Compex Systems SP6.0: instruction

Instruction for use

Mode d’emploi

Anweisungen

Istruzioni

Instrucciones

Instructies

Instruções

Инструкция

Bruksanvisning

Instructions

EN

TABLE OF CONTENTS

1. Explanation of symbols 02

2. How does electrostimulation work? 03

3. How does MI technology work (Muscle Intelligence)? 05

4. Instructions 07

Composition of kits and accessories 07

Device description 08

First use 10

Device function 11

Charging 25

5. Troubleshooting 29

6. Device maintenance 33

Guarantee 33

Maintenance 33

Storage/transport and use 33

Disposal 33

7. Technical specifications 34

General information 34

Neurostimulation 34

RF data 35

Standards 35

Information about electromagnetic compatibility (EMC) 35

8. EMC table 36

It is strongly recommended to read these instructions and the contra-indications and safety

measures carefully before using your stimulator.

01

EN

1. EXPLANATION OF SYMBOLS

See the instructions

The stimulator is a category II device with built-in power supply and BF applied parts type.

Manufacturer’s name and address and date of manufacture

Name and address of approved representative in the European Community

This device must be separated from household waste and sent to special recycling plants

The stand-by button is multi-functional

Protect from sunlight

Store in a dry place

IP20

Protected against solid bodies with a diameter equal to or greater than

On the unit

12.5 mm (0.5 po.)

IP02

IP02 on the carrying case means: Protected from the ingress of water droplets from a shower of

On the case

rain.

Latex-free

Reference number

Batch number

02

EN

2. HOW DOES ELECTROSTIMULATION WORK?

Electrostimulation involves stimulating nerve fibres by electrical impulses transmitted by electrodes. The

electrical impulses produced by Compex stimulators are high-quality impulses that are safe, comfortable

and effective and stimulate various types of nerve fibres:

1. Motor nerves to stimulate a muscle response referred to as electrical muscle stimulation (EMS).

2. Certain types of sensitive nerve fibres to obtain analgesic effects or pain relief.

1. STIMULATION OF MOTOR NERVES (EMS)

With voluntary activity, the brain orders muscles to contract and a command is then sent to nerve fibres

in the form of an electrical signal. This signal is then sent to muscle fibres, which contract. The principle

of electrostimulation correctly reproduces the process involved in a voluntary contraction. The stimulator

sends an electrical impulse to nerve fibres to excite them. This excitation is then transmitted to muscle

fibres and results in a mechanical response (= a twitch). This is the basic requirement for muscular

contraction. The muscular response is to all intents and purposes identical to the muscular work

controlled by the brain. In other words, the muscle does not distinguish between a command sent by the

brain or the stimulator.

Programme settings (number of impulses per second, duration of contraction, rest time, total programme

duration) subject the muscle to various types of workout, depending on the muscle fibre. Various types

of muscle fibres can be identified depending on their respective contraction speeds: slow, intermediate

and rapid fibres. A sprinter clearly has more rapid fibres and a marathon runner has more slow fibres.

With good knowledge of human physiology and perfect control of stimulation settings in the various

programmes, muscular workout can be very accurately directed to achieve the desired objective

(muscular strengthening, increased blood circulation, firming, etc.).

03

EN

2. STIMULATION OF SENSORY NERVES

Electrical impulses can also excite sensory nerve fibres to obtain analgesic effects or pain relief.

Stimulating tactile sensory nerve fibres blocks pain being transmitted to the nervous system. Stimulating

another type of sensory fibre increases the production of endorphins and therefore reduces pain. With

pain relief programmes, electrostimulation can be used to treat acute or chronic localised pain and

muscle pain.

Note: Do not use pain relief programmes for an extended period without medical advice.

BENEFITS OF ELECTROSTIMULATION

Electrostimulation is a very effective method for making muscles work:

• with a significant improvement in various muscle qualities

• with no cardiovascular or mental fatigue

• with limited stress exercised on joints and tendons. Electrostimulation thereby enables more muscular

workout than voluntary activity.

For optimum results, Compex recommends supplementing your electrostimulation sessions with other

exercise, such as:

• regular physical exercise

• balanced and healthy diet

• balanced life style

04

EN

3. HOW DOES MI TECHNOLOGY WORK

(MUSCLE INTELLIGENCE)?

