microlife BPA6PC Upper Arm Blood Pressure Monitor Instruction Manual

microlife BPA6PC Upper Arm Blood Pressure Monitor

Specifications

• Manufacturer: Microlife Corporation
• Model: BP A6 PC
• Display: LCD Display
• Measurement Parameters: Systolic value, Diastolic value, Pulse rate
• Features: Battery display, Traffic light indicator, Cuff check indicator, Atrial Fibrillation Indicator (AFIB)
• Operating Temperature: 10°C to 40°C
• Storage Temperature: -20°C to 50°C
• Humidity Limitation: 15% to 85% RH
• Power Source: Batteries

Product Usage Instructions

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.
• 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 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: before taking medications and eating / in the evening: before going to bed, bathing, or taking medication) and average the measurements.

Safety, Care, Accuracy Test, and Disposal

• Ensure the device is kept dry and clean. Store it in a safe place away from children.

Cleaning the Cuff

• Clean the cuff with a damp cloth and mild soap. Do not immerse the cuff in water.

Accuracy Test

• Regularly check the accuracy of the device by comparing its readings with those obtained from a professional healthcare provider.

Disposal

• Dispose of batteries and electronic devices according to local regulations. Do not dispose of them with domestic waste.

FAQ

Q: How often should I measure my blood pressure?

A: It is recommended to measure your blood pressure at least twice a day, in the morning before taking medications and eating, and in the evening before going to bed, bathing, or taking medication.
Always follow your healthcare provider’s advice on monitoring frequency.

Q: Can this device detect atrial fibrillation?

A: Yes, the Microlife BP A6 PC is equipped with an Atrial Fibrillation Indicator (AFIB) to help detect irregular heart rhythms like atrial fibrillation. Consult your doctor for an interpretation of AFIB readings.

OVERVIEW

1. START/STOP Button
2. Display
3. Cuff socket
4. Mains Adapter Socket
5. Battery compartment
6. Cuff
7. Cuff connector
8. AFIB/MAM Switch
9. User switch
10. Time button
11. M-button (memory)
12. + «Forward» Button
13. – «Backward» Button
14. Lock switch
15. USB Port
16. Display
17. Date/Time
18. Systolic value
19. Diastolic value
20. Pulse rate
21. Battery display
22. Traffic light indicator
23. Stored value
24. Pulse indicator
25. Cuff check indicator
26. Atrial Fibrillation Indicator (AFIB)
27. AFIB/MAM Mode
28. Arm movement indicator
29. User indicator
30. BS AFIB/MAM Interval time

SYMBOLS

• 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 under 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 for operating and storage
• Temperature limitation for operating or storage
• 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 pressure measurement technology for the detection of atrial fibrillation (AF) and arterial hypertension.
• These are the two top risk factors for 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 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 investigators and showed that the device detects patients with AFIB at a certainty of 97-100%. 1,2
• If you have any questions, or 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 Corporation!

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.

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.
• 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 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: before taking medication and eating / in the evening: before going to bed, bathing, or taking medication) and average the measurements.
• It is quite normal for two measurements taken in quick succession 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 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 unusually 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.

How do I evaluate my blood pressure?

Table for classifying home blood pressure values in adults per the international Guidelines (ESH, ESC, JSH).

Data in mmHg.

advice
5.| blood pressure dangerously high| ≥ 160| ≥ 100| Urgently seek medical advice!

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».

Important Facts about Atrial Fibrillation AF

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 irregularly (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 a stroke as compared to elder people.
• For more information visit our website: www.microlife.com/afib.
• Microlife AFIB detection provides a convenient way to screen for AF (only in AFIB/MAM mode)
• Knowing your blood pressure and knowing whether you or your family members have AF can help reduce the risk of stroke. Micro-life AFIB detection provides a convenient way to screen for AF whilst taking your blood pressure.

Risk factors you can control

• Early diagnosis of AF followed by adequate treatment can significantly reduce the risk of getting a stroke. Knowing your blood pressure and knowing whether you have AF is the first step in proactive stroke prevention.

