Instructions / Assembly

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Limited Warranty
The Blood Pressure Monitor is guaranteed for 1-year from the date of purchase.Within the
warranty period, should there be any manufacturing defect found and repair is needed,
please contact your local retailer accordingly. The warranty does not cover damages
to your Blood Pressue Monitor due to improper handling. Please contact local retailer
for details.
29
Specifications
Product Description
Model
Display
Measurement Method
Measurement Range
Pulse
Measurement Accuracy
Pressurization
Memory
Function
Power Source
Battery Life
Unit Weight
Unit Dimensions
Cuff Circumference
Oscillometric Method
Pressure
Pressure
Pulse
Arm-type Fully Automatic Blood Pressure Monitor
80-5101
LCD Digital Display Size:102.1mm×68.9mm (4.02" x 2.71")
0mmHg～300mmHg
30 to 180 Beats/Minute
±3mmHg
±5%
120 Memories in Two Groups with Date and Time
Irregular Heartbeat Detection
WHO Classification Indicator
Last 3 Tests Average
Low Battery Detection
Automatic Power-Off
4 AA batteries or Medical AC Aadapter (DC6.0V, 600mA)
(recommended, not provided)
Approximately 2 m at 3 tests per dayonths
Approx.480g (16.93 oz.) (excluding battery)
Approx.164 x 110x 58mm (6.46" x 4.33" x 2.28" )(L x W x H)
Approx.135 (W)×485(L) mm
(Medium cuff: Fits arm circumference 22-36 cm)
Operating Environment
Humidity
Temperature
10℃ ℃ ℉ ℉ ~ 40 (50 ~104 )
15% ~ 90%RH
Pressure
Atmospheric Pressure
Automatic Pressurization
28
Maintenance
4. Do not soak cuff in water!
5.
Cuff Cleaning: Apply a small amount of rubbing alcohol to
a soft cloth to clean cuff's surface. Use a damp cloth (water-based) to wipe clean.
Allow cuff to dry naturally at room temperature.
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.
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30
Specifications
International Standards:
AAMI / ANSI SP10:2002/(R) 2008 & 2002/A1:2003/(R)2008 & 2002/A2:2006/(R)2008
Manual, electronic, or automated sphygmomanometers
European Directive 93/42 EEC for Medical Products Act
EN 60601-1 Medical electrical equipment part 1: General requirements for safety
EN 60601-1-2 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.
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.
Storage Environment
Humidity
Classification:
Temperature:
Internal Powered Equipment,Type BF . Cuff is the Applied Part
15% ~ 90% RH
-20 ~55 (-4 ~131 )℃ ℃ ℉ ℉
Ingress Protection
Rating
IP22
27
Maintenance
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.
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