How To Set Up Microlife Blood Pressure Monitor

microlife BP B6 Blood Force per unit area Monitor

OVERVIEW

1. ON/OFF Button
2. Display
3. M Button (Retentivity)
4. Bluetooth/Time Button
5. User Button
6. Gage Socket
7. MAM Switch
8. Traffic LED Light indicator
9. USB Port
10. Mains Adapter Socket
11. Battery Compartment
12. Cuff
13. Cuff tube
14. Cuff Connector
    Display
15. Active Bluetooth
16. Systolic Value
17. Diastolic Value
18. Pulse Rate
19. Battery Display
20. Cuff Fit Check
    – A: Suboptimal Cuff Fit
    – B: Arm Motility Indicator<<Err2>>
    – C: Cuff Pressure Check<<Err3>>
21. Cuff Indicate Indicator <<Err1>>
22. Irregular heartbeat Indicator (IHB)
23. User indicator
24. MAM Mode
25. Stored Value
26. Clinical Claret Pressure Average « MyBP »
27. Date/Time
28. Pulse Indicator
29. Average Indictor « MyCheck »
30. MAM Interval Time

Read the instructions carefully before using this device.
Type BF applied function
Keep dry out

Important Product and Rubber Information

Follow Instructions for Use. This document provides important product operation and condom information regarding this Claret Pressure Monitor. Please read this certificate thoroughly before using the device and keep for future reference.

Indications for Use
The Upper Arm Blood Pressure Monitor, Model BP3KV1-5W is a device intended to mensurate the systolic and diastolic blood pressure and pulse rate of an developed private by using a non-invasive oscillometric technique in which an inflatable gage is wrapped around the upper arm for a circumference range from 22 to 42cm. The device detects the appearance of irregular heartbeat during measurement and gives a warning bespeak with the reading once the irregular heartbeat is detected.
The device can be used in connectedness with a smartphone running the APP. The memory information can be transferred to the smartphone via Bluetooth.

Alarm – Potentially hazardous situation that if not avoided may upshot in serious injury or expiry.

• Self-measuring means monitoring, non diagnosis or treatment. Unusual values must always be discussed with your dr.. Under no circumstances should you independently alter the dosages of any drugs prescribed by your dr.
• Consult your doctor before using this device if any of the following or similar conditions are nowadays: arrhythmias such as atrial or ventricular premature beats or atrial fibrillation, arterial sclerosis, poor perfusion, diabetes, historic period, pregnancy, preeclampsia, renal diseases. Motion during measurement, including trembling or shivering may touch the measurement.
• Though not for use with children under 12, ensure that any children around this device are supervised; some parts are small enough to be swallowed.
  Practise NOT:
• Utilize this device if you think it is damaged or anything appears unusual (due east.thou. sporadic operation, open up packaging upon purchase).
• Use the displayed pulse for checking the frequency of heart pacemakers as this device is non suitable for this activity.
• Open/modify this device; inaccuracy and/or harmful injury may result.
• Acquit many frequent measurements as this may upshot in harmful injury due to claret menses interference.
• Identify the Cuff over a wound equally this may crusade further injury.
• Place and pressurize the Gage over/near any present intravascular access or therapy, or arteriovenous shunt, as this may cause blood flow interference and result in harmful injury.
• Place and pressurize the Cuff over a limb near the side of a mastectomy as this may cause harmful injury.
• Utilize the Blood Pressure Monitor on a limb simultaneously with other medical equipment on the same limb due to possible interference with such medical equipment.
• Maintain force per unit area in the Gage applied to the limb for a prolonged amount of time. Ensure that circulation in the limb is not impaired by checking circulation if prolonged/repeated exposure to pressure occurs.
• Service the device when being used or when ability is supplied. When the device is not in use and power is removed, batteries may exist replaced by the user. No other parts/components are accessible.
  CAUTION – Potentially hazardous state of affairs that if not avoided may result in modest/moderate injury, property harm, and/or damage to the device
• This device contains sensitive electronics components. Avert strong electrical or electromagnetic fields in the directly vicinity of the device (e.g., mobile telephones, microwave ovens). These can atomic number 82 to temporary impairment of the measuring accuracy. Move the device to another location if interference is determined.
• When not using the Blood Pressure Monitor for extended lengths of time, remove the batteries to avoid potential battery leakage and harm to the monitor.
• When replacing the batteries, ensure all the batteries are replaced simultaneously to avoid battery damage and potential damage to the monitor. Microlife USA does not recommend using rechargeable batteries.
• To avert inaccurate measurements and to lessen any discomfort from Gage pressure, ensure the Gage is placed correctly on the limb and fits correctly when snug (not tight), as indicated by markings with the Cuff.
• Consult your physician in cases of frequent irregular heartbeat detections.
• This Risk Indicator feature is provided in order to help y'all empathise your potential blood force per unit area risk. However, this feature is neither a diagnosis nor a substitute for a medical examination. It is important to consult with your physician to make up one's mind your take a chance.
  Exercise Non:
• Drop this device or expose it to strong vibrations; sensitive components may be affected resulting in inaccuracies and/or operational issues.
• Use the Claret Pressure Monitor exterior of its specified functioning temperature and humidity rating, or if stored outside of its specified storage temperature and humidity rating. Avoid storage in direct sunlight.
• Use this monitor in areas containing high frequency (HF) surgical equipment, magnetic resonance imaging (MRI) equipment, computerized tomography (CT) scanners. This may issue in incorrect functioning of the monitor and/or cause an inaccurate reading
• Utilize this device in a moving vehicle; inaccurate measurements may result. Only utilize this device in a home healthcare environment.
• Use third party accessories. Simply employ Microlife authorized accessories, such equally cuffs or Air-conditioning adapters, equally those not canonical for use with the device may provide inaccurate measurements, injury, and/or damage the device.
  STANDARDS
  This medical device is compliant with:
• Medical device and not-invasive blood pressure monitor standards IEC 60601-i, IEC 60601-1-two, IEC 60601-1-xi, and AAMI/ANSI/IEC 80601-2-30, and
• Electromagnetic standards IEC 60601-1-2, along with FCC Role 15, and
• Clinical Testing per standard ISO 81060-2:2013 was conducted on blood force per unit area device using the same measurement technology.