N.B.: The activation/deactivation of MI functions is performed via the Settings menu

MI-SCAN

Just before starting a workout session, the MI-scan function probes the chosen muscle group and

automatically adjusts the stimulator settings to the excitability of this area of the body, depending on your

physiology.

This function results in, at the start of the programme, a short test sequence during which measurements are

taken.

At the end of the test, intensities must be increased to start the programme.

MI-TENS

The MI-tens function limits unwanted muscle contractions in painful areas.

With each intensity increase, a test phase occurs and if a muscular contraction is detected, the device

automatically reduces the intensity of the stimulation.

This function is only accessible in the TENS, Epicondylitis and Tendinitis programmes.

MI-RANGE

The MI-range function allows the user to select the ideal level of stimulation intensity for recovery, massage,

capillarisation or even muscle pain programmes.

At the beginning of the programme, the device prompts the user to increase stimulation intensity. During this

increase, the device analyses the response of each stimulated muscle, and deduces their optimal level. As

soon as a muscle reaches its optimal level, the related channel is automatically deselected and the stimulation

intensity cannot be increased. To recover control, simply re-select the channel in question and raise or lower

the stimulation intensities.

MI-AUTORANGE

The MI-autorange function pursues the same objective as MI-range except that in this case everything is

done automatically.

At the beginning of the programme, a single press of the up key of the multifunction pad allows the device to

automatically increase the stimulation intensities until it detects the ideal level of intensity. Pressing the down

key of the multifunction pad cancels the MI-autorange function. The device then goes into manual mode and

intensities must be managed by the user.

05

EN

MI-ACTION

The MI-action function allows you an electro-induced contraction to be initiated by means of a voluntary

action. Thus the electro-induced contraction is perfectly controlled, the workout becomes more comfortable,

more thorough and more complete.

At the end of each active rest phase the remote control emits a beep. From this point the start of voluntary

contraction is possible. If no voluntary contraction has occurred after a certain period of time, the device will

automatically pause.

This work mode is available only for programmes inducing powerful muscle contractions.

N.B.: To function properly, the MI-action function needs good muscle twitches during the active rest phase.

If they are not significant enough, the device emits beeps and a + sign appears on the channels. Similarly, in

order to render these twitches possible, it is imperative that muscles be well relaxed during the rest phase.

At the end of each contraction phase, it is necessary to ensure that you return to a position allowing for best

muscle relaxation.

The table below shows which functions are available with each device.

SP 6.0 SP 8.0 FIT 5.0

MI-SCAN

✓ ✓ ✓

MI-TENS -

✓

-

MI-RANGE

✓

-

✓

MI-AUTORANGE -

✓

-

MI-ACTION -

✓

-

06

EN

4. INSTRUCTIONS

COMPOSITION OF KITS AND ACCESSORIES

SP 6.0 SP 8.0 FIT 5.0

REF QTY REF QTY REF QTY

REMOTE CONTROL 001047 1 001046 1 001048 1

MODULES 001061 4 001061 4 001055 2

DOCKING STATION 001068 1 001068 1 001073 1

CHARGER 64902X 1 64902X 1 00108X 1

BAG OF SMALL 5X5

42215 2 42215 2 42215 1

ELECTRODES

BAG OF LARGE 5X10

42216 2 42216 2 42216 1

ELECTRODES, 2 SNAP

BAG OF LARGE 5X10

42222 2 42222 2 42222 2

ELECTRODES, 1 SNAP

INSTRUCTIONS ON

880054 1 880054 1 880054 1

CD-ROM

QUICK START GUIDE 885625 1 885625 1 885625 1

CARRY CASE 680043 1 680042 1 680043 1

REMOTE CONTROL

NA NA 1094 1 NA NA

PROTECTION SLEEVE

Only use this device with cables, electrodes, battery, power adaptor and accessories

recommended by Compex.

07

EN

3. SELECT ELECTRODE PLACEMENT

A Select the desired electrode placement

A

B Confirm your selection

C

B

C Return to the previous step

A

4. CONNECT THE MODULES TO THE ELECTRODES

Stick the electrodes to your skin. The module is attached to the electrode from the side. Slide the module

onto the electrode’s snap until it clips into place.

