anko DBP-1358 Arm-Type Fully Automatic Digital Blood Pressure Monitor Owner’s Manual

DBP-1358 Arm-Type Fully Automatic Digital Blood Pressure Monitor
Owner’s Manual Owner’s Manual
Arm-type Fully Automatic Digital Blood Pressure Monitor Model DBP-1358
Arm Type

Safety Notice

Thank you for purchasing the DBP-1358 Blood Pressure Monitor. The unit has been constructed using reliable circuitry and durable materials. Used properly, this unit will provide yeas of satisfactory use.
This device is intended for non-invasive measuring an adult individual’s systolic, diastolic blood pressure and heart rate using the oscillometric method. The device is not intended for use on infants and children. The device is designed for home or clinical use. All functions can be used safely andvalues can be read out in one LCD DISPLAY. Measurement position is on adult upper arm only. Please read this manual thoroughly before using the unit. Please retain this manual for future reference. For specific information about your blood pressure, please CONSULT YOUR DOCTOR.
To avoid risk and damage follow all warning precautions. Operate unit only as intended. Read all instructions prior to use.

WARNING SIGNS AND SYMBOLS USED

| Caution
| Mandatory
| Prohibited
| Type BF Equipment
| Instructions For Use MUST be Consulted
| Serial Number
| Discard the used product to the recycling collection point according to local regulations
| The product conforms to the requirements of the EC Directive(93/427EEC) on medical devices
| Manufacturer
| Authorised Representative in the European Community
| Keep Dry
| Keep off Sunlight
| Manufacturing Date

Safety Notice

Caution

Individuals with serious circulation problems may experience discomfort. Consult your physician prior to use.|
Contact your physician if test results regularly indicate abnormal readings. Do not attempt to self-treat these symptoms without consulting your physician first.
Product is designed for its intended use only. Do not misuse in any way.|
Product is not intended for infants or individuals who cannot express their intentions.
Do not disassemble or attempt to repair.
Do not use cell phones and other devices, which generate strong electrical or electromagnetic fields, near the device, as they may cause incorrect readings and interference or become interference source to the device.
Only use a recommended AC adaptor double-insulated complying with EN 60601-1 and EN 60601-1-2 (see page 6). An unauthorized adapter may cause fire and electric shock.
Battery Precautions

Do not mix new and old batteries simultaneously.
Replace batteries when Low Battery Indicator ” ” appears on screen.
Be sure battery polarity is correct.
Do not mix battery types. Long-life alkaline batteries are recommended.
Remove batteries from device when not in operation for more than 3 months.
Dispose batteries properly; observe local laws and regulations.

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 oscilloscope measurement method can produce incorrect readings.
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.
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.
20. The system might produce incorrect readings if stored or used outside the manufacturer’s specified temperature and humidity ranges.
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. Do not use the device during patient transport outside healthcare facility for interference source existing as well.
22. Do not mix new and old batteries simultaneously
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. Do not insert the batteries with their polarities incorrectly aligned.
27. Dispose batteries properly; observe local laws and regulations.
28. Only use a recommended AC adaptor double-insulated complying with EN 60601-1 and EN 60601-1-2.An unauthorized adapter may cause fire and electric shock.
29. Advising operator that Instruction manual/ Booklet must be consulted

Unit Illustration

Monitor Unit

Important Testing Guidelines

1. Avoid eating, exercising, and bathing for 30 minutes prior to testing.
2. Situational environment for at least 5 minutes prior to testing.
3. Do not stand while testing. Siting relaxed position while keeping your arm level with your heart.
4. Avoid speaking or moving body parts while testing.
5. While testing, avoid strong electromagnetic interference such as microwave ovens and cell phones.
6. Wait 3 minutes or longer before re-testing.
7. Try to measure your blood pressure at the same time each day for consistency.
8. Test comparisons should only be made when monitor is used on the same arm, in the same position, and at the same time of day.
9. This blood pressure monitor is not recommended for people with severe arrhythmia.
10. Do not use this blood pressure monitor if the device is damaged.

