BTL 4000 User manual

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BTL-4000

Series

USER’S MANUAL

GENERAL CHARACTERISTICS | Page 1 of 62

110DA03/03/2008EN

BEFORE YOU START

Take a moment to reflect on the advantages of the BTL-4000 Electrical Stimulation,

Ultrasound, Laser and Magnet technology in your own clinic. The BTL-4000 system has

many benefits not available in other systems. For an example, a choice of therapy

protocols offers maximum flexibility in a variety of clinical applications.

The combination electrical stimulation / ultrasound / laser or magnet therapy system also

offers substantial benefits since it eliminates the need to purchase separate units. We

sincerely believe the latest BTL physiotherapy system is technically superior to any other

physiotherapy products available and will provide years of trouble-free and profitable

use.

All of us at BTL wish you every success with your BTL-4000 system. We pride ourselves

on being as responsive as possible to our customers’ needs. Your suggestions and

comments are always welcome since we believe an ongoing relationship with our

customers is critically important to our future product line. Please call or email us your

suggestions.

While we would like you to start using your equipment right away, we encourage you to

thoroughly read this manual in order to fully understand the operational features of the

BTL-4000 system.

Again, thank you for being a BTL customer. In the event of any problem, or if you require

service, please make an initial call to your local distributor, who will decide whether to

refer the problem to our office.

PAGE 2 OF 62

CONTENTS

1 GENERAL CHARACTERISTICS........................................................................................................................ 5

2 INSTRUCTIONS FOR USE ................................................................................................................................ 6

2.1 Top Panel ...................................................................................................................................................... 6

2.2 Rear Panel..................................................................................................................................................... 7

2.3 Front Panel .................................................................................................................................................... 8

2.4 Unpacking And Assembly.............................................................................................................................. 8

2.5 Operating the Unit ....................................................................................................................................... 11

2.6 Therapy Setting ........................................................................................................................................... 13

2.6.1 Therapy Flow Chart................................................................................................................................ 13

2.6.2 Welcome Screen and Selection of Channels, Tabs and Accessories.................................................... 14

2.6.3 Setting of Therapy Parameters Via the Selection of Diagnosis – "DIAG" Key ....................................... 15

2.6.4 Setting of Therapy Parameters Via the Selection of Program – "PROG" Key........................................ 16

2.6.5 Setting of Therapy Parameters Manually Via The ‘MAN' Key ................................................................ 17

2.6.6 Therapy Parameters Screen .................................................................................................................. 18

2.7 Course of Therapy ....................................................................................................................................... 19

2.7.1 Start, Interrupt and End of Therapy........................................................................................................ 19

2.7.2 Running Therapy Screen ....................................................................................................................... 20

2.7.3 Electrotherapy – Setting During Therapy ............................................................................................... 20

2.7.4 Accessories / Applicators – Visual Signalization. ................................................................................... 21

2.7.5 Indication of Operation – Energy On Operation ..................................................................................... 22

2.8 Therapy Parameters.................................................................................................................................... 24

2.9 Encyclopaedia ............................................................................................................................................. 24

2.10 Therapy Saving ........................................................................................................................................... 25

2.10.1 Save Therapy......................................................................................................................................... 25

2.11 Interconnection of Units ............................................................................................................................... 27

2.11.1 Interconnection of BTL 4000 Puls (COMBI) and Vacuum Unit BTL Vac................................................ 27

2.11.2 Interconnection of BTL-4000 Puls and BTL-4000 Sono ......................................................................... 27

2.11.3 Interconnection of BTL-4000 Puls, BTL-4000 Sono and BTL Vac ......................................................... 28

2.11.4 Setup and Operation of Combined Therapy in Individual Devices ......................................................... 29

2.11.5 Stopping Combined Therapy in Individual Devices................................................................................ 29

3 DEVICE MENU ................................................................................................................................................. 30

3.1 Accessories ................................................................................................................................................. 30

3.1.1 Installation of Accessories...................................................................................................................... 30

3.1.2 Information about Accessories............................................................................................................... 30

3.1.3 Connectors – Information....................................................................................................................... 30

3.2 Unit Settings ................................................................................................................................................ 31

3.2.1 Password Setting ................................................................................................................................... 31

3.2.2 Sound Setting ........................................................................................................................................ 31

3.2.3 Auto Switch Off Setting .......................................................................................................................... 31

3.2.4 Setting of Display Contrast..................................................................................................................... 32

3.2.5 setting Contrast of Small Display ........................................................................................................... 32

3.2.6 setting of Backlight................................................................................................................................. 32

3.2.7 Date and Time Setting ........................................................................................................................... 32

3.2.8 Language Setting................................................................................................................................... 32

3.2.9 Setting of HW Key.................................................................................................................................. 32

3.2.10 New Operation ....................................................................................................................................... 32

3.2.11 Style of Operation .................................................................................................................................. 32

3.2.12 Unit Information...................................................................................................................................... 32

3.2.13 Unlock Code .......................................................................................................................................... 32

PAGE 3 OF 62

3.2.14 Service Functions .................................................................................................................................. 33

3.3 Special Settings........................................................................................................................................... 33

4 USER SETTINGS OPTION............................................................................................................................... 34

4.1 User Sequences .......................................................................................................................................... 34

4.1.1 Creating New Sequence ........................................................................................................................ 34

4.1.2 Parameters of Sections in Sequence..................................................................................................... 36

4.1.3 Saving New Sequence........................................................................................................................... 36

4.2 User Diagnoses / Programs......................................................................................................................... 37

4.3 List of Recent Therapies.............................................................................................................................. 37

5 ACCESSORIES ................................................................................................................................................ 38

5.1 Power Supply Adapter 60W / Adapter 90W................................................................................................. 38

5.2 Accumulator................................................................................................................................................. 38

5.3 Lithium Battery............................................................................................................................................. 39

5.4 Accessories Common for All Units .............................................................................................................. 39

5.5 Accessories for Electrotherapy .................................................................................................................... 39

5.6 Accessories for Ultrasound Therapy............................................................................................................ 40

5.7 Accessories for Laser Therapy .................................................................................................................... 40

5.8 Accessories for Magnetotherapy ................................................................................................................. 40

6 MAINTENANCE AND SAFETY INSTRUCTIONS ............................................................................................ 41

6.1 Safety .......................................................................................................................................................... 42

6.2 Contraindications......................................................................................................................................... 46

6.2.1 Contraindications for Electrotherapy ...................................................................................................... 46

6.2.2 Contraindications for Ultrasound............................................................................................................ 47

6.2.3 Contraindications for Laser Therapy ...................................................................................................... 47

6.2.4 Contraindications for Magnetotherapy ................................................................................................... 48

6.3 Warranty ...................................................................................................................................................... 48

7 TECHNICAL PARAMETERS ........................................................................................................................... 49

7.1 Technical Parameters of The BTL-4000 Series Devices .............................................................................49

7.2 Technical Parameters of Power Supply Adapter 60W / Adapter 90W ......................................................... 50

7.3 Basic Parameters of Electrotherapy Generator ........................................................................................... 51

7.4 Basic Parameters of Ultrasound Generator ................................................................................................. 51

7.5 Basic Parameters of Laser Generator ......................................................................................................... 52

7.6 Basic parameters of Magnet Generator....................................................................................................... 52

7.7 Technical Parameters of Ultrasound Heads ................................................................................................ 53

7.8 Technical Parameters of Laser Probes........................................................................................................ 53

7.9 Technical Parameters of Laser Clusters...................................................................................................... 54

7.10 Technical parameters of Magnetic Applicators ............................................................................................ 55

7.11 Applicable Standards................................................................................................................................... 55

7.12 Interconnection of Devices .......................................................................................................................... 56

7.13 Manufacturer ............................................................................................................................................... 56

8 UNITS CONFIGURATIONS.............................................................................................................................. 57

8.1 Table of Configurations of the Combined Devices BTL 4000 Series ........................................................... 57

8.2 Table of Configurations of the Electrotherapy Devices BTL-4000 Puls ....................................................... 60

8.3 Table of Configurations of the Ultrasound Therapy Devices BTL-4000 Sono.............................................. 61

8.4 Table of Configurations of the Laser Therapy Devices BTL-4000 Laser ..................................................... 61

8.5 Table of Configurations of the Magnetotherapy Devices BTL-4000 Magnet................................................ 62

PAGE 4 OF 62

1 GENERAL CHARACTERISTICS

The BTL-4000 Series offers advanced and well designed physiotherapy units for professional use. Depending on

the required configuration, each system can consist of up to two units with combinations - for electrotherapy,

ultrasound, laser or magnet therapy treatment.

The modular design of the BTL-4000 equipment allows you to build the combination you require. Combine an

electrotherapy unit of your choice with either ultrasound, laser or magnet all in a single unit. This can save

considerable money in your physiotherapy investment.

Selecting a diagnosis from a list of alphabetically organized treatment protocols, or selecting a program, will make

an easy and efficient start of the therapy. Naturally, you can adjust any treatment parameter manually by the

simple use of the unit keys and buttons. Throughout the whole therapy, the display informs you about the

remaining therapy time, channel and therapeutic method used, the type of therapy applied, attached accessories,

and other necessary data.

If several accessories are attached to your unit at the same time, you can easily recognize the accessory required

for a specific treatment. Select a treatment on the display (electrotherapy, ultrasound, laser or magnet), and the

control light on the corresponding accessory (electrotherapy cable, ultrasound head, or magnet disc / double disc

/ linear or solenoid applicator) will start blinking to indicate that this accessory should be used.

Save your time by using the pre-programming of the BTL-4000 units. Based on detailed research and practical

use of the units, the well-organized pre-programmed protocols will give you recommendations for treating various

conditions. The unit also includes up to 50 free lots to define your own protocols. Moreover, you can recall the last

20 treatments.

Prepare your own protocols and later invoke them from easily accessible option.

With every BTL unit, you can purchase a cart specially designed for BTL products. Its versatile design allows you

to conveniently store and use 1 or 2 physiotherapy units and a vacuum unit. The cart includes a range of

accessory trays and baskets. Four well-built and steady castors ensure easy movement of the unit in the office or

hospital.

Please visit our corporate website at http://www.btlnet.com

services.

GENERAL CHARACTERISTICS | PAGE 5 OF 62

for the latest information on BTL products and

2 INSTRUCTIONS FOR USE

2.1 TOP PANEL

1. - 6 outputs for patient cables on the rear panel of the device, see chapter Rear Panel

7. display

8 diag key, for quick selection of diagnosis or programs

9 prog key, for quick selection of therapy program

10 man key, for manual setting of all therapy parameters

11 menu key, to set date, time, language, display contrast, sounds, user options, etc.

12 select/intensity knob, to select individual parameters

13 enter key, to confirm selection or setting

14 esc key, to cancel selection or setting and return to the original setting

15 tab key, for switching between the buttons on the display

16 next key, for fast entering the therapy parameters subscreens

17 key 1 for switching to the tab of the first generator

18 key 2 for switching to the tab of the second generator

INSTRUCTIONS FOR USE | PAGE 6 OF 62

2.2 REAR PANEL

1 -6 patient outputs – for exact configuration, see table Configuration of Output Connectors

19 mains switch, for switching the device on/off – positions I / 0.

20 socket for connection of external power supply Adapter 60W / Adapter 90W

21 warning label with parameters of power supply and input of the device

INSTRUCTIONS FOR USE | PAGE 7 OF 62

2.3 FRONT PANEL

22 display of the remaining time of therapy for the first channel

23 display of the remaining time of the therapy for the second channel (or current intensity in case the

channel is only one)

24 start / stop1 key, for starting or pausing the therapy on the first channel

25 start / stop2 key, for starting or pausing the therapy on the second channel

26 on / off switch – serves for switching the device on/off

27 service connector placed under the cover and then the type, manufacture and warning labels (they are

placed on the bottom cover of the device)

2.4 UNPACKING AND ASSEMBLY

Inspect the box for damage and report any damage to the carrier and your distributor. Do not proceed with

installation and assembly if the box is damaged.

Unpack the equipment and place it on a stable horizontal surface suitable for the equipment's weight, out of reach

of sunlight. During the operation the equipment gets warm, therefore it must not be located close to heat-

producing devices. Cooling of the equipment is provided by forced air circulation. Cooling vents are located on the

rear panel and at the bottom of the equipment and must not be covered. Place the equipment so, that the free

space behind the rear side is at least 10 cm. Do not position the equipment on a soft surface which may obstruct

air flow to the bottom cooling vents. Do not put any heat-producing devices or objects containing water or other

liquid on the equipment. Do not place the equipment close to devices producing strong electromagnetic, electric

or magnetic field (diathermy, X-rays, etc.), as equipment electronics could be undesirably influenced. In case of

any questions, please call your distributor or service agent.

