JOYTECH DBP-6282L Fully Automatic Digital Blood Pressure Monitor User Manual

JOYTECH DBP-6282L Fully Automatic Digital Blood Pressure Monitor

Safety Notice
Thank you for purchasing the DBP-6275B Blood Pressure Monitor. The unit has been constructed using reliable circuitry and durable materials. Used properly, this unit will provide years of satisfactory use. Indications for use The Arm-type Fully Automatic Digital Blood Pressure monitors are intended to measure blood pressure(systolic and diastolic) and pulse rate of adults and adolescents over 12 years of age.All functions can be used safely and values can be read out in one LCD DISPLAY. The measurement position is on the adult’s upper arm only.

The PATIENT is an intended OPERATOR

Blood pressure measurements determined with this device are equivalent to those obtained

by a trained observer using the cuff/ stethoscope auscultation method, within the limits prescribed by the Recognized Consensus Standard (IEC 80601-2-30) for electronic sphygmomanometer.

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. Otherwise, the cuff may not inflate properly.
6. If the unit has been stored at temperatures above 40 ℃, leave it in a cool place for about 15 minutes before using it. Otherwise, the cuff may not inflate properly.
7. Do not store the unit in direct sunlight, high humidity or dust.
8. To avoid any possibility of accidental strangulation, keep this unit away from children and do not drape tubing around your neck.
9. Ensure that children do not use the instrument unsupervised; some parts are small enough to be swallowed.
10. some may get skin irritation from the cuff taking frequent readings over the day, but this irritation typically goes away on its own after the monitor is removed.

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.
6. Monitoring the trends in your blood pressure taken at either the arm or the wrist is nevertheless useful and important.
7. 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.
8. Different values may be obtained due to their condition.
9. 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.
10. In certain cases oscillometric measurement method can produce incorrect readings.
11. Too frequent measurements can cause injury to the patient due to blood flow interference.
12. The cuff should not be applied over a wound as this can cause further injury.
13. 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.
14. 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.
15. Pressurization of the cuff can temporarily cause loss of function of simultaneously used ponitoring equipment on the same limb.
16. A compressed or kinked connection hose may cause continuous cuff pressure resulting in blood flow interference and potentially harmful injury to the patient.
17. check that operation of the unit does not result in prolonged impairment of the circulation of the patient.
18. Product is designed for its intended use only. Do not misuse in any way.
19. Product is not intended for infants or individuals who cannot express their intentions.
20. Prolonged over-inflation of the bladder may cause ecchymoma of your arm.
21. Do not disassemble the unit or arm cuff. Do not attempt to repair.
22. Use only the approved arm cuff for this unit. Use of other arm cuffs may result in incorrect measurement results.
23. The system might produce incorrect readings if stored or used outside the manufacturer’s specified temperature and humidity ranges.
24. Make sure to store the blood pressure monitor, children, pets and pests are outside of accessible range.
25.  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.
26.  Do not mix new and old batteries simultaneously.
27. Replace batteries when Low Battery Indicator“ ”appears on screen. Replace both batteries at the same time.
28. Do not mix battery types. Long-life alkaline batteries are recommended.
29. Remove batteries from device when not in operation for more than 3 months.
30. Dispose batteries properly; observe local laws and regulations.
31. Only use a recommended class II AC Medical approved adaptor which comply with 2MOPP, and pass IEC 60601-1, IEC 60601-1-2 (or FCC) standard . An unauthorized adapter may cause fire and electric shock.
32. Advising operator that Instruction manual/ Booklet must be consulted.
33. Do not use the device during transport vehicles for influencing measurement accuracy, such as patient transport in an ambulance or helicopter.
34. Contains small parts that may cause a chocking hazard if swallowed by infants.
35. Please align the polarities of each battery with the +ve and -ve signs imprinted on the battery housing when you replace the batteries .
36. use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation.
37. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
38. 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.
39. 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.

