Setup modeTo enter setup mode, press the key marked with symbol during self-test.
The following information will be shown on the display:
The following functions are available:
• Sounds
• Contrast
• Dose unit
• Removal of user programs
• Language
• Start-up menu
The function is selected with keys . To enter the selected option press
the key. To exit the setup mode, switch off unit supply or in setup mode press
the (then the unit restarts, and the suitable information is shown on the display).
5.2.1 SoundsWith the Magneris unit the user may confi gure settings of acoustic signals, which
occur during unit operation. Description of available confi guration options:
• Keys sounds – sound signal is generated whenever a key is pressed
• Sounds during treatment – while performing treatment procedure sound
signals are generated at 1-second interval
• End of treatment sound – the end of a treatment procedure is signalled
by sequence of short sound signals
To select arrow position use the keys, switching on and off particular
option takes place with keys . That a particular option is on is confi rmed
by the „tick” symbol visible in the fi eld just opposite the option name. If the fi eld
is empty, this particular option has not been selected.
Approval of selection is performed by pressing the key. Escape without
approval (settings from before modifi cation remain) is performed by pressing
the key.
page 24 MAGNERIS – USER GUIDE
5.2.2 ContrastIn the Magneris unit it is possible to adjust display contrast. With the key
the level of contrast is increased and with the key decreased. Approval of settings
is performed by pressing the key. Escape without approval (settings from
before modifi cation remain) is performed by pressing the key.
5.2.3 Dose unitIn the Magneris unit it is possible to choose units indication:
• mT – militesla
• Gs – Gauss
To select arrow position use the keys, switching on and off particular
option takes place with keys . That a particular option is on is confi rmed by
the „tick” symbol visible in the fi eld just opposite the option name. If the fi eld
is empty, this particular option has not been selected. Approval of selection is per-
formed by pressing the key. Escape without approval (settings from before
modifi cation remain) is performed by pressing the key.
5.2.4 Removal of user programsSelection of this option enables overall deletion of programs saved by the user.
In order to delete all user-defi ned programs, follow the instructions shown on
the display.
While editing settings, it is unnecessary to repeat deletion of user-defi ned
programs several times.
5.2.5 LanguageWith the Magneris unit information in the display may be presented in diff erent
languages. The user is free to select language option.
To change of language version use the keys, switching on particular
option takes place with the key. That a particular option is on is confi rmed
by the “tick” symbol visible in the fi eld just opposite the option name. Approval
of selection is performed by pressing the key. Escape without approval (settings
from before modifi cation remain) is performed by pressing the key.
5.2.6 Start-up menuThis option enables selection of mode, in which after switching on the mains supply
the Magneris unit will be started. Two options are available:
• Program mode
• Recently selected program
In the fi rst case, after switching on main supply, general menu will appear, when
one of the following options may be selected:
• Preset programs
• User programs
In the second case after switching on mains supply the list of preset programs will be
displayed at the program, which was recently selected in the last treatment cycle
or in manual mode.
5 DEVICE INSTALLATION AND START-UP
ISSUE DATE 05.11.2010 page 25
6 UNIT OPERATION
6 Unit operation
The unit can be operated in one of the two modes:
• program mode
• manual mode
In the program mode you can take advantage of preset procedures:
• treatment programs
• user defi ned programs
In the program mode you cannot edit the introduced parameters. Such option
is available in the manual operation mode.
Transition between program operation mode and manual mode (and vice versa)
follows after pressing the key.
Under no circumstances should the applicators be connected or disconnected
during the treatment. This procedure should be performed when the unit is not
generating the magnetic fi eld!
Figure 6.1 shows an example treatment procedure.
Figure 6.1. Example of treatment procedure.
6.1 Operation with preset treatment programsThe simplest method to use the unit is to use its preset programs or treatment
sequences. The unit includes a base of several dozens of most frequently met
disorders together with suggested treatment types and parameters. The list of all
diseases with parameters is included in Appendix A at the end of the manual.
page 26 MAGNERIS – USER GUIDE
6 UNIT OPERATION
Parameter values of treatment programs are selected on the basis of available
literature data and determined as average values. Sole responsibility for applica-
tion of preset programs rests with the user.
