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When using your blood pressure monitor, basic precautions should always be followed. Please read and follow all instructions and warnings before using this product. Save these instructions for future reference.
Blood pressure measurements determined with this device are equivalent to those obtained by a trained observer using the cuff/stethoscope auscultatory method within the accuracy limits prescribed by the American National Standard for manual, electronic, or automated sphygmomanometers.
What is blood pressure?
Blood pressure is the pressure exerted on the artery walls while blood flows through the arteries. The pressure measured when the heart contracts and sends blood out of the heart is systolic (highest) blood pressure. The pressure measured when the heart dilates with blood flowing back into the heart is called diastolic (lowest) blood pressure.
Why measure your blood pressure?
Among today's various health problems, those associated with high blood pressure are very common. High blood pressure dangerously correlates with cardiovascular diseases. Therefore, blood pressure monitoring is important for identifying those at risk.
Why do my readings vary?
Blood pressure is a body parameter that is subject to normal variations throughout the day. A single reading that is different from your and your doctor's readings are not necessarily inaccurate. The average of several readings, taken under similar conditions, using the same arm, is preferred for accurate blood pressure readings.
Why are my readings different than those taken at my doctor's office?
Many experience a phenomenon called "White Coat Hypertension" when measured by a doctor. White Coat Hypertension refers to blood pressure that rises above its usual level when measured in a clinical setting, such as a doctor's office.
The table below contains defined levels of hypertension that are publicly available from the American Heart Association® (AHA 2017) (www.heart.org/HEARTORG/Conditions/HighBloodPressure/KnowYourNumbers/UnderstandingBlood-Pressure-Readings_UCM_301764_Article.jsp#.WusfWogvy71). Users can compare their own blood pressure readings against these defined levels to determine if they may be potentially at increased risk.
This table is applicable to most adults age 18 and older.
Blood Pressure Category | Systolic mm Hg (upper number) | Diastolic mm Hg (lower number) | LED Indicator Color | |
Normal | <120 | and | <80 | Green |
Elevated | 120-129 | and | <80 | Yellow |
High Blood Pressure (hypertension) Stage 1 | 130-139 | or | 80-89 | Red |
High Blood Pressure (hypertension) Stage 2 | 140-180 | or | 90-120 | |
Hypertension Crisis (consult your doctor immediately) | >180 | and/or | >120 |
Blood pressure tends to go up and down, even in people who normally don't have high readings. If your numbers stay above the "normal" range most of the time, you may be at increased risk and should consult your physician.
Although one can easily find where their own blood pressure readings fall on this table, this monitor comes equipped with a Risk Category Index that automatically compares each reading to the defined levels and provides a helpful cue if your reading falls into one of the stages that could potentially indicate an increased risk.
Please note that cues provided by this monitor are only intended to assist you in using this table. The table and cues are only provided for convenience to help you understand your non-invasive blood pressure reading as it relates to the AHA 2017 information. They are not a substitute for a medical examination by your physician. It is important for you to consult with your physician regularly. Your physician will tell you your normal blood pressure range as well as the point at which you may actually be considered to be at risk.
Replace the batteries if:
NOTE:
Press the DATE/TIME SET buttonand the YEAR will flash on the screen. Press USER/ + button to increase to desired YEAR; press DATE/TIME SET button
to confirm. Repeat steps for MONTH, DAY, HOUR, and MINUTE.
![]() | Low Battery Symbol: Appears when batteries should be replaced. |
![]() | Pulse Symbol: Shows the heart rate per minute. |
![]() | Risk Category Indicator: See Blood Pressure Standard section for more information. |
![]() | Irregular Heartbeat Detector: See below for more information. |
![]() | Memory Average: Displays average of last 3 readings. |
EE | Measurement Error: Adjust the cuff and keep wrist steady during measurement. |
The appearance of theicon indicates that a pulse irregularity consistent with an irregular heartbeat was detected during measurement. Usually, this is not a cause for concern. However, if the symbol appears often, we recommend you seek medical advice. Please note that the device does not replace a cardiac examination, but serves to detect pulse irregularities at an early stage.
Movement, shaking, or talking during the measurement can result in pulse irregularities that may cause the appearance of this icon. Therefore, it is of great importance to not move or talk during measurement.
