Beurer BM 47: ENGLISH
ENGLISH: Beurer BM 47
15
E N G L IS H
Dear
Cust
omer
,
Thank
you
for
choosing
one
of
our
pr
oducts.
Our
name
stands
for
high-quality,
thor
oughly
test
ed
pr
oducts
for
the
applications
in
the
ar
eas
of
heat,
weight,
blood
pr
essur
e,
body
temper
atur
e,
pulse,
gentle
ther
apy,
massage
and
air
.
Please
read
these
instructions
for
use
car
efully
and
keep
them
for
lat
er
use,
be
sur
e
to
mak
e
them
accessible
to
other
users
and
obser
ve
the
information
they
contain.
Best
regar
ds,
Your
Beur
er
Team
1.
Getting
to
know
your
instrument
The
upper
arm
blood
pr
essur
e
monit
or
is
used
for
non-
invasive
measur
ement
and
monit
oring
of
adults’
ar
terial
blood
pr
essur
e.
You
can
use
it
to
measur
e
your
blood
pr
essur
e
quickly
and
easily,
st
oring
the
results
and
displaying
the
pr
ogr
ession
of
readings
together
with
the
aver
age.
A
warning
is
issued
for
anyone
suffering
from
car
diac
ar
-
rhythmi
a.
The
values
det
ermined
ar
e
classified
and
gr
aphically
evalu
-
at
ed
accor
ding
to
WHO
guidelines.
K
eep
these
instructions
car
efully
for
fur
ther
use
and
also
let
other
users
have
access
to
them.
2.
Impor
tant
information
Signs
and
symbols
The
following
symbols
ar
e
used
in
these
instructions
for
use,
on
the
packaging
and
on
the
type
plat
e
for
the
device
and
accessories:
C
aution
Not
e
Not
e
on
impor
tant
information
Follow
instructions
for
use
Type
BF
applied
par
t
Dir
ect
curr
ent
16
D
is
po
sa
l i
n
ac
co
rd
an
ce
w
ith
E
C
D
ire
ct
iv
e
20
02
/9
6/
EC
–
W
EE
E
(W
as
te
E
le
ct
ric
al
a
nd
El
ec
tro
ni
c
Eq
ui
pm
en
t).
Manufactur
er
St
o
rage
RH ≤85%
-20°C
+50°C
Permissible
st
or
age
temper
atur
e
and
humidity
Operating
RH ≤85%
+10°C
+40°C
Permissible
oper
ating
temper
atur
e
and
humidity
K
eep
dr
y
SN
Serial
number
0483
The
CE
labelling
cer
tifies
that
the
pr
od
-
uct
complies
with
the
essential
requir
e-
ments
of
Dir
ective
93/42/EEC
on
medical
pr
oducts.
Advice
on
use
š
In
or
der
to
ensur
e
compar
able
values,
always
measur
e
your
blood
pr
essur
e
at
the
same
time
of
day
.
š
Befor
e
ever
y
measur
ement,
relax
for
about
five
minut
es.
š
If
you
want
to
per
form
sever
al
measur
ements
on
the
same
person,
wait
five
minut
es
between
each
measur
ement.
š
Do
not
tak
e
a
measur
ement
within
30
minut
es
aft
er
eating,
drinking,
smoking
or
ex
er
cising.
š
Repeat
the
measur
ement
if
you
ar
e
unsur
e
of
the
measu
-
red
value.
š
The
measur
ements
tak
en
by
you
ar
e
for
your
information
only
–
they
ar
e
not
a
substitut
e
for
a
medical
examination!
Discuss
the
measur
ements
with
your
doct
or
, and
never
base
any
medical
decisions
on
them
(e.g.
medicines
and
their
administr
ation)!
š
Do
not
use
the
blood
pr
essur
e
monit
or
on
newborns,
pr
egnant
women
or
patients
with
pr
eeclampsia.
š
C
ar
diovascular
diseases
may
lead
to
incorr
ect
measur
e-
ments
or
have
a
detrimental
effect
on
measur
ement
accu
-
racy
. The
same
also
applies
to
ver
y
low
blood
pr
essur
e,
diabet
es,
cir
culat
or
y
disor
ders
and
arrhythmias
as
well
as
chills
or
shaking.
