.1
Specifications
Specifications
Product Description
Model
Display
Measurement Method
Measurement Range
Measurement Accuracy
Pressurization
Memory
Function
Power Source
Battery Life
Unit Weighl
Unit Dimensions
Cuo-Circumference
Operating Eovirooment
Arm-type Fully Automatic Blood
Pre
ss
ure
Monitor
80-5101
LCD Digital Display Size: 102. 1 mm X68.9mm (4.02" x 2.
71
~')
Oscillometric Method
Pressure
OmmH
g-
300mmHg
Pulse
30
to
180 Bcats/Minute
Pressure
±3mmHg
Pulse
I ± 5%
Automatic Pressurization
120
Memorie:o.
in
Two Groups
v.'ith
Dale
and
Time
lrregular
Hl.!artbc:at
Dcl~ction
WHO
Classification Indicator
Last 3 Tests Average
Low Battery Detection
Automatic Power-Off
4
AA
batteries or Medical
AC
Aadapter
(DC6.0V, 600mA)
(recommended. nol provided)
Appro:<imatcly 2 months
at
31CS1S
per day
Approx.480g (16.93 oz.)
("xeluding
ballery)
Approx.164 x
II0x
58mm (6.46" x 4.33" x
2.28")(L
x W x
H)
Approx.135 (W) X485(L) mm
(Medium cuff: Fil S
3rm
circurnfen:ncc 22· 36 cm)
Temperature
10"C
-40"c
(50r
-
104r)
Humidity
15%.-90%RH
Pr
essure
Atmospheric
Pre
ss
ure
Storage Environment
Temperature:
-20'C- 55'C (-4"F
-131"F)
HumidilY
15%-90%RH
Ingress Protection
IP22
Rating
Classification:
Internal Powered Equipment,Type
BF[!].
Cuffis
the
Applied
Part
Specifications
are
subject
10
change
without
notice
.
International
Standards:
AAMI
1
ANSI
SP
I
0:2002/(R)
2008
& 2002/A I :
2003/(R)2008
& 20021
A2:2006/(R)2008
Manual,
eleclronic
,
or
automated
sphygmomanometers
European
Direetive
93
/42
EEC
for
Medical
Products
Act
EN
6060
I-I
Medical
electrical
equipment
part
I:
General
requirements
for
safety
EN
6060
1-1·2
Medical
electrical
equipment
part
1-2:
General
requirements
for
safety-
Collateral
standard:
Electromagnetic
compatibility-
Requirements
and
tests
EN
1060·1
Non-invasive
sphygmomanometers·
General
requirements
EN
1060-3
Non-invasive
sphygmomanometers
-
Supplementary
requirements
for
electromechanical
blood
pressure
measuring
systems.
EN
1060-4
Non-invasive
sphygmomanometers
-
Test
procedures
to
determine
the
overall
system accuracy
of
automated
non-invasive sphygmomanometers .
)t
Correct
Disposal
of
This
Product
(Waste
Electrical
&
Electronic
Equipment)
_
This
marking
shown
on
the
product
indicates
that
it
should
not
be
disposed
with
other
household
wasleat
the
end
of
its
life. To
prevent
potential
harm
to
Ihe
environment
or
to
human
health,
please
separate
this
product
from
other
types
of
wastes
and
recycle
it
responsibly.
When
disposing
this
type
of
product,
contact
the
retailer
where
product
was
purchased
or
contact
your
local
governmenl
office
for
details
regarding
how
Ihis
item
can
be
disposcd
in
an
environmentally
safe
recycling
cenler.
Business
users
should
contact
their
supplier
and
check
the
terms
and
conditions
of
the
purchasing
agreement.
This
produci
should
not
be
mixed
with
other
commercial
wastes
for
disposal.
This
product
is free
of
hazardous
materials.
a.
.
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