OxiPro BP2 Wireless Blood Pressure Monitor Instruction Manual

OxiPro BP2 Wireless Blood Pressure Monitor

Thank you for purchasing the Arm Blood Pressure Monitor. The device uses the oscillometric method of blood pressure measure­ment. It is intended for professional and domestic use in monitoring diastolic and systolic blood pressure and pulse rate. The device is suitable for use at home, at work, and on vacation. It is also suitable for daily blood pressure checks.

Unpacking Inspection

Before use, please open the package carefully and check whether all the parts are available according to the following packing list and whether the parts are damaged during transportation, and then install and operate in strict accordance with the manual.

Packing List

Safety Precautions

The warnings and illustrations shown in the manual are intended to enable you to use the device safely and correctly, thus preventing harm to you and others, specific meanings of which are shown as follows:

Product Composition

This device is composed of the main body and cuff.

Intended Use / Instructions for Use
The Arm Blood Pressure Monitor is intended to measure the systolic pressure and diastolic pressure, as well as the pulse rate of an adult person via a non-invasive oscillometric technique at medical facilities or at home.

Contraindication
No known contraindication exists.

Product Parts

1. Main Body

2. Display Outline

3. Systolic Blood Pressure Icon

4. Diastolic Blood Pressure Icon

5. Pulse Rate Icon

6. Pulse Rate Value

7. “Irregular Heartbeat” Indication

8. Blood Pressure Unit

9. Battery Indication

10. “User 1” Icon

11. “User 2” Icon

12. “User (guest)” Icon

13. “Keep Still” Indication

14. Memory Number

15. “Cuff Worn” Indication

16. Memory Icon

17. Average/Triple
    Measurement Indication

18. Date & Time

19. WHO Blood Pressure Indication

20. Systolic Blood Pressure Value

21. Diastolic Blood Pressure Value

22. Bluetooth Icon

3-color Backlit Indicator

Red for High Blood Pressure

Systolic Blood Pressure(mmHg)| Diastolic Blood Pressure(mmHg)| Color| Hierarchical Relationship
---|---|---|---
160| 100| Red| and (or)
140-159| 90-99| Yellow| and (or)
90-139| 60- 89| Green| and (or)
<90| <60| Yellow| and

Charging with USB-C

Please check the device’s power before using it. When the battery runs out, please use the manufacturer-provided Type-C charging cable to charge the device till the ‘ ” indicator stops flashing powered from a mobile phone charger or device with powered USB output.

Function Setting

To Select User
In power-off mode, press the ” ” button to enter the user group selection interface. Then press the “ ” button again to switch and select user groups.

(2)Year/Month/Date Setting
In power-off mode, press the ” fl1. ” button for about 3 seconds to enter the date setting, and “year” will flash. Press the button to adjust to the desired year, and then press the “ ” button to confirm the selection. When the “year’ is set, ii will automatically enter the month setting. At this time, the “month” icon will flash. You can switch to the desired value by pressing the” “button. Follow the same step to set “date”, “hour”, and “minute”.

(3) Unit Display Setting
In power-off mode, keep pressing the” “button for about 3 seconds to enter the unit selection. Press the” “button to switch between mmHg and kPa, and then press the ” ” button to confirm the selection. The default unit is mmHg.

How to Take Proper Measurements

Preparation before measurement

• Always measure in the same arm (generally the left arm). –Remain still and keep quiet during measurement.

• Relax as much as possible and do not talk during measurement.

• Measure your blood pressure at about the same time every di3y.

• Do not measure right after physical exercise or a bath. Rest for 20 to 30 minutes before taking the measurement.

• Readings under the conditions Tisted below may affect results:
  Within an hour after dinner, after having wine, coffee, tea, sports; talking, being nervous, being in unsteady mood, bending forward, moving, room temperature dramatically changing during measuring; inside a moving vehicle, repeated and continuous measuring.

• (2) Wearing the cuff correctly

• 1. Unroll the cuff. Place your arm inside it. (We strongly recommend to use your left arm.)

Make sure that the device’s screen is positioned on your inner arm as illustrated in the diagram. The bottom edge of the cuff should be 0. 79-1.18 inches (2 to 3 cm) above lhe inside elbow.

Tighten the cuff around your arm, so it can not move around your arm.
Note: Repeated measurements may result in blood congestion in the arm, which will affect the measurement result. To avoid this situation, we advise that you can raise the left hand and hold the fist for several times, or take off the cuff and rest for at least 2-3 minutes before taking the measurement.

