EasyManua.ls Logo

Sirona c8+ turn - Safety Information

Sirona c8+ turn
42 pages
Print Icon
To Next Page IconTo Next Page
To Next Page IconTo Next Page
To Previous Page IconTo Previous Page
To Previous Page IconTo Previous Page
Loading...
1 Preparations Sirona Dental Systems GmbH
Installation Requirements C8
+
/C8
+
Tu r n
60 28 000 D3417
6 D3417.021.04.11.02
ATTENTION
It is essential that you comply with the warning and safety
information contained in the Installationsvoraussetzungen.
All such information is highlighted by the signal words
NOTE, CAUTION or WARNING.
ATTENTION
The unit may only be operated by properly trained person-
nel. On-site installation must be performed in accordance
with our specifications.
In our capacity as a manufacturer of medical electr ical
equipment, we only consider ourselves to be responsible for
the safety characteristics of the unit if we perform mainte-
nance and repair work on it ourselves or if this is performed
by centers that we have expressly authorized to do so; and if
defective components are replaced with original spare
parts.
When this work is carried out, we recommend that you ask
those responsible for the work to provide a certificate indi-
cating the nature and scope of the work, including details of
changes to rated data or the working area where applicable.
This certificate should also be signed and dated, and should
show information about the relevant company.
ATTENTION
By law, any changes to this unit which may compromise the
safety of operators, patients or third par ties are not permis-
sible.
For reasons of product safety, this product may only be op-
erated with original Sirona accessories or accessories from
third parties approved by Sirona. The user assumes the risk
of using non-approved accessories.
If any devices not approved by Sirona are connected, they
must comply with the applicable standards, e.g.:
IEC 60950 for information technology equipment
(e.g. PCs) and
IEC 60601-1 for medical equipment.
The monitor used at the treatment center must meet the re-
quirements of IEC 60950. The loudspeaker port of the mon-
itor may only be connected to a device that complies with
IEC 60950 (e.g. a PC) or IEC 60601-1. Under no circum-
stances may it be connected to a stereo system, for exam-
ple.
If a system is being assembled during installation, the re-
quirements of IEC 60601-1 (3rd edition) must be adhered
to. The person assembling the system assumes responsi-
bility for ensuring that it conforms to Directive 93/42/EEC.
ATTENTION
The floor must be flat and level (DIN 18 202). A mounting
plate must be used for uneven floors (see Section 1.5,
"Mounting plates C8
+
(not for C8
+
Turn)" on page 12).
ATTENTION
The floor must have a minimum loading capacity of 0.5N/
cm².
ATTENTION
Wireless phone interference with medical electrical equip-
ment:
To ensure safe operation of medical electrical equipment,
the use of mobile wireless phones in practice or hospital en-
vironments is prohibited.
ATTENTION
Electromagnetic compatibility: The unit should not be op-
erated in the immediate vicinity of other devices. If this
proves to be unavoidable, the unit should be monitored to
ensure that it is operating properly.
1.1 Safety

Related product manuals