š
The
blood
pr
essur
e
monit
or
must
not
be
used
in
connec
-
tion
with
a
high-fr
equency
sur
gical
unit.
š
Only
use
the
device
on
people
who
have
the
specified
upper
arm
measur
ement
for
the
device.
š
Please
not
e
that
when
inflating,
the
functions
of
the
limb
in
question
may
be
impair
ed.
17
š
During
the
blood
pr
essur
e
measur
ement,
blood
cir
cula
-
tion
must
not
be
st
opped
for
an
unnecessarily
long
time.
If
the
device
malfunctions,
remove
the
cuff
from
the
arm.
š
A
void
any
mechanical
restriction,
compr
ession
or
bending
of
the
cuff
line.
š
Do
not
allow
sustained
pr
essur
e
in
the
cuff
or
frequent
measur
ements.
The
resulting
restriction
of
the
blood
flow
may
cause
injur
y.
š
Ensur
e
that
the
cuff
is
not
placed
on
an
arm
in
which
the
ar
teries
or
veins
ar
e
under
going
medical
tr
eatment,
e.g.
intr
avascular
access
or
ther
apy,
or
an
ar
teriovenous
(A
V)
shunt.
š
Do
not
use
the
cuff
on
people
who
have
under
gone
a
mast
ect
omy
.
š
Do
not
place
the
cuff
over
wounds
as
this
may
cause
fur
ther
injur
y.
š
The
blood
pr
essur
e
monit
or
can
only
be
oper
at
ed
with
batt
eries.
Please
not
e
that
data
transfer
and
data
st
or
age
is
only
possible
when
your
blood
pr
essur
e
monit
or
is
sup
-
plied
with
power
. As
soon
as
the
batt
eries
ar
e
empty,
the
blood
pr
essur
e
monit
or
loses
the
dat
e
and
time.
š
T
o
conser
ve
the
batt
eries,
the
monit
or
switches
off
aut
o-
matically
if
no
butt
ons
ar
e
pr
essed
for
one
minut
e.
š
The
device
is
only
int
ended
for
the
purpose
described
in
these
instructions
for
use.
The
manufactur
er
is
not
liable
for
damage
resulting
from
impr
oper
or
car
eless
use.
S
tor
age
and
C
ar
e
š
The
blood
pr
essur
e
monit
or
is
made
up
of
pr
ecision
elec
-
tr
onic
components.
Accur
acy
of
readings
and
the
instru
-
ment’
s
ser
vice
life
depend
on
car
eful
handling.
–
You
should
pr
ot
ect
the
device
from
impact,
moistur
e,
dir
t,
major
temper
atur
e
fluctuations
and
dir
ect
exposur
e
to
the
sun’
s
rays.
–
Never
dr
op
the
device.
–
Do
not
use
near
str
ong
electr
omagnetic
fields,
i.e.
keep
it
away
from
any
radio
syst
ems
and
mobile
phones.
–
Only
ever
use
the
cuffs
pr
ovided
with
the
monit
or
or
original
replacement
cuffs.
Other
wise
err
oneous
results
will
be
recor
ded.
š
Do
not
pr
ess
any
butt
ons
until
the
cuff
is
in
position.
š
If
the
instrument
is
not
used
for
any
length
of
time,
we
recommend
removing
the
batt
eries.
Advice
on
batt
eries
š
Batt
eries
can
be
fatal
if
swallowed.
You
should
ther
efor
e
st
or
e
the
batt
eries
and
pr
oducts
wher
e
they
ar
e
inacces
-
sible
to
small
childr
en.
If
a
batt
er
y
has
been
swallowed,
call
a
doct
or
immediat
ely
.
š
Batt
eries
should
not
be
char
ged
or
reactivat
ed
with
any
other
means,
nor
should
they
be
tak
en
apar
t,
thr
own
in
the
fir
e
or
shor
t-cir
cuit
ed.
18
š
Remove
the
batt
eries
from
the
instrument
if
they
ar
e
worn
out
or
if
you
ar
e
not
going
to
use
the
instrument
for
any
length
of
time.
This
pr
events
any
damage
as
a
result
of
leakage.
Always
replace
all
the
batt
eries
at
the
same
time.
š
Never
use
differ
ent
types
of
batt
er
y,
batt
er
y
br
ands
or
batt
eries
with
differ
ent
capacities.