Federal Communication Commission (FCC) Interference Statement

This device complies with part 15 of the FCC Rules. Operation is subject to the condition that this device does not cause harmful interference. This device is verified to comply with part 15 of the FCC Rules for use with cable television service. This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions:

This device may not cause harmful interference, and  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. 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.

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

Essential performance

Unit Illustration 6

Monitor Unit

Arm Cuff Medium size cuff (fits arm circumference: 22.0 cm -36.0 cm). If air is leaking from the arm cuff, replace the arm cuff with a new one. It is generally recommended to have the cuff replaced timely to ensure correct functioning and accuracy. Please consult your local authorized Sejoy distributor or dealer.

Unit Illustration

Contents

Important Testing Guidelines

1.  Avoid eating, exercising, and bathing for 30 minutes prior to testing.
2. Sit in a calm environment for at least 5 minutes prior to testing.
3. Do not stand while testing. Sit in a relaxed position while keeping your arm level with your heart.
4. Avoid speaking or moving body parts while testing.
5. White 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 the 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. Any blood pressure recording can be affected by the following factors
11. The position of the subject, his of her physiologic condition
12. The performance and accuracy of the device
13. Cuff size small cuff (bladder) will produce a higher blood pressure value than usual, big cuff (bladder) will produce a lower blood pressure value;
14. Measuring position does not keep level with your heart;
15. Speaking or moving body parts while feasting;
16. Not relaxing for about 5 minutes before faking the measurement.

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 deskor 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 ” START/STOP ” Button to start testing.

Lithium Battery Charging
The device has a built-in lithium battery that must be recharged using a specific power adapter. When low battery indicator icon “ ”appears on the screen Please connect the power adapter to charge. When charging, the screen will be displayed in a cycle from ” ” to” “. Insert the adapter connector into the adapter interface, then insert the adapter into the socket, and then connect the adapter to the cable endInsert the adapter interface on the device and press the on/off button to measure normally. (if this model has been packed)When you plug in the adapter, the screen power display changes, indicating that you are using the adapter for power. AC Adapter jack is on the back side of the monitor. Medical AC adapter(DC 5.0 V,1000mA) can be used with the device (Optional,If users want to purchase other adapters, they need to meet the requirements of IEC 60601-1). Do not use any other type of AC adapter as it may harm the unit.
Note :Power supply is specified as part of ME EQUIPMENT

Unit Operation

Applying the Arm Cuff

Firmly insert air plug into opening located on left side of monitor unit. With sticky nylon section facing outward, insert end of cuff underneath metal ring of cuff Fasten cuff about above the elbow joint. For best results apply cuff to bare arm and keep level with heart while testing 1-2cm (0.4-0.8”)
Note: Do not insert air plug into opening located on back side of monitor unit. This opening is designed for an optional power supply only.

Testing

Power On Press and hold the “START/STOP” button to turn the unit on. The LCD screen will appear full 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 residual air from previous testing is present in cuff. The LCD will flash “ ” until pressure is stabilized. After cuff inflation, air will slowly rise 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. Unit Operation 17 Unit Operation 18

Result Display
The screen will display measurements for systolic and diastolic blood pressure with voice broadcast. An indicator representing the current measurement will appear next to the corresponding WHO Classification.

Note: Refer to Page 24~25 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.

Power Off turn off the power itself about 3 minutes no operation in any mode.

The ” START/STOP ” button can be pressed to turn off the unit in any mode. The unit can Note: Refer to Page 24~25 for detail WHO Blood Pressure Classification Information. Safety Precaution: If pressure 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.

Arm Shake Indicator
If there is arm movement during the measurement, the “ ” icon may flash. Indicates that the measurement results may be inaccurate, and the situation will be recorded at the end of the measurement as a reminder.

Memory Deletion
Memory for a selected group may be deleted while in Memory Check mode. Press and hold the for approximately 3 seconds to delete all memory records from the selected group with voice broadcast “Memory Clear” and then transfer into testing mode. Press the “START/STOP ” button to turn the unit off.
Note: Memory cannot be recovered once it has been deleted.

Low Battery Indicator
The unit will broadcast “Low Battery” 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 ” START/STOP” button, and then install the batteries.

