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TECHNICAL SPECIFICATIONS
Rated power supply
Max Electrical power absorbed
Operational frequency
Intermittent Operation
Water Supply:
Classification:
LED Illumination
Applicable standards
For the correct operation of the device it must be connected to the specific power supply and control electronic circuit,
designed by the manufacturer, by way of suitable hose connection.
The manufacturer promises to provide, upon request, wiring diagrams, component parts lists, calibration instructions or
other information that may be needed by authorised technical service personnel.
The manufacturer reserves the right to bring about modifications at any moment without notice.
Intended Use
Medical device, or a medical device accessory for professional use in Dentistry, possibly assisted by authorised office
personnel. The device is meant for use on dental units complying with the 93/42/EEC Directive and subsequent
amendments made, and installed in locales for medical use with electrical system that complies with the IEC 60364-7-
710 Standards.
IMPORTANT WARNINGS
Before use it is required that the instructions in this manual be read carefully. The use of the device must be performed
with respect for those instructions supplied. For the correct interpretation of the indications in this manual the Italian
text is binding.
The device is not suitable for use with blends of inflammable anaesthetics and oxygen or Nitrous Oxide.
The instrument is provided in a non-sterile state. Before its use see to it suitable cleaning and disinfection.
Use of electrically powered devices may interfere with the operation of pacemakers or other active implants. In
case of doubt on the treatment of patients with implanted cardiac stimulators it is recommended that an expert
in cardiology or other field concerned be consulted.
During use dust and fragments from the patient's oral cavity or from the same device may be projected into the
environment (organic and inorganic dust and metal dust, fragments of the device or its tips and potentially
infected biological material)
- Protect the patient, when possible, by way of the use of the dam.
- Instruct the patient to breathe with the nose in cases where the dam is not applicable.
- Medical personnel must put on suitable personal protection equipment.
Suitably cool the surgical field during use.
In case of visible damage, the emission of unusual noises and/or vibrations or if overheating is noticed, do not
use the device and call authorised technical service assistance.
Ablators must be used exclusively with the inserts provided, with original spare parts or inserts approved by the
manufacturer.
Before use verify that the insert is seated tightly.
Do not work with worn or damaged inserts. Handle the insert with care; wear protective gloves.
Use only inserts with the CE Mark of compliance with 93/42/EEC Directive and subsequent amendments made
with biocompatible materials in compliance with IEC 10993-1 Regulations.
Use only original spare parts and accessories, or those authorised by the manufacturer.
Do not modify the structure of the inserts through bending or filing.
Do not use the handpiece on metal or ceramic dental work the high frequency oscillations could damage it.
Inserts may be particularly pointed or sharp. To avoid accidental puncture wounds or cuts pay particular
attention when the inserts are being attached to the handpiece and remove them when finished.
All manuals and user guides at all-guides.com
"PIEZOSTERIL 6" AND "PIEZOLIGHT 6" SCALER
Piezosteril 6
and subsequent amendments made – (ECC Directive 2007/47)
32 V DC
15 W
25,000 - 32,000 Hz
20 min of work - 10 min of rest
90 - 140 kPa (0.9 - 1.4 bar)
Class IIa (Directive 93/42 CEE)
Class II type B (IEC 60601-1)
IEC 60601-1 – IEC 60601-2 - ISO 10993-1
IEC 60825-1:1993 + A1:1997 + A2:2001
31/01/2011 - 97050183-03-GB - 66
Piezolight 6
3500 K - 20000 mlm
λ 400 ÷ 600 nm
P
< 1 mW
max
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