orliman Pantbrace PF010 Betriebsanleitung Seite 2

Ref.: PF010
Pantbrace
The manufacturing date is included in the batch number which can be found on the packaging
EN
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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
PF010
Fecha de emisión/Date of issue: 2021-09
Fecha de revisión/Revision date: 2022-02 | v.02
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
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
imising the existing risks. Tests have been in accordance with European Regulation UNE-EN ISO 22523 on Prostheses
and Orthoses.
INDICATIONS
Girdle-trousers of this type are indicated for persons with flaccid muscle tissue with prominent pendulous abdomen,
sagging glutei and soft thigh musculature associated with lower back pain incisional hernias, post-abdominal wall sur-
gery, arthritis and rheumatic problems, etc. in which cosmetic appearance is important as well as compression which
gathers and contains al the associated musculature, obtaining elevation of the lower abdomen and creating an upwards
compression, preventing chafing of the inner thighs.
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.
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When fitting the product, you must adhere to the following instructions:
It is recommended to be used with underwear so as to obtain greater comfort and hygiene.
With the opening systems open, place each leg into its corresponding trouser leg.
Then lift the girdle-trousers up to the pubic area, gathering the glutei. Raise the rest of the girdle as high as possible,
up to about just below the ribs, and close the girdle starting below and going upwards, starting with the hook-and-eye
system, then closing the zip.
Adaptation of the lumbosacral support:
The lumbosacral support is an elastic element in the back zone of girdle-trousers. At both ends it has 4 rows of hooks
which allow us to regulate the pressure of the elastic lumbosacral system. On the front (abdominal), there are 2 tabs
which on their ends, a row of male hooks. Pull the back elastic bands toward the abdomen, fastening them with the
hooks on the desired row in order to obtain the necessary compression, always starting from the lowest, and going to
the highest hook. Carry out this procedure on both sides.
Attachment of the lumbar cushion:
The panty girdle has an anatomically designed lumbar pad.
Before putting in place, it needs to be adapted to the patient's lumbar area. Once this has been done, remove the astra-
khan Velcro straps and position the fastener area on the velour provided for this purpose.
The widest area should be positioned upwards and the narrowest edge downwards. For proper positioning, the Velcro
face should be attached to the rear internal side of the girdle, positioned in accordance with the female Velcro and
properly aligned.
The plate should be adapted to the patient's lumbar curve, which we can do using our hand. Take care to ensure that
the Velcro fastener does not come into contact with the external part of the orthosis, in order to avoid chaffing with the
fabric.
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 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
to latex.
Products marked with the
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 characteristics due to improper use, defects
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This article is defined as a class I medical device. A Risk Analysis (UNE EN ISO 14971) has been carried out, min-
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symbol contain natural rubber latex and can cause allergic reactions in people sensitive
o
symbol contain ferromagnetic components and, therefore, extreme precaution must be
ENGLISH