Anthos A3 Plus - General Warnings and Safety; Symbols and Icon Interpretation

A3 PLUS - A5 - A6 PLUS - L6
SURGICAL SINGLE CART
4
EN
1. GENERAL WARNINGS
• These instructions explain how to correctly use the following dental unit:
A3 PLUS (SN.71IF, 71IG)
A5
A6 PLUS
L6
A3 PLUS CONTINENTAL
(SN.71HU)
A5 CONTINENTAL
(SN.71IA)
A6 PLUS CONTINENTAL
(SN.71HW)
L6 CONTINENTAL
(SN.71H1)
A3 PLUS INTERNATIONAL
(SN.71HV)
A5 INTERNATIONAL
(SN.71IB)
A6 PLUS INTERNATIONAL
(SN.71HX)
L6 INTERNATIONAL
(SN.71H2)
A5 CART
(SN.71IC)
L6 SIDE DELIVERY
(SN.71H3)
A5 SINGLE CART
(SN.71IE)
L6 CONTINENTAL, HYBRID
version (SN.71H4)
A5 IDRICO SINGOLO
(SN.71ID)
SURGICAL SINGLE CART
(SN. 71HS)
Please carefully read this manual before using the device.
• The dental units described in this manual are manufactured by CEFLA s.c. - via Selice Provinciale 23/A - 40026 Imola (BO) Italia, a manufacturer
complying with the European Directive on medical 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.
• 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; this is a translation from the original in Italian.
• The manufacturer’s website contains a list of authorised agents of the various countries.
• EU REG. 2016/679 - GDPR INFORMATION: we inform the user that by activating the connection of the devices to the Internet, the device will
automatically direct data to the Easycheck and Di.V.A. web portals. CEFLA s.c. declares that this data collection exclusively concerns telemetry data
on the operation of the devices, that this data collection does not concern and does not involve the processing of personal data. The Easycheck and
Di.V.A. web portals comply with the requirements of ISDP©10003:2020 - Control rules and requirements for the certification of data processing
processes with regard to the assessment of respect for the fundamental rights of natural persons and the free movement of data.
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.
Accessory compliant with the requirements set out by
Regulation
(EU) 2017/745.
(Class I Medical Device).
WARNING!
Failure to observe may result in equipment damage or
injury to the user and/or patient.
Disposal symbol in accordance with Directive
2012/19/EU.
“See the operator’s manual”
It indicates that it is advisable to consult the operator’s
manual
before using the relevant part of the equipment.
WARNING: biological hazard.
It provides information about possible risks of
contamination deriving from contact with fluids, storage of
infected biological waste.
NOTE:
Identifies information that is especially important for the
user and/or the assistant.
Manufacturer.
Protective ground contact.
Equipment date of manufacture.
Alternating current.
Device serial number.
Part that can be sterilized in a steam autoclave up to 135°
C.
ON / OFF button.
Product/equipment identification code.
"Refer to the operator's manual"
It means that for reasons of safety you need to consult
the operator’s manual before using the equipment.
Pushing prohibited.
Off (a part of the unit).
WARNING: foot crushing hazard.