The same installation conditions should be observed for the Adapter 60W / Adapter 90W power supply adapter.

INSTRUCTIONS FOR USE | PAGE 8 OF 62

Retain the original packaging to ensure future possible transportation of the device.

Plug the device into the mains socket by means of the Adapter 60W / Adapter 90W power supply adapter

(see chapter Technical Parameters).

PLUG THE POWER SUPPLY ADAPTER DIRECTLY INTO THE MAINS SOCKET; DO NOT USE ANY MULTI-

CONNECTION EXTENSION CABLE OR ADAPTOR.

In case of any questions, please call your distributor or service agent.

Switching the device on:

Connect the power supply adapter to the device and plug its mains cable into the mains socket, switch the I/ 0

rocker switch (19) on the rear panel to the I position and finally press the ON/OFF switch (26) on the front panel.

The system will then run a self-test. If the self-test finds no faults, the screen will display the equipment type and it

is ready for use - see note below.

Connection of accessories

Connect the accessories to the output connectors (1) - (6) on the rear panel in this way:

Put in the cable connector and secure the fluted ring by pressing and turning in clockwise. ATTENTION WHEN

DISCONNECTING THE CONNECTOR, first of all, it is necessary to take by the fingers the fluted ring NOT THE

WHOLE connector. TURN THE FLUTED RING ANTICLOCKWISE and then after releasing the ring, disconnect

the connector by pulling the fluted ring still held in the fingers!

ATTENTION!!! DO NOT TURN THE WHOLE CONNECTOR USING FORCE, THE DEVICE COULD BE

DAMAGED.

For configuration of the output connectors (1) to (6), see the table Configuration of Output Connectors

The unit will automatically detect the accessories type and display it on the screen. If a wrong one is connected,

the equipment will not operate and the screen will display a warning and help about where to connect which

accessory.

Recharging the accumulator

The device accumulator is sold in half-charged status. That is why we recommend formatting the accumulator

after purchase of the device: connect the device to the mains via the external adapter for at least 48 hours without

interruption, with the mains rocker switch (18) in position I. The device will be recharged and the accumulator

will be properly formatted. A properly formatted accumulator enables longer operation of the device without mains

supply. For details, see the chapter Accumulator.

Restart of the device - reset

If for any reason (electromagnetic interference, etc.) the device stops responding to the user's commands and the

message "please wait..." with small moving squares is not displayed, the device can be put into the initial state by

simultaneously pressing the prog (9) and menu (11) keys. After this, the device immediately goes into the initial

status as well as after switch-on of power supply.

The mains switch (19) on the rear panel has the same effect – the whole device switches off; however, we

recommend using the above described combination of keys prog + menu which is more friendly to the electronics

of the device.

Note:

After switching on, the unit tests for about 10 - 15 secs all internal functions. If any fault exists, the screen will

display a warning. If any fault that compromises patient safety exists, the system will 'lock' itself into ‘secure’

mode. If this situation occurs, please call your local distributor for service advice.

INSTRUCTIONS FOR USE | PAGE 9 OF 62

Tab. 2.1 Configuration of output connectors

Device Type

BTL-4610 Puls Optimal BTL-4615 Puls Optimal BTL-4620 Puls Optimal BTL-4625 Puls Optimal BTL-4110 Laser Optimal BTL-4710 Sono Optimal BTL-4210 Sono Optimal BTL-4810 S Combi Optimal BTL-4815 S Combi Optimal BTL-4810 L Combi Optimal BTL-4815 L Combi Optimal BTL-4800 SL Combi Optimal BTL-4800 TL Combi Optimal BTL-4810 M Combi Optimal BTL-4815 M Combi Optimal BTL-4810 T Combi Optimal BTL-4815T Combi Optimal BTL-4816 S Combi Professional BTL-4818 S Combi Professional BTL-4816 L Combi Professional BTL-4818 L Combi Professional BTL-4816 M Combi Professional BTL-4818 M Combi Professional BTL-4800 LM Combi Optimal BTL-4800 SM Combi Optimal BTL-4920 Magnet Optimal BTL-4610 Puls Professional* BTL-4615 Puls Professional* BTL-4620 Puls Professional BTL-4625 Puls Professional BTL-4110 Laser Professional BTL-4710 Sono Professional BTL-4210 Sono Professional BTL-4810 S Combi Professional BTL-4815 S Combi Professional BTL-4810 L Combi Professional BTL-4815 L Combi Professional BTL-4800 SL Combi Professional BTL-4800 TL Combi Professional BTL-4810 M Combi Professional BTL-4815 M Combi Professional BTL-4810T Combi Professional BTL-4815T Combi Professional BTL-4800 LM Combi Professional BTL-4800 SM Combi Professional BTL-4920 Combi Professional

output 1 output 2 output 3 output 4 output 5 output 6

E1opti E1opti E2opti E1opti E2opti E1opti

L1A L1B door acup. U1A U1B E input E output T1A T1B E input E output U1A U1B E1opti U1A U1B E1opti

L1A L1B door E1opti

L1A L1B door E1opti U1A U1B door L1A T1A T1B door L1A

M1A M1B E1opti

M1A M1B E1opti T1A T1B E1opti T1A T1B E1opti E1A E1B U1B U1A E1A E1B U1B U1A E1A E1B door L1A E1A E1B door L1A E1A E1B M1 M2 E1A E1B M1 M2

L1A Door M1A M1B

U1A U1B M1A M1B

M1A M1B

E2 E1

L1A L1B door acup. U1A U1B E input E output T1A T1B E input E output U1A U1B E1 U1A U1B E1

L1A L1B door E1

L1A L1B door E1 U1A U1B door L1A T1A T1B door L1A

E1 M1A M1B

E1 M1A M1B T1A T1B E1 T1A T1B E1

L1A door M1A M1B

U1A U1B M1A M1B

M1A M1B

* can be extended by the HVT module

INSTRUCTIONS FOR USE | PAGE 10 OF 62

Notes:

E1 connector for connection of electrotherapy accessories (BTL-236-1(2), BTL vac) to the E1 generator

E2 connector for connection of electrotherapy accessories (BTL-236-1(2), BTL vac) to the E2 generator

E1opti connector for connection of electrotherapy cables (BTL-226, BTL vac) to the E1 generator

E2opti connector for connection of electrotherapy cables (BTL-226, BTL vac) to the E2 generator

E1A, E1B connector for connection of electrotherapy accessories (BTL-236-1(2), BTL vac) to the double

generator E1

L1A, L1B connector for connection of laser probe/ cluster BTL-448 / BTL-445 to the L1 generator

L2A, L2B connector for connection of laser probe/ cluster BTL-448 / BTL-445 to the L2 generator

U1A, U1B connector for connection of ultrasound head BTL-237, e.g. 1 / 4 cm

M1A, M1B connector for connection of magnetotherapy applicators (BTL-239) to the M1 generator

E input connector for input of external electrotherapy BTL-46xx, BTL-56xx on the ultrasound device at

combined therapy

E output connector for output of external electrotherapy BTL-46xx, BTL-56xx on the ultrasound device at

combined therapy

door connector for the open door sensor

acup. connector for the acupuncture electrode

How many patients and which outputs you can simultaneously connect to can be seen on the display after

pressing the menu key, in menu / accessories / connectors – information.

, to the U1 generator

2.5 OPERATING THE UNIT

The display contains several graphic elements. Some of them are only for information, some can be activated.

The basic elements are the following:

• buttons (it is possible to activate them by the tab key (15) and to change their values.) The activated

buttons are displayed inversely.

• information texts

• channel tabs (switching between the tabs, selection)

The buttons can be enabled or disabled. The disabled buttons are crossed out.

All the displayed enabled buttons can be successively activated by pressing the tab key (15). By repeated

pressing of this key further buttons on the screen are successively activated.

If the button contains one numeric value, this value can be directly changed by the select/intensity knob (12). If

the button contains more numeric values or an item selected from a list, pressing of the enter key (13) opens the

detailed subscreen of the button. In the bottom right corner of the selected parameters screens there is a button

shaped like a folded corner of paper. It has the same function as the NEXT key (16) and opens the parameters

subscreens. To leave the subcscreen press esc (14) – all data you have changed will remain changed.

Information texts

The text is displayed directly on the display, in a menu or in a button. If a text is too long and does not fit on the

display in full, after a while it starts scrolling automatically.

Selected channel

Although most of the devices of the BTL-4000 Series can run more therapies at a time, only one channel can be

controlled at the particular moment. That channel is called the "selected channel". The tab of the "selected

channel" in the bottom part of the screen is coloured dark. All information on the screen and all controls are relate

to this channel. The most important information about the therapies on the other channels remains visible on their

tabs.

INSTRUCTIONS FOR USE | PAGE 11 OF 62

INSTRUCTIONS FOR USE | PAGE 12 OF 62

2.6 THERAPY SETTING

2.6.1 THERAPY FLOW CHART

INSTRUCTIONS FOR USE | PAGE 13 OF 62

2.6.2 WELCOME SCREEN AND SELECTION OF CHANNELS, TABS AND ACCESSORIES

Besides the initial information, this screen contains channel tabs with description of the connected accessories.

The number of channels – tabs depends on the required configuration of the device. To display all information of

the channel press key 1 (17) or 2 (18) under the tab. The information set on the "invisible channels" remain

preserved. The following scheme shows that almost the entire screen is available for the "selected channel".

Keys 1(17) and 2(18) located directly under the tabs serve for switching between the tabs.

On the channels where more accessories can be connected to one generator (ultrasound generator and two

ultrasound heads, laser generator and laser probes, magnet generator and magnet applicators), repeated

pressing of the tab's key serves for switching between these accessories.

The tab of the channel which is selected (i.e. its information is just on the display) is black.

Examples of information on the tabs:

tab of the selected E channel, to which no accessory is connected

tab of the E channel, which is not selected, with connected accessory BTL-236-2

tab of the U generator , which is not selected, with

connected ultrasound head; pressing of keys 1 (17) and 2

(18) under the tab serves for switching between the

connected heads – 1 cm

/4 cm

tab of the selected L generator with connected laser

probe; pressing of keys 1 (17) and 2 (18) under the tab

serves for switching between the connected probes–

685nm/830nm (red/infrared)

tab of selected M generator with connected disc applicator;

tab of the selected E2 channel with unsuitable connected accessory, which this

generator cannot work with

INSTRUCTIONS FOR USE | PAGE 14 OF 62

2.6.3 SETTING OF THERAPY PARAMETERS VIA THE SELECTION OF DIAGNOSIS – "DIAG" KEY

To view the list of diagnoses press the diag key (8). Each channel tab has its own list of therapy protocols. The

letter in front of each number corresponds to the type of selected therapy: E – electrotherapy; U – ultrasound;

L – laser; M – magnetotherapy. For example, the channel tab of the ultrasound generator includes a list of

therapy protocols for ultrasound treatment. If the tab depicts an HVT or combined therapy symbols, the list

includes protocols for HVT or combined therapies.

For moving in the list of diagnoses use the select/intensity knob (12). The currently selected diagnosis is

displayed in bold.

For fast finding of a diagnosis, select its initial letter by the tab key (15).

After finding of the required diagnosis, select it by pressing the enter key (13). If to the diagnosis are assigned

more therapies – e.g. the treatment can be done by several various types of current – the list of therapies appears

after selection of the diagnosis. Select the required therapy by the select knob (12) and press enter (13) again.

Saved by user protocols can easily be find in the “*user diagnoses / programs” item, which appears at the top of

the diagnoses list.

INSTRUCTIONS FOR USE | PAGE 15 OF 62

2.6.4 SETTING OF THERAPY PARAMETERS VIA THE SELECTION OF PROGRAM – "PROG" KEY

Press the prog (8) key to set the required program number. The program numbers generally correspond to the

program numbers used in the traditional BTL physiotherapy line. The letter in front of each number corresponds to

the type of therapy selected: E – electrotherapy; U – ultrasound; L – laser; M – magnetotherapy.

Combined therapies

ultrasound head symbol. They are in the positions E-35xx - E-39xx.

Your own therapy protocols

electrotherapy, U-80xx - U-89xx for ultrasound therapies, L-80xx - L-89xx for laser therapies and

M-80xx - M-89xx for magnetotherapy.

Your own sequences

U-95xx - U-99xx for ultrasound therapies, L-95xx - L-99xx for laser therapies and M-95xx - M-99xx for

magnetotherapy.