You
should
pr
efer
ably
use
alkaline
batt
eries.
Repair
and
disposal
š
Batt
eries
do
not
belong
in
domestic
refuse.
Used
bat
-
teries
should
be
disposed
of
at
the
collection
points
pr
ovided.
š
Never
open
the
instrument.
If
these
instructions
ar
e
not
heeded,
the
warr
anty
will
be
null
and
void.
š
Never
att
empt
to
repair
the
instrument
or
adjust
it
your
-
self.
W
e
can
no
longer
guar
ant
ee
per
fect
functioning
if
you
do.
š
Repairs
may
only
be
per
formed
by
Cust
omer
Ser
vice
or
authoriz
ed
dealers.
However
, always
check
the
batt
eries
and
replace
them
if
necessar
y
prior
to
making
any
com
-
plaint.
š
The
appliance
should
be
disposed
of
accor
ding
to
Regulation
2002/96/EC
–
WEEE
(W
ast
e
Electrical
and
Electr
onic
Equipment).
In
case
of
queries,
please
contact
the
municipal
authorities
responsible
for
wast
e
disposal
in
your
ar
ea.
3.
Unit
description
1.
Cuff
2.
Cuff
line
3.
Cuff
connect
or
4.
ST
AR
T/S
TOP
butt
on
5.
function
butt
ons
-
/
+
6.
LED
WHO
scale
7.
Connection
for
cuff
connect
or
8.
Display
9.
Memor
y
butt
on
M
2
1
3
8
7
6
5
4
9
19
Information
on
the
display:
1.
Time
and
dat
e
2.
S
yst
olic
pr
essur
e
3.
Diast
olic
pr
essur
e
4.
C
alculat
ed
pulse
value
5.
Batt
er
y
replacement
symbol
6.
Memor
y
display:
aver
age
value
(
),
morning
(
),
even
-
ing
(
),
memor
y
space
number
7.
Release
air
8.
WHO
classification
9.
User
memor
y
10.
C
ar
diac
arrhythmia
symbol
4.
P
reparing
the
measur
ement
Inser
t the
batt
eries
š
Open
the
batt
er
y
compar
t-
ment
lid.
š
Inser
t four
1.5
V
AA
(alka
-
line
type
LR6)
batt
eries.
Mak
e
sur
e
that
the
batt
er
-
ies
ar
e
inser
ted
with
the
corr
ect
polarity,
accor
ding
to
the
label.
Do
not
use
rechar
geable
batt
eries.
š
Close
the
batt
er
y
compar
tment
lid
again
car
efully
.
š
W
ith
inser
ted
batt
eries,
the
unit
permanently
displays
the
time,
dat
e
and
select
ed
user
memor
y.
If
the
low
batt
er
y
indicat
or
is
permanently
displayed,
you
can
no
longer
per
form
any
measur
ements
and
must
re
-
place
the
batt
eries.
Once
the
batt
eries
have
been
removed
from
the
unit,
the
time
must
be
set
again.
Used
batt
eries
should
not
be
disposed
of
in
normal
household
wast
e.
Dispose
of
them
via
your
electr
onics
retailer
or
your
local
recycling
point.
You
ar
e
legally
obligat
ed
to
do
so.
Not
e:
The
codes
below
ar
e
ed
on
batt
er
-
ies
containing
harmful
substances:
Pb:
batt
er
y
contains
lead,
Cd:
batt
er
y
contains
cadmium,
Hg:
batt
er
y
contains
mer
cur
y.
1
10
9
8
5
6
7
2
3
4
4
x
A
A
(L
R
6
) 1
,5
V
20
Setting
the
dat
e
and
time
It
is
essential
to
set
the
dat
e
and
time.
Other
wise,
you
will
not
be
able
to
save
your
measur
ed
values
corr
ectly
with
a
dat
e
and
time
and
to
access
them
again
lat
er
.
The
time
is
displayed
in
the
24-hour
format.
To
set
the
dat
e
and
time,
pr
oceed
as
follows:
š
P
re
ss
th
e
m
em
or
y
bu
tto
n
M
fo
r a
t l
ea
st
th
re
e
se
co
nd
s.
š
T
he
y
ea
r d
is
pl
ay
w
ill
s
ta
rt
to
fl
as
h.
