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The following symbols are used on the device, in these instructions for use, on the packaging and on the type plate for the device:
Indicates a potentially impending danger. If it is not avoided, death or serious injury will occur.
Indicates a potentially impending danger. If it is not avoided, slight or minor injuries may occur.
Product information Note on important information | |
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![]() | Disposal in accordance with the Waste Electrical and Electronic Equipment EC Directive – WEEE |
![]() | Do not dispose of batteries containing harmful substances with household waste |
![]() | Manufacturer |
![]() | CE labelling This product satisfies the requirements of the applicable European and national directives. |
![]() | Dispose of packaging in an environmentally friendly manner |
![]() | Marking to identify the packaging material. A = material abbreviation, B = material number: 1–7 = plastics, 20–22 = paper and cardboard |
![]() | Separate the product and packaging elements and dispose of them in accordance with local regulations. |
![]() | Protected against solid foreign objects 12.5 mm in diameter and larger |
![]() | Direct current The device is suitable for use with direct current only |
![]() | Unique device identifier (UDI) Identifier for unique product identification |
![]() | Batch designation |
![]() | Item number |
![]() | Serial number |
![]() | Medical device |
![]() | Type BF applied part Galvanically isolated applied part (F stands for "floating"); meets the requirements for leakage currents for type B |
![]() | Temperature range |
![]() | Humidity range |
![]() | Atmospheric pressure limitation |
![]() | Importer symbol |
![]() | Type number |
![]() | Date of manufacture |
Intented purpose
The blood pressure monitor (hereinafter, device) is intended for the fully automatic, non-invasive measurement of arterial blood pressure and pulse values on the upper arm.
It is designed for self-measurement by adults in a domestic environment.
Intended users
The blood pressure measurement is suitable for adult users whose upper arm circumference is within the range printed on the cuff.
Clinical benefits
The user can record their blood pressure and pulse values quickly and easily using the device. The recorded values are classified according to internationally applicable guidelines and evaluated graphically. Furthermore, the device can detect any irregular heart beats that occur during measurement and inform the user via a symbol in the display. The device saves the recorded measurements and can also output average values of previous measurements. The recorded data can provide healthcare service providers with support during the diagnosis and treatment of blood pressure problems, and therefore it plays a part in the long-term monitoring of the user's health.
Indications
In the event of hypertension or hypotension, the user can independently monitor their blood pressure and pulse values at home. However, the user does not need to be suffering from hypertension or arrhythmia in order to use the device.
Contraindications
Undesirable side effects
Check that the exterior of the cardboard delivery packaging is intact and make sure that all contents are present. Before use, ensure that there is no visible damage to the device or accessories and that all packaging material has been removed.
If you have any doubts, do not use the device and contact your retailer or the specified Customer Services address.
If the symbol is displayed and does not disappear, measurement is no longer possible. Replace all the batteries. Once the batteries have been removed from the device, the date and time must be set again. Any saved measured values are retained.
You can also operate this device with a mains part (not included in delivery). However, before connecting the device with the mains part, please ensure that you have removed the batteries from the device. During mains operation, there must not be any batteries in the battery compartment, as this could damage the device.
Make sure that the device's settings have been set correctly so you can make full use of all its functions. Otherwise you will not be able to save your measured values with the date and time and access them later.
There are two different ways to access the settings menu:
Set these settings in the order shown below:
Press to confirm your selection each time.
Time format flashes:
The year flashes:
The month flashes:
The day flashes:
If the time format is set to the 12-hour format, the order in which the day and month are displayed is reversed.
The hour flashes:
The minutes flash:
The Bluetooth® symbol flashes on the display.
Bluetooth® data transfers will shorten the battery life.
You can measure your blood pressure on either arm. Some deviations between the values in the right and left arm are perfectly normal. Always perform the measurement on the arm with the higher blood pressure values. Consult your doctor about this before starting self-measurement.
This device has two users with 120 memory spaces each in order that you can save measurements from two different people separately from each other.
If multiple people are using the device, make sure that the correct user has been selected before each measurement:
Requirement: cuff attached, user selected.
The device can identify heart rhythm abnormalities during the blood pressure measurement. If is displayed after the measurement, this indicates that an irregularity has been detected in your pulse.
Repeat the measurement if is displayed.
