beurer BC 87 Series 800W Wrist Blood Pressure Monitor Instruction Manual

beurer BC 87 Series 800W Wrist Blood Pressure Monitor

SAVE THESE INSTRUCTIONS FOR FUTURE REFERENCE
If the instruction manual is damaged or if you no longer have the instruction manual in your possession, please contact customer service. See warranty for service contact.
Dear Valued Customer,
Thank you for choosing one of our products. Our name stands for high-quality, thoroughly tested products for application in the areas of heating, weight management, blood pressure, body temperature, pulse, gentle therapy, massage, and beauty.
Register your product today to receive further benefits:

•  added protection for your purchase
• health and wellness tips
•  new product information
• continual outstanding customer service and support.

Visit www.registerbeurer.com or contact customer service at 1-800-536-0366.
Please read these instructions for use carefully and keep them for later use. Make them accessible to other users and observe the information they contain.
With kind regards,
Your Beurer team

IMPORTANT SAFETY NOTES

Signs and symbols
Whenever used, the following signs identify safety and property damage messages and designate a level of hazard or seriousness.
READ THIS ENTIRE MANUAL, THE SAFETY SECTION AND ALL INSTRUCTIONS AND WARNINGS COMPLETELY AND CAREFULLY BEFORE USING THIS PRODUCT. FOLLOW ALL SAFETY INSTRUCTIONS AND WARNINGS TO AVOID HAZARDOUS SITUATIONS AND TO MAKE CORRECT USE OF THIS PRODUCT.

| This is the safety alert symbol. It alerts you to potential personal injury hazards. Obey all safety messages that follow this symbol to avoid possible injury or death.
---|---

WARNING

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

CAUTION

| Indicates a hazardous situation which, if not avoided, may result in minor or moderate injury

NOTICE

| Addresses practices not related to personal injury, such as product and/or property damage.
| Isolation of applied parts Type BF
Galvanically isolated applied part (F stands for “floating”); meets the requirements for leakage currents for type B
| Observe the instructions
Read the instructions before starting work and/or operating devices or machines
**| Direct current The device is suitable for use with direct current only
Storage/Transport **| Permissible storage and transport temperature and humidity
| Permissible operating temperature and humidity
| Serial number

WARNING – To reduce the risk of fire, electric shock, or serious personal injury:

• Do not use the blood pressure monitor on newborns or patients with pre-eclampsia. Consult your doctor before using the blood pressure monitor during pregnancy.
• This device is not intended for use by people (including children) with restricted physical, sensory or mental skills or a lack of experience and/or a lack of knowledge, unless they are supervised by a person who has responsibility for their safety or they receive instructions from this person on how to use the device. Supervise children around the device to ensure they do not play with it.
• Small parts may present a choking hazard for small children if swallowed. They should therefore always be supervised.
• Cardiovascular diseases may lead to incorrect measurement accuracy. The same also applies to very low blood pressure, diabetes, circulatory disorders, and arrhythmias as well as chills or shaking.
• The blood pressure monitor must not be used in connection with a high-frequency surgical unit. Do not mastectomy. which the arteries or veins are undergoing medical treatment, e.g. intravascular access or intravascular or therapy, or an arteriovenous (AV) shunt.
• Do not use the device at the same time as other medical electrical devices (ME equipment). This could lead to a malfunction of the device and/or an inaccurate measurement.
•  During the blood pressure measurement, the blood circulation must not be stopped for an unnecessarily from the wrist.
• The device is not suitable for use on the women who are or may be pregnant.
• The device is not suitable for use on patients with implanted, electrical devices, such as cardiac pacemakers, defibrillators.

CAUTION – To reduce the risk of personal injury or product/ property damage:

• Place on other parts of the body.
• Please note that when inflating, the functions of the limb in question may be impaired.
• Do not perform measurements more frequently than necessary. The resulting restriction of the blood flow may cause injury.