In order to perform the treatment procedure by means of a preset treatment
program:
1. Switch on the unit. Depending on the Menu function confi guration, after
powering on (see section 5.2.6) the unit starts up either in the PROGRAM
GROUPS menu mode or in a set treatment program (or user program) that was
used during the previous treatment procedure. In the latter case, in order
to select a diff erent program from the PROGRAM GROUPS menu, press the
key. When no program change is necessary, proceed to step 5.
The PROGRAM GROUPS menu screen:
2. Press the keys to choose the Preset programs option, and press the
key to confi rm.
3. Press the keys to choose the treatment program.
Press the key to display an information screen containing parameters
of the relevant treatment program (example shown below):
Defi nitions of symbols are provided in section 4.5.
In order to close the information window (showing the name or parameters),
press the or key.
4. Prepare the patient for treatment. Set up the applicator that will be used
during the treatment procedure.
5. To start the treatment procedure, press the START key.
6. Press the keys to adjust the magnetic-fi eld induction, if required.
ISSUE DATE 05.11.2010 page 27
6 UNIT OPERATION
NOTE
If two magnetic fi eld applicators are connected, the applicator selection window
displays when the START key is pressed. The applicator selection window is shown
below:
Press the buttons to select an applicator. When the applicator type is selected,
press the START key again. The unit starts generating magnetic fi eld. An indicator
denoting the selected applicator lights up on the keyboard.
An example screen during the treatment procedure is shown below:
If during the treatment procedure the induction value is reduced to 0 [mT]/0 [Gs],
the following message displays on the screen:
In order to continue the treatment procedure, press the key. If you wish
to return to the Preset programs menu, press the key.
When the treatment procedure is fi nished, a message displays on the screen
and an audible signal is emitted (provided this feature is enabled; see section
5.2.1).
In order to pause the treatment procedure, press the STOP key. The time counter
will stop. In order to continue the treatment procedure, press the START key. If you
wish to return to the Preset programs menu, press the key.
page 28 MAGNERIS – USER GUIDE
6 UNIT OPERATION
6.2 Operation in the manual modeIn the manual mode the user can set up custom treatment parameters. Perform
the following procedure:
1. Switch on the unit. Press the key in order to enter the manual mode.
2. Press the keys to choose a parameter or applicator selection fi eld.
The selected fi eld is highlighted. An example screen is shown below:
Defi nitions of symbols are provided in section 4.5
3. Press the keys to change the parameter values or the applicator type.
4. Prepare the patient for treatment. Set up the applicator that will be used
during the treatment procedure.
5. To start the treatment procedure, press the START key.
6. Press the keys to adjust the magnetic-fi eld induction, if required.
If when starting or during the treatment procedure the induction value is reduced
to 0 [mT]/0 [Gs], the following message displays on the screen:
In order to continue the treatment procedure, press the key. If you wish
to return to the treatment parameters screen, press the key.
When the treatment procedure is fi nished, a message displays on the screen
and an audible signal is emitted (provided this feature is enabled; see section
5.2.1).
In order to pause the treatment procedure, press the STOP key. The time counter
will stop. In order to continue the treatment procedure, press the START key. If you
wish to return to the treatment parameters screen, press the key.
6.3 User defi ned programsThe user may save up to twenty own treatment programs. Each program may be
given a name consisting of letters (19 signs max.).
ISSUE DATE 05.11.2010 page 29
To edit and save a user defi ned program:
1. Start the unit in manual mode in compliance with rules given in section 6.2.
2. Set up treatment procedure parameters, as in section 6.2.
3. Press the key marked with symbol
4. With keys select the number, under which the edited program will be
saved. Confi rm your choice with key.
5. Enter program name – with keys select the sign, with keys
move the arrow. Below an example of screen after entering program name
is shown:
6. Press the key. On the screen the following information is displayed:
7. Pressing of key results in saving user defi ned program and return to
parameter edition menu.
