WEPERE LOB User manual

USER MANUAL
Magnetize your sport

3 USER MANUAL
Introduction
Magnetotherapy 5
Manufacturer 6
Declaration of conformity 6
Classifications 7
Intended purpose and scope of use 8
Technical characteristics 8
Labelling 10
Device labels in detail 10
Description of the symbols (device and packaging) 11
Contents of the pack 12
How to use the device
Warnings 12
Electromagnetic interference 13
Contraindications and side effects 13
Radiation emitted for therapeutic purposes 13
Fortuitous radiation 14
Quick use of the device with preset parameters 14
Use of the therapeutic belts and solenoids,
main applications and suggestions 16
Instructions for using the preset programs 17
List of stored programs 20
Settings (language selection) 23
How to look after the device
Checking device operation 23
Cleaning the device 24
Transport and storage 24
Disposal 25
Maintenance 25
Support 25
Spare parts 26
EMC Tables 26
Warranty 29

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Magnetotherapy
The treatment of certain conditions through low frequency and high intensity pulsed magnetic
fields has garnered great consensus amongst international scientific circles for many years,
especially as regards chronic and degenerative diseases.
Magnetotherapy uses low frequency and high intensity pulsed magnetic fields induced by the
electric current that runs through a coil; due to its characteristics it is now universally recogni-
sed as the most suitable technique for the treatment of bone conditions and in particular for
osteoporosis.
The biological modifications induced by the magnetic fields on the cell membranes guarantee a
biostimulation able to restore the correct functionality of the cell itself.
According to the experiences of several authors, in cases of osteoporosis, already starting from
the sixth treatment session there is a remarkable regression of pain symptoms and even more
striking is that a significant increase in BMD (Bone Mass Density) is noted. The high magnetic
field flux value (Gauss) generated by the device allows the treatment of the user even in the
presence of braces or plaster casts.

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Classifications
In compliance with article 2, point 1, of REGULATION (EU) 2017/745, the LOB device is a medical
device as it consists of a device intended by the manufacturer to be used on humans for the tre-
atment or mitigation of illnesses.
In compliance with point 1.2 of Annex VIII of REGULATION (EU) 2017/745, the LOB device is a type of
device designed for continuous use for less than 24 hours, whose duration of use is therefore “short
term”. According to point 2.4 of the same annex, the device is an active therapeutic device as it
depends on a source of electrical energy (active medical device), and is intended for the treatment
of various types of pathologies (therapeutic device). In accordance with point 6.1 rule 9, annex VIII
of regulation (EU) 2017/745, all therapeutic active devices intended to supply or exchange energy
are classified as class IIa unless their characteristics are such as to allow them to supply energy to
the human body or exchanging energy with the human body in a potentially dangerous form, taking
into account the nature, density and point where the energy is applied, in which case they are in
class IIb. Considering the fact that pulsed magnetic fields do not fall into the category of either
ionizing radiation or potentially dangerous radiation, it can be said that the energy exchanged by
the device with the human body is absolutely not dangerous. Therefore, the LOB device is a class
IIa active medical device. With regard to point 3.5 of the aforementioned annex, which states “If
different rules or, within the same rule, more sub-rules apply to the same device according to its
intended use, the more stringent rule and sub-rules that involve the higher classification must be
applied ”, it is stated that there are no other stricter rules to apply to the LOB device.
Therefore, the classification is IIa.”
Basic UDI-DI: 8019781PEMFLFDEVP2 - UDI-DI: 08019781202208
The LOB device assumes the following classifications:
• Class II with type BF applied part (Classif. IEC EN 60601-1);
• Device with IP21 degree of protection against the penetration of solid objects,
powders and liquids.
• Device and accessories supplied non-sterile and not subject to sterilisation;
• Device and accessories supplied do not contain or incorporate a medicine, including a
derivative of human blood or plasma;
• Device and accessories supplied do not contain or incorporate tissues or cells of human
origin, or their derivatives;
• Device and accessories supplied do not contain or incorporate tissues or cells of animal
origin, or their derivatives;
• Device not suitable for use in the presence of a flammable anaesthetic mixture with air,
with nitrous oxide, with any flammable agent of any kind and in environments with a
high concentration of oxygen;
• Device intended for continuous operation;
• Device not suitable for external use.
Manufacturer
I.A.C.E.R. S.r.l.
via Enzo Ferrari 2 • 30037 Scorzè (VE) - Italy
Tel. [phone] • Fax [phone]
IACER S.r.l. is an Italian manufacturer of medical devices (UE certificate No. ITH13442941 issued by the Noti-
fied Body No. 1936 TÜV Rheinland Italia srl).
Declaration of conformity
IACER S.r.l., with registered office in via Enzo Ferrari 2 - 30037 Scorzè (VE) - Italy, declares that
the LOB device complies with general safety and performance requirements of Regulation (EU)
2017/745 of 5 April 2017 concerning medical devices, amending Directive 2001/83/EC, Regu-
lation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives
90/385/EEC and 93/42/EEC.
Notified body:TÜV Rheinland Italia srl, Via Mattei 3 - 20010 Pogliano Milanese (MI) Italy.
Certification path: Annex IX.
The LOB device is a class IIa equipment according to Annex VIII, paragraph 3, point 6.1 rule 9 of
Regulation (EU) 2017/745 (and subsequent amendments).
Scorzè, 16/01/2023 MASSIMO MARCON
The legal representative