NOTICE:

• We recommend that the batteries be removed if the device is not to be used for a prolonged period.
• Do not use the device outside of the specified storage and operating conditions. This could lead to incorrect measurements.
• The device is only intended for the purpose described in these instructions for use. The manufacturer is not liable for damage resulting from improper or careless use.
• Using the blood pressure monitor outside your home environment or whilst on the move (e.g. whilst travelling in a car, ambulance or helicopter, or whilst undertaking physical activity such as playing sport) can influence the measurement accuracy and cause incorrect measurements.
• Only  values will be recorded.
• Protect the device from impacts, humidity, dirt, marked temperature fluctuations and direct sunlight.
• Do not drop the device.
• Do not use the device in the vicinity of strong electromagnetic fields and keep it away from radio systems or mobile telephones.
•  Never immerse or spill water or any other liquid onto the monitor or any components, otherwise liquid will enter it and cause damage.
• Never attempt to repair, open and/or disassemble the adjust it yourself. This may damage the unit and impair the functions. If you need to have the unit repaired, please contact our customer service. Please see warranty for service contact. Before submitting any complaint, first check the batteries and replace them if necessary.
• Bring the device to room temperature before taking measurements. If the measuring device has been stored near to the maximum or minimum storage and transport temperature and is brought into an environment with a temperature of 68 °F (20 °C), it is recommended that you wait 2 hours before using the measuring device.

Battery Handling Safety Precautions

• Use only the size and type of batteries specified.
• Be sure to follow the correct polarity when installing the batteries. Reversed batteries may cause damage to the device.
• D Alkaline and Carbon-zinc or rechargeable batteries) or old batteries with fresh ones. Always replace batteries as a simultaneous set.
• If the batteries in the device are depleted or the device will not be used for a long period of time, remove the batteries to prevent damage or injury from possible battery leakage.
• Do not try to recharge batteries not intended to be recharged; they can overheat and rupture (follow battery manufacturer’s directions).
•  Do not dispose of batteries in fire, batteries may explode or leak.
• Clean the battery contacts and also those of the device prior to battery installation.
• Remove discharged batteries from the product and dispose/recycle in compliance with all applicable laws.
• Keep batteries away from children and pets. Batteries may be harmful if swallowed. Should a child or pet swallow a battery, seek medical assistance immediately.
•  If your skin or eyes come into contact with battery fluid, assistance.
• Do not disassemble, open or crush the batteries.
• If a battery has leaked, put on protective gloves and clean the battery compartment with a dry cloth.

Notes on electromagnetic compatibility

• The device is suitable for use in all environments listed in these instructions for use, including domestic environments.
• The use of the device may be limited in the presence of electromagnetic disturbances. This could result in issues such as error messages or the failure of the display/device.
• Avoid using this device directly next to other devices or stacked on top of other devices, as this could lead to faulty operation. If, however, it is necessary to use the device in the manner stated, this device as well as the other devices must be monitored to ensure they are working properly.
• The use of accessories other than those specified or provided by the manufacturer of this device can lead to an increase in electromagnetic emissions or a decrease in the device’s electromagnetic immunity; this can result in faulty operation.
•  Failure to comply with the above can impair the performance of the device.

GETTING TO KNOW YOUR INSTRUMENT

This blood pressure monitor performs non-invasive measurement and monitoring of adult arterial blood pressure and heart rate on adult patients with wrist circumference from 5.3 to 8.5 in. You can use it to measure your blood pressure quickly and easily, store the results, and display stored readings and their average. This device comes with a resting indicator which shows if the user’s circulatory
It also features an irregular heartbeat indicator, with values classified and graphically evaluated according to industry guidelines. The recorded data can provide healthcare service providers with support during the diagnosis and treatment of blood pressure problems, and therefore plays a part in the long- term monitoring of the user’s health. The Blood Pressure Monitor is intended for use indoors and by adults only. For consistency, always measure your blood pressure at the same time each day. Before each measurement, relax for about five minutes. When performing multiple measurements on an individual, wait five minutes between each measurement. Do not take a measurement within 30 minutes of eating, drinking, smoking or exercising. Repeat the measurement if you are unsure of the results. Measurements are for your information only – they are no substitute for a medical examination. Discuss the measurements with your doctor and never base any medical decisions on them (e.g. medicines and their administration).

