KSP N305-150, Инструкция по эксплуатации и техническому обслуживанию, Страница: 6 / 42

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General mandatory conduct Mandatory conduct
Refer to instruction leaflet On device
Alternating current On device
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3. Intended use
This manual was drawn up taking into account the characteristics, knowledge, education and
training of the Operator/End user.
The Operator handling the device must:
 Be perfectly acquainted with the product;
 Be over the age of 18;
 Be physically strong and in good mental health (e.g. not be under the influence of alcohol or
drugs and not suffering from any mental illness which might cause hallucinations, loss of
balance, or similar symptoms; if in doubt, please contact the Manufacturer);
 Be capable of assessing any dangerous situations, tackling them with composure and
cautiously;
 Have an excellent grasp of written and spoken English in order to be able to read and
understand the manual;

Know the meanings of the symbols and markings;
 Be able to move the device forward and backward;
 Have no trouble standing up or keeping their balance;
 Be physically capable of handling and supporting the patient when the latter is
raised/lowered, lifted and transferred.
CHECK THE SUITABILITY OF THE ENVIRONMENT BEFORE USE!!
The Operator/End user is fully responsible for the suitability/compatibility of the rooms where the
product is to be used.
To verify the suitability of the space where the device will be used, it is also possible to request a
demonstration visit performed by authorised personnel for the purpose of determining the
compatibility of the medical device and the site where it will be used.
THE DEVICE IS NOT SUITABLE FOR OUTDOOR USE BUT IS INTENDED FOR DOMESTIC
INDOOR USE ONLY.
The device is an aid for the disabled that allows individuals with reduced mobility to move with the
help of an operator.
It is a Class I medical device as envisaged in Annex IX to Directives 93/42/EEC; 2007/47/EC and Italian
Leg. Decree. 37/2010. It was manufactured in compliance with Italian and international regulations
relating to medical devices and aids for the disabled, and is duly registered in the database of the
Italian Ministry of Health for medical devices.
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