microlife AFIB Advanced Easy Blood Pressure Monitor User Manual

microlife AFIB Advanced Easy Blood Pressure Monitor

Product Information

The Microlife AFIB ADVANCED EASY is a blood pressure monitor that also detects Atrial Fibrillation. It is manufactured by Microlife AG, a company based in Switzerland. The device is equipped with a cuff, display, and several indicators such as systolic value, diastolic value, pulse rate, battery display, traffic light indicator, stored value, pulse indicator, Atrial Fibrillation Indicator (AFIB), cuff check indicator, AFIB/MAM mode,and arm movement indicator. The device operates on batteries or can be connected to the mains adapter socket. The Microlife AFIB ADVANCED EASY is a medical device that should be kept away from children of age 0-3.

Product Usage Instructions

1. Before using the device, read the instructions for use carefully.
2. Fit the cuff closely around your upper arm but not too tight.
3. Perform the measurement before medication intake.
4. If it is your first time using the device, insert the batteries and select the correct cuff size and mode.
5. Press the START/STOP button to begin the measurement.
6. The device will display your systolic and diastolic values, pulse rate, and other indicators such as battery display and traffic light indicator.
7. The Atrial Fibrillation Indicator (AFIB) will only be active in AFIB/MAM mode.
8. After use, turn off the device and store it in a dry place.
9. Dispose of batteries and electronic devices according to locally applicable regulations.

Preparazione

1. Sit on a back-supported chair and keep your legs uncrossed.
2. Avoid thick or close-fitting garments on the upper arm.
3. Place the artery-mark on the cuff over your artery.
4. Fit the cuff closely, but not too tight.
5. Position the cuff 1-2 cm above your elbow.
6. Keep your arm still and do not speak during the measurement.

Microlife AFIB ADVANCED EASY

BP A6 Advanced Easy

Prima di ogni misurazione

1. Avoid eating, bathing, smoking or caffeine (approx. 30 min).
2. Avoid activity and relax for 5-10 min.
3. Measure before medication intake.

Microlife BP A6 Advanced Easy

1. START/STOP Button

2. Display

3. Cuff socket

4. Mains Adapter Socket

5. Battery compartment

6. Cuff

7. Cuff connector

8. Cuff tube

9. AFIB/MAM Switch

10. Lock switch
    Display

11. Systolic value

12. Diastolic value

13. Pulse rate

14. Battery display

15. Traffic light indicator

16. Stored Value

17. Pulse indicator

18. Atrial Fibrillation Indicator (AFIB)

19. Cuff check indicator

20. AFIB/MAM Mode

21. Arm movement indicator

22. AFIB/MAM Interval time

Read the important information in these instructions for use before using this device. Follow the instructions for use for your safety and keep it for future reference.

Type BF applied part

Keep dry

Manufacturer

Batteries and electronic devices must be disposed of in accordance with the locally applicable regulations, not with domestic waste.

Authorized representative in the European Community

Catalogue number

Serial number
(YYYY-MM-DD-SSSSS; year-month-day-serial number)

Caution

Humidity limitation

Temperature limitation

Medical device

Keep away from children of age 0 – 3

CE Marking of Conformity

Intended use:
This oscillometric blood pressure monitor is intended for measuring non- invasive blood pressure in people aged 12 years or older.
It is clinically validated in patients with hypertension, hypotension, diabetes, pregnancy, pre-eclampsia, atherosclerosis, end-stage renal disease, obesity and the elderly.
The device can detect an irregular pulse suggestive of Atrial Fibrillation (AF). Please note that the device is not intended to diagnose AF. A diagnosis of AF can only be confirmed by ECG. The patient is advised to see a physician.