PACKAGE CONTENTS

• 1 x Storage Box
• 2 x 1.5 V AAA batteries
• 1 x Quick Start Guide
• 1 x Instruction manual

PARTS AND CONTROLS

1. Blood Pressure Risk Indicator
2.  LCD Display
3. M1 Memory Button
4.  START/STOP Button with position indicator
5.  M2 Memory Button
6. Battery Compartment
7. Wrist cuff

LCD Display Information

1. Time and Date
2. Low Battery Icon
3. Bluetooth® Icon
4. Resting Indicator
5. User Number /
6.  Memory Space Number/
7. Pulse Rate
8. Irregular Heartbeat Pulse Icons
9. Risk Indicator
10. Diastolic Pressure
11. Systolic Pressure

PREPARING FOR MEASUREMENT

Inserting/changing batteries:

1. Push the tab on the middle of the Battery Compartment Cover to remove it from the bottom of the device.

2. Insert two AAA alkaline batteries (included) according to the polarity markings inside the compartment.
   NOTE: Do not use rechargeable batteries.

3. Reattach the Battery Compartment Cover.

4. ” ” will flash. Set the hour format, date and time as described below. Any saved measurements will be retained.

Setting the hour format, date, time, Bluetooth connectivity, and default user number:
If date and time are not set, stored measurements will not have a valid timestamp associated with them.
NOTE: Press and hold the M1 or M2 Buttons to advance values rapidly.
Before first use and after every battery
change:
When you insert batteries into the device, you will automatically arrive at the relevant menu.
If batteries have already been inserted: STOP Button for 5 seconds.

1. Select an hour format (12 or 24 hour display) with the M1/M2 Buttons and press the START/STOP Button to confirm.

2. The year flashes on the LCD Display. Set the year with the M1/M2 Buttons and press the START/STOP Button to confirm. .

3. The month flashes on the LCD Display. Set the month with the M1/M2 Buttons and press the START/STOP Button to confirm.

4. The day flashes on the LCD Display. Set the day with the M1/M2 Buttons and press the START/STOP Button to confirm.
   NOTE: If the hour format is set to , the day/month display sequence is reversed.

5. The hour flashes on the LCD Display. Set the hour with the M1/M2 Buttons and press the START/STOP Button to confirm.

6. The minutes flash on the LCD Display. Set the minutes with the M1/M2 Buttons and press the START/STOP Button to confirm.

7. The Bluetooth icon flashes on the LCD Display. Use the M1/M2 Buttons to select (Bluetooth icon appears in the LCD Display) or deselect (Bluetooth icon disappears from the LCD Display) automatic Bluetooth data transfer. Note that Bluetooth transfers may impact battery life. See the “Bluetooth Setup” subsection below for details. Press the START/STOP Button to confirm.

8. The User Number icon flashes on the LCD Display. Select a User Number (U1 or U2) with the M1/M2 Buttons and then press the START/STOP Button to confirm and exit. Measurement will start after settings.

Bluetooth® Setup

In addition to displaying and saving measurements locally on the blood pressure monitor itself, you can also transfer measurements to your mobile device via Bluetooth®. To do so, you will need to install the “Beurer HealthManager Pro” app. These apps are freely available in either the Apple App Store or Google Play Store.
System requirements:

• iOS ≥ 14.0, Android ≥ 8.0
•  Bluetooth® ≥ 4.0

For a list of compatible devices, scan the QR Code below:
To transfer the measured values, proceed as follows:

• Start the app and follow the instructions.
•  Select your blood pressure monitor in the app.
• Confirm the pairing request on your smartphone.
• Take a measurement
• If the Bluetooth® function is activated, data will be automatically transferred after the measurement.
•  (Data transfer at a later point): Go into the memory recall mode for the desired user memory (see “Saving, accessing and deleting measured values”). The data transfer starts automatically.
•  Make sure the Beurer mobile app on your smartphone is always activated and open before you start data transfer from the blood pressure monitor.
• Data transfer is in progress when the Bluetooth® symbol appears on the LCD Display.

MEASURING BLOOD PRESSURE

The blood pressure monitor needs to be at room temperature when measuring. Fundamentally, blood pressure can be measured on both wrists. Blood pressure can vary between the right and left arm, which may mean Always perform the measurement on the same arm. If the consult your doctor to determine which arm should be used for the measurement.

Positioning the cuff

1. With your palm up, place the cuff.
2. Position device about half an inch (1 cm) below the bottom of your hand.
3. Secure the cuff with hock.

Correct Posture:

1.  Rest for at least five minutes before each measurement.
2. Perform the measurement sitting upright with your arms and back supported and comfortably. Place your feet flat on the floor, do not cross your legs.
3. Keep still during the measurement and do not talk.