Using the device for the first time

Inserting the batteries

• Switch the lock switch AN to the «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.

Setting the date and time

1. After the new batteries are fitted, the year number flashes in the display. You can set the year by pressing either the «+» AM or the «-» AL button. To confirm and then set the month, press the time button AT.
2. Press the «+» AM or the «-» AL button to set the month. Press the time button AT to confirm and then set the day.
3. Follow the instructions above to set the day, hour, and minutes.
4. Once you have set the minutes and pressed the time button, the date and time are set and the time is displayed.
5. If you want to change the date and time, press and hold the time button for approx. 3 seconds until the year number starts to flash. Now you can enter the new values as described above.

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 center 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.

Selecting standard or AFIB/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 6 on the side of the device downwards to position «1» and select
• AFIB/MAM mode, slide this switch upwards to position «3».

AFIB/MAM mode (highly recommended)

• In AFIB/MAM mode, 3 measurements are automatically taken in succession and the result is then automatically analyzed and displayed.
• Because blood pressure constantly fluctuates, a result determined in this way is more reliable than one produced by a single measurement. AF detection is only activated in AFIB/MAM mode.
• When you select the 3 measurements, the AFIB/MAM symbol BN 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 countdown 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 is questionable, a fourth one is automatically taken.

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 patient’s first visit 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).
   • Fit the cuff closely, but not too tight.
   • Make sure that the cuff is positioned 1-2 cm above the elbow.
   • 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.
   • Support your arm so it is relaxed.
   • Ensure that the cuff is at the same height as your heart.
6. Slide the lock switch AN down to the «unlock» position. Press the START/STOP button 1 to start measuring.
7. 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.
8. When the correct pressure is reached, the pumping stops and the pressure falls gradually. If the required pressure is not reached, the device will automatically pump some more air into the cuff.
9. During the measurement, the pulse indicator BM flashes in the display.
10. The result, comprising the systolic AQ the diastolic AR blood pressure, and the pulse rate AS are displayed. Note also the explanations on further display symbols in this booklet.
11. When the device has finished measuring, remove the cuff.
12. Switch off the device. (The monitor does switch off automati-cally after approx. 1 min.).

How not to store a reading

• As soon as the reading is displayed press and hold the START/STOP button 1 until «M» BL is flashing. Confirm to delete the reading by pressing the M-button AK.
• You can stop the measurement at any time by pressing the ON/OFF button or opening the cuff (e.g. if you feel uneasy or have an unpleasant pressure sensation).
• 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 1 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.

Appearance of the Atrial Fibrillation Indicator for early Detection (Active only in AFIB/MAM mode)

• This device can detect atrial fibrillation (AF). This symbol BO 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 the 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 measurements). If the AFIB symbol appears again, we recommend the patient 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.
• In the presence of atrial fibrillation, the diastolic blood pressure value may not be accurate.
• 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.

Traffic light indicator in the display

• The bars on the left-hand edge of the display BK show you the range within which the indicated blood pressure value lies.
• Depending on the height of the bar, the readout value is either within the optimum (green), elevated (yellow), too high (orange), or dangerously high (red) range.
• The classification corresponds to the 4 ranges in the table as defined by the international guidelines (ESH, ESC, JSH), as described in «Section 1.».

PC-Link functions

• This device can be used in conjunction with a personal computer (PC) running the Microlife Blood Pressure Analyzer+ (BPA+) software. The memory data can be transferred to the PC by connecting the monitor via a cable.
• If no download-voucher and cable is included download the BPA+ software from www.microlife.com/software and use a USB cable with a Mini-B 5-pin connector.
• During the connection, the device is completely controlled by the computer.

Data memory

• This device automatically stores up to 99 measurement values for each of the 2 users.

Viewing the stored values

• Select either user 1 or 2 with the user switch 9.
• Switch the lock switch AN to the «unlock» position. Press the M-button AK briefly. The display first shows «M» BL and «28A», which stands for the average of all stored values.
• Pressing the «+» AM or the «-» AL button repeatedly enables you to move from one stored value to another. Press the M-button again to exit the memory mode.

