Sirona Dental Systems GmbH
1 Warning and safety information
Operating Instructions HELIODENT DS
60 81 744 D 3302
D 3302.201.01.25.02
5
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Electromagnetic compatibility (EMC)
The HELIODENT DS complies with the requirements of
IEC 60601-1-2:2001.
Medical electrical devices are subject to special precau-
tionary measures regarding EMC. They must be
installed and operated as specified in the document
"Installation Requirements".
Portable and mobile HF communication devices can
influence medical electrical equipment. The use of
mobile telephones in the practice or hospital area there-
fore must be prohibited.
Disposal
It applies generally that the national regulations have to
be complied with when disposing of this product. Please
observe the regulations applying in your country.
Within the European Economic Community the directive
2002/96/EEC (WEEE) for electrical and electronic
devices requires environmentally compatible recycling /
disposal.
Your product is marked with the adjacent symbol. With
the goal of environmentally compatible recycling / dis-
posal, your product must not be disposed of with the
domestic refuse.
The black bar under the "refuse bin" symbol means that
it has been put onto the market after 13.08.2005. (See
EN 50419:2005)
Please note that this product is subject to the directive
2002/96/EEC (WEEE) and laws applicable in your coun-
try and must be sent for environmentally compatible
recycling / disposal.
The X-ray tube assembly
of this product contains a
tube with a potential implosion hazard, a lead lining and
mineral oil.
Please contact your dealer if your product should be
finally disposed of.
Dismantling and reassembly
When dismantling and reassembling the unit, always
proceed as outlined in the instructions for reassembly.
This is necessary to ensure the unit’s proper functioning
and stability.
Summary of Contents for HELIODENT DS
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