5. TURN ON THE MODULES

A Return to the previous step

B Confirm your selection

BA

To launch the programme, see the section entitled “Start a stimulation programme.”

14

EN

HOW TO ACCESS OBJECTIVES

The Objectives menu displays the objectives downloaded from your personal account (see section

entitled “Creating your personal account”).

N.B.: The Objectives menu is only available for the SP 8.0 device.

A

A Select the Objectives menu

B Confirm your selection

B

A

The progress bar under the objective shows the progress of the objective and what remains to be done.

The bell indicates that there is an element of the objective to perform today.

A

BC

A Indicates an element of the objective to perform today

B What remains to be done

C What has already been accomplished:

- What has been completed appears in green

- What has not been completed appears in red

1. SELECT AN OBJECTIVE

A Select the desired objective

A

B Confirm your selection

C

B

C Return to the previous step

A

15

EN

2. SELECT AN ELEMENT TO DO

A Select the desired element

A

B Confirm your selection

B

C Return to the previous step

A

The element to do can be a programme or a task. The element to do is selected by default, but it is

possible to select another.

The next to a programme or a task signifies that it has been done.

3. SELECT ELECTRODE PLACEMENT

A Select the desired electrode placement

A

B Confirm your selection

C

B

C Return to the previous step

A

N.B.: In most cases a different electrode placement cannot be selected because it is directly linked to the

objective.

4. CONNECT THE MODULES TO THE ELECTRODES

Stick the electrodes to your skin. The module is attached to the electrode from the side. Slide the module

onto the electrode’s snap until it clips into place.

16

EN

5. TURN ON THE MODULES

A Return to the previous step

B Confirm your selection

BA

To launch the programme, see the section entitled “Start a stimulation programme.”

17

EN

HOW TO ACCESS SETTINGS

The Settings menu enables certain elements to be configured such as backlighting, volume, language,

etc. Some settings are not available in all devices.

A

A Select the Settings menu

B Confirm your selection

B

A

1. SELECT A SETTING

A Select the desired setting

A

B Confirm your selection

BC

C Return to the previous step

A

Language: Allows you to change the device’s language

MI-autorange: Turns the MI-autorange function on (ON) or off (OFF)

MI-range: Turns the MI-range function on (ON) or off (OFF)

MI-scan: Turns the MI-scan function on (ON) or off (OFF)

MI-tens: Turns the MI-tens function on (ON) or off (OFF)

MI-action: Turns the MI-action function on (ON) or off (OFF)

N.B.: For an explanation of MI functions see the section entitled “3. How does MI technology work?”.

18

EN

Cycles: Turns the Cycles function on (ON) or off (OFF)

The Cycles function is for people who are already accustomed to electrostimulation and want to perform

several training cycles. If the Cycles function is turned on (ON) an additional screen will appear for certain

programmes (programmes inducing powerful muscle contractions) enabling the training cycle to be

selected.

The cycle logic refers to the workload performed by electrostimulation. And just like a normal workout,

one has to to start with an amount of work then increase it over the course of the cycles. Thus, it is

recommended starting with the 1st cycle and going on to the next level when the cycle is finished,

normally after 4 to 6 weeks of stimulation based on 3 sessions per week. It is also important to have

reached significant stimulation intensities in sessions before going on to another cycle.

Power saving: Turns the Power saving function on (ON) or off (OFF). Decreases the intensity and the

backlighting time.

Sound: Turns the Sound function on (ON) or off (OFF).

Contraction sound: Turns the contraction arrival warning sound on (ON) or off (OFF).

Set time: Allows you to set the time on the device.

Set date: Allows you to set the date on the device.

Pair a new module: Enables a new module to be paired to the remote control.

Reset the device: Enables the device to be re-set and return to the basic settings (Favourites deleted,

Objectives cleared, Default settings).

System info: Enables information related to the device to be viewed.

19

EN

START A STIMULATION PROGRAMME

Before beginning any stimulation programme, you must turn the modules on.

