REF.: ET-210
English
INSTRUCTIONS FOR USE AND PRESERVATION
Dear customer,
Thank you for your trust in this Orliman product. You have acquired a quality product with a high
medicinal value. Please, read the instructions carefully. If you have any doubt, get in contact with
your doctor, your orthopaedist specialist or our customer service department. Orliman appreci-
ates your choice and wishes you a speedy recovery.
REGULATION
These products satisfy the European Medical Device Directive 93/42/CEE (RD. 1591/2009). A Risk
Analysis has been carried out (UNE EN ISO 14971) minimising all the existing risks. The trials have
been carried out in accordance with the European regulation UNE-EN ISO 22523 of Prosthesis and
Orthesis.
SUITABLE FOR
⋅ Treatment of clavicular fractures, as a figure-of-eight bandage.
⋅ Description of posture. As a method of rest, limiting mobility and preventing gravity-induced cap-
sulo-ligamentous strain by obtaining a functionally correct position.
⋅ It acts as a method of support, shifting the weight of the upper arm to the back, thereby reducing
the biomechanical load on the respective joints. Additionally, it acts as a means of positioning
the shoulder in a certain position to minimize the action of certain muscle groups which need to
be relaxed, and aligning the fractured segments of the injury in the collarbone.
FITTING INSTRUCTIONS
THE PRODUCT SHOULD BE ADJUSTED BY YOUR ORTHOPAEDIC TECHNICIAN OR IN ACCORDANCE
WITH DOCTOR'S ORDERS.
In order to obtain a greater degree of therapeutic effectiveness in the different pathologies and to
prolong the life and utility of the product, it is fundamental that the correct size adequate for each
patient or user is chosen (enclosed in the packet is a diagram with all the sizes and the equivalent
in centimetres). An excess compression can produce intolerance, therefore we recommend that
the compression be regulated to an optimum degree.
To fit observe the following aspects:
IC-30:
The aim of this device is to provide the maximum shoulder retropulsion possible, for which there
are 4 adjustment straps.
Situated on the back plate, between D2 and D5, immediately adjust the traction strap in a balanced
manner and exert the force necessary to obtain the desired support. In cases where an anatomi-
cal revision is required, gradually increase the tension in the straps to the tolerance limit of the
patient, until the correct posture is obtained.
To apply treatment to reduce fractures and align the clavicle, tighten the straps until the clavicle
is correctly aligned.
When using the device in hemiplegic patients with a scapulohumeral subluxation, the back plate
(interscapular) is placed at the C7 and D1 level. This is achieved by tightening as much as possible
then slightly releasing the lower straps.
Once the plate is in position, tighten all the straps to the maximum extent possible. This supplies
the force required to raise the dislocated shoulder and reduce the subluxation.
ET-210:
With the patient in the standing position, centre the back plate by placing the upper straps over the
shoulders and the lower straps below, on both sides.
Wrap the lower straps around the stomach below the ribs and fasten them using the velcro in the
area above the abdomen.
Then place the upper straps over the shoulders and below the armpit, crossing them across the
back and wrap them around the sides in the direction of the abdomen.
Tighten the lower straps as much as necessary to get the desired support for the shoulders, then
fasten the straps with the Velcro in the area below the abdomen.
PRECAUTIONS
The constructive material is inflammable.
Do not expose these products to situations where they could ignite. If this were the case remove
them quickly and use the necessary measures to put it out. The material used is hypoallergenic,
however we cannot guarantee 100% that in some determined cases it will not produce allergies, if
this occurs, remove the product and see the doctor that prescribed it.
In case of minor irritations due to sweat, we recommend the use of a cotton sock, to separate
the skin from contact with the material. For small inconvenience caused by sweat, we recommend
using an interface to separate the skin from contact with the tissue. If rash, irritation or swell-
ing to remove the product and consult a doctor or prosthetist. Contraindicated in open scars with
swelling, redness and accumulation heat. The product contains natural rubber latex and may elicit
allergic responses in individuals who are sensitised to latex.
RECOMMENDATION-WARNINGS
These products are to be used only by those which have been medically prescribed to do so. Per-
sons unconnected to such prescriptions should not use them. When the product is not being used,
store in its original packaging. In order to dispose of the packaging and the product, strictly com-
ply with the legal norms of your community.
The use of the orthesis is conditioned to the recommendations of the prescribing doctor, therefore
it must not be used for any other means than those prescribed.
For the validity of the guarantee, the issuing establishment should comply with this sheet of in-
structions.
MANUFACTURE-CHARACTERISTICS
The material features used in production have been tested and approved and meet all the Euro-
pean quality requirements.
All the products are produced with high quality materials and offer an unbeatable comfort and
quality of use. All products offer restraint, stability and compression for the optimum treatment of
the pathologies for which they have been designed.
RECOMMENDATIONS FOR PRESERVATION AND CLEANING
Stick the velcros to each other (if the orthesis has any), wash periodically by hand with a damp
cloth and a neutral soap. To dry the orthesis, use a dry towel to absorb most of the dampness and
leave to dry at room temperature. Do not hang up or iron and do not expose to direct heat sources
such as stoves, heaters, radiators, direct sun light etc. During use or during washing do not use al-
cohols, ointments or dissolvent liquids. If the orthesis is not properly dried any detergent residues
could irritate the skin and deteriorate the product.
GUARANTEES
ORLIMAN, S.L.U. Guarantees all its products, as long as these have not been manipulated or al-
tered from their original state. Does not guarantee those products in which as a result of misuse,
deficiencies or breakage of any kind, its original state has been altered. If you observe any defi-
ciency or anomaly, communicate this immediately to the establishment from which it was obtained
in order for it to be changed.
ORLIMAN, S.L.U. Appreciates your choice and wishes you a speedy recovery.