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Idiomas disponibles
Idiomas disponibles
Ref.: TC300
Dorsotech
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
TC300
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 de-
partment.
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 prod-
ucts, replacement parts or systems, make sure they are
compatible and made by Orliman
any products with altered characteristics due to improper
use, defects or breakage of any kind. The statutory regula-
tions 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 Orli-
man 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
Risk Analysis (UNE EN ISO 14971) has been carried out,
minimising the existing risks. Tests have been in accord-
ance with European Regulation UNE-EN ISO 22523 on
Prostheses and Orthoses.
®
INDICATIONS
⋅ Stable osteoporotic fracture.
⋅ Osteoporosis.
⋅ Muscle weakness.
⋅ Scheuermann's juvenile kyphosis.
⋅ Kyphosis with back pain.
⋅ Vertebral misalignments.
⋅ Postural rehabilitation.
FITTING INSTRUCTIONS
For best therapeutic results considering different pathol-
ogies and to extend the useful life of the product, it is es-
sential 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:
Wearing lightweight clothing underneath the brace can
improve comfort.
A Fitting the brace to the patient:
A.1. Adjusting the metal plate.
1-Peel off the micro hook closure of the lower textile com-
ponent of the rear area.
2-Separate both components, removing the metal plate
inside the lower component.
3-Remove the closure in a micro-hook that fixes the plate
to the upper textile component to access the complete
metal plate.
4-With the patient standing and looking forwards, po-
sition the stabiliser plate on the patient's back so that
the upper edge is approximately 4 cm below C7 and the
lower edge is at the level of the coccyx.
5-If it is necessary to adjust the height of the plate, remove
the 4 screws with a 2.5 mm Allen key, slide both pieces
to the desired height and re-fix all of the screws to the
ends of the upper and lower plates.
6-Adjust the plate to the anatomical shape of the patient's
spine beginning with the lumbar lordosis. It is not nec-
essary to use tools for this process.
7-Once the adaptation of the metal plate has been com-
pleted, you must insert it into the upper textile compo-
nent and close the respective micro-hook.
8-Insert the lower part of the plate into the lower textile
component and close the respective micro-hook.
A.2. Adjusting the straps.
1-After closing the brace in the abdominal area, begin
by adjusting the tension and length of the 4 straps
that connect this part to the rear plate. Special atten-
tion should be paid to the lower straps, which should
be tight. To adjust the length of the straps, release the
Velcro fasteners fixed to their ends, trim the straps to the
desired length and reattach the fasteners.
2-With the patient standing and looking forwards, adjust
the tension and length of the 2 shoulder straps in order
obtain a correct posture when they are fixed to the ab-
dominal area.
3-The intermediate actuation point of these straps can be
adjusted in the rear area by moving the Velcro piece that
. It does not guarantee
®
This article is defined as a class I medical device. A
joins the two buckles.
A.3. Adjusting the armpit protectors.
1-To move the armpit protectors, detach the 2 Velcro fas-
teners on their ends and move the protectors until they
are in contact with the front area of the shoulder and
the armpit area to prevent discomfort from rubbing.
2-After situating them correctly, fix their position with the
Velcro fasteners on the ends.
B Placement of the brace by the patient:
After the orthopaedic technician has carried out the
fitting, it will not be necessary to move the positions
of the straps. For the placement of the brace, only the
abdominal closure needs to be handled.
1-With the abdominal closure open, insert the arms
through the openings of the shoulder straps, as if it were
a backpack.
2-Insert the fingers into the respective loops on the left
and right-hand sides of the closure.
3-Press the left-hand side of the closure on the abdomen
and pull the right-hand side until the Velcro can be
closed.
4-To close the Velcro, firstly remove the fingers from the
left-hand loop and then from the right-hand loop.
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 establish-
ment.
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 rec-
ommend using some type of cotton fabric to separate
the skin from contact with the product material. For dis-
comfort 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 swell-
ing, 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 ferro-
magnetic components and, therefore, extreme pre-
caution 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 indica-
tions. 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 com-
munity.
RECOMMENDATIONS FOR STORAGE AND WASHING
When not using the product, store it in the original pack-
aging in a dry place at room temperature. Stick the Velcro
to each other (if the orthotic device has them), frequent-
ly 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 temper-
ature. Do not hang it up or iron the product and do not
expose it to direct heat sources such as stoves, dryers, di-
rect sun exposure, etc. When using or cleaning the prod-
uct, 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 prod-
uct to deteriorate.
t o y m U
ENGLISH
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