S
et
th
e
ye
ar
w
ith
th
e
fu
nc
-
tio
n
bu
tto
ns
-
/
+
a
nd
c
on
fir
m
w
ith
th
e
m
em
or
y
bu
tto
n
M
.
š
S
et
th
e
m
on
th
, d
ay
, h
ou
r a
nd
m
in
ut
es
a
nd
c
on
fir
m
e
ac
h
se
tti
ng
w
ith
th
e
m
em
or
y
bu
tto
n
M
.
5.
Measuring
blood
pr
essur
e
Please
ensur
e
the
unit
is
at
room
temper
atur
e
befor
e
meas
-
uring.
A
ttach
the
cuff
Place
the
cuff
on
to
the
bar
e
left
upper
arm.
The
cir
culation
of
the
arm
must
not
be
hinder
ed
by
tight
clothing
or
similar
.
The
cuff
must
be
placed
on
the
upper
arm
so
that
the
bott
om
edge
is
positioned
2
– 3
cm
above
the
elbow
and
over
the
ar
ter
y.
The
line
points
to
the
centr
e
of
the
palm.
N
ow
ti
gh
te
n
th
e
fre
e
en
d
of
th
e
cu
ff,
but
mak
e
sur
e
that
it
is
not
too
tight
ar
ound
the
arm
and
close
the
Velcr
o
fast
ener
. The
cuff
should
be
fast
ened
so
that
two
fingers
fit
under
the
cuff.
Now
inser
t the
cuff
line
int
o
the
connection
for
the
cuff
connect
or
.
C
aution:
The
unit
may
only
be
oper
at
ed
with
the
original
cuff.
The
cuff
is
suitable
for
an
arm
cir
cumfer
ence
of
22
to
35
cm.
A
lar
ger
cuff
for
upper
arm
cir
cumfer
ences
from
30
to
42
cm
is
available
from
retailers
or
the
ser
vice
addr
ess
under
or
der
no.
162.795.
21
Please
ensur
e
that
the
cuff
is
not
bent
at
any
point
and
that
the
reinfor
ced
end
lies
flat
against
your
arm.
Adopt
the
corr
ect
postur
e
š
Befor
e
ever
y
measur
ement,
relax
for
about
five
minut
es.
Other
wise
deviations
can
occur
.
š
Y
ou
can
per
form
the
measur
ement
while
sitting
or
lying.
Mak
e
sur
e
that
the
cuff
is
at
hear
t level.
š
T
o
carr
y
out
a
blood
pr
essur
e
measur
ement,
mak
e
sur
e
you
ar
e
sitting
comfor
tably
with
your
arms
and
back
lean
-
ing
on
something.
Do
not
cr
oss
your
legs.
Place
your
feet
flat
on
the
gr
ound.
š
T
o
avoid
falsifying
the
measuring
result,
it
is
impor
tant
to
remain
still
during
the
measur
ement
and
not
to
speak!
Selecting
memor
y
Pr
ess
the
-
or
+
function
butt
on.
Select
the
desir
ed
user
memor
y
(
...
)
by
pr
essing
the
-
/
+
function
butt
on.
You
have
4
memories
with
30
spaces
each
to
st
or
e
the
measur
ements
of
4
differ
ent
people
separ
at
ely
. Confirm
your
selection
with
the
ST
AR
T/S
TOP
butt
on
.
P
er
forming
the
blood
pr
essur
e
measur
ement
š
As
described
befor
e,
attach
the
cuff
and
adopt
the
pos
-
tur
e
in
which
you
want
to
per
form
the
measur
ement.
š
S
tar
t the
blood
pr
essur
e
monit
or
with
the
ST
AR
T/S
TOP
butt
on
. Aft
er
the
full-scr
een
display,
the
most
recently
st
or
ed
measur
ement
appears.
If
ther
e
is
no
measur
ement
in
the
memor
y,
the
unit
displays
the
value
“0”
.
š
The
cuff
aut
omatically
inflat
es.
The
cuff
’s
air
pr
essur
e
is
slowly
released.
If
the
device
alr
eady
recognise
a
ten
-
dency
for
high
blood
pr
essur
e,
it
will
reinflat
e
and
incr
ease
the
cuff
pr
essur
e
again.
As
soon
as
a
pulse
is
found,
the
pulse
symbol
is
displayed.
