Canon DelftDI LLS-1, Руководство пользователя

Страница: 5 / 36

User Manual: LLS-1
ODB-118-0070ENG
Page 5 of 36
14-01-2022
Symbols
Symbol Meaning Remarks
Location: Near or on the
type identification plate.
Symbol for separated collection of electrical
and electronic equipment per Directive
2002/96 of the European Parliament and
the Council of the European Union
(Directive on Waste of Electrical and
Electronic Equipment -
WEEE ). If applicable
to the type of device, it indicates legally
imposed obligations within EU member
states, Iceland, Norway and Switzerland
when the equipment is disposed of, at the
end of its life-time.
Owners of marked equipment should
contact the organization that imported
the equipment into their country, when
they want to dispose of the equipment,
at the end of its lifetime. The Directive
prioritizes re-use of equipment over re-
use of components over re-use of
materials over disposal as waste. Article
5 part 2d allows producers to decline
the return of any used equipment that is
or may be biologically or radiologically
contaminated.
Medical device
Legal manufacturer
Date of manufacture
Serial number
UDI code
Unique Device Identification
This mark indicated that this is CLASS II
Equipment according to EN60601-1.
This mark indicated that this is a Type B
Applied Part according to EN60601-1.
Consult Instructions for Use
Consulting the accompanying documents is
a mandatory action.
General warning sign Placed together with a supplementary
symbol or text. The text associated shall
be an affirmative statement (i.e., a
safety notice) describing the principal
risk(s) foreseen (e.g.
“Causes burns”,
“Risk of explosion”, etc.).
The CE Mark is a declaration by the
manufacturer that the product complies with
the requirements of the applicable
European Union (EU) medical device
directive and that the product has been
subject to conformity assessment
procedures as provided in that directive.