Introduction; Warnings - Acteon satelec Piezotome 2 Benutzerhandbuch

I - INTRODUCTION
Congratulations! You have just taken possession
of your P ™ 2.
IEZOTOME
Designed by SATELEC
multifunction device intended for:
• surgical procedures (osteotomy, osteoplasty,
periodontal and implant surgery) with its
P 2 or P
IEZOTOME IEZOTOME
• mechanical ultrasonic treatment (prophylaxis,
periodontics, endodontics) with its N
N L handpiece (according to option).
EWTRON ED
In order to get the most out of this high-
technology device and ensure it has a long
working life, please read this manual carefully
before using or maintaining it.
Points preceded by the symbol
particular attention.
II - WARNINGS
CAUTION:
United States Federal Law restricts the use of
this device solely to qualified, trained and
competent dental health practitioners or under
their supervision.
The tips designed for P
C 2 are not compatible with P
ENTER
I C , and vice versa.
MPLANT ENTER
To reduce the risk of accidents, the precautions
stipulated below must be taken:
5
® , the P 2 is a
IEZOTOME
2 L handpiece.
ED
EWTRON
should be given
2 and I
IEZOTOME
IEZOTOME
Device users:
- Use of the P
qualified, trained and competent dental health
practitioners in the normal context of their
work.
- If you have received this device by error, please
contact the supplier so that it can be removed.
Interactions:
- P
IEZOTOME
and/or the operator has a cardiac stimulator
(pacemaker) or any other active implant (e.g. a
® or cochlear implant).
- The device
electromagnetic compatibility standards. The
user should nevertheless ensure that any
potential electromagnetic interference does
not cause an additional risk (presence of
radiofrequency emitters, electronic devices,
etc.).
- The device is not designed to withstand shocks
delivered by an electric defibrillator.
- Do not attempt to connect to the P
connectors any other accessories than those
supplied by SATELEC.
Electrical connection:
- Your P
IEZOTOME
electric power supply by a certified dental
installation technician.
- Warning: To avoid any risk of electric shock, this
device must be connected to an electrical
power supply with a protective ground.
MPLANT
and - The electric supply to which the device is
connected must comply with the standards in
force in your country.
- If loss of electrical power during use is likely to
generate an unacceptable risk, the device must
be connected to a suitable power source (e.g.
UPS).
2 is restricted solely to
IEZOTOME
2 must not be used if the patient
complies with
2 must be connected to the
applicable
2
IEZOTOME