Globus Genesy 3000 User manual

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DEAR CUSTOMER
THANK YOU FOR CHOOSING A GLOBUS PRODUCT. WE REMAIN AT YOUR
ENTIRE DISPOSAL FOR ANY ASSISTENCE OR ADVICE YOU MAY NEED
The electrostimulators GL3K (Genesy 3000) are manufactured and distributed
by:
DOMINO s.r.l.
via Vittorio Veneto 52
31013 - Codognè - TV - Italy
Tel. [phone]
Fax. [phone]
E-Mail: [email protected]
www.globuscorporation.com
This product has been manufactured according to the technical regulations in
force and is certified according to Directive 93/42/EEC updated by 2007/47
directive for medical devices, by KIWA CERMET ITALIA S.P.A. Scrl (authorization n.
0476), in order to ensure the product's safety.
Genesy 3000

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Table of contents
TECHNICAL FEATURES .......................................................................................................................... 7
Device ............................................................................................................................................... 7
Technical features of the currents EMS and TENS: ...................................................................... 7
EQUIPMENT ........................................................................................................................................... 9
INTENDED USE ..................................................................................................................................... 10
CONNECTIONS ................................................................................................................................... 11
Battery: how to charge the batteries.......................................................................................... 11
How to connect the cables ......................................................................................................... 11
Electrode application ................................................................................................................... 12
LABELLING AND SYMBOLS................................................................................................................. 13
Device ............................................................................................................................................. 14
PANEL AND KEYBOARD ..................................................................................................................... 16
Display and interface.................................................................................................................... 17
ALARMS ............................................................................................................................................... 18
Compliance.................................................................................................................................... 18
WARNINGS AND CONTRAINDICATIONS ......................................................................................... 18
Mandatory behavior ..................................................................................................................... 18
Warnings before use...................................................................................................................... 18
Warnings during the use ............................................................................................................... 19
Side effects ..................................................................................................................................... 20
Contraindications .......................................................................................................................... 20
MAINTENANCE AND CLEANING ..................................................................................................... 20
Device ................................................................................................................................................. 20
Battery ............................................................................................................................................. 21
Accessories ..................................................................................................................................... 22
Disposal of the device................................................................................................................... 22
INSTRUCTIONS FOR USE...................................................................................................................... 22

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“Program List” menu...................................................................................................................... 23
“Last 10” menu ............................................................................................................................... 25
“Favorites” menu ........................................................................................................................... 26
“Treatments” menu........................................................................................................................ 26
“Programming” menu................................................................................................................... 27
“Advanced” menu........................................................................................................................ 28
ACTION PRINCIPLES ........................................................................................................................... 32
Muscular electrostimulation ................................................................................................................... 32
Tens........................................................................................................................................................ 35
Microcurrents...................................................................................................................................... 36
Ionophoresis ........................................................................................................................................ 36
Denervated......................................................................................................................................... 37
Interferential current......................................................................................................................... 38
Kotz ........................................................................................................................................................ 38
PROGRAM LIST.................................................................................................................................... 39
WARRANTY.......................................................................................................................................... 54

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TECHNICAL FEATURES
Device
Size: 220x170x60 mm
Weight: 790 gr.
Case: in Food Grade ABS
Protection level: IP 20
Storage and transportation temperature: from -10°C to 45°C
Max. relative humidity: 30% - 75%
The values indicate the limits allowed if the product or its accessories are not in the
original package.
Use conditions
Temperature: from 0°C to 35°C
Max. relative humidity: from 15% to 93%
Atmospheric pressure: from 700 hPa to 1060 hPa
Technical features of the currents
EMS and TENS:
Channels available: Channels 1-2-3-4
Constant current: Yes
Intensity: 0-120 mA with 1000 Ohm load
Wave form: Rectangular, biphasic, symmetrical,
compensated
Working frequency: 1-150 Hz
Recovery frequency: 1-150 Hz
Pulse amplitude: 50-450 µs
Working time: from 1 to 30 seconds
Recovery time: from 0 to 1 minute
Frequency mod. range: continuous variation from 1 to 150 Hz
Min. modulation time: 3 seconds
Amplitude modulation range: continuous variation from 50 to
450 µseconds
Microcurrents:
Channels available: Channels 1-3
Constant current: Yes
Min. frequency: 5Hz
Max. frequency: 200Hz

