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REF.: BE-165 | BE-175 

REF.: BE-165 | BE-175 

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

A-Lumbosacral Back Support:

Lumbago, lumbosciatica, degenerative processes, weak and atonic muscles, disc hernia, pre and 

post-surgical treatment.

In the case of prominent abdomens the pendulum abdomen support is recommended.

B-Dorsolumbar Back Support: 

Dorsalgias, degenerative processes, kyphosis, dorsal treatment, osteoporosis, crushed verte-

brae, pre and post-surgical treatment.

In the case of prominent abdomens the pendulum abdomen support is recommended. 

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:

A-Lumbosacral Back Support:

Place the orthesis around the body so that the bones are placed in the centre of the back and 3 cm 

above the gluteal fold, then proceed with the tightening and closure.

Velcros: Adjust the velcro closing systems to achieve the desired compression.

Elastic or crossed straps: Adjust the posterior elastic or crossed straps sticking them to the front 

side by means of the front velcro fasteners.

B-Dorsolumbar Back Support:

*For dorso lumbar support, carry out the procedure as described above, then tighten the shoulder 

pins at the back towards the front, passing them under the armpit, subsequently crossing them 

and carrying the ends to the abdominal wall, sticking them to each other, until the necessary trac-

tion is obtained in order to achieve a tolerable retropulsion of the shoulders for the patient

Both fasteners should be placed above the pubis lifting the abdominal wall.

*In some cases includes a removable lumbar foam cushion (heat effect) and better adaptation of 

lordosis.

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 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 Europe-

an 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.

 › For proper use of the orthosis it is advisable not to modify its height position once the Velcro straps are adjusted, since the fabric could tear.  If you need to 

adjust the height of the orthosis, first loosen the Velcro straps, re-position the orthosis at the desired height, and adjust the tension of the Velcro straps.

Summary of Contents for BE-165

Page 1: ...aciones que pudieran producir su ignici n Si as fuera despr n dase r pidamente de ellos y utilice los medios adecuados para apagarlo El material empleado es hipoalerg nico sin embargo no podemos garan...

Page 2: ...te 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...

Page 3: ...nt nous ne pouvons pas garantir 100 qu il ne produise pas d aller gies dans certains cas Si tel tait le cas retirer le produit et consulter le m decin prescripteur Au cas o vous auriez de petites g ne...

Page 4: ...immten F llen nie ganz ausgeschlossen werden In einem solchen Fall das Produkt abnehmen und den verschreibenden Arzt aufsuchen Sollte die Orthese aufgrund der Schwei bildung unbequem sein empfehlen wi...

Page 5: ...ilize os meios adequados para apagar o fogo O material utilizado hipoalerg nico no entanto n o se pode garantir a 100 que em determinados casos estes n o provoquem alergias Nesse caso retire o produto...

Page 6: ...ombustione In tal caso rimuoverlo al pi presto ed usare i mezzi adatti per l estinzione Il materiale impiegato ipoal lergenico tuttavia non possiamo garantire al 100 che in determinati casi non si pos...

Page 7: ...by ulec podpaleniu W takim wypadku nale y natychmiast zdj produkt i u y odpowiednich rodk w w celu jego ugaszenia Zastosowane materia y s hipoalergiczne niemniej jednak nie mo emy zagwarantowa w 100 e...

Page 8: ...kunnen we niet 100 garanderen dat er zich in bepaalde gevallen geen aller gie n kunnen voordoen Als dit gebeurt verwijder dan het product en raadpleeg de arts die het product voorgeschreven heeft In h...

Page 9: ...expune i produsele la situa ii ce ar putea conduce la combustie Dac acest lucru se nt mpl desprinde i v rapid de produs i folosi i mijloacele adecvate pentru stingere De i materialul fo losit este hi...

Page 10: ...REF BE 165 BE 175 REF BE 165 BE 175 Orliman Orliman 93 42 CEE RD 1591 2009 UNE EN ISO 14971 UNE EN ISO 22523 A B A 3 B 100 ORLIMAN S L U Orliman...

Page 11: ...gevel skulle ske skal De hurtigt tage produktet af og slukke ilden med en passende ildslukker Selvom materialet er hyperallergisk kan vi ikke garantere 100 at der i specifikke tilf lde ikke kan foreko...

Page 12: ...stempel van de orthopedie RO Semnatura si stampila vanzatorului RU DA Underskrift og stempel es Para la validez de la garant a es necesario cumplimentar estos datos eN To validate the warranty your lo...

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