Measurement tips

• To take a measurement, you need to be relaxed and comfort­ably seated in a room with a comfortable temperature.

• Sit in a comfortable chair with your back and arm supported.

• Keep your feet flat and your legs uncrossed.

• The device should be placed on your inner arm at the same level as your heart, with the arm resting comfortably on a table.

• Please use only the manufacturer-provided cuff, as it has passed all required clinical trials.

Any replacement of the original components with materials not specified or provided by the manufacturer may result in measure­ment errors.

Taking a measurement
Press the “ ” button and the monitor will begin to inflate. Please do not move or talk during the measurement.

Note: If you feel uncomfortable during the measurement, press the “ “button immediately to stop measure. When the air pressure is filled to a certain value, the value on the display screen will slowly drop at a certain speed, and the heartbeat symbol will flash. After measurement 1s completed, the systolic pressure, diastolic pressure, and pulse measurements will be displayed on the screen.

Note: Consult your doctor if unexpected readings are obtained.

Memory function

1. 1. Each measured value is stored automatically under the appropriate “User” group. This device can store up to 120 sets of measurements for each user. (Note: There is no memory for “Guest”.) Once the memory log is full, old values are refreshed with new ones.
2. 2. In power-off mode, press the ” ” button once and the device will display the average value of the blood pressure measurements of the last 2 or 3 times. Press the ” ” button again, and the latest measured value will be displayed. Press the “? ” button again and the rest memories will be displayed one by one.

Delete memory
In the power-off mode, press the button to select the
user group whose measured values need to be deleted.
Press the ” ” to power off the device, then press the ” once, and then keep pressing the button for 3 seconds to delete memories of the selected user and the ” ” icon will appear on the screen.

“Cuff Worn” Detection

The “ ” icon is always displayed on the screen when the cuff is worn correctly. When the cuff is worn too loosely, the “ ” icon will always flash to remind you. If the” 0)” icon is flashing all the time, please press the “ ” button to stop the measurement.

“Keep Still” indication
The ” ” icon flashes when you move the body or shake the hand during the measurement, which may cause incorrect measurement results. Please measure again.

Contraindications, Precautions, Warnings and Prompt Instructions

• No maintenance or servicing when using.

• Do not operate when charging.

• Dispose of the monitor when its service life is reached. Follow local regulations regarding the disposal of such products.

• Maintenance should be done by the operator as suggested

• Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30cm (12 inches) to any part of this device, including the cable specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.

• When the ambient temperature is less than 5°C, please take the device to the place where the ambient temperature is between° 5 C-40°C at least 1 hour; When the ambient temperature is higher than 40°C, please take the device to the place where the ambient temperature is between 5°C-40°C at least 2 hours.

• DO NOT use this monitor on infants, toddlers, children or persons who cannot express themselves.

• DO NOT take medicine based on readings from the device. Contact your physician for specific information about your blood pressure. The user should not self-diagnose or self-medicate per measured results. Kindly adhere to the instructions of your physician or health provider.

• DO NOT use this monitor on an injured arm or an arm under medical treatment.

• DO NOT use the device while you are on an intravenous drip or blood transfusion.

• DO NOT use this monitor in areas containing high-frequency (HF) surgical equipment, magnetic resonance imaging (MRI) equipment, or computer tomography (CT) scanners. This may result in incorrect operation of the monitor and/or cause an inaccurate reading.

• Consult with your physician before using this monitor if you have common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation, arterial sclerosis, poor
  Perfusion, diabetes, pregnancy, pre-eclampsia or renal disease. NOTE that any of these conditions in addition to patient motion, trembling, or shivering may affect the measurement reading.

• NEVER diagnose or treat yourself based on your readings. ALWAYS consult with your physician.

• To avoid strangulation, keep the type C cable away from infants, toddlers and children.

• Stop using this monitor and consult with your physician if you experience skin irritation or discomfort.

• Consult with your physician before using this monitor on an arm where intravascular access or therapy, or an
  arterio-venous (A-V) shunt, is present because of temporary interference to blood flow which could result in injury.

• Consult with your physician before using this monitor if you have had a mastectomy.

• Consult with your physician before using this monitor if you have severe blood flow problems or blood disorders as cuff inflation can cause bruising.

• DO NOT use this monitor for any purpose other than measuring blood pressure and pulse rate.

• DO NOT disassemble or attempt to repair this monitor or other components. This may cause an inaccurate reading.