Quick Start

1. Install batteries. (See Figure A )
2. Insert cuff air plug into the left side of monitor unit. (See Figure B)
3. Remove thick clothing from the arm area.
4. Rest for several minutes prior to testing. Sit down in a quiet place, preferably at a desk or table, with your arm resting on a firm surface and your feet flat on the floor. (See Figure C )
5. Apply cuff to your left arm and keep level with your heart. Bottom of cuff should be placed approximately 1-2cm (0.4-0.8″) above elbow joint. (See Figures D&E)
6. Press” ” Button to start testing.

Unit Operation

Battery Installation
Slide battery cover off as indicated by arrow.
Install 4 new AAA alkaline batteries according to polarity.
Close battery cover.

AC adapter jack is on the back side of the monitor. Medical AC adapter(DC 6.0 V,600mA) can be used with the device (recommended, not provided). The adapter connect  pin should be positive inside and negative outside with a 2.1mm coaxial joint. Do not use another type of AC adapter as it may harm the unit.

Note:Power supply is specified as part of ME EQUIPMENT.

System Settings
With power off, press “SET” button to activate System Settings. The Memory Group icon flashes.

1. Select Memory Group
   While in the System Setting mode, you may accumulate test results into 2 different groups. This allows multiple users to save individual test results (up to 60 memories per  group.) Press” M” button to choose a group setting. Test results will automatically store in each selected group.

2. Time /Date Setting
   Press “SET” button again to set the Time/Date mode. Set the month first by adjusting the “M'” button. Press “SET” button again to confirm current month. Continue setting the day, hour and minute in the same way. Every time the “SET” button is pressed, it will lock in your selection and continue in succession (month, day, hour, minute.)

3. Saved Settings
   While in any setting mode, press “ ” button to turn the unit off.
   All information will be saved.

Applying the Arm Cuff

1. Firmly insert air plug into opening located on left side of monitor unit.
2. With sticky nylon section facing outward, insert end of cuff underneath metal ring of cuff.
3. Fasten cuff about 1-2cm (0.4-0.8″) above the elbow joint. For best results apply cuff to bare arm and keep level with heart while testing.

Note: Do not insert air plug into opening located on right side of monitor unit.
This opening is designed for an optional power supply only.

Testing

1. Power On
   Press and hold “  ” button until a beep sounds. The LCD screen will appear for one second as unit performs a quick diagnosis. A long tone indicates device is ready for testing.
   Note: Unit will not function if residual air from previous testing is present in cuff.
   The LCD will flash ” “until pressure is stabilized.

2. Pressurization
   The unit will automatically inflate to the proper shelf and stop inflating. During this time, please keep quiet. Note: Pressurization will gradually subside and ultimately stop when cuff is not properly applied to the arm. If this occurs, press “ ” button to turn the unit off.

3. Testing
   After cuff inflation, air will slowly subside as indicated by the corresponding cuff pressure  value. A flashing” ” will appear simultaneously on screen signaling heart  beat detection. Note: Keep relaxed during testing. Avoid speaking or moving body parts.

4. Result Display
   Three short beeps sound when testing is complete. The screen will display measurements for systolic and diastolic blood pressure. An indicator representing the current  measurement will appear next to the corresponding WHO Classification. Note: Refer to Page 23~24 for detail WHO Blood Pressure Classification Information.
   Irregular Heartbeat Indicator
   If the monitor detects an irregular heart rhythm two or more times during the measuring process, the Irregular Heartbeat Symbol ” “appears on screen along with measurement results. Irregular heartbeat rhythm is defined as rhythm that is either 25% slower or faster than the average rhythm detected while measuring systolic blood  pressure and diastolic blood pressure. Consult your physician if the Irregular Heartbeat Symbol “ ” frequently appears with your test results.

