Specifications; Warranty; Electromagnetic Compatibility Information - JOYTECH DBP-1359b Owner's Manual

Specifications

Product Description Arm-type Fully Automatic Blood Pressure Monitor
DBP-1359b
Model
Display
LCD Digital Display
Measurement Method Oscillometric Method
Systolic Pressure
Diastolic Pressure
Pressure
Measurement Range
Pressure
Pulse
Pulse
Pressurization Automatic Pressurization
Memory 120 Memories in Two Groups with Date and Time
Irregular Heartbeat Detection
WHO Classification Indicator
Last3 Tests Average
Low Battery Detection
Function
Automatic Power-Off
voice
Backlight
Bluetooth
4 AA Abatteries or Medical AC Adapter(DC6.0V, 600mA)
Power Source
(recommended, not provided)
Battery Life Approximately 2 months at 3 tests per day
Unit Weight Approx.480g (16.93 oz.) (excluding battery)
Unit Dimensions Approx.131.2 x 101.8 x 44.1mm (L x W x H)
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-year 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: 69mm 67mm
60mmHg～28 0 mmHg
30mmHg～200 mmHg
0mmHg～3 00 mmHg
±3mmHg or ±2% of the reading above 200 mmHg
30 ~ 180 Beats/Minute
±5%
℃ ℃ ℉ ℉
10 ~ 40 (50 ~104 )
15% ~ 93% RH
700hPa~1060hPa
Specifications
31
Temperature:
Storage Environment
Humidity
Classification:
Internal Powered Equipment,Type BF
Ingress Protection Rating: IP20, Indoor Use Only
Specifications are subject to change without notice.
International Standards:
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. ANSI/AAMI ISO 81060-2, non-invasive sphygmomanometers - part 2: clinical validation
of automated measurement type. (Cardiovascular)
3. AAMI / ANSI ES60601-1:2005/(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.
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.
33

Electromagnetic Compatibility Information

The device satisfies the EMC requirements of the international standard IEC
60601-1-2. The requirements are satisfied under the conditions described in the
table below. The device is an electrical medical product and is subject to special
precautionary measures with regard to EMC which must be published in the
instructions for use. Portable and mobile HF communications equipment can affect
the device. Use of the unit in conjunction with non-approved accessories can affect
the device negatively and alter the electromagnetic compatibility. The device
should not be used directly adjacent to or between other electrical equipment.
Table 1
Guidance and declaration of manufacturer-electromagnetic emissions
The device is intended for use in the electromagnetic environment specified below.
The customer or the user of the device should assure that it is used in such an environment.
Emissions test Compliance
Radiated emission CISPR 11 Group 1,
class B.
Group 1,
Conducted emission CISPR 11
class B.
Harmonic emissions
Class A
IEC 61000-3-2
Voltage fluctuations/
flicker emissions
Complies
IEC 61000-3-3
32
℃ ℃ ℉ ℉
-25 ~70 (-13 ~158 )
≤93% RH
. Cuff is the Applied Part
34
Electromagnetic environment
-guidance
The device uses RF energy only for
its internal function. Therefore, its
emissions are very low and are not
likely to cause any interference in
nearby electronic equipment.
The device is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage
power supply network that supplies
buildings used for domestic
purposes.