Please note: According to international standards, your monitor should be checked for accurateness every 2 years.
Blazon
IP20: Protected against solid foreign objects of 12.v mm diameter and greater.

MR Unsafe
Expected Life
Monitor 5 Years
Cuff 2 Years
Batteries and electronic instruments must exist disposed of in accordance with the locally applicable regulations, not with domestic waste product.
Data Manual
This product emits radio frequencies (RF) in the two.4 GHz band. Practice Not use this product in locations where RF is restricted, such equally on an aircraft or in hospitals. Plow off the Bluetooth® feature in this monitor, remove batteries when in RF restricted areas. For farther data on potential restrictions refer to documentation on the Bluetooth usage by the FCC.

FCC

This device complies with office 15 of the FCC Rules. Operation is subject to the post-obit 2 conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired performance. Changes or modifications to the production are not approved by Microlife United states and could void the user's authority to operate the equipment under FCC jurisdiction.
This equipment has been tested and found to comply with the limits for a Form B digital device, pursuant to Office xv of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses, and can radiate radio frequency energy, and if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. Nonetheless, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or tv reception, which can be adamant past turning the equipment off and on, the user is encouraged to try to correct the interference past one or more of the post-obit measures: i) Reorient or relocate the receiving antenna. 2) Increase the separation betwixt the equipment and receiver. 3) Connect the equipment into an outlet on a excursion different from that to which the receiver is continued. iv) Consult the dealer or an experienced radio/Tv set technician for assistance.
This device complies with FCC radiation exposure limits set forth for an uncontrolled environment. End users must follow the specific operating instructions for satisfying RF exposure compliance.
Trademark Usage:
Apple tree, the Apple tree logo, iPad, and iPhone are trademarks of Apple tree Inc., registered in the U.S. and other countries. App Store is a service marker of Apple tree Inc.
Android and Google Play are both trademarks of Google Inc.
The Bluetooth® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any use of such marks in this Blood Pressure Monitor is under license. Other trademarks and trade names are those of their respective owners.

Using the Device for the First Fourth dimension

Inserting the batteries
Later on you have unpacked your device, starting time insert the batteries. The battery compartment 11 is on the bottom of the device. Insert the batteries (4 x 1.five V, size AA), thereby observing the indicated polarity.