Programs recommended for diagnoses can be found in the User’s Guide.

For faster setting, the program numbers are arranged into pairs. For change of the number use the select knob

(12), for switching between the pairs of digits use the tab key (15).

E+U are listed among E programs and can be found on the electrotherapy tab with the

(except sequences) can be saved under the following numbers: E-80xx - E-89xx for

are saved under the following numbers: E-95xx - E-99xx for electrotherapy,

INSTRUCTIONS FOR USE | PAGE 16 OF 62

2.6.5 SETTING OF THERAPY PARAMETERS MANUALLY VIA THE ‘MAN' KEY

Press the man (9) key to select manual setting for the therapy. All therapy parameters can be set and saved as a

user program or diagnosis.

It is obvious that the therapy parameters screens of individual currents of electrotherapy, ultrasound therapy and

laser therapy differ in dependence on the options which can be set in the particular moment. For more details see

the respective User's Guide.

To open the required menu or setting dialog select the respective button by the tab key (15) and then press enter

(13). For fast entering the therapy parameters subscreens use the “next” key. Most dialogs are accompanied

with illustration pictures and symbols. See the scheme of possibilities of individual settings in this mode.

INSTRUCTIONS FOR USE | PAGE 17 OF 62

2.6.6 THERAPY PARAMETERS SCREEN

This screen opens after selection of therapy after pressing the diag (8), prog (9) or man (10) key, (see the

chapter Therapy Setting Flow Chart). Before the start of therapy you can change all parameters.

• SETTING THERAPY TIME

The time of the therapy can be set only on the therapy parameters screen, either by activation of the time button

and pressing of the enter key (13) after which the time setting dialog opens, or by fast selection using the

select / intensity knob (12).

enter

select

Select/intensity

By pressing the start / stop1 (24) or start / stop2 (25) keys you can start or interrupt therapy – see chapter Start,

Interruption and End of Therapy

• INTENSITY SETTING

For the ultrasound, laser and magnet

therapies, the intensity (power) can be set only on the therapy parameters

screen and only when the therapy is not running. To set the intensity, select the intensity option and adjust the

required value by turning the select/intensity knob. For the laser therapy, the power option is situated in the

therapy parameters subscreen, which can be accessed by pressing the next key.

To the electrotherapy,

the intensity is set during therapy running, and can only be adjusted by turning the

select/intensity knob (12).

INSTRUCTIONS FOR USE | PAGE 18 OF 62

2.7 COURSE OF THERAPY

2.7.1 START, INTERRUPT AND END OF THERAPY

To start therapy on the first channel (tab) press the start / stop1 key (24). To start therapy on the second channel

press the start / stop2 key (25). Therapy can be started only if the display of the selected channel is displaying

the therapy parameters screen.

The paused therapy can be resumed by pressing the start / stop1 (or start / stop2) key or stopped by pressing

the esc (14) key.

While the therapy is paused, you can adjust the time (except for laser therapies and all types of sequences) by

the select / intensity (12) knob.

For electrotherapy, you can adjust the intensity during therapy running by turning the select / intensity (12)

knob to the right (to increase intensity) or to the left (to decrease intensity).

Direction of

intensit

Laser therapy can also be started / paused by the start / stop key on the laser probe.

START / STOP

INSTRUCTIONS FOR USE | PAGE 19 OF 62

2.7.2 RUNNING THERAPY SCREEN

2.7.3 ELECTROTHERAPY – SETTING DURING THERAPY

• SETTING THE INTENSITY IN 4-ELECTRODE THERAPIES

Making a therapy with four electrodes, you can set different intensities between each pair of electrodes. In case of

4-pole interference, the output intensity is set by the select / intensity (12) knob on both channels at the same

time (the screen button 1+2 is pressed) or on each channel separately (the screen button 1 or 2 is pressed). For

switching among the buttons use the tab key (15).

If the intensity on one of the channels is set to zero, the therapy is terminated.

• 4-POLE ELECTROTHERAPY GENERATOR

Devices equipped with 4-pole electrotherapy generator enable starting of 4-pole interference and special

interference just with using of single channel. This way the second channel stays active for starting another

therapy. Between individual pairs of electrodes is possible to set different intensity values. Setting of output

intensity is the same as in precedent.

Note:

Devices equipped with 4-pole electrotherapy generator cannot be connected with HVT module and they do not

allow starting the therapy with microcurrents.

INSTRUCTIONS FOR USE | PAGE 20 OF 62

• MANUAL CONTROL OF VECTOR IN DIPOLE INTERFACE

In manually-controlled dipole interference, the dipole angle in the intersection of the electrodes is set during

therapy by the enter knob (13) for turning to the right, and by the esc knob (14) for turning to the left. The position

of the dipole is symbolized on the screen above the time value.

When rotating the dipole, the unit automatically switches to diagnostic mode (Spectrum value = 0Hz). After 1 or 2

seconds the unit returns to therapeutic mode (Spectrum value = preset value).

2.7.4 ACCESSORIES / APPLICATORS – VISUAL SIGNALIZATION.

Accessories BTL-236 (for electrotherapy) and BTL-237 (ultrasound heads) and BTL-239 (magnetic applicators)

feature blue pilot lights that signal their operating conditions:

BTL-236-1: patient cable with two electrodes – blue and yellow pilot light signals:

•slow blinking – accessories ready for therapy – therapy settings screen displayed

•continuous light – therapy in process, possible dangerous voltage on electrodes

BTL-236-2: patient cable with four electrodes – blue and yellow pilot light signals:

•slow blinking – accessories ready for therapy – therapy settings screen displayed; always the

pilot light at the selected pair of electrodes A or B is blinking

•blinking in rhythm of generated currents or continuous light – therapy in process, dangerous

voltage may be on the pair of electrodes A or B at which the pilot light is blinking

BTL-237:

•slow blinking – accessories ready for therapy – therapy settings screen displayed

•continuous light – the therapy in process

ultrasound head 1 cm2 or 4 cm2 – blue pilot on the head:

•rapid blinking – wrong contact of head with patient's tissue, therapy paused; contact must be re-

established to continue therapy

BTL-448:

•blinking in rhythm of generated laser or continuous light – the device is generating laser

radiation, during generation the device indicates occurrence of laser radiation by acoustic signal

BTL-445

•blinking in rhythm of generated laser or continuous light. Laser irradiation is also indicated

by acoustic signal

laser probes 635 nm and 830 nm – green pilot light and focusing beam:

: laser clusters: red, infrared and combined – focusing beam:

INSTRUCTIONS FOR USE | PAGE 21 OF 62

BTL vac:

For detailed information please refer to the leaflet which is enclosed to each accessory supplied.

BTL-239-1:

•slow blinking – accessories prepared for therapy, therapy settings screen displayed.

•continuous light or blink in therapy rhythm – therapy in process.

BTL-239-2:

•slow blinking – accessories prepared for therapy, therapy settings screen displayed.

•continuous light or blink in therapy rhythm – therapy in process.

BTL-239-3:

•slow blinking – accessories prepared for therapy, therapy settings screen displayed.

•continuous light or blink in therapy rhythm – therapy in process.

BTL-239-4:

•slow blinking – accessories prepared for therapy, therapy settings screen displayed.

•continuous light or blink in therapy rhythm – therapy in process.

BTL-239-5:

vacuum unit for electrotherapy – see separate manual for BTL vac unit.

disc magnetic applicator – blue pilot light signals:

solenoid ø30 cm magnetic applicator – blue pilot light signals:

solenoid ø60 cm magnetic applicator – blue pilot light signals:

double disc magnetic applicator – blue pilot light signals:

multi disc magnetic applicator – blue pilot light signals:

•slow blinking – accessories prepared for therapy, therapy settings screen displayed.

•continuous light or blink in therapy rhythm – therapy in process.

BTL-239-6:

•slow blinking – accessories prepared for therapy, therapy settings screen displayed.

•continuous light or blink in therapy rhythm – therapy in process.

BTL-239-8

• slow blinking - accessories prepared for therapy, therapy settings screen displayed.

•continuous light or blink in therapy rhythm – therapy in process

2.7.5 INDICATION OF OPERATION – ENERGY ON OPERATION

Electrotherapy

Presence of electrotherapy voltage on output is indicated:

• on the screen:

• on the channel tab – by value of intensity or running time

– by value of intensity of output current

– by an animated icon of running electrotherapy current

linear magnetic applicator – blue pilot light signals:

: solenoid ø70 cm magnetic applicator with couch – blue pilot light signals:

• on the electrotherapy accessory BTL-236 – by continuously lit blue pilot light.

INSTRUCTIONS FOR USE | PAGE 22 OF 62

Disconnection of electric circuit (such as in the case of wrong contact between electrode and patient) is indicated

by blinking information about intensity and time on the corresponding electro generator tab, or by audio signalling.

This function can be switched on and off in the menu of the unit (press menu key (11), select menu – specific

settings – check contact of electrodes). Its current state is marked by a figure symbol (crossed-out if disabled).

Audio signalling can be switched on and off - marked by a bell symbol on the screen (crossed-out if disabled).

Note:

Some types of the generated currents do not allow monitoring of the contact with the patient. In such cases the

crossed-out figure is displayed, regardless of the user setting of detection.

Ultrasound Therapy

Generation of ultrasound energy by ultrasound head BTL-237 is indicated:

• on the screen:

– by value of intensity

– by bar-graph showing contact of head with tissue

• on the channel tab – by value of intensity and time

• on the ultrasound accessory BTL-237 – by blue light ring.

Insufficient contact between the ultrasound head and the tissue

on the head and blinking of the information on intensity and time on the channel tab of the corresponding

ultrasound generator. This function is indicated by a figure symbol on the screen. This function is indicated by a

figure symbol on the screen.

Laser Therapy

Laser irradiation by BTL-448 laser probe is indicated:

• on the screen:

– by power value

is indicated by rapid blinking of the blue light ring

– by signal icon

• on the channel tab – by value of intensity and time

• by acoustic signal. Signalling can be enabled or disabled from the menu (press menu key (11), select

menu – specific settings – sound in running therapy)

• by green pilot light on laser probe

• by green or red focused beam.

Laser irradiation by BTL-445 laser cluster is indicated:

• on the screen:

– by intensity value

– by icon of the signal

• on the channel tab – by value of intensity and time

• by acoustic signal. Signalling can be enabled or disabled from the menu (press menu key (10), select

menu – specific settings – sound in running therapy)

• by blue focusing beam.

INSTRUCTIONS FOR USE | PAGE 23 OF 62

Magnetotherapy

Presence of magnetotherapy field on output is indicated:

• on the screen:

– by value of intensity of output magnetic field

– by icon of running magnetic field

• on the channel tab – by value of intensity and remaining time

• on the magnetic applicator BTL-239 – by blue pilot light.

2.8 THERAPY PARAMETERS

Therapy parameters are variable. Only the parameters that characterize the therapy and that can be set in

manual mode are displayed - by pressing the man (10) key. For a detailed description of parameters for individual

therapies, refer to the User’s Guide.

2.9 ENCYCLOPAEDIA

The encyclopaedia provides information about individual therapies, examples of electrode and magnet applicator

placement and application areas for ultrasound and laser. Each unit is supplied with a hard copy of the

encyclopaedia. Its electronic format is included in the unit, and is available from menu / encyclopaedia.

Treatment protocols and related information are only a guide and are not intended as a replacement for

Note:

good clinical judgment and experience!

After opening of the encyclopaedia you get to its contents – the list of diagnoses. For browsing in the list use the

select/intensity knob (12). After selection of the required diagnosis press the enter key (13) to get the specific

information about the diagnosis:

INSTRUCTIONS FOR USE | PAGE 24 OF 62

2.10 THERAPY SAVING

Pressing the save button on the screen, the user can save the particular therapy setting under a name of

diagnosis and number of program.

2.10.1 SAVE THERAPY

Therapy can be saved always after setting of the therapy parameters – i.e. from the therapy parameters screen.

The following information is saved with each therapy:

Electrotherapy:

• All parameters of currents (pulse length, pause length, modulation, etc.)

• Therapy time

• Polarity

• Output mode (current / voltage)*

Ultrasound therapy:

• All therapy parameters (for example, ultrasound frequency, duty factor - DF, pulse frequency, etc.)

• Therapy time

• Intensity

Combined therapies electro + ultrasound:

• All electrotherapy parameters (pulse length, pause length, modulation, etc.)

• All ultrasound therapy parameters (ultrasound frequency, duty factor - DF, pulse frequency, etc.)