• DO NOT use in a location where there is moisture or a risk of water splashing this monitor. This may damage this monitor.

• DO NOT use this monitor in a moving vehicle such as in a car.

• DO NOT drop or place this monitor to strong shocks or vibrations.

• DO NOT use this monitor in places with high/low humidity and temperatures.

• 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.

• 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.

Common Q &A on Blood Pressure

• Why is the blood pressure value obtained at home lower than that obtained at the hospital?
  • The blood pressure difference between home and hospital measurements is about 20 mmHg – 30 mmHg (2.7 kPa – 4.0 kPa). This is because individuals tend to be more relaxed at home than at the hospital.
  • Also, when the device is placed at a position over the heart, the blood pressure value tends to be much lower than it actually is. Ensure the device is positioned right at the heart level.
• Why is the blood pressure value obtained at home higher than that obtained at the hospital?
  • The anti-hypertensive drug the patient might be using has lost its efficacy. Kindly adhere to your doctor’s instructions.
  • The cuff might not be in the correct position. If the cuff is not placed right, no arterial pressure value will be obtained, and the blood pressure value might be much higher than it is. Therefore, properly position the cuff.
  • The cuff is not tight enough. If the cuff is loose, the compres­sion force might fail to transmit to the artery, causing the blood pressure value to be much higher than it is. Therefore, re-adjust and tighten the cuff further.
  • The patient is not sitting correctly during measurement. Slouching, tilting, bending, and sitting cross-legged are not encouraged while taking blood pressure measurements due to increased abdominal pressure or the arm position being below the heart. Kindly take readings in the correct posture.
• Q3: When can I obtain better measurements?
  • Measurements are best taken in the mornings right after you urinate or when your mind and body are stable. We recom­mend taking readings at the same time of the day, every time.
• Abnormal Phenomena and Handling
  If the measurement is abnormal, any of the following symbols may appear. Kindly use the recommended method for measurement.

Error codes are displayed on page 25

Cleaning and Disinfection

Cleaning

• The device can be cleaned with a soft, clean cloth dampened with a small amount of neutral detergent or water.
• Do not use corrosive cleaning agents, and take care not to o immerse any part of the monitor in any fluid.
• It is suggested to clean once every week. Complete the cleaning in 3min each time.

Disinfection
Recommended Disinfecting Agent 75% medical alcohol

Steps:

1. Carefully wipe the device with a soft, clean cloth dampened with a small amount of the above disinfectant, and dry immediately with a soft, clean, dry cloth.
2. The body of the device can also be cleaned with a soft, clean cloth dampened with a small amount of 75% medical alcohol for disinfection.
3. Do not disinfect through methods like high-temperature steam or ultraviolet radiation. These might damage the device and reduce its service life.
   It is suggested to disinfect the monitor before and after use each time. Each time of disinfection shall be completed within 1 min. The number of repeated disinfection of each lime shall not exceed 2 limes.

Disposal

• Dispose of your monitor, other components, and optional accesso­ries according to applicable local regulations.
• Unlawful disposal may cause environmental pollution.

Notes

• Do not bend or crease the air tube excessively.
• Do not store the monitor or its components:
  • if the monitor or its parts is wet
  • in locations with extreme temperatures, humidity, direct sunlight, dust, or corrosive gases.
  • in areas with a high risk of vibrations or shocks.

Upkeep and Maintenance

• Always keep the surface of the monitor clean and tidy, which helps to prolong the service life of the Blood Pressure Monitor.
• If the host is dirty, please wipe with a dry soft cloth. If the dirt cannot be eliminated easily, wipe with a soft cloth stained with water or neutral detergent, and then dry with a dry cloth.
• No maintenance or maintenance is required when using the device.

WARNING: Do not allow water or other liquids to flow into the host.

Specifications

Pneumatic Pressure

Measuring Range

| 0-295 mmHg (0-39.3 kPa)
---|---
Maximum Pressure

Protection

| 295 mmHg (39.3 kPa)

Measurement Range

| Blood Pressure Va lue| SYS: 57-255 mmHg

(7.6-33.4 kPa);

DIA: 25-195 mmHg

(3.33-26 kPa);

Pulse Rate| 40-199 bpm

Accuracy

| Blood

Pressure Value

| ****

±3 mmHg (±0.4 kPa)

Pulse Rate| ±5%

Memory

| It can be used for 3 users (user 1,

user 2 and guest mode) .