Setting the date and time

1. After the new batteries are fitted, the twelvemonth number flashes in the brandish. You can set the yr by pressing Retentiveness button 3. To confirm and and so set the month, printing the fourth dimension button 4.
2. Press retentiveness button three to fix the month. Press the time button 4 to confirm and then set the day.
3. Follow the instructions above to set the 24-hour interval, hour and minutes.
4. Once you have set the minutes and pressed the time push button, the date and time are set and the fourth dimension is displayed.
5. If you want to change the engagement and time, press and hold the time button down for approx. 7 – 8 seconds until the year number starts to wink. Now yous can enter the new values as described above
   Exercise non Select this gage
   Microlife offers different cuff sizes. Select the gage size to friction match the circumference of your upper arms (measured by close-fitting in the middle of the upper arm).

Cuff size	for circumference of upper arm
S	17 – 22 cm
K	22 – 32 cm
One thousand-L	22 – 42 cm
Fifty	32 – 42 cm
50-XL	32 – 52 cm

Merely use Microlife cuffs.

• Contact your local Microlife Service if the enclosed cuff 12 does not fit.
• Connect the cuff to the device by inserting the cuff connector 14 into the cuff socket three every bit far equally it volition go.

Selecting the user
This device allows to store the results for 2 individual users.

→ Select the intended user (User ane or User 2) 23 by pressing the user button v.
→ Before each measurement, ensure that the correct user is selected.

Select the measuring mode: standard or MAM mode

Before each measurement, select standard (single measurement) or MAM mode(automatic double measurement). In MAM way, 2 measurements are automatically taken in succession and the result is then automatically analysed and displayed. Considering claret force per unit area constantly fluctuates, a result determined in this way is more reliable than a single measurement is performed.

• When yous select MAM mode, the MAM symbol 24 appears in the display.
• To select standard mode, slide the MAM switch 7 on the side of the device downwardly to position «1» and to select MAM style, slide this switch upwards to position «3».
• The bottom, right hand section of the display shows a 1 or 2 to indicated which of the two measurements is currently being taken.
• At that place is a break of 15 seconds between the measurements. A count down indicates the remaining fourth dimension. The circle icon 30 will go circle too during interval time.
• The individual results are non displayed. Your blood pressure will but be displayed afterwards all measurements are taken.
• Do not remove the gage between measurements.
• If one of the private measurements was questionable, an additional 1 is automatically taken.

Checklist for taking a reliable measurement

1. Avert activity, eating or smoking immediately before the measurement.
2. Sit down for at least 5 minutes before the measurement and relax.
3. Ever measure on the same arm (normally left). It is recommended that doctors perform double-arm measurements on a patient-get-go visit in lodge to determine which arm to mensurate in the time to come. 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 non be rolled up – they exercise not interfere with the cuff if they are laid apartment.
5. Always ensure that the correct cuff size is used (marking on the gage).
   • Fit the gage closely, but not too tight.
   • Brand certain that the gage is positioned 2 cm above the elbow.
   • The avenue marking located on the cuff (ca. 3 cm long bar) must lie over the artery which runs downwardly the inner side of the arm.
   • Back up your arm then it is relaxed.
   • Ensure that the gage is at the aforementioned height as your heart.

Taking a Blood Pressure Measurement

1. Select standard (single measurement) or MAM (Automatic double measurements); see details in affiliate «1».
2. Press the ON/OFF button 1, the backlight will exist plough on and to start the measurement.
3. The cuff will at present pump up automatically. Relax, do not move and do not tense your arm muscles until the measurement result is displayed. Exhale commonly and do not talk.
4. The cuff fit check 20 on the display indicates that the cuff is perfectly placed. If the icon 20-A appears, the cuff is fitted suboptimally, but it is still ok to measure.
5. When the correct force per unit area 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 gage.
6. During the measurement, the pulse indicator 28 flashes in the display.
7. The result, comprising the systolic sixteen and the diastolic 17 blood pressure level and the pulse rate xviii, Cuff Fit Bank check 20 (and MyCheck 29) is displayed. Note besides the explanations on further display symbols in this booklet.
8. When the device has finished measuring, remove the cuff.
9. Switch off the device. (The monitor does switch off automatically after approx. 1 min.).
   * You tin stop the measurement at any time by pressing the ON/OFF button ane (e.thou. if you feel uneasy or an unpleasant pressure sensation).
   * The monitor is particularly tested for utilise in pregnancy and pre-eclampsia. When you detect unusual loftier readings in pregnancy, you should measure after a short while once more (eg. 1 hour). If the reading is still too high, consult your doctor or gynecologist.

