Jumper Medical HAA11 Bluetooth Electronic Blood Pressure Monitor User Manual

Jumper Medical HAA11 Bluetooth Electronic Blood Pressure Monitor

Product Composition
The product is comprised of the host machine and the cuff of the Electronic Blood Pressure Monitor.

Intended use
The Electronic Blood Pressure Monitor is intended to measure the systolic and diastolic blood pressure as well as the pulse rate of an adult person via a non-invasive oscillometric technique at medical facilities or at home.

Safety Precautions

The warnings and illustrations shown in the User Manual enable you to use the product safely and correctly, thus preventing you and others from being injured, specifically as follows:

Legend, mark and meaning

| Warning message
| Anti-electric shock degree is Type BF of the

application part

| When the product life expires and the end users discard the products, send them to the designated collecting and separating place for disposal according to the requirements of the local

environmental protection authority.

|

Consult the instructions for use.

| This product complies with the MDD93/42/EEC

requirements.

| Degree of protection against the ingress of water.
| Information of manufacturer
| Date of manufacture
| Authorized European Representative

Quick Start Guide

Avoid smoking, eating, drinking caffeinated drinks or exercising for 30 minutes before taking measurements.

1. Sit upright in a chair with both feet on the floor.
2. Remove tight-fitting clothing from your upper arm along with any thick clothing.
3. Pull on the end of the cuff until it wraps securely around your upper arm. Place your arm on a table so that the cuff will be at the same level as your heart.
4. The cuff will automatically inflate and the measurement will start, upon pressing the “ ” button.
5. When the measurement is complete, the cuff will automatically deflate and your systolic and diastolic pressure values and pulse rate will be displayed.

Overview

Structure

1. Air Jack
2. User Button
3. Power Button
4. Memory Button
5. USB External Power Supply Interface
6. Volume Switch

Features

• Dual users and guest mode
• 199 Readings * 2 Users
• Voice Reminder Function
• Average Of Last 3 Readings
• Irregular Heartbeat Detector
• Auto-off Power Saving Feature
• Operated by 4 AA Batteries (USB 5V optional)
• Universal Cuff

Display

Packing List

Preparation

Battery Installation

• Open the battery cover as shown in the picture.
• Place 4 AA dry batteries. Pay attention to the battery electrode indication.

Battery power indication and replacement

• After the product is turned on, if a low power symbol appears on the screen, the measurement cannot be performed, and the battery must be replaced.
• Do not use any expired battery;
• If the product is not used for over 3 months, please take out the batteries.

USB Power Supply
USB line can be connected to the power supply of the product without battery.

Cuff
The applicable arm circumference range of the cuff is 22-36cm or 22-42cm.

Connection: Insert the air plug of cuff air tube into the air jack of the Electronic Blood Pressure Monitor. Figure as shown above.

Function Setting Mode

User mode

• Switch between “User 1” 、“User 2” and “Guest” can be processed in the shutdown state or upon the measurement completion, by a short press on the “User ” button.

(Note: In the shutdown state, press the “User ” button to view the current time and the current user)

Year/Month/Date/Time setting

In the “OFF” state, enter the setting mode by long pressing the “User ” button over 3s, then enter the “Year” setting mode. After entering the “Year” setting mode, 20XX will flash on the screen. Press the “Memory ” button, and the value will be incremented between 2019 and 2039. Press the “User ” button for “Year” value confirmation and move to the “Month” setting mode. After entering the “Month” setting mode, 1-1 will flash on the screen. Press the “Memory ” button and the value will be incremented between 1 and 12. Press the “User ” button for “Month” value confirmation and enter the “Date” setting mode. After entering the “Date” setting mode, 1- 1 will flash on the screen. Press the “Memory ” button and the value will be incremented between 1 and 31. Press the “User ” button for “Date” value confirmation and enter the “Time” setting mode. After entering the “Time” setting mode, XX: XX will flash on the screen. Press the “Memory ” button, and the “Hour” value can be set. Press the “User ” button for “Hour” value confirmation and enter the “Minute” setting mode. Press the “Memory ” button, and the “Minute” value can be set.

