63 76 482 D 3572
10
D 3572
.
031.01.04
.
02 12.2015
3 Safety instructions
Sirona Dental Systems GmbH
3.1 Modifications to the unit
Installation Instructions Facescan
3
Safety instructions
3.1
Modifications to the unit
Modifications to this unit which might affect the safety of the system
owner, patients or other persons are prohibited by law!
For reasons of product safety, this product may be operated only with
original Sirona accessories or third-party accessories expressly approved
by Sirona. The user is responsible for any damage resulting from the use
of non-approved accessories.
3.2
Fixed connection
3.3
Electromagnetic compatibility
The unit complies with the requirements of standard IEC 60601-1-2.
Medical electrical equipment is subject to special EMC preventive
measures. It must be installed and operated as specified in the document
"Installation Requirements".
If high-voltage systems, radio link systems or MRI systems are located
within 5 m of the unit, please observe the specifications stated in the
installation requirements.
Portable and mobile RF communications equipment may interfere with
medical electrical equipment. Therefore, the use of mobile wireless
phones in medical office or hospital environments must be prohibited.
Reference to ESD protective measures in operating instructions
Please also observe the ESD protective measures in the chapter entitled
"Electrostatic discharge".
3.4
Electrostatic discharge
Electrostatic discharge (abbreviated: ESD – ElectroStatic Discharge)
Electrostatic discharge from people can damage electronic components
when the components are touched.
Touch a ground point to discharge static electricity before touching any
boards.
3.5
Switching the unit on
Safety information for switching on the unit: Service engineer
Due to the risk of injury caused by malfunction, no person may be
positioned in the unit when it is switched on.
DANGER
Potentially lethal shock hazard!
Fixed connection!
Installing a mains plug instead of the specified fixed connection infringes
international medical regulatory actions and is prohibited. In case of
error, this puts patients, users, and other parties seriously at risk.