Manual Aggrandizement
In case of loftier systolic blood pressure (due east.1000. above 135mmHg), it tin exist an reward to set the force per unit area individually, Press the ON/OFF push 1 after the monitor has been pumped up to a level of approx. 30 mmHg (shown on the brandish). Keep the push pressed until the pressure is almost 40 mmHg above the expected systolic value –so release the push.

How not to shop a reading
Every bit soon equally the reading is displayed, printing and hold the ON/OFF button 1 until «M» 25 is flashing. Confirm to delete the reading past pressing the Bluetooth/Time button 4.
* « CL » is displayed when the reading is deleted from the retention successfully.

How do I evaluate my blood force per unit area?
The LED traffic light indicator on the left-paw side of the display 8 indicates within which range the measured claret pressure level lies. The value is either within the optimum (green), elevated (yellow) or loftier (red) range. The classification corresponds to the following range divers by ACC, AHA 2022 Guidelines. Data in mmHg.

Range		Systoli c		Diastolic	Recommendation
1	blood pressure level too high	≧130	or	≧80	Seek medical advice
2	blood pressure level elevated	120 -130	and	＜80	Self-cheque
3	blood force per unit area optimum	＜120	and	＜80	Self-check

The higher value is the 1 that determines the evaluation.
Example: a blood pressure value of 140/fourscore mmHg or a value of 130/90 mmHg indicates «claret pressure besides high».
Average Indicator « MyCheck »
This symbol 29 indicates after each measurement, if the almost recent measured value lies beneath, above or on the aforementioned level equally your stored average value (see also chapter « 4 Information Memory »)

• If the measured Systole or Diastole is more than 5mmHg high than the stored average, the arrow shows upwards.
• If the measured Systole or Diastole is more than 5mmHg lower than the stored average, the arrow shows downwards.
• If the measured Systole and Diastole do non differ by more than 5mmHg from the stored average, the pointer directly on.
• If the measured systole and diastole differ in different direction from the stored average, this is indicated first with the systole effigy flashing, together with the upwardly or down arrow for the seconds, Thereafter, the diastole figure flashes with the pointer pointing up or downwards for ii seconds.

Appearance of the Irregular heartbeat Indicator
This irregular heartbeat indicator 22 is displayed, when pulse irregularities occurred during the measurement. If the symbol appears, it is recommended to select MAM Mode and repeat measurement to double confirm the blood force per unit area reading: see details in chapter «1»
The irregular heartbeat symbol indicates that sure pulse irregularities were detected during the measurement. In this case, the event may deviate from your normal basal blood force per unit area – repeat the measurement. In most cases, this is no cause for concern.

However, if the symbol appears on a regular footing (due east.g., several times a calendar week with measurements taken daily), we propose yous to tell your doc.
Please show your medico the following caption:
Data for the doctor on frequent appearance of the irregular heartbeat symbol
This instrument is an oscillometric blood pressure monitor device that also analyzes pulse frequency during measurement. The instrument is clinically tested. If pulse irregularities occur during measurement, the irregular heartbeat symbol is displayed later on the measurement. If the symbol appears more than frequently (e.g., several times per week on measurements performed daily) or if it all of a sudden appears more than often than usual, nosotros recommend the patient to seek medical advice.
The musical instrument does not replace a cardiac examination but serves to detect pulse irregularities at an early phase.

Data Retentiveness

This device automatically stores up to 99 measurement values for each of the 2 users. Select either user1 or two by pressing the user button v
Viewing the average of the concluding 28 days
Press the Memory button three briefly, when the device is switched off. The display first shows «M» 25 and previous «28A», which stands for the average of measurement values of the final 28 days.
* Blood pressure readings with suboptimal cuff fit xx-A are not considered in the boilerplate value.
Viewing the clinical blood pressure average « MyBP »
Press the M-button again, allows you lot to see the clinically relevant blood pressure level boilerplate« MyBP ». The display first shows «K» 25 and «MyBP» 26. This clinical blood pressure average is just shown when 12 clinically relevant measurement values in the last 28 days accept been performed.

• Just measurement that were performed in the morning betwixt (05:00-ten:59) or in the evening (17:00-22:59)
• A maximum of 4 readings per day are considered (2 from the morning and 2 from the evening)
• Measurements performed in standard mode and in MAM-mode are considered in the average when they have been performed during the right time of the twenty-four hour period.
• Measurements performed in MAM-modes or single standard fashion are both classed as unmarried measurements for working out the «MyBP average».
• Blood pressure level reading with suboptimal cuff fit 20-A are non considered in the average value.

