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Idiomas disponibles
Idiomas disponibles
Ref.: AB100
Boxia
The manufacturing date is included in the batch number which can be found on the packaging
EN
x
label as
, in the following way: the second and third digits represent the year of manufacture and
the fourth and fifth digits represent the month.
ORLIMAN S. L. U.
C/ Ausias March, 3 - Pol. Ind. La Pobla-L´Eliana
Apdo. de correos 49 · C.P.: 46185
La Pobla de Vallbona Valencia - España (Spain)
Tel.: +34 96 272 57 04 - Fax: +34 96 275 87 00
Tel. Exportación: +34 96 274 23 33
E-mail: orto@orliman.com · Export mail: export@orliman.com
www.orliman.com
AB100
Fecha de emisión/Date of issue: 2021-09
Fecha de revisión/Revision date: 2022-02 | v.02
Plus
®
USE AND MAINTENANCE INSTRUCTIONS
INSTRUCTIONS FOR USE, STORAGE AND WARRANTY
Dear Customer,
Thank you very much for placing your trust in an Orliman
product. Please read the instructions carefully. Keep these
instructions and the packaging for future reference. If
you have any questions or concerns, please contact your
doctor, orthopaedic specialist or our customer service de-
partment.
ORLIMAN S.L.U. guarantees all its products as long as
the original configuration has not been manipulated or
altered except for the intended use as described in these
instructions.
If the products are used in combination with other prod-
ucts, replacement parts or systems, make sure they are
compatible and made by Orliman
. It does not guarantee
®
any products with altered characteristics due to improper
use, defects or breakage of any kind. The statutory regula-
tions of the country of purchase apply. Please first contact
the retailer from whom you obtained the product directly
in the event of a potential claim under the warranty. If any
serious incidents related to the product occur, notify Orli-
man S.L.U. and the corresponding competent authority in
your country.
Orliman would like to thank you for choosing this product
and hopes you a speedy recovery.
REGULATIONS
d
This article is defined as a class I medical device. A
Risk Analysis (UNE EN ISO 14971) has been carried out,
minimising the existing risks. Tests have been in accord-
ance with European Regulation UNE-EN ISO 22523 on
Prostheses and Orthoses.
INDICATIONS
⋅ Weakness or inability to dorsiflex the ankle (dropfoot)
as a result of neurological injuries, congenital altera-
tions or muscular disorders.
⋅ Flaccid paralysis associated with hemiparesis.
FITTING INSTRUCTIONS
For best therapeutic results considering different pathol-
ogies and to extend the useful life of the product, it is es-
sential to choose the correct size for each patient or user.
Excessive compression may be intolerable; adjusting the
compression to be firm yet comfortable is recommended.
If the product must be adapted, any such adjustments
must be done by an orthopaedic specialist or healthcare
professional legally certified to do so who must make sure
the end user or person responsible for fitting the product
properly understands how it works and should be used.
When fitting the product, you must adhere to the
following instructions:
Using an interface (i.e. a sock) is recommended.
A ADJUSTING THE PERIMETER
A.1-The product can be adapted to a specific ankle
perimeter by adjusting the part containing the
elastic guide (pin).
A.2-Depending on the patient's ankle perimeter in the
malleolus area, position this part between the
first and last of the 4 holes on the supramalleolar
part. See the following table for guidance:
•
Size
• (cm)
(cm)
(cm)
●
(cm)
1
14
16
18
20
2
20
22
24
26
3
26
28
30
32
B SECURING THE HOOKS
B.1-If using the anti-slip part with a hook, until the
laces on the footwear and position it between the
shoe tongue and laces so it is centred. Secure the
lower micro-hook by holding the laces.
B.2-If using the "S" hooks, you must insert them in the
eyelets with the longest part inside the shoe. The
elastic traction strap must go through both hooks.
C ADAPTING THE SUPRAMALLEOLAR PART
C.1-Open the supramalleolar part until you hear a
click; the part will be flat.
C.2-Position the supramalleolar part in the back of the
ankle so it coincides with the centre of the silicone
pad against the Achilles tendon.
C.3-Press the ends of the part toward the leg until you
hear a click which unlocks the part to be wrapped
around the ankle.
C.4-Secure the tip of the widest micro-hook so the
buckle is between the 2 narrowest straps.
C.5-Pull and secure the narrowest straps.
C.6-Insert the elastic traction band through the guide
(pin) on the front.
C.7-Secure the elastic band to the hook (or hooks) and
pull on the ends with the micro-hook and then se-
cure them to get the desired traction.
D FITTING THE INNER STRIP Ref.: AB12/AB22
D.1-Secure the strip in the middle of the foot with the
Velcro closures in the instep. Make sure the clo-
sure hook is in the right direction. Then, insert
the elastic traction band through the guide on
the front of the supramalleolar part. Secure it to
the hook and pull on the ends to get the desired
traction.
E INSERTING THE SHIN SUPPORT Ref.AB14/AB24
E.1-The shin support must correspond to the size of the
Boxia AB100, after being previously adapted and
checked for the patient.
E.2-Secure using the micro-hook on the inside and
front of the supramalleolar part.
E.3-The "Y"-shaped shin support has 3 ends. The short-
est one along with the longest and narrowest will
hug the shin at the height of the top of the fibula.
The remaining end will go over the front of the
tibia to be secured to the supramalleolar part on
the inside.
p
PRECAUTIONS
Before each use, check that all product components are
present as per the fitting process. Periodically check the
conditions of the product. If you observe any defect or
anomaly, immediately report it to the issuing establish-
ment.
This product is made of inflammable material. Do not
expose the products to situations that could set them on
fire. In the event of a fire, quickly get them off your body
and use the proper resources to extinguish the fire.
To avoid minor discomfort caused by sweating, we rec-
ommend using some type of cotton fabric to separate
the skin from contact with the product material. For dis-
comfort such as chafing, irritation and swelling, remove
the product and see a doctor or orthopaedic specialist.
The product should only be used on healthy skin. It is
not recommended for use over open scars with swell-
ing, redness or hotspots.
l
Products marked with the
symbol contain natural
rubber latex and can cause allergic reactions in people
sensitive to latex.
o
Products marked with the
symbol contain ferro-
magnetic components and, therefore, extreme pre-
caution must be taken if you undergo an MRI scan or
are exposed to radiation associated with diagnostic or
therapeutic procedures.
RECOMMENDATIONS-WARNINGS
The use of these products is conditioned by the indica-
tions. Although the product is not defined as a single-use
device, using it on a single patient only is recommended
and only for the intended purposes as described in these
instructions or by a healthcare professional.
When disposing of the product and its packaging, you
must strictly adhere to the legal regulations in your com-
munity.
RECOMMENDATIONS FOR STORAGE AND WASHING
When not using the product, store it in the original pack-
aging in a dry place at room temperature. Stick the Velcro
to each other (if the orthotic device has them), frequent-
ly wash by hand with warm water (30º C max.) and mild
soap. To dry the product, use a dry towel to absorb as
much moisture as possible and let it dry at room temper-
ature. Do not hang it up or iron the product and do not
expose it to direct heat sources such as stoves, dryers, di-
rect sun exposure, etc. When using or cleaning the prod-
uct, do not use abrasive or corrosive substances, alcohol,
ointments or liquid solvents. If not dried off properly, the
detergent residue may irritate the skin and cause the prod-
uct to deteriorate.
t o y m U
ENGLISH
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