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• Device and accessories supplied do not contain or incorporate tissues or cells of animal
origin, or their derivatives;
Intended purpose and scope of use
Clinical purpose: Therapeutic
Scope of use: Outpatient Clinic/Hospital and home
LaMagneto is a magnetotherapy device designed and indicated for the rehabilitation and functio-
nal recovery treatments of pathologies affecting:
• joints of the wrist, hand, shoulder, foot, ankle and knee
• the musculoskeletal system
• muscular atrophies and dystrophies
• bruises;
• sprains;
• benign lesions and pulled muscles
and for the care treatments of:
• osteoporosis;
• bone edema;
• osteonecrosis;
• ulcers;
• neuropathies;
• arthrosis;
• bursitis
• periarthritis;
• tendinitis and tendinosis
LOB is also particularly suitable for the treatment of fractures and consolidation delays.
Thanks to the high intensity of the magnetic field it is able to generate, LOB is particularly indi-
cated in the treatment of bone fractures even in the presence of rigid bandages or plaster casts.
LOB is a device intended for both professional users (doctor, therapist etc.) and for in-home the-
rapy. With regard in-home therapy, it is recommended that the device only be used following
advice from your doctor/therapist.
The patient population intended for magnetotherapy treatment using the LOB device includes
patients of both sexes, men and women, and adult (unless otherwise indicated by medical practi-
tioners). For further details, please refer to the Contraindications and Side Effects section.
In accordance with guidelines for medical devices, the manufacturer suggests a check of the ef-
ficiency and safety of the device every 24 months. Useful life of the device and its accessories
(period after which it is suggested to send the device to the manufacturer): 3 years
Technical characteristics
Feature Specification
Power supply Pow. UES36LCP1-150200SPA, out 15VDC-2A
Max. current consumption 1 A
Insulation class (CEI EN 60601-1) II
Applied part (CEI EN 60601-1) BF
Dimensions (length x width x height)(mm) 180x110x50
Intensity of the field Adjustable with increasing scale up to 100 Gauss
(per channel).
Frequency of the square wave 1-75 Hz
Therapy time User-settable
The maximum magnetic field intensity is 100 Gauss per channel with a professional applicator
with a pair of solenoids (optional accessory).
The values of intensity, frequency and time are supplied with an accuracy of ± 20%.
Ambient operating conditions:
temperature from +5 to + 40°C
relative humidity from 15 to 93%
pressure from 700 to 1060 hPa

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Follow the "instructions for use"
Waste disposal (WEEE Directive)
Class II device
Applied part type BF
This product complies with Regulation (EU) 2017/745 and subsequent
amendments
Medical device
SN Serial number
Temperatures permitted
Relative humidity
Manufacturer's data
IP21 Degree of protection against the entry of solids, powders and liquids
UDI vector for device traceability
Center positive symbol
Unique device identifier. Affixed near UDI vector
Model
Batch number
Power supply (model and specifications)
Labelling
Label 1 (on the back)
Device labels in detail
Description of the symbols (device and packaging)
Label 2
DC 15V/2.0A
UES36LCP1-150200SPA
Label 3
ON/OFF
Label 4
CH1 CH2
Label 1
Label 3 Label 4
Label 2