Viewing the stored single values
Pressing the K-button again, allows yous to see the concluding performed measurement. The brandish first shows« M » 25 and a value, e.g. « M17 ».single values in memory. Pressing the Yard-push again displays the previous value. Pressing the 1000-button repeatedly enables yous to move from on stored value to another.

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

Immigration all values
Make sure the correct user is activated.
If yous are sure that yous desire to permanently remove all stored values, hold downwards the Memory push button (the device must have been switched off beforehand) until «CL» appears and so release the push. To permanently clear the retention, press the Memory push button while «CL» is flashing. Individual values cannot be cleared.
* Abolish deletion: press ON/OFF push button 1 while «CL» is flashing.

Battery Indicator and Battery change

Low bombardment
When the batteries are approximately ¾ empty the battery symbol xix will flash as soon as the device is switched on (partly filled bombardment displayed). Although the device will continue to measure reliably, you should obtain replacement batteries.
Flat battery – replacement
When the batteries are apartment, the battery symbol xix will flash every bit before long as the device is switched on (flat bombardment displayed). You cannot take any further measurements and must supercede the batteries.

1. Open the bombardment compartment 11 at the back of the device.
2. Replace the batteries – ensure right polarity as shown past the symbols in the compartment.
3. To set date and fourth dimension, follow the procedure described in «Section one».
   The memory retains all values although date and time must be reset – the year number therefore flashes automatically after the batteries are replaced.

Which batteries and which procedure?

• Apply four new, long-life 1.5 5, size AA alkaline batteries.
• Do non use batteries beyond their date of death.
• Remove batteries if the device is not going to exist used for a prolonged period.
  Using rechargeable batteries
  You can also operate this device using rechargeable batteries.
• Only utilize «NiMH» type reusable batteries.
• Batteries must be removed and recharged when the flat battery symbol appears. They should non remain inside the device as they may become damaged (full discharge as a effect of low use of the device, even when switched off).
• Ever remove the rechargeable batteries if y'all 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.

6. Using a Mains Adapter
You tin operate this device using the Microlife mains adapter (DC 6V, 600 mA).

• Only employ the Microlife mains adapter available every bit 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 level monitor.
  2. Plug the adapter plug into the wall socket. When the mains adapter is continued, no battery electric current is consumed.

Bluetooth® Function

Employ the Bluetooth function to transfer data to <Microlife Connected Wellness+> App on a smartphone (Android Bone or iOS). Information bachelor on:
https://world wide web.microlife.com/technologies/connect
Bluetooth operations:
The Bluetooth® icon indicator on your blood pressure monitor, located in the upper right portion of the screen, is designed to provide information about the connectedness between your device and the monitor. Please note the following:

• The Bluetooth® of this monitor is a medical device information system (MDDS) every bit its merely function is for transfer of records and no boosted functions. The Bluetooth® is not active when the monitor is recording data or during blood pressure level measurement. The monitor will not audio whatever alert with or without Bluetooth®. The Bluetooth® is used only to transfer data from point A to signal B. The App on your smart devices cannot be used to start or stop the monitor, nor update the firmware of monitor via Bluetooth®.
• The Bluetooth® icon on your blood pressure monitor will flash initially when set to connect with a device, and continue flashing for 2 minutes until a connectedness occurs.
  The blood pressure monitor volition also display "Id" and a 6-digit number to indicate the unique, monitor-specific MAC ID for the recognition of the monitor unit.
  • Manually plow on Bluetooth: Press Bluetooth/Time push iv to activate Bluetooth, Bluetooth symbol 15 on display volition blink.
  • Automatically plow on Bluetooth: Bluetooth will activate automatically later on a measurement. Bluetoooth symbol 15 on brandish will glimmer.
  • Manually plow off Bluetooth: Press ON/OFF button 1 to turn off Bluetooth.
  • Automatically plow off Bluetooth: Bluetooth will plough off automatically later 2 minutes if a smartphone does not connect to the device.