Dear Customer,
This device was developed in collaboration with physicians and clinical tests carried out prove its measurement accuracy to be of a very high standard.*
Microlife AFIB detection is the world’s leading digital blood pres-sure measurement technology for the detection of atrial fibrillation (AF) and arterial hypertension. These are the two top risk factors of getting a stroke or heart disease. It is important to detect AF and hypertension at an early stage, even though you may not experi-ence any symptoms. AF screening in general and thus also with the Microlife AFIB algorithm, is recommended for people of 65 years and older. The AFIB algorithm indicates that atrial fibrillation may be present. For this reason, it is recommended that you visit your doctor when the device gives an AFIB signal during your blood pressure measurement. The AFIB algorithm of Microlife has been clinically investigated by several prominent clinical investiga-tors and showed that the device detects patients with AFIB at a
certainty of 97-100%. 1,2

If you have any questions, problems or want to order spare parts please contact your local Microlife-Customer Service. Your dealer or pharmacy will be able to give you the address of the Microlife dealer in your country. Alternatively, visit the internet at www.microlife.com where you will find a wealth of invaluable infor-mation on our products.

Stay healthy – Microlife AG!

• This device uses the same measuring technology as the award winning «BP 3BTO-A» model tested according to the British and Irish Hypertension Society (BIHS) protocol.
  1 Kearley K, Selwood M, Van den Bruel A, Thompson M, Mant D, Hobbs FR et al.: Triage tests for identifying atrial fibrillation in primary care: a diagnostic accuracy study comparing single-lead ECG and modified BP monitors. BMJ Open 2014; 4:e004565.
  2 Wiesel J, Arbesfeld B, Schechter D: Comparison of the Microlife blood pressure monitor with the Omron blood pressure monitor for detecting atrial fibrillation. Am J Cardiol 2014; 114:1046-1048.
  Beime B, Kruger R, Hammel G, Bramlage P, Deutsch C. Validation of the microlife bp a3 pc upper arm blood pressure monitor in patients with diabetes mellitus according to the ansi/aami/iso 81060-2: 2013 protocol. Blood Press Monit. 2018;23:52-57.

Appearance of the Atrial Fibrillation Indicator for early Detection (Active only in AFIB/MAM mode)
This device is able to detect atrial fibrillation (AF). This symbol AR indicates that atrial fibrillation was detected during the measure-ment. Please refer to the next paragraph for information regarding the consultation with your doctor.

Information for the doctor on frequent appearance of the atrial fibrillation indicator
This device is an oscillometric blood pressure monitor that also analyses pulse irregularity during measurement. The device is clinically tested.
The AFIB symbol is displayed after the measurement, if atrial fibrillation occurred during measuring. If the AFIB symbol appears after having performed a full blood pressure measure-ment episode (triplicate measurements), the patient is advised to perform another measurement episode (triplicate measure- ments). If the AFIB symbol appears again, we recommend the patient to seek medical advice.
If the AFIB-symbol appears on the screen of the blood pressure monitor, it indicates the possible presence of atrial fibrillation. The atrial fibrillation diagnosis however, must be made by a cardiologist based on ECG interpretation.

• Keep the arm still during measuring to avoid false readings.
• This device may not or wrongly detect atrial fibrillation in people with pacemakers or defibrillators.
• In the presence of atrial fibrillation the diastolic blood pressure value may not be accurate.
• In the presence of atrial fibrillation using AFIB/MAM-mode is recommended for more reliable blood pressure measurement.

What is Atrial Fibrillation (AF)?
Normally, your heart contracts and relaxes to a regular beat. Certain cells in your heart produce electrical signals that cause the heart to contract and pump blood. Atrial fibrillation occurs when rapid, disorganized electrical signals are present in the heart’s two upper chambers, called the atria; causing them to contract irregu-larly (this is called fibrillation). Atrial fibrillation is the most common form of heart arrhythmia. It often causes no symptoms, yet it significantly increases your risk of stroke. You’ll need a doctor to help you control the problem.

Who should be screened for Atrial Fibrillation?
AF screening is recommended for people over 65 years of age, since the chance of having a stroke increases with age.
AF screening is also recommended for people from the age of 50 years who have high blood pressure (e.g. SYS higher than 159 or DIA higher than 99) as well as those with diabetes, coronary heart failure or for those who have previously had a stroke.
In young people or in pregnancy AF screening is not recom-mended as it could generate false results and unnecessary anxiety. In addition, young individuals with AF have a low risk of getting stroke as compared to elder people.