A Return to the previous step

B Confirm your selection and start the

A B

programme

To turn on the modules, press their respective On/Off button. As soon as the module is turned on, its

battery level appears on the screen. Turn on the number of modules desired according to the electrode

placement selected. As soon as a sufficient number of modules is turned on, a small arrow appears on

the right of the screen.

If the MI-scan function is activated, the programme starts with a short sequence during which

measurements are taken. For the duration of the measurement test, it is important to stand still and be

perfectly relaxed. Once the test is completed, the programme can start. Stimulation always starts at 000.

A Contraction phase

B Warm up phase

A

G

F

C Active rest phase

E

D Relaxation phase

D

B

E Number of contractions performed / Total number of contractions

C

F Indication of the active MI function

G Pop-up help indicating information or actions to be taken

20

EN

A Select the channels on which to act. When a channel is

active the LED button emits a strong blue light.

B Pause

A A

A

A

C Increase or decrease the stimulation intensities on the

C

selected channels

B

C

Increase the stimulation intensities on the selected channels.

By default, all of the channels are active at the beginning of the session. To deselect a channel, simply

press the corresponding button.

In this case only channel 1 is active. Any change of intensity will only be performed on channel 1.

21

EN

Depending on the programme, the diagram on the middle of the screen can change.

CONTRACTION/ACTIVE REST PROGRAMME

These programmes always begin with a warm-up phase. After this warm-up phase, a contraction cycles

phase followed by active rest occurs (the number of cycles depends on the programme) and when all

cycles are completed, the programme ends with a relaxation phase.

E

A Warm up phase

D

B Active rest phase

C Relaxation phase

A

C

D Contraction phase

B

E Work phase which consists of a contraction/active rest cycle

MASSAGE, RECOVERY TYPE PROGRAMME

These programmes consist of a single phase and have no contraction/active rest cycle. These are

recovery, massage, capillarisation, or even pain type programmes. During this type of programme,

frequency variations can occur.

A

A Work phase

22

EN

CONTINUE A STIMULATION PROGRAMME

A Skip the current phase or exit the

programme

B Resume the stimulation session

CBA

C Skip the current phase or exit the

B

A

programme

A Average stimulation intensity

B Maximum stimulation intensity

By pressing on the central button of the remote control or on the On/Off button of one of the modules

during the stimulation, the device goes into pause. At this point it is possible to skip the current phase or

exit the programme.

Depending on the programme, maximum and average intensities statistics may appear.

N.B.: The session restarts with intensities equal to 80% of those used prior to the interruption.

23

EN

SYNCHRONIZATION PROBLEM

If the synchronization process was discontinued or cannot run successfully for any reason (remote control

disconnected, power failure, etc.) the remote control may, in some cases, display this screen.

• Reconnect the remote control to the computer and restart the synchronization process.

BEHAVIOUR OF THE MODULE’S LED

The LED alternately flashes green and red: the module is out of range or not recognized by the remote

control.

• Ensure the remote control is on.

• Ensure that the module and the remote control are less than 2 metres away from each other.

The LED is still red.

• Ensure the module is charged.

• Try to restart the remote control and modules.

• If despite this the LED is still red, contact customer service provided and approved by Compex.

The LED does not turn on.

• Ensure the module is charged.

• If despite this the LED still does not turn on, contact customer service provided and approved by Compex.

30

EN

MODULE UNCHARGED

During the stimulation a module may be uncharged. In this case the symbol for an uncharged battery

appears and an arrow flashing on the channel where the problem was detected (in this case, channel 1).

• Stop the stimulation and recharge the uncharged module.

• Abandon the uncharged module and continue the stimulation session without it.

THE MODULE WILL NOT PAIR WITH THE REMOTE CONTROL

At the time of first use, if the remote control is unable to pair all modules, an error message may appear.

• Ensure that the module is charged, and repeat the pairing step.

• If despite this the message returns, contact customer service provided and approved by Compex.

STIMULATION DOES NOT PRODUCE THE USUAL SENSATION

• Check that all settings are right and check electrodes are properly positioned.

• Change the positioning of the electrodes slightly.

STIMULATION CAUSES DISCOMFORT

• Electrodes lose their adhesive capacity and no longer provide adequate contact with skin.