Memory full

• Pay attention that the maximum memory capacity of 99 memories per user is not exceeded.
• When the 99 memory is full, the oldest value is automatically overwritten with the 100th value.
• Values should be evaluated by a doctor before the memory capacity is reached – otherwise, data will be lost.

Clearing all values

Make sure the correct user is activated.

1. Firstly unlock the device 14 then select either 1 or 2 with the user switch 9.
2. Hold down the M-button 11 until «CL» appears and then release the button.
3. Press the M-button while «CL» is flashing to permanently clear all values of the selected user.
   • Cancel deletion: press START/STOP button 1 while «CL» is flashing.
   • Individual values cannot be cleared.

Battery indicator and battery change

Low battery

• When the batteries are approximately ¾ empty the battery symbol BT 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 20 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
3. To set a date and time, follow the procedure described in Section
4. Using the device for the first time».

• The memory retains all values although the date and time must be reset – the year number therefore flashes automatically after the batteries are replaced.
• The memory retains all values although the date and time must be reset – the year number therefore flashes automatically after the batteries are replaced.

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 orig-inal 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»

BQ

| 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.
Error| Description| Potential cause and remedy
---|---|---
«Err 3»

BN

| 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 necessary. Repeat the measurement.
«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 taking a reliable measurement 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 measurement.
«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 1.» 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 it 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 individual sections of this instruction manual.
• The measurement results given by this device are not a diagnosis. It does not replace the need for the consultation of a physician, especially if not match 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, infants, or neonates).
• The 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 intravenous drip) making it unsuitable for surface contact or pressurization, 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 environmental 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 an oscillometric method to determine blood pressure. The arm being measured should have normal perfusion.
• The device is not intended to be used on a limb with restricted or impaired blood circulation. If you suffer from perfusion or blood disorders, consult your doctor before using the device.
• Avoid taking measurements on the arm on the side of a mastectomy 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’s medication and treatment based on the result of one or multiple measurements. Treatment and medication changes should be prescribed only by a medical professional.
• Inspect the device, cuff, and other parts for damage. DO NOT USE the device, cuff, or parts if they appear damaged or operating 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.
• 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 lose the cuff to depressurize the cuff.
• Do not use this device in oxygen oxygen-rich environment or near flammable gas.
• The device is not water-resistant or waterproof. 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’s 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 in the 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) equipment 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) equipment, 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 result 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
• This device has 2 user settings. Please ensure it is cleaned and disinfected between users to prevent any cross-contamination.
• 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 the 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 ovens 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 soap suds.
• 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 under 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 the 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 conditions: 10 – 40 °C / 50 – 104 °F 15 – 90 % relative maximum humidity
• Storage conditions: -20 – +55 °C / -4 – +131 °F 15 – 90 % relative maximum humidity
• Weight: 354 g (including batteries)
• Dimensions: 160 x 80 x 32 mm
• Cuff size: from 17 – 52 cm according to the cuff sizes (see «Using the device for the first time»)
• Measuring procedure: oscillometric, corresponding to Korotkoff
• method: Phase I systolic, Phase V diastolic
• Measurement range: SYS: 60 – 255 mmHg
• DIA: 40 – 200mmHg
• Pulse: 40 – 199 beats per minute
• 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: IEC 80601-2-30; 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.

Guarantee Card

• Name of Purchaser- ———————-
• Serial Number– ————————–
• Date of Purchase—————————–
• Specialist Dealer—————————-
• Microlife Corporation
• 9F, 431, RuiGuang Road, NeiHu
• Taipei 11492, Taiwan, China
• www.microlife.com

Documents / Resources

| microlife BPA6PC Upper Arm Blood Pressure Monitor [pdf] Instruction Manual
BPA6PC Upper Arm Blood Pressure Monitor, Upper Arm Blood Pressure Monitor, Pressure Monitor, Monitor
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References

• The Most Iconic Photographs of All Time - LIFE
• Hypertension and Fever Management - Microlife AG
• Support - Microlife AG

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