Risk factors you can control
Early diagnosis of AF followed by adequate treatment can signifi-cantly reduce the risk of getting stroke. Knowing your blood pres-sure and knowing whether you have AF is the first step in proactive stroke prevention.
For more information visit our website: www.microlife.com/afib.

Important facts about blood pressure and self-measurement

• Blood pressure is the pressure of the blood flowing in the arteries generated by the pumping of the heart. Two values, the systolic (upper) value and the diastolic (lower) value, are always measured.
• The device indicates the pulse rate (the number of times the heart beats in a minute).
• Permanently high blood pressure values can damage your health and must be treated by your doctor!
• Always discuss your values with your doctor and tell them if you have noticed anything unusual or feel unsure. Never rely on single blood pressure readings.
• There are several causes of excessively high blood pressure values. Your doctor will explain them in more detail and offer treatment where appropriate.
• Under no circumstances should you alter the dosages of drugs or initiate a treatment without consulting your doctor.
• Depending on physical exertion and condition, blood pressure is subject to wide fluctuations as the day progresses. You should therefore take your measurements in the same quiet conditions and when you feel relaxed! Take at least two readings every time (in the morning and in the evening) and average the measurements.
• It is quite normal for two measurements taken in quick succes-sion to produce significantly different results.
• Deviations between measurements taken by your doctor or in the pharmacy and those taken at home are quite normal, as these situations are completely different.
• Several measurements provide much more reliable information about your blood pressure than just one single measurement.
• Leave a small break of >5 minutes between two measurements.
• If you suffer from a cardiac arrhythmia consult with your doctor before using the device. See also chapter «Appearance of the Atrial Fibrillation Indicator for early Detection (Active only in AFIB/MAM mode)» of this user manual.
• The pulse display is not suitable for checking the frequency of heart pacemakers!
• If you are pregnant, you should monitor your blood pressure regularly as it can change drastically during this time.
  • This monitor is specially tested for use in pregnancy and pre-eclampsia. When you detect unusual high readings in pregnancy, you should measure after a short while again (eg. 1 hour). If the reading is still too high, consult your doctor or gynecologist.
  • In pregnancy the AFIB symbol can be ignored.

Using the device for the first time

Inserting the batteries
Switch the lock switch AT to «unlock» position. The battery compartment 5 is on the bottom of the device. Insert the batteries (4 x 1.5 V, size AAA), thereby observing the indicated polarity.

Selecting the correct cuff
Microlife offers different cuff sizes. Select the cuff size to match the circumference of your upper arms (measured by close fitting in the centre of the upper arm).

Only use Microlife cuffs.

• Contact your local Microlife Service if the enclosed cuff 6 does not fit.
• Connect the cuff to the device by inserting the cuff connector 7 into the cuff socket 3 as far as it will go.

If you buy a spare Microlife cuff, please remove the cuff connector 7 from the cuff tube 8 from the cuff supplied with the original device and insert this cuff connector into the tube of the spare cuff (valid for all cuff sizes).
Spare part cuffs are delivered with different cuff connectors 7. If you exchange/replace the cuff for this device please ensure that is the same connector as the one supplied with the original cuff.

Selecting standard or MAM mode
This device enables you to select either standard (standard single measurement) or AFIB/MAM mode (automatic triple measure-ment). To select standard mode, slide the AFIB/MAM switch 7 on the side of the device downwards to position «1» and to select AFIB/MAM mode, slide this switch upwards to position «3». MAM-Mode
In AFIB/MAM mode, 3 measurements are automatically taken in succession and the result is then automatically analysed and displayed. Because the blood pressure constantly fluctuates, a result determined in this way is more reliable than one produced by a single measurement.

