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as long as a copy of the proof of purchase can
be supplied.
On receipt, LANAFORM will repair or replace
your appliance at its discretion and will return
it to you. The guarantee is only valid through
LANAFORM’s Service Centre. Any attempt to
maintain this product by a person other than
LANAFORM’s Service Centre will render this
guarantee void.
EUROPEAN DIRECTIVE ON
MEDICAL PRODUCTS
The device corresponds to the requirements
of the European directive on medical prod-
ucts //EC and to the legislation on medical
products. In accordance with “the regulation
on medical products //EC”, regular tech-
nical checks must be carried out if the device is
used for professional or commercial purposes.
We recommend asking the manufacturer to
carry out a technical check every  years, in-
cluding when used privately.
GUIDANCE AND MANUFACTURER’S DECLARATION :
ELECTROMAGNETIC EMISSIONS
The device is intended for use in the electromagnetic environment specied below.
The customer or the user assures that it is used in such an environment.
Emissions test Compliance
Electromagnetic
environment - guidance
RF emissions CISPR 11 Group 1
RF emissions CISPR 11 Class B
Harmonic emissions
lEC 61000-3-2
Not applicable
Voltage uctuations / icker
Emissions lEC 61000-3-3
Not applicable
E-IM-MediStim-001.indd 17 19/12/2017 14:45:35
17


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