Bluetooth pairing & App setup:

1. Open Microlife Connected Health+ App on the smartphone. (Brand certain the App is running on the foreground, not in the groundwork.)
2. Plough on Bluetooth manually to connect device to smartphone.
3. Find the name and the unique MAC ID of blood pressure monitor in the pairing list displayed on your telephone, check if MAC ID displayed on the monitor and on the phone are matching; if the name and MAC ID data are right, select to proceed with the pairing, then Bluetooth® icon showed without blinking. If the name and MAC ID shown on the phone is not the aforementioned every bit displayed on the monitor, please abort the connection and make sure the correct monitor and phone are used.
4. For 1st pairing, both phone and monitor will show 6 digits "Passkey" earlier pairing. Make sure the numbers are the aforementioned between phone & monitor to avert misconnection to wrong BT device. It will be paired automatically without Passkey from next connexion. If the "Passkey" on the monitor and on the phone are non the aforementioned, the monitor peradventure connected to an wrong phone, and the pairing should be aborted.
5. After pairing, the App volition bear witness message to setup device user selection (1 or ii) to the App user profile. Ostend to proceed with setup. Cancel to abort setup (if user option is incorrect).
6. After setup, the device will automatically commutation measurement data and
   engagement/fourth dimension settings with the app. Bluetooth turns off automatically later on data exchange.

Bluetooth status:

• Bluetooth symbol 15 blinking slowly: Bluetooth is activated and waiting for connexion.
• Bluetooth symbol 15 not blinking: Bluetooth connection established.
• Bluetooth symbol 15 blinking rapidly: Bluetooth connection error.
  In case of Bluetooth connection error, turn off device Bluetooth, wait for a minute,then re-try Bluetooth connection. Refer to Chapter vii for details.

Wireless advice interference
This product operates in an unlicensed ISM band at 2.4 GHz. In the event this product is used near other wireless devices such as microwave and wireless LAN, which operate on the same frequency band as this product, there is a possibility that interference may occur. If interference occurs, stop the functioning of the other devices or relocate this product away from other wireless devices before attempting to utilise it.

PC-Link Functions

This device tin can be used in conjunction with a personal computer (PC) running the Microlife Blood Force per unit area Analyser (BPA+) software. The retentivity information tin 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/technologies/connect/bpaplus and use a Micro-USB cable.

Error Letters

If an fault occurs during the measurement, the measurement is interrupted and an error bulletin, e.g. «ERR 3», is displayed

Error	Description	Potential cause and remedy
«ERR 1» 21	Indicate too weak	The pulse signals on the cuff are besides weak. Re-position the gage and repeat the measurement.*
«ERR 2» 20-B	BP Mistake signal	During the measurement, error signals were detected by the cuff, caused for instance by move or muscle tension. Repeat the measurement, keeping your arm still.
«ERR 3» 20-C	BM No pressure in the cuff	An adequate pressure cannot be generated in the cuff. A leak may take occurred. Check that the gage is correctly connected and is not too loose. Replace the batteries if necessary. Repeat the measurement.
«ERR 5»	Aberrant result	The measuring signals are inaccurate and no result can therefore exist displayed. Read through the checklist for performing reliable measurements and then echo the measurement.*
«ERR 6»	MAM Mode	In that location were too many errors during the measurement in MAM mode, making it incommunicable to obtain a terminal result. Read through the checklist for performing reliable measurements so echo the measurement.*

15	Bluetooth symbol blinks rapidly.	Bluetooth connection mistake. Turn off the device Bluetooth and shut the App on the smartphone. Wait for i minute, open the App on the smartphone and manually activate Bluetooth on device, to re-try Bluetooth connection & data transfer.
«ERR bt»	Bluetooth cocky-bank check error.	Bluetooth is malfunctioning. Contact your local Microlife benefactor.
«HI»	Pulse or cuff Force per unit area also high	The pressure in the cuff is too high (over 300 mmHg) OR the pulse is too high (over 200 beats per minute). Relax for five minutes and echo the measurement.*
«LO»	Pulse too depression	The pulse is too low (less than twoscore beats per minute). Repeat the measurement.*

Please consult your doctor, if this or whatsoever other problem occurs repeatedly.
If you call back the results are unusual, delight read through the information in «Department two» advisedly.

