Globus GENESY 1500 User manual

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Rev.05.15

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Rev.05.15
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 GL4 (Genesy 1500) are manufactured and distributed by:
DOMINO s.r.l.
via Vittorio Veneto 52
31013 - Codognè - TV - Italy
Tel. [phone]
Fax. [phone]
E-Mail: [e-mail]
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. (authorization n. 0476), in
order to ensure the product safety.

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Rev.05.15
Table of contents
TECHNICAL FEATURES .......................................................................................................................................... 6
Device ............................................................................................................................................................ 6
Technical features of the currents EMS and TENS: ............................................................................. 6
EQUIPMENT.......................................................................................................................................................... 8
INTENDED USE......................................................................................................................................................9
CONNECTIONS .................................................................................................................................................... 10
How to connect the cables ................................................................................................................... 10
Electrode application .............................................................................................................................. 11
Battery: how to charge the batteries.................................................................................................. 11
LABELLING AND SYMBOLS.................................................................................................................................. 12
Device .......................................................................................................................................................... 13
PANEL AND KEYBOARD....................................................................................................................................... 14
Display and interface............................................................................................................................... 15
ALARMS .............................................................................................................................................................. 16
Compliance................................................................................................................................................ 16
WARNINGS AND CONTRAINDICATIONS ............................................................................................................. 16
Mandatory behavior ................................................................................................................................ 16
Warnings before use................................................................................................................................. 16
Warnings during use ................................................................................................................................. 17
Side effects.................................................................................................................................................. 18
Contraindications...................................................................................................................................... 18
MAINTENANCE AND CLEANING ......................................................................................................................... 19
Device .......................................................................................................................................................... 19
Battery .......................................................................................................................................................... 19
Accessories ................................................................................................................................................. 20
Disposal of the device ............................................................................................................................. 20

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Rev.05.15
INSTRUCTIONS FOR USE.....................................................................................................................................21
“Program List” menu................................................................................................................................. 21
“Last 10” menu........................................................................................................................................... 23
“Favorites” menu....................................................................................................................................... 24
“Treatments” menu................................................................................................................................... 25
“Programming” menu.............................................................................................................................. 25
“Advanced” menu................................................................................................................................... 26
ACTION PRINCIPLES ............................................................................................................................................31
Muscular electrostimulation ................................................................................................................... 31
Stimulation intensity .................................................................................................................................. 32
Tens........................................................................................................................................................ 33
Microcurrents...................................................................................................................................... 34
Ionophoresis ........................................................................................................................................ 35
Denervated......................................................................................................................................... 35
Interferential current......................................................................................................................... 36
Kotz ........................................................................................................................................................ 37
PROGRAM LIST ...................................................................................................................................................38
WARRANTY ......................................................................................................................................................... 55

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Rev.05.15
TECHNICAL FEATURES
Device
Size: 160x99x35.4 mm
Weight: 404 g
Case: in Food Grade ABS
Protection level: IP 22
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.
Conditions of use
Temperature: from 0°C to 35°C
Max. relativity 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: 0.3-150 Hz
Recovery frequency: 0.3-150 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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Rev.05.15
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: GTM4160-2512
PRI: 100-240Vac 50-60Hz Max 0,6A
SEC: 12V 2,08A
Polarity:
Battery
Battery pack: Ni-MH 7,2 V 1,8 Ah

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Rev.05.15
EQUIPMENT
The electrostimulator is supplied complete of cables and electrodes: therefore,
please check that the package contains the complete equipment. If some
elements are not contained in the package, please contact immediately the
authorized retailer where you purchased the product.
Control the integrity of the device and its electrodes carefully.
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 electrodes (50 x 50 mm)
(Use these electrodes for small areas such as upper limbs, calves, cervical…)
C. A bag containing 4 reusable self-adhesive electrodes (50 x 90 mm)
(Use these electrodes for large areas such as thighs, abdomen and glutei...)
D. Power supply unit (See technical features)
E. GL4 Unit
F. User manual
G. Carrying bag
All the supplied information can be modified without prior notice.
The device can be used with some optional accessories (for further info, visit the
website www.globuscorporation.com ).
If you are interested in buying these accessories, please contact the retailer.
Accessories not included (available on charge)
- Motor point pen
- Kit of 8 elastic bands for legs and thighs
- Kit of 4 elastic bands for thighs
- Face electrodes
A B- C D E F G

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Rev.05.15
- Kit Y cables
- Gel
- Rectangular electrodes for ionophoresis (60x85 mm)
- Fast band
- Fast pad
- Anal and vaginal probes
INTENDED USE
The service life of the product is estimated at 5 years. It is advisable to return the
product for maintenance and security checks every two years. The device can be
plugged to the mains for a continuous use. The number of treatments depends on
the battery charge. The duration of the battery is 6 months; thereafter its
replacement is recommended.
The Genesy 1500 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 device can be used by medical and physiotherapy staff only.

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Rev.05.15
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 them instantly.
Device
Power supply by electricity grid. Genesy 1500 can operate also connected to the
mains 230 V. To connect the power supply to the connector, plug it as shown
below.
To isolate the charger from the mains you have to disconnect it from the mains
outlet.
How to connect the cables
Plug the connectors in the slots in the upper part of the unit to connect the diffusers
to the device, (see pic.) When plugging in the cable, the grooves of the cable have
to be oriented downward. The inlets are placed exactly under the corresponding
channels.