www.humancaregroup.com
25
ENGLISH
Product label
Symbols on the unit and product label
The product label contains information about
the lift. This label is located on top of the lift.
The product has been tested by an accredited
test institute and complies with the necessary
requirements in accordance with the Medical
Devices Directive for Class 1 products (MDD
93/42/EEC and Regulation 2017/745).
The lift is CE marked and complies with the re-
quirements of EN 10535, EN 60601-1 (Electrical
Safety) and EN 60601-1-2 (EMC).
Wireless transmission equipment, mobile
telephones, etc. must not be used close to the
device as it may affect its function. Particular
caution must be observed when using strong
sources of interference (such as diathermy, etc.)
to ensure that no cables or electrical compo-
nents are placed on or near the device.If in
doubt, ask the person in charge of the equip-
ment or the supplier.
f
CE marking
g
Date of manufacture
h
Manufacturer
j
Max. load
Instructions: Read the instruc-
tions and make sure you under-
stand them before using this
product
l
Article number/reference number
”-XX” = country specific code
n
Serial number
MD
Medical Device
o
Warning
q
The lift contains lead batteries
and electronics and it must be
recycled appropriately
Third party certification marking
(not applicable for all regions and
versions)
p
Type-B product
Switch the product off/Switch the
product on