• Therapy time

• Polarity of electrotherapy output

• Electrotherapy output mode (current / voltage)

• Intensity of ultrasound

Laser therapy:

• All therapy parameters (frequency, course of signal, etc.)

• Irradiated area

• Dosage

Magnetotherapy:

• All magnetotherapy parameters (pulse, pause, modulation, random frequency)

• Pulse shapes

• Therapy time

• Intensity of magnetic field

When saving a therapy, enter:

• name of diagnosis (therapy) – will be displayed in the list of diagnoses under the diag key (8)

• number of program – will be displayed in the list of diagnoses under the prog key (9)

INSTRUCTIONS FOR USE | PAGE 25 OF 62

The number of the saved program falls within the interval from 8000 to 8999. and adds the letter of the

corresponding generator (E for electrotherapy and combined therapies, U for ultrasound therapies, L for laser

therapies and M for magnetotherapy).

The unit suggests the lowest available number (from the range of 8000-8999) and adds the letter of the

corresponding generator (E for electrotherapy and combined therapies, U for ultrasound therapies, L for laser

therapies and M for magnetotherapy).

Saved therapy goes in the list with the user diagnoses / program, which appear as an option at the top of the list

with diagnose.

List of diagnoses List of programs

enter

List of programs

INSTRUCTIONS FOR USE | PAGE 26 OF 62

2.11 INTERCONNECTION OF UNITS

2.11.1 INTERCONNECTION OF BTL 4000 PULS (COMBI) AND VACUUM UNIT BTL VAC

Combine any BTL-4000 Puls or Combi unit with the vacuum unit BTL vac to apply electrotherapy currents by

means of suction cup electrodes. Adjustable vacuum pressure ensures simple and convenient attachment of

patient electrodes, especially on parts of the body hard to reach with classic electrodes. Moreover, the pulse

mode provides mechanical massage of the tissue improves body metabolism and increases blood supply.

The electrotherapy unit has its outputs connected to the vacuum unit. Both vacuum and flat electrodes are

attached to the vacuum unit. Each channel on the vacuum unit has a switch. When the switch is on, current is

brought to the vacuum electrodes. When the switch is off, current is brought to the standard electrodes.

BTL-4000

Puls (Combi)

The picture is only an illustration. For the actual interconnection follow the table Configuration of Output

Connectors.

For interconnection, use the interface cables leading from BTL-4000 Puls outputs E1, E2 (and connected to BTL

vac inputs IN1 and IN2. For more information, see the User's Guide of BTL vac.

2.11.2 INTERCONNECTION OF BTL-4000 PULS AND BTL-4000 SONO

If combined therapy is used, connect the ultrasound and electrical stimulation units together.

Electrotherapy BTL-46xx Puls or BTL-56xx Puls Ultrasound BTL-4710 Sono or BTL-5710 Sono

Connector Connected accessories Connector Connected accessories

E2*

interface cable to ultrasound U1A ultrasound head 1 cm

electrodes E2* U1B ultrasound head 4 cm

E input interface cable to electrotherapy

* if installed E output electrodes E1

INSTRUCTIONS FOR USE | PAGE 27 OF 62

Setting of polarity between the ultrasound head and the electrode

After interconnection with the electrotherapy device, the ultrasound head becomes the anode (+). The other pole

is the cathode (-), which is the electrode with the black banana plug. If the ultrasound head is required to be the

cathode (-) during combined therapy, select ‘negative polarity’ in the therapy parameters screen of the

electrotherapy unit.

ATTENTION

In the case of accessories „1>>2“connected to the electrotherapy device, the ultrasound head becomes the

anode (+). The cathode (-) is connected thru the black banana plug with minus sign “-„ on it.

In the case of accessories „1>>4“” (optional) connected to the electrotherapy device, the ultrasound head

becomes the anode (+). The cathode (-) is connected thru red banana plug with plus sign “+„ on it, independent

of selected output A or B.

If you want to apply only electrotherapy with such interconnected devices, it is no problem. Uncheck the option

"with electro" on the BTL-4000 Sono device, and the electrotherapy electrodes are automatically connected to

the electrotherapy output. Connectors E-input and E-output are interconnected inside the ultrasound device even

if the BTL-4000 Sono device is off.

2.11.3 INTERCONNECTION OF BTL-4000 PULS, BTL-4000 SONO AND BTL VAC

To connect the units, follow this diagram:

BTL-4000

Puls

BTL-4000

Sono

BTL vac

The picture is only an illustration. For the actual interconnection follow the below-stated table as well as the Table

Configuration of Output Connectors.

Electrotherapy BTL-46xx or BTL-56xx Puls Ultrasound BTL-4710 Sono or BTL-5710 Sono

Connector Connected accessories Connector Connected accessories

E1 interface cable to ultrasound U1A ultrasound head 1 cm2

E2* interface cable to BTL vac (IN2) U1B ultrasound head 4 cm2

E input interface cable to electrotherapy

* if installed E output interface cable to BTL vac (IN1)

INSTRUCTIONS FOR USE | PAGE 28 OF 62

2.11.4 SETUP AND OPERATION OF COMBINED THERAPY IN INDIVIDUAL DEVICES

After checking for correct interconnection of the electrotherapy and ultrasound units, select a diagnosis or

program that utilizes combined therapy. Select these separately on the electrotherapy and on the ultrasound

units. Set the electrotherapy unit to CV mode. Then attach the respective electrode to the patient to close the

electric circuit ultrasound head-patient-electrode (see the above diagrams). It is now possible to run the

ultrasound by the start /stop1 key. Position the ultrasound head in contact with tissue and notice that the timer

commences counting down. Slowly increase the intensity on the electrotherapy by turning the select / intensity

knob to the right (in the "+" direction). Combined therapy is now running. If the contact between the ultrasound

head and the treated tissue during the therapy was not continuous, the times shown on both devices can differ,

because timer countdown on the ultrasound device does not run when the contact is interrupted.

2.11.5 STOPPING COMBINED THERAPY IN INDIVIDUAL DEVICES

Delivery of combined therapy ends after expiration of the set time on both units' timer devices. To stop or interrupt

therapy before the set time expires, it is necessary first to interrupt the therapy on both units by pressing the

start / stop keys.

INSTRUCTIONS FOR USE | PAGE 29 OF 62

3 DEVICE MENU

Press the menu (11) key - two options appear, menu and user. Enter the menu option and scroll through the

following options:

• accessories

• encyclopaedia – see chapter Encyclopaedia

• unit settings

• special settings

3.1 ACCESSORIES

The available options are:

• installation of accessories

• information about connected accessories

• information about the number of patients and connection of connectors on the rear panel of the device

3.1.1 INSTALLATION OF ACCESSORIES

Each connected accessory has a memory that includes identification data of this accessory. According to these

data, the unit recognizes which accessory is connected, if it is compatible or not and if the unit can work with the

connected accessory or not. The memory also contains the serial number of the accessory. Since the accessory

memory contains quite a lot of information, their upload lasts approximately from 30 second to 2 minutes. The

installation of accessories serves for faster functioning of the unit. After the installation, only the serial number of

the accessory is read from the accessory memory and the other information is read from the unit’s memory.

During the installation process, follow the instructions on the screen. In particular:

• switch off all therapies

• do not have connected other accessories than the one that is being installed. Make sure the installed

accessory is connected directly, not via interface cable and vacuum or BTL-4000 Sono devices.

This will help decrease electromagnetic interference, which could cause improper reading of memory data.

3.1.2 INFORMATION ABOUT ACCESSORIES

Allows identification of connected accessories (name, serial number, for

which generator - output / input - the accessory has been designed).

3.1.3 CONNECTORS – INFORMATION

This menu item will inform you about the way of connection of the

connectors on the rear panel of the device and up to how many patients

you can connect safely to the device.

DEVICE MENU | PAGE 30 OF 62

3.2 UNIT SETTINGS

This submenu provide a list of settings of parameters and user preferences:

• Access Password setting

• Sound setting

• Auto-switch off setting

• Setting of display contrast

• Setting of contrast on small (digital) 99 display

• Setting of display backlight

• Date and time setting

• Language setting

• Setting of HW key

• New operation

• Style of operation

• Unit Information

• Unlock code

• Service functions

3.2.1 PASSWORD SETTING

This option enables the change of the password, which is required by the device after switch-on. Without entering

of this password the device does not allow any further work the password required to operate the unit after power-

up. The units as standard come with this function disabled.

If the unit includes a laser generator - BTL-4000 Laser, BTL-48xx L, BTL-48xx xL, you cannot disable the

password code (in compliance with the applicable standards). In this case, the four-digit code is factory-set to

0000.

Note:

If you happen to forget the password, you can always use the universal one: "00000000"

3.2.2 SOUND SETTING

Sets audio signalling of keys and provides warnings of various operational conditions (start of therapy, stop or

pause of therapy). The factory-set standard sounds are sounds of therapy processes. You can set another

sound scheme or switch the sounds completely off (sound scheme 0)..

Units with laser generator - BTL-4000 Laser, BTL-48xx L, BTL-48xx xL, the sound signalling of running therapy

can be enabled or disabled from the menu (press menu key (11), select menu – specific settings – sound in

running therapy)

3.2.3 AUTO SWITCH OFF SETTING

Here you can set the time after which the display will be switched off, and

the idle time after which to switch off the entire device.

DEVICE MENU | PAGE 31 OF 62

3.2.4 SETTING OF DISPLAY CONTRAST

After selection of this menu you can set the optimum contrast (readability) of the display by the select/intensity

knob (12).

Since the display contrast depends on many factors (e.g. temperature of the display), there is also another fast

and direct way of setting the contrast. Press simultaneously the enter (13) and esc (14) keys and set the contrast

by the select/intensity knob (12) (when holding the two keys enter and esc pressed).

3.2.5 SETTING CONTRAST OF SMALL DISPLAY

After selection of this menu you can set the optimum contrast (readability) of the lower digital display on the front

panel by the select/intensity knob (12).

3.2.6 SETTING OF BACKLIGHT

In this item you can select by the select/intensity knob (12) whether the main display shall be backlighted

permanently, shall not be backlighted at all or shall be backlighted only if the device is connected to the mains.

This setting has strong influence on the time for which the device can be supplied from the accumulators* without

recharging. The switched-on backlighting is considerable load for the accumulators* and reduce the time of

operation without recharging.

*) refers only to the devices of the Professional series.

3.2.7 DATE AND TIME SETTING

Sets the date and time.

3.2.8 LANGUAGE SETTING

Selects the language of the text on the display of the device. Factory pre-set is English.

3.2.9 SETTING OF HW KEY

Via this option the type of unit can be changed by inserting a special 64-digit code.

3.2.10 NEW OPERATION

In older devices the enter and esc keys were arranged the other way round; in this item you can select the new

arrangement (enter on the right, esc on the left) or the old arrangement (enter on the left, esc on the right).

3.2.11 STYLE OF OPERATION

Here you can select whether the set time and intensity values on the display after the end of therapy shall be zero

or equal to the values of the last performed therapy.

3.2.12 UNIT INFORMATION

Displays info about the unit (serial number, firmware version, etc.). It also contains information till when the device

will work – so called "device validity". If the functioning of the device is temporary, this item contains information

until which date the device will be fully functional.

3.2.13 UNLOCK CODE

If the functioning of the device is temporary, in this item can be inserted the code which can prolong the

functionality of the unit or removes the time restriction.

DEVICE MENU | PAGE 32 OF 62

3.2.14 SERVICE FUNCTIONS

• SCAN DISK

Checks the file system in the unit for possible errors. Recommended for use in case of lack of memory, if the

unit refuses to save data, or if you think that some data have been lost.

• FILE SYSTEM FORMATTING

Clears all data and programs created by the user.

• DELETE ACCESSORIES

Deletes all installed accessories. Use only in case of improper installation – e.g. a bad "scattered" picture on

the tab, connected accessories are not detected (the “?” symbol is displayed), etc.

• DRIVES INFO

Displays the current free space in the memory that can be used for user data. User data are, for example

saved user diagnoses, I/t curves, etc.

The user can use the memory marked "E:"; the memory marked "S:" and “L:” are intended for internal use.

• DEFAULT SETTING WITHOUT LOSING USER DATA

This option is available in the subscreen, which could be accessed by pressing the next key from the “service

functions” submenu. All factory settings are restored. User data, such as user saved therapies, sequences etc.

are preserved.

• GENERS INFO

This option also is available in the subscreen, which could be accessed by pressing the next key from the

“service functions” submenu. It shows information about the generators in the unit - their type, ID, FW version,

position (master or slave) and temperature.