Unit setting
Either mmHg or KPa will show up on the screen, upon entering the “Unit” setting mode by pressing the “User ” button (after the “Minute” setting mode). Display of mmHg indicates that the mmHg unit is selected; display of KPa indicates that the kPa unit is selected. Unit will be switched upon every press on the “Memory ” button. After the unit is selected, press the “User ” button again to save the unit setting.

Talking function
The talking function can be turned on/off by toggling the voice switch button on the left side of the device. The voice icon will be displayed on the screen when the voice is on, and will disappear when the voice is off. The switch button is shown as below:

Correct Method of Use

How to use the cuff

1. Place the cuff flat on the table, leave the hook & loop downwards, and pass the end of cuff through the metal ring to form a loop. The hook & loop shall point outwards.
2. Pull the cuff through the upper arm to be measured, and wear the cuff correctly based on the downward icon “ Φ ”, the air tube runs down the inside of your arm. Hook up the cuff on the upper arm according to the illustration, and ensure that the lower edge of cuff is 2~3cm away from the elbow joint. Tighten the free edge of the cuff to stick the hook & loop.
3. The cuff should be wrapped on the upper arm comfortably, with tight space for two fingers. Before measurement, remove tight-fitting clothing from your upper arm along with any thick clothing.
4. Place the lower arm flat on the desktop, leaving the centre of the palm naturally upwards, sitting upright, and ensuring the centre of cuff and the heart are at the same level. Note that the tube of cuff cannot be folded or bent.

Note: If you cannot use the left arm for measurement, please use the right arm for measurement. All the measurements must be performed on the same arm for comparison.

Starting measurement

Power on state, after you wear the cuff correctly, the “cuff detection icon ” lights up, then you can start the measurement:

1. Press the “Power ” button, and the device will return to zero automatically, the air pump will start to inflate the cuff, and the screen will display the change of the pressure in the cuff.
2. When reaching the stable pressure upon inflation, the air pump will stop the inflation, and the pressure in the cuff will be reduced gradually and displayed on the screen. If the inflated pressure is insufficient, the device will reinflate the cuff automatically for a higher pressure.
3. When the pulse is measured, the screen will display the “heart” symbol and start flashing. The flashing “heart” symbol will be displayed on the screen.
4. Upon measurement completion, the measured values of systolic pressure, diastolic pressure and pulse rate will be displayed on the screen.
5. The screen will continue to display the measurement results unless your long-press on the “Power ” button to turn off the device. If there is no operation, the device will be powered off automatically in 30s.

Note

1. When the icon shows up, it means body movements during the measurement, which may result in incorrect measurement.
2. An irregular heartbeat symbol appears in the result when an irregular rhythm is detected 2 or more times during a measurement. If it continues to appear, we recommend you to consult with and follow the directions of your physician. (An irregular heartbeat rhythm is defined as a rhythm that is 25 % less or 25 % more than the average rhythm detected while your monitor is measuring blood pressure)
3. If you suffer from an irregular heartbeat, measurements taken with this device should be evaluated with your doctor.

Using memory function

This blood pressure monitor is available for 2 users with 199 memories per user(The data of guest mode is not stored). If the 199 groups of memory data are full, they will be replaced automatically. After the blood pressure monitor has been used for several times, in the OFF state, you can press the “Memory ” button to display the latest measurement result, and track the rest data one by one via pressing the “Memory ” button. When there are over 3 measurement data, press the “Memory ” button for the average values of the latest 3 measurement data, recorded as “3 AVG”. Track the memory data by pressing The “Memory ” button from the latest measurement, recorded as “ 1 ”. Then track “ 2 ”, “ 3 ” or more via the same operation.

