Mo-vis Foot Control Omni Manual de usuario

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Foot Control
Foot Control Omni (P021-51) - Foot Control LiNX (P021-53)
User manual
Edition D-P021-51-70-M9-0200, August 2023

Other languages
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DA: Du kan finde denne manual på dansk på vores websted.
DE: Auf unserer Website finden Sie diese Anleitung in Deutsch.
EN: You can find this manual in English on our website.
ES: Este manual está disponible en español en nuestro sitio web.
FR: Vous pouvez trouver ce manuel en français sur notre site Web.
IT: nostro sito web è disponibile il presente manuale in italiano.
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SL: Slovenski priročnik je na voljo na naši spletni strani.
SV: Du hittar den här handboken på svenska på vår webbplats.
You can find the latest version of all our manuals on the website.
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About this manual
User manual
Thank you for choosing a mo-vis product!
Ta priročnik vsebuje uporabne in pomembne informacije o vaši napravi. Pred uporabo ga
skrbno preberite in varno shranite za prihodnjo uporabo.
Our team (or your authorized dealer) will be happy to answer your questions.
mo-vis bv
Biebuyckstraat 15D 9850 Deinze Belgija
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User manual
Warning labels
Please read this manual, the safety instructions and warning texts carefully, in order
to reduce the risks associated to the device. Our products are safe under normal and
reasonably foreseeable operating conditions.
NOTE: This symbol indicates general notes and information.
CAUTION: This symbol indicates caution for a hazardous situation that, if not
avoided, could result in minor or moderate injury.
WARNING: This symbol indicates a warning for a hazardous situation that, if not
avoided, could result in death or serious injury.
Other labels:
Catalogue number: indicates the
manufacturer's catalogue number so that
the medical device can be identified.
Batch code: indicates the manufacturer's
batch code so that the batch or lot can be
identified.
Medical device: indicates that the item is a
medical device.
Date of manufacture: indicates the date
when the medical device was manufac-
tured.
Serial number: indicates the
manufacturer's serial number so that a spe-
cific medical device can be identified.
Consult instructions for use or consult elec-
tronic instructions for use: indicates the
need for the user to consult the instruc-
tions for use.
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Keep dry: indicates a medical device that
needs to be protected from moisture.
Do not use if package is damaged and con-
sult instructions for use: indicates that a
medical device should not be used if the
package has been damaged or opened and
that the user should consult the instruc-
tions for use for additional information.
CE label: indicates that the manufacturer
or importer affirms the good's conformity
with European health, safety, and environ-
mental protection standards.
WEEE: indicates that the product should
not be discarded as unsorted waste but
must be sent to separate collection facili-
ties for recovery and recycling.
Manufacturer: indicates the medical device
manufacturer.
Support, scrapping & recycling
Technical support
TROUBLE: Ob tehničnih težavah:
• Contact your dealer
• If your dealer is not available or unknown, please contact mo-vis: contact@mo-
vis.com or +32 9 335 28 60.
Pri stiku z nami vedno navedite šifro izdelka in serijsko številko naprave. Le tako vam
lahko zagotovimo pravilne informacije.
Spare parts and accessories
Za več informacij o nadomestnih delih in dodatni opremi se obrnite na podjetje mo-vis ali
svojega trgovca.
Scrapping & recycling
CAUTION: For scrapping, adhere to your local waste legislation. Dispose of obsolete
electronic parts responsibly in accordance with local recycling regulations.
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Limited liability
mo-vis accepts no liability for personal injury or damage to property that may arise from
the failure of the user or other persons to follow the recommendations, warnings and
instructions in this manual.
CAUTION: This product should only be installed by a qualified service engineer.
NOTE: All mo-vis user manuals can be found at http://www.mo-vis.com where they
can be consulted in PDF format.
NOTE: In case any serious incident occurs in relation to this device, this should be
reported immediately to mo-vis and the competent authority of the Member State in
which the user is established.
Intended use
The Foot Control:
• is a proportional enota s krmilno palico, ki jo je mogoče povezati neposredno z
elektroniko invalidskega vozička za upravljanje funkcij invalidskega vozička.
• can be operated by foot
• is specifically designed for people with hand or arm function problems, but with
relatively good foot control
• enables people to move and control the wheelchair through movements of their foot
Features
The Foot Control:
• is low and proportional
• is available with optional safety brackets for the front side
• can be controlled by the foot
• allows to add straps to position and tighten the foot
• ima 2 stikali, ki se lahko povežeta z ločenim vmesnikom: (1) vklop/izklop električnega
invalidskega vozička – (2) način delovanja električnega invalidskega vozička.
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• se povsem prilagodi posameznikovim zmožnostim in potrebam z zelo domišljeno
elektroniko (povezava mini USB).
• je združljiv z različnimi vrstami elektronike invalidskega vozička.
• ima lučko LED na vmesniku, ki začne utripati zeleno v primeru napake ali oranžno pri
nagibanju (glejte Priročnik za vgradnjo).
• also has a LED light on the Foot Control itself, which will indicate warnings and errors.
Operation
The movements of the control are translated into according movements of the wheelchair,
e.g. driving or menu navigation.
Common practice to navigate the wheelchair with the joystick is as follows:
•Direction: point the control into the direction you want the wheelchair to move. The
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wheelchair then moves in that direction.
•Speed: the further you move the control from the default (center) position, the faster
the wheelchair moves.
•Stop: whenever you release the control, the control moves back to the default (center)
position and the wheelchair stops.
CAUTION: Izogibajte se udarcem ob ovire med vožnjo.
WARNING: Ko lučka LED utripa in/ali po vsakem dogodku z invalidskim vozičkom ali
napravo mo-vis, se obrnite na trgovca, da preveri delovanje.
LED status
The illumination of the LED on the joystick interface indicates the operational status of the
joystick.
JOYSTICK
STATUS
COLOUR LED TIMING COUNT STATE DESCRIPTION
Configuring Orange Fast Wheelchair is configuring
Powercycle Orange Heartbeat Wheelchair waits for power
cycle
Focus Green Always on System is in focus
Out of focus Green Heartbeat System is out of focus
Out of neu-
tral
Green Medium
Not applica-
ble
Joystick is out of neutral
Error Red Errors See Something went wrong
Parts and accessories
The Foot Control package consists of:
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• A Foot Control Sensor (P021-41) which includes:
A Foot Control Pedal
B 2x Foot Control Set Pin Short
C 2x Foot Control Set Pin Long
D Foot Control Strap Mounting Plate
• A Foot Control Strap (M021-80)
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• A Joystick Interface (Omni or LiNX, see Installation manual for more information).
Accessories
There is an optional Foot Control Safety Bracket Set (M021-61) available as accessory. This
can be mounted on the Foot Control itself, in the dedicated mounting slots (see Installation
manual).
The Foot Control Set Pin Short is designed in such a way that a strap can be added. This is
not available through mo-vis.
Qualifications
CAUTION: Only a qualified service engineer may install the device.
CAUTION: An incorrect programming of the wheelchair or device electronics, may
cause damage to the devices or injury to the user.
First time use
CAUTION: A qualified service engineer should assist during first time use of the
device and make sure that all functions are clear to the user, including what to do in
case of problems or doubt.
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Otros manuales para Foot Control Omni
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Este manual sirve para los siguientes modelos
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