3.3 SPECIAL SETTINGS

Variable for each generator. See your User’s Guide for details.

DEVICE MENU | PAGE 33 OF 62

4 USER SETTINGS OPTION

Press menu, select the user settings option - opens a screen allowing access to special features of the unit, as

well as to data saved by the user. The following items can be selected:

• user sequences

• user diagnoses / programs

• recent therapies

• motor point detection*

• accommodation coefficient*

• I/t curve*

* Available only with electrical stimulator equipped with electrodiagnostics (optional).

4.1 USER SEQUENCES

This item enables to work with the list of sequences of programs created by

the user. The selected sequence can be run, edited and deleted in this menu.

A new sequence can be created in the therapy parameters screen in the

manual settings.

4.1.1 CREATING NEW SEQUENCE

There is limitation of the choice of currents in one sequence when there is no pause set between the sections:

If the option pause between sections is set, the unit stops generation after each current and the intensity of the

next current has to be set manually. In this case, there is no limitation and the user can select and combine any

current in one sequence. We suggest setting this option for electrotherapy sequences.

If the pause between sections is not set, the unit generates the same intensity for all currents. Be careful when

setting sequences. Each current is felt differently by the patient. Whereas in case of TENS the patient tolerates an

intensity of about 100 mA, the maximum tolerated intensity in case of diadynamic currents is 10 times lower.

Combine in one sequence only currents that are perceived by the patient in a similar way – such as currents with

the same pulse length and with maximum difference in frequency 1:10. Monophasic, symmetric and alternating

currents should not be mutually combined.

The following combinations are recommended if the pause between sections is not set:

• diadynamic currents

• monophasic pulses of the same length with DC component (differing in frequency or modulation)

• symmetric pulses of the same length with zero DC component (differing in frequency or modulation)

• alternating pulses of the same length with zero DC component (differing in frequency or modulation)

• mid-frequency bipolar currents (differing in frequency or modulation)

• interferences

• TENS (differing in frequency or modulation)

• ultrasound therapies

• laser therapies

USER SETTINGS OPTION | PAGE 34 OF 62

For the electro generator it is possible to select sequence in the therapy parameters screen (in the manual

mode). For the laser generator, laser sequence is in the therapy parameter screen, accessible by means of the

next key (from the manual mode). Creation of a new sequence for the electro generator is displayed in the

following diagram.

select

Repeat the process to insert additional

program (section) in the sequence

USER SETTINGS OPTION | PAGE 35 OF 62

4.1.2 PARAMETERS OF SECTIONS IN SEQUENCE

A sequence consists of a few currents / programs that are called sections. Parameters of sections must be set

when creating a sequence.

Each program includes basic current parameters such as frequency, pulse length, modulation, etc. For more

information, please refer to the chapter Save Therapy. Set all data in the manual setting screen and save them

as a user-designed program (diagnosis). Insert the program/diagnoses in the sequence. Set the length of time of

the section when inserting the program/diagnoses in the sequence (except laser, where the time of the section

depends on the currently connected laser probe). Obviously, the factory-preset programs can also be inserted in

the sequences. In the section only the polarity can be set (for electrotherapy sequence). The other parameters

must be specified and saved in the inserted program.

Example: you want to create a sequence of diadynamic DF current (without base, positive polarity, CC mode,

time of stimulation: 1 minute) and CP-ISO current (base 10%, reversal of polarity in the middle of the set time, CC

mode, 10 minutes). Press man to select the manual mode, set diadynamic currents, DF type, without base,

positive polarity, CC mode. Save this setting as (for example) program E-8001. Then set the parameters of the

CP-ISO current: base 10%, positive, reversal, CC mode, and save it as (for example) program E-8002. Select

therapy and press new sequence then press new, set the program number 8001, set the time of section 1:00,

positive polarity, and press enter. Then add the second section in the same way – new, program number 8002,

time of section 10:00, positive polarity with reversal, and press enter. Then press enter again to return to the

manual settings screen, press save/copy and save the sequence (for example, as number 9501). The cv/cc

mode is set globally for the whole sequence before starting it.

4.1.3 SAVING NEW SEQUENCE

Sequence created according to the chapter Creating New Sequences can be saved as follows:

Either directly from the screen for setting of new sections.

Or from the main manual screen in the same way as the new diagnosis.

User-made sequences are saved under numbers 9500 - 9999. They can be found in the list of programs, in the

list of diagnoses or in the list of sequences.

USER SETTINGS OPTION | PAGE 36 OF 62

4.2 USER DIAGNOSES / PROGRAMS

Use this feature to run user designed therapies, to edit and delete their

parameters and names. It is very similar to the creation of a new

diagnosis / program – see the chapter Therapy Saving. On each

channel tab, you can see only those therapies that were created on this

tab. An icon before the name of the therapy will tell you which type of

generator the therapy has been designed for.

4.3 LIST OF RECENT THERAPIES

Allows the user to select a recent therapy on the selected tab, run it again after pressing the load button or view

its parameters.

USER SETTINGS OPTION | PAGE 37 OF 62

5 ACCESSORIES

The equipment is not designed for use in connection with other medical devices except those stated in this

manual.

Following is a list of accessories that can be supplied with the units, both standard and optional. For detailed

information on individual accessories, see the enclosed leaflet and/or the User's manual.

5.1 POWER SUPPLY ADAPTER 60W / ADAPTER 90W

The devices of the BTL-4000 series can be connected to the mains exclusively via the supplied power supply

Adapter 60W or Adapter 90W. Adapter 90W is more powerful and is used only for the connection of specific

device configurations. Your device always includes the proper type of adapter.

It is forbidden to connect another adapter than mentioned to the device.

5.2 ACCUMULATOR

BTL-4000 devices have a built-in accumulator. Its type is specified in the chapter Technical Parameters.

Replacement of the accumulator is provided by the authorized service of BTL devices.

During operation, the accumulator is continuously being recharged from the mains. Its recharging and keeping

charged is running even if the equipment is switched off and connected to the mains, and the mains switch (18)

on the rear panel is in position I. At switching off, the device checks the status of the accumulators and if it finds

them low, it switches to the charging mode; in the charging mode the display is dark and the main display shows

the symbol of a recharging battery. After recharging of the accumulator, the device automatically switches off

completely. Note that the charging process runs only if the device is plugged into the mains and the rocker mains

switch (18) on the rear panel is in position I.

Determination of the accumulator status may take some time, therefore, the device may respond with a delay

after switching off and then on again.

If the device is supplied from the mains, this status is signalled by the plug picture. In case the device is

supplied from the mains and the accumulator is low, there is shown an animation of a recharging battery

on the display.

For full charging of the accumulator, let it recharge for approximately 6 hours – preferably overnight.

A charged accumulator is signalled by a "full battery" picture.

If the accumulator is low, it is still possible to work with the device for a short time. But when the picture of

a low accumulator starts to blink, the accumulator is dead and no therapy can be started, the running

therapy will be finished and the device will switch off automatically.

To ensure long lifetime of the accumulator, we recommend keeping it permanently charged. When possible,

connect the device to the mains via the adapter and switch the mains switch (14) to position I. The indication of

recharging is displayed, after recharging it goes out and the accumulator will automatically be kept charged.

ACCESSORIES | PAGE 38 OF 62

If the device is left unplugged from the mains for a longer time (even in the OFF status), the accumulators

gradually spontaneously discharge. This effect is characteristic of the accumulators and cannot be removed;

therefore, if the device has been off and unplugged for a longer time than approximately 2-3 months, we

recommend recharging it, preferably for 48 hours without interruption.

For the same reason, we recommend charging the device continuously for at least 48 hours immediately after

purchase, regardless of the accumulator status indication (you can work with the device normally, only do not

unplug it from the adapter, the accumulator recharges even during standard operation of the device). Thus the

accumulator becomes “formatted” and will keep working longer without recharging.

5.3 LITHIUM BATTERY

The device contains a lithium battery for backing up the date and time. The type of battery is stated in the chapter

Technical Parameters. Replacement is provided by the authorized service of BTL devices.

5.4 ACCESSORIES COMMON FOR ALL UNITS

• External power supply Adapter 60W / Adapter 90W including the mains cable

• User’s manual

• Markers for output cables

• Trolley

5.5 ACCESSORIES FOR ELECTROTHERAPY

• user’s guide for electrotherapy

• patient cable BTL-236-1

• patient cable BTL-236-2 (optional)

• flat rubber electrodes 7 x 5 cm

• flat rubber electrodes 12 x 8 cm

• sponge covers 7 x 5 cm

• sponge covers 12 x 8 cm

• set of fixation belts

• point electrode (optional)

- ball point attachment – diameter 2 mm

- ball point attachment – diameter 6 mm

- HVT attachment

• self-adhesive electrodes (optional)

• vaginal electrode (optional)

• rectal electrode (optional)

• interface cable between BTL-4000 and BTL vac (optional)

ACCESSORIES | PAGE 39 OF 62

5.6 ACCESSORIES FOR ULTRASOUND THERAPY

• user's guide for ultrasound therapy

• 1cm

• 4cm

• ultrasound gel 235ml, 5l, 10l

• interface cable between BTL-46xx Puls and BTL-47xx Sono (optional)

ultrasound head BTL-237-1-13 for 1 and 3MHz, ERA 0.7 cm2 (optional)

ultrasound head BTL-237-4-13 for 1 and 3MHz, ERA 3.24 cm2

5.7 ACCESSORIES FOR LASER THERAPY

• user's guide for laser therapy

• laser probes - red BTL-448

• laser probes – infrared BTL-448

• laser clusters - red BTL-445

• laser clusters - infrared BTL-445

• laser clusters - combined (red and infrared) BTL-445

• holder for laser probe and laser cluster

• holder for optical attachment

• optical attachments for laser probes

• warning labels

• safety goggles OPTE BS 2, L3, 630 – 1350nm

5.8 ACCESSORIES FOR MAGNETOTHERAPY

• user’s guide for magnetotherapy

• disc applicator - BTL-239-1

• solenoid small applicator - BTL-239-2

• solenoid big applicator - BTL-239-3

• double disc applicator - BTL-239-4

• multi disc applicator - BTL-239-5

• linear applicator - BTL-239-6

• solenoid applicator ø70cm with couch- BTL-239-8

• interface cable for connection of old type of applicators from BTL-09

• fixation belts

ACCESSORIES | PAGE 40 OF 62

6 MAINTENANCE AND SAFETY INSTRUCTIONS

The service inspection including measuring of all parameters of the device and possible recalibration must be

performed at intervals shorter than 30 months. The inspection and recalibration is performed by the authorized

BTL service department on the basis of the user's order. If the inspection is not done within the stated term, the

manufacturer does not guarantee the technical parameters or safe operation of the product.

Safe operation of any item of medical equipment requires close attention to detail. Please check the following on

a regular basis:

Power cord and plug: Check for frays and kinks. Ensure that the insulation is not damaged in any way.

Ultrasound head surface: Gel should always be thoroughly cleaned from the surface of the head. Always maintain

this surface in as clean a condition as possible. Do not use any abrasive products for cleaning this surface as they

could damage this delicate accessory.

Wires, cables and electrodes: Check for frays, cuts or tears in the insulation. Always route electrical cords and

cables away from user or patient foot traffic areas where they could increase the chance of a tripping-related

accident.

Check the unit before each use to determine that all controls function normally.

Calibration of heads and probes / clusters must be done by authorized personnel.

Cleaning

To keep the device clean, do not store or use it in a dusty environment and do not spill any liquid on the surface.

To clean, turn the equipment off and unplug the power supply. Clean the unit with a damp cloth. Do not use

abrasive materials. Do not use agents containing alcohol, ammonia, benzine, or thinners. Clean the accessories

that come into contact with the patient after each treatment. Use appropriate agents. No part of the equipment

needs to be aseptic or sterilized.

Laser probes/clusters: Keep the lens clean. After each application, wipe the head of the probe with a cotton cloth

(divergent probes). Unscrew the head, wipe the lens and blow compressed air through the head (convergent

probes). In laser clusters, wipe the laser aperture with a cotton cloth so as to keep the protective glass clean.

Laser optical attachments: Can be sterilized for 20 minutes at a temperature of 180°C.

Fuse replacement

A protective fuse is located inside the BTL-4000 device. The type of fuse is specified in the chapter Technical

Parameters. The user should not replace the fuse; for replacement of the fuse, always contact the authorized

service of BTL devices.