• Electrodes are worn and must be replaced.

• Change the positioning of the electrodes slightly.

31

EN

THE DEVICE IS NOT WORKING

• Ensure that the remote control and modules are charged.

• Try to restart the remote control and modules.

• If despite this the device still does not work, contact customer service provided and approved by Compex.

32

EN

6. DEVICE MAINTENANCE

GUARANTEE

See the attached leaflet.

MAINTENANCE

Your stimulator does not require any calibration or periodic maintenance. Use a soft cloth and solvent-free

alcohol-based detergent to clean your device. Use as little liquid as possible to clean the device. Do not

dismantle the stimulator or the charger because they contain high voltage components which could cause

electrocution. This must be carried out by Compex-approved technicians or repair services. If your stimulator

contains parts that appear to be worn or faulty, please contact the closest Compex customer service centre.

STORAGE/TRANSPORT AND USE

STORAGE AND TRANSPORT USE

TEMPERATURE -20° C to 45° C 0° C to 40° C

MAXIMUM RELATIVE HUMIDITY 75% 30% to 75%

ATMOSPHERIC PRESSURE from 700 hPa to 1060 hPa from 700 hPa to 1060 hPa

Do not use in areas at risk of explosion.

DISPOSAL

Batteries must be disposed of in accordance with national current regulations. Any product bearing the

WEEE label (a bin crossed out with a cross) must be separated from household waste and sent to special

recycling plants.

33

EN

7. TECHNICAL SPECIFICATIONS

GENERAL INFORMATION

Remote control battery: Rechargeable 3.7[V] / ≥ 1,500[mAh] lithium polymer (LiPo) battery.

Module battery: Rechargeable 3.7[V] / ≥ 450[mAh] lithium polymer (LiPo) battery.

SP 6.0 and 8.0 AC power adapter: Only 5[V] / 3.5 [A] AC power adapters bearing reference number 64902X

can be used to recharge your device.

FIT 5.0 AC power adapter: Only 5[V] / 1.5 [A] AC power adapters bearing reference number 00108X can be

used to recharge your device.

Product and accessories expected service life: 5 years

Electrode shelf life: refer to electrodes bag

NEUROSTIMULATION

All the electrical specifications are supplied for an impedance from 500 to 1000 ohms per channel.

Outputs: four independent and individually adjustable channels, electrically insulated from one another.

Impulsion form: constant rectangular current with compensated impulses to eliminate any direct element of

continuous current to avoid any residual polarisation from the skin.

Maximum impulse intensity: 120 mA.

Impulse intensity increments: manual adjustment of stimulation intensity from 0 to 999 (energy) by minimum

increments of 0.25 mA.

Duration of impulses: from 50 to 400 μs.

Maximum quantity of electricity per impulse: 96 microcoulombs (2 x 48 μC, compensated).

Typical impulse rise time: 3 μs (20%-80% of maximum current).

Frequency of impulses: 1 to 150 Hz.

34

EN

RF DATA

Transmission frequency band: 2.4[GHz] ISM

The characteristics of the type and frequency of modulation: GFSK, +/-320[kHz] deviation

Effective emission power: 4.4 [dBm]

STANDARDS

To ensure your safety, the stimulator has been designed, manufactured and distributed in accordance with

the requirements of the amended European Directive 93/42/CEE covering medical devices.

The stimulator also complies with the CEI 60601-1 standard covering general safety requirements for

electromedical devices, with the CEI 60601-1-2 standard covering electromagnetic compatibility and the CEI

60601-2-10 standard covering special safety requirements for nerve and muscle stimulators

In accordance with current international standards, a warning must be given about applying electrodes to the

thorax (increased risk of cardiac fibrillation).

The stimulator also complies with Directive 2002/96/CEE covering electrical equipment and electronic waste

(WEEE).

INFORMATION ABOUT ELECTROMAGNETIC COMPATIBILITY (EMC)

The Compex is designed to be used in typical domestic approved environments in accordance with the

safety standard EMC EN 60601-1-2.

This device emits very low levels in the radiofrequency interval (RF) and is therefore not likely to cause

interference with electronic equipment nearby (radios, computers, telephones, etc.).

