Instructions for use ARCUSevo
2 Safety
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2.2 Proper use
2.2 Proper use
2.2.1 General information
The user must ensure that that the device works properly and is in a satisfactory
condition before each use.
This KaVo product is intended only for use in the field of dentistry. It is impermissible
to use the product for a purpose for which it was not intended.
"Proper use" includes following all the instructions for use and ensuring that all in‐
spections and service tasks are performed.
Apply and meet the overarching guidelines and/or national laws, national regulati‐
ons and the rules of technology for medical devices applicable for startup and use
of the KaVo product for the intended purpose.
Responsibility is accepted for the safety, reliability and performance of the compo‐
nents supplied by KaVo provided:
▪ installation, upgrades, adjustments, changes or repairs are carried out by tech‐
nicians trained by KaVo or third parties authorised by KaVo, or by the personnel
of authorised distributors.
▪ The unit is operated in accordance with the instructions for use, care and instal‐
lation.
▪ The IT components supplied by the operator meet the technical requirements in
these instruction for use for hardware and software, and they are installed and
set up according to the descriptions of these components.
▪ If it is repaired, the requirements of VDE 0751-1 "Repeat tests and tests before
start-up of electrical items of medical equipment and systems - general regula‐
tions" must be met in full.
The user must observe the following:
▪ - only use properly operating equipment.
▪ protect himself or herself and third parties from danger.
▪ avoid contamination from the product.
During use, national legal regulations must be observed, in particular:
▪ the applicable health and safety regulations.
▪ the applicable accident prevention regulations.
Authorised to repair and service the KaVo product:
▪ The technicians of KaVo branches.
▪ Technicians of authorised dealers specially trained by KaVo.
In Germany, the operator, person responsible for the device and user must operate
their devices in accordance with the provisions of the Medical Device Law.
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