Positioning indicator

This device has a positioning indicator below the START/STOP Button to help determine the correct measuring position of the device at heart level. It changes color depending on the angle of observation.

• Position indicator appears red

  • Incorrect wrist position; wrist is either too high or too low.

• Position indicator appears green and “OK” shows in the indicator window

  • Correct wrist position; start measurement using the START/STOP Button.

In the vast majority of use cases, the position indicator provides an excellent guide as to whether the measuring
as size and/ or physique on the user side, this function may not be helpful in all cases. If you feel that the wrist position according to the position indicator does not match the level of the heart, use your own judgement.

User Number Selection

This device has two user memories with 120 memory spaces each so you can save measurements from two
the device, make sure to set the appropriate user number before measurement. See the “Setting the hour format, date, time, Bluetooth connectivity, and default user number” section for instructions on selecting a desired User Number. The user can also be chosen by pressing the M1/M2

Performing a Measurement

1. press the START/STOP Button. All LCD Display elements will briefly display, before HI appears on the display and measurement will begin after about three seconds. To cancel a measurement at any time, press the START/STOP Button.

2. An icon will appear in the LCD Display to indicate whether you were sufficiently rested during the measurement ( = Rested, = Not rested). See the „Resting Indicator“ subsection below for details.

3. Er_ (where the blank space is a number 1-8) will appear if the measurement was not performed properly. Refer to the „Troubleshooting Guide“ section for details about specific error message numbers and then repeat the measurement.

4. To select a desired user memory, press the M1 or M2 Button. Each of the two user memories can store 120 sets of measurements. If you do not select a user memory, the measurement will be stored in the most recently-used user memory.

5. If Bluetooth® data transfer is active, the unit will transmit measurement data to the “beurer HealthManager Pro” mobile app installed on your paired mobile device. The Bluetooth® icon will flash while the unit establishes communication with your mobile device and will display when a link is successful. After data unsuccessful, the error message ” ” will display. Also, if the unit cannot establish a Bluetooth®
   NOTE: Remember that you must add the SERIES 800W blood pressure monitor to the “beurer HealthManager Pro” app to enable data transfer.

6. Press the START/STOP pressure monitor if needed. The measurement is stored in the selected user memory. The device will also shut

7. Wait at least five minutes before taking another measurement.

EVALUATING RESULTS

Irregular Heartbeat

This device can detect irregular heartbeat patterns during measurement and will indicate them by displaying the Irregular Heartbeat Icon . This could be an indicator for arrhythmia, a condition where the heart rhythm is abnormal. These symptoms (omitted or premature heartbeats, slow or excessively fast heart rate) may be caused, among other things, by heart disease, age, physical predisposition, excessive use of stimulants, stress, or lack of sleep. This function is not designed for diagnosing or treating an arrhythmic disorder. Only your doctor can determine if you do have arrhythmia.
Repeat the measurement if the Irregular Heartbeat Icon displays after a measurement. Rest for at least five minutes between measurements and do not talk or move during measurement. If the icon appears often, contact your doctor, since self-diagnosis and treatment based solely on the test results may be dangerous. It is vital to follow your doctor‘s instructions.

Risk Classification

Measurements can be classified and assessed by the table below. However, these standard values are only a general

Hypertension Category| Systolic
(in mmHg)| Diastolic
(in mmHg)| Action| Color for the risk indcator
---|---|---|---|---
Grade 3: Severe hypertension| ≥ 180| ≥ 110| Seek medical advice| Red
Grade 2: Moderate hypertension| 160 – 179| 100 – 109| Seek medical advice| Orange
Grade 1: Mild hypertension| 140 – 159| 90 – 99| Have your doctor check your blood pressure regularly| Yellow
High Normal| 130 – 139| 85 – 89| Have your doctor check your blood pressure regularly| Green
Normal| 120 – 129| 80 – 84| Continue self- monitoring| Green
Optimal| < 120| < 80| Continue
self- monitoring| Green

Source: WHO, 1999
Consult your doctor regularly for advice. Your doctor will tell you your individual values for normal blood pressure as well as the value above which your blood pressure is classified as dangerous.
The classification on the LCD Display shows where the recorded blood pressure values fall. If the systolic and
Classification Indicator shows the higher category.