2 user **s* 120 memories and guest mode w ithout memory .**

Po wer Source| 3.7V rechargeable lithium battery
Charging Method| Type-C charg ng port ; Charging voltage: d.c. 5V
Low Battery| Whe n the power is lower than 3.4V , the device will be turned off .
Dimension| 123 mm (L) x 59 mm (W) x 28mm (H)

(4.84 nchesx2.32inchesx1 . 10 nches)

Screen Size| 75mm (L) x 35 mm (W) (3.2 nches)
Cuff Size| 22-42 cm (8.66-16.53 inches)
Weight| About 225g
Anti Electroni c

Shock Type

| Internal Power Supply
Auto Power-off| 1 Minute W ithout Operation
Anti Electronic

Shock Degree

| Type BF
Protection Against Harmful Ingress of Wa ter or Particular Matter| ****

IP22

Service Life| 5 years
Protection Against Electric Shock| Internally powered supply
---|---

Operating Environment

| 6  i  ure| 5’C-40 ‘C| s r y nd

: i: ! !ed and hum d ty

gb s I properly.

Humidity Condition| 15%-90% RH
Atmospheric Condition| 70kPa- 106kPa

Transportation and Storage Environment

| Avoid strong impact, direct impact, exposure or rain during transportation. The device shall be stored ndoors at the temperature of -20’C -55 ‘C and the relative hum d ty of 10%-93%, atmospheric condition:

70kPa-106kPa without corrosive gas and with good ventilation.

Appendix 1 EMC lnfonnation

Guidance and manufacturer’s declaration –

Electromagnetic emission

Arm Blood Pressure Monitor is intended for use in the electromagnetic environment specified below. The customer or the user of the Arm Blood Pressure Monitor should assure that it is used in such an environment.
Emissions| Complian

ce

| Electromagnetic

environment

– guidance

RF emissions CISPR 11

|

Group 1

| The Arm Blood Pressure Monitor

uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions CISPR 11

|

Class B

| The Arm Blood Pressure

Monitor 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| NA
IEC61000-3-2|
Voltage|
fluctuations/flick|
| NA
emissions|
IEC61000-3-3|
Guidance and manufacturer’s declaration

– Electromagnetic immunity

The Arm Blood Pressure Monitor is intended for use in the electromagnetic

environment specified below. The customer or the user of Arm Blood Pressure Monitor should assure that it is used in such an environment.

Immunity test| IEC 60601

test level

| Compliance level
Electrostatic

discharge (ESD) IEC 61000-4-2

| ±8kV contact

±2 kV,±4kV,±8 kV,

±15kV air

| ±8 kV contact

±2 kV,±4 kV,

±8 kV,±15 kV air

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

transienVburst IEC 61000-4-4

| Not applicable| Not applicable
Surge

IEC 61000-4-5

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

61000-4-11

| Not applicable| Not applicable
Power frequency

Magnetic field IEC 61000-4-8

| 30A/m, 50/60Hz| 30Nm , 50/60Hz
Conducted RF

IEC61000-4-6

| Not applicable| Not applicable
Radiated RF IEC61000-4-3| 10 V/m

80 MHz- 2,7 GHz

80 %AM at 1 kHz

| 10V/m

80 MHz – 2,7 GHz

80%AMat1 kHz

NOTE: UT is the a.c. mains voltage prior to application of the test level
Guidance and manufacturer’s declaration – electromagnetic Immunity

The Arm Blood Pressure Monitor is intended for use in the electromagnetic

environment specified below. The customer or the user of the Arm Blood Pressure Monitor should assure that it is used in such an environment.

Radiate

d RF IEC6100 0-4-3

(Test specifica tionsfor ENCLO SURE PORT IMMUNI

TY to RF

wireless

ications equIpme ot)

| Test

Frnq, ency( MHz)

|

Band (MHz)

| Service| Modula

lion

| Ma,

P=

ec

(W)

| o;

st

00

(m)

| IEC

60601-1-2

Test level (V/m)

| Comp

liance level (V/m)

385| 380

390

| TETRA

400

| Pulse

modula lion 18Hz

| 1,8| 0.3| 27| 27
450| 430

470

| GMRS

460, FRS 460

| FM

t5kHz deviation 1 kHz

| | 0.3| 28| 28
| 710| 704| LTE

Band

| Pulse

modula

| 0,2| 0.3| 9|
| 787| 13.17| lion| | |
| | | 217Hz| | |
810| 800| GSM

800/900.

