MANUAL
Doc. HBE090-3
Installation and User Manual EVOSTYLE N.G.
Mod. MQI006-0
NEW LIFE RADIOLOGY S.R.L. Corso Giuseppe Canonico Allamano 13/15 INT.G - 10095
Grugliasco (TO) Italy Phone and fax + 39.011. 781994 [email protected]
www.newliferadiology.it
1
GENERAL ASPECTS
Introduction
Dear Customer,
thank you for the preference granted to our product. We invite you to attentively read the
present instructions that will help you to get the maximum of your X-ray diagnostic
information with minimal x-ray use.
This manual has the purpose to provide the User with instructions for proper, safe and
efficient operation.
The equipment must be used in accordance with the procedures contained in the manual
and never for purposes other than those specified herein.
The User is responsible for what concern the fulfilments in legal matters facing installation
and equipment functioning.
The plant can only be used by medical personnel in possession of the related licenses
enablers and aware of the risks associated with the use of ionizing radiation sources. The use
of X-ray sources for purpose of medical diagnostics is subject to specific authorizations
and/or communications to the Authorities responsible for vigilance. The User is responsible
for the use unauthorized of the plant. The User of the X-ray plant for dental complementary
radiology is also required, without exception, to observe the regulations governing the
safety of exposure to ionized radiations sources for workers, for member of the public, for
population and patients.
If the equipment is not operated correctly or it is not made proper maintenance, the
manufacturer cannot be held responsible for any breakages, lesions and mal functioning.
Descriptions
“CAUTION: Do not modify this equipment without the manufacturer’s permission.”
EVOSTYLE N.G. radiological unit is an equipment designed to obtain intraoral dental
radiographs arranged to be use with acquisition systems (conventional films, phosphor
plates and video radiographic).
According to Directive 2007/47/CE (Legislative Decree 37/2010) it is classified in CLASS IIb.
The unit is manufactured in accordance with the actual international standards on the
protection of ionizing radiation, electrical safety, mechanical safety and electromagnetic
compatibility for electro medical equipment.
