Manual de uso Walgreens WGNBPA-220 Tensiómetro

Manual de uso

19

MEASUREMENT PROCEDURE

IMPORTANT NOTES:

• Blood pressure changes with every heartbeat and is in constant

fluctuation throughout the day.

• Blood pressure measurement can be affected by the position of the

user, his or her physiologic condition, and other factors.

Before Measurement:

To help ensure an accurate reading, follow these instructions before

taking a measurement:

• Wait 1 hour after exercising, bathing, eating, drinking beverages with

alcohol or caffeine, or smoking to measure blood pressure.

• Sit quietly and rest for 15 minutes.

• Stress raises blood pressure. Avoid taking measurements during

stressful times.

• Take your reading in a comfortable environment as measurements

can be affected by hot or cold temperatures. Take your blood

pressure at normal body temperature.

During Measurement:

• DO NOT talk or move your arm or hand muscles.

• DO NOT cross your legs. Sit with feet flat on the floor.

• DO NOT touch cuff or monitor during measurement.

20

1. With the cuff wrapped around your arm, press the “START/STOP”

button. Do not inflate the cuff unless it is wrapped around your arm.

All digits will light up to check the display functions. The checking

procedure will be completed after about 3 seconds.

NOTE:

• The Check-with-Confidence

TM

icon will stay on the screen if this

is the 1st or 30th use and the feature is “ON”. The monitor will then

perform a self-check to ensure it is working properly.

2. After all symbols disappear, the display will show “00”. The monitor is

ready to measure and will automatically inflate the

cuff to start measurement.

3. When the measurement is completed, the cuff

will deflate entirely. Systolic pressure, diastolic

pressure, and pulse will be shown simultaneously

on the LCD screen. The measurement is

then automatically stored into memory.

NOTE:

• This monitor automatically turns off approximately 1 minute after last

operation. You may also press the “START/STOP” button to turn

the unit off.

• To interrupt the measurement, you may press the “START/

STOP” (recommended) or “MEM” buttons. The cuff will deflate

immediately after a button is pressed.

21

RISK CATEGORY INDEX

This monitor comes equipped with a Risk Category Indicator that

automatically compares each reading to defined levels established by

the American Heart Association

®

(AHA 2017) as described earlier in this

manual, and provides a helpful cue if your reading falls into one of the

stages that could potentially indicate increased risk. Please note that

cues provided by this monitor are only intended to assist you in using

this table.

The table is only provided for your convenience to help you understand

your noninvasive blood pressure readings 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.

Blood Pressure Category

Systolic mmHg

(upper number)

Diastolic mmHg

(lower number)

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

Hypertensive Crisis (consult your doctor

immediately)

>180

and/

or

>120

*Source: AHA 2017

22

IRREGULAR HEARTBEAT DETECTOR

The appearance of the icon 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.

Important Information:

This blood pressure monitor is not designed for use by people with

arrhythmias nor for diagnosing or treating an arrhythmia problem. As a

safeguard, we recommend that if you have arrhythmias, such as atrial

or ventricular premature beats and atrial fibrillation or any other special

conditions, you should check with your physician before using your

blood pressure monitor.

Irregular Heartbeat Detector

23

EXCESSIVE BODY MOTION DETECTOR

The icon is displayed if body movement is detected during

measurement, especially the movement of the arm the blood pressure

monitor is worn on.

NOTE:

• The measured blood pressure reading may not be accurate if the icon

is displayed.

RECALLING VALUES FROM MEMORY

1. Press the “MEM” button to access

the memory.

2. Every new press of the “MEM” button

will recall a previous reading. The latest

reading will be recalled first.

Excessive

Body Motion

Detector

24

CLEARING VALUES FROM MEMORY

Press and hold the “MEM” and “START/STOP” buttons at the

same time while in memory recall mode, and the data will be erased

automatically.

NOTE:

• Once deleted, your readings cannot be restored.

• Once deleted, the device will automatically perform a self-check on

the next measurement.

IMPORTANT NOTES REGARDING YOUR

BLOOD PRESSURE MEASUREMENT

• It is suggested that you take your measurements at the same time

each day and use the same arm for consistency.

• Users should wait a minimum of 5 minutes before taking additional

measurements. More time may be necessary depending upon your

physiology.

• The measurement results that users receive are for reference only. If

users have any blood pressure concerns, please consult a physician.

• Once inflation reaches 300 mmHg, the unit will deflate automatically

for safety reasons.

• This product is not suitable for people with arrhythmias.

• This device may have difficulty determining the proper blood

pressure for pregnant women and for users with irregular heartbeat,

diabetes, poor circulation of blood, kidney problems, or for users

who have suffered a stroke.