| Pulse

modula

| | 03| 28| 28
| 960| TETRA

800,

| lion

18Hz

| | |
| | iDEN| | | |
| | 820,| | | |
| | CDMA| | | |
| | 850,| | | |
| | LTE| | | |
| | Bands| | | |
1720| | GSM| Pulse| | 0.3| 28| 28
| | 1800;| modula| | |
| | CDMA| lion| | |
1845| 1700| 1900;| 217Hz| | |
| 1990| GSM

1900;

| | | |
| | DECT;| | | |
| | LTE| | | |
| | Band| | | |
| | 1.3,| | | |
| | 4,25;| | | |
| | UMTS| | | |
2450| | Bluelo| Pulse| | 0.3| 28| 28
| | oth,| modula| | |
| | WLAN,| lion| | |
| 2400| 802.11

blgln,

| 217Hz| | |
| 2570| RFID| | | |
| | 2450,| | | |
| | LTE| | | |
| | Band7| | | |
5240| | WLAN| Pulse| 0,2| 03| 9|

5500

| 5100

5800

| 802.11

alo

| modula lion

217Hz

| | |
5785| | | | | |
Guid a n ce a nd m a nuf a ctu re r ‘ s de cl a r at ion – e l e ctrom a gn etic Immun i t y

Radiated RF IEC61000-4·39

(Test specifications for ENCLOSURE PORT IMMUN I TY

toproxmty magneticlelds)

| Test Frequency| Moduation| IEC 60601 · 1 – 2

Test Level (Alm)

| Compliance level (Alm)
30k H Z| CW| |
|

modulatioo

2.1 kHz

| |
13.56kHZ| Pulse modulation SO kHz| 7.5| 7.5

NOTE

• Optional AC adaptor should comply with the requirement of IEC 60601-1 standard.
• Use only the exclusive AC adapter specified by authorized dealers. Other AC adapters may vary in output voltage and polarities and may represent a risk to your life and damage the device.

Limited Warranty Terms

WARRANTOR
This Limited Warranty is granted by and this Limitation of Liability is stipulated for the benefit of OxiPro, a trademark of OxiPro Medical Ltd, at the address displayed on www.OxiPro.io.

WHAT THIS WARRANTY COVERS
OxiPro Medical Ltd. (“OxiPro”) warrants to you that the Hardware will be free from defects in workmanship and materials under normal use (“Defects”) for two (2) years (unless the country of purchase requires a longer period under local legislation) from the date that the Hardware was first purchased by you from an authorized OxiPro dealer (“Warranty Period”). During the Warranty Period, the Hardware will be repaired or replaced at OxiPro’s choice (“Limited Warranty”) without charge to you for either parts or labor. This Limited Warranty covers the replacement of the Hardware only. If the Hardware is repaired after the Warranty Period has expired (at your cost), the Warranty Period for the repair will expire six (6) months after the date of repair.

WHAT THIS WARRANTY DOES NOT COVER
The Limited Warranty does not apply to normal wear and tear, does not apply when the Hardware is opened or repaired by someone not authorized by OxiPro, and does not cover repair or replacement of any Hardware or part thereof damaged by: misuse, moisture, liquids, proximity or exposure to heat and accident, abuse, non-compliance with the instructions supplied with the Hardware, neglect or misapplication. The Limited Warranty does not cover physical damage to the surface of the Hardware or calibration of the Hardware.

HOW TO MAKE A WARRANTY CLAIM
To claim a Defect, you must contact OxiPro by email or telephone during the Warranty Period via www.OxiPro.io to explain the Defect and to obtain an RMA number (Return Materials Authorisation) if necessary. You must return the Hardware during the Warranty Period, along with an explanation of the Defect, to the address provided to you by OxiPro. If a defect arises and a valid claim under this Limited Warranty is received by OxiPro after the first one hundred and eighty (180) days of the Warranty Period, OxiPro is entitled to charge you for any reasonable shipping and handling costs made in connection with the repair or replacement of the Hardware. You must comply with any other return procedures stipulated by OxiPro, if any.