š
S
yst
olic
pr
essur
e,
diast
olic
pr
essur
e
and
pulse
readings
ar
e
displayed.
š
Measuring
can
be
cancelled
at
any
time
by
pr
essing
the
ST
AR
T/S
TOP
butt
on
.
22
š
_
appears
if
the
measur
ement
has
not
been
per
formed
pr
operly
. T
ak
e
not
e
of
the
chapt
er
on
err
or
messages/
tr
ouble-shooting
in
these
instructions
for
use
and
repeat
the
measur
ement.
š
The
measur
ement
is
aut
omatically
st
or
ed.
š
T
o
switch
off,
pr
ess
the
ST
AR
T/S
TOP
butt
on
.
If
you
for
get
to
turn
off
the
unit,
it
will
switch
off
aut
omati-
cally
aft
er
appr
ox.
1
minut
e.
W
ait
at
least
5
minut
es
befor
e
taking
another
measur
ement.
6.
E
valuating
results
C
ar
diac
arrhythmia:
This
unit
can
identify
pot
ential
disruption
of
the
hear
t rhythm
when
measuring
and
if
necessar
y,
indicat
es
this
aft
er
the
measur
ement
with
the
symbol
. This
can
be
an
indicat
or
for
arrhythmia.
Arrhythmia
is
an
illness
in
which
the
hear
t
rhythm
is
abnormal
because
of
flaws
in
the
bioelectrical
syst
em
that
regulat
es
the
hear
tbeat.
The
sympt
oms
(skipped
or
pr
ematur
e
hear
t beats,
pulse
being
slow
or
too
fast)
can
be
caused
by
fact
ors
such
as
hear
t disease,
age,
physical
mak
e-up,
ex
cess
stimulants,
str
ess
or
lack
of
sleep.
Ar
-
rhythmi
a
can
only
be
det
ermined
thr
ough
an
examination
by
your
doct
or
. If
the
symbol
is
shown
on
the
display
aft
er
the
measur
ement
has
been
tak
en,
it
should
be
repeat
ed.
Please
ensur
e
that
you
rest
for
5
minut
es
befor
ehand
and
do
not
speak
or
move
during
the
measur
ement.
If
the
symbol
appears
frequently,
please
consult
your
doct
or
. Self-
diagnosis
and
treatment
based
on
the
measur
ements
can
be
danger
ous.
Always
follow
your
GP’
s
instructions.
WHO
classification:
In
accor
dance
with
the
guidelines/definitions
of
the
W
orld
Heath
Or
ganization
and
the
lat
est
findings,
the
measur
e-
Blood
pr
essur
e
value
cat
egor
y
S
yst
ole
(in
mmHg)
Dia
st
ole
(in
mmHg)
Action
Gr
ade
3:
sever
e
hyper
tension
>
=
180
>
=
110
seek
medical
att
ention
Gr
ade
2:
moder
at
e
hyper
tension
160
–
179
100
–
109
see
k
medical
att
ention
Gr
ade
1:
mild
hyper
tension
140
– 159
90
–
99
regular
monit
oring
by
doct
or
High
normal
130
– 139
85
–
89
regular
monit
oring
by
doct
or
Normal
120
– 129
80
–
84
self-monit
oring
Optimal
<
120
<
80
self-monit
oring
Sour
ce:
WHO
, 1999
23
ments
can
be
classified
and
assessed
accor
ding
to
the
following
table.
However
, these
standar
d
values
ser
ve
only
as
a
gener
al
guideline,
as
the
individual
blood
pr
essur
e
varies
in
differ
ent
people
and
differ
ent
age
gr
oups
etc.
It
is
impor
tant
to
consult
your
doct
or
regularly
for
advice.
Your
doct
or
will
tell
you
your
individual
values
for
normal
blood
pr
essur
e
as
well
as
the
value
above
which
your
blood
pr
essur
e
is
classified
as
danger
ous.
The
bar
char
t on
the
display
and
the
scale
on
the
unit
show
which
cat
egor
y
the
recor
ded
BMI
values
fall
int
o.