Until the LCD screen is full, release the ” START/STOP” button. When the LCD screen displays the double zero, the blood pressure meter is in static state. Software version is displayed:10 is a software version in the figure.

Note : Only Service personnel permitted to access to this mode, the mode unavailable in normal use.

Bluetooth requirements

The monitor requires a device with:

• Bluetooth 4.0 or later
• Android 5.0 or later
• IOS 9.0 or later
• And works with
• iphone , iPod, iPad
• Android Phones and Tablets

Wireless communication

• Frequency range : 2.4 Ghz (2400-2483.5 MHz)
• Modulation : GFSK
• Antenna gain:0.5dBi

Bluetooth connection

1. Download the free “JoyHealth” App: On your mobile phone or table go to www.sejoy.com.
2. Open the App on your phone or tablet. If requested, you should enable Bluetooth on your dvice. You can enable Bluetooth under the Settings menu on your smart phone or table.
3. Create a new user login, or login with your existing user name and password.
4.  Selection device “Blood pressure monitor”.

Pairing your monitor with a Smart Device

1. Long press the “memory” button (or the “M” key) on your monitor until the word “boo” flashes on your monitor
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 pictureA film or text can be used to pair the device.
3. After the pairing is complete, the device interface switches from boo interface, indicating that the pairing is successful.

Transfer your readings
As soon as your measurement is complete, open the app on your smart phone to transfer your reedings.
Note: On the paired smartphone, Bluetooth must be enabled. You can view your blood pressure readings on the app.

Troubleshooting

Abnormal sphygmomanometer

| The armband is tied too tight or too loose, Or the arm strap is tied incorrectly;| Roll the armband correctly
Move the arm during measurement or Electronic sphygmomanometer| Stay quiet, keep your arm steady, and do not move the monitor
Speaking, nervous or emotional during measurement| Instead of talking, take deep breaths to calm your mood and relax your body
Incorrect measurement posture| Adjust posture, see

“Blood pressure gauge Wearing”

There is interference in charging process or improper operation in measuring

process

| See operation Instructions.

The following table shows the error signs that may occur during measurement, possible causes and handling methods. Please measure again using the correct method

Note: If you cannot solve the abnormal situation by yourself, you can consult the manufacturer or the manufacturer’s designated unit by phone. It is forbidden to disassemble and repair without permission. If necessary, professional maintenance personnel can ask the manufacturer for the list of components and circuit schematic diagram.

Blood Pressure Information
Blood pressure is the force of blood pushing against the walls of arteries. It is typically measured in millimeters of mercury (mmHg.) 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-6282L 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.

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.
4. Use a damp cloth to remove dirt and excess detergent.
5. 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.
6. Do not use petrol, thinners or similar solvents.
7. Remove batteries when not in operation for an extended period of time.
8. Do not disassemble product.
9. It is recommended the performance should be checked every 2 years.
10. Expected service life: Approximately three years at 10 tests per day.
11. 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

Measurement Range

| Systolic Pressure| 60mmHg～260 mmHg
Diastolic Pressure| 40mmHg～200 mmHg
Pressure| 0mmHg～299mmHg
Pressure| ±3mmHg
Pulse| 30 ~ 180 Beats/Minute
Pulse| ±5%
Pressurization| Automatic Pressurization
Memory| 2×150 Memories in Two Groups with Date and Time

Function

| Irregular Heartbeat Detection
WHO Classification Indicator
Last 3 Tests Average
Low Battery Detection
Automatic Power-Off
Voice
Backlight
Bluetooth
Power Source| Lithium battery 3.7 V or DC5.0v 1000mA medical external power supply (DC5.0V, 1000mA)(Optional,If users want to purchase other adapters, they need to meet the requirements of IEC 60601-1 )
Battery Life| Approximately 2 months at 3 tests per day
Unit Weight| Approx.255g (8.99 oz) (excluding battery)
Unit Dimensions| Approx.150mm X 108mm X 65mm（5.90″ x 4.25″ x 2.56″）
Cuff Circumference| Approx.135 (W) x 485(L) mm

