A7 Plus – OPERATOR'S MANUAL
1. GENERAL WARNINGS
• These instructions explain how to correctly use the following dental units:
Please carefully read this manual before using the device.
• The dental units described in this manual are manufactured by CEFLA s.c. - via Selice Prov.le 23/A - 40026 Imola (BO) Italy, a manufacturer
complying with the European Directive on devices.
• These instructions describe all the versions of the dental units with the maximum possible accessories, therefore not all the paragraphs are applicable
to the unit you have purchased.
• It is forbidden to reproduce, store and transmit this publication by any means (electronically, mechanically, by photocopying, translating or in other
ways) without a written authorisation issued by CEFLA s.c..
• The information, technical specifications and illustrations contained in this publication are not binding.
CEFLA s.c. reserves the right to introduce modifications and technical improvements without having to modify these instructions.
• The manufacturer has a company policy of continual development. Although every effort is made to keep technical documentation up-to-date at all
times some of the instructions, specifications and figures given in this manual may slightly differ from the purchased product. The manufacturer
reserves the right to make changes without prior notice.
• The original text is in Italian; translation from the original in Italian.
• This equipment is equipped with a device that prevents liquid back flow.
• The manufacturer’s website contains a list of authorised agents of the various countries.
1.1. SYMBOLS
Note the meaning of the following symbols and expressions:
Type of protection against direct and indirect contact:
Class I.
Type of protection against direct and indirect contact:
Type B.
Equipment in compliance with essential requirements of
directive 93/42/EU and subsequent changes
( Class IIa Medical Device).
Notified body: IMQ spa.
WARNING!
Failure to observe may result in equipment damage or
injury to the user and/or patient.
Accessory in compliance with essential requirements of
directive 93/42/EU and subsequent changes
( Class I Medical Device).
"Consult the instruction manual"
It means that it is advisable to consult the instruction
manual before using that part of the device.
Disposal symbol in accordance with Directive
2012/19/EU
NOTE:
Identifies information that is especially important for the
user and/or the assistant.
“Warning biological hazard”.
It provides information about possible risks of
contamination deriving from contact with fluids, storage of
infected biological waste.
Protective ground contact.
Month and year of construction.
Part that can be sterilised in a steam autoclave up to 135°
C.
DVGW mark (Quality assurance kitemark regarding
supply of drinking water).
"Refer to the instruction manual"
Means that for reasons of safety you need to consult the
instruction manual before using the equipment.
Product/equipment identification code.
Off (a part of the unit).
Equipment equivalent to Class 2 light source.
Ukrainian national symbol of conformity.
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