Orliman MANUTEC FP-75 Скачать руководство пользователя страница 2

REF.: FP-75 | MANUtEc®

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-For thumb splints:

Arthrosis trapezium-metacarpal joint, cubital ligament injuries, metacarpophalangeal of the 

thumb, post-operative care, Bennet fracture, surgical repair of ligament injuries. Prosthesis of 

the trapezium-metacarpal joint, thumb surgery support. Rhizarthrosis of the thumb.

B-For Quervain splints:

Combined injuries of the wrist and thumb joints. Tendinitis, tendovaginitis painful and inflam-

matory episodes of tendovaginitis. Instabilities of the metacarpophalangeal and carpometacar-

pal joints. Injuries of the lateral ligaments of the primary metacarpal (sports and post-traumatic 

injuries). Eg: Skier’s thumb. Rhizoarthrosis of the thumb.

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:

Insert thumb, allowing for flexion at distal interphalangeal joints, if necessary trim the plastic.

Carry out the necessary adjustments for a perfect fit. The splint can be thermo shaped with a hot 

air gun (by the orthopaedic technician).

Ref.: FP-74

Orthosis Ref.: FP-74, thumb immobiliser including a perspirable fabric interface. First position the 

interface directly on the hand, introducing the thumb through the orifice as with a glove. Then 

adjust the splint, introducing the thumb and ensuring the flexion of the distal interphalange, cut-

ting the plastic if necessary.

Make all necessary adjustments for a perfect fit.

The splint can be thermo-shaped with a hot air pistol (to be carried out by the orthopaedic techni-

cian).

There is a micro-fastener sealer at the end of the attachment strap. The strap can be cut to fit to the 

required length; to do this, release the Velcro strap micro-fastener, cut off the excess Velcro and 

seal the micro-fastener again on the Velcro distal end.

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 tem-

perature. 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 alcohols, 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.

Содержание MANUTEC FP-75

Страница 1: ...ar para ajustarla a la longitud deseada para ello libere el microgancho de la cincha velour corte el velour sobrante y vuelva a fijar el cierre de microgancho sobre el extremo distal de velour PRECAUC...

Страница 2: ...e Velcro strap micro fastener cut off the excess Velcro and seal the micro fastener again on the Velcro distal end PRECAUTIONS The constructive material is inflammable Do not expose these products to...

Страница 3: ...eau la fermeture en micro crochet sur l extr mit distale en velours PR CAUTIONS Le mat riau de fabrication est inflammable N exposez pas le produit des situations qui pourraient l enflammer Si tel tai...

Страница 4: ...rsch ssigen Velours ab und bringen Sie den Mikrohaken wieder am u eren Ende des Veloursgurtes an VORSICHTSMASSNAHMEN Das Material der Orthese ist entflammbar Die Produkte nicht in Situationen bringen...

Страница 5: ...ho da correia velour corte o velour restante e fixe novamente o fecho de micro gancho na extremidade distal de velour PRECAU ES O material de constru o inflam vel N o exponha os produtos a situa es qu...

Страница 6: ...rla alla lunghezza desiderata a tal fine rilasciare il microgancio della cinghia di velour tagliare il velour in eccesso e fissare nuovamente la chiusura a microgancio sull estremit distale di velour...

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Страница 10: ...REF FP 75 MANUtec Orliman Orliman 93 42 CEE RD 1591 2009 UNE EN ISO 14971 UNE EN ISO 22523 A B Ref FP 74 Ref FP 74 100 ORLIMAN S L U Orliman...

Страница 11: ...men klip nu den overskydende velour af og s t velcroen p igen i enden af velour remmen FORSIGTIG Materialet er br ndbart Uds t ikke produktet for situationer hvor det kan ant ndes Hvis dette alligevel...

Страница 12: ...ning en 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...

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