• When you select the 3 measurements, the AFIB/MAM-symbol BT appears in the display.
• The bottom, right hand section of the display shows a 1, 2 or 3 to indicate which of the 3 measurements is currently being taken.
• There is a break of 15 seconds between the measurements. A count down indicates the remaining time.
• The individual results are not displayed. Your blood pressure will only be displayed after all 3 measurements are taken.
• Do not remove the cuff between measurements.
• If one of the individual measurements was questionable, a fourth one is automatically taken.
  • Microlife AFIB is also activated in standard mode. If the device detects AF in standard mode, the cuff pressure will stop at a level of approx. 60 mmHg to receive more data. The hourglass 15 will appear in the display.

Taking a blood pressure measurement

Checklist for taking a reliable measurement

1. Avoid activity, eating or smoking immediately before the measurement.

2. Sit down on a back-supported chair and relax for 5 minutes. Keep your feet flat on the floor and do not cross your legs.

3. Always measure on the same arm (normally left). It is recom-mended that doctors perform double arm measurements on a patients first visit in order to determine which arm to measure in the future. The arm with the higher blood pressure should be measured.

4. Remove close-fitting garments from the upper arm. To avoid constriction, shirt sleeves should not be rolled up – they do not interfere with the cuff if they are laid flat.

5. Always ensure that the correct cuff size is used
   (marking on the cuff).

6. Fit the cuff closely, but not too tight.

7. Make sure that the cuff is positioned 1-2 cm above the elbow.

8. The artery mark on the cuff (ca.3 cm long bar) must lie over the artery which runs down the inner side of the arm.

9. Support your arm so it is relaxed.

10. Ensure that the cuff is at the same height as your heart.

11. Slide the lock switch AT down to the «unlock» position. Press the START/STOP button 1 to start measuring.

12. The cuff will now pump up automatically. Relax, do not move and do not tense your arm muscles until the measurement result is displayed. Breathe normally and do not talk.

13. When the correct pressure is reached, the pumping stops and the pressure falls gradually. If the required pressure was not reached, the device will automatically pump some more air into the cuff.

14. During the measurement, the pulse indicator AQ flashes
    in the display.

15. The result, comprising the systolic AK and the diastolic AL blood pressure and the pulse rate AM are displayed. Note also the explanations on further display symbols in this booklet.

16. When the device has finished measuring, remove the cuff.

17. Switch off the device. (The monitor does switch off automati-cally after approx. 1 min.).

18. You can stop the measurement at any time by pressin g the START/STOP button or open the cuff (e.g. if you feel uneasy or an unpleasant pressure sensation).

19. If the systolic blood pressure is known to be very high,it can be an advantage to set the pressure individually. Press the START/STOP button after the monitor has been pumped up to a level of approx. 30 mmHg (shown on the display). Keep the button pressed until the pressure is about 40 mmHg above the expected systolic value – then release the button.

How do I evaluate my blood pressure
The LED traffic light indicator on the left-hand side of the display AP indicates within which range the measured blood pressure lies. The value is either within the optimum (green), elevated (yellow) or high (red) range. The classification corresponds to the following ranges defined by international guidelines (ESH, ESC, JSH). Data in mmHg.

elevated

| 130 – 134| 80 – 84| Self-check
3.| blood pressure normal| < 130| < 80| Self-check

The higher value is the one that determines the evaluation. Example: a blood pressure value of 140/80 mmHg or a value of 130/90 mmHg indicates «blood pressure too high».

Data memory

This device always stores the last result at the end of the measure-ment. To recall the reading, press and hold the ON/OFF button 1 while the device is switched off. Release the button as soon as all display elements are shown. The stored result will then be shown, indicated with the letter «M» AP.

Battery indicator and battery change

Low battery
When the batteries are approximately ¾ empty the battery symbol AN will flash as soon as the device is switched on (partly filled battery displayed). Although the device will continue to measure reliably, you should obtain replacement batteries.

Flat battery – replacement
When the batteries are flat, the battery symbol AN will flash as soon as the device is switched on (flat battery displayed). You cannot take any further measurements and must replace the batteries.

