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DN:KD-7961N-SMSY01 V3.0 

Operation Guide 

Template version:1

 

5/15 

10.  Blood pressure measurements determined  by  this monitor are equivalent to those obtained by  a trained 

observer  using  the  cuff/stethoscope  auscultation  method,  within  the  limits  prescribed  by  the  American 

National Standard Institute, Electronic or automated sphygmomanometers. 

11.  Information regarding potential electromagnetic or other interference between the blood pressure monitor 

and  other  devices  together  with  advice  regarding  avoidance  of  such  interference  please  see  part 

ELECTROMAGNETIC COMPATIBILITY INFORMATION. 

12.  If Irregular Heartbeat (IHB) brought by common arrhythmias is detected in the procedure of blood pressure 

measurement, a signal of 

  will be displayed. Under this condition, the Electronic Sphygmomanometer 

can keep function, but the results may not be accurate, it’s suggested that you consult with your physician 

for accurate assessment. 

There are 2 conditions under which the signal of IHB will be displayed: 

1)    The coefficient of variation (CV) of pulse period >25%. 
2)    The  difference  of  adjacent  pulse  period≥0.14s,  and  the  number  of  such  pulse  takes  more  than  53 

percentage of the total number of pulse.   

13.  Please do not use the cuff other than supplied by the manufacturer, otherwise it may bring biocompatible 

hazard and might result in measurement error. 

14. 

The  monitor  might  not  meet  its  performance  specifications  or  cause  safety  hazard  if  stored  or  used 

outside the specified temperature and humidity ranges in specifications. 

15. 

Please do not share the cuff with other infective person to avoid cross-infection. 

16.  This blood pressure monitor is verified by auscultatory method. It is recommended that you check annex B 

of ANSI/AAMI SP-10:2002+A1:2003+A2:2006 for details of verification method if you need. 

17.  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. 

SETUP AND OPERATING PROCEDURES 

1. BATTERY LOADING 

a.  Open battery cover at the back of the monitor. 

b. 

Load two ―AAA‖ size batteries. Please pay attention to polarity. 

c.  Close the battery cover. 

When LCD shows battery symbol

, replace all batteries with new ones. 

Rechargeable batteries are not suitable for this monitor. 

Summary of Contents for KD-7961N

Page 1: ...TERY LOADING 5 2 TOUCH BUTTON SWITCH 6 3 CLOCK AND DATE ADJUSTMENT 6 4 VOICE SETTING 6 5 CONNECTING THE CUFF TO THE MONITOR 7 6 APPLYING THE CUFF 7 7 BODY POSTURE DURING MEASUREMENT 7 8 TAKING YOUR BLOOD PRESSURE READING 8 9 DISPLAYING STORED RESULTS 8 10 DELETING MEASUREMENTS FROM THE MEMORY 9 11 ASSESSING HIGH BLOOD PRESSURE FOR ADULTS 9 12 TECHNICALALARM DESCRIPTION 10 13 TROUBLESHOOTING 1 10 1...

Page 2: ...ht Typically the value begins to increase at around 3 00AM and reaches to highest level in the daytime while most people are awake and active Considering the above information it is recommended that you measure your blood pressure at approximately the same time each day Too frequent measurements may cause injury due to blood flow interference please always relax a minimum moment of 1 to 1 5 minute...

Page 3: ...1 General requirements for basic safety and essential performance IEC60601 1 2 2007 EN 60601 1 2 2007 AC 2010 Medical electrical equipment Part 1 2 General requirements for basic safety and essential performance Collateral standard Electromagnetic compatibility Requirements and tests IEC 80601 2 30 2009 Cor 2010 EN 80601 2 30 2010 Medical electrical equipment Part 2 30 Particular requirements for ...

Page 4: ...cuff should be placed at the same level as your heart 4 During measurement neither speak nor move your body and arm 5 Measuring on same wrist for each measurement 6 Please always relax a minimum moment of 1 to 1 5 minutes between measurements to allow the blood circulation in your arm to recover Prolonged over inflation cuff pressure exceed 300 mmHg or maintained above15 mmHg for longer than 3 min...

