29
28
30
Specifications
Specifications
Maintenance
4. Cuff Cleaning and Disinfection:
A) Spread the cuff (skin-contact surface) upwards onto a clean table. Use a damp clean cloth
(water-based) to wipe the skin-contact surface with a force.
B) Soak the cloth clean with drinking water and wring it dry. Repeat A) with the damp cloth
(water-based) for 3 times.
C) Apply 70%-80% alcohol to a new cloth (or 75% alcohol cotton-ball), use it to
wipe the skin-contact surface with a force. Then soak the cloth with the alcohol again
(or change a new 75% alcohol cotton-ball), repeat the disinfection procedure for 3 times.
D
)
When
the
disinfection
towards
the
skin
-
contactsurface is
finished
,
wipe
thenon
-
skin
contact surface
with
a
cloth (alcohol-based) or alcohol cotton-ball
thoroughly
for
3 times.
E
)
Leave
the
cuff
naturally
dry
,
then
it
is
ready
for
reuse
.
Notice: Do not soak in water or splash water on it.
5. Do not use petrol, thinners or similar solvents.
6. Remove batteries when not in operation for an extended period of time.
7. Do not disassemble product.
8. It is recommended the performance should be checked every 2 years.
9. Expected service life: Approximately three years at 10 tests per day.
10.No service and maintenance while it is in use and maintenance only be performed by service
personnel. Service and maintenance require parts, repair, technical support will be provided.
Maintenance
27
Product Description
Model
Display
Measurement Method
Oscillometric Method
Arm-type Fully Automatic Blood Pressure Monitor
BM 92
Pressurization
Memory
Function
Power Source
Battery Life
Unit Weight
Unit Dimensions
Cuff Circumference
2x120 Memories in Two Groups with Date and Time
Irregular Heartbeat Detection
WHO Classification Indicator
Low Battery Detection
Automatic Power-Off
Voice
4 AAA batteries
Approximately 2 months at 3 tests per day
Approx.180g (6.35 oz.) (excluding battery)
Operating Environment
Automatic Pressurization
Humidity
Temperature
10 ~ 40 (50 ~104 )
℃
℃
℉
℉
15% ~ 93% RH
Storage Environment
Humidity
Ingress Protection
rating:
Battery Shelf life:
Battery Storage
Temperature:
Temperature:
IP 21,Indoor Used Only
60 months
-25
℃
~55
℃
(-13
℉
~131
℉
)
-25 ~55 (-13 ~131 )
℃
℃
℉
℉
Measurement Range
Pulse
Systolic Pressure
Pulse
60mmHg
～
2
60
mmHg
30 ~ 180 Beats/Minute
±
5%
Diastolic Pressure
40mmHg
～
20
0
mmHg
Pressure
0mmHg
～
299mmHg
Pressure
±
3mmHg
Backlighting
≤
93% RH
Medium cuff: Fits arm circumference 22-36 cm
Operating Environment
Pressure
800hPa~1060hPa
Bluetooth
Last 7 days average
1. Avoid dropping, slamming, or throwing the unit.
2. Avoid extreme temperatures. Do not expose unit directly under sunshine.
3. When cleaning the unit, use a soft fabric and lightly wipe with mild detergent.
Use a damp cloth to remove dirt and excess detergent. If the previous cleaning instructions
are not successful, repeat several times until the visible dirt is removed.
Approx.125mm X 95mm X 44mm(4.92" x 3.74" x 1.73"
）
LCD Digital Display Size:71mm x 76mm(
2.80" x 2.99")
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 waste at the end of its life. To prevent potential harm to the 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 government office for details regarding how this item can
be disposed in an environmentally safe recycling center.
Business users should contact their supplier and check the terms and conditions of the
purchasing agreement. This product should not be mixed with other commercial wastes
for disposal. This product is free of hazardous materials.
Specifications are subject to change without notice.
Safety
Standard
(
included
but
not
limited
):
1
.
IEC
80601
-
2
-
30
,
medical
electrical
equipment
-
part
2
-
30
:
particular
requirements
for
the
basic
safety
and
essential
performance
of
automated
noninvasive
sphygmomanometers
. (
Cardiovascular
)
2
.
ISO
81060
-
2
,
non
-
invasive
sphygmomanometers
-
part
2
:
clinical
validation
of
automated
measurement
type
. (
Cardiovascular
)
3
.
AAMI
/
ANSI
ES
60601
-
1
:
2005
/(
R
)
2012
and
C1
:
2009
/(
R
)
2012
and
,
a2
:
2010
/(
r
)
2012
(
consolidated
text
)
medical
electrical
equipment
--
part
1
:
general
requirements
for
basic
safety
and
essential
performance
4
.
AAMI
/
ANSI
/
IEC
60601
-
1
-
2
,
Medical
Electrical
Equipment
--
Part
1
-
2
:
General
Requirements
For
Basic
Safety
And
Essential
Performance
--
Collateral
Standard
:
Electromagnetic
Disturbances
--
Requirements
And
Tests
(
General
II
(
ES
/
EMC
)).
5
.
IEC
60601
-
1
-
11
,
medical
electrical
equipment
-
part
1
-
11
:
general
requirements
for
basic
safety
and
essential
performance
-
collateral
standard
:
requirements
for
medical
electrical
equipment
and
medical
electrical
systems
used
in
the
home
healthcare
environment
.
收缩
压
Average for the last 7 days
Afternoon average for the last 7 days
HSD