5. Deleting/Storing Test Results
   User may delete their current test result due to unfavorable testing conditions or for any other reason. To delete the last test result, press the “SET” button after result is  displayed. If result is not deleted, it will automatically store by date within the previously configured Memory Group.
   Note: Be sure the appropriate Memory Group selection is made prior to testing.
   If the number of tests surpasses the allotted 60 memories per group, the most recent tests will appear first, thus eliminating the oldest readings.

Power Off
The “ ” button can be pressed to turn off the unit in any mode. The unit can turn off the power itself about 3 minutes no operation in any mode.
Safety Precaution: If pressure in arm cuff becomes too extreme while testing, press the “ ” button to turn power off. The cuff pressure will rapidly dissipate once the unit is off.

Memory Check
With power off, you may check past test results by using the” M” buttons. The most recent test result and oldest test result in memory can be viewed by pressing and holding  the “M” button upon activating test results you can press the “ M ” button to scroll through all test results stored in memory.

Note: Previous test results will only be displayed from the most recently used memory group. To check previous test results in other memory groups, you must first select the desired group and then turn monitor off. (See “Select Memory Group” on Page 10.)
Memory Deletion
Memory for a selected group may be deleted while in Memory Check mode. Press and hold the” SET” button for approximately 3 seconds to delete all memory records from  the selected group. The monitor will beep indicating successful deletion and then transfer into testing mode. Press the “ ” button to turn the unit off. Note: Memory cannot be recovered once it has been deleted.

Last 3 Tests Average
With power off, press the “M” button to activate screen display. After the unit performs a self diagnosis, the screen will display the average test results from the last 3 readings  of the last group used. The”. AVG “symbol will appear along with the corresponding WHO Blood Pressure Indicator. The Memory Check mode can be accessed  by pressing the “M” buttons. To check the average results from other groups, select the desired group first prior to activating the “SET ” button in the off position. (See  “Select Memory Group” on Page 10.)

Low Battery Indicator
4 short warning beeps sound when battery life is depleting and unable to inflate cuff for testing. The” ” appears simultaneously for approximately 5 seconds prior to  shutting off. Replace batteries at this time. No memory loss will occur throughout this process. Static Pressure Measurement
In the power down state, press and hold the “ ” button, and the install the batteries. Until the LCD screen is full, release the “ ” button.
When the LCD screen displays the double zero, the blood pressure meter is in static state.
Software version is displayed at the heart rate .

Note:Power supply is specified as part of ME EQUIPMENT.

Troubleshooting

Blood pressure results are not
within typical range| Cuff is too tight or not properly positioned on the arm| Firmly reposition cuff approximately1-2cm (1/2″) above the elbow joint ( See Page 12)
Inaccurate test results due to body movement or monitor movement| Sit in a relaxed position with arm placed near heart. Avoid speaking or moving body parts while testing. Make sure the monitor unit is placed in a stationary position throughout the testing period. ( See Page 7)
” Err “displayed| Cuff fails to inflate properly| Make sure hose is properly fastened to cuff and monitor unit
Improper operation| Read user manual carefully and re-test properly.
Pressurization is over cuff rated pressure 300mmHg| Read user manual carefully and re-test properly.

Blood Pressure Information

Blood Pressure
Blood pressure is the force of blood pushing against the walls of arteries. It is typically measured in millimeters of mercury (mg.) Systolic blood pressure is the maximum force exerted against blood vessel walls each time the heart beats. Diastolic blood pressure is the force exerted on blood vessels when the heart is resting between beats.
An individual’s blood pressure frequently changes throughout the course of a day.
Excitement and tension can cause blood pressure to rise, while drinking alcohol and bathing can lower blood pressure. Certain hormones like adrenaline (which your body  releases under stress) can cause blood vessels to constrict, leading to a rise in blood pressure.
If these measuring numbers become too high, it means the heart is working harder than it should.

WHO Blood Pressure Classification Indicator
The DBP-1358 is equipped with a classification indicator based on established guidelines from the World Health Organization. The chart below (color coded on monitor  unit) indicates test results.

