________________________________________________________________________________________________________________________________
TensioMed®
TensioDay
Plus™
9
The
symbols
on
the
bottom
of
the
device
are
sown
in
Figure
2.
5
Name
of
the
Manufacturer
6
The
name
of
the
device
7
The
type
ID
of
the
device
8
The
classification
of
the
MDD
requirements:
II
a
9
The
nominal
voltage
range
applicable
with
batteries
10
The
classification
of
the
protection
against
electric
shock
Classification:
patient's
side:
CF.
11
Calling
the
attention
to
read
thoroughly
the
present
User's
Manual
12
Certification
mark
guaranteeing
that
the
apparatus
complies
with
the
prescriptions
and
requirements
of
the
European
Union.
13
Serial
number
14
Operating
ambient
temperature
range
15
Year
of
the
manufacturing
16
Head
office
of
the
Manufacturer
17
The
permanently
placed
in
unused
equipment
must
be
collected
in
order
to
get
more
efficient
reuse
and
recycling
,
as
well
as
harmful
effects
on
human
health
and
for
the
environment
of
the
ingredients
are
selectively
18
Level
of
protection
against
any
liquid
or
grainy
material
filtering
into
the
device
(IP
N
1
N
2
)
N
1
=2:
Protected
against
solid
foreign
objects
of
12,5mm
and
greater
N
2
=2:
Protection
against
vertically
falling
water
drops
when
enclosure
tilted
up
to
15°
Figure
2.
13
14
9
8
10
11
12
5
6
7
15
16
18
17