1. Open the battery compartment 5 on the bottom of the device.
2. Replace the batteries – ensure correct polarity as shown by the symbols in the compartment.

Which batteries and which procedure?

• Use 4 new, long-life 1.5 V, size AAA alkaline batteries.
• Do not use batteries beyond their date of expiry.
• Remove batteries if the device is not going to be used for a prolonged period.

Using rechargeable batteries
You can also operate this device using rechargeable batteries.

• Only use «NiMH» type reusable batteries.
• Batteries must be removed and recharged when the flat battery symbol appears. They should not remain inside the device as they may become damaged (total discharge as a result of low use of the device, even when switched off).
• Always remove the rechargeable batteries if you do not intend to use the device for a week or more.
• Batteries cannot be charged in the blood pressure monitor. Recharge batteries in an external charger and observe the information regarding charging, care and durability.

Using a mains adapter

You can operate this device using the Microlife mains adapter (DC 6V, 600 mA).

• Only use the Microlife mains adapter available as an original accessory appropriate for your supply voltage.
• Ensure that neither the mains adapter nor the cable are damaged.
  1. Plug the adapter cable into the mains adapter socket 4 in the blood pressure monitor.
  2. Plug the adapter plug into the wall socket.

When the mains adapter is connected, no battery current is consumed.

Error Messages

If an error occurs during the measurement, the measurement is interrupted and an error message, e.g. «Err 3», is displayed.

Re-position the cuff and repeat the measurement.*
«Err 2»

BK

| Error signal| During the measurement, error signals were detected by the cuff, caused for instance by movement or muscle tension. Repeat the measurement, keeping your arm still.
«Err 3»

BT

| No pressure

in the cuff

| An adequate pressure cannot be

generated in the cuff. A leak may have occurred. Check that the cuff is correctly connected and is not too loose. Replace the batteries if neces- sary. Repeat the measurement.

If the 2-year warranty period has expired, it is recommended to replace with a new Microlife cuff available at your pharmacy.

«Err 5»| Abnormal result| The measuring signals are inaccurate and no result can therefore be displayed. Read through the checklist for taking a reliable measurement and then repeat the measurement.*
«Err 6»| AFIB/MAM

Mode

| There were too many errors during the

measurement in AFIB/MAM mode, making it impossible to obtain a final result. Read through the checklist for performing reliable measurements and then repeat the measurement.*

«HI»| Pulse or cuff pressure too high| The pressure in the cuff is too high (over 299 mmHg) OR the pulse is too high (over 200 beats per minute). Relax for 5 minutes and repeat the measure- ment.
---|---|---
«LO»| Pulse too low| The pulse is too low (less than 40 beats per minute). Repeat the measurement.

Please immediately consult your doctor, if this or any other problem occurs repeatedly.
If you think the results are unusual, please read through the information in «Section 2.» carefully.

Safety, care, accuracy test and disposal

Safety and protection

• Follow instructions for use. This document provides important product operation and safety information regarding this device. Please read this document thoroughly before using the device and keep for future reference.
• This device may only be used for the purposes described in these instructions. The manufacturer cannot be held liable for damage caused by incorrect application.
• This device comprises sensitive components and must be treated with caution. Observe the storage and operating condi-tions described in the «Technical Specifications» section.
• The cuffs are sensitive and must be handled with care.
• Only pump up the cuff once fitted.
• Do not use this device if you think it is damaged or notice anything unusual.
• Never open this device.
• Read the additional safety information provided within the indi-vidual sections of this instruction manual.
• The measurement results given by this device is not a diag-nosis. It is not replacing the need for the consultation of a physi-cian, especially if not matching the patient’s symptoms. Do not rely on the measurement result only, always consider other potentially occurring symptoms and the patient’s feedback. Calling a doctor or an ambulance is advised if needed.
  Ensure that children do not use this device unsupervised; some parts are small enough to be swallowed. Be aware of the risk of strangulation in case this device is supplied with cables or tubes.