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Min. intensity: 0 µA/1000 Ohm Step 10 µA
Max. Intensity: 800 µA/1000 Ohm
Amplitude value: included between 1 and 250 µseconds
Interferential:
Channels available: Channels 1-3
Max. intensity: 60 mA
Main frequency: 2500 Hz - 4000 Hz - 10000 Hz
Frequency modulation: 0 - 200 Hz
Pulse modulation: Variable in duration and period
Russian:
Channels available: Channels 1-3
Max. intensity: 60 mA
Main frequency: 1250 - 2500 Hz
Modulating wave: 6-12-25-50-100Hz
Denervated muscles:
Channels available: Channels 1-3
Max. Intensity: 60 mA
Pulses: Triangular 1000 ms,
Rectangular/trapezoidal 500 ms
Ionophoresis:
Channels available: Channel 1
Constant current: Yes
Min. intensity: 0 mA/1000 Ohm
Max. intensity: 10 mA/1000 Ohm steps of 0.1 mA/1000
Ohm
Min. time: 1 minute
Max. time: 99 minutes
Power supply unit:
Brand: Globtek
model: GTM91099-6024-6.0-T2
PRI: 100-240V~ 50-60Hz 1,5A
SEC: 18 V = 3,33 A
Polarity:
Battery
Battery pack: Ni-MH 12 V 2000 mA

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EQUIPMENT
The electrostimulator is supplied complete of cables and electrodes to use:
therefore, opening the package, it is necessary to check that the basic equipment
is complete. If some elements should be missing, contact immediately the
authorized retailer where you purchased the product.
A. 4 colored electrode connection cables (for EMS, TENS, DENERVATED,
INTERFERENTIAL, RUSSIAN treatments) and 2 gray cables for electrode connection
(for MICROCURRENT and IONOFORESIS treatments)
B. A bag containing 4 reusable self-adhesive electrode (50 x 50 mm)
(Use these electrodes for small areas such as upper limbs, calves, cervical…)
C. A bag containing 4 reusable self-adhesive electrode (50 x 90 mm)
(Use these electrodes for big areas such as thighs, abdomen and glutei...)
D. Power supply unit (See technical features)Carrying bag
E. GL3K Unit
F. User manual
G. Carrying bag
H. Ionophoresis kit
The device can be used with some optional accessories (it is possible to see their
features on the website www.globuscorporation.com). If you are interested in
buying these accessories, please contact the retailer.
Accessories not included (available on charge)
- Find Motor point pen
- Kit of 8 elastic bands for legs and thighs
- Kit of 4 elastic bands for thighs
- Face electrodes
- Kit Y cables
- Gel
AB- C D E F G H

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- Rectangular electrodes for ionophoresis (60x85 mm)
- Fast band
- Fast pad
- Anal and vaginal probes
INTENDED USE
The after sales service is guaranteed for 5 years. We suggest having a check of the
device every 2 years for the maintenance and to ensure the safety.
The device can be used continuously when connected to the mains. The numbers
of treatments depends on the battery charge. The duration of the battery is 6
months, we suggest replacing it after that period.
The Genesy 3000 devices are not designed to be used at home and are intended
to be used in the following operating environments:
- clinics;
- physiotherapy centers;
- rehabilitation centers;
- general pain treatments (in medical field).
The use of this device is permitted to medical and physiotherapy staff.

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CONNECTIONS
Cable connection outlets and power supply
Attention:
If the package, the cable or the connector of the charger show signs of wear or
damage, replace it instantly.
Device
Power supply by electricity grid. Genesy 3000 can operate also connected to the
mains 115-230 V. To connect the power supply to the connector, plug it as shown
below (see how to charge the batteries).
To isolate the charger from the mains you have to disconnect it from the mains
outlet.
Battery: how to charge the batteries
The device is supplied with a set of rechargeable nickel-metal hydrate batteries
(12V, 2mAh) which have high performance without storage effect.
Recharge the batteries when the battery indicator on the display indicates ¼.
To charge the batteries, turn off the electrostimulator and disconnect the
electrodes, then connect the elctrostimulator to the power supply unit provided by
inserting the plug in the appropriate inlet (see picture above).
Do not use a different charger from the one provided with the device. To replace
the electrostimulator's batteries, contact the authorized service center.
How to connect the cables
To connect the cables to the device, plug them in the intended inlets in the upper
part of the unit (see picture). Insert the cables with the grooves facing downwards.
The inlets are placed exactly under the corresponding channels.

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NOTE: for EMS and TENS currents use indifferently the 4 channels with colored
cables.
NOTE: for microcurrent programs use only channels 1 and 3 with gray cables.
NOTE: for denervated muscles programs (rectangular, triangular, trapezoidal) use
only channles 1 and 3 with gray cables.
NOTE: for interferential programs use only the channels 1 and 3 with colored cables.
NOTE: for ionophoresis programs use only the channel 1 with gray cables.
Electrode application
Take the electrodes from the original package; all new electrodes have a seal on
the package. Be sure that the device is off. To start, connect the two cable plugs to
the electrodes, then disconnect the electrodes from their position and apply them
on the skin. To place the electrodes correctly, see the pictures included in this
manual.
After the use, place the electrodes in their original position again.
ATTENTION: do not unplug the electrodes if the unit is working.

