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Ref.: AB11
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
AB11
Fecha de emisión/Date of issue: 2021-09
Fecha de revisión/Revision date: 2022-02 | v.02
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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 care-
fully. Keep these instructions and the packaging for future reference. If you have any questions or con-
cerns, please contact your doctor, orthopaedic specialist or our customer service department.
ORLIMAN S.L.U. guarantees all its products as long as the original configuration has not been manipu-
lated or altered except for the intended use as described in these instructions.
If the products are used in combination with other products, replacement parts or systems, make sure
they are compatible and made by Orliman
teristics due to improper use, defects or breakage of any kind. The statutory regulations 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 Orliman 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 accordance with European Regulation
UNE-EN ISO 22523 on Prostheses and Orthoses.
INDICATIONS
Forefoot lift during walking in patients with flaccid paralysis that cause equinism, due to injuries in
the lower extremities, cerebrovascular accidents (CVA-strokes) peripheral nervous system injuries, etc.
FITTING INSTRUCTIONS
For best therapeutic results considering different pathologies and to extend the useful life of the prod-
uct, it is essential 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 responsi-
ble for fitting the product properly understands how it works and should be used.
When fitting the product, you must adhere to the following instructions:
1-Attach the strap above the ankle suprameleolar matching gel pad with Achilles tendon.
2-Open the shoelaces of the shoe and put the plate hook attachment between the tongue of the shoe
and shoelaces, trying to stay focused and with the hook in the direction of traction.
3-Then enter the stretch drive by the guide at the front of the ankle.
4-Set the hook and proceed to pull the ends with velcro fixing it after obtaining the desired traction.
Type of footwear laces.
PRECAUTIONS
p
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 establishment.
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 recommend using some type of cotton fabric to
separate the skin from contact with the product material. For discomfort 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 swelling, redness
or hotspots.
Products marked with the
l
symbol contain natural rubber latex and can cause allergic reactions in
people sensitive to latex.
Products marked with the
o
symbol contain ferromagnetic components and, therefore, extreme
precaution 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 indications. 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 community.
RECOMMENDATIONS FOR STORAGE AND WASHING
When not using the product, store it in the original packaging in a dry place at room temperature. Stick
the Velcro to each other (if the orthotic device has them), frequently 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 temperature. Do not hang it up or iron the product and do not expose it to direct
heat sources such as stoves, dryers, direct sun exposure, etc. When using or cleaning the product, 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 product to deteriorate.
t o y m U
. It does not guarantee any products with altered charac-
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