To determine the presence of an irregular heartbeat, the average of the heartbeat intervals is calculated with the first 3 normal effective heartbeat values. It is important to note that the average is not a strict mathematical averaging of all recorded intervals. At least 3 beats with 25% or greater difference from the average heartbeat interval will generate the icon on the screen.
It is extremely important that the cuff be at the same height as the heart. Having the cuff higher or lower may cause inaccurate results.
NOTE:
This monitor can be used by 2 individuals. Each user can store up to 30 measurements.
Note: Once deleted, your readings cannot be restored.
If any abnormality arises during use, please check the following points.
SYMPTOMS | POSSIBLE CAUSES | CORRECTION |
Unit does not turn on when the START/STOP button is pushed. | Batteries have run down. | Replace them with 2 new AAA alkaline batteries. |
Battery polarities (+/ -) have been positioned incorrectly. | Re-insert the batteries in the correct positions. | |
EE measurement error symbol shown on display or the blood pressure value is displayed excessively low (or high). | The wrist cuff has been positioned on the arm incorrectly. | Re-wrap the cuff properly so that it is positioned correctly. Take new measurement. |
Did you talk or move during measurement? | Keep arm steady during measurement. Measure again. Refer to "Measurement Procedure" instructions. | |
Shaking of the arm with the cuff on. | ||
E1 error symbol shown on display. | Air circuit abnormality. Cuff tube may not be plugged into monitor correctly. | Check cuff connection. Take new measurement. See "Using the Wrist Cuff" section. |
E2 error symbol shown on display. | Inflation pressure exceeding 300 mmHg. | Switch the unit off and then turn back on. Take new measurement. |
E3 error symbol shown on display. | Error determining measurement data. | Re-wrap the cuff properly so that it is positioned correctly. Take new measurement. |
EP error symbol shown on display. | System error. | Remove batteries. After 1 minute, re-insert the batteries. Take new measurement. |
Note: If the unit still does not work, contact HoMedics Consumer Relations. Under no circumstance should you disassemble or attempt to repair the unit by yourself. Contact information for HoMedics Consumer Relations can be found on the Warranty page.
Measurement Method: | Oscillometric |
Rated Range of Cuff Pressure: | 0-300 mmHg |
Measurement Range: | Pressure: 40~280 millimeters Mercury (mmHg) Pulse: 40~199 beats/minute |
Rated Range of Determination: | 40-280 mmHg |
Accuracy: | Pressure: ±3 mmHg Pulse: +5% Max. |
Pressure Sensor: | Semi-conductor |
Inflation: | Automatic inflation (air pump) |
Deflation: | Automatic air release control valve |
Display: | Liquid Crystal Display |
Memory: | 60 memory total for 2 users |
Unit Dimensions: | 75 x 75 x 26 mm (L x W x H) 2.95 x 2.95 x 1.02 inch (L x W x H) |
Unit Weight: | 79.5 g + 5 g (2.80 oz + 0.18 oz) (without cuff and batteries) |
Cuff Size: | 135 ~ 195 mm (approx. 5.3 ~ 7.7 inch) |
Storage/Transportation Environment: | Temperature: -25°C ~ 70°C (-13°F ~ 158°F) Humidity: < 93% RH |
Operation Environment: | Temperature: 5°C ~ 40°C (41°F~104°F) Humidity: 15% ~ 93% RH |
Atmospheric pressure: | 700 hPa ~ 1060 hPa |
Power Supply: | DC 3 V, AAA "LR03" (1.5 V) alkaline battery x 2 |
Battery Life: | Approx. 250 measurements |
Product Life: | 5 years (4 times a day) |
Sleeping Mode: | Without any operation for 1 minute, device automatically shuts off |
Accessories: | Instruction manual, storage case, 2 AAA (LR03) alkaline batteries |
![]() | Internally powered equipment Type BF equipment IP22-degrees of protection provided by enclosures Not suitable for use in presence of flammable anesthetic mixture with air, oxygen, or nitrous oxide. Continuous operation with short-time loading. |
![]() | Follow instructions for use. |
Note: These specifications are subject to change without notice.
POTENTIAL FOR ELECTROMAGNETIC INTERFERENCE
To avoid inaccurate results caused by electromagnetic interference between electrical and electronic equipment, do not use the device near a cell phone or microwave oven. For most wireless communication devices, it is recommended to maintain a distance of 10.8 feet (3.3m) in order to avoid electromagnetic interference.
