1.2 MARKING
The lift device is manufactured in compliance with the relevant EC directives applicable on the date of
entering the market. Considered a "medical device" pursuant to article 2, point 1), letter a), first
paragraph of directive 2007/47/EC, the device carries a specific identification plate which, in addition to
the specific technical data also includes the CE marking, guarantee of the compliance of the device to
the directives/standards referred to the enclosed Declaration of Conformity.
The plate, a facsimile of which is shown here, is stamped with the data indicating the specific model and
unit.
To Next Page
Loading...
