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Lanaform Medi Stim Mode D'emploi page 17

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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.
GUIDANCE AND MANUFACTURER'S DECLARATION :
ELECTROMAGNETIC EMISSIONS
The device is intended for use in the electromagnetic environment specified below.
The customer or the user assures that it is used in such an environment.
Emissions test
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissions
lEC 61000-3-2
Voltage fluctuations / flicker
Emissions lEC 61000-3-3
M-MediStim-001.indd 17
EUROPEAN DIRECTIVE ON
MEDICAL PRODUCTS
The device corresponds to the requirements
of the European directive on medical prod-
ucts 93/42/EC and to the legislation on medical
products. In accordance with "the regulation
on medical products 93/42/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 3 years, in-
cluding when used privately.
Compliance
Group 1
Class B
Not applicable
Not applicable
EN
Electromagnetic
environment - guidance
English
FR NL
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19/12/2017 14:45:35

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