Clearing stored measurement data

In the off state, long press the “Memory ” and “User ” button at the same time for 3 seconds until “ “and” ” are displayed on a screen, thus all of the memory values are deleted.

Classification standard for blood pressure condition
There is no definition of hypotension yet. Generally, if the systolic blood pressure is less than 90mmHg (12kPa), it is hypotension.

Contraindications, Precautions, Warnings & Prompt Instruction

Warning

• Keep the device out of the reach of children under 12 and people who can’t express their intentions. When children of 12~18 use the device, they should be accompanied by adults. Pregnant women shall use it under the guidance of doctors.
• Do not wrap the cuff over a wound, as this can cause further injury.
• This model of Electronic Blood Pressure Monitor is suitable for the arm circumference range of 22-36cm or 22-42cm, and if the arm circumference exceeds this range, you might fail to obtain the correct measured value of blood pressure.
• This model of Electronic Blood Pressure Monitor is not suitable for newborns or young children.
• The blood pressure is constantly changing. You shall not judge the blood pressure condition with just one measurement result. The repeated measurement data over a while will be more reliable.
• Do not make self-diagnosis according to the measurement results. Please consult your professional doctor with the measurement result record(s). The treatment based on the self-diagnosis of measurement results is very dangerous.

Precautions

• Do not repair, disassemble or modify the Electronic Blood
• Pressure Monitor without permission.
• Do not collide or drop the host to avoid collision or strong impact on the device.
• Do not mix old and new batteries of different brands for use.
• Indoor temperature, environment, noise, user’s body position, speech or exercise might affect the blood pressure measurements.
• The body movement, magnetic field and improper wearing of cuff and sensor will affect the measurement as well.

Troubleshooting

If you have troubles using the device, please check the following instruction.

No display when press the Power button

| Low battery| Replace new batteries or use the USB for power supply.
The polarities of batteries are installed wrongly.| Install the batteries in correct polarities.

No pressurizing

| The air plug is loosely installed.| Make sure the air plug is securely inserted in the main

unit

The air tube is broken or leaked.| Purchase a new cuff.

The cuff leaks

| The cuff wrapped too loose| Please tighten the cuff
The cuff is broken| Replace with a new cuff

“Er 1”

displayed

| The leakage is too fast or the pulse signal is too weak|

Please check the cuff, tie it up and try again

“Er 2”

displayed

| The blood pressure signal cannot be detected due to too much noises.|

Please remove the noise sources and measure again

“ Er 3 ”

displayed

| The result of blood pressure is abnormal.|

Please remeasure in the right way.

---|---|---

“Er P”

displayed

|

The inflation fails

|

Please check the cuff, tie it up and try again.

“HI” displayed

|

The inflation pressure is greater than 295 mmHg (39kPa )

|

Please measure again.

Note: If your problem cannot be solved by the above, please contact customer service. Do not disassemble the device!

Storage & Maintenance

• Keep the device away from direct sunlight, extreme temperatures, humidity or moisture.
• Use a dry, soft cloth to clean the device, or if desired, use a cloth lightly dampened with water.
• Do not use corrosive cleaner, benzene, thinner or other volatile liquids to clean the device.
• Do not wash or expose the arm cuff to liquid.
• Remove batteries from the device when it will not be used for more than 3 months.

Disinfection

• Recommended disinfecting agent:
• Isopropanol solution with 70% concentration
• Medical alcohol with 75% concentration

Specifications

EMC Information-Guidance and Manufacture’s Declaration

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. 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.”
3. WARNING: 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 ME equipment, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.”