If
the
values
of
syst
ole
and
diast
ole
fall
int
o
two
differ
ent
WHO
cat
egories
(e.g.
syst
ole
in
the
‘High
normal’
cat
egor
y
and
diast
ole
in
the
‘Normal’
cat
egor
y),
the
gr
aphical
WHO
classification
on
the
unit
always
shows
the
higher
cat
egor
y;
for
the
example
given
this
would
be
‘High
normal’
.
7.
Saving,
displaying
and
deleting
measur
ements
š
The
results
of
ever
y
successful
measur
ement
ar
e
st
or
ed
together
with
the
dat
e
and
time.
If
ther
e
ar
e
mor
e
than
30
measur
ements,
the
oldest
measur
ements
ar
e
lost.
š
P
ress
the
-
or
+
function
butt
on.
Select
the
desir
ed
user
memor
y
(
...
)
by
pr
essing
the
-/+
function
butt
on.
Confirm
your
selection
with
the
ST
AR
T/S
TOP
butt
on
.
š
If
you
pr
ess
the
memor
y
butt
on
M
, the
aver
age
value
of
all
the
st
or
ed
measur
ed
values
in
the
user
memor
y
will
be
displayed.
If
you
pr
ess
the
memor
y
butt
on
M
again,
the
aver
age
value
of
the
morning
measur
ements
for
the
last
7
days
will
be
displayed.
(morning:
5.00
–
9.00,
display
).
If
you
pr
ess
the
memor
y
butt
on
M
again,
the
aver
age
value
of
the
evening
measur
ements
for
the
last
7
days
will
be
displayed.
(evening:
18.00
–
20.00,
display
).
If
you
continue
to
pr
ess
the
memor
y
butt
on
M
, the
most
recent
individual
measur
ed
values
ar
e
displayed
in
turn
with
the
dat
e
and
time.
š
Y
ou
c
an
d
el
et
e
th
e
m
em
or
y
by
p
re
ss
in
g
an
d
ho
ld
in
g
th
e
m
em
or
y
bu
tto
n
M
fo
r 3
s
ec
on
ds
.
š
T
o
switch
off,
pr
ess
the
ST
AR
T/S
TOP
butt
on
.
š
If
you
for
get
to
switch
off
the
unit,
it
will
switch
off
aut
o-
matically
aft
er
1
minut
e.
8.
Err
or
message/tr
ouble
shooting
In
the
event
of
err
ors,
the
err
or
message
_
appears
on
the
display
.
Err
or
messages
may
appear
if:
š
syst
olic
or
diast
olic
pr
essur
e
could
not
be
measur
ed
(
or
appears
on
the
display)
š
syst
olic
or
diast
olic
pr
essur
e
was
outside
the
measur
e-
ment
range
(
or
Lo
appears
on
the
display)
š
the
cuff
is
fast
ened
too
tightly
or
loosely
(
or
appears
on
the
display)
š
the
pump
pr
essur
e
is
higher
than
300
mmHg
(
appears
on
the
display)
24
š
pumping
up
tak
es
longer
than
160
seconds
(
appears
on
the
display)
š
ther
e
is
a
syst
em
or
device
err
or
(
,
,
or
appears
on
the
display)
š
the
batt
eries
ar
e
almost
empty
.
In
such
cases,
repeat
the
measur
ement.
Ensur
e
that
you
do
not
move
or
speak.
If
necessar
y,
reinser
t or
replace
the
batt
eries.
T
echnical
alarm
–
description
Should
the
recor
ded
blood
pr
essur
e
(syst
olic
or
diast
olic)
lie
outside
the
limits
specified
in
the
section
“T
echnical
speci
-
fications”
, the
technical
alarm
will
appear
on
the
display
indicating
either
“
”
or
“
Lo
”.
In
such
cases,
you
should
seek
medical
assistance
and
check
the
accur
acy
of
your
pr
oce
-
dur
e.
The
limit
values
for
the
technical
alarm
ar
e
fact
or
y
set
and
cannot
be
adjust
ed
or
deactivat
ed.
These
alarm
limit
val
-
ues
ar
e
accor
ded
second
priority
under
the
standar
d
IEC
60601-1-8.
The
technical
alarm
is
a
non-locking
alarm
and
must
not
be
reset.
The
signal
shown
on
the
display
will
disappear
aut
o-
matically
aft
er
about
8
seconds.
9.
Cle
aning
and
st
oring
the
unit
š
Clean
your
blood
pr
essur
e
device
car
efully
with
a
slightly
damp
cloth
only
.