Resting Indicator

A common error made when taking a blood pressure measurement is not ensuring the user’s circulatory system
and diastolic blood pressure values do not correspond to proper blood pressure levels. This blood pressure monitor uses integrated hemodynamic stability diagnostics (HSD) to indicate whether the blood pressure was taken when the this can be caused by various factors such as physical or mental strain or distraction, speaking, or experiencing irregular heartbeat 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 taking a blood pressure measurement or chronic mental conditions may remain hemodynamically 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 can lead to incorrect results in some cases. Nevertheless, the blood pressure measurements
represent particularly reliable results.

DISPLAYING AND DELETING MEASUREMENTS

User Memory

Every successful measurement is stored along with its date and time. If there are more than 120 measurements in a user memory bank, the oldest measurement is deleted.
M1 (for user 1) or M2 (for user 2) Button to select a user memory. Confirm selection by pressing the START/STOP button.

Average Values

1. The average of all saved measurements in the selected user memory is displayed. If Bluetooth® is activated (the symbol flashes on the display), the blood pressure monitor attempts to connect to the app. If you press the M1 Button in the meantime, the transfer is cancelled and the average values of the morning are displayed.
2. Press the relevant Memory Button again; ” ” is shown on the display. The average value of the morning measurements for the last seven days is displayed (morning: 5:00 AM – 9:00 AM).
3. Press the Memory Button a third time; ” ” is shown on the display. The average value of the evening measurements for the last seven days is displayed (evening: 6:00 PM – 8:00 PM).

Individual Measured Values

1. Press the M1 Button again and the last individual measurement is displayed. Press the M1 Button once more to view all previous measurements.
2. START/STOP Button. You can exit the menu at any time by pressing the START/STOP Button.

Clearing Memory

1. To clear one of the user memories, you must first select it.
2. Start individual measurement access as described above and select a user memory.
3. Press and hold the M1 and M2 Buttons for five seconds. CL01 appears on the LCD Display and all values in the selected user memory will be deleted.

NOTE: To exit the menu at any time, press the START/STOP Button.

CARE, MAINTENANCE AND DISPOSAL

• C cloth.
• Do not use detergents or solvents.
•  Never immerse the device in water or other liquids.
• When storing the device, make sure no heavy objects are placed on top of it. Remove the batteries. Ensure the Air Tube does not have any sharp kinks.

Disposal

Observe the local regulations for material disposal. Dispose of the device in accordance with local regulations. If you have any questions, please contact the local authorities responsible for waste disposal.

TROUBLESHOOTING GUIDE

In case of errors, ” ” will appear in the LCD Display, where “ ” is a number 1-8. Error messages may appear if:

Er5 inflate properly or readings are outside measurement range Data not transferred via Bluetooth® Other device error

ER 1
ER 2
ER 3
ER 4
ER 5
BAT 10
ER 7
ER 8| Pressure or pulse| Please wait one
could not be| minute and repeat the
measured| measurement. Ensure
| that you do not talk
| or move during the
| measurement
Movement or speech during measurement| Please wait five minutes and then repeat the measurement.
attached correctly| Remove and before repeating the measurement
An unknown error occurred during measurement| Please wait five minutes and repeat the measurement. Ensure that you do not talk or move during the measurement
Remove and before repeating the measurement
Batteries are almost depleted| Replace the batteries
Please refer to the instructions in “Bluetooth® Setup” subsection in the “Preparing for Measurement” section.
Please wait five minutes and then repeat the measurement.

TECHNICAL SPECIFICATIONS

the upper arm
Measurement Range| ** Systolic 60-230 mmHg,
Diastolic 40-130 mmHg,
Pulse 40-199 beats/minute
Display Accuracy| Pressure ± 3 mmHg, Pulse ± 5%
Measurement inaccuracy| Max. permissible standard deviation according to clinical testing: systolic 8 mmHg / diastolic 8 mmHg
Memory| 2 x 120 memory spaces
Dimensions| 2.8 in L x 3.8 in W x 2.8 in H
(72 mm L x 96 mm W x 71 mm H)
Weight| batteries
| 5.3 in – 8.5 in (135 – 215 mm)
Operating Range| 41° F – 104° F (5° C – 40° C),
15-90% relative humidity (non-condensing)
Storage Range| -4° F – 140° F (-20° C – 60° C),
≤93% relative humidity (non-condensing)
Power Supply| 2 x 1,5 V AAA batteries
Battery Life| Approx. 300 measurements**

FCC COMPLIANCE INFORMATION

Upper Arm Blood Pressure Monitor SERIES 800W
Responsible Party – U.S. Contact InformationBeurer North America LP
1 Oakwood Boulevard, Suite 255
Hollywood, FL 33020
United States
1-800-536-0366 info@beurer.com

FCC Compliance Statement

This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:

1. This device may not cause harmful interference, and
2. This device must accept any interference received, including interference that may cause undesired operation.