When assessing your blood pressure, only use the results that have been recorded without any irregularities in your pulse.
Consult your doctor if is displayed frequently. Only they can determine, through an examination, whether there is an abnormality.
Measured blood pressure value range | Classification | Risk indicator colour | |
Systolic (in mmHg) | Diastolic (in mmHg) | ||
≥ 180 | ≥ 110 | Stage 3 high blood pressure (severe)1 | Red |
160 – 179 | 100 – 109 | Stage 2 high blood pressure (moderate)1 | Orange |
140 – 159 | 90 – 99 | Stage 1 high blood pressure (mild)1 | Yellow |
130 – 139 | 85 – 89 | High normal1 | Green |
120 – 129 | 80 – 84 | Normal1 | Green |
< 120 | < 80 | Optimal1 | Green |
< 90 | < 60 | Low blood pressure2 | Orange |
The risk indicator indicates which category the recorded blood pressure values fall into. If the measured values are in two different categories (e.g. systolic pressure in the "high normal" range and diastolic pressure in the "normal" range), the risk indicator always indicates the higher range – "high normal" in the example described.
Note that these default values are for general guidance only, as individual blood pressures may vary.
Please note that self-measurement at home usually results in values lower than those recorded at a doctor's surgery. Consult your doctor at regular intervals. Only they are able to give you personal target values for controlled blood pressure, particularly if you are receiving medical therapy.
Low blood pressure (hypotension) can be a health hazard and cause dizziness or fainting. Blood pressure is considered low if systolic and diastolic pressure are below 90/60 mmHG (source: National Health Service, 2023).
Seek medical attention if you suddenly suffer from low blood pressure.
Atrial fibrillation is one of the most common forms of cardiac arrhythmia and is characterised by an irregular heartbeat associated with an increased risk of stroke, heart failure and other heart complications.
While the final diagnosis of atrial fibrillation can only be made by a medical examination, the Beurer AFIB technology of this device enables it to be detected with a high level of accuracy. During the blood pressure measurement, possible atrial fibrillation is detected and displayed after the measurement with the symbol in combination with the
symbol. If arrhythmias, such as atrial fibrillation, are present, the displayed blood pressure value may be incorrect. If the
symbol is displayed after a blood pressure measurement, repeat the measurement. Rest for 5 minutes beforehand. Do not move or speak during the measurement. If the
symbol appears for the first time and more frequently, please promptly consult your doctor. If you have previously been diagnosed with atrial fibrillation, follow your doctor's instructions regarding what to do in the event that AFIB is detected by the device.
Do not perform self-diagnosis and self-treatment based on the measurements, but rather always follow the doctor's instructions.
One of the most common errors made when taking a blood pressure measurement is not ensuring that the user's circulatory system is sufficiently at rest when taking the measurement. In this case, the measured systolic and diastolic blood pressure values do not represent the blood pressure at rest. However, it is this blood pressure at rest that should be used to assess the measured values.
This blood pressure monitor uses integrated haemodynamic stability diagnostics (HSD) to measure the user's haemodynamic stability when taking the blood pressure measurement. This enables it to indicate whether the blood pressure was taken when the user's circulatory system was sufficiently at rest.
![]() | The measured blood pressure value was obtained when the user's circulatory system was sufficiently at rest and reliably represents the blood pressure at rest. |
![]() | Indicates that the value was obtained when the user's circulatory system was not sufficiently at rest. The blood pressure values measured in this case generally do not represent the blood pressure at rest. The measurement should therefore be repeated after a period of physical and mental rest lasting at least 5 minutes. |
No resting indicator symbol is displayed | During the measurement it was not possible to determine whether the user's circulatory system was sufficiently at rest. In this case too, the measurement should be repeated after a period of rest lasting at least 5 minutes. |
The user's circulatory system not being sufficiently at rest can be the result of various factors, such as physical stress, mental strain/distraction, speaking or experiencing cardiac arrhythmia during the measurement.
In an overwhelming number of cases, HSD will give a very good guide as to whether the user's circulatory system is rested when a blood pressure measurement is taken. However, certain patients suffering from cardiac arrhythmia or chronic mental conditions may remain haemodynamically unstable even in the long-term, something which persists even after repeated periods of rest. The accuracy of the results for the blood pressure at rest is reduced in these users. Like any medical measurement method, the precision of HSD is limited and it can lead to incorrect results in some cases. Nevertheless, the blood pressure measurements taken when the user's circulatory system is sufficiently at rest represent particularly reliable results.
