background image

31

Warranty

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

Table 2

Guidance and declaration of manufacturer-electromagnetic immunity

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 environm-
ent.

Floors should be wood, concrete 
or ceramic tile. If floors are 
covered with synthetic material, 
the relative humidity should be 
at least 30 %.

Electromagnetic environment
 -guidance

Compliance
level

IEC 60601
test level

IMMUNITY test

±

 8 kV 

contact

±

2 kV,

±

4 kV,

 

±

8 kV, 

±

15 kV air

Electrostatic
discharge (ESD)
IEC 61000-4-2

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.

Electromagnetic environment
 -guidance

Compliance

Emissions test

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.

Group 1,
class B.

Radiated emission CISPR 11

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.

Conducted emission CISPR 11

Harmonic emissions
IEC 61000-3-2

Class A

Voltage fluctuations/
 flicker emissions
 IEC 61000-3-3

Complies

Electrostatic
transient/burst
IEC 61000-4-4

Surge
IEC 61000-4-5

±0.5kV, ±1kV 
(differential 
mode)

Voltage dips, 
short interrupti-
ons and voltage
variations on p-
ower supply in-
put lines

IEC 61000-4-11  

0 % UT; 
0,5 cycle
At 0°, 45°, 90°, 
135°, 180°, 225°
, 270° and 315°

0 % UT; 1 cycle
and
70 % UT; 
25/30 cycles
Single phase:
 at 0°

0 % UT; 
250/300 cycle

Power frequency
(50/60 Hz)
magnetic field

IEC 61000-4-8 

30 A/m; 50Hz 
or 60Hz 

Power frequency magnetic fields 
should be at levels charactertic of a 
typical location in a typical comme-
rcial or hospital environment.

30 A/m; 50Hz 
or 60Hz

±

 8 kV 

contact

±

2 kV,

±

4 kV,

 

±

8 kV, 

±

15 kV air

Electromagnetic Compatibility Information

32

33

±

 2 kV ,

100kHz, for 
AC power port

0 % UT; 
0,5 cycle
At 0°, 45°, 90°, 
135°, 180°, 225°
, 270° and 315°

0 % UT; 1 cycle
and
70 % UT; 
25/30 cycles
Single phase:
 at 0°

0 % UT; 
250/300 cycle

±0.5kV, ±1kV 
(differential 
mode)

±

 2 kV ,

100kHz, for 
AC power port

Mains power quality should be that
of a typical commercial or hospital
environment.

Mains power quality should be that
of a typical commercial or hospital
environment.

Mains power quality should be that
of a typical commercial or hospital
environment.

Group 1,
class B.

Table 2(continued)

Guidance and declaration of manufacturer-electromagnetic immunity

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 environm-
ent.

Electromagnetic environment
 -guidance

Compliance
level

IEC 60601
test level

IMMUNITY test

Electromagnetic Compatibility Information

34

Radiated RF EM 
         fields
IEC 61000-4-3  

3V/m or 10 V/m
80MHz-2.7
Ghz 80%AM at 
1kHz

3V/m or 10 V/m
80MHz-2.7
Ghz 80%AM at 
1kHz

Portable and mobile RF communications 
equipment should be used no closer to any 
part of the device, including cables, than 
the recommended separation distance 
calculated from the equation applicable to 
the frequency of the transmitter.
Recommended seperation distance 80 MHz 
to 800 MHz 800 MHz to 2.7 Ghz where P is 
the maximum output power rating of the 
transmitter in watts (W) according to the 
transmitter manufacturer and d is the 
recommended separation distance in 
metres (m). Field strengths from fixed RF 
transmitters, as determined by an 
electromagnetic site survey, a should be 
less than the compliance level in each 
frequency range. Interference may occur in 
the vicinity of equipment marked with the 
following symbol: 

Conducted 
disturbances 
Induced by RF 
fields
IEC 61000-4-6

3 V in 0.15 
MHz- 80 MHz 
6 V in ISM 
and/or amateur 
radio bands 
between 0.15 
MHz and 80 
MHz 80 % 
AM at 1kHz

Portable and mobile RF communications 
equipment should be used no closer to any 
part of the device, including cables, than the 
recommended separation distance 
calculated from the equation applicable to 
the frequency of the transmitter.
Recommended seperation distance 80 MHz 
to 800 MHz 800 MHz to 2.7 Ghz where P is 
the maximum output power rating of the 
transmitter in watts (W) according to the 
transm- itter manufacturer and d is the 
recommended separation distance in 
metres (m). Field strengths from fixed RF 
transmitters, as determined by an 
electromagnetic site survey, a should be less 
than the compliance level in each frequency 
range. Interference may occur in the 
vicinity of equipment marked with the 
following symbol: 