Table 1

declaration – electromagnetic emission

Emissions test| Compliance
RF emissions| Group 1
CISPR 11|
---|---
RF emissions

CISPR 11

| Class B
Harmonic emissions

IEC 61000-3-2

| Not applicable
Voltage fluctuations/ flicker emissions

IEC 61000-3-3

| Not applicable

Table 2

declaration – electromagnetic immunity

Immunity test| IEC 60601 test level| Compliance level
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

Electrical              fast transient/burst

IEC 61000-4-4

| ± 2 kV for power supply lines

± 1 kV for input/output

lines

| Not applicable
Surge

IEC 61000-4-5

| ± 0.5kV, ± 1 kV line(s) to lines

± 0.5kV, ± 1 kV, ± 2 kV

line(s) to earth

| Not applicable
Voltage dips, short interruptions and voltage variations on power supply input 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 cycles

| Not applicable
---|---|---
Power frequency (50/60 Hz) magnetic field

IEC 61000-4-8

| 30 A/m| 30 A/m
NOTE: UT is the a.c. mains voltage prior to application of the test

level.

Table 3

declaration – electromagnetic immunity

Immunity test| IEC 60601 test level| Compliance level
Conducted RF IEC 61000-4-6| 3 V

0.15 MHz to 80 MHz

6 V in ISM bands between

0.15 MHz and 80 MHz

| Not applicable
Radiated RF

IEC 61000-4-3

| 10V/m

80 MHz to 2.7 GHz

| 10V/m

Table 4

declaration – IMMUNITY to proximity fields from RF wireless

communications equipment

Immu nity test| IEC60601 test level| Compli ance level
Test frequency| Modulation| Maxim

um power

| Immunit y level
Radiat| 385 MHz| *Pulse| 1.8W| 27 V/m| 27 V/m
ed RF|  | Modulation:|  |  |
IEC|  | 18Hz|  |  |
61000| 450 MHz| FM+ 5Hz| 2 W| 28 V/m| 28 V/m
-4-3|  | deviation:|  |  |  
 |  | 1kHz sine|  |  |
 | 710 MHz| Pulse| 0.2 W| 9 V/m| 9 V/m
 | 745 MHz| Modulation:|  |  |
 | 780 MHz| 217Hz|  |  |
 | 810 MHz| Pulse| 2 W| 28 V/m| 28 V/m
 | 870 MHz| Modulation:|  |  |
 | 930 MHz| 18Hz|  |  |
 | 1720 MHz| Pulse| 2 W| 28 V/m| 28 V/m
 | 1845 MHz| Modulation:|  |  |
 | 1970 MHz| 217Hz|  |  |
 | 2450 MHz| Pulse

Modulation: 217Hz

| 2 W| 28 V/m| 28 V/m
---|---|---|---|---|---
5240 MHz

5500 MHz

5785 MHz

| **Pulse Modulation:

217Hz

| 0.2 W| 9 V/m| 9 V/m
**Note*** – As an alternative to FM modulation, 50 % pulse modulation at

18 Hz may be used because while it does not represent actual modulation, it would be worst case.

Note** – The carrier shall be modulated using a 50 % duty cycle square

wave signal.

FCC Statements

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.

Note: 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.

Caution: Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.

US Radiation Exposure Statement
This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment. End user must follow the specific operating instructions for satisfying RF exposure compliance. This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.

After-sale Service

• After-sale service unit: Shenzhen Jumper Medical Equipment Co., Ltd.
• Address: D Building, No. 71, Xintian Road, Fuyong Street, Baoan,
• Shenzhen, Guangdong, China
• Tel: +86-755-26696279
• E-mail: [email protected]
• Website: www.jumper-medical.com
• Postal Code: 51810

Authorized European Representative

• MedPath GmbH
• Mies-van-der-Rohe-Strasse 8, 80807 Munich,
• Germany

CONTACT

• Shenzhen Jumper Medical Equipment Co., Ltd.
• D Building, No. 71, Xintian Road, Fuyong Street, Baoan,
• Shenzhen, Guangdong, China,518103
• Tel: +86-755-26696279
• E-mail: [email protected].
• Website: www.jumper-medical.com.

References

• medical.com is for sale | www.brandforce.com
• 京柏医疗-智慧妇幼专科能力建设解决方案提供商

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