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Ref.: OSL3100
marca
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
OSL3100
Fecha de emisión/Date of issue: 2022-02
Fecha de revisión/Revision date: 2022-02 | v.01
®
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 department.
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 products, replacement parts or systems, make sure they are
compatible and made by Orliman
. It does not guarantee any products with altered characteristics due to im-
®
proper 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
⋅ Prevention and/or relief of pain in the cervical and upper dorsal paravertebral muscles.
FITTING INSTRUCTIONS
For best therapeutic results considering different pathologies and to extend the useful life of the product, 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 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:
1-Place the pillow underneath the appropriate part of the body.
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 thera-
peutic 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
Washing the outer cover:
BEFORE WASHING, REMOVE THE FILLING AND THEN REPLACE IT ONCE DRY. Close the zip before washing.
Machine washable: machine wash at maximum temperature 95°C with neutral detergent. Spin dry at 800-1000
rpm. Can be dried in a dryer, maximum temperature 60°C. Ironing, maximum temperature 150°C. Do not use
bleach. Do not dry clean.
2 o s b U
Washing the inner cover with the filling:
Machine washable: machine wash with delicate programme and tepid water (30°C) with neutral detergent.
Spin dry gently (400 rpm). Leave to dry at room temperature. Do not hang up, iron or expose to direct heat
sources like stoves, heaters, radiators, direct sunlight, etc. Do not use bleach. Do not dry clean.
e o y m U
When using or cleaning, do not use bleach, alcohol, ointments or liquid solvents. If the product is not well
wrung out, detergent residue can remain and cause irritation to the skin and damage to the product.
Store in a dry place at room temperature.
EN
COMPOSITION
> Outer cover:
· Fabric: 65% polyester, 35% cotton.
· Closure system: 100% polyester zip.
> Inner cover:
· Fabric: 100% polyester.
· Filling: 100% siliconised and conjugated hollow polyester fibre.
ENGLISH
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