Anthos SMART TOUCH R7, Operating Instruction

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42 42 EN
R7
- OPERATING INSTRUCTION
Turbine rotation speed change.
With the instrument in working position, select turbine speed change mode
by touching the following icon buttons:
Linear change proportional to the movement of the
the foot control lever
ON/OFF change that results in delivery of the maximum power
set upon activation of the foot control lever
The active mode icon is shown on the TOUCH DISPLAY.
NOTE : the data is automatically stored.
Instrument spray control button.
With the instrument in working position, select the type of spray delivered
by the instrument by touching the following icon buttons:
Water + air spray operation
Water-only spray operation
Operation without spray
The change is cyclic each time the button is touched and the active mode icon
is shown on the TOUCH DISPLAY.
NOTE : the data is automatically stored.
Removable cord
The turbine has a removable cord to ease cleaning (see paragraph 5.).
Cleaning and care.
Refer to the specific instructions furnished with the instrument.
It is recommended to use Daily Oil ( CEFLA s.c. ) for lubrication.
Sterilization.
Only instrument handpiece: see paragraph 1.5.
WARNING!
Carefully read the operating instructions supplied with the handpiece before attempting to sterilize.
Instructions for use.
WARNING!
• The instrument is supplied NOT STERILE and must be sterilized before use (see paragraph 1.5.).
Before performing sterilization, check the instructions for use included with the device.
• Only for American and Canadian markets: instruments must be FDA-approved.
• The turbine must never be started without attaching the chuck or false chuck.
• The chuck release button must be held down during operation!
Friction between the button and micromotor rotor overheats the head and may cause burns.
• The patient’s internal tissues (tongue, cheeks, lips, etc...) must be protected against contact with the button by using suitable instruments (mirror,
etc...).
• The chucks and various instruments attached to the handpieces must comply to the standard ISO 10993-1 Biological evaluation of medical devices.