š
Do
not
use
any
cleaning
agents
or
solvents.
š
Und
er
no
cir
cumstances
should
you
hold
the
unit
under
wat
er
, as
this
can
cause
liquid
to
ent
er
and
damage
the
uni
t.
š
If
you
st
or
e
the
unit,
no
heav
y
objects
should
be
placed
on
top
of
it.
Remove
the
batt
eries.
The
cuff
line
should
not
be
bent
sharply
.
10.
Technical
specifications
Model
no.
BM
47
Measur
ement
method
Oscillometric,
non-invasive
blood
pr
essur
e
measur
ement
on
the
upper
arm
Measur
ement
range
Cuff
pr
essur
e
0-300
mmHg
,
syst
olic
60-260
mmHg
,
diast
olic
40-199
mmH
g,
Pulse
40-180
beats/minut
e
Display
accur
acy
S
yst
olic
±
3
mmHg
,
diast
olic
±
3
mmHg,
pulse
±
5
%
of
the
value
shown
25
Measur
ement
inac
-
cur
acy
Max.
permissible
standar
d
deviation
accor
ding
to
clinical
testing:
syst
olic
8
mmH
g
/diast
olic
8
mmH
g
Memor
y
4
x
30
memor
y
spaces
Dimensions
L
134
mm
x
W
102
mm
x
H
52,5
mm
W
eight
Appr
oximat
ely
280g
(without
batt
er
-
ies
and
cuff
)
Cuff
siz
e
22
to
35
cm
Permissible
oper
ating
conditions
+10
°C
to
+40
°C,
≤
85
%
relative
air
humidity
(non-condensing)
Permissible
st
or
age
conditions
-20
°C
to
+50
°C,
≤
85
%
relative
air
humidity,
800-1050
hP
a
ambient
pr
essur
e
Power
supply
4
x
1,5
V
AA
batt
eries
Batt
er
y
life
For
appr
ox.
500
measur
ements,
depending
on
the
blood
pr
essur
e
level
and/or
pump
pr
essur
e
Accessories
Instruction
for
use,
4
x
1.5
V
AA
bat
-
teries,
st
or
age
pouch
Classification
Int
ernal
supply,
IPX0,
no
AP
or
APG
, continuous
oper
ation,
type
BF
applied
par
t
Technical
information
is
subject
to
change
without
notifica
-
tion
to
allow
for
updat
es.
š
This
unit
is
in
line
with
Eur
opean
S
tandar
d
EN
60601-
1-2
and
is
subject
to
par
ticular
pr
ecautions
with
regar
d
to
electr
omagnetic
compatibility
(EMC).
Please
not
e
that
por
table
and
mobile
HF
communication
syst
ems
may
int
er
fer
e
with
this
unit.
Mor
e
details
can
be
request
ed
from
the
stat
ed
Cust
omer
Ser
vice
addr
ess
or
found
at
the
end
of
the
instructions
for
use.
š
This
device
is
in
line
with
the
EU
Medical
Devices
Dir
ec
-
tive
93/42/EC,
the
„Medizinpr
odukt
egesetz“
(German
Medical
Devices
Act)
and
the
standar
ds
EN
1060-1
(non-
invasive
sphygmomanomet
ers,
Par
t 1:
Gener
al
requir
e-
ments),
EN
1060-3
(non-invasive
sphygmomanomet
ers,
Par
t 3:
Supplementar
y
requir
ements
for
electr
o-mechani
-
cal
blood
pr
essur
e
measuring
syst
ems)
and
IEC
80601-2-
30
(Medical
electrical
equipment
–
Par
t 2
–
30:
Par
ticular
requir
ements
for
the
safety
and
essential
per
formance
of
aut
omat
ed
non-invasive
blood
pr
essur
e
monit
ors).
š
The
accur
acy
of
this
blood
pr
essur
e
monit
or
has
been
car
efully
check
ed
and
developed
with
regar
d
to
a
long
useful
life.
If
using
the
device
for
commer
cial
medical
pur
-
poses,
it
must
be
regularly
test
ed
for
accur
acy
by
appr
o-
priat
e
means.
Pr
ecise
instructions
for
checking
accur
acy
may
be
request
ed
from
the
ser
vice
addr
ess.
