Faro ALYA - INTENDED USE; INTENDED USER; GENERAL STANDARDS AND MAIN WARNINGS

ALYA INSTALLATION AND USER’S MANUAL - EN
Edition 2.0 Sept 2018 Pag. 4 di 32
Symbol to adjust light intensity
Symbol to switch on/off the light
Symbol to switch on/off the light on the rear arm (Alya with Theia Tech)
1.1.3 Symbols on the pakaging
High
Fragile
Do not wet
Do not Roll
Do not use hooks
Maximum stackable weight
Storage and Trasportation temperatures
Storage and Trasportation Relative Humidity
Storage and Trasportation Atmospheric Pressure
Recyclable cardboard
1.2 INTENDED USE
The device is used in dental office and is intended for illuminating the oral cavity and oral structures of
patients in dentistry.
In the normal use, the device is positioned distance of 700mm from the operative area, the distance for
which the lighting features were designed.
Patients can be of all ages with typical dental pathologies.
1.3 INTENDED USER
The intended users are Dentists (all specializations) or Dental Nurse
1.3.1 Professional qualification:
 Degree in Medicine with Dentistry Specialization
 Degree in Dentistry
 Degree in dental nursery
1.3.2 Minimum skills
Those planned for the professional qualification
Understanding of language: Those acquired for the professional qualification
1.3.3 Experience
Those outlined to conduct the profession
1.3.4 Possible user handicaps
For the use it is necessary at least one upper limb;
Visual faculty compatible with the profession;
The user with these characteristics does not require any special training
1.4 GENERAL STANDARDS AND MAIN WARNINGS
 The device can be installed in a dental unit, but also on specific applications to ceiling, floor or wall.
 The device can be powered both by the dental unit and by a power supply connected directly to the
mains. See the specific installation paragraph.
 The device does not have Essential Performances for which inadequacy of the device performance
prejudices patient safety.
 The device does not provide life support.
 The device must be cleaned before use (see Device Cleaning paragraph).
 The packaging of the light is suitable to protect it adequately from penetration of external agents.
 The device must never be modified without written authorization of FARO S.p.A. For maintenance
only original FARO’s spare parts are allowed. Fail to comply with this warning will immediately make
decay the warranty and the conformity of the product to international regulations and directives on
Medical Devices.