Antar AT52304 Manual De Usuario página 21

Silla de ruedas eléctrica

Idiomas disponibles

ENG

NOTE:

For intensive use of the product, it is recommended to replace the ba eries/ba eries every 6 months.

The guarantee for the ba eries/ba eries is 6 months.

NOTE: Check rear tyre pressure (2.4-3bar) before ﬁ rst use. The pressure should also be checked

periodically.

NOTE:

In the event of a product-related 'serious incident' that directly or indirectly led to, could have led to

or is likely to lead to any of the following:

(a) the death of a pa ent, user or other person; or

(b) temporary or permanent deteriora on of the health of a pa ent, user or other person, or

this 'serious incident' should be reported to the manufacturer and to the competent authority of the

Member State in which the user or pa ent is resident. For Poland, the competent authority is the

Oﬃ ce for Registra on of Medicinal Products, Medical Devices and Biocidal Products.

NOTE:

If you experience pain, allergic reac ons or other distressing, unclear symptoms related to the use of

the medical device, consult a healthcare professional.

WARNING: During use and handling of the product and when assembling and adjus ng the

mechanisms, there may be a danger of trapping and/or pinching parts of the user's/companion's body

in the openings/gaps between components. Perform these opera ons with par cular care.

NOTE: There may be a risk of pping over if the product is used incorrectly. Please follow the

instruc ons for ge ng on/oﬀ / moving. Once the adjustment is complete, stabilise the posi on by

ghtening the nuts/bolts carefully.

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 this

instruc on manual). 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 and variants of the device, the indica ons and contraindica ons for use and

the informa on provided by the manufacturer.

HOW TO DISPOSE OF THE PRODUCT

Dispose of the electrical medical device in accordance with the obligatory rules. Handle in a manner

appropriate to the disposal of electrical and electronic equipment.

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2023-12-22 13:27:30