En Abdominal Support For Stoma - Thuasne Stomex Mode D'emploi

Entretien
Fermer les auto-agrippants avant lavage.
Lavable en machine à 60 °C (cycle délicat). Ne
pas laver le dispositif en machine au-delà de
10 lavages. Ne pas nettoyer à sec. Ne pas utiliser
de détergents, adoucissants ou de produits
agressifs (produits chlorés...). Ne pas utiliser
de sèche-linge. Ne pas repasser. Essorer par
pression. Sécher loin d'une source directe de
chaleur (radiateur, soleil...). Sécher à plat. En cas
de souillure de la ceinture, il est recommandé et
possible exceptionnellement de la laver à 90 °C.
Stockage
Stocker à température ambiante, de préférence
dans l'emballage d'origine.
Élimination
Éliminer conformément à la réglementation
locale en vigueur.
* Non applicable aux dispositifs médicaux sur-
mesure patient, les mesures sont prises de
manière individuelle.
Premier marquage CE : 1997
Conserver cette notice.
en
ABDOMINAL SUPPORT FOR
STOMA
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
Compact elastic fabric. ❶
Abdominal panel in elastic, ladder-proof fabric
to enable openings to be cut out. ❷
Closure with self-fastening surface and thumb-
loops. ❸
Flexible and removable dorsal stays. ❹
Flexible and removable lateral stays. ❺
Texile components: cotton - elastane -
elastodiene - polyamide - polyester -
polyether - viscose.
Non-textile components: brushed tempered
steel - polyamide
Properties/Mode of action
The device ensures strong support and
adaptable compression to the abdomen thanks
to the elastic compact fabric.
Indications
Stoma.
Post-operative abdominal conditions.
Contraindications
Do not apply the product in direct contact with
broken skin.
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.
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.
It is recommended that a healthcare professional
supervises the first application.
Do not wear the product in a medical imaging
machine.
Do not wear the product while sleeping.
In the event of discomfort, significant hindrance,
pain, abnormal sensations, remove the device
and consult a healthcare professional.
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 without excessive
compression.
Do not use the device in case of application of
certain products on the skin (creams, ointments,
oils, gels, patches...).
The use of a medical device by a child, should
be done under the supervision of an adult or a
healthcare professional.
Undesirable side-effects
This device can cause skin reactions (redness,
itching, burns, blisters,etc.) or wounds of various
degrees of severity.
In postoperative conditions, the restrictive effect
of the device could alter respiratory function and
decrease lung capacity and tidal volume.
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
Fit the belt so as to determine where to cut
the opening.
Position the belt around the waist, using the
thumb-loops. Ⓐ
Outline the opening on the abdominal panel of
the belt at the level of the stoma. Ⓑ
Remove the belt and cut out with scissors the
opening. Ⓒ
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