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Contents of the pack
The LOB pack contains:
• N°1 LOB device;
• N°1 medical power supply (approx 1.5mt cable);
• N°1 Use and maintenance manual;
• N°1 belt applicator with 3 solenoids (approximately 1.5mt cable);
• N°1 device carry bag;
• Magnet for verifying therapy operation
• Non-woven fabric strip 15x150 cm (see page 16 for further details)
The professional applicator with a pair of solenoids is available as an optional accessory.
OSTEOMAT solenoid mattresse are available as accessories. Visit the website
www.wepere.com/en for more information.
How to use the device
Warnings
It is recommended to read this manual carefully before using the device. For any further infor-
mation and details we advise you to visit our website www.wepere.com/en and refer to the
section dedicated to magnetotherapy. In that section, within the LOB product page, a copy of the
most updated revision of this user manual can be consulted under the heading “User Manual”.
Nevertheless, please follow the following instructions:
• Check the location and meaning of all labels affixed to the device;
• Do not damage the applicator by acting on the connecting wire, also avoid winding the wire
around the applicator or around the device;
• Check the integrity of the power supply each time it is used. Avoid use in the case of signs of
damage to the casing or to the connecting wire;
• People who are not properly trained and who have not read this manual must not use the
device;
• Avoid using the device while using ointments containing free ions of magnetisable metals;
• Avoid using the device in humid environments and/or in the presence of flammable agents;
• During therapy, the user and the patient are advised not to wear metal objects;
• Position the applicator in such a way that the green side is in contact with the user’s skin;
• Use only cables and applicators supplied by the Manufacturer. Inadequate cables and
applicators could damage the device and/or cause harm to the patient;
• The user must periodically check the insulation (integrity) of the applicators and their cables
and check that they are not damaged (contacting the manufacturer if needed);
• The user must pay attention when using the connecting cables of the belt and the power
supply: strangulation risk.
• The materials used for producing the device exceed the required standards regarding
material toxicity. In case of allergic reactions, discontinue therapy and consult a doctor.
• Do not connect the device and its accessories to other devices not indicated in this manual.
• Keep out of the reach of children and animals.
• Avoid exposing the device and its accessories to excessive direct light and dust.
Refer to the indications in the paragraph “How to look after the device”;
• Use the device only with the supplied power supply model.
CAUTION.
Disconnect the power supply from the wall socket at the end of the therapy session.
The manufacturer is to be considered responsible for the safety, reliability and performance of
the device provided that:
• any additions, modifications and/or repairs are carried out by personnel authorised directly
by the manufacturer.
• the electrical system of the environment in which LOB is inserted complies with
national laws.
• the devices are used in strict compliance with the instructions reported in this manual.
Electromagnetic interference
It is advisable to use the device at a distance of at least 3 meters from televisions, monitors, mo-
bile phones, WI-FI routers or any other electronic equipment as these devices could affect the
operation of the device.
The device must be installed and operated in accordance with the electromagnetic compatibility
information contained in this manual. See also the paragraph EMC tables.
The use of accessories, transducers and cables other than those specified, with the exception
of those sold by the manufacturer as replacement parts for internal components, may result in
increased emissions and decreased immunity.
The device should not be used near or placed on top of other equipment and, if it is necessary to
use it near or placed on top of other equipment, it should be observed to check normal operation
in the configuration in which it is used.
Radiation emitted for therapeutic purposes
The radiation emitted by the LOB device is the one produced by a pulsed electromagnetic field
(CEMP). The magnetic field is induced by the passage of electric current through coils, made up
of windings of copper cable. This magnetic field is pulsed as the generating electric current is not
continuous (stationary) but pulsed (square wave electric pulse) with specific frequencies (fixed,
if the programs with preset parameters are used, free if the Free Memory programs are used. ).
The maximum intensity of the magnetic field generated by the LOB device is 100 Gauss per
channel with the use of the professional applicator with a pair of two solenoids.
The frequency range of the square wave generating the CEMP is 1-75 Hz.

