Antar AT53037 Instrucciones De Uso página 5

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 notified 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.
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 fit the correct size, measure the circumference above the ankle):
- S(19-22cm),
- M(22-26cm),
- L(26-30cm)
TARGET PATIENT GROUP
The healthcare professional indicates the use of the device to adults and children at their own risk, taking into account the available
variants/sizes/necessary functions/sizes and indications, bearing in mind the information provided by the manufacturer.
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