KaVo ERGOcom 3, Инструкция по эксплуатации

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Instructions for use ERGOcom 3
2 Safety
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2.2 Intended purpose
2.2 Intended purpose
2.2.1 General
It is mandatory that country-specific regulations be adhered to during final decom‐
missioning of the KaVo product. Should you have any questions relating to the
proper disposal of the KaVo product, please contact your nearest KaVo office.
Note
According to the EC directive concerning electrical and electronic used devices,
this product is subject to the cited directive and must be disposed accordingly within
Europe.
Before disassembling and disposing of the product, it must be completely proces‐
sed (disinfected, sterilized) according to the section "Preparation methods".
Additional information can be obtained from KaVo or your dental supplier.
The user must ensure that that the device works properly and is in a satisfactory
condition before each use.
During use, national legal regulations must be observed, in particular:
▪ the applicable health and safety regulations.
▪ the applicable accident prevention regulations.
The appropriate, comprehensive guidelines for this product and/or national laws,
national regulations and technlogical rules for starting up and operating have to be
applied and fulfilled in line with the specified, intended purpose of the KaVo product.
Note
Dispose of or recycle the waste materials produced without endangering human
health or the environment and under observance of the applicable national regu‐
lations.
Should you have any questions relating to the proper disposal of the KaVo product,
contact your nearest KaVo office.
2.2.2 Product-specific
TheERGOcom 3 shows the multimedia content of external image and audio
sources.
In a dental practice outside of the patient environment and together with
aKaVo Display , it corresponds to a medical product of protection class 1.
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