Use And Maintenance Instructions - Orliman IR-6500 Instrucciones De Uso Y Conservación

Ref.: IR-6500
marca
GUARANTEE 6 months since purchase date
EN
Reference
EN
lot no.
EN
Purchase date
EN
Stamp and signature of local
EN
stockist
To validate the warranty your local stockist should indicate the purchase
EN
date.
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
IR-6500
Fecha de emisión/Date of issue: 2021-07
Fecha de revisión/Revision date: 2021-07 | v.01
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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
istics due to improper use, defects or breakage of any kind. To use the warranty, go to the place where
you bought the product as they must complete the warranty information table on this instructions
sheet. 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
⋅ Fracture.
⋅ Sprain.
⋅ Pre and postoperative knee treatment.
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-Open the immobiliser and put it around the leg.
2-The knee cap should be positioned between the 2 previously adjusted middle straps (strap 1 and 2).
3-Close the immobiliser with the straps in the defined order.
4-If necessary, readjust the tightness of the straps to comfortable pressure.
PRECAUTIONS
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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 symbol contain ferromagnetic components and, therefore, extreme
o
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 character-
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