The Compex is designed to support anticipated disturbance originating from electrostatic discharge,

magnetic fields for the power supply or radiofrequency emitters.

However, it is not possible to guarantee that the stimulator will not be affected by powerful RF fields

(radiofrequency) originating from other sources.

For more information about electromagnetic emission and immunity, please contact Compex.

35

EN

8. EMC TABLE

The Compex Stimulator requires special precautions regarding EMC and needs to be installed and put into

service according to the information provided on the EMC in this manual.

All RF wireless transmission devices can affect the Compex Stimulator. The use of accessories, sensors,

and cables other than those specified by the manufacturer, may result in greater emissions or reduce the

immunity of the Compex Stimulator.

The Compex Stimulator should not be used beside or stacked on other equipment, if adjacent or stacked

use is necessary, one must check the correct functioning of the Compex Stimulator within the context of the

configuration used.

RECOMMENDATIONS AND DECLARATION BY THE

MANUFACTURER CONCERNING ELECTROMAGNETIC EMISSIONS

The Compex Stimulator is intended for use in the electromagnetic environment specified below.

The customer or user of the Compex Stimulator should ensure that it is used in this environment

ELECTROMAGNETIC ENVIRONMENT

EMISSIONS TEST COMPLIANCE

- GUIDE

The Compex Stimulator uses RF

energy only for its internal operation.

RF emissions

Consequently, its RF emissions are

Group 1

CISPR 11

unlikely to interfere with any adjacent

electrical device (radios, computers,

telephones etc.).

RF emissions

Class B

CISPR 11

Compex Stimulator is suitable for use in

any establishment, other than a private

Harmonic emissions

Class A

dwelling or a place connected directly

IEC 61000-3-2

to the low voltage mains supply which

Voltage fluctuations/ emission

powers residential buildings.

Not applicable

oscillations IEC 61000-3-3

36

EN

RECOMMENDATIONS AND DECLARATION BY THE MANUFACTURER CONCERNING

ELECTROMAGNETIC IMMUNITY

Compex Stimulator is designed for use in the electromagnetic environment stipulated below. The buyer or user of the

Compex Stimulator must ensure it is used in this recommended environment.

ELECTROMAGNETIC

IMMUNITY TEST TEST LEVEL IEC 60601 OBSERVANCE LEVEL

ENVIRONMENT -

RECOMMENDATIONS

Floors must be wood,

concrete or ceramic tile.

±6 kV at the contact

Electrostatic discharge (DES)

±6 kV at the contact

If floors are covered with

CEI 61000-4-2

±8 kV in air

synthetic material the relative

±8 kV in air

humidity must be maintained

at a minimum of 30%.

±2 kV for power supply lines

The quality of the electrical

Fast transient electrical

±2 kV for power supply lines

power supply should be that

bursts

Not Applicable for input/

of a typical commercial or

CEI 61000-4-4

±1 kV for input/output lines

output lines

hospital environment.

The quality of the power

±1 kV differential mode

±1 kV differential mode

Surge

supply should be that of

CEI 61000-4-5

a typical commercial or

N/A

±2 kV joint mode

hospital environment.

<5 % VT (dips >95 % de UT)

<5 % VT (dips >95 % de UT)

for 0.5 cycle

for 0.5 cycle

The quality of the power

supply should be that of

<40 % VT

<40 % VT

a typical commercial or

Voltage dips, short

(dips >60 % de UT)

(dips >60 % de UT)

hospital environment. If the

interruptions and voltage

for 5 cycles

for 5 cycles

Compex Stimulator user

variations on power supply

requires continuous operation

lines

<70 % VT

<70 % VT

during mains power cuts, it is

CEI 61000-4-11

(dips >30 % de UT)

(dips >30 % de UT)

recommend that the Compex

for 25 cycles

for 25 cycles

Stimulator is powered by a

UPS or a battery.

<5 % VT (dips >95 % de UT)

<5 % VT (dips >95 % de UT)

for 5 seconds

for 5 seconds

Magnetic fields at the mains

frequency should be at a

Magnetic field at grid

level characteristic of a

frequency (50/60 Hz)

3 A/m 3 A/m

typical location in a typical

CEI 61000-4-8

commercial or hospital

environment.

