Antar AT53052 Instrucciones De Uso página 5

ENG
CONTRAINDICATIONS
Physical or mental limitations (e.g. visual impairment) that prevent the safe handling of the product.
If soreness or a rash occurs, discontinue use immediately and consult a physician.
USE:
1. The orthosis should be put on in a standing position.
2. Place the left side of the brace on your stomach, then attach the right side to it with Velcro. Make sure that the brace is
compressed enough so that it does not fall off (for additional cuffs, do the same). The possibility of tensioning the elastic
straps with a Velcro end will ensure appropriate pressure adjustment.
3. Loosen and remove in the reverse order.
Warning: do not use the product if liquids or warming ointments have been used, do not use in the event of skin damage!
Daily use and duration of use should be agreed with a doctor, recommended use time 3-4 hours / day. Long-term use of the
orthosis can weaken the muscles.
PRODUCT CLEANING AND MAINTENANCE INSTRUCTIONS:
• The brace may only be washed by hand in lukewarm water (at 30-40°C) with a mild detergent (eg gray soap). Before
taking out, be sure to remove the stays. In order to maintain the adhesion of Velcro fasteners, they should be closed before
washing.
• Do not dry clean.
• Do not use bleach.
• Protect against moisture.
• Do not expose to high temperature or sunlight.
• Do not tumble dry.
• Dry when unfolded, do not dry in a hanging position.
Note: The product may only be used again when it is completely dry.
STORAGE
The product should be stored in a dry and cool place, away from direct sunlight and moisture. It is recommended to store
in the original packaging
SIZES (in order to choose the right size, measure the waist circumference).
S: 75-85 cm, M: 85-95 cm, L: 95-105 cm, XL: 105-115 cm, XXL: 115-125 cm, XXXL: 125-135 cm
NOTE: In the event of a product-related „serious incident" that led, directly or indirectly, could or could have led to any of
the following events:
a) death of a patient, user or other person or
b) temporary or permanent deterioration in the health of a patient, user or other person, or
c) a serious threat to public health
this „serious incident" must be reported to the manufacturer and to the competent authority of the Member State in which
the user or patient is resident. In the case of Poland, the competent authority is the Office for Registration of Medicinal
Products, Medical Devices and Biocidal Products.
NOTE: In the event of pain, allergic reactions or other disturbing, unclear for the user symptoms related to the use of a
medical device, please consult a healthcare professional.
ATTENTION: it is forbidden to use the product other than in accordance with its intended purpose
ATTENTION: The manufacturer is not responsible for damage caused by neglect of maintenance, inadequate servicing or
resulting from failure to comply with the recommendations contained in this manual.
NOTE: If the doctor recommends using the preparation at night, make sure that it does not interfere with blood circulation;
loosen the belt in case of any numbness and remove it if necessary. In case of persistent discomfort, consult a doctor.
TARGET PATIENT GROUP
The healthcare professional shall indicate the use of the device to adults and children on his/her own responsibility, taking
into account the available variants/sizes/necessary functions/sizes and indications, bearing in mind the information provided
by the manufacturer.
METHOD OF DISPOSAL OF THE PRODUCT AFTER REMOVING FROM SERVICE
After the device is withdrawn from use, the medical device can be disposed of as normal household waste, except for
electrical products - proceed in the manner appropriate for the disposal of electrical and electronic equipment.
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