Contra-indications
Do not use this device if the patient’s condition meets the following contra- indications, to avoid inaccurate measurements or injuries.

• The device is not intended for measuring blood pressure in pediatric patients of age younger than 12 years old (children, infant, or neonates).
• Presence of significant cardiac arrhythmia during measurement may interfere with blood pressure measurement and affect the reliability of blood pressure readings. Consult with your doctor about whether the device is suitable for use in this case.
• The device measures blood pressure using a pressured cuff. If the measuring limb suffers from injuries (for example open wounds) or under conditions or treatments (for example intrave-nous drip) making it unsuitable for surface contact or pressur-ization, do not use the device, to avoid worsening of the injuries or conditions.
• Patient motions during measurement may interfere with the measurement process and influence results.
• Avoid taking measurements of patients with conditions, diseases, and susceptible to environment conditions that lead to incontrollable motions (e.g. trembling or shivering) and inability to communicate clearly (for example children and unconscious patients).
• The device uses oscillometric method to determine blood pres-sure. The arm being measure should have normal perfusion. The device is not intended to be used on a limb with restricted or impaired blood circulation. If you suffer with perfusion or blood disorders, consult your doctor before using the device.
• Avoid taking measurement on the arm on the side of a mastec-tomy or lymph node clearance.
• Do not use this device in a moving vehicle (for example in a car or on an aircraft).

WARNING
Indicates a potentially hazardous situation, which if not avoided, could result in death or serious injury.

• This device may only be used for the intended uses described in this Instructions for Use. The manufacturer cannot be held liable for damage caused by incorrect application.
• Do not change the patient medication and treatment based the result of one or multiple measurements. Treatment and medica-tion changes should be prescribed only by a medical profes-sional.
• Inspect the device, cuff, and other parts for damage. DO NOT USE the device, cuff or parts if they appear damaged or oper-ating abnormally.
• Blood flow of the arm is temporarily interrupted during measure-ment. Extended interruption of blood flow reduces peripheral circulation and may cause tissue injury. Beware of signs (for example tissue discoloration) of impeded peripheral circulation if taking measurements continuously or for an extended period of time.
• Prolonged exposure to cuff pressure will reduce peripheral perfusion and may lead to injury. Avoid situations of extended cuff pressurization beyond normal measurements. In the case of abnormally long pressurization, abort the measurement or loose the cuff to depressurize the cuff.
• Do not use this device in oxygen rich environment or near flam-mable gas.
• The device is not water resistant or water proof. Do not spill or immerse the device in water or other liquids.
• Do not dissemble or attempt to service the device, accessory and parts, during use or in storage. Access to the device internal hardware and software is prohibited. Unauthorized access and servicing of the device, during use or in storage, may compromise the safety and performance of the device.
• Keep the device away from children and people incapable of operating the device. Beware of the risks of accidental ingestion of small parts and of strangulation with the cables and tubes of this device and accessories.

CAUTION
Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the user or patient, or cause damage to the device or other property.

The device is intended only for measuring blood pressure at upper arm. Do not measure other sites because the reading does not reflect your blood pressure accurately.

• After a measurement is completed, loosen the cuff and rest for > 5 minutes to restore limb perfusion, before taking another measurement.
• Do not use this device with other medical electrical (ME) equip-ment simultaneously. This may cause device malfunction or measurement inaccuracies.
• Do not use this device in proximity of high frequency (HF) surgical equipment, magnetic resonance imaging (MRI) equip-ment, and computerized tomography (CT) scanners. This may cause device malfunction and measurement inaccuracies.
• Use and store the device, cuff and parts in temperature and humidity conditions specified in the «Technical Specifications». Usage and storage of the device, cuff and parts in conditions outside ranges given in the «Technical Specifications» may results in device malfunction and the safety of usage.
•  Protect the device and accessories from the following to avoid damaging the device:
  • water, other liquids, and moisture
  • extreme temperatures
  • impacts and vibrations
  • direct sunlight
  • contamination and dust
• Stop using this device and cuff and consult with your doctor if you experience skin irritation or discomfort.

