I - Introduction; Warnings - Satelec Acteon Mini LED III Supercharged User Manual

MLED III Supercharged U2
I – INTRODUCTION
You have just taken possession of your Mini LED
SuperCharged unit, congratulations.
Created by SATELEC®, the Mini LED SuperCharged is a
photopolymerizer allowing dental care to be given using
the suitable light guide supplied with the unit.
To take full advantage of the technology of this product,
we request that you read carefully the chapter covering
all safety recommendations.
The manufacturer's warranty is applicable only if these
indications relating to the unit's operation and safety
have been correctly applied. All of these safety
measures require a sound knowledge of dentistry,
photopolymerization and of the specific instructions
regarding the operation of the Mini LED SuperCharged
given in this operating manual.
Sections with the symbol are
would like to attract your attention.
II – WARNINGS
United States Federal Law restricts on its
territory the use of this unit exclusively to trained,
capable and qualified dental healthcare professionals,
or under their control.
To reduce the risk of accidents, it is imperative to
comply with the following precautions:
Users of the unit
Use of the Mini LED SuperCharged is limited exclusively
to trained dental healthcare professionals, apt and
qualified in the usual context of their activity.
If you have received this unit in error, contact the unit's
supplier to arrange for its return.
Interactions/contraindications
Do not use on persons currently suffering from, or that
have suffered from in the past, photo-biological
reactions (including solar urticaria or erythropoietic
protoporphyria) or on persons undergoing treatment
using photosensitizing
methoxsalen or chlortetracycline).
Any person, practitioners or patients who have
previously suffered from a retina or lens condition or
who have undergone eye surgery, in particular cataract
surgery, must consult their ophthalmologist before using
this unit.
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Even in the event of agreement, it is strongly
recommended to be prudent as the light intensity may
cause accidents.
It is particularly recommended to continuously wear
protective glasses suited to the use of equipment
emitting radiation of wavelengths less than 500 nm.
The light radiation produced by this type of equipment
can be dangerous and must never be directed towards
the eyes, even if the practitioner or the patient is
wearing protective glasses suited to the use of
equipment emitting radiation of wavelengths less than
500 nm.
The lighting produced by this lamp must be directed
only at the part to be treated in the oral cavity.
The equipment must not be used if the patient and/or
the operator has a pacemaker or any other active
implant (cochlear implant...).
The equipment has not been designed to withstand
shocks from an electrical defibrillator.
The unit complies with current electromagnetic
compatibility standards, nevertheless, the user shall
ensure that any electromagnetic interference does not
create an additional risk (presence of radiofrequency
emitters, electronic equipment...).
Overexposure to light radiation of the pulp and
soft tissues can result in the release of heat and can
result in injury to the patient.
To use your equipment in the best possible
conditions, it is important to comply with the
specifications given in sections II - WARNINGS
Equipment users and V – ROUTINE USE.
As far as possible, avoid the accumulation of heat due
to a dental dam.
To avoid a sensation of heat, it is recommended to
separate cycles by 10 seconds for polymerization
times of 10 seconds or less, and by 30 seconds for
polymerization times greater than 10 seconds.
Connection to AC power supply
Ensure that your equipment is connected to the AC
power supply by an authorized dentistry installation
technician.
Do not tilt the unit at an angle of greater than 5°.
Before connecting the unit, check that the AC voltage is
compatible with that indicated on the AC power adapter
allowing lamp charging.
A different voltage would result in damage to the unit
and could injure the patient and/or the user.
The AC power supply used to power the unit must
comply with the applicable standards of your country.