25

CARE, MAINTENANCE, & CLEANING

• Clean the blood pressure monitor body and cuff carefully with a

slightly damp, soft cloth. Do not press. Do not wash cuff or use

chemical cleaner on it. Never use thinner, alcohol or petrol (gasoline)

as cleaner.

• Leaky batteries can damage the unit. Remove the batteries when the

unit will not be used for a long time.

• Follow local ordinances and recycling instructions regarding disposal

or recycling of the device and device components, including batteries.

• If the unit is stored near freezing, allow it to acclimate to room

temperature before use.

• This blood pressure monitor is not field serviceable. You should not

use any tool to open the device nor should you attempt to adjust

anything inside the device. If you have any problems with this device,

please contact HoMedics Consumer Relations (contact information

can be found in the Warranty section).

• DO NOT immerse the unit in water as this will result in damage to the

unit.

• DO NOT subject the monitor or cuff to extreme temperatures,

humidity, moisture, or direct sunlight. Protect from dust.

• DO NOT fold the cuff and tubing tightly.

• DO NOT disassemble the monitor or cuff. If in need of repair, refer to

the Warranty section of this manual.

• DO NOT subject the monitor to extreme shock (do not drop on floor).

26

• DO NOT inflate the cuff unless wrapped around arm.

• DO NOT wrap the cuff around body parts other than your arm.

• DO NOT drop or insert any object into any opening or hose.

• To avoid accidental strangulation, keep this product away from

children. Do not drape tube around neck.

• This monitor may not meet its performance specifications if stored or

used outside of these temperature and humidity ranges:

Storage/Transportation

Environment

Temperature:

-13°F~158°F (-25°C~70°C)

Humidity:

less than 93% RH

Operating

Environment

Temperature:

41°F~104°F (5°C ~40°C)

Humidity:

15% ~ 93% RH

Atmospheric pressure:

700hPa-1060hPa

27

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 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 operation.

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:

• Reorient or relocate the receiving antenna.

• Increase the separation between the equipment and receiver.

• Connect the equipment into an outlet on a circuit different from that

to which the receiver is connected.

• Consult the dealer or an experienced radio/TV technician for help.

28

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.

9ROWDJHÛXFWXDWLRQVÛLFNHU

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

In the case of air discharge testing, the climatic

conditions shall be within the following ranges:

Ambient Temperature: 15°C~35°C

Relative Humidity: 30%~60%

Power frequency

PDJQHWLFÚHOG

IEC 61000-4-8

30 A/m

50 or 60 Hz

30 A/m

50 or 60 Hz

3RZHUIUHTXHQF\PDJQHWLFÚHOGVVKRXOGEHDW

levels characteristic of a typical location in a typical

commercial or hospital environment.

29

• 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

3V rms

At 0.15-80 MHz

6V rms

At ISM & Radio Amateur

Freq.

Not Applicable Portable and mobile RF communications equipment should be used no

closer to any part of the device, including cables, than the recommended

separation distance calculated from the equation applicable to the frequency

of the transmitter.

Radiated RF

IEC 61000-4-3

3UR[LPLW\ÚHOGV

from RF wireless

communications

equipment

IEC 61000-4-3)

10 V/m at 80-2700 MHz

AM Modulation And

9-28V/m at 385-

6000MHz, Pulse Mode

and other Modulation.

The system shall be

WHVWHGDVVSHFLÚHGLQ

IEC60601-1-2 Table

IRUSUR[LPLW\ÚHOGV

from RF wireless

communications

equipment using the

WHVWPHWKRGVVSHFLÚHG

in IEC 61000-4-3

10 V/m at 80-2700 MHz

AM Modulation And

9-28V/m at 385-

6000MHz, Pulse Mode

and other Modulation.

The system shall be

WHVWHGDVVSHFLÚHGLQ

IEC60601-1-2 Table

IRUSUR[LPLW\ÚHOGV

from RF wireless com-

munications equipment

using the test methods

VSHFLÚHGLQ,(&

61000-4-3

Recommended separation distance

Considering to reduce the minimum separation distance, based on RISK

MANAGEMENT, and using higher IMMUNITY TEST LEVELS that are

appropriate for the reduced minimum separation distance. Minimum

separation distances for higher IMMUNITY TEST LEVELS shall be calculated

using the following equation:

E = 6/d

where P is the maximum power in W, d is the minimum separation distance in

m, and E is the IMMUNITY TEST LEVELS in V/m.

)LHOGVWUHQJWKVIURPÚ[HG5)WUDQVPLWWHUVDVGHWHUPLQHGE\DQ

electromagnetic site survey,

a

should be less than the compliance level in

each frequency range.

b

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.

