HIL
1
–
USER
MANUAL
9
the
general
population;
consult
Safety
Code
6,
obtainable
from
Health
Canada’s
website.
CE
compliance
This
product
is
carrying
the
CE
‐
Mark
in
compliance
withthe
related
European
Directives
(1999/5/EC).
Responsible
for
CEMarking
isIpteq
S.A.,
Avenue
du
Casino
52
1820,
Montreux
–
Switzerland.
NOTE
:
Observe
the
national
local
regulations
in
the
location
where
the
device
is
to
be
used.
This
device
may
be
restricted
for
use
in
some
or
all
member
states
of
the
European
Union
(EU)
Caution:
Exposure
to
Radio
Frequency
Radiation.
The
SAR
limit
of
Europe
is
2.0
W/kg.
Device
types
HIL
1
has
also
been
tested
against
this
SAR
limit.
The
highest
SAR
value
reported
under
this
standard
during
product
certification
when
properly
worn
on
the
body
is
0.147
W/kg.
This
device
was
tested
for
typical
body
‐
worn
operations
with
the
back
of
the
device
contact
with
the
body.
The
use
of
belt
clips,
holsters
and
similar
accessories
should
not
contain
metallic
components
in
its
assembly.
The
use
of
accessories
that
do
not
satisfy
these
requirements
may
not
comply
with
RF
exposure
requirements,
and
should
be
avoided.
Working
environment
The
Electromagnetic
Compliance
(EMC)
of
this
product
has
been
verifiedtypically
for
this
product
category
for
a
so
called
Residential,
Commercial
&Light
Industry
Environment.
Any
other
working
environment
has
not
been
verified
by
Ipteq
and
the
use
of
this
product
in
these
working
environments
is
maybe
restricted
or
cannot
be
recommended.
Possible
consequences
of
the
use
of
this
product
in
not
verified
working
environments
can
be:
Disturbances
of
other
products
or
of
this
product
in
the
nearby
surrounding
area
with
temporarily
malfunction
or
data
loss/corruption
as
result.
Example
of
not
verified
working
environments
and
related
advices:
Industrial
environment
(e.g.
where
3
‐
phase
380V
mains
is
being
used
mainly):
Danger
of
disturbances
of
this
product
due
to
possible
strong
electromagnetic
fields
especially
near
to
big
machinery
or
power
units.
Medical
environment:
The
compliance
to
the
Medical
Product
Directive
has
not
been
verified
by
Ipteq,
therefore
this
product
cannot
be
used
as
a
medical
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