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
FEDERAL COMMUNICATIONS COMMISSION COMPLIANCE STATEMENT
Changes or modifications to this equipment not expressly approved by the manufacturer could void the user's authority to operate the equipment. 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 determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:
ELECTROMAGNETIC COMPATIBILITY (EMC)
Guidance and manufacturer's declaration – electromagnetic emissions The device is intended for use in the electromagnetic environments listed below, and should only be used in such environments:
Emissions test | Compliance | Electromagnetic environment - guidance |
RF emissions CISPR 11 | Group 1 | RF energy is used only to maintain device's operation. Therefore, its RF emissions are so low that it's not likely to cause any interference in nearby electronic equipment. |
RF emissions CISPR 11 | Class B | |
Harmonic emissions IEC 61000-3-2 | Not Applicable | The device is suitable for use in all establishments, including domestic establishments, and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes. |
Voltage fluctuations/flicker emissions IEC 61000-3-3 | Not Applicable |
Guidance and manufacturer's declaration – electromagnetic immunity
The device is intended for use in the electromagnetic environments listed below, and should only be used in such environments:
Immunity test | IEC 60601 test level | Compliance level | Electromagnetic environment-guidance |
Electrostatic discharge (ESD) IEC 61000-4-2 | ± 8 kV contact discharge ± 15 kV air discharge | ± 8 kV contact discharge ±15 kV air discharge | The relative humidity should be at least 5% |
Power frequency magnetic field IEC 61000-4-8 | 30 A/m 50 or 60 Hz | 30 A/m 50 or 60 Hz | Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. Recommended separation distance![]() where I is the current in amperes in a power bus or an appliance wire and r is the recommended separation distance between your device and the power bus or application wire, in meters (m). |
Recommended separation distances between portable and mobile RF communication equipment and the device.
The device is intended for use in an electromagnetic environment where radiated RF disturbances are under control. User can help prevent electromagnetic interference by keeping the device at a minimum distance from portable and mobile RF communications equipment (transmitters). Below table details the maximum output power of transmitter:
Rated maximum output power of transmitter W | Separation distance according to frequency of transmitter m | ||
150 kHz to 80 MHz Not applicable | 80 MHz to 800 MHz d = 1.2 | 800 MHz to 2.5 GHz d = 2.3 ![]() | |
0.01 | N/A | 0.12 | 0.23 |
0.1 | N/A | 0.38 | 0.73 |
1 | N/A | 1.2 | 2.3 |
10 | N/A | 3.8 | 7.3 |
100 | N/A | 12 | 23 |
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation ls affected by absorption and reflection from structures, objects, and people. |
Guidance and manufacturer's declaration – electromagnetic immunity
The device is intended for use in the electromagnetic environments listed below, and should only be used in such environments:
Immunity test | IEC 60601 test level | Compliance level | Electromagnetic environment- guidance |
Conducted RF IEC 61000-4-6 Radiated RF IEC 61000-4-3 | 3Vrms At 0.15-80MHz 6Vrms At ISM & Radio Amateur Freq. 3 V/mat 80 -2700 MHz (10V/m Home Healthcare) AM Modulation And 9-28V/mat 385-6000MHz, Pulse Mode and other Modulation |
Not Applicable
3 V/mat 80 -2700 MHz (10V/m Home Healthcare) AM Modulation And 9-28V/mat 385-6000MHz, Pulse Mode and other Modulation |
where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya, should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol: |
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. | |||
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, the device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the device. |
LIMITED 5-YEAR WARRANTY
HoMedics sells its products with the intent that they are free of defects in manufacture and workmanship for a period of 5 years from the date of original purchase, except as noted below.
To obtain warranty service on your HoMedics product, contact a Consumer Relations representative by telephone at 1-800-466-3342 for assistance. Please make sure to have the model number of the product available.
©2018 HoMedics, LLC. All rights reserved. HoMedics is a registered trademark of HoMedics, LLC. Distributed by Homedics, LLC, 3000 N Pontiac Trail, Commerce Township, MI 48390
Here you can download full pdf version of manual, it may contain additional safety instructions, warranty information, FCC rules, etc.
Download HoMedics BPW-O200 - Wrist Blood Pressure Monitor Manual
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