Active Living BP-1307 Manual do Proprietário - Página 8
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Specifications
Product Description
Arm-type Fully Automatic Blood Pressure Monitor
BP-1307 (LA137)
Model
Display
LCD Digital Display
Measurement Method
Oscillometric Method
Pressure
Measurement Range
Pulse
Pressure
Measurement Accuracy
Pulse
Pressurisation
Automatic Pressurisation
Memory
120 Memories in Two Groups with Date and Time
Irregular Heartbeat Detection
WHO Classification Indicator
Test Average
Function
Low Battery Detection
Automatic Power-Off
Optional chosen by manufacture
4 AA batteries or Medical AC Aadapter (DC6.0V, 600mA)
Power Source
(recommended, not provided)
Battery Life
Approximately 2 m
Unit Weight
Approx.480g (16.93 oz.) (excluding battery)
Unit Dimensions
Approx.166 x 114x 72mm (6.54
Approx.135 (W)×485(L) mm
Cuff Circumference
(Medium cuff: Fits arm circumference 22-36 cm)
Temperature
Operating Environment
Humidity
Pressure
Warranty
The Blood Pressure Monitor is guaranteed for 2-years from the date of purchase. If the Blood
Pressure Monitor does not function properly due to defective components or poor
workmanship, we will repair or replace it freely. The warranty does not cover damages to your
Blood Pressure Monitor due to improper handling. Please contact local retailer for details.
Size:102.1mm×68.9mm (4.02" x 2.71")
0mmHg～300mmHg
30 to 180 Beats/Minute
±3mmHg
±5%
onths
at 3 tests per day
"
"
"
x 4.49
x 2.83
)(L x W x H)
1
~ 40
(50 ~104 )
0℃
℃
15% ~ 90%RH
Atmospheric Pressure
27
Specifications
Temperature:
Storage Environment
Humidity
Ingress Protection Rating:
IP 22
Internal Powered Equipment,Type BF
Classification:
Specifications are subject to change without notice.
This Blood Pressure Monitor complies with the European regulations and bears the CE mark
"CE 0197".This blood pressure monitor also complies with mainly following standards
(included but not limited):
Safety standard:
EN 60601-1 Medical electrical equipment part 1: General requirements for safety
EMC standard:
EN 60601-1-2 Medical electrical equipment part 1-2: General requirements for
safety- Collateral standard: Electromagnetic compatibility- Requirements and tests
Performance standards:
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.
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.
29
-20 ~55
(-4
~131
)
℃
℃
℉
℉
15% ~ 90%RH
.Cuff is the Applied Part
RoHS2
Compliant
Directive
2011/65/EU
28