127(7KHVHJXLGHOLQHVPD\QRWDSSO\LQDOOVLWXDWLRQV(OHFWURPDJQHWLFSURSDJDWLRQLVDIIHFWHGE\DEVRUSWLRQDQGUHÛHFWLRQIURPVWUXFWXUHV

objects and people.

D)LHOGVWUHQJWKVIURPÚ[HGWUDQVPLWWHUVVXFKDVEDVHVWDWLRQVIRUUDGLRFHOOXODUFRUGOHVVWHOHSKRQHVDQGODQGPRELOHUDGLRVDPDWHXUUDGLR

AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment

GXHWRÚ[HG5)WUDQVPLWWHUVDQHOHFWURPDJQHWLFVLWHVXUYH\VKRXOGEHFRQVLGHUHG,IWKHPHDVXUHGÚHOGVWUHQJWKLQWKHORFDWLRQLQZKLFKWKH

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.

E2YHUWKHIUHTXHQF\UDQJHN+]WR0+]ÚHOGVWUHQJWKVVKRXOGEHOHVVWKDQ9P

Test specifications for enclosure port immunity to RF wireless communications equipment.

Test frequency (MHz) Modulation IMMUNITY TEST LEVEL (V/m)

385 Pulse modulation 18 Hz 27

450 FM ± 5 kHz deviation 1kHz sine 28

710

745

780

Pulse modulation 217 Hz 9

810

870

930

Pulse modulation 18 Hz 28

1720

1845

1970

Pulse modulation 217 Hz 28

2450 Pulse modulation 217 Hz 28

5240

5500

5785

Pulse modulation 217 Hz 9

NOTE: If necessary to achieve the IMMUNITY TEST LEVEL, the distance between the transmitting antenna and the ME EQUIPMENT or ME

SYSTEM may be reduced to 1 m, the 1 m test distance is permitted by IEC 61000-4-3.

a). The carrier shall be modulated using a 50% duty cycle square wave signal.

b). AS an alternative to FM modulation, 50% pulse modulation at 18 Hz may be used because while it does not represent actual modulation, it

would be worst case.

30

TROUBLESHOOTING

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 4 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).

Cuff has been placed incorrectly. Wrap the cuff properly so

that it is positioned correctly.

Measure again.

E1 error symbol shown on

display.

Air circuit abnormality. Cuff tube may not

be plugged into monitor correctly.

Check cuff connection.

Measure again.

E2 error symbol shown on

display.

Inflation pressure exceeding 300 mmHg. Switch the unit off, then

measure again.

E3 error symbol shown on

display.

Error determining measurement data. Measure again.

If the circumference of the upper arm

differs largely from the circumference of

the forearm, an excessive gap may occur

between the arm and the arm cuff.

Ensure the cuff is wrapped

correctly. Please consult your

healthcare professional if you

have questions on how to

properly wear the arm cuff.

EP error symbol shown on

display.

System error. Turn off monitor and measure

again. If EP error still appears

on the display, please call

a Consumer Relations

representative.

Excessive body motion

detector symbol shown

on display

Excessive body movement, especially of

the arm the cuff is worn, occurred during

the measurement. Ex: talking, moving or

shaking of the arm with the cuff on while

measurement.

Measure again. Keep arm

steady during measurement.

Cuff may not be wrapped correctly, or the

circumference of the upper arm differs

largely from the circumference of the

forearm, an excessive gap may occur

between the arm and the arm cuff.

Ensure cuff is wrapped

correctly, see “Using the

Ultrasoft

®

Arm Cuff” section

for more information. Please

consult your healthcare

professional if you have

questions on how to properly

wear the arm cuff.

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 Department can be found in the Warranty

section.

31

Power Source: Four 1.5V DC “AAA” alkaline batteries

Measurement Method: Oscillometric

Rated Range of Cuff Pressure: 0~300 mmHg

Rated Range of Cuff

Determination:

40~280 mmHg

Measurement Range of

Heart Rate:

40~199 beats/minute

Accuracy:

Pressure: ±3 mmHg

Pulse: ±5% of reading

Pressure Sensor: Semi-conductor

,QÛDWLRQ Pump driven

'HÛDWLRQ Automatic pressure release valve

Memory Capacity: 60 memories

Auto Shutoff: 1 minute after last button operation

Battery Life: Approx 300 Measurements

Product Life: 5 Years (4 times per day)

Operation Environment:

Temperature: 41°F~104°F (5°C ~40°C)

Humidity: 15% ~ 93% RH

Atmospheric pressure: 700 hPa~1060 hPa

Storage/Transportation

Environment:

7HPSHUDWXUHå)a)&a&

Humidity: Less Than 93% RH

Weight: 0.48 lbs (216 g) (without batteries)

Arm Circumference:

One Size UltraSoft™ Cuff—Fits Most Arms: 9"–17"

(23cm-43cm)

Dimensions:

3.78"(L) x 4.41"(W) x 1.93"(H)

96mm(L) x 112mm(W) x 49mm(H)

Accessories:

(4) “AAA” alkaline batteries, arm cuff with tube,

Instruction Manual

SPECIFICATIONS

32

Internally powered equipment

Type BF equipment

1RWVXLWDEOHIRUXVHLQSUHVHQFHRIÛDPPDEOH

anesthetic mixture with air, oxygen, or nitrous oxide.