Transport and Storage

We recommend keeping the original packaging of this equipment to ensure its maximum protection during

transportation. Unplug the power supply adapter and the accessories cables. The equipment must be stored or

transported as defined in the chapter Technical Parameters.

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 41 OF 62

6.1 SAFETY

ATTENTION!

The consumed current or voltage of the connectors marked with this label can exceed safety values.

The protection of the equipment is BF-type floating applied part (only if original accessories including power

supply Adapter 60W / Adapter 90W are used).

The equipment does not use any medicaments which would be an integral part or would be applied by means of

it.

ATTENTION!

This system has no user-serviceable parts or assemblies. Do not remove the instrument covers under

any circumstances. Call your distributor for advice about any malfunction.

The device is equipped with a protection system that prevents connection of accessories other than

those supplied from the manufacturer.

General safety precautions:

• Before first switch-on of the equipment, carefully read the User's Manual.

• All staff who will use the equipment must be instructed in the way of operation, maintenance and checking of

the equipment, and the safety principles.

• The electrical cabling which the equipment will be connected to must be installed and tested according to

the existing valid standards (IEC 364). If you are not sure that the mains are completely OK, get them

inspected by an inspection engineer.

• Check whether the parameters of the mains correspond to the requirements of the equipment according to

the chapter Technical Parameters. It must not be used in an environment which implies the danger of

explosion or penetration of water into the equipment. It must not be used in connection with flammable

anaesthetics or oxidizing gasses (O

• Do not place the equipment in direct sunshine or strong electromagnetic fields so as to prevent undesirable

mutual influence. In case this undesirable influence occurs, place the equipment further from the source of

interference or contact the authorized service of BTL devices.

• Inspect the equipment thoroughly before each use (loose cables, broken insulation of cables, functions of

displays and controls, etc.); in case of any inconsistency, stop using the equipment and contact the

authorized BTL service department. If the equipment's behaviour differs from the function described in this

Manual, stop using the equipment and contact the BTL service department.

, N2O, etc.).

• If the equipment shows any defect or if you have doubts about its correct functioning, terminate therapy

immediately. If you do not determine the source of uncertainty after thorough study of the Manual, contact

the BTL service department. If the equipment is not used in accord with this Manual or is used even if it

shows functional differences from this Manual, the user is responsible for the damage caused by the

equipment.

• Do not dismantle the equipment in any case; removal of the protective covers implies the danger of

electrical injury. Replacement of the lithium battery, fuses or accumulators may only be done by the

authorized BTL service department.

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 42 OF 62

• All material and parts which come into direct contact with the patient's body (as well as, for example, agents

for cleaning the electrodes) must comply with the respective standards related to irritability, allergization,

toxicity, genotoxicity, carcinogeneity (ISO 10993-1, ISO 10993-3, ISO 10993-5). The user is responsible for

all these materials and parts if not supplied by the BTL equipment supplier.

• The connectors for accessories as well as the other connectors must not be used for connection of anything

else than they are designed for, otherwise there is a danger of electrical injury and serious damage to the

equipment.

• The equipment does not use or produce any toxic substances during its operation, storage or transport

under the stated conditions.

• After bringing the equipment from a cold environment into warmth, do not plug it into the mains until the

temperatures become equal (i.e. for at least 1 hour).

• Before the start of therapy, check whether all set parameters correspond to your intents.

• Do not apply therapy on damaged skin!

• To terminate the application, do not switch off the mains switch but press the stop knob (20). The time

interval between switching the mains switch on and off must be at least 3 seconds.

• If after many years of operation it is necessary to discard the equipment, it can be done in a way which is

usual for this type of devices after removal of the lithium battery and the lead accumulator. The removed

batteries shall be disposed of in the way designated for hazardous waste - not within municipal waste. The

equipment does not contain any toxic materials which could harm the environment in case of normal

liquidation.

Warning: removal of batteries causes irreversible damage to the unit. Perform only environmental liquidation

of the unit!

Procedure:- unscrew the bottom cover of the unit

- remove the batteries with a suitable tool (placing of batteries - see the picture)

The equipment and the accessories must not be used in a way not stated in this User's Manual.

During work with this device, use the recommended protective equipment.

• Keep the equipment out of reach of children.

• The equipment does not contain any components which can be repaired by the user. Do not remove any

covers from the equipment. All repairs should be done by the authorized BTL service department.

• Don’t connect equipment to the patient when it is still connected to the computer (via service connector).

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 43 OF 62

Safety precautions for electrotherapy:

• When applying DC currents (the polarity button is enabled), it is necessary to pay attention to the set

intensity and time of application of currents. Wrong values can cause burning of the patient's skin.

• The maximum secure effective value of current density on the electrodes is 2 mA/cm

(according to IEC

601-2-10). BTL-4000 Series can exceed this value (according to the place of used electrodes type). In such

case it is necessary to pay greater attention to the application of currents! Wrong values can cause burning

of the patient's skin.

• Application of electrodes near the thorax may increase the risk of cardiac fibrillation.

• For contraindications, see the chapter Contraindications. Use of electrotherapy in cases of contraindication

must be approved by a specialist.

• Simultaneous connection of the patient to a high-frequency surgical device may cause burning in the place

of the electrodes and possible damage to the electrotherapy device.

• Simultaneous connection of the patient to an ECG monitor or an ECG alarm system may cause temporary

malfunctioning of the ECG systems or unreliability of the values measured by the ECG systems.

• Operation of the equipment close to (within 1 m of) a short-wave or micro-wave therapeutic device may

cause instability of the equipment's output.

• All supplied electrodes can be used at the maximum intensity of currents and voltage that can be set on the

device.

Safety precautions for ultrasound:

• Protect the heads consistently from shocks and frost. Do not unnecessarily bend the mains cable.

• During therapy, hold the head so that you do not touch its metallic parts.

• An impact on the metal part of the head as well as an intense impact on the head's case may negatively

change the parameters of the therapeutic head.

• For contraindications, see chapter the Contraindications. Use of ultrasound therapy in cases of

contraindication must be approved by a specialist.

• For therapy, use only the BTL ultrasound gel; the head is not tested for other gels or oils and their use could

damage the head. If you still want to use other gels, we recommend them to be only water-based gels.

Never use paraffin-based gels.

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 44 OF 62

Safety precautions for laser:

• Mark the laser workplace with the respective warning notices and connect the door switch.

• Equip the laser workplace with an operating code which must be approved by a competent health officer.

• When using a laser probe with an output of 200 mW or more (300 mW, 400 mW) and if the laser power is

set higher than 150 mW, the duration of therapy must not exceed 15 min.

• Attention – use of any other than the stated control and setting elements and processes may cause

dangerous exposure to radiation.

• The equipment works with laser beam of the 3B class. When working with the beam, follow all the

instructions stated in this Manual and in the laser therapy User's Guide. Prevent the laser beam from hitting

the eyes, thyroid and other endocrine glands, the head, etc. (see the User's Guide). Both the therapist and

the patient must wear the supplied protective goggles during therapy. Incorrect handling of the equipment

(not in accord with this Manual) may cause dangerous radiation and even damage to the eyes! In such a

case, the user is responsible for all damage.

• During radiation, do not disconnect the probe from the equipment and do not switch the equipment off.

• Protect the laser probe consistently from impacts!!!! The probe is not waterproof!

• Protect yourself and your surroundings from being directly hit by the laser beam.

• For contraindications, see the chapter Contraindications. Use of laser therapy in cases of contraindication

must be approved by a specialist.

Safety precautions for magnet:

• Never use damaged applicators. Electric shock to personal or patient may occur.

• Attending personnel should keep away from the patient applicator side when the applicator is in use. The

relevant channel should be switched off during necessary manipulation.

• Stop the therapy at once in case of any failure.

• Check all parameters before you start the therapy.

• Place the instrument on an even hard board to assure proper cooling.

• Watches, electronic devices and magnetic recording carriers can be damaged when closely exposed to

applicators and cables.

• Do not connect anything else to the connectors – there is a danger of injury by electric shock and / or

serious damage to the instrument.

• The instrument must not be used in the presence of pregnant women!

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 45 OF 62

6.2 CONTRAINDICATIONS

The list of contraindications the cases when the manufacturer does not recommend applying the selected

therapy. If a specialised medical workplace decides to apply the therapy in spite of it, they bear all the

responsibility for this action.

6.2.1 CONTRAINDICATIONS FOR ELECTROTHERAPY

• Active tuberculosis

• Allergy to solutions used for dampening electrode cover sponges

• Applications in the area of the heart and eyes

• Groundless stimulation - "placebo effect"

• Cardiovascular diseases

• Electronic implants (i.e. Cochlear implants, neural implants, pacemaker, defibrillator, chip implants...)

• Metal implants

• Malignancies in the current path

• Skin defects and skin inflammations

• Bleeding conditions

• Menstruation

• Tumour diseases

• Sensitivity disorders (relative KI) in the area of electrode placement

• Psychopathological syndromes and organic psychosyndromes

• Multiple sclerosis

• Pregnancy

• Inflammations of veins and lymphatic paths

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 46 OF 62

6.2.2 CONTRAINDICATIONS FOR ULTRASOUND

• Active tuberculosis

• Allergies to used ultrasound gels

• Applications on peripheral nerves (located on the bone, close to skin surface)

• Applications on glands with inner secretion

• Applications on areas around the eyes, brain, spinal cord

• Blood diseases

• Children - epiphyses of growing bones

• Gonads

• Pregnancy

• Pacemaker

• Cardiovascular diseases

• Cochlear implants

• Metal implants

• Skin defects and skin inflammations

• Bleeding conditions

• Menstruation

• Tumour diseases

• Blood circulation deficiency

• St. p. Laminectomii

6.2.3 CONTRAINDICATIONS FOR LASER THERAPY

• Applications in the area of the eyes – possibility of direct eye irradiation and retina damage

• Menstruation

• Tumour diseases

• Irradiation of malignancies and potentially precancerous growths

• Irradiation of patients with cochlear implants

• Irradiation of glands with inner secretion

• Patients with febrile conditions

• Pulse modes (both red and infrared beam) are not used on patients with anamnesis of epilepsy

• Pregnancy

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 47 OF 62

6.2.4 CONTRAINDICATIONS FOR MAGNETOTHERAPY

• Bleeding conditions, hypothalamus and hypophysis disorders

• Electronic implants (i.e. Cochlear implants, neural implants, pacemaker, defibrillator, chip implants...)

• Hyperthyroidism, hyperfunction of adrenals, myastenia gravis

• Malignancies

• Menstruation

• Metal implants

• Onychomycosis

• Paroxysm neurologic diseases

• Pregnancy

• Psychoses

• Serious mycosis, active tuberculosis, acute virosis

• Special attention must be paid to patients with hypotonia or otherwise with hypertension

• Tumour diseases

• Children – growth discs of bones (epiphysis)

6.3 WARRANTY

The Manufacturer of this product guarantees the product is free of defects in workmanship and material for the

period and conditions defined in the BTL General Service Conditions.

MAINTENANCE AND SAFETY INSTRUCTIONS | PAGE 48 OF 62

7 TECHNICAL PARAMETERS

7.1 TECHNICAL PARAMETERS OF THE BTL-4000 SERIES DEVICES

Device Type:

Display:

•dimensions:

•resolution:

Low battery indication:

Design

Weight – device only 2.9 kg Dimensions (l x h x w) 160 x 140 x 350mm Covering grade according to EN 60 529

Operating conditions:

Temperature: + 10 °C to + 40 °C Relative humidity: 30 % to 75 % Atmospheric pressure Position Type of operation

Transport and storage conditions:

Temperature: - 10 °C to + 55 °C Relative humidity: 25 % to 85 % Atmospheric pressure Position Max time of storage: max. 1 year

Additional conditions:

Power supply:

Input max: 60 W / 90 W Input voltage 24 V DC Frequency: 50 Hz to 60 Hz Protection class: II (according to IEC 536, ČSN 33 0600)

Internal fuse:

Mains switch: on the rear panel of the device, positions 0 and I Power switch on the front panel of the device, marked on/off Covering: IP20

Internal chemical sources:

Battery: lithium battery CR2032 Lead accumulator: 2x 6 V / 1.2 Ah, maintenance-free

capacity of the accumulator:

charger: internal, time needed for 100 % charging is approx. 6 hours

Classification

Applied parts type BF Class according to MDD 93/42/EEC IIb

*the stated values do not apply to Magnet therapy, which always must be supplied from the AC mains.

