microlife BP A2 Easy Blood Pressure Meter Instruction Manual
- August 20, 2024
- microlife
Table of Contents
- Product Overview
- Symbol
- Important facts about blood pressure
- Using the device for the first time
- Taking a blood pressure measurement
- Appearance of the Pulse Arrhythmia (PAD)
- Traffic light indicator in the display
- Data memory
- Battery indicator and battery change
- Using a mains adapter
- Error messages
- Safety, care, accuracy test and disposal
- Disposal
- Guarantee
- Technical specifications
- References
- Read User Manual Online (PDF format)
- Download This Manual (PDF format)
microlife BP A2 Easy Blood Pressure Meter Instruction Manual
Product Overview
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ON/OFF button
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Display
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Cuff socket
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Mains Adapter Socket
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Battery compartment
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Cuff
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Cuff connector
Display -
Battery display
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Systolic value
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Diastolic value
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Pulse rate
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Traffic light indicator
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Pulse indicator
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Cuff check indicator
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Arm movement indicator
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Pulse Arrhythmia Indicator (PAD)
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Stored value
Symbol
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Batteries and electronic devices must be disposed of in accordance with the locally applicable regulations, not with domestic waste.
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Read the instructions carefully before using this device.
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Type BF applied part
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Keep dry
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Type approval of measuring device
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Unified sign of circulation of products on the market of the member states of the
Eurasian Customs Union. -
Serial number (WW-YY-SSSSSS; week-year-serial number)
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Catalogue number
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Manufacturer
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Class II equipment
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Operating temperature restriction 10 – 40 °C
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Storage temperature restriction -20 – +55 °C
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Keep away from children of age 0 – 3
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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.
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.
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 information 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.
Important facts about blood pressure
- 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: before taking medications 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 suffer from a cardiac arrhythmia consult with your doctor before using the device. See also chapter «Appearance of the Pulse Arrhythmia (PAD)» 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.
A number of factors can affect the accuracy of measurements taken on the wrist. In some cases, the result may differ from the measurement taken on the upper arm. We therefore advise you to compare these values with those produced by the upper arm measurement and discuss them with your doctor
How do I evaluate my blood pressure
Table for classifying home blood pressure values in adults in accordance with the international Guidelines (ESH, ESC, JSH). Data in mmHg.
Range | Systolic | Diastolic | Recommendation |
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1. | blood pressure normal | < 120 | < 74 |
2. | blood pressure optimum | 120 – 129 | 74 – 79 |
3. | blood pressure elevated | 130 – 134 | 80 – 84 |
4. | blood pressure too high | 135 – 159 | 85 – 99 |
medical 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».
Using the device for the first time
Inserting the batteries
After you have unpacked your device, first insert the batteries. The battery compartment 5 is on the bottom of the device. Insert the batteries (4 x 1.5 V, size AA), 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).
Cuff size | for circumference of upper arm |
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S | 17 – 22 cm |
M | 22 – 32 cm |
M – L | 22 – 42 cm |
L | 32 – 42 cm |
L – XL | 32 – 52 cm |
Pre-shaped cuffs are optionally available.
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.
Taking a blood pressure measurement
Checklist for taking a reliable measurement
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Avoid activity, eating or smoking immediately before the measurement.
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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. -
Always measure on the same arm (normally left). It is recommended 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.
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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.
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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.
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Press the ON/OFF button 1 to start the measurement.
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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.
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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.
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During the measurement, the pulse indicator AM flashes in the display.
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The result, comprising the systolic 9, the diastolic AT and the pulse rate AK are displayed.
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When the device has finished measuring, remove the cuff.
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Switch off the device. (The monitor does switch off automatically after approx. 1 min.)
You can stop the measurement at any time by pressing the ON/OFF button or open the cuff (e.g. if you feel uneasy or 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 ON/OFF 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 Pulse Arrhythmia (PAD)
This symbol AP indicates that certain pulse irregularities were detected during the measurement. In this case, the result may deviate from your normal blood pressure – repeat the measurement. In most cases, this is no cause for concern. However, if the symbol appears on a regular basis (e.g. several times a week with measurements taken daily) we advise you to tell your doctor. Please show your doctor the following explanation:
Information for the doctor on frequent appearance of the Arrhythmia indicator
This device is an oscillometric blood pressure monitor that also analyses pulse frequency during measurement. The device is clinically tested.
The arrhythmia symbol is displayed after the measurement, if pulse irregularities occur during measurement. If the symbol appears more frequently (e.g. several times per week on measurements performed daily) we recommend the patient to seek medical advice.
This device does not replace a cardiac examination, but serves to detect pulse irregularities at an early stage.
Traffic light indicator in the display
The bars on the left-hand edge of the display AL 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.».
Data memory
This device always stores the last result at the end of the measurement. 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» 17.
Battery indicator and battery change
Low battery
When the batteries are approximately ¾ empty the battery symbol 8 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 8 will flash as soon as the device is switched on (flat battery displayed). You cannot take any further measurements and must replace the batteries.
- Open the battery compartment 5 on the bottom of the device.
- 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 AA 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
- Plug the adapter cable into the mains adapter socket 4 in the blood pressure monitor.
- 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.
Error | Description | Potential cause and remedy |
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«Err 1» | Signal too weak | The pulse signals on the cuff are too |
weak. Re-position the cuff and repeat the measurement.*
«Err 2»
Ae
| 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»
AN
| 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.
«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.*
«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 measure- ment.*
- 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 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 conditions 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 is not a diagnosis. It is not replacing the need for the consultation of a physician, 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.
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The device is not intended for measuring blood pressure in pediatric patients of age younger than 12 years old (children, infant, or neonates).
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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.
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Patient motions during measurement may interfere with the measurement process and influence results.
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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).
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The device uses oscillometric method to determine blood pressure. 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.
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Avoid taking measurement on the arm on the side of a mastectomy or lymph node clearance.
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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 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 measurement. 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 nearflammable 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.
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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.
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After a measurement is completed, loosen the cuff and rest for > 5 minutes to restore limb perfusion, before taking another measurement.
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DO NOT use this device with other medical electrical (ME) equipment simultaneously. This may cause device malfunction or measurement inaccuracies.
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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.
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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
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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: Do not wash the cuff in a washing machine or dishwasher
WARNING: Do not dry the cuff cover in a tumble dryer!
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 inaccordance 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.
Guarantee Card
- Name of Purchaser
- Serial Number
- Date of Purchase
- Specialist Dealer
Technical specifications
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Operating conditions:
- 10 – 40 °C / 50 – 104 °F
- 15-90 % relative maximum humidity
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Storage conditions: -20 – +55 °C / -4 – +131 °F 15-90 % relative maximum humidity
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Weight: 338 g (including batteries)
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Dimensions: 135.5 x 82 x 57 mm
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Cuff size: from 17-52 cm according to the cuff sizes (see «Selecting the correct cuff»)
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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
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Cuff pressure display range: 0 – 299 mmHg
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Resolution: 1 mmHg
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Static accuracy: within ± 3 mmHg
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Pulse accuracy: ± 5 % of the readout value
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Voltage source:
- 4 x 1.5 V alkaline batteries; size AA
- Mains adapter DC 6V, 600 mA (optional)
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Battery lifetime: approx. 920 measurements (using new batteries)
- IP Class: IP 20
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Reference to standards:
- EN 1060-1 /-3 /-4; IEC 60601-1;
- IEC 60601-1-2 (EMC); IEC 60601-1-11
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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.