Antar AT53037 Instrucciones De Uso página 5

ENG
HOW TO DISPOSE OF THE PRODUCT AT END-OF-LIFE
Once the device has been withdrawn from service, the medical device can be disposed of as normal
municipal waste.
NOTES:
In the event of a device-related „serious incident" that directly or indirectly led to, could have led to, or is likely
to lead to any of the following:
(a) death of a patient, user or other person, or
(b) temporary or permanent deterioration of the health of a patient, user or other person, or
(c) a serious risk to public health
the above ‚serious incident' must be noti ed 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
O ce for Registration of Medicinal Products, Medical Devices and Biocidal Products.
NOTES:
In the event of pain, allergic reactions or other disturbing symptoms unclear to the user related to the use of
the medical device, a healthcare professional should be consulted.
DIAGRAM OF HOW TO PUT ON THE ORTHOSIS:
REMOVAL
Remove the orthosis by following all the above steps in reverse order.
SIZING TABLE (To t the correct size, measure the circumference above the ankle):
- S (19-22cm),
- M (22-26cm),
- L (26-30cm)
TARGET PATIENT GROUP
Persons suff ering from diseases, dysfunc ons or injuries for the treatment/rehabilita on or
compensa on of which this device is intended (see sec on on intended use of the device in these
instruc ons). The device can be purchased by the user on their own or on the recommenda on
of a doctor, therapist or other specialist. Whether you purchase the device yourself or on the
recommenda on of a doctor/therapist/other specialist, you must take into account the available
sizes/necessary func ons/sizes/variants of the device, the indica ons and contraindica ons for use,
as well as the informa on provided by the manufacturer.
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