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Unit Illustration

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Safety Notice

Safety Notice

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Important Instructions Before Use
1. Do not confuse self-monitoring with self-diagnosis. Blood pressure measurements should
    only be interpreted by a health professional who is familiar with your medical history.
2. Contact your physician if test results regularly indicate abnormal readings.
3. If you are taking medication, consult with your physician to determine the most appropriate
    time to measure your blood pressure. NEVER change a prescribed medication without first
    consulting with your physician.
4. Individuals with serious circulation problems may experience discomfort. Consult your
    physician prior to use.
5. For persons with irregular or unstable circulation resulting from diabetes, liver disease,
    arteriosclerosis or other medical conditions, there may be variations in blood pressure
    values measured at the wrist versus at the upper arm. Monitoring the trends in your blood
    pressure taken at either the arm or the wrist is nevertheless useful and important.
6. People suffering from vascular constriction, liver disorders or diabetes, people with
    cardiac pacemakers or a weak pulse, and women who are pregnant should consult their
    physician before measuring their blood pressure themselves. Different values may be
    obtained due to their condition.
7. People suffering from arrhythmias such as atrial or ventricular premature beats or atrial
    fibrillation only use this blood pressure monitor in consultation with your doctor. In
    certain cases oscillometric measurement method can produce incorrect readings.

15. Product is designed for its intended use only. Do not misuse in any way.
16. Product is not intended for infants or individuals who cannot express their intentions.
17. Prolonged over-inflation of the bladder may cause ecchymoma of your arm.
18. Do not disassemble the unit or arm cuff. Do not attempt to repair.
19. Use only the approved arm cuff for this unit. Use of other arm cuffs may result in
       incorrect measurement results.

8.Too frequent measurements can cause injury to the patient due to blood flow interference.
9.The cuff should not be applied over a wound as this can cause  further injury.
10.

DO NOT 

attach the cuff to a limb being used for IV infusions or any other intravascular 

    access, therapy or an arterio-venous  (A-V) shunt. The cuff inflation can temporarily 
   block blood flow, potentially causing harm to the patient.
11.The cuff should not be placed on the arm on the side of a mastectomy. In the case of a 
     double mastectomy use the side of the least dominant arm.
12.Pressurization of the cuff can temporarily cause loss of function of simultaneously used 
     monitoring equipment on the same limb.
13.A compressed or kinked connection hose may cause continuous cuff pressure resulting 
     in blood flow interference and potentially harmful injury to the patient.
14.Check that operation of the unit does not result in prolonged impairment of the circulation 
      of the patient.

23. Replace batteries when Low Battery Indicator

          

appears on screen. Replace both

      batteries at the same time.
24. Do not mix battery types. Long-life alkaline batteries are recommended.
25. Remove batteries from device when not in operation for more than 3 months.
26. Dispose batteries properly; observe local laws and regulations.
27. 

Only use a recommended class II AC Medical approved adaptor which comply with 2MOPP, and pass

 IEC 60601-1, IEC 60601-1-2 (FCC) standard  . An unauthorized adapter may cause fire and electric shock.

28.                  Advising operator that Instruction manual/ Booklet must be consulted. 
29. Do not use the device during transport vehicles for influencing measurement accuracy,
      such as patient transport in an ambulance 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 equipment and 
      the other equipment should be observed to verify that they are operating normally.
33.Portable RF communications equipment (including peripherals such as antenna cables 
      and external antennas) should be used no closer than 30 cm (12 inches) to any part of the 
      unit, including cables specified by the manufacturer. Otherwise, degradation of the 
      performance of this equipment could result.
34.the blood pressure monitors equipped with bluetooth(BT) module is only  transmit historical blood pressure (BP) 
from the subject device to a user-supplied digital device, and is not intended for active patient monitoring.

20. The system might produce incorrect readings if stored or used outside the manufacturer's
       specified temperature and humidity ranges. Make sure to store the blood pressure monitor,
       children, pets and pests are outside of accessible range. 
21. Do not use the device near strong  electrical or electromagnetic fields generated by cell 
      phones or other devices, they may cause incorrect readings and interference or become 
      interference source to the device. 
22. Do not mix new and old batteries simultaneously.