BTL-4000 Series – physiotherapy

LCD diagonal: 10.922 cm (4.3”) 480 x 272

on the display

700 hPa to 1060 hPa horizontal – on legs continuous

650 hPa to 1100 hPa any

transport only in the supplied packing recharge the accumulators at least 2x a year

supply only via the external supply Adapter 60W / Adapter 90W

T6.3A / 250V, safety fuse on the printed circuit, acc. to IEC 127-2 (replacement may only be done by the authorized service)

20 min. – 45 min. in dependence on the ener

intensiveness of the therapies applied*

TECHNICAL PARAMETERS | PAGE 49 OF 62

Therapy duration

For electro and laser therapies 0 to 100 minutes For ultrasound therapies 0 to 30 minutes For magnetotherapies 0 to 100 minutes Step of setting 1 second Accuracy of therapy time Accuracy of time values 5 seconds per day

± 2 % of the set value

7.2 TECHNICAL PARAMETERS OF POWER SUPPLY ADAPTER 60W /

ADAPTER 90W

Device Type: Adapter 60W

Operating conditions:

Temperature: + 10 °C to + 40 °C Relative humidity: 30 % to 75 % Atmospheric pressure Position Type of operation

Transport and storage conditions:

Temperature: - 10 °C to + 55 °C Relative humidity: 25 % to 85 % Atmospheric pressure Position Time of storage: max. 5 years

Power supply of the device:

Maximum input: 100 W Input mains voltage 100V – 240V ~ (alternating) Frequency: 50 – 60 Hz Protection class: II (according to IEC 536, ČSN 33 0600) Fuse: internal Covering: IP20 Type of connector of the device mini 2 poles

Output parameters:

Output voltage 24V Output current 2.5A Output power: 60W

Insulation barriers:

Mains – output (output connector) 4kV

700 hPa to 1060 hPa

continuous, use indoor only

650 hPa to 1100 hPa

horizontal

any

Adapter 90W

120 W

3.75A 90W

TECHNICAL PARAMETERS | PAGE 50 OF 62

7.3 BASIC PARAMETERS OF ELECTROTHERAPY GENERATOR

Output current* max. 140 mA (maximum instantaneous value) Output current - HVT** max. 4 A (maximum instantaneous value) Output current - microcurrents** max. 999 µA (maximum instantaneous value) Output voltage max. 130 V (maximum instantaneous value) Output voltage - HVT** max. 390 V (maximum instantaneous value) *maximum value for some currents is limited according to IEC 601-2-10 **presence of these currents depends on the ordered configuration of the device

Tolerance of output amplitude

Tolerance of time parameters of current

Nominal load impedance Internal output resistance in CV mode Internal output resistance in CC mode Output capacity standard 150 pF Output polarity – can be selected positive / negative / with reversal in the middle of therapy Positive polarity red banana plug = + = anode; black banana plug = - = cathode Negative polarity red banana plug = - = cathode; black banana plug = + = anode

± 10 % for 5 mA (5 V, 5 µA) and higher; otherwise ± 30 % ± 10 % for 35 V and higher; otherwise ± 30 % (for HVT)

standard ± 5 %; maximum ± 15 % standard ± 20 % for modulation of HVT from 5 s; otherwise ± 30 % 500 Ω 96 Ω ± 10 % 47 kΩ ± 10 %

7.4 BASIC PARAMETERS OF ULTRASOUND GENERATOR

Adjustable values

Effective intensity Continuous operation Pulse operation Working frequency Modulation frequency Duty factor Duty factor – default

0.1 to 2 W/cm

0.1 to 3 W/cm 1 MHz ± 5 % and 3.2 MHz ± 5 % 10 to 150 Hz ± 5 % 6 to 100 % ± 5 % of the set value

6.25 % (1:16); 12.5 % (1:8); 25 % (1:4); 50 % (1:2), 100% (1:1) ± 5 % of the set value

Maximum output power 12W

Parameters of pulses

Duty factor

Pulse

Frequency 10 Hz period 100 ms

Pause

length

Frequency 50 Hz period 20 ms Pulse length

Pause

length 50 % 50 ms 50 ms 10 ms 10 ms 5 ms 5 ms 3.33 ms 3.33 ms 25% 25 ms 75 ms 5 ms 15 ms 2.5 ms 7.5 ms 1.67 ms 5 ms 10% 10 ms 90 ms 2 ms 18 ms 1 ms 9 ms 0.67 ms 6 ms 6% 6 ms 94 ms 1.2 ms 18.8 ms 0.6 ms 9.4 ms 0.40 ms 6.27 ms

Steps of adjustable values

Intensity 0.1 W/cm Modulation frequency 10 Hz Duty factor 1%

± 20 % for output intensity higher than 0.2W/cm2

Frequency 100Hz period 10 ms Pulse length

Pause length

Frequency 150 Hz period 6.67 ms Pulse length

Pause length

TECHNICAL PARAMETERS | PAGE 51 OF 62

7.5 BASIC PARAMETERS OF LASER GENERATOR

Indication of emission of laser radiation green pilot light on the probe, supplementary lighting of the

probe/cluster, sound Indication of readiness for emission on the screen Indication of not being ready for emission on the screen Additional safety means - warning labels on the device case and on the probe/cluster

- warning label for the entrance door of the workplace

- connector of the remote control

Connector of the remote control (door switch)

input voltage AC / DC 5 V to 35 V (external power supply) / automatic polarity

recognition input current max. 10mA active level settable positive / negative logic

Adjustable values

Frequency***

0 – 10000 Hz with laser probe BTL-448

0 – 500 Hz with laser cluster BTL-445

accuracy of frequency

Dose*

accuracy of dose

Area*

± 3 % of the stated value

0.1 – 100.0 J/cm2

±20% (according to IEC 60601-2-22)

0.1 – 100.0 cm

accuracy of area see BNR

Output*

5.0 – 500 mW (depending on the connected laser probe)

20 – 1800 mW (depending on the connected laser cluster)

accuracy of output

Duty factor**

accuracy of duty factor

*) The stated values are maximum. The actual values depend on the type of connected laser generator and on the ordered configuration of the device **) Can be set only in pulsed mode, in continuous mode it is always 100% ***) Zero frequency means continuous operation

±20% (according to IEC 60601-2-22)

10 – 90 %

±1% of the range of DF

7.6 BASIC PARAMETERS OF MAGNET GENERATOR

Adjustable values

Magnetic field max. 128 mT / 1280 Gauss* (max. value on the surface of applicator) Mode of magnetic field pulses / series of pulses / continuous Shape of magnetic pulses rectangular, rectangular protracted, exponential, triangular, sinusoidal Pulse frequency 0 – 166 Hz Modulation none, burst, sine / trapezoid / symmetric surge Random frequency yes / no Accuracy: amplitude of magnetic field ±30% time parameters ±10%

*) The stated value is maximum for disk applicator. The actual value depends on the type of connected applicator and on the

settings of the device.

TECHNICAL PARAMETERS | PAGE 52 OF 62

7.7 TECHNICAL PARAMETERS OF ULTRASOUND HEADS

BTL-237-1-13 – small head

Effective radiation area (ERA) ERA (EN 61689) ERA (21 CFR 1050) Maximum effective intensity Maximum effective acoustic power Radiation frequency

0.7 cm

0.9 cm

± 20%

3 W/cm2 ± 20%

2.1 W ± 20%

1 MHz and 3.2 MHz ± 5% Type of beam collimated BNR < 8 Covering grade according to EN 60 529 IP 67

BTL-237-4-13 – large head

Effective radiation area (ERA) ERA (EN 61689) ERA (21 CFR 1050) Maximum effective intensity Maximum effective acoustic power Radiation frequency

3.2 cm

4.4 cm

3 W/ cm

± 20%

9.6 W ± 20%

1 MHz and 3.2 MHz ± 5% Type of beam collimated BNR < 8 Covering grade according to EN 60 529 IP 67

7.8 TECHNICAL PARAMETERS OF LASER PROBES

Laser probes with red (visible) radiation:

Type: BTL-448-03RD BTL-448-03RC BTL-448-05RD BTL-448-05RC Output power:

30 mW ± 20 % 30 mW ± 20 % 50 mW ± 20 % 50 mW ± 20 % Wavelength: 685 nm 685 nm 685 nm 685 nm Class*: 3B 3B 3B 3B Beam: divergent collimated divergent collimated Aperture: Ø 2 mm Ø 4.4 mm Ø 2 mm Ø 4.4 mm BNR:

0.28 rad ± 0.05 rad 0.015 rad ± 0.005 rad 0.28 rad ± 0.05 rad 0.015 rad ± 0.005 rad

NOHD**: 0.2 m 2.3 m 0.2 m 3.4 m

Laser probes with infrared (invisible) radiation:

Type: BTL-448-05IC BTL-448-10IC BTL-448-20IC BTL-448-30IC Output power:

50 mW ± 20 % 100 mW ± 20 % 200 mW ± 20 % 300 mW ± 20 % Wavelength: 830 nm 830 nm 830 nm 830 nm Class*: 3B 3B 3B 3B Beam: collimated collimated collimated collimated Aperture: Ø 4.4 mm Ø 4.4 mm Ø 4.4 mm Ø 4.4 mm BNR:

0.015 rad ± 0.005 rad 0.015 rad ± 0.005 rad 0.015 rad ± 0.005 rad 0.015 rad ± 0.005 rad

NOHD**: 8.5 m 12.1 m 12.5 m 16.6 m

TECHNICAL PARAMETERS | PAGE 53 OF 62

Type: BTL-448-40IC Output power:

400 mW ± 20 % Wavelength: 830 nm Class*: 3B Beam: collimated Aperture: Ø 4.4 mm BNR:

0.015 rad ± 0.005 rad

NOHD**: 19.2 m

* Laser class is classified according to IEC 60601-2-22:1995 and IEC 60825-1:1993/A2:2001.

**NOHD – nominal ocular hazard distance (nominal distance from the laser aperture in which eye damage by laser beam should

not happen)

7.9 TECHNICAL PARAMETERS OF LASER CLUSTERS

Laser clusters with red (visible) radiation:

Type: Output power:

445-C25R02

200 mW ± 20 % (4x 50 mW) Wavelength: 4x 685 nm Class*: 3B Beam: 4x divergent Aperture: 4x Ø 1.5 mm Active area: Ø 56 mm (25 cm2) BNR:

4x 0.35 rad ± 0.05 rad NOHD**: 0.2 m

Laser clusters with infrared (invisible) radiation:

Type: Output power:

445-C25I08 445-C25I16

800 mW ± 20 % (4x 200 mW) 1600 mW ± 20 % (4x 400 mW) Wavelength: 4x 830 nm 4x 830 nm Class*: 3B 3B Beam: 4x divergent 4x divergent Aperture: 4x Ø 3.5 mm 4x Ø 3.5 mm Active area: Ø 56 mm (25 cm2) Ø 56 mm (25 cm2) BNR:

4x 0.52 rad ± 0.17 rad 4x 0.52 rad ± 0.17 rad NOHD**: 8.5 m 12.1 m

Combined laser clusters with red and infrared radiation:

Type: Output power:

Wavelength: red: 4x 685 nm

445-C25RI10 445-C25RI18

red: 200 mW ± 20 % (4x 50 mW)

infrared: 800 mW ± 20 % (4x 200 mW)

infrared: 4x 830 nm

red: 200 mW ± 20 % (4x 50 mW) infrared: 1600 mW ± 20 % (4x 400 mW) red: 4x 685 nm

infrared: 4x 830 nm Class*: 3B 3B Beam: 8x divergent 8x divergent Aperture: red: 4x Ø 1.5 mm

infrared: 4x Ø 3.5 mm

red: 4x Ø 1.5 mm

infrared: 4x Ø 3.5 mm Active area: Ø 56 mm (25 cm2) Ø 56 mm (25 cm2) BNR:

red: 4x 0.35 rad ± 0.05 rad infrared: 4x 0.52 rad ± 0.17 rad

red: 4x 0.35 rad ± 0.05 rad

infrared: 4x 0.52 rad ± 0.17 rad NOHD**: 8.5 m 12.1 m

* Laser class is classified according to IEC 60601-2-22:1995 and IEC 60825-1:1993/A2:2001.

**NOHD – nominal ocular hazard distance (nominal distance from the laser aperture in which eye damage by laser beam should

not happen).