At the fi rst attempt to save user program all memory locations are free. Saving
of consecutive user defi ned programs may follow to free locations or already
saved by their overwriting. In the second case, when attempting to save,
on the screen the following message will be displayed:
Pressing of key results in change to program name entry mode, method
of entering program name – see stage 5.
At every stage of user defi ned program edition you may return to an earlier
level by pressing the key.
In order to perform a treatment procedure based on user defi ned program,
follow the instruction of using preset treatment programs (see 6.1.1). Choose
User programs option in the PROGRAM GROUPS menu.
6 UNIT OPERATION
page 30 MAGNERIS – USER GUIDE
7 INDICATIONS AND CONTRAINDICATIONS
7 Indications and contraindications
7.1 Indications• delayed union of fractured bone
• pseudoarthrosis
• osteoporosis
• degenerative joint disease
• rheumatoid arthritis
• ulcerations and trophic shank changes
• bacterial infection of skin and soft tissues
• keloids
• condition after cerebral stroke
• hemicrania and vasomotor headaches
• functional disorders of cranial and peripheral nerves
• multiple sclerosis
• cornea infection diseases
• optic atrophy
• arterial hypertension
• ischaemic heart disease
• heart arrhythmia
• hypersensitive large intestine
• chronic pancreatitis
7.2 Contraindications• pregnancy
• neoplastic disease
• active tuberculosis
• juvenile diabetes
• thyrotoxicosis
• bleeding from alimentary system
• severe infections
• presence of electronic implants (e.g. cardiac pacemaker)
ISSUE DATE 05.11.2010 page 31
8 Maintenance, cleaning, disinfection
8.1 Cleaning, disinfectionCAUTION!
Before approaching the below operations separate the unit from the mains!
Cleaning of the unit shall be performed with lightly humid sponge or soft cloth
with delicate soap solution or soft detergent.
Do not use solvents! Do not also use excessively wet sponges, which could
bring about penetration of water inside the unit.
Cleaning of the applicators shall be performed with lightly humid sponge or soft
cloth with delicate soap solution or soft detergent, then dry the cleaned accessories
with dry cloth and leave for complete drying.
Do not use humid or wet cables!
Do not disinfect or sterilise unit casing.
Disinfection of accessories, which are not intended for contact with patient’s body
(for example cables), shall be carried out with liquid or spray agents dedicated
to that purpose at least once a week.
Applicator casing may contact with patient’s body during treatment procedure.
Perform disinfection after each such treatment procedure, it is recommended
to use 70 % alcohol solution. After disinfection, accessories must be washed
with clean, tepid water to avoid allergic reaction.
8.2 Fuse replacementWARNING
Before approaching the operations below separate the unit from the mains!
In case of burnt fuses replace them. The parameters are listed in section 9. and
in the name plate.
To replace fuses:
1. Isolate the device from the mains.
2. Disconnect the mains cable from the mains socket.
3. With fl at screwdriver lever the fuse socket until the moment of its slipping
from the socket.
4. Remove the socket with your fi ngers, replace the fuses, install them in the socket
again and press fi rmly.
5. Connect the mains cable – fi rst to the socket placed in the back panel
of the controller and then to the mains.
6. Check the device operation.
8 MAINTENANCE, CLEANING, DISINFECTION
page 32 MAGNERIS – USER GUIDE
9 SPECIFICATION AND ACCESSORIES
9 Specifi cation and accessories
9.1 Technical specifi cation
Operation mode
Unit is intended for continuous operation.