The results of every successful measurement are saved with the date and time. If there are more than 120 measurements, the oldest measurements are deleted.
Press on the start screen and select the desired user using the slider.
Bluetooth® activated in the display: Measurement data is transferred automatically.
is displayed:
The average value of all this user's saved measured values is displayed.
Transfer via Bluetooth®
List of system requirements and compatible devices
* This product satisfies the requirements of the applicable European directives.
Accessories and replacement parts are available on the homepage www.beurer.de, under "Service". Please state the corresponding order number.
Designation | Item number and/ or order number |
Universal cuff | 164.503 |
Mains adapter (EU) | 072.78 |
Mains adapter (UK) | 072.79 |
Error message | Possible cause | Solution |
![]() | Unable to record a pulse. | Please wait one minute and repeat the measurement. Ensure that you do not speak or move during the measurement. |
![]() | The measured blood pressure is outside the measurement range. | |
![]() | There is a pneumatic system error. | Repeat the measurement. Ensure that the cuff line is correctly connected and that you do not move or speak. |
![]() | An error occurred during the measurement. | Please wait one minute and repeat the measurement. Ensure that you do not speak or move during the measurement. |
![]() | The inflation pressure is higher than 300 mmHg. | Please take another measurement to check whether the cuff can be correctly inflated. Make sure that neither your arm nor other heavy objects are pressing on the line, and that the line is not bent. |
![]() | There is a system error. | If this error message appears, please contact Customer Services. |
![]() | There are problems with the connection between the smartphone/ tablet and the app. | Switch off the main unit, close the app and first deactivate Bluetooth® on your smartphone/tablet before reactivating the function. Try to establish the connection again. |
![]() | The batteries are nearly flat. | Insert new batteries into the device. |
Type | BM 64 |
Measurement method | Oscillometric, non-invasive blood pressure measurement on the upper arm |
Measurement range | Cuff pressure 300 mmHg, systolic pressure 50 – 280 mmHg, diastolic pressure 30 – 200 mmHg, pulse 40 – 199 beats/minute |
Display accuracy | Systolic pressure ± 3 mmHg, diastolic pressure ± 3 mmHg, pulse ± 5% of the displayed value |
Measurement uncertainty | Max. permissible standard deviation according to clinical testing: systolic pressure 8 mmHg, diastolic pressure 8 mmHg |
Memory | 2 x 120 memory spaces |
Dimensions | L 143 mm x W 105 mm x H 60 mm |
Weight | Approx. 450 g (without batteries, with cuff) |
Cuff size | 22 to 42 cm upper arm circumference |
Operating conditions | + 10°C to + 40°C, < 90% relative humidity, 800 – 1050 hPa ambient pressure |
Storage conditions | -20°C to + 55°C, < 90% relative humidity (non-condensing) |
Power supply | 4 x 1.5V ![]() |
Battery life | Lasts for approx. 300 measurements depending on the blood pressure and inflation pressure as well as the number of Bluetooth® connections |
Expected service life | At least 20.000 measurements |
Classification | Internal power supply, IP20 no AP or APG, continuous operation, type BF applied part |
Data transfer via Bluetooth® wireless technology | The device uses Bluetooth®, Frequency band 2.400 – 2.483 GHz, max. transmission power 5 dBm. |
The serial number is located on the device or in the battery compartment.
Technical specifications are subject to change without notification to allow for updates.
Mains part
Model no. | LXCP12X-050100BG |
Input | 100 – 240 V, 50 – 60 Hz, 0.5 A max |
Output | 5 V DC, 1 A, in conjunction with Beurer blood pressure monitors only |
Manufacturer | Shenzhen Iongxc power supply co., ltd. |
Protection | This device is double protected and has a primary-side cutout switch which disconnects the device from the mains in case of malfunction. Ensure that you have removed the batteries from the battery compartment before you use the mains part. |
![]() | Polarity |
General warnings
General precautions
Notes on handling batteries
Notes on electromagnetic compatibility
Here you can download full pdf version of manual, it may contain additional safety instructions, warranty information, FCC rules, etc.
Download Beurer BM 64 - Upper arm blood pressure monitor Manual
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