FCC Radiation Exposure Statement

This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment.
This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.
Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.
NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 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. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be encouraged to try to correct the interference by one or more of the following measures:

• Reorient or relocate the receiving antenna.
• Increase the separation between the equipment and receiver.
• Connect the equipment into an outlet on a circuit
• Consult the dealer or an experienced radio/TV technician for help.

WARRANTY

Limited Lifetime Warranty For Original Purchaser

Your Beurer Upper Arm Blood Pressure Monitor, model BC 87, is warranted to be free from defects in materials and workmanship for the life of the product under normal conditions of intended use and service. This warranty extends only to the original retail purchaser and does not extend to retailers or subsequent owners.
We will, at our option, repair or replace the Beurer Upper Arm Blood Pressure Monitor, model BC 87, without additional charge, for any part or parts covered by these written warranties. No refunds will be given. Repair or replacement is our only responsibility and your only remedy under this written warranty. If replacement parts for defective materials are not available, Beurer reserves the right to make product substitutions in lieu of repair or replacement.
For warranty service contact our customer service department at 1-800-536-0366 or at info@beurer.com to provide a description of the problem. If the problem is deemed to be within the scope of the limited lifetime warranty, you will be asked to mail the product at your costs in its original package with proof of purchase, your name, address and phone number. If the problem is not deemed to be within the scope of the limited lifetime warranty, we will provide a quotation for repair respectively replacement and return shipping fee. This warranty does not cover damage caused by misuse or abuse; accident; the attachment of unauthorized accessory; alteration to the product; improper installation; misapplication; lack of reasonable care with respect to the product; unauthorized repairs or modifications; improper use of electrical/power supply; old worn batteries; normal wear; loss of power; dropped product; malfunction or damage of an operating part as a result of failure to comply with instructions for use or to provide manufacturer’s recommended maintenance; transit damage; theft; neglect; vandalism; or environmental conditions; loss of use during the period the product is at a repair facility or otherwise awaiting parts or repair; or any other conditions whatsoever that are beyond the control of Beurer. This warranty is void if the product is ever used in a commercial or business environment. The maximum liability of Beurer under this warranty is limited to the purchase price actually paid by the customer for the product covered by the warranty, as confirmed by proof of purchase, regardless of the amount of  operated in the country in which the product is purchased. A product that requires modifications or adaptation to enable it to operate in any other country than the country for which it was designed, manufactured, approved and/or authorized,  or repair of products damaged by these modifications is not covered under this warranty.
THE WARRANTY PROVIDED HEREIN SHALL BE THE SOLE AND EXCLUSIVE WARRANTY. ANY IMPLIED WARRANTIES, OBLIGATIONS, OR LIABILITES, INCLUDING BUT NOT LIMITED TO THE IMPLIED WARRANTY OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE, ARE LIMITED IN DURATION TO THE DURATION OF THIS APPLICABLE WRITTEN WARRANTY. Some states do not allow limitations on how long an implied warranty lasts, so the above limitations may not apply to you.
IN NO EVENT SHALL BEURER BE LIABLE FOR ANY SPECIAL, INCIDENTAL, INDIRECT OR CONSEQUENTIAL DAMAGES FOR BREACH OF THIS OR ANY OTHER WARRANTY, EXPRESS, IMPLIED OR ANY OTHER THEORY OF LIABILITY, WHATSOEVER. Some states do not allow the exclusion or limitation of special, incidental, or consequential damages, so the above limitation may not apply to you.
Beurer does not authorize anyone, including, but not limited to, retailers, the subsequent consumer purchaser of the product from a retailer or remote purchaser, to obligate Beurer in any way beyond the terms set forth herein. This warranty does not extend to the purchase of opened, used, repaired, repackaged and/or resealed products, including but not limited to sale of such products on Internet auction sites and/or products by surplus or bulk resellers. Any and all warranties or guarantees shall immediately cease and terminate in connection with any products or parts thereof which are repaired, replaced, altered, or modified, without the prior explicitly written consent of Beurer.
This warranty gives you specific legal rights, and you may also have other rights which may vary from state to state. For more information regarding our product line in the USA, please visit: www.beurer.com
Distributed by:
Beurer North America LP
1 Oakwood Boulevard, Suite 255
Hollywood, FL 33020, USA
www.beurer.com
Questions or comments? Call our US-based customer service toll free at 1-800-536-0366.
Assembled in China