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The intensity and frequency values are given with ± 20% accuracy.
The therapeutic electromagnetic radiations generated during the operation of the device are lo-
cated near the surface of the applicators in contact with the skin (green side). Outside the afo-
rementioned distribution area, the intensity of the radiation is such that it does not entail any
clinical benefit or decisive interaction with the tissues to be treated.
The radiation emitted by the device is not ionizing.
Fortuitous radiation
Given the nature and distribution of electromagnetic radiation emitted, no means of protection
from accidental radiation is necessary either for patients, users or people close to them.
Contraindications and side effects
Pregnant women, patients with tuberculosis, juvenile diabetes, viral diseases (in the acute pha-
se), mycosis, subjects with heart disease, those suffering from tumours, severe arrhythmias or
pacemaker wearers, children, those with magnetisable prostheses, acute infections, epileptics
(unless otherwise prescribed by doctors).
There are no known significant side effects related to therapy, nor have there been any problems
reported related to excessive exposure to the electromagnetic field generated by the device.
Quick use of the device with preset parameters
To start using LOB quickly and easily, we recommend that you follow the steps below:
1. Connect the applicator (or applicators) to the device by connecting the plug of the applicator
cable to one of the two ports (CH1-CH2) on the panel at the top of the appliance;
2. Connect the mains cable to the power supply and then connect the power supply outlet to
the circular connector on the panel at the top of the appliance, near the ON/OFF switch:
3. Connect the plug of the mains cable to the mains socket (100-240VAC, 50-60 Hz);
4. Press the ON/OFF switch on the small panel on the upper part so it is in the ON position: the
display will show the I-TECH MEDICAL DIVISION logo and then the main menu screen; for quick
standard use, now select the first item “Single user” by pressing the “OK” button.
5. Scroll through the program using the buttons sand tselect the desired program;
6. Press OK. The display will show the basic setting time of the therapy (2 hours) and
magnetic field intensity. These are the average values suggested by IACER to immediately
start the treatment effectively.
7. Press the OK button. The device will start the treatment, displaying the magnet icon with the
magnetic field flux. The green light below the display notifies the therapy is underway.
8. At the end of the therapy, the device will automatically return to the program menu screen.
Note: it is possible to temporarily suspend therapy at any time by pressing the OK button. To resu-
me therapy, press the OK button again. During the pause phase the green LED goes off, and then
comes back on when the therapy is restarted.
Note: it is possible to exit the treatment at any time by pressing the / nbutton once: the devi-
ce will go back to the screen of the selected programme (point 6). By pressing the / n button
again the device will go back to the initial screen of the program menu (point 5).
Note: the device recognises if the applicators are connected correctly. During the therapy phase,
the connection status is displayed below the magnet icon. The presence of the symbol ✓next to
the channel number (1 or 2) confirms the applicator is connected correctly and recognised.The X
symbol next to the channel number (1 or 2) tells you that the applicator is not connected correctly,
missing or not working correctly (see paragraph “Checking device operation”).
Use of the therapeutic belts and solenoids, main applications and suggestions
Some of the main positions for applying the therapeutic belt and the solenoids are given below.
N.B: it is recommended to interpose the non-woven fabric strip between the skin and the applicator.
This recommendation is also to be applied if the TAP2000 or OSTEOMAT applicators are used.
Wrap the 3-solenoid belt (applicator) around the area to be treated (or place it over the area, such
as in the treatment of the vertebral column) taking care that the green side of the belt is placed in
contact with the skin. Two photos are given below by way of example

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The professional solenoids (accessory to be purchased separately) must be placed on the area
to be treated, opposite each other, taking care that the green side is placed on the same side of
the skin.
The photos below are for illustration purposes only concerning applicator placement. Remem-
ber that between the applicator and the skin it is necessary to interpose the non-woven fabric
strip contained in the pack.
Suggestions for correct use:
• The device and the applicators are designed to operate in the temperature ranges indicated
with treatments of up to 12 consecutive hours;
Instructions for using the preset programs
To use LOB by freely setting the parameters related to treatment time and magnetic field intensi-
ty, follow the following simple steps:
1. Connect the applicator (or applicators) to the device by connecting the plug of the applicator
cable to one of the two ports (CH1-CH2) on the panel at the top of the appliance;
2. Connect the mains cable to the power supply and then connect the power supply outlet to
the circular connector on the panel at the top of the device, near the ON/OFF switch;
3. Connect the plug of the mains cable to the mains socket (100-240VAC, 50-60 Hz);
4. Press the ON/OFF switch on the small panel in the upper part so it is in the ON position: the
display will show the I-TECH MEDICAL DIVISION logo and then the main menu screen;
5. Select “Single user” and scroll through the programs using the sand tbuttons and select
the desired program
Ankle
Wrist
Ankle
Vertebral column Lumbar
Hip
Elbow
Shoulder
Back (lumbar)
Cervical vertebrae
Femoral head Femur
Knee
Knee
Shoulder
Tibia / fibula

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6. Press OK. The display will show the basic setting of therapy time (2 hours) and intensity of
magnetic field that we will modify;
a) Press the button tso that the spanner is highlighted. At this point press OK: the display
shows a moving spanner icon on the left-hand side;
b) Use the sand tbuttons to set the desired therapy hours (from 0 to 24) and confirm by
pressing the OK button. The display will highlight the minutes of therapy;
c) Use the sand tbuttons to set the desired therapy minutes (from 0 to 59) and confirm by
pressing the OK button. The display will highlight the intensity of the treatment;
d) Use the sand tbuttons to set the treatment intensity and confirm by pressing the
OK buttons.
7. The device will return to the screen in point 6. Press OK: the device will start the treatment,
displaying the magnet icon with the magnetic field flux. The green light tells you the
therapy is underway.
8. At the end of the therapy, the device will automatically return to the program menu screen.

