EasyManua.ls Logo

Acteon Mini LED - Required information; Indication for use; Operating principle; Using accessories not supplied by the manufacturer

Acteon Mini LED
40 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...
2 Required information
2.1 Indication for use
This medical device is designed to cure photosensitive composites and bonding composites used in dentistry. The
target clinical uses relate to conservative and restorative dentistry.
This medical device is used with an optical guide and a rigid protection shield.
2.2 Operating principle
Designed to light-cure dental composites, the Mini LED is fitted with electroluminescent diodes (LED) that emit a visible
blue light in a spectrum of wavelengths between 440 nm - 460 nm.
The wavelength of the light source corresponds to that of the photo-initiators used in dental curing composites.
A removable optical guide is attached to the end of the medical device. The optical guide concentrates and directs the
light produced to the clinical site.
2.3 Using accessories not supplied by the manufacturer
The Mini LED is designed to be used with SATELEC, a company of Acteon Group accessories. The use of optical guides,
protection shields or mains adapters made by other manufacturers will damage the Mini LED.
2.4 Connecting and disconnecting accessories during use
Never release the battery when the Mini LED is in use. When handling the mains adapter and the battery
disconnected from the handpiece, avoid all contact between these parts and the patient or any other party.
Do not disconnect the optical guide or the rigid protection shield when using your Mini LED.
2.5 Repairing or modifying the medical device
Contact the supplier of your device. Using the services of an unapproved repairer could render your device dangerous
for you and your patients.
Do not repair or modify the device without seeking the prior permission of SATELEC, a company of Acteon Group.
If the device is modified or repaired, specific checks and tests must be carried out to ensure that the medical device is
still safe to use.
In the event of doubt, contact an approved dealer or the SATELEC, a company of Acteon Group Customer Service team:
www.acteongroup.com
satelec@acteongroup.com
SATELEC, a company of Acteon Group, at the request of technical personnel working for the network of
approved dealers, will provide any information required to repair defective parts on which they may perform
repairs.
2.6 Warranty
The user must not disassemble the base, the battery or the handpiece as this will void the medical device's warranty.
2.7 Latest document update
01/2017
2.8 Date of first CE marking
2007
User Manual | Mini LED™ | J02541|V8|(07)| 01/2017|NG13EN010H - Page 7/38

Table of Contents

Related product manuals