Continuous operation with short-time loading.

Follow instructions for use.

To avoid inaccurate results caused by electromagnetic

interference.

NOTE: 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 device. Otherwise,

degradation of the performance of this equipment

could result.

Waste of electrical and electronic equipment (WEEE)

Serial number

YYMMXXXX

Ingress Protection Rating

First characteristic numeral - Degree of protection

against access to hazardous parts and against foreign

objects.

IP22 N1 =2 (Protected against solid foreign objects of

12.5 mm ∅ and greater).

Second characteristic numeral - Degree of protection

against ingress of water.

N2=2 (Protected against vertically falling water drops

when ENCLOSURE tilted up to 15°).

Non-ionizing electromagnetic radiation.

NOTE: These specifications are subject to change without notice. If the device needs to be

calibrated, please contact Consumer Relations.

33

©2020 HoMedics, LLC. All rights reserved.

Homedics, Ultrasoft, and GentleInflate are registered trademarks ofHoMedics, LLC.

American Heart Association is a registered trademark of the American Heart Association.

IB-WGNBPA220B

P/N: 323103321 VER:001

For service or repair,

do not return this unit

to the retailer. Contact

HoMedics Consumer

Relations at:

Email:

cservice@

homedics.com

Phone:

1-800-466-3342

Business Hours:

8:30am-7pm ET

Monday-Friday

Distributed by

HoMedics, LLC

3000 N Pontiac Trail

Commerce Township, MI

48390

Made in Vietnam

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. HoMedics warrants that its products will be free of defects in material and

workmanship under normal use and service. This blood pressure monitor meets the simulated

measurement cycles test requirement per EN1060-3, part 8.10. This warranty extends only to

consumers and does not extend to Retailers.

To obtain warranty service on your HoMedics product, contact a Consumer Relations

Representative for assistance. Please make sure to have the model number of the product

available.

HoMedics does not authorize anyone, including, but not limited to, Retailers, the subsequent

consumer purchaser of the product from a Retailer or remote purchasers, to obligate

HoMedics in any way beyond the terms set forth herein. This warranty does not cover

damage caused by misuse or abuse; accident; the attachment of any unauthorized accessory;

alteration to the product; improper installation; unauthorized repairs or modifications;

improper use of electrical/power supply; loss of power; dropped product; malfunction

or damage of an operating part from failure to provide manufacturer’s recommended

maintenance; transportation 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 HoMedics.

This warranty is effective only if the product is purchased and operated in the country in

which the product is purchased. A product that requires modifications or adoption 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.

THERE SHALL BE NO OTHER WARRANTIES EXPRESS OR IMPLIED INCLUDING ANY IMPLIED

WARRANTY OF MERCHANTABILITY OR FITNESS OR ANY OTHER OBLIGATION ON THE

PART OF THE COMPANY WITH RESPECT TO PRODUCTS COVERED BY THIS WARRANTY.

HOMEDICS SHALL HAVE NO LIABILITY FOR ANY INCIDENTAL, CONSEQUENTIAL OR SPECIAL

DAMAGES. IN NO EVENT SHALL THIS WARRANTY REQUIRE MORE THAN THE REPAIR OR

REPLACEMENT OF ANY PART OR PARTS WHICH ARE FOUND TO BE DEFECTIVE WITHIN THE

EFFECTIVE PERIOD OF THE WARRANTY. NO REFUNDS WILL BE GIVEN. IF REPLACEMENT

PARTS FOR DEFECTIVE MATERIALS ARE NOT AVAILABLE, HOMEDICS RESERVES THE RIGHT

TO MAKE PRODUCT SUBSTITUTIONS IN LIEU OF REPAIR OR REPLACEMENT.

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 sales of such products by surplus or bulk resellers. Any and all warranties or guarantees

shall immediately cease and terminate as to any products or parts thereof which are repaired,

replaced, altered, or modified, without the prior express and written consent of HoMedics.

This warranty provides you with specific legal rights. You may have additional rights which

may vary from state to state. Because of individual state regulations, some of the above

limitations and exclusions may not apply to you.

Made exclusively for

B

323103623

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