Beurer BM 47 - Manual (Page 25)

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.