YOUR LEGAL RIGHTS

• Some countries may not allow the exclusion or limitation of damages. If any part of this Limited Warranty is held to be invalid or unenforceable, the remainder of the Limited Warranty shall nonetheless remain in full force and effect.
• This Limited Warranty is the only express warranty made to you and is provided instead of any other express warranties or similar obligations (if any) created by any advertising, documentation, packaging, or other communications.
• Except for the Limited Warranty and to the maximum extent permitted by applicable law, OxiPro and its suppliers provide the Hardware “AS IS AND WITH ALL FAULTS”, and hereby disclaim all other warranties and conditions, whether express, implied or statutory, including, but not limited to, any (if any) implied warranties, duties or conditions of satisfactory quality, of fitness for a particular purpose, of reliability or availability, of accuracy or completeness of responses, of results, of workmanlike effort, of lack of viruses, and reasonable care and skill, all concerning the Hardware, and the provision of or failure to provide support or other services, information, software, and related content through the Hardware or otherwise arising out of the use of the Hardware. Also, there is no warranty or condition of quiet enjoyment, quiet possession, or non-infringement about the Hardware. This exclusion does not apply to (i) any implied condition as to title and (ii) any implied warranty as to conformity with description.
• This Limited Warranty does not affect any legal rights under applicable national legislation governing the sale of consumer goods.
• This Limited Warranty cannot be transferred to any other person.

LIMITATION OF LIABILITY

1. Neither OxiPro Medical Ltd nor its suppliers shall be liable to you or to any third party for any damages either direct, indirect, incidental, consequential, or otherwise (including in each case, but not limited to, damages for the inability to use the equipment, loss of business, loss of profits, business interruption or the like) arising out of the use of or inability to use the Hardware even if OxiPro Medical Ltd has been advised of the possibility of such damages.

2. Notwithstanding any damages that you might incur for any reason whatsoever
   (including, without limitation, all damages referenced herein and all direct or general damages in the contract or anything else), the entire liability of OxiPro Medical Ltd and any of its suppliers shall be limited to the amount actually paid by you for the Hardware.

3. OxiPro Medical Ltd shall not be liable for (i) any fraud on the part of its employees and/or agents; or (ii) any fraudulent misrepresentation on the part of its employees and/or agents.

4. Notwithstanding the above, neither party’s liability for death or personal injury resulting from its own negligence shall be limited.

5. If any of these terms shall become or be declared illegal, invalid or unenforceable for any reason whatsoever such term shall be divisible from these terms and shall be deemed to be deleted from them.

Troubleshooting & Error Codes

indicator

stops fiash ng

Error displayed| Check error codes and remedies| Keep your arm and body still

Check error codes in this manual

Air cuff leakage| The airbag of the

cuff is ripped

| Please contact the dealer to replace with

a new cuff. Don’t change the cuff by yourself

If the blood pressure still cannot be measured after trying the

A above-stated solutions, please contact us. Do NOT

attempt to disassemble the device by yourself.

Error codes are displayed on the next page

12 seconds. Check the cuff is secured round the arm correctly.

ErH| Cuff pressure has reached 295mmHg, and

deflates automatically after 20 seconds. Please contact us.

Er1| The pulse rate is not detected correctly. Please reposition the cuff and try again.
Er2| Movement or interference is detected during

measurement. Please read section 11 and retry the measurement.

Er3| The measurement result is unexpected, please read section 11 and retry the measurement.
Er23| SYS value is lower than 57mmHg, please read section 11 and retry the measurement.
Er24| SYS value is higher than 255mmHg, please read section 11 and retry the measurement.
Er25| DIA value is lower than 25mmHg, please read section 11 and retry the measurement.
Er26| DIA value is higher than 195mmHg, please read section 11 and retry the measurement.

Product support & warranty

• Web: oxipro.io
• Email: hello@oxipro.io
• UK: 01628 778885
• IE: 015137065
• Lines open Mon-Fri 0900-1700
• OxiPro Medical Lid
• Unit 3, Maidenhead Enterprise Centre,
• Cordwallis Street, Maidenhead
• SL6 7BE. United Kingdom
• Shenzhen AOJ Medical Technology Co., Ltd.
• Room 301&4F, Block A, Building A, Jingfa Intelligent Manufacturing Park, Xiaweiyuan, Gushu Community, Xixiang Street, Baoan District, 518126 Shenzhen, CHINA

Share Info GmbH

• Heerdter. Lohweg 83, 40549 DLlsseldorf, GERMANY
• Tel: 0049 179 5666 508
• E-mail: EU-Rep@share-info.com
• UK: Share Info Ltd
• Responsible:
• Person:  House, Park Street Walsall, West Midlands, WSl lNS, UK
• Model: AOJ-33A

Made in China

Read User Manual Online (PDF format)

Read User Manual Online (PDF format)  >>

Download This Manual (PDF format)

Download this manual  >>