NOTE :VT is the AC supply voltage before application of the test level.

37

EN

RECOMMENDATIONS AND DECLARATION BY THE MANUFACTURER

CONCERNING ELECTROMAGNETIC IMMUNITY

Compex Stimulator is designed for use in the electromagnetic environment stipulated below. The buyer or user of the

Compex Stimulator must ensure it is used in this recommended environment.

TEST LEVEL IEC

OBSERVANCE

ELECTROMAGNETIC ENVIRONMENT -

IMMUNITY TEST

60601

LEVEL

RECOMMENDATIONS

Portable and mobile RF communication devices must

only be used relative to the Compex Stimulator and its

wiring at a distance which is not less than the spacing

recommended and calculated using the appropriate

equation for the transmitter’s frequency.

Recommended spacing

d = 1.2 √P

Conducted RF IEC

d = 1.2 √P 80 MHz to 800 MHz

61000-4-6

3 Vrms

d = 2.3 √P 800 MHz to 2.5 GHz

150 kHz to 80 MHz

3 Vrms

where P is the maximum output power of the transmitter

Radiated RF

in watts (W) set by the manufacturer’s specifications and

3 V/m

3 V/m

IEC

where d is the recommended spacing in metres (m).

80 MHz to 2.5 GHz

61000-4-3

The field intensity of RF fixed transmitters, as determined

by an electromagnetic survey a must be less than the

observance level to be found in each frequency rangeb.

Interference may occur close to any appliance identified

by the following symbol:

NOTE 1 At 80 MHz and at 800 MHz ,the high frequency amplitude is applied

NOTE 2 These guidelines may not be appropriate for some situations. Electromagnetic wave propagation

is modified by absorption and reflection due to buildings, objects and persons.

a The field intensity from fixed transmitters, such as radio telephone base stations (cellular/wireless) and a mobile radio, amateur

radios, AM and FM radio transmissions and TV transmissions cannot be predicted with any accuracy. It may therefore be necessary

to consider an analysis of the electromagnetic environment of the site to calculate the electromagnetic environment coming from

fixed RF transmitters. If the field intensity measured in the environment where the Compex Stimulator is located exceeds the

appropriate RF observance level above, the Compex Stimulator should be monitored to ensure it is operating properly. In the event

of abnormal operation, new measures may then be imposed, such as realignment or movement of the Compex Stimulator.

b Above the frequency amplitude from 150 kHz to 80 MHz, the field intensity must be < 3 V/m.

38

EN

RECOMMENDED SPACING BETWEEN A PORTABLE AND MOBILE COMMUNICATION DEVICE

AND THE COMPEX STIMULATOR

The Compex Stimulator is designed for use in an electromagnetic environment in which radiated RF waves are controlled.

The buyer or user of the Compex Stimulator can contribute to preventing electromagnetic interference by maintaining a

minimum distance between portable and mobile RF communication devices (transmitters) and the Compex Stimulator

according to the table of recommendations below and according to the maximum output power of the telecommunication

device.

SPACING ACCORDING TO THE FREQUENCY OF THE TRANSMITTER M

MAXIMUM TRANSMITTER OUTPUT

FROM 150 KHZ

FROM 80 KHZ

FROM 800 MHZ

POWER W

TO 80 MHZ

TO 800 MHZ

TO 2.5 GHZ

D = 1.2 √P

D = 1.2 √P

D = 2.3 √P

0.01 0.12 0.12 0.23

0.1 0.38 0.38 0.73

1 1.2 1.2 2.3

10 3.8 3.8 7.3

100 12 12 23

In the case of transmitters whose maximum output power is not shown in the table above, the recommended spacing of d in

metres (m) can be calculated using the appropriate equation for the transmitter frequency, where P is the maximum output power

of the transmitter in watts (W) as set by the transmitter manufacturer

NOTE 1 At 80 MHz and at 800 MHz ,the spacing for high frequency amplitude is applied.

NOTE 2 These guidelines may not be appropriate for some situations. Electromagnetic wave propagation is modified by absorption

and reflection due to buildings, objects and persons.

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