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REINFORCED LUMBAR SUPPORT
BELT
Description/Destination
The device is intended only for the treatment
of the indications listed and for patients whose
measurements correspond to the sizing table.
Composition
Aerated and breathable Combitex fabric. ❶
Optimized back comfort due to a fleecy-foam
complex.
Abdominal panels with self-fastening surface and
finger-loop. ❷
Additional strap with thumb-loops. ❸
Conformable dorsal stays. ❹
Texile components: Polyamide - Polyester - Elastane
Non-textile components: Brushed tempered steel -
Polyoxymethylene - Polypropylene - PVC
Properties/Mode of action
The device relieves low back pain, supporting the
lumbar spine: compartmental lumbar unloading is
therefore achieved via increased intra-abdominal
pressure.
Indications
Non-specific low back pain (acute, subacute and
chronic phases).
Spinal stenosis.
Contraindications
Do not use in the event of known allergy to any of the
components.
Do not use on pregnant women.
Do not use in the event of a hiatus hernia.
Do not use in the event of bone cancer with spinal
metastases.
Do not use in the event of circulatory, pulmonary
or cardiovascular problems in patients for whom
an increase in arterial blood pressure is not
recommended.
Precautions
Verify the product's integrity before every use.
Wear the device above thin clothing.
Do not use the device if it is damaged.
Choose the appropriate size to fit the patient, referring
to the size chart.
Strictly comply with your healthcare professional's
prescription and recommendations for use.
It is recommended that a healthcare professional
adjust the stays to the shape of the patient's back
before the belt is worn for the first time.
Do not wear the product in a medical imaging
machine.
Do not wear the product while sleeping.
Consult a health professional if discomfort or pain
occurs.
The use of a medical device by a child, should be done
under the supervision of an adult or a healthcare
professional.
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Undesirable side-effect
This device can cause skin reactions (redness, itching,
irritations...).
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
Position the belt around the waist, placing your hands
in the finger loop located on the front panel. Ⓐ
The belt must be centered on the spine: the dorsal
stays should be positioned on either side of the spine.
The bottom of the belt must stop at the top of the
crease between the buttocks.
The inside label must be positioned upwards.
Hold the left end flat using your left hand.
Pull the finger loop on the abdominal panel
simultaneously and evenly. Ⓑ
Fasten the belt, right side over left side, adjusting to
the desired compression. Ⓒ
For an adapted compression,
additional strap.
Pull the thumb loops on the additional strap
simultaneously and evenly. Ⓓ
Attach the self-fastening parts onto the centre of the
abdominal panels of the belt. Ⓔ
The level of compression can be adjusted as required
throughout the day.
Care
Close the self-fastening tabs before washing. Machine
washable at 40 °C. Do not machine wash the device
more than 10 times. Do not dry clean. Do not use
detergents, fabric softeners or aggressive products
(products containing chlorine). Do not tumble-dry. Do
not iron. Squeeze out excess water. Dry away from any
direct heat source (radiator, sun, etc.). Dry flat.
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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VERSTÄRKTE
LWS-STABILISIERUNGSORTHESE
Beschreibung/Zweckbestimmung
Das Produkt ist ausschließlich für die Behandlung
der aufgeführten Indikationen und für Patienten
vorgesehen, deren Körpermaße der Größentabelle
entsprechen.
Zusammensetzung
Elastisches, luftdurchlässiges und atmungsaktives
Combitex Gewebe. ❶
Optimierter Rückenkomfort dank einer Kombination
aus Velours und Schaumstoff.
you can use the