Safe, Care, Accurateness Exam and Disposal

Safety and protection

• This device may just be used for the purposes described in these instructions. The manufacturer cannot be held liable for harm caused by incorrect application.
• This device comprises sensitive components and must be treated with caution. Notice the storage and operating conditions described in the «Technical Specifications» section.
• Protect it from:
  • h2o and moisture
  • farthermost temperatures
  • impact and dropping
  • contamination and dust
  • direct sunlight
  • heat and cold
• The cuffs are sensitive and must be handled with care.
• Do not exchange or utilize any other kind of cuff or cuff connector for measuring with this device.
• Only pump up the cuff once fitted.
• Practice non use this device close to strong electromagnetic fields such as mobile telephones or radio installation. Continue a minimum distance of 3.3m from such devices when using this device.
• No not use this device if you retrieve it is damaged or discover anything unusual.
• Never open this device.
• If the device is non going to be used for a prolonged period the batteries should be removed.
• Read the additional safety data provided within the private 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 md, specially if non matching the patient's symptoms. Do non rely on the measurement result only, always consider other potentially occurring symptoms and the patient'southward feedback. Calling a dr. or an ambulance is advised if needed.
  • Ensure that children do not use this device unsupervised; some parts are small enough to exist swallowed. Be aware of the risk of strangulation in case this device is supplied with cables or tubes.

Device care
Clean the device only with a soft, dry cloth.
Cleaning the cuff
Carefully remove spots on the cuff with a damp textile and soapsuds. To avoid cross-infection, rub seventy% Isopropyl alcohol on the surface of cuff for disinfection before using afterwards some other user.
Alert: Practice not wash the cuff in a washing machine or dishwasher!
Accuracy test
We recommend this device is tested for accuracy every 2 years or afterward mechanical impact (eastward.thou. existence dropped). Please contact your local Microlife-Service to accommodate the test (run into foreword).
Disposal
Batteries and electronic devices must exist tending of in accordance with the locally applicative regulations, non with domestic waste product.

Guarantee

This device is covered by a 5 year guarantee from the date of purchase. The guarantee is valid only on presentation of the guarantee card completed by the dealer (run across dorsum) confirming appointment of purchase or the receipt.

• Batteries and parts that become worn with use are not included.
• Opening or altering the device invalidates the guarantee.
• The guarantee does not cover impairment caused by improper treatment, discharged batteries, accidents or non-compliance with the operating instructions.
• The cuff has a functional guarantee (bladder tightness) for ii years. Please contact your local Microlife-Service (see foreword).

Technical Specifications

• Operating conditions: ten – forty °C / 50 – 104 °F
  15 – 95 % relative maximum humidity
• Storage weather condition: -20 – +55 °C / -four – +131 °F
  15 – 95 % relative maximum humidity
• Weight:                      415 g (including batteries)
• Dimensions:          157.5 x 105 x 61.v mm
• Measuring process: oscillometric, respective to Korotkoff method: Stage I systolic, Phase V diastolic
• Measurement range: SYS: 60-255 mmHg DIA: 40-200 mmHg, 40 – 199 beats per minute – pulse
• Cuff pressure level display range: 0 – 299 mmHg
• Resolution: 1 mmHg
• Static accuracy: pressure within ± 3 mmHg
• Pulse accurateness: ± 5 % of the readout value
• Atmospheric pressure range: 70KPa -106KPa
• Transmission method: Bluetooth® Depression Energy
• Wireless communication: Frequency range: 2.4 GHz (2400 – 2483.5 MHz)
• Modulation: GFSK
• Effective radiated power: < 20 dBm
• Compatibility: iOS: iOS 8.0 or newer Android: Android four.iv.ii or newer
• Voltage source: four x ane.5 V alkaline batteries; size AA
• Mains adapter DC 6V, 600 mA (optional)
• Battery lifetime: approx. 920 measurements (using new batteries)
• IP Course: IP20
• Reference to Standards: EN 1060-1 /-3 /-4; IEC 60601-1; IEC 60601-ane-2 (EMC); IEC 60601-1-11
• Expected service life: Device: 5 years or 10000 measurements
  Accessories: ii years

This device complies with the requirements of the Medical Device Directive 93/42/EEC.
Technical alterations reserved.
The Bluetooth® word mark and logos are registered trademarks owned by Bluetooth SIG, Inc. and any apply of such marks by Microlife Corp. is nether license. Other trademarks and trade names are those of their respective owners.

How to contact u.s.a.

Distributed by:
Microlife U.s., Inc.
1617 Gulf to Bay Blvd. Clearwater, FL 33755
Price Free Help Line: ane-800-568-4147 Email: [electronic mail protected] www.microlifeusa.com

Documents / Resource

Source: https://manuals.plus/microlife/bp-b6-blood-pressure-monitor-manual

Share this post