Treatment parameters
shapes of magnetic fi eld rectangular, sinusoidal, triangular,
half-rectangular, half-sinusoidal, half-triangular
frequency 2 – 60 Hz, step variable
accuracy of frequency ±20 % preset value
pulse time in interrupted mode 1 s
accuracy of pulse time in interrupted mode ±20 %
pause time in interrupted mode 0,5; 1,0; 1,5; 2,0; 3,0; 4,0; 6,0; 8,0 s
accuracy of pause time ±20 % preset value
maximum induction 2,5 mT
maximum induction spread 5 mT
accuracy of preset induction ±20 % maximum value
for given applicator in his geometrical centre
available to preset induction values
• applicator CP 0,0; 0,5; 1,0; 1,5; 2,0; 2,5 mT
• applicator CSL60 0,0; 0,5; 1,0; 1,5; 2,0; 2,5 mT
Treatment programs
preset 50 programs
user-defi ned 10
Treatment timer
treatment time setting range 1 – 30 minutes
treatment time setting step 1 minutes
accuracy ±10 %
General
mains supply 230 V ±10 %, 50 Hz
power consumption 200 W, 250 VA
safety class I, typ BF
degree of protection provided by enclosure IP20
mains fuses time lag T 2 A, 250 V
unit dimensions (width x depth x height) 30x30x13 cm
unit weight max 6 kg
CP weight max 5,5 kg
CSL60 weight max 14 kg
stand with CP weight max 17,5 kg
total weight max 29 kg
dimensions of the stand area 65x75 cm
height adjustment range 40 – 110 cm
ISSUE DATE 05.11.2010 page 33
9 SPECIFICATION AND ACCESSORIES
CP – angle of rotation 150°
wheels 4 wheels with brakes
Storage conditions
temperature range +5 – +45°C
relative humidity 30 – 75 %
pressure range 700 – 1060 hPa
Operation conditions
temperature range +15 – +30°C
relative humidity 30 – 75 %
pressure range 700 – 1060 hPa
Transport conditions
temperature range -10 – +45°C
relative humidity 20 – 95 %
pressure range 700 – 1060 hPa
page 34 MAGNERIS – USER GUIDE
9 SPECIFICATION AND ACCESSORIES
9.2 EMC parameters In compliance with EN60601-1-2 standard
Compliance
Group 1
Class B
Class A
Complies
Electromagnetic environment – guidance
The LFMF unit Magneris uses RF energy only for its internal functions. Therefore, its RF emissions are very low and it is not probable, that they will cause any disturbances in the opera-tion of electronic equipment located nearby.
The Magneris unit is suitable for use in all establishments includ-ing domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
Emissions test
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissionsIEC 61000-3-2
Voltage fl uctuations/Flicker emissionsIEC 61000-3-3
Guidance and manufacturer’s declaration – electromagnetic emissions
The LFMF unit Magneris is intended for use in the electromagnetic environment specifi ed below. The customeror user should assure that the LFMF unit Magneris is used in such an environment.
ISSUE DATE 05.11.2010 page 35
9 SPECIFICATION AND ACCESSORIES
Immunity test
Electrostatic discharge (ESD)IEC 61000-4-2
Electrical fast transient/burstIEC 61000-4-4
SurgeIEC 61000-4-5
Voltage dips, short interruptions and voltage variations on power supply input linesIEC 61000-4-11
Power frequency (50/60 Hz) Magnetic fi eldIEC 61000-4-8
IEC60601test level
±6 kV contact±8 kV air
±2 kV for power supply lines±1 kV for input/output lines
±1 kV diff erential mode±2 kV common mode
<5 % UT
(>95 % dip in UT)
for 0,5 cycle40 % U
T
(60 % dip in UT)
for 5 cycles70 % U
T
(30 % dip in UT)
for 25 cycles<5 % U
T
(>95 % dip in UT)
for 5 sec
3 A/m
Compliance level
±6 kV contact±8 kV air
±2 kV for power supply lines±1 kV for input/output lines
±1 kV diff erential mode±2 kV common mode
<5 % UT
(>95 % dip in UT)
for 0,5 cycle40 % U
T
(60 % dip in UT)
for 5 cycles70 % U
T
(30 % dip in UT)
for 25 cycles<5 % U
T
(>95 % dip in UT)
for 5 sec
3 A/m
Electromagnetic environment – guidance
Floors should be wood, concrete or ceramic tile. If fl oors are covered with synthetic material, the relative humidity should be at least 30 %
Mains power quality should be that of a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital environment. If the user of the Magneris requires continued operation during power mains interrup-tions, it is recommended that Magneris be powered from an interruptible power supply or a battery.