Electromagnetic Compatibility Information
This device is compliant with EN60601-1-2: 2015 Electromagnetic Disturbances standard.
This device is not certified to be used in vicinity of High Frequency (HF) medical equipment.
Do not use this device close to strong electromagnetic fields and portable radio frequency communication devices (for example microwave oven and mobile devices). Keep a minimum distance of 0.3 m from such devices when using this device.

Device care
Clean the device only with a soft, dry cloth.

Cleaning the cuff
Carefully remove spots on the cuff with a damp cloth and soapsuds.

WARNING: Under no circumstances may you wash the inner bladder!

Accuracy test
We recommend this device is tested for accuracy every 2 years or after mechanical impact (e.g. being dropped). Please contact your local Microlife- Service to arrange the test (see foreword).

Disposal

Batteries and electronic devices must be disposed of in accordance with the locally applicable regulations, not with domestic waste.

Guarantee

This device is covered by a 5 year guarantee from the date of purchase. During this guarantee period, at our discretion, Microlife will repair or replace the defective product free of charge. Opening or altering the device invalidates the guarantee.
The following items are excluded from the guarantee:

• Transport costs and risks of transport.
• Damage caused by incorrect application or non-compliance with the instructions for use.
• Damage caused by leaking batteries.
• Damage caused by accident or misuse.
• Packaging/storage material and instructions for use.
• Regular checks and maintenance (calibration).
• Accessories and wearing parts: Batteries, power adapter (optional).

The cuff is covered by a functional guarantee (bladder tightness) for 2 years.
Should guarantee service be required, please contact the dealer from where the product was purchased, or your local Microlife service. You may contact your local Microlife service through our website: www.microlife.com/support
Compensation is limited to the value of the product. The guarantee will be granted if the complete product is returned with the original invoice. Repair or replacement within guarantee does not prolong or renew the guarantee period. The legal claims and rights of consumers are not limited by this guarantee.

Technical Specifications

• Operating 10 – 40 °C / 50 – 104 °F

• conditions: 15 – 90 % relative maximum humidity

• Storage conditions: -20 – +55 °C / -4 – +131 °F

• Weight: 294.2 g (including batteries)

• Dimensions: 160 x 80 x 32 mm

• Cuff size: from 17 – 52 cm according to the cuff sizes (see «Selecting the correct cuff»)

• Measuring procedure: oscillometric, corresponding to Korotkoff method: Phase I systolic, Phase V diastolic

• Measurement range: 20 – 280 mmHg – blood pressure 40 – 200 beats per minute – pulse

• Cuff pressure display range: 0 – 299 mmHg

• Resolution: 1 mmHg

• Static accuracy: within ± 3 mmHg

• Pulse accuracy: ± 5 % of the readout value

• Voltage source:  4 x 1.5 V alkaline batteries; size AAA

• Mains adapter DC 6V, 600 mA (optional)

• Battery lifetime: approx. 400 measurements

• (using new batteries)

• IP Class: IP 20

• Reference to standards: EN 1060-1 /-3 /-4; IEC 60601-1;
  IEC 60601-1-2 (EMC); IEC 60601-1-11

• Expected service life: Device: 5 years or 10000 measurements,whichever comes first Accessories: 2 years or 5000 measurements, whichever comes first

This device complies with the requirements of the Medical Device
Directive 93/42/EEC.
Technical alterations reserved.

Colpharma s.r.l.
Parma – Italy
www.colpharma.com

Microlife UAB
P. Lukšio g. 32
08222 Vilnius
Lithuania

Microlife AG
Espenstrasse 139
9443 Widnau
Switzerland
www.microlife.com

IB BP A6 Advanced Easy 4G IT-V4 1123
Revision Date: 2023-02-14

References

• The Most Iconic Photographs of All Time - LIFE
• Aerosol, termometri, repellenti antizanzare - Colpharma
• Hypertension and Fever Management - Microlife AG
• Support - Microlife AG

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