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List of stored programs
N° Condition Hz Duration
hours Session cycles Interval between
sessions
1. Osteoporosis 8 2 – 6 30 – 60 24 hours
2. Arthrosis 30 2 – 6 30 – 60 24 hours
3. Arthritis 30 2 – 6 30 – 60 24 hours
4. Cervical arthrosis 10 2 – 6 30 – 60 24 hours
5. Articular pain 30 2 – 6 30 – 60 24 hours
6. Cervicalgias 20 2 – 6 30 – 60 24 hours
7. Chronic pain 10 2 – 6 30 – 60 24 hours
8. Fractures 25 2 – 6 30 – 60 24 hours
9. Epicondylitis 25 2 – 6 30 – 60 24 hours
10. Epitrocleitis 25 2 – 6 30 – 60 24 hours
11. Pseudoarthrosis 75 2 – 6 30 – 60 24 hours
12. Lumbalgy 50 2 – 6 30 – 60 24 hours
13. Lumbar-sacral pain 50 2 – 6 30 – 60 24 hours
14. Shoulder Arthrosis 30 2 – 6 30 – 60 24 hours
15. Knee arthrosis 30 2 – 6 30 – 60 24 hours
16. Scapulohumeral periarthritis 4 2 – 6 30 – 60 24 hours
17. Coxarthrosis 30 2 – 6 30 – 60 24 hours
18. Muscle atrophy 30 2 – 6 30 – 60 24 hours
19. Muscle treatment 30 2 – 6 30 – 60 24 hours
20. Osteonecrosis 75 2 – 6 30 – 60 24 hours
21. Algodystrophy 30 2 – 6 30 – 60 24 hours
22. Cartilage lesion 75 2 – 6 30 – 60 24 hours
23. Ligament lesion 75 2 – 6 30 – 60 24 hours
24. Bone oedema 75 2 – 6 30 – 60 24 hours
25. Tendinitis 73 2 – 6 30 – 60 24 hours
26. Chondropathy 30 2 – 6 30 – 60 24 hours
27. Anti-inflammatory 75 2 – 6 30 – 60 24 hours
28. Whiplash syndrome 20 2 – 6 30 – 60 24 hours
29. Healing 12 2 – 6 30 – 60 24 hours
30. Cutaneous ulcers 12 2 – 6 30 – 60 24 hours
31. Discopathy 25 2 – 6 30 – 60 24 hours
List of stored programs
N° Condition Hz Duration
hours Session cycles Interval between
sessions
32. Myalgia 1 2 – 6 30 – 60 24 hours
33. Neuropathy 10 2 – 6 30 – 60 24 hours
34. Muscle strain 1 2 – 6 30 – 60 24 hours
35. Muscular cramp 1 2 – 6 30 – 60 24 hours
36. Rhizarthrosis 25 2 – 6 30 – 60 24 hours
37. Impingement syndrome 50 2 – 6 30 – 60 24 hours
38. Carpal tunnel 50 2 – 6 30 – 60 24 hours
39. Titanium prosthesis 75 2 – 6 30 – 60 24 hours
40. Rotator cuff 73 2 – 6 30 – 60 24 hours
41. Tarsal tunnel 30 2 – 6 30 – 60 24 hours
Osteoporosis: specific program for stimulating bone regeneration.
Arthrosis: program designed to reduce pain and slow down the degenerative process.
Arthritis: program designed to reduce pain and slow down the degenerative process.
Cervical arthrosis: program designed to reduce pain and slow down the degenerative process
in the cervical area.
Articular pain: analgesic program designed for the joints.
Cervicalgias: specific program for the reduction of cervical pain.
Chronic pain: program designed to reduce pain and inflammatory processes. It is recommended
to use the applicators on the area where the pain is felt.
Fractures: specific program for the stimulation of bone regeneration in a post-traumatic condition.
Epicondylitis: specific program for this condition, aimed at promoting the recovery of the joint in
an inflammatory condition of the tendons.
Epitrocleitis: specific program for this condition, aimed at promoting the recovery of the joint in
an inflammatory condition of the tendons.
Pseudoarthrosis: specific program for the stimulation of bone regeneration in the tibia in situa-
tions where there is no union.
Lumbalgy: program designed for the treatment of lower back pain with a view to reducing pain.
Lumbar-sacral pain: program designed for the treatment of lumbar-sacral pain with a view to
reducing pain.
Shoulder arthrosis: program designed to reduce pain and slow down the degenerative process
in the shoulder area.
Knee arthrosis: program designed to reduce pain and slow down the degenerative process in
the knee area.