Page 5: ...umidity ranges in specifications 15 Please do not share the cuff with other infective person to avoid cross infection 16 This blood pressure monitor is verified by auscultatory method It is recommended that you check annex B of ANSI AAMI SP 10 2002 A1 2003 A2 2006 for details of verification method if you need 17 This equipment has been tested and found to comply with the limits for a Class B digi...

Page 6: ...nd LCD will display time and date See picture 3 Picture 3 Picture 3 1 Picture 3 2 Picture 3 3 Picture 3 4 b While the monitor is in Clock Mode pressing both the START and MEM button simultaneously touch button switch in ON position the month will blink at first See picture 3 1 Press the button START repeatedly the day hour and minute will blink in turn See picture 3 2 3 3 3 4 While the number is b...

Page 7: ...he monitor until the plugs and brackets are securely attached 6 APPLYING THE CUFF a Place the cuff around a bare wrist 1 2cm above the wrist joint on the palm side of the wrist b While seated place the arm with the cuffed wrist in front of your body on a desk or table with the palm up If the cuff is correctly placed you can read the LCD display c The cuff must be neither too tight nor too loose No...

Page 8: ...pressure has built up for a measurement Then the monitor slowly releases air from the cuff and carries out the measurement Finally the blood pressure and pulse rate will be calculated and displayed on the LCD See picture 8 3 The irregular heartbeat symbol if any and blood pressure classification indicator will blink on the screen The result will be automatically stored in the memory If the voice f...

Page 9: ...pressing button MEM for three seconds all results in the memory bank will be deleted after three beep See picture 10 picture 10 1 Press the button MEM or START the monitor will turn off Picture 10 Picture 10 1 11 ASSESSING HIGH BLOOD PRESSURE FOR ADULTS The following guideline for assessing high blood pressure without regard to age or gender has been established by the World Health Organization WH...

Page 10: ...ng Review the BODY POSTURE DURING MEASUREMENT sections of the instructions and re test Speaking arm or body movement angry excited or nervous during testing Re test when calm and without speaking or moving during the test Irregular heartbeat arrhythmia It is inappropriate for people with serious arrhythmia to use this Electronic Sphygmomanometer 14 TROUBLESHOOTING 2 PROBLEM POSSIBLE CAUSE SOLUTION...

Page 11: ...priately qualified technical personnel to repair those parts of equipment which are designated repairably can be supplied 9 The monitor can maintain the safety and performance characteristics for a minimum of 10 000 measurements or three years and the cuff integrity is maintained after 1 000 open close cycles of the closure 10 It is recommended the cuff should be disinfected 2 times every week if ...

Page 12: ...magnetic emissions The KD 7961N is intended for use in the electromagnetic environment specified below The customer or the user of the KD 7961N should assure that it is used in such an environment Emissions test Compliance Electromagnetic environment guidance RF emissions CISPR 11 Group 1 The KD 7961N uses RF energy only for its internal function Therefore its RF emissions are very low and are not...

Page 13: ...terial the relative humidity should be at least 30 Power frequency 50 60 Hz magnetic field IEC 61000 4 8 3 A m 3 A m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment Table 3 For ME EQUIPMENT and ME SYSTEMS that are not LIFE SUPPORTING Guidance and manufacturer s declaration electromagnetic immunity The KD 7961N...

Page 14: ...magnetic propagation is affected by absorption and reflection from structures objects and people a Field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy To assess the electromagnetic environment due to fixed RF transmitters a...

Page 15: ...W Separation distance according to frequency of transmitter m 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 10 3 8 3 8 7 3 100 12 12 23 For transmitters rated at a maximum output power not listed above the recommended separation distance d in meters m can be determined using the equation applicable to the frequency of the transmitter wh...

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