Safety Notice

Federla Commulcation Commission (FCC) Interference Statement

1.This device complies with part 15 of the FCC Rules. Operation is subject to the condition 
that this device does not cause harmful interference.
2.This device is verified to comply with part 15 of the FCC Rules for use with cable television 
service.
3.This device complies with part 15 of the FCC Rules. Operation is subject to the following two
 conditions:
(1) This device may not cause harmful interference, and
(2) this device must accept any interference received, including interference that may cause 
undesired operation. Please note that changes or modifications not expressly approved by the 
party responsible for compliance could void the user's authority to operate the equipment.
4.This equipment has been tested and found to comply with the limits for a Class B digital
 device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable 
protection against harmful interference in a residential installation. This equipment generates, 
uses and can radiate radio frequency energy and, if not installed and used in accordance with the 
instructions, may cause harmful interference to radio communications. However, there is no 
guarantee that interference will not occur in a particular installation. If this equipment does 
cause harmful interference to radio or television reception, which can be determined by turning 
the equipment off and on, the user is encouraged to try to correct the interference by one or more 
of the following measures:

Reorient or relocate the receiving antenna.

Increase the separation between the equipment and receiver.

Connect the equipment into an outlet on a circuit different from that to which the receiver

 is connected.

Consult the dealer or an experienced radio/TV technician for help.

5.This equipment complies with radio frequency exposure limits set forth by the FCC for an 
uncontrolled environment.
6. This device must not be co-located or operating in conjunction with any other antenna or
transmitter.

WARNING SIGNS AND SYMBOLS USED 

Keep off Sunlight

Type BF Equipment

Discard the used product to the recycling 

collection point according to local 

regulations

Instructions For Use MUST be Consulted

Keep Dry

The Bluetooth® Smart word mark and logos are 

registered trademarks owned by Bluetooth SIG, 

Inc. and any use of such marks by JOYTECH 

Healthcare Co.,Ltd. 

Limits of the error of
the manometer

Reproducibility of the
BLOOD PRESSURE
DETERMINATION

Refer 202.12.1.102    IEC 80601-2-30 

Refer 201.12.1.107    IEC 80601-2-30 

7.Essential performance:

Electrosurgery
interference recovery

Refer 202.6.2.101      IEC 80601-2-30 

Monitor Unit

MR

IP21

     21 indicate dustproof and waterproof grade. Number 2 indicate that 
Protected against solid foreign objects of 12.5 mm and greater; Number 
1 indicate that Protection against vertically falling water drops .

 

Magnetic Resonance unsafe

IP

 MEM  

"

 

Button

ON/OFF  

"

 

Button

LCD

SET  

"

 

Button

Summary of Contents for DBP-6293B

Page 1: ...EC 81060 2 30 for electronic sphygmomanometers Precautions to Ensure Safe Reliable Operation 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 leave it in a warm place for about 15 minutes before using it Otherw...

Page 2: ...uipment should be avoided because it could result in improper operation If such use is necessary this equipment and the other equipment should be observed to verify that they are operating normally 33 Portable RF communications equipment including peripherals such as antenna cables and external antennas should be used no closer than 30 cm 12 inches to any part of the unit including cables specifie...

Page 3: ...ee 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 arm and middle of the cuff at the level of your heart Bottom of cuff should be placed appr...

Page 4: ... format ON or OFF by pressing the MEM button 8 Saved Settings 7 Volume Setting Press SET button to enter volume setting mode Set the voice volume by adjusting the MEM button There are six volume levels While in any setting mode press ON OFF 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 s...

Page 5: ...ure in arm cuff becomes too extreme while testing press the START STOP button to turn power off The cuff pressure will rapidly dissipate once the unit is off Testing 1 Power On Press and hold START STOP button to turn the unit on The LCD screen will appear for one second as unit performs a quick diagnosis A voice tone will indicate when unit is ready for testing Note Unit will not function if resi...

Page 6: ...emory button or the M key on your monitor until the word boo flashes on your monitor The MAC address Bluetooth SMART AM 2 Open the APP and click pair device button a popup window will appear Click Search device button to display all sphygmomanometer devices The display information includes the device model and MAC address then you can find the sphygmomanometer through the device Name click the pic...

Page 7: ... 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 your heart Q What is the best ...

Page 8: ...00mmHg Pressure 0mmHg 299mmHg Pressure 3mmHg Backlight Medium cuff Fits arm circumference 22 42 cm Operating Environment Pressure 80kPa 106kPa Bluetooth Last 3 Tests 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 ...

Page 9: ...er 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 ...

Page 10: ... product leaves the factory Patients can use the method described in the section Verify Manometer Pressure Accuracy to verify the accuracy If the accuracy deviation is large please contact the manufacturer to recalibration 10 Mechanical strength and resistance to heatThe resistance to heat will be retained by device during the EXPECTED SERVICE LIFE of the ME EQUIPMENT Additional Notes 38 11 Do not...

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