Power frequency magnetic fi elds should be at levels characteristic of a typical location in a typical commercial or hospital environment.
Indications and declaration of manufacturer – electromagnetic immunity
The LFMF unit Magneris is intended for use in the electromagnetic environment specifi ed below. The customeror user should assure that the LFMF unit Magneris is used in such an environment.
NOTE UT is the a.c. mains voltage prior to application of the test level.
page 36 MAGNERIS – USER GUIDE
9 SPECIFICATION AND ACCESSORIES
Immunity test
Conducted RFIEC 61000-4-6
Radiated RFIEC 61000-4-3
IEC60601test level
3 Vrms
150 kHz to 80 MHz
3 V/m
26 MHz to 2,5 GHz
Compliance level
3 Vrms
3 V/m
Electromagnetic environment – guidance
Portable and mobile RF communications equipment should be used no closer to any part of the Magneris, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.
Recommended separation distanced = 1,2√Pd = 1,2√P 26 MHz to 800 MHzd = 2,3√P 800 MHz to 2,5 GHzwhere P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m).
Field strengths from fi xed RF transmitters, as determined by an electromagnetic site surveya, should be less than compliance level in each frequency rangeb.
Interference may occur in the vicinity of equipment marked with the following symbol.
Indications and manufacturer’s declaration – electromagnetic immunity
The LFMF unit Magneris is intended for use in the electromagnetic environment specifi ed below. The customer or user should assure that the LFMF unit Magneris is used in such an environment.
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
a Field strengths from fi xed transmitters, such a base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagneticenvironment due to fi xed RF transmitters, an electromagnetic site survey should be considered. If the measured fi eld strength in the location in which the Magneris is used exceeds the applicable RF compliance level above, the unit should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the unit.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
ISSUE DATE 05.11.2010 page 37
9 SPECIFICATION AND ACCESSORIES
Radiated maximum outputpower of transmitter W
Separation distance according to frequency of transmitter m
150 kHz to 80 MHzd = 1,2√P
0,12
0,38
1,20
3,80
12,00
0,01
0,10
1,00
10,00
100,00
80 MHz to 800 MHzd = 1,2√P
0,12
0,38
1,20
3,80
12,00
800 MHz to 2,5 GHzd = 2,3√P
0,23
0,73
2,30
7,30
23,00
Recommended separation distances between portable and mobile RF communications equipment and LFMF unit Magneris
The Magneris unit is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the unit can help prevent electromagnetic interference by main-taining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Magneris as recommended below, according to the maximum output power of the communications equipment.
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can beestimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitterin watts (W) according to the transmitter manufacturer.NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is aff ected by absorption and refl ection from structures, objects and people.
page 38 MAGNERIS – USER GUIDE
9 SPECIFICATION AND ACCESSORIES
9.3 Accessories• controller Magneris
• stand dedicated to CP type applicator
• CP type applicator
• CSL60 type applicator – optional
• protective glasses for the patient
• mains cable
• User guide
• Warranty certifi cate
• Post inspection report
• Electrical safety test – inspection report
• spare fuses – time lag T 2 A/250 V type
ISSUE DATE 05.11.2010 page 39
APPENDIX A LIST OF PRESET TREATMENT PROGEAMS
Ite
m 1 2 3 4 5 6 7 8 9
10
11
12
13
14
15
16
17
18
19
20
21
22
Ind
uct
ion
[mT
]
2,5
2,5
1,0
2,5
2,5
2,5
1,0
1,5
2,5
1,5
2,5
1,0
2,5
1,5
2,5
1,0
2,5
1,5
1,0
2,0
2,5
1,0
Fre
qu
en
cy[H
z] 30
35
12
20
40
35 6
30
40
10
30
10
40
10
35
12
40
20
10
40
27 4
Tre
atm
en
t ti
me
[min
.]
