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Idiomas disponibles
Idiomas disponibles
Ref.: OSL1260
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
OSL1260
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 compat-
ible 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 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, min-
imising the existing risks. Tests have been in accordance with European Regulation UNE-EN ISO 22523 on Prostheses
and Orthoses.
INDICATIONS
⋅ Prevention of pressure sores in people with high risk and as an auxiliary treatment method.
⋅ Fractures and other painful processes in the sacrococcygeal region.
⋅ Chronic idiopathic anal pain.
⋅ Bursitis of the hip.
⋅ Help with postural changes.
⋅ Slight postural asymmetries.
⋅ Incontinent or non-incontinent people who spend long periods of time seated.
⋅ Conditions that require postural control and stability from the pelvic area.
⋅ Postpartum pain relief and post-operative recovery in general.
⋅ Pelvic stability and moderate mediolateral and anteroposterior postural support.
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 profes-
sional 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:
Can be used on a wheelchair or any type of seat (chair, armchair, etc.).
1-Place the cushion on the seat.
2-Make sure that the bottom face of the cushion in contact with the seat is flat.
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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 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.
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 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
Maintenance: Wipe the outer cover with a damp cloth.
Use a dry towel to absorb any moisture.
Washing the outer cover:
BEFORE WASHING, REMOVE THE VISCOELASTIC AND THEN REPLACE IT ONCE DRY.
AVOID WETTING THE VISCOELASTIC FOAM.
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 80°C. Do not use bleach. Do not iron. Do not dry clean.
2 o a 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.
The use and the conditions of use of the viscoelastic foam can limit the useful life of the product. Avoid direct light and
sudden temperature changes. Always use with your cover.
COMPOSITION
EN
> Outer cover:
· Fabric: 100% polyester.
· Coating: 100% breathable and impermeable polyurethane, with flame retardant and anti-microbial (fungicide and anti-
bacterial) BIO -PRUF treatment.
· Closure system: 100% polyester zip.
· Handle: 100% polyester.
> Inner foams:
· Viscoelastic polyurethane foam - density 80 kg/m
· Discharge pad: 100% Silicone with polyurethane coating.
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