Villa Sistemi Medicali
ARCOVIS 3000 S/R
User's Manual
[File:201175-G-01-01.doc]
Rev. A - Pag. 5/76
1.6. General disposal
Villa Sistemi Medicali produces radiological systems that are advanced in terms of safety
and environmental protection. Assuming that the unit is properly used, there is no risk to
people or the environment.
In order to comply with applicable safety requirements, it is necessary to use materials that
may be harmful to the environment (for example: monobloc oil, protective lead, monitor
kinescope, boards and electronic components). Therefore, when necessary, proper disposal
methods, according to the regulations of the country where the unit is installed, should be
followed.
For this reason, the unit may not be disposed of along with industrial or
domestic waste and must be regarded as hazardous waste.
This symbol indicates that the waste of electrical and electronic equipment must
not be disposed as unsorted municipal waste and must be collected separately.
The proper differentiated collection for the following start of the unit disused to the
recycle, treatment and disposal, compatible with the environment, aid to prevent
possible negative effects on the environment and health and it favours the recycle
of materials that compose the unit.
The abusive disposal of the product from the user implies the application of
administrative sanctions according to the Standards in force of the unit installation
country.
For information concerning the dismantling modes of the units out of use, stick to
the local provisions or contact a representative authorized by the manufacturer.
For additional information, contact Villa Sistemi Medicali.
1.7. Interfaceability
The device does not forecast any interaction with devices for medication.
It is possible to interface the unit with certain devices such as DVD Recorder, thermal printer,
Network (DICOM System). Such devices must be in full compliance with the safety
requirements specified by 93/42/EEC Directive. The liability of the interface, if it has not been
evaluated and authorized by Villa Sistemi Medicali in writing, is of the operator and/or of the
person who has performed this interface.
1.8. Copyright
The original release of this manual is in Italian language (file: 201175-C-01-00.doc). For
further information, please refer to the Italian version.
The software contained in the unit belongs to Technix S.p.A.. Upon receipt of the unit, the
user acquires the right to use the software.
This right is neither exclusive nor
transferable.
Written authorization to Technix S.p.A. is mandatory prior to any modifications for the unit
use with functions other than the ones foreseen.