Health Reminder
Hypertension is a dangerous disease that can affect the quality of life. It can lead to a lot of problems including heart failure, kidney failure, and cerebral hemorrhaging. By  maintaining a healthy lifestyle and visiting your physician on a regular basis, hypertension and relative diseases are much easier to control when diagnosed in their early stages.

Note: Do not be alarmed if an abnormal reading occurs. A better indication of an individual’s blood pressure occurs after 2-3 readings are taken at the same time each day  over an extended period of time. Consult your physician if test results remain abnormal.

Blood Pressure Q&A

Q: What is the difference between measuring blood pressure at home or at a professional healthcare clinic?****

– A: Blood pressure readings taken at home are now seen to give a more accurate account as they better reflect your daily life. Readings can be elevated when taken in a clinical  or medical environment. This is known as White Coat Hypertension and may be caused by feeling anxious or nervous.
– Note: Abnormal test results may be caused by:
– 1. Improper cuff placement
– Make sure cuff is snug-not too tight or too loose.
– Make sure bottom of the cuff is approximately 1-2cm (1/2″) above the elbow joint.
– 2. Improper body position
– Make sure to keep your body in an upright position.
– 3. Feeling anxious or nervous
– Take 2-3 deep breaths, wait a few minutes and resume testing.

Q: What causes different readings?****

– A: Blood pressure 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 your heart.

Q: What is the best time of day for testing?****

– A: Morning time or any time you feel relaxed and stress free.

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.

4. Cuff Cleaning: Do not soak cuff in water! 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. The cuff must be cleaned and disinfected before use between different users

5. 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.

10. No service and maintenance while it is in use and maintenance only be performed by service personnel. Service and maintenance require parts, repair, technical support will be provided.

Specifications

WHO Classification Indicator
Last 3 Results Average
Low Battery Detection
Automatic Power-Off
Power Source| 4 AAA batteries or Medical AC Adapter(DC6.0V, 600mA) (recommended, not provided)
Battery Life| Approximately 2 months at 3 tests per day
Unit Weight| Approx.425g (14.99 oz.) (excluding battery)
Unit Dimensions| Approx.131.2 x 101.8 x 44.1 mm (L x W x H)
Cuff Circumference| Approx.135 (W) X 485(L) mm (Medium cuff: Fits arm circumference 22-42 cm)
Operating Environment| Temperature| 10°C 40°C (50 °F-104 °F)
Humidity| 15% – 93% RH
Pressure| 700hPa-1060hPa
Storage Environment| Temperature:| -25*C-70t (-13T-158T)
---|---|---
Humidity| ≤ 93% RH
Classification:| Internal Powered Equipment,Type BF .Cuff is the Applied Par
Ingress Protection Rating:| IP20, Indoor Use Only

Specifications are subject to change without notice.
This Blood Pressure Monitor complies with the European regulations and bears the CE mark“CE 0197”. This blood pressure monitor also complies with mainly following standards (included but not limited):
Safety standard:
EN 60601-1 Medical electrical equipment part 1: General requirements for safety
EMC standard:
EN 60601-1-2 Medical Electrical Equipment — Part 1-2: General Requirements For Basic Safety And Essential Performance — Collateral Standard: Electromagnetic Disturbances — Requirements And Tests.
Performance standards:
IEC81060-2-30, Medical electrical equipment — Part 2-30: Particular requirements for the basic safety and essential performance of automated non- invasive  sphygmomanometers.
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.
ISO 81060-2, non-invasive sphygmomanometers – part 2: clinical validation of automated measurement type.
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.

