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Thuasne Genu Dynastab Manual Del Usuario página 5

Rodillera ligamentaria articulada
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Bilateral product.
Available in 6 sizes.
The device is composed of:
• an anatomically-shaped knitting integrating a light and soft knit at the back of
the knee,
• 2 rigid hinged uprights providing knee stability ❶,
• a bi-axial hinge ❷,
• 1 anterior half-straps Ⓒ and 2 posterior half-straps Ⓐ Ⓑ (including a suspension
strap Ⓐ),
• a patellar insert to support patella ❸.
Composition
Textile components: polyamide - polyester - polyurethane - elastane.
Rigid components: polyamide - silicone.
Properties/Mode of action
Stabilisation of knee joint ligaments provided by the rigid hinged side uprights.
An anatomically-shaped knitting for even compression.
The brace is maintained on the leg thanks to:
• the Suspension Strap Ⓐ;
• the silicone-coated threads at the top of the knee brace.
Staggered straps to prevent tourniquet effect.
Indications
Conservative treatment of knee ligament injuries (lateral ligaments).
Joint instability/laxity.
Knee pain and/or swelling management.
Sport activities resumption.
Contraindications
Do not use the product if the diagnosis has not been confirmed.
Do not use in the event of known allergy to any of the components.
Do not apply the product in direct contact with broken skin.
History of venous or lymphatic disorders.
Do not use in the event of major venous thromboembolic history without
thromboprophylaxis.
Precautions
Verify the product's integrity before every use.
Do not use the device if it is damaged.
Choose the appropriate size to fit the patient, referring to the size chart.
It is recommended that a healthcare professional supervises the first application.
Strictly comply with your healthcare professional's prescription and
recommendations for use.
This product is intended for the treatment of a given condition. Its duration of use
is limited to this treatment only.
For hygiene and performance reasons, do not re-use the product for another
patient.
It is recommended to adequately tighten the device to achieve support/
immobilisation without restricting blood circulation.
In the event of discomfort, significant hindrance, pain, variation in limb volume,
abnormal sensations or change in colour of the extremities, remove the device and
consult a healthcare professional.
In the event of any modification in the product's performance, remove it and
consult a healthcare professional.
Before any sports activity, check the compatibility of the use of this medical device
with your healthcare professional.
Do not wear the product in a medical imaging device.
Do not use the device in case of application of certain products on the skin (creams,
ointments, oils, gels, patches...).
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Undesirable side-effect
This device can cause skin reactions (redness, itching, burns, blisters...) or wounds
of various degrees of severity.
Any serious incidents occurring related to the device should be reported to the
manufacturer and to the competent authority of the Member State in which the
user and/or patient is resident.
Instructions for use/Application
It is recommended to wear the device directly on the skin, unless contraindicated.
To avoid damage to the knit fabric, please make sure that the self-griping pads
are always fastened to the designated self-griping surfaces when putting it on
and taking it off.
• Slip the knee brace on the leg with your foot extended, making sure the patella
is properly positioned at the centre of the patellar insert.
• To make it easier to put on, use the pull tabs at the top of the brace and turn it by
approx. 90° beforehand.
• First tighten and fasten the suspension strap Ⓐ located above the calf.
• Tighten strap Ⓑ, the back strap over the thigh.
• Tighten strap Ⓒ, the front strap over the thigh.
If you feel the need to tighten the straps during an activity, make sure you tighten
them following the steps indicated in the fitting instructions.
Care
Remove lateral uprights before washing.
To do this:
• Remove the straps, making a note of their original positions.
• Pull on the top of the product to disengage the upper end of the lateral uprights
from of their casings.
• Remove the uprights via the top opening.
Replace after washing:
• Insert the hinge via the top opening, with the domed part outwards and flexed
towards the back.
• Insert the upper and lower ends of the uprights into their casings.
• Check that the loops protrude properly through the openings.
• Replace the straps, placing strap Ⓐ at the back of the calf, strap Ⓑ at the back of
the thigh and strap Ⓒ at the front of the thigh.
Close the self-fastening tabs before washing. Machine wash at 30°C (delicate
programme). If possible use a washing net. Do not use detergents, fabric softeners
or aggressive products (products containing chlorine, etc.). Squeeze out excess
water. Dry away from any direct heat source (radiator, sun, etc.). If the device is
exposed to seawater or chlorinated water, make sure to rinse it in clear water and
dry it.
Storage
Store at room temperature, preferably in the original packaging.
Disposal
Dispose of in accordance with local regulations.
Keep this instruction leaflet
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KNIEFÜHRUNGSORTHESE
Beschreibung/Zweckbestimmung
Das Produkt ist ausschließlich für die Behandlung der aufgeführten Indikationen
und für Patienten vorgesehen, deren Körpermaße der Größentabelle entsprechen.
Beidseitig tragbares Produkt.
Erhältlich in 6 Größen.
Das Gerät besteht aus:
• einem anatomisch geformten Gewebe mit feinem und flexiblem Strickgewebe
in der Kniekehle,
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