15
15
12
15
15
15
12
15
15
12
15
12
15
12
15
15
15
10
10
10
10
10
Fie
ld s
ha
pe
Re
cta
ng
ula
r
Re
cta
ng
ula
r
Sin
uso
ida
l
Re
cta
ng
ula
r
Re
cta
ng
ula
r
Re
cta
ng
ula
r
Ha
lf-s
inu
soid
al
Tria
ng
ula
r
Re
cta
ng
ula
r
Sin
uso
ida
l
Re
cta
ng
ula
r
Ha
lf-r
ect
an
gu
lar
Re
cta
ng
ula
r
Ha
lf-r
ect
an
gu
lar
Re
cta
ng
ula
r
Sin
uso
ida
l
Re
cta
ng
ula
r
Sin
uso
ida
l
Sin
uso
ida
l
Re
cta
ng
ula
r
Sin
uso
ida
l
Sin
uso
ida
l
Na
me
of
dis
ea
se
De
laye
d u
nio
n o
f fr
act
ure
d b
on
e
Pse
ud
oa
rth
rosi
s
Fra
ctu
res
– in
fl a
mm
ato
ry s
tag
e
Fra
ctu
res
– c
art
ilag
e f
orm
ati
on
sta
ge
Fra
ctu
res
– c
linic
al a
dh
esi
on
sta
ge
Ne
cro
sis
of
he
ad
of
fem
ur
Su
de
ck s
ynd
rom
e –
acu
te s
tag
e
Sud
eck
syn
dro
me
– d
ystr
op
hy
and
atr
op
hy
stag
e
Ost
eo
po
rosi
s
De
ge
ne
rati
on
of
join
ts –
acu
te s
tag
e
De
ge
ne
rati
on
of
join
ts –
ch
ron
ic s
tag
e
Rh
eu
ma
toid
art
hri
tis
– a
cute
sta
ge
Rh
eu
ma
toid
art
hri
tis
– r
em
issi
on
sta
ge
De
ge
ne
rati
ve c
ha
ng
es
of
spin
e C
-se
ctio
n
– a
cute
sta
ge
De
ge
ne
rati
ve c
ha
ng
es
of
spin
e C
-se
ctio
n
– c
hro
nic
sta
ge
De
ge
ne
rati
ve c
ha
ng
es
of
spin
e jo
ints
, T
h-
an
d L
-se
ctio
ns
– a
cute
sta
ge
De
ge
ne
rati
ve c
ha
ng
es
of
spin
e jo
ints
, T
h-
an
d L
-se
ctio
ns
– c
hro
nic
sta
ge
Ulc
era
tio
ns
an
d t
rop
hic
ch
an
ge
s o
f lim
bs
Bu
rns
– e
xud
ate
sta
ge
Bu
rns
– g
ran
ula
tio
n
Ch
elo
id
Mig
rain
e
Ap
pe
nd
ix A
L
ist
of
pre
set
tre
atm
en
t p
rog
ram
s
page 40 MAGNERIS – USER GUIDE
APPENDIX A LIST OF PRESET TREATMENT PROGEAMS
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
2,0
1,5
1,5
2,5
1,5
2,5
1,0
2,5
1,5
2,5
2,0
2,5
1,0
2,5
1,5
1,5
2,5
2,0
2,0
1,5
2,5
1,5
1,5
2,5
1,0
4 8
10
35
10
40
10
40
10
36 6 8
10
40
12 8
36
10 6 8
40
35 6
30 6
Sin
uso
ida
l
Re
cta
ng
ula
r
Tria
ng
ula
r
Re
cta
ng
ula
r
Sin
uso
ida
l
Re
cta
ng
ula
r
Sin
uso
ida
l
Re
cta
ng
ula
r
Sin
uso
ida
l
Re
cta
ng
ula
r
Re
cta
ng
ula
r
Sin
uso
ida
l
Sin
uso
ida
l
Re
cta
ng
ula
r
Re
cta
ng
ula
r
Sin
uso
ida
l
Re
cta
ng
ula
r
Sin
uso
ida
l
Sin
uso
ida
l
Tria
ng
ula
r
Re
cta
ng
ula
r
Sin
uso
ida
l
Sin
uso
ida
l
Re
cta
ng
ula
r
Sin
uso
ida
l
Ne
ura
lgia
s (g
en
era
l)
Lum
ba
lgia
Sta
tus
aft
er
imp
lan
tati
on
of
en
do
pro
the
sis
– a