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Scapulohumeral periarthritis: program designed to reduce pain and slow down the degenera-
tive process of the scapulohumeral structure.
Coxarthrosis: program designed to reduce pain and slow down the degenerative process in the
hip area.
Muscle Atrophy: program designed to stimulate muscle tissues.
Muscular treatment: program designed to stimulate muscle tissues and reduce pain.
Osteonecrosis: specific program for the stimulation of bone tissue in cases of osteonecrosis, in
order to counter the progress of the disease and alleviate pain.
Algodystrophy: analgesic program designed for pain relief in forms of algodystrophy.
Cartilage lesion: program designed for the regeneration of cartilaginous tissues.
Ligament lesion: program designed for post-surgery recovery.
Bone oedema: specific program for the stimulation of bone tissues in cases of bone oedema.
Tendinitis: program designed for the treatment of inflammation of tendon tissues.
Chondropathy: specific program for osteoarthritis (a particular type of chondropathy), designed
for the reduction of inflammation of cartilaginous tissues.
Anti-inflammatory: program to mitigate inflammatory and painful conditions. Useful also in ca-
ses of post-surgery recovery.
Whiplash syndrome: program designed for post-traumatic recovery, with a view to reducing pain.
Healing: specific program for increasing circulation and reducing the damaged area.
Cutaneous ulcers: specific program to increase circulation and decrease the damaged area,
even in cases of diabetic foot.
Discopathy: specific program for the treatment of diseases affecting vertebral discs, relative to
bone and cartilage tissues, also useful in post-surgery.
Myalgia: program designed to stimulate muscle tissues and increase oxygenation.
Neuropathy: specific program to obtain an analgesic and anti-inflammatory effect on the peri-
pheral nerves.
Muscle strain: program designed to stimulate muscle tissues and increase oxygenation.
Muscular cramp: program designed to stimulate muscle tissues and increase oxygenation.
Rhizarthrosis: program designed to reduce pain and slow down the degenerative process in the
hand area.
Impingement syndrome: specific program for the reduction of inflammation in the shoulder tis-
sues for this type of condition, also known as the subacromial impingement syndrome.
Carpal Tunnel: specific program to relieve painful symptoms.
Titanium prosthesis: specific program to promote osseointegration with the implanted hip pro-
sthesis.
Rotator cuff: program designed for functional recovery and pain reduction for this type of condition.
Tarsal tunnel syndrome: program designed to reduce the pain of this condition and other poly-
neuropathies.
The therapy duration values are those recommended by IACER S.r.l. and can be altered by the user.
The LOB magnetotherapy device incorporates the indications regarding magnetic field, frequen-
cy of therapy and power delivered that are found in scientific and medical literature, the result of
experiments and clinical evaluations carried out (Barker - Lunt 1983, Bassett - Pawluk - Pilla 1974,
Bassett - Valdes - Hernandez 1982).
Settings (language selection)
Press the ON/OFF switch located on the small panel in the upper part so it is in the ON position.
After the I-TECH MEDICAL DIVISION logo appears, press and select the “Settings” menu. At this
point select “Language” and use the and buttons to select the desired language.
N.B.: to turn off the device, press the ON/OFF switch on the back or press the / n button until
the screen turns off.
How to look after the device
Checking device operation
A magnet (small ring or disc in metal or metal/plastic) is supplied with the appliance to check
device operation.
Procedure for checking:
1. switch on the device following all the safety instructions provided in this manual;
2. start any therapy, following the instructions for use of this manual;
3. hold the supplied magnet and bring it closer to the applicator;
4. check that the magnet vibrates (proportional to the frequency of the selected therapy).
Contact the manufacturer if the magnet fails to vibrate.
Cleaning the device
Use a soft dry cloth to remove any dust from the device.
More difficult stains can be removed using a sponge soaked in a water and alcohol solution (20% alcohol).
To clean the 3-solenoid belt or the circular cases of the professional applicator with a pair of so-
lenoids, it is recommended to disconnect the applicator from the device before carrying out any
operation.
• Remove the 3-solenoid cable by removing the 2 silver studs with a screwdriver or open the
circular cases using the side zip.
• Clean the fabric with water and neutral soap and wait for it to dry completely before
replacing the applicators. The fabric used is designed to withstand 10 cleaning cycles while still
maintaining its original characteristics.
CAUTION: always respect the polarity of the applicators taking care to insert the coils with the
side indicated by the + sign towards the green part of the belt (therapeutic side).
Respect the temperature, humidity and pressure limits indicated in this manual even when clea-