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LABELLING AND SYMBOLS
Warning
This symbol on your device indicates that it complies with
the directives on medical devices (93/42/CEE
47/2007CEE). The number of the notified unit is 0476
It indicates that this is a II class device
It indicates that this device has type BF parts
WEEE symbol (Waste of Electrical and Electronic
Equipment). Recycling symbol. The WEEE symbol used for
this product indicates that the device may not be
disposed of as a household product. Properly dispose of
the product to help protect the environment. For more
information on recycling this product, contact the local
competent department, the household waste
management company or the store in which the
product was purchased
It indicates that the product has been produced
respecting the directive 2002/95/CE
It indicates the optimal temperatures for the storage and
transportation of the product
It informs the operator that before using the device he
must read the manual
IP20
It indicates the water protection degree
It informs the operator of a compulsory conduct
It refers to the pressure of the storage and transport
environment where the device and its accessories are
used
It refers to the humidity of the storage and transport
environment where the device and its accessories are
used

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PRI
Mains voltage
SEC
Power supply voltage
Input
Input: it indicates the value of the mains voltage for the
power supply unit
Output
Output:
- it indicates the power supply unit outbound voltage
- it indicates the maximum power value of the magnetic
field emitted by the device
- it indicates the range of frequencies of the magnetic
field emitted by the device
Type
It indicates the device type
Power
It indicates the power supply unit model of the device
Battery
It indicates the battery pack inside the device
It refers to the manufacturer
It refers to the expiry date
It refers to the production lot
It refers to the manufacturing date
Polythene symbol
Device
Input PWR: GlobTek
Model: GTM91099-6024-6.0-T2
PRI: 100-240V~50-60Hz 1.5A
SEC: 18 V = 3.33A
Input Power: 18Vdc 1.65A
Output: 120mApk (1000Ω)
Nerve and Muscle stimulator: GENESY 3000
SN: E3KR201700001
Internal Battery: 12V 2000mAh Ni-MH

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Accessories
Electrodes
Clean and degrease the skin.
Do not apply the electrode on wounds or injured skin.
Connect the cable connector to the electrode connector.
Remove the electrode.
Apply on the skin.
Start the program.
At the end, put the electrode back in the package.
Electrodes are for personal use.
Do not remove the electrode by grabbing the connector.
Electrodes should not touch each other.
Do not apply the electrodes on the temples, the neck and in a transthoracic way.
It indicates the dimensions of the electrode
It indicates the number of electrodes contained in the
package
It indicates the product code
It refers to product certification and indicates that it
complies with directive 2001/95/EC updated as
2014/357/EU
It indicates the storage temperature of the electrodes

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Do not leave the electrodes in the car.
All the provided information can be modified without previous notice.
PANEL AND KEYBOARD
NOTE : When the 3” message appears, it means that pressing the button for 3
seconds the function is activated.
ON/OFF/OK Button
To confirm the selection. While a program is running, it
activate the pause.
3” = ON/OFF.
Left/BACK Button
To move the selection to the left.
To go back to the previous selection.
3” = While a program is running, it returns to the previous
phase.
P+ Button
To move the selection upwards.
While a program is running, it increments the intensity of
the 4 channels simultaneously.
P- Button
To move the selection downwards.
While a program is running, it decrements the 4 channels
intensity simultaneously.
Right/USER Button
To move the selection to the right.
3” = While a program is running, it goes to the next phase.
Increase/Decrease
intensity button
Function button
Left/Back button
P- button
ON/OFF/OK button
Right/User button
P+ button
*button

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* Button
To start and stop the contraction during the execution of
the “Action Now” programs (in the devices that have
these functions).
fn (Runtime)
Pressed together with other buttons, it modifies their
function, while pressed alone during the stimulation, it
permits to access to the Runtime function (to modify time,
frequency and amplitude).
Intensity button
To increase/decrease the stimulation intensity of the
corresponding channel.
Display and interface
-On/off indicator
-PAUSE indicator (during the treatment)
-General error indicator. If the lights turns on, check the
cable/electrode connections. If the light is still on, please contact
the service center.
CH1-4 -Active channel indicator
Program name
Time indicators
Battery indicator
Time of the
working phase
and of the rest
phase
Stimulation
intensity
Type of currents
and indicator of
the phase
number and of
the phase in
progress