EMC Guidance

The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments
Warning: Don’t use near active HF surgical equipment and the RF shielded room of an ME system for magnetic resonance imaging, where the intensity of EM disturbances is high.
Warning: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
Warning: Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.”
Warning: Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the equipment , including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.
Technical description:

1. All necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFORMANCE with regard to electromagnetic disturbances for the excepted service life.
2. Guidance and manufacturer’s declaration
   • electromagnetic emissions and Immunity

Table 1
Guidance and manufacturer’s declaration – electromagnetic emissions

Table 2
Guidance and manufacturer’s declaration – electromagnetic Immunity

| Immunity Test| IEC 60601-1-2
Test level| Compliance level
---|---|---|---
| Electrostatic discharge (ESD) IEC 61000-4-2| ±8 kV contact
±2 kV, ±4 kV, ±8
kV, ±15 kV air| ±8 kV contact
±2 kV, ±4 kV, ±8
kV, ±15 kV air
| Electrical fast transient/burst IEC 61000-4-4| Not applicable| Not applicable
| Surge
IEC 61000-4-5| Not applicable| Not applicable
| Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11| Not applicable| Not applicable
| Power frequency magnetic field IEC 61000-4-8| 30 A/m

50Hz/60Hz

| 30 A/m

50Hz/60Hz

| Conducted RF IEC61000-4-6| Not applicable| Not applicable
| Radiated RF IEC61000-4-3| 10 V/m
80 MHz – 2,7
GHz
80 % AM at 1
kHz| 10 V/m
80 MHz – 2,7
GHz
80 % AM at 1
kHz
NOTE UT is the a.c. mians voltage prior to application of the test level.|

Table 3
Guidance and manufacturer’s declaration – electromagnetic Immunity

1700-1990GSM 1800;CDMA 1900;GSM 1900; DECT; LTEBand 1, 3,4, 25; UMTS Pulse modulation 217 Hz  2  0.3  28  28  2400-2570Bluetooth, WLAN,802.11 b/g/n, RFID 2450, LTE Band 7 Pulse modulation 217 Hz  2  0.3  28  28 5100-5800 WLAN 802.11a/nPulse modulation 217 Hz 0.2 0.3 9 9

Radiated RF IEC61000-4-3
(Test specifications for ENCLOSURE PORT IMMUNITY to
RF wireless communications equipment)

| Test frequency (MHz)| Band (MHz)| Service| Modulation| Maximum Power (W)| Distance (m)| Test Level (V/m)| Compliance level

(V/m)

---|---|---|---|---|---|---|---|---
385| 380-390| TETRA 400| Pulse modulation 18 Hz| 1,8| 0.3| 27| 27
450| 430-470| GMRS 460,
FRS 460| FM ± 5 kHz
deviation 1 kHz sine| 2| 0.3| 28| 28
710| 704-787| ****

LTE Band 13, 17

| Pulse modulation 217 Hz| 0.2| 0.3| 9| 9
745
780
810| 900-960| GSM 800/900, TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5| ****

Pulse modulation 18 Hz

| 2| 0.3| 28| 28
870
930
1720
1845

1970

2450
5240
5500
5785

Documents / Resources

| beurer BC 87 Series 800W Wrist Blood Pressure Monitor [pdf] Instruction Manual
TMB-1976, TMB1976, OU9-TMB-1976, OU9TMB1976, BC 87, Series 800W, Wrist Blood Pressure Monitor, Series 800W Wrist Blood Pressure Monitor, BC 87 Wrist Blood Pressure Monitor, BC 87 Series 800W Wrist Blood Pressure Monitor
---|---

Read User Manual Online (PDF format)

Read User Manual Online (PDF format)  >>

Download This Manual (PDF format)

Download this manual  >>