Antar AT51026 Bedienungsanleitung Seite 6

ENG
GENERAL WARNING
Thank you for purchasing our product. Please read the contents of this manual. Do not use the
product until you have read and thoroughly understood the instructions. If you do not understand
the warnings, cautions or instructions, please contact your healthcare professional or dealer to avoid
damage to the product.
It is mandatory to read the contents of this manual before using the product. Do not use if the weight
of the user exceeds 136 kg.
Store away from direct sunlight and heat source.
The toilet chair is designed for use on flat and level surfaces.
Standing on the toilet chair is not permitted.
Check the product regularly for damage and wear. If you notice any damage, stop using the product
immediately and contact your dealer.
PRODUCT DESCRIPTION
The height-adjustable toilet chair is a modern product designed for people with limited mobility.
Assembly, the product is quick, easy and tool-free. The product is made of a stable steel frame,
equipped with soft comfortable armrests. The chair's legs are finished with non-slip feet to ensure
stability. The set includes a bucket with lid and a toilet seat with lid. The product is easy to handle and
convenient to fold for transport or storage.
PRODUCT CHARACTERISTICS:
- steel frame
- soft, comfortable armrests
- height adjustable
- anti-slip feet
- bucket with lid
- easy-to-clean toilet seat
APPLICATION
The toilet chair allows patients with limited mobility to attend to their physiological needs. It can be
used in close proximity to the bed or patient area. In addition, the chair can be used without
buckets over the toilet seat.
CONTRAINDICATIONS
physical or mental limitations (e.g. visual impairment) that prevent safe handling .
NOTES:
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 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 threat to public health
this 'serious incident' should be reported to the manufacturer and to the competent authority of the
Member State in which the user or patient is resident. For Poland, the competent authority is the
Office for Registration of Medicinal Products, Medical Devices and Biocidal Products.
NOTES:
If you experience pain, allergic reactions or other distressing, unclear symptoms related to the use of
the medical device, consult a healthcare professional.
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