3 V in 0.15 
MHz- 80 MHz 
6 V in ISM 
and/or amateur 
radio bands 
between 0.15 
MHz and 80 
MHz 80 % 
AM at 1kHz

The Blood Pressure Monitor is 

 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 Pressue Monitor due to improper handling. Please contact local retailer for 

details.

guaranteed

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.

Summary of Contents for DBP-6281B

Page 1: ...peration 1 Do not drop the unit Protect it from sudden jars or shocks 2 Do not insert foreign objects into any openings 3 Do not attempt to disassemble the unit 4 Do not crush the pressure cuff 5 If the unit has been stored at temperatures below 0 oC leave it in a warm place for about 15 minutes before using it Otherwise the cuff may not inflate properly 6 If the unit has been stored at temperatur...

Page 2: ...ce or helicopter 30 Contains small parts that may cause a chocking hazard if swallowed by infants 31 Please align the polarities of each battery with the ve and ve signs imprinted on the battery housing when you replace the batteries 32 Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation If such use is necessary this equ...

Page 3: ...k Start 1 Install batteries 2 Insert cuff air plug into the behind side of monitor unit See Figure B See Figure A 3 Remove thick clothing from the arm area 4 Rest for several minutes prior to testing Sit down in a quietplace comfortably back and arm support on a desk or table withyour legs uncrossed your arm resting on a firm and your feet flat on the floor See Figure C 5 Apply cuff to your left a...

Page 4: ... enter volume setting mode Set the voice volume by adjusting the MEM button There are six volume levels While in any setting mode press START STOP button to turn the unit off All information will be saved Note If unit is left on and not in use for 3 minutes it will automatically save all information and shut off Unit Operation System Settings With power off press GROUP1 button or to activate Syste...

Page 5: ...ldest test result in memory can be viewed by pressing and holding the MEM button Upon activating test results you can press the MEM button to scroll through all test results stored in memory To check the average results from other groups please press corresponding GROUP1 button or GROUP2 button With power off press the MEM button to activate screen display After the unit performs a self diagnosis ...

Page 6: ...2483 5 MHz Modulation GFSK Antenna gain 0 5dBi Troubleshooting Problem Solution displayed Connection failure Data is not being transmitted Cuff is too tight or not properly positioned on the arm Firmly reposition cuff approximately above the elbow joint See Page 12 1 2cm 1 2 Inaccurate test results due to body movement or monitor movement Sit in a relaxed position with arm placed near heart Avoid ...

Page 7: ...essure varies throughout the course of a day Many factors including diet stress cuff placement etc may affect an individual s blood pressure Q Should I apply the cuff to the left or right arm What is the difference A Either arm can be used when testing however when comparing results the same arm should be used Testing on your left arm may provide more accurate results as it is located closer to yo...

Page 8: ...rating Environment Automatic Pressurization LCD Digital Display Size 87 5mm X 85mm 3 44 x 3 34 Humidity Temperature 10 40 50 104 15 93 RH Storage Environment Humidity Classification Ingress Protection rating Battery Shelf life Battery Storage Temperature Temperature Internal Powered Equipment Type BF Cuff is the Applied Part IP 20 Indoor Used Only 60 months 25 55 13 131 25 55 13 131 Measurement Ra...

Page 9: ...al environment Group 1 class B Table 2 continued Guidance and declaration of manufacturer electromagnetic immunity 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 environm ent Electromagnetic environment guidance Compliance level IEC 60601 test level IMMUNITY test Electromagnetic Compa...

Page 10: ...e use and are non invasive blood pressure measurement systems designed to measure the systolic and diastolic blood pressure and pulse rate of adolescents and adults individual by using a non invasive technique which is a well known technique in the market called the oscillometric method it can measure the systolic blood pressure diastolic blood pressure and pulse rated on up arm and the device is ...

Reviews: