Pyle PHBPB16TL User guide

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Automatic Blood Pressure Monitor w/ Arm Cuff

Instruction Manual

PHBPB16TL

Table of Contents

1. Safety Information ................................................................................................... 2

1.1 Warning .............................................................................................................................. 2

1.2 Precaution .......................................................................................................................... 2

2. Product Feature ....................................................................................................... 3

3. Pre Measurement ..................................................................................................... 5

3.1 Battery ................................................................................................................................ 5

3.2 Power Adapter（Optional） ............................................................................................ 5

3.3 Setting ................................................................................................................................. 6

4 Take a measurement ................................................................................................. 6

4.1 Important Noted ................................................................................................................ 6

4.2 Fitting the cuff ................................................................................................................... 6

4.3 Body posture during measurement.................................................................................. 7

4.4 Take Measurement ............................................................................................................ 7

4.5 Data Transmission ............................................................................................................. 8

4.6 Memory .............................................................................................................................. 9

5. Error Indication ....................................................................................................... 9

6. Trouble Shooting ...................................................................................................... 9

7. Specification ........................................................................................................... 10

8．About Blood Pressure .......................................................................................... 14

8.1 What is Blood Pressure? ................................................................................................. 14

8.2 What is high blood pressure? ......................................................................................... 14

8.3 What is morning hypertension (morning surge)? ........................................................ 15

Reference Standard .................................................................................................... 15

Blood Pressure Measurement Chart ........................................................................ 16

Guarantee Card ............................................................. Error! Bookmark not defined.

Product label................................................................... Error! Bookmark not defined.

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1. Safety Information

1.1 Warning  Self diagnosis and treatment which use measured results may be dangerous. Follow the

instructions of your physician or licensed healthcare provider.

 Those who have arrhythmia, diabetes, blood circulation or apoplexy problem, please use

under the physician’s instruction.

 If cuff inflation doesn’t stop, remove the cuff or power off the unit, otherwise, it may result in

a hazardous condition.

 This equipment is not suitable for the neonate, infant and who can't communicate or interact

independently.

 Do not use the blood pressure monitor for any other purpose except measuring the blood

pressure of human body.

 Only take measurement with the manufacturer supplied cuff or AC adapter, or else it will lead

to inaccurate results.

 Do not use the blood pressure monitor when you are close proximity to strong static

electricity or electromagnetic fields, and avoid using the mobile during measurement.

 Do not use in combination with a hyperbaric oxygen therapy device, or in an environment

where combustible gas may be generated.

 Do not install the unit in the following locations:

- Locations subject to vibration such as ambulances and emergency helicopters.

- A location where there is gas or flame.

- A location where there is water or steam.

- A location where chemicals are stored.

- A location where the unit may easily fall.

 The common arrhythmia such as atrial premature beats, premature ventricular and atrial

fibrillation will lead to inaccurate results or error.

 Measurements or stores need to take into account environment variables, or else it would lead

to the inaccurate measurement.

 When using or replacing the AC adapter and batteries, the operator not to touch those parts

and the patient simultaneously.

 The battery has positive/negative polarity. If the battery does not connect well to the unit, do

not forcibly connect it.

 Do not use Luer lock. If Luer lock connectors are used in the construction of tubing, there is a

possibility that they might be inadvertently connected to intravascular fluid systems, allowing air to be pumped into a blood vessel.

1.2 Precaution

 Do not attempt to disassemble, repair or modify the blood pressure monitor or hand cuff.  Avoid high temperature, moisture, dust and direct sunlight.

 Clean the body with soft and clean wet cloth. Do not clean the unit with alcohol and other

corrosive liquids.

 Do not wet or cleaning the cuff with water.  Clean the cuff with soft dry cloth after measurement.

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 Do not use at extremely high temperature, high humidity, or high altitude. Use only within the

Back of unit

required ambient conditions.

 Do not place heavy objects on the AC adapter cable, or allow the unit to sit on the cord.  Do not plug in or unplug the AC adapter with wet hands.  Do not drop or expose the device to heavy shock.  Do not use the unit near large equipment that uses a switching relay for power ON/OFF.  Remove the batteries if the unit will not use for a long time.  Clinical testing has not been conducted on newborn infants and pregnant women. Do not use

on newborn infants and pregnant women.

 The blood pressure monitor has gone through several trials of testing to ensure the

measurement accuracy. The end user should conduct a manufacturer recommended inspection and calibration annually.

 Blood pressure measurements determined with the device are equivalent to those obtained by

a trained observer using the cuff/stethoscope auscultatory method, within the limit prescribed by the American National Standard, Manual, electronic or automated sphygmomanometers.

 Keep out of reach of infants, small children, and compromised people who cannot express

their consent.

 This product is suitable for use to self- monitoring of blood pressure in home or used by the

licensed healthcare personnel in hospital.

Precaution！Please read the enclosed instruction.

2. Product Feature

Scope：Measurement of Human Blood Pressure and Pulse Rate for adults

Body

Fig 1

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Cuff (Type BF Applied Part)

Model：PHBPB16TL

Applicable Arm Circumference: 8.6" to 14" inches

Note:

Symbol for”TYPE BF APPLIED PART”

Display

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3. Pre Measurement

Please use the same brand battery and be aware of battery polarity during installation

Fig 5

Electric outlet

AC adapter

AC Adapter connector

3.1 Battery

3.1.1 Installation and replacement

1） Remove battery cover 2） Load 4 standard AAA alkaline battery as indicated in figure below

Fig 4

3） Install back the battery cover 4） Replace the battery if low battery icon is displayed

 If the low battery symbol is displayed, replace with new batteries, otherwise

the unit will not function properly.

 Use 4 same brand 1.5 Volt AAA alkaline batteries.  Do not mix the new and old batteries.  Remove the battery if the unit is to remain unused for an extended period.  Reset the time and date after battery replacement.

3.1.2 Battery Life

 Four new LR03 (AAA) batteries will last for approximately 200 measurements, if

measurements are taken once a day at room temperature (70°F).

 The batteries enclosed in the package are used for demonstration purpose. It is possible

these batteries will therefore not last for 200 measurements.

 The battery life can be confirmed in the bottom right of the display. If the low battery

symbol is displayed, remaining power is low, replace with new batteries.

3.2 Power Adapter（Optional）

1) Connect the AC adapter to the AC adapter connector of the main unit

2) Plug the socket into electric outlet.( Fig 5)

 AC adapter model: UE08WCP-060050SPA  Use the correct adapter designed for your local voltage (AC 100~240 V)  Do not plug in multiple plugs into same power outlet.  Power adapter specification: Input: AC 100~240 V,

50/60Hz, 400mA; Output: 6.0V 0.5A

 Use the manufacturer power adapter only.  Unplug the AC adapter or wires if the device is damaged.  Do not touch the AC adapter with wet hand.  When operating the unit please do not tangle the power cords.

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3.3 Setting

1) With monitor power off

2) Hold the【S】button for 3 seconds, Year digits blinking a) Change number

ⅰPress the memory button to advance one number ⅱHold down the 【M】memory button, the number will change rapidly

b) Enter the two digit of the year number c) Press the 【S】button will proceed to month setting d) Repeat step a) to c) to set month, day, hour and minutes

3) Unit Conversion (mmHg to kPa) a) Press the memory button will automatically change the unit conversion either from

mmHg or kPa as shown on Fig 6 or Fig 7.

b) Complete setting, press Start/Stop button to exit.

Fig 6 Fig 7

4 Take a measurement

4.1 Important Noted

 Don't eat, drink alcohol, smoke, take a shower or exercise for at least 30 minutes before you

take your blood pressure and don't use any medicines that can raise blood pressure.

 Try not to take your blood pressure if you are nervous or upset. If you are nervous, anxious,

or agitated your blood pressure will rise.

 Rest for 5～10 minutes before taking a reading. Sit in a comfortable, relaxed position. Don't

move around or talk while taking the blood pressure. Leave your legs in one position, breath freely and calmly.

 The blood pressure cuff should fit over about 3/4 of your upper arm. It should easily go

around the arm and the Velcro should close tightly.

 If you can, use the same arm for every reading.  Measuring blood pressure at the same time on different days should give about the same

reading (excluding outside influences like exercise).

 Changes in medication or nutritional supplement can alter your result. Please consult your

doctor before taking or stopping medications or supplement.

4.2 Fitting the cuff

1) Plug in the air tube connector into the main unit

2) Wrap the cuff around the upper left arm or upper right arm.

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3) Tighten the cuff around the arm, make sure the cuff is approximately 2～3cm ( 1～2 inches)

above the elbow.（Fig 8）

Fig 8

4) Make sure cuff air tube outlet is facing your finger. Do not over tighten. Approximate one finger should be able to fit underneath the cuff after tightening.

5) Relax, place the elbow on the desk with palm facing up; the cuff should be level with your heart. If the cuff doesn’t fit your arm, the reading accuracy may be affected.

 Do not bend with the cuff or the air tube.  To detach the cuff, unplug the air tube connector from the main unit  Do not inflate prior fitting the cuff.  Change the cuff, if it there is a leakage or if the cuff is not working properly.  Only use the manufacturer cuff to ensure the measurement accuracy

4.3 Body posture during measurement

Relax, place the elbow on the desk with palm facing up; cuff should be at the heart level (Fig

9). The reading accuracy may be affected if the cuff is not fitted properly. The arm should be

at the same level of your heart. If your arm is too low, your reading will be too high. If your arm is too high, your reading will be too low.

Fig 9

4.4 Take Measurement

After installing the batteries and wearing the cuff, the unit is ready for measurement:

1) For the most accurate result please relax, do not smoke, take deep breath, speak loudly or move around during the measurement.

2) Turn on the on/off button; display will lit-up for 1 second as shown on fig 10

3) Then the display on switch to fig 11, a beep sound indicates the monitor has begun taking the measurement.

4) When the device detects a pulse, the heart symbol will flash as shown on fig 12. The

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cuff inflates, and your pulse and blood pressure measurement is taken.

5) When completing the test, the cuff will automatically deflate and the test result will display on the screen as shown on fig 13.

6) You may turn off the unit or compare with the previous results

7) Automatic shut off in 3 minutes.

8) If a problem occur during the test, “Err ” will display on the screen.

9) In the end of measurement, “ ” will display on the screen when irregular pulse is detected.

Fig 10 Fig 11 Fig 12 Fig 13

Notes:  Do not self-diagnosis according to measurement results. Follow the instructions of your

physician or licensed healthcare provider.

 The blood pressure monitor only will remind the end user on high blood pressure as follows:

When the systolic pressure is greater or equal to 140mmHg and/or when the diastolic pressure is greater or equal to 90mmHg as abnormal. The display will flash to remind the end user of the blood pressure abnormality.

 If the device caused any discomfort during measurement or fail to perform as indicated, turn

off the power or discontinue use.

 The time of the pressure reduced from 260mmHg (34.67kPa) to 15mmHg (2kPa) does not

exceed 10s.

 If cuff inflated up to 300 mmHg (40 kPa) doesn’t stop, please remove the cuff or power off

the unit

4.5 Bluetooth Connection and Data Transmission

The Bluetooth can be turned on after the device is connected to the AC adapter or you have installed the batteries, the device can transmit data to the PHBP Blood Pressure App by Bluetooth. Download and install the PHBP Blood Pressure App on your Android or iOS device Please be sure that Bluetooth is turned on your device Search for the PHBPB16TL on your device. Once the device is found select it for automatic pairing. Start the PHBP Blood Pressure App and follow the directions included in App.

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4.6 Memory

Error

Cause

How to correct

Er 30

Power on, cuff inflation rate is too low or main unit does not connect with the cuff.

（1） Reconnect the air tube connector

with the main unit

（2） Cuff or bladder leakage, if