TECHNICAL PARAMETERS | PAGE 54 OF 62

7.10 TECHNICAL PARAMETERS OF MAGNETIC APPLICATORS

Type Name Dimension [mm] Weight [kg] Max. intensity BTL-239-1 disk 130 x 130 x 30 1.05 128.0 mT (1280 G) BTL-239-2 solenoid 30 340 x 340 x 300 5.75 9.0 mT (90 G) BTL-239-3 solenoid 60 620 x 540 x 300 10.00 8.5 mT (85 G) BTL-239-4 double disk 2x 130 x 130 x 30 2.15 95.0 mT (950 G) BTL-239-5 multi disk 4x 130 x 130 x 30 4.30 75.0 mT (750 G) BTL-239-6 linear 290 x 600 x 30 6.05 46.4 mT (464 G) BTL-239-8 solenoid 70 with couch 2000x740x1100 67.00 7.6 mT (76 G)

These mentioned parameters for applicators are basic. The exact values and shape of the magnetic field – please

see 2

part of manual – BTL-4000 Magnetotherapy User’s Guide.

7.11 APPLICABLE STANDARDS

Name IEC, EN, ISO, MDD

Medical electrical equipment. Part 1: General requirements for safety Amendments to IEC 601-1 A2, A11, A12 Medical electrical equipment Part 1: General requirements for safety

1.Collateral standard: Safety requirements for medical electrical systems Medical electrical equipment Part 1: General requirements for safety

2. Collateral Standard: Electromagnetic compatibility. Requirements and tests Industrial, scientific and medical (ISM) radio-frequency equipment - Radio disturbance characteristics - Limits and methods of measurement Electromagnetic compatibility (EMC) - Part 4: Testing and measurement techniques

- Section 2: Electrostatic discharge immunity test - Basic EMC Publication Electromagnetic compatibility (EMC) - Part 4: Testing and measurement techniques

- Section 3: Radiated, radio frequency, electromagnetic field immunity test Electromagnetic compatibility (EMC) - Part 4: Testing and measurement techniques

- Section 4: Electrical fast transients/burst immunity test - Basic EMC Publication Electromagnetic compatibility (EMC) - Part 4: Testing and measurement techniques

- Section 5: Surge immunity test Medical electrical equipment Part 1: General requirements for safety

4.Collateral standard: Programmable electrical medical systems Medical devices – Risk analysis EN 1441 / ISO 14971 Biological evaluation of medical devices - Part 1: Evaluation and testing ISO 10 993-1

The Medical Devices Directive 93/42/EEC MDD 93/42/EEC

Medical electrical equipment Part 2: Particular requirements for the safety of ultrasonic therapy equipment Medical electrical equipment - Part 2: Particular requirements for the safety of nerve and muscle stimulators Medical electrical equipment Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment Safety of laser products. Part 1: Equipment classification, requirements and user's guide Amendments to IEC 60 825-1 A1, A2

IEC 601-1

IEC 60601-1-1

IEC 60601-1-2

EN 55011

IEC 61000-4-2

IEC 61000-4-3

IEC 61000-4-4

IEC 61000-4-5

IEC 601-1-4

IEC 601-2-5

IEC 601-2-10

IEC 601-2-22

IEC 60 825-1

TECHNICAL PARAMETERS | PAGE 55 OF 62

7.12 INTERCONNECTION OF DEVICES

BTL-4000 Puls can be interconnected with: BTL vac, BTL-4000 Sono, BTL-12, BTL-07p, BTL-4000

Sono, BTL-5000 Sono

BTL-4000 Combi can be interconnected with: BTL vac, BTL-12

BTL-4000 Sono can be interconnected with: BTL-4000 Puls, BTL-4000 Puls, BTL-5000 Sono

Other combinations are not allowed.

7.13 MANUFACTURER

This product is manufactured in accordance with the EU Medical Devices Directive by:

BTL Industries Ltd.

161 Cleveland Way

Stevenage

Hertfordshire

SG1 6BU

United Kingdom

E-mail: sales@btlnet.com

http://www.btlnet.com

For service, please contact the service department at service@btlnet.com.

electronic, mechanical, photographic or other records without previous approval from BTL Industries Limited

BTL Industries Limited operates a policy of continuous development. Therefore, it reserves the right to make changes and

improvements to the Product described in this manual without prior notice.

The contents of this document are provided "as is". Except as required by the applicable law, no warranties of any kind, either

expressed or implied, are made in relation to the accuracy, reliability or contents of this document. BTL Industries Limited

reserves the right to revise this document or withdraw it at any time without prior notice.

TECHNICAL PARAMETERS | PAGE 56 OF 62

8 UNITS CONFIGURATIONS

8.1 TABLE OF CONFIGURATIONS OF THE COMBINED DEVICES BTL 4000 SERIES

Type:

mains supply x x x x x x built-in accumulator x x x manual mode x x x x x x predefined programs x x x x x x predefined diagnoses x x x o o o user programs 50 50 50 5 5 5 ultrasound head 1MHz x x ultrasound head 1/3MHz x x el. patient cables – basic x x el. p. cab. with visual detection x x possibility to connect BTL-vac x x x x electrotherapies 1 1 1 1 ultrasound therapies 1 1 1 1 magnetic therapies laser therapies 1 1 1 1 number of simultaneously running therapies number of simultaneously running electrotherapies number of simultaneously running magnetotherapies number of simultaneously connected magnetic applicators sound schemes x x x x x x number of simultaneously treated patients

4810S

Professional

2 2 2 1 1 1

1 1 1 1

2 2 2 1 1 1

4810L

Professional

4800SL

Professional

4810S

Optimal

4810L

Optimal

4800SL

Optimal

Type:

mains supply x x x x built-in accumulator x x manual mode x x x x predefined programs x x x x predefined diagnoses x x o o user programs 50 50 5 5 ultrasound head 1MHz x ultrasound head 1/3MHz x el. patient cables – basic x x el. p. cab. with visual detection x x possibility to connect BTL-vac x x x x electrotherapies 1 1 1 1 ultrasound therapies 1 1 magnetic therapies laser therapies 1 1 number of simultaneously running

therapies number of simultaneously running

electrotherapies number of simultaneously running

magnetotherapies number of simultaneously

connected magnetic applicators sound schemes x x x x number of simultaneously treated

patients

4815S

Professional

2 2 1 1

1 1 1 1

2 2 1 1

4815L

Professional

4815S

Optimal

4815L

Optimal

UNITS CONFIGURATIONS | PAGE 57 OF 62

Type:

mains supply X X X X X X built-in accumulator x x x manual mode X X X X X X predefined programs X X X X X X predefined diagnoses x x x o o o user programs 50 50 50 5 5 5 ultrasound head 1MHz x ultrasound head 1/3MHz x el. patient cables – basic x el. p. cab. with visual detection x possibility to connect BTL-vac x x electrotherapies 1 1 ultrasound therapies 1 1 laser therapies 1 1 magnetic therapies 1 1 1 1 1 1

number of simultaneously running therapies

number of simultaneously running electrotherapies.

number of simultaneously

running magnetotherapies

number of simultaneously connected magnetic applicators

sound schemes X X X X X X number of simultaneously

treated patients

481xM

Professional

2 2 2 1 1 1

1 1 1 1

1 1 1 1 1 1

2 2 2 2 2 2

4800LM

Professional

4800SM

Professional

481xM

Optimal

4800LM Optimal

4800SM Optimal

2 2 2 1 1 1

Type:

mains supply x x x x x x built-in accumulator x x x x x x manual mode x x x x x x predefined programs x x x x x x predefined diagnoses x x x x x x user programs 50 50 50 50 50 50 ultrasound head 1MHz ultrasound head 1/3MHz x x el. patient cables – basic el. p. cab. with visual detection x x x x x x possibility to connect BTL-vac x x x x x x electrotherapies 1 1 1 1 1 1 ultrasound therapies 1 1 laser therapies 1 1 magnetic therapies 1 1 number of simultaneously running therapies number of simultaneously running electrotherapies. number of simultaneously running magnetotherapies number of simultaneously connected magnetic applicators sound schemes x x x x x x number of simultaneously treated patients

4816S

Professional

2 2 2 1 1 1

1 1 1 1 1 1

1 1

2 2

2 2 2 1 1 1

4816L

Professional

4816M

Professional

4818S

Optimal

4818L

Optimal

4818M

Optimal

UNITS CONFIGURATIONS | PAGE 58 OF 62

Type:

mains supply x x x x x x built-in accumulator x x x manual mode x x x x x x predefined programs x x x x x x predefined diagnoses x x x o o o user programs 50 50 50 5 5 5 ultrasound head 2MHz x x x x x el. patient cables – basic x x el. p. cab. with visual detection x x possibility to connect BTL-vac x x x x electrotherapies 1 1 1 1 ultrasound therapies 1 1 1 1 1 1 magnetic therapies laser therapies 1 1 number of simultaneously running therapies number of simultaneously running electrotherapies number of simultaneously running magnetotherapies number of simultaneously connected magnetic applicators sound schemes x x x x x x number of simultaneously treated patients

4810T

Professional

2 2 2 1 1 1

1 1 1 1

2 2 2 1 1 1

4815T

Professional

4800TL

Professional

4810T

Optimal

4815T

Optimal

4800TL

Optimal

UNITS CONFIGURATIONS | PAGE 59 OF 62

8.2 TABLE OF CONFIGURATIONS OF THE ELECTROTHERAPY DEVICES BTL-4000

PULS

Type:

mains supply x x x x x x x x built-in accumulator x x x x manual mode x x x x x x x x pre-defined programs x x x x x x x x pre-defined diagnoses x x x x o x o o user programs 50 50 50 50 5 5 5 5 ultrasound head 1MHz ultrasound head 1/3MHz el. patient cables – basic x x x x el. p. cab. with visual detection possibility to connect BTL-vac electrotherapy outputs 1 1 2 2 1 1 2 2 ultrasound outputs laser outputs number of simultaneously running therapies number of simultaneously running electrotherapies. sound schemes x x x x x x x x number of simultaneously treated patients galvan x x x x x x x x träbert, farad, neofarad x x x x x x x x diadynamics x x x x x x x x TENS x x x x x x x x rectangular pulses x x x x x x triangular pulses x x x x x x exponential pulses x x x x x x combined pulses x x x x x x intermittent pulses stimulation pulses x x x x x x russian stimulation x x x x x x x x 2-pole interference x x x x x x x x 4-pole interference x x x x isoplanar field (interference) vector field (interference) x x HVT o o h – waves x x spastic currents micro currents x x leduc current x x mid-frequency waves pulses with exponential rise preset sequences 20 20 20 5 5 5 electrodiagnostics

4610

Professional

x x x x

x x x x x x x x

1 1 2 2 1 1 2 2

1 1 2 2 1 1 1 1

x x

x x x x x x

4615

Professional

4620

Professional

4625

Professional

4610

Optimal

4615

Optimal

4620

Optimal

4625

Optimal

UNITS CONFIGURATIONS | PAGE 60 OF 62

8.3 TABLE OF CONFIGURATIONS OF THE ULTRASOUND THERAPY DEVICES

BTL-4000 SONO

Type:

mains supply x x x x built-in accumulator x x manual mode x x x x number of ultrasound therapies 1 1 1 1 user programs 50 5 50 5 predefined diagnoses x o x o preset programs x x x x language versions x x x x sound schemes x x x x recent therapies 20 20 20 20 Ultrasound parameters: head 1 MHz x head 1 and 3 MHz x head 2 MHz x x detection of contact continuous continuous continuous continuous continuous mode of operation x x x x pulse mode of operation x x x x duty factor x x x x

4710

Professional

4710

Optimal

4210

Professional

4210

Optimal

8.4 TABLE OF CONFIGURATIONS OF THE LASER THERAPY DEVICES BTL-4000

LASER

Type:

mains supply x x built-in accumulator x manual mode x x number of laser therapies 1 1 user programs 50 5 predefined diagnoses x o preset programs x x language versions x x sound schemes x x recent therapies 20 20

4110

Professional

4110

Optimal

UNITS CONFIGURATIONS | PAGE 61 OF 62

8.5 TABLE OF CONFIGURATIONS OF THE MAGNETOTHERAPY DEVICES BTL-

4000 MAGNET

Type:

mains supply x x built-in accumulator x manual mode x x number of magnetotherapies user programs 50 5 predefined diagnoses x o preset programs x x language versions x x sound schemes x x recent therapies 20 20 number of simultaneously running magnetotherapies number of simultaneously connected magnetic applicators Magnetic parameters: Rectangular pulses x x Rectangular protracted x x Exponential x x Triangular x x Sinusoidal x x Continuous mag. field x x Series of pulses x x Random frequency x x Modulation x x

4920

Professional

1 1

2 2

4920

Optimal

UNITS CONFIGURATIONS | PAGE 62 OF 62

BTL 4000 User manual

Specifications and Main Features

Frequently Asked Questions

User Manual