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REF.: OP1195D | OP1195I
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
OP1195 | OP1198:
⋅ Hyperextension of the knee.
⋅ Incapacity or weakness of plantar flexion and/or dorsiflexion.
⋅ Excessive plantar flexion (toe walking).
⋅ Instability as a result of low or high muscle tone.
⋅ Lack of coordination or balance.
OP1196:
⋅ Moderate or severe pronosupination.
⋅ Instability in the subtalar joint, midfoot and forefoot as a result of low or high muscular tone.
⋅ Severe flat foot.
⋅ Lack of coordination or balance.
OP1197:
⋅ Incapacity or weakness of dorsiflexion.
⋅ Excessive plantar flexion.
⋅ Hyperextension of the knee.
⋅ Instability as a result of low or high muscle tone.
⋅ Lack of coordination or balance.
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:
*(It is advisable to fit the orthoses with the patient seated). Place an interface over the patient's
skin (sock or stocking).
1-Insert the foot in the orthoses by opening the sides that surround the dorsal midfoot.
2-Position the protective pad for the dorsal midfoot by slightly opening the sides of the orthoses
that surround the dorsal midfoot.
3-Without removing the backing, place the toe pad under the toes and mark the cuts to be made
so that the pad ends up level with the distal edge of the orthoses. Peel off the backing and stick
the pad.
4-Adjust the length of the straps. Cut them if necessary.Close the orthoses using the velcro system
then place into the child's shoe.
After placing the orthoses into the shoe, the patient may feel their feet are somewhat squeezed.
If so, adjust the pressure of the shoe's closure system, always ensuring however that the shoe is
firmly held to the foot.
Adjusting the dorsiflexion limit of the articulated model Ref.: OP1197:
Using a 3mm hex key, turn the screw anti-clockwise to increase the dorsiflexion angle. If a greater
dorsiflexion limit is required, it is possible to replace the screw with a longer one.
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 us-
ing an interface to separate the skin from contact with the tissue. If rash, irritation or swelling to
remove the product and consult a doctor or prosthetist. Contraindicated in open scars with swell-
ing, redness and accumulation heat.
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.
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