cute
co
nd
itio
n
Sta
tus
aft
er
imp
lan
tati
on
of
en
do
pro
the
sis
– c
hro
nic
co
nd
itio
n
Sta
tus
aft
er
reco
nst
ruct
ion
of
liga
me
nts
–
acu
te c
on
dit
ion
Sta
tus
aft
er
reco
nst
ruct
ion
of
liga
me
nts
–
ch
ron
ic c
on
dit
ion
Po
st t
rau
ma
tic
inju
rie
s o
f p
eri
art
icu
lar
soft
ti
ssu
es
– a
cute
co
nd
itio
n
Po
st t
rau
ma
tic
inju
rie
s o
f p
eri
art
icu
lar
soft
ti
ssu
es
– c
hro
nic
co
nd
itio
n
Po
st t
rau
ma
tic
wo
un
ds
– in
fl a
mm
ato
ry s
tag
e
Po
st t
rau
ma
tic
wo
un
ds
– g
ran
ula
tio
n
an
d r
eco
nst
ruct
ion
sta
ge
Ba
ck p
ain
s in
an
kyl
osi
ng
sp
on
dyl
itis
Hyp
ert
on
ia –
La
xato
r
Po
st s
urg
ica
l wo
un
ds
– a
cute
sta
ge
Po
st s
urg
ica
l wo
un
ds
– c
hro
nic
sta
ge
Ove
rlo
ad
ch
an
ge
s o
f m
usc
le a
tta
chm
en
ts
MS
– M
ult
iple
scl
ero
sis
– L
axa
tor
Be
dso
res
Bra
in s
tro
ke
Sto
ma
ch u
lce
rati
on
Torn
lig
am
en
ts –
acu
te c
on
dit
ion
Torn
lig
am
en
ts –
ch
ron
ic c
on
dit
ion
Bro
nch
ial a
sth
ma
Bra
chia
l ne
ura
lgia
– a
cute
co
nd
itio
n
Bra
chia
l ne
ura
lgia
– c
hro
nic
co
nd
itio
n
Acu
te c
ata
rrh
al b
ron
chit
is
12
10
10
15
12
15
10
15
10
15
15
15
10
15
10
15
15
12
10
10
15
10
10
15
10
ISSUE DATE 05.11.2010 page 41
APPENDIX A LIST OF PRESET TREATMENT PROGEAMS4
8
49
50
1,0
1,5
2,5
6 8
40
10
10
15
Sin
uso
ida
l
Sin
uso
ida
l
Re
cta
ng
ula
r
Acu
te c
olla
tera
l sin
usi
tis
an
d t
on
silli
tis
Sci
ati
ca –
acu
te c
on
dit
ion
Sci
ati
ca –
ch
ron
ic c
on
dit
ion
page 42 MAGNERIS – USER GUIDE
APPENDIX B DESCRIPTION OF THE SYMBOLS, WHICH ARE PLACED ON THE UNIT CASING
Appendix B Description of the symbols, which are placed on the unit
casing
Explanation
Caution, see the ASSOCIATE DOCUMENTS
Application components of BF type
Date of manufacture : year
Protection level provided for by casing
Susceptibility to electrostatic discharges
Fuse
Unit version
Serial number
Disposal of worn-out device together with other waste is prohibited
Follow operating instructions
Background colour: blueSymbol/text: white
Stepping prohibited
Background colour: whiteCicular band and slash: red Symbol/text: black
Sitting prohibited
Background colour: whiteCicular band and slash: red Symbol/text: black
Symbol
IP20
VER
SN
or
or
or
ISSUE DATE 05.11.2010 page 43
Notes