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Verfügbare Sprachen
Verfügbare Sprachen
REF.: J001G | J001AG | JEWETT
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
⋅ Fractures due to crushing.
⋅ Vertebral pain caused by secondary metastasis.
⋅ Spondyloarthrosis associated or not with arthritic sclerosis.
⋅ Lumbalgia, lumbosciatica, and chronic dorsalgia.
⋅ Mid-term immobilisation after intervertebral disc surgery.
⋅ Stable vertebral fractures of the lower dorsal column and the lumbar column.
⋅ Mid-term immobilisation after intervertebral disc surgery.
⋅ Temporary orthosis care after surgery on fractures of unstable body of vertebrae.
⋅ Permanent orthosis care after surgery on tumours and metastasis of body of vertebrae.
⋅ Post-surgical care after spine surgery by decompression with or without internal attachment.
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:
Select the correct size according to the table of measurements.
Adjust the frame via the system of screws both lengthways and widthways (A-B).
Adjust the orthosis to the patient via the nylon belt (C).
Then insert the plastic pin on the patient's right-hand side (D). Finally push the block clip situated
on the patient's left-hand side forwards, until it is blocked (E-F).
The orthosis must enable the patient to adopt the correct seated position without compressing the
thighs with the pelvic band and without exceeding the sternum on its top edge (G).
The PELVIC BAND can be adjusted in one of two modes:
1-MOBILE (as delivered).
2-FIXED, without any kind of mobility:
Immobilise the plate by inserting the screws into the holes located on the tab next to the plate
joint on both sides.
Ref.: J001G/J001AG. Jewett brace with three-dimensional sternal adjustment:
A- Adjusting the height of the sternal support: This support can be set to two different positions.
When supplied, it is always set to the lower position. To increase the height:
1-Remove the foam fabric padding to access the screws that connect the sternal pad to the hinges.
2-Remove these screws using the Allen key and invert the position of the pad keeping the Velcro
pointed towards the chest.
3-Reattach the sternal pad to the hinges using the screws.
B- Adjusting the position of the sternal support: The sternal pad can be repositioned by sliding it
along its horizontal grooves. To do so:
1-Remove the foam fabric padding to access the screws that connect the sternal pad to the hinges.
2-Loosen these screws using the Allen key and move the sternal pad to the required position.
3-Reattach the screws.
C- Adjusting the stability of the sternal piece: The lateral stability of the pad can be increased or
decreased by changing the distance between the hinges. To do so:
1-Remove the foam fabric padding to access the screws that connect the sternal pad to the hinges.
2-Remove these screws using the Allen key, detach the sternal pad and remove the hinges and
washers, leaving the black axes accessible.
3-Remove these axes and change their position: moving them further apart produces less pad
mobility and, therefore, greater stability. Moving them closer together produces greater pad mo-
bility and, therefore, less stability. The position of the hinges must be symmetrical.
4-After fixing the black axes, reattach the hinges, washers and sternal pad, fastening the assem-
bly with the screws.
Ref.:J001A/J002A/J001AG. Jewett brace – chest support adjustment:
The adjustment system located on both sides of the chest support enables the position of the
chest support to be varied to adapt to the shape of the patient.
The five holes enable the support to be adjusted at 20° intervals. To do so, remove the screw and
position it in the desired hole.
Ref.: J003/J004. Jewett brace with Pubic Support:
The pubic support can be adjusted to the patient's physiology by adjustment of the screws and
threaded holes.
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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