USER MANUAL 24 25 USER MANUAL
ning the device and its accessories.
Transport and storage
Transport precautions
There is no particular care to be taken during transport as LOB is a portable device.
It is recommended to store LOB and its accessories in the bag supplied after each use and store
everything inside the original box.
It is recommended not to twist the power supply and applicator cables.
Storage precautions
The storage location should have the following characteristics:
ambient temperature from +5° to +40°C.
relative humidity from 15 to 93%
pressure from 700 to 1060 hPa
Disposal
The product is subject to the WEEE regulation (the symbol is present on the label )
concerning separate collection: to dispose of the product, make use of special areas equipped to
collect electronic material by contacting the competent authorities in your country or the manu-
facturer directly.
Maintenance
If used in accordance with the information reported herein, this device requires no particular rou-
tine maintenance operations.
In the event of malfunction, first follow these simple steps:
• make sure that the power outlet to which the device is connected is working properly by
connecting another working device;
• check the connection to the power supply and the integrity of all connection cables;
• check the connection with the applicator (or applicators);
• verify that all operations have been performed correctly;
• every two years check that all functions of the device work correctly (contact the manufacturer).
If you discover a problem or you require further information, please contact the manufacturer
immediately at:
I.A.C.E.R. S.r.l.
via Enzo Ferrari 2 • 30037 Scorzè (VE) - Italy
Tel. [phone] • Fax [phone]
Support
The manufacturer is the only point of contact for technical support regarding the device. For all
technical support matters, please contact:
I.A.C.E.R. S.r.l.
via Enzo Ferrari 2 • 30037 Scorzè (VE) - Italy
Tel. [phone] • Fax [phone]
Technical documentation concerning repairable parts may be provided, but only with prior com-
pany authorisation and only after giving proper training to the maintenance personnel.

USER MANUAL 26 27 USER MANUAL
Spare parts
Original spare parts for this device can be ordered at any time from the manufacturer. To order
them contact:
I.A.C.E.R. S.r.l.
via Enzo Ferrari 2 • 30037 Scorzè (VE) - Italy
Tel. [phone] • Fax [phone]
Use only original spare parts supplied by the manufacturer; if non-original spare parts are used,
the operation and safety of the product might be affected and the warranty will be null and void.
EMC Tables
Emission aspects
Emission test Compliance Electromagnetic environment - guidance
RF emissions
Cispr 11 Group 1
The LOB product uses RF energy only for its internal
operation.
Therefore, its RF emissions are very low and not likely to
cause interference in nearby electronic equipment.
RF emissions
Cispr 11 Class B
The LOB can be used in all buildings, including domestic
buildings, and those directly connected to the
public low-voltage power supply network that supplies
buildings for domestic use.
Harmonic emissions
IEC 61000-3-2 Class A Complies
Voltage fluctuations
and flicker
IEC 61000-3-3 Complies
Immunity aspects
The LOB is intended to work in the electromagnetic environment specified below. The customer
or user should make sure that it is used in such environment
Immunity test Test level EN
60601-1-2 Compliance level Electromagnetic environment - guidance
Electrostatic
discharge (ESD)
EN 61000-4-2
± 8kV contact
± 15kV air ± 8kV contact ± 15kV air Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30%.
Electrical fast
transient/burst
EN 61000-4-4
± 2kV power
supply lines ± 2kV power supply lines Mains power quality should be that of a
typical business or hospital environment.
Impulsi
EN 61000-4-5 ± 1kV differential
mode ± 1kV differential mode
Voltage dips,
short interrup-
tions and voltage
variations on
power supply
input lines
EN 61000-4-11
0% UT
for 0.5 cycles,
different angles
0% UT
for 1 cycle
70% UT
for 25/30 cycles
0% UT
for 5 seconds
0% UT
for 0.5 cycles,
different angles
0% UT
for 1 cycle
70% UT
for 25/30 cycles
0% UT
for 5 seconds
Mains power quality should be that of a
typical business or hospital environment. If
the user requires continuous operation even
during the interruption of the mains voltage,
it is recommended to power the device with
an uninterruptible power supply (UPS) or
with batteries.
Magnetic field at
mains frequency
EN 61000-4-8 30 A/m 30 A/m The magnetic fields at mains frequency
should be at levels typical of a business or
hospital environment.