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.
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| Electromagnetic environment -guidance
Radiated emission CISPR 11| Group 1, class B.| 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.
Conducted emission CISPR 11| Group 1, class B.| 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.
Harmonic emissions IEC 61000-3-2| Class A
Voltage fluctuations/ flicker emissions IEC 61000-3-3| Complies

Electromagnetic Compatibility Information
Table 2Guidance 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 environment.
IMMUNITY test| IEC 60601 test level| Compliance level| Electromagnetic environment -guidance
Electrostatic discharge (ESD) IEC 61000-4-2| ± 8 kV contact
±2 kV,±4 kV, +8 kV,
±15 kV air| ± 8 kV contact
±2 kV,±4 kV, +8 kV,
±15 kV air| Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.
Electrostatic transient/burst IEC 61000-4-4| ± 2 kV , 100kHz, for AC power port| ± 2 kV , 100kHz, for AC power port| Mains power quality should be that of a typical commercial or hospital environment.
Surge
IEC 61000-4-5| ±-0.5kV, ±1 kV (differential mode)| ±0.5kV, ±1kV (differential mode)| Mains power quality should be that of a typical commercial or hospital environment.
Voltage dips, short interruptions and voltage variations on power supply in- put lines
IEC 61000-4-11| 0 % UT; 0,5 cycle
At 0°, 45°, 90°, 135°, 180°, 225’1350, , 270° and 315°
0 % UT; I cycle0 and
70 % UT; 25/30 cycles Single phase: at 0°
0 % UT; 250/300 cycle| 0 % UT; 0,5 cycle At 0°, 45°,  90°, 180°, 225) , 270° and 315° % UT; 1 cycle and
70 % UT; 25/30 cycles Single phase: at 0°
0 % UT; 250/300 cycle| Mains power quality should be that of a typical commercial or hospital environment.
Power frequency (50/60 Hz) magnetic field
IEC 61000-4-8| 30 A/m; 50Hz or 60Hz| 30 A/in; 50Hz or 60Hz| Power frequency magnetic fields should be at levels character tic of a typical location in a typical commercial or hospital environment.

Table 3Guidance 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 environment.
IMMUNITY test| IEC 60601 test level| Compliance level| Electromagnetic environment -guidance
Conducted RF IEC
61000-4-6
Radiated RF IEC 61000- 4-3| 3V for 0.15- 80MHz; 6V in ISM and
amateur radio bands between0.15- 80MHz
385MHz, 27V /m
450MHz, 28V /m
710MHz,745 MHZ,780MHz 9V/m
810MHz,870 MHZ,930MHz 28V/m
1720MHz,1845 28V/m
2450MHz, 28V /m
5240MHz,5500 9V/m| MHZ,1970MH2MHZ,1970MH7electromagnetic
MHZ,5785M1-12MHZ,5785MHOOV
3V for 0.15- 80MHz; 6V in ISM and amateur radio bands between0.15- 80MHz
385MHz, 85MHz, 27V
450MHz, 28V /in
710MHz,745 MHZ,780MHz 9V/m
810MHz,870 MHZ,930MHz 28V/m
1720MHz,1845 28V/m
2450MHz, 28V /m
5240MHz,550( 9V/m| Portable and mobile RF communications equipment s
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 separation distance
80 MHz to 800 MHz c
800 MHz to 2.7 Gaz Eid
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
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:
h x%

Table 4

Recommended separation distances between portable and mobile RF communications equipment and the device

The device is intended for use in an electromagnetic environment in which radiated therefore disturbances are controlled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the device as recommended below, according to the maximum output power of the communications equipment.
Rated maximum output power of transmitter W| Separation distance according to frequency of transmitter m
80 MHz to 800 MHz| 800 MHz to 2.7 GHz
0.01| 0.12| 0.23
0.1| 0.38| 0.73
I| 1.| 2.
10| 4.| 7.
100| 12| 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

Document No. JDBP-5404-013
Version: .Z
Date of Issue:2016.11
The product is in compliance with the requirements of MDD 93/42/EEC,
“0197” is the identification number of notify body;
JOYTECH Healthcare Co., Ltd.
No.365, Suzhou Hangul Economic Development Zone,
Hangzhou City,311100 Zhejiang,China
Shanghai International Holding Corp. GmbH (Europe)
Weierstrass 80, 20537 Hamburg, Germany

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