(Medium cuff: Fits arm circumference 22-36 cm)

Operating Environment

| Temperature| 10℃ ~ 40℃ (50 ℉ ~104 ℉ )
---|---|---
Humidity| 15% ~ 93%RH
Pressure| 800hPa~1060hPa

Storage Environment

| Temperature:| -25℃~55℃ (-13℉~131℉)
Humidity| ≤93% RH
Classification:| Internal Powered Equipment,Type BF           ,Cuff is the Applied Part
Ingress Protection Rating:| IP21, Indoor Use Only

Bluetooth

| Modulation Type| GFSK
Version| 5.0.1 BT Signal mode
Operation frequency| 2. 4GHz( 2400~ 2483. 5MHz)
Antenna gain| 0 dBi
Bandwidth| 2.0 MHz

Specifications are subject to change without notice.

Safety Standard( included but not limited)

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. ISO 81060- 2, non-invasive sphygmomanometers – part 2: clinical validation of automated measurement type. ( Cardiovascular)
3. AAMI / ANSI ES 60601- 1: 2005/ ( R) 2012 and C1: 2009/ ( R) 2012 and, a2: 2010/ ( r) 2012 ( consolidated text) medical electrical equipment
4. part 1: general requirements for basic safety and essential performance
5. AAMI/ ANSI/ IEC 60601- 1- 2, Medical Electrical Equipment – – Part 1- 2: General Requirements For Basic Safety And Essential Performance
6. Collateral Standard: Electromagnetic Disturbances – – Requirements And Tests ( General II ( ES/ EMC) ) .
7. IEC 60601- 1- 11, medical electrical equipment – part 1- 11: general requirements for basic safety and essential performance
8. collateral standard: requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment.

Warranty

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.

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 environmen

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

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.
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, ±1kV

(differential mode)

|

±0.5kV, ±1kV

(differential mode)

|

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

| 0 % UT;| 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

|

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

| 0,5 cycle
| At 0°, 45°, 90°,
| 135°, 180°, 225
| , 270° and 315°
Voltage dips, short interrupti- ons and voltage variations on p- ower supply in- put lines| 0 % UT; 1 cycle and

70 % UT;

25/30 cycles Single phase: at 0°

IEC 61000-4-11| 0 % UT;

250/300 cycle

Power frequency (50/60 Hz)

magnetic field

IEC 61000-4-8

|

30 A/m; 50Hz or 60Hz

|

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.

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.
IMMUNITY test| IEC 60601

test level

| Compliance level| Electromagnetic  environment

-guidance

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

|

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 th 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 les

than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol:

Table 3

Guidance and declaration of manufacturer-electromagnetic immunity Nowadays, many RF wireless equipments have being used in various healthcare locations where medical equipment and/or systems are used. When they are used in close proximity to medical equipment and/or systems, the medical equipment and/or systems’ basic safety and essential performance may be affected. Arm-type Fully Automatic Digital Blood Pressure Monitor has been tested with the immunity test level in the below table and meet the related requirements of IEC 60601-1-2:2014. The customer and/or user should help keep a minimum distance between RF wireless communications equipment and this medical equipment and/or systems as recommended below.

Test frequency (MHz)| Band (MHz)| ****

Service

| ****

Modulation

| Maximum power (W)| Distance (m)| Immunity test level (V/m)|
---|---|---|---|---|---|---|---
385| 380-390| TETRA 400| Pulse

modulation 18Hz

| 1.8| 0.3| 27|
450| 430-470| GMRS 460

FRS 460

| FM

± 5 kHz deviation 1 kHz sine

| 2| 0.3| 28|
710| ****

704-787

| ****

LTE

Band 13, 17

| ****

Pulse modulation

217Hz

| ****

0.2

| ****

0.3

| ****

9

|
745
780
810| | GSM 800/900,| ****

Pulse modulation

18Hz

| | | |
800-960| TETRA 800,

iDEN 820,

CDMA 850,

| 2| 0.3| 28|
870
930
| LTE Band 5| | | |
1720| | ****

GSM 1800;

| ****

Pulse modulation

217Hz

| | | |
| CDMA 1900;| | | |
1845
1700-1990| GSM 1900; DECT;| 2| 0.3| 28|
| LTE Band 1, 3,| | | |
| | 4, 25; UMTS| | | |
1970| | | | | |
2450| 2400-2570| Bluetooth,WLAN,

