AUTOLIFT ONDA OB Series, Instruction Manual

Page: 3 / 38

GENERAL WARNINGS
1
Lift
DEVICE
ONDA
MODEL
3
1.1 MANUFACTURER
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.
CUSTOMER NAME:
INSTALLER NAME:
DATE OF INSTALLATION:
SERIAL NUMBER:
IT IS PROHIBITED TO REMOVE OR TAMPER WITH THE
IDENTIFICATION PLATE.
AUTOLIFT SRL
Via Trentin8
– 46020 Pegognaga (MN) - Italy
Tel. +39 0376 550375
– info@autoliftsrl.com