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ALARMS
Compliance
Certifications: CE MDD certificate.
The sound and acoustic signals are in compliance with directive 60601-1-8.
Meaning of the “Electrode error” alarm
If one or more cables are not connected to the mains, or if microcurrents cables are
used to an EMS program, on the display the following alarm will appear: "Electrode
error"
WARNINGS AND CONTRAINDICATIONS
Mandatory behavior
For safety reasons, the device must be used in the prescribed manner and within
the limits of use explained in this manual.
Do not carry out any treatments in case of skin lesions. If the package, the cable or
the connector of the charger show signs of wear or damage, replace it instantly.
The unit should be connected to the mains by its power supply unit. Before starting
the treatment, make sure that the power system specifications comply with the
directives in force within your country. Make sure that the power supply unit will be
in a comfortable position and that it will be easy to be removed.
The manufacturer declines any responsibility due to a different use from what it is
indicated in this manual.
No part of this manual (texts and photos) may be reproduced by electronic or
mechanical manner without the prior written authorization of the manufacturer.
Warnings before use
We suggest avoiding the use of the device together with other electronic devices,
especially with those used to maintain vital functions. For a correct use of the
Electromedical device, refer to the tables attached. If it is necessary to use the
device near or together with other devices, pay attention to its working.
- It is recommended to read carefully the entire operating manual before using the
device.
- The device can emit current value above 10mArms.
- Before each use always check the integrity of the unit. This is a fundamental
requirement for carrying out therapies, do not use the unit if either the buttons or
cables are defective or malfunctioning.
- It should not be used for purposes other than transcutaneous neuromuscular
stimulation.

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- It must be used with the supplied electrodes intended for transcutaneous
neuromuscular stimulation.
- It must be kept out of the reach of children.
- ECG monitoring devices may not operate properly when electrostimulation is
working.
- Do not use the device in transthoracic modality because it may cause cardiac
arrhythmia, imposing its frequency over the heart one. Do not stimulate the pectoral
and dorsal muscles simultaneously.
- A simultaneous connection of the patient to a high frequency electrosurgery
device can cause burns where the electrodes are placed and the electrostimulator
can result damaged.
- After turning on the device, make sure that in the display the software version and
the model of the device appear, it means that the device is working and it is ready
to be used.
If not, or in the display all the segments do not appear, turn it off and on again. If
the problem persists, contact the service center and do not use the device.
- An unexpected switching-off of the device means that the battery has run-down.
Charge it according to the instructions in the paragraph: how to charge the
batteries.
Warnings during the use
While using the electrostimulator some warnings should be followed:
- Be sure that the cables and the electrodes are clean before each application.
- In case of damaged cables, they must be replaced with original parts and no
longer used.
- Use only Globus branded electrodes.
- Pay particular attention when the current density for every electrode is above
2mA/cm2 (effective value).
- The cables of the electrostimulation should not be wrapped around people's neck
to avoid any risk of strangulation and suffocation.
- The mobile and fixed radio communications devices could influence the
functioning of the electromedical device: see the tables attached to this manual.
Preventative measures to take using the device for incontinence treatments.
- Patients with extra-urethral incontinence should not be treated with the
electrostimulator.
- Patients suffering excessive incontinence due to evacuation problems should not
be treated with the electrostimulator.
- Patients with severe urinary retention to the upper urinary passages should not be
treated with the stimulator.
- Patients with total peripheral denervation of the pelvic floor should not be treated
with the stimulator.

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- Patients suffering of a total/subtotal prolapse of the uterus/vagina should be
stimulated with extreme care.
- Patients with infections to the urinary passages should be treated for these
symptoms before starting the stimulation treatment.
- Before removing or touching the probe it is necessary to turn off the stimulator or to
regulate the intensity of both the channels on 0,0 mA.
- The treatment is a personalized medical prescription: do not borrow the stimulator
to other persons.
Side effects
Isolated incidents of skin irritation may occur in subjects with high epidermal
sensitiveness.
In case of an allergic reaction to the electrode gel, suspend the treatment and
contact a specialist.
If during the treatment signs of tachycardia and extrasystole appear, suspend the
treatment and contact your physician.
Contraindications
Do not use the device in the following cases:
- Stimulation of the front part of the neck (carotid sinus).
- Pacemaker weavers.
- Patients with tumor diseases (seek the oncologist’s advice).
- Stimulation of the brain region.
- Pains whose etiology is unknown.
- Sores and dermatological diseases.
- Stimulation on recent scars.
- Pregnancy.
- It is strictly forbidden to use the electrostimulator in the ocular area.
- Near body areas with metallic implants or infratissue metals (prostheses,
osteosynthetic devices, coils, screws, orthopedic plates), when using monophasic
current, interferential, or continuous current, ionophoresis.
It is recommended to use the device with caution in people with capillary fragility,
as an excessive stimulation could cause capillary ruptures.
MAINTENANCE AND CLEANING
Device
- In case of damaged case, this should be replaced and no longer used.
- In case of real or alleged malfunction, do not tamper with the device or try to
repair it yourself.