USER MANUAL 28 29 USER MANUAL
RF immunity aspects
The LOB is intended to work in the electromagnetic environment specified below. The customer
or user should make sure that it is used in such environment
Immunity test Test level EN
60601-1-2 Compliance level Electromagnetic environment - guidance
Immunity to con-
ducted disturban-
ces induced by
radio-frequency
fields
EN 61000-4-6
3 Veff. 150kHz to
80MHz 3 Veff. 150kHz to 80MHz
Portable and mobile RF communications
equipment should not be used near any part
of the equipment, including cables, except
when respecting the recommended separa-
tion distances calculated from the equation
applicable to the transmitter frequency
Recommended separation distances
d = 1.2 .√P from 150kHz to 80MHz
d = 0.35 .√P from 80 MHz to 800 MHz
d = 0.7 .√P from 800 MHz to 2.7 GHz
where P is the maximum output power
of the transmitter in watts (W) according
to the transmitter manufacturer and d is
the recommended separation distance in
meters (m).
Radiated RF
EN 61000-4-3 10 V/m 80 MHz to 2.7 GHz 10 V/m 80 MHz to 2.7 GHz
The field strength from fixed RF transmitters, as determined by an electromagnetic site survey, may be
less than the compliance level in each frequency range.
Interference may occur in the vicinity of equipment marked with the following symbol:
Recommended separation distance between portable and mobile radio communication devi-
ces and the LOB device
The LOB is intended to operate in an electromagnetic environment in which RF irradiated disturbances are
controlled. The customer or the operator of the device can help prevent electromagnetic interference by
ensuring a minimum distance between mobile and portable RF communications devices (transmitters)
and the device, as recommended below, in relation to the maximum output power of the radio communi-
cation devices.
Maximum rated output
power of the transmit-
ter (W)
Separation distance to the frequency of the transmitter (m)
From 150kHz to 80MHz
d = 1.2 .√P From 80MHz to 800MHz d = 0.35 .√P From 800MHz to 2.7GHz d = 0.7 .√P
0,01 0,12 0,04 0,07
0,1 0,38 0,11 0,22
11,2 0,35 0,7
10 3,8 1,1 2,2
100 12 3,5 7,0
For transmitters specified for a maximum output power not listed above, the recommended separation
distance d in metres (m) can be calculated using the equation applicable to the frequency of the tran-
smitter, where P is the maximum output power of the transmitter in watts (W) according to the transmitter
manufacturer.
Note:(1) At 80 MHz and 800 MHz the highest frequency range applies.
(2) These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects and people.
Incident reporting
In compliance with the provisions of Regulation (EU) 2017/745, the manufacturer places the need
to report any serious accident in relation to the device to the attention of the user.
The report must be addressed:
• to the device manufacturer:
I.A.C.E.R. Srl
Via Enzo Ferrari 2 – 30037
Scorzè (VE) ITALY
Tel. [phone] – Fax [phone]
e-mail: [e-mail]
Warranty
LOB is covered by a 2 year warranty starting from the date of purchase on the electrical and
electronic parts. The parts subject to normal wear and tear are not covered by the warranty (fabric
case of applicators as well as velcro elastic closure of the same) and all parts that may be defecti-
ve due to negligence or neglect of use, incorrect maintenance or in case of tampering with the
device and intervention on the same by personnel not authorized by the manufacturer or autho-
rized dealer. The warranty conditions are those described in the following paragraph “Warranty
conditions”.

LOB. All rights reserved.
LOB and the logo WEPERE the exclusive property of
I.A.C.E.R. Srl and are registered trademarks
Edition: MNPG507-00 of the 31/03/2023
In the event of subsequent warranty intervention, the equipment must be packaged so as to avoid
damage during transport and sent to the manufacturer together with all accessories. To be eligi-
ble for warranty work, the purchase must send the appliance with the receipt or invoice proving
the correct origin of the product and the date of purchase.
Warranty conditions
1. Should assistance be needed, enclose the purchasing receipt when sending the device to the
manufacturer.
2. The warranty period (2 years) is valid only on the electronic parts. The warranty will be granted
by the shop or directly by the manufacturer.
3. The warranty covers only the product damages, which causes its malfunctioning.
4. Warranty means that only the manufacturing defect components or material are covered by
reparation or free substitution, hand work included.
5. Warranty is not applied to damages caused by negligence or use not compliant to the given
instructions, by intervention on the device from personnel not authorized, accidental causes
or negligence form the purchaser.
6. Warranty is not applied in case of damages caused by unsuitable power supplies.
7. Warranty does not apply to wearing parts.
8. Warranty does not include transportation costs which have to be covered by the purchaser.
9. After the warranty period (2 years) the warranty is no more applicable. In this case all the
assistance interventions will be performed by debiting the costs of the substitution of the
parts, the hand work and the transportations costs.
10.The court of Venice has exclusive jurisdiction over any dispute.

I.A.C.E.R. Srl
via Enzo Ferrari 2 - 30037 Scorzè (VE) - Italy
www.wepere.com