802.11 b/g/n,RFID 2450,LTE Band 7

| Pulse modulation 217Hz| 2| 0.3| 28|
5240| ****

5100-5800

| ****

WLAN 802.11

a/n

| ****

Pulse modulation

217Hz

| ****

0.2

| ****

0.3

| ****

9

|

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
1| 1.2| 2.3
10| 3.8| 7.3
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 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.

Additional Notes

Important Instructions Before Use

1.  WARNING: 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.

2. WRNING: 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 Fully Automatic Digital Blood Pressure Monitor, including cables specified by the MANUFACTURER. Otherwise, degradation of the performance of this equipment could result.

3. The software identifier refer to the software evaluation report , and the file code is

4. verify manometer pressure accuracy: In the power down state, press and hold the ” START/STOP” button, and then install the batteries. Until the LCD screen is full, release the ” START/STOP” button. When the LCD screen displays the double zero, the blood-pressure meter is in static state. At this point, 500ml gas capacity, calibrated standard pressure gauge and manual pressure device can be connected to the sphygmomanometer through the sleeve interface of the sphygmomanometer and manual pressure can be applied to the effective display range of the sphygmomanometer, and then the difference between the reading of the sphygmomanometer and that of the standard pressure gauge can be compared.This mode can be used to verify manometer pressure accuracy.

5.  Contraindications: Product is not intended for infants or individuals who cannot express their intentions.

6. Indications for use: The digital blood pressure monitor is used to measure blood pressure and pulse rate from upper arm.

7. The patient is the operator: the PATIENT is an intended OPERATOR. the PATIENT Do not carry out other maintenance operations except to replace the battery. NYRJ211220003

8. WARNING: Do not modify this equipment without the authorization of the manufacturer.

9. ESSENTIAL PERFORMANCE Maintenance advice: Pressure calibration will be carried out when this 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 the device during the EXPECTED SERVICE LIFE of the ME EQUIPMENT.

11. Do not place the blood pressure monitor and cuff at will. It will cause asphyxiation if the child swallows or twine around his neck.

12. The cuff and the case of the blood pressure monitor have been tested for biocompatibility and do not contain allergenic or harmful materials.Please stop using it if allergy occurs during use.

13. Warning: Non-professionals do not modify the equipment, otherwise it will make the equipment measurement is not accurate.

14. Warning: Do not expose the equipment for a long time, otherwise it will reduce the performance of the equipment.

15. Warning: This device is not used for children and pets

16. Clean: The equipment can be cleaned by lay operator according to the cleaning procedures in the instructions

17. Warning: Do not use a damaged cuff for blood pressure measurement.

18. Warning: When measuring with the cuff, if the tester feels seriously uncomfortable, press the button of the blood pressure monitor to deflate the cuff, or remove the cuff directly from the arm.

19. Warning: If an unexpected reading occurs, the operator can take several more measurements and consult a doctor.

20. Warning: This equipment is used outside the specified environment, may damage the equipment, and may be inaccurate measurement.

21. Warning: The Operator should not use the system and should inform the customer service, if the ESSENTIAL PERFORMANCE is lost or degraded due to EM DISTURBANCES.

22. Warning: Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this
    equipment and result in improper operation.

23. Warning: Failure to use this equipment in the specified type of shielded location could result in degradation of the performance of this equipment, interference with other equipment or interference with radio services

24. ME equipment not intended for use in conjunction with flammable agents “ME equipment not intended for use in oxygen rich 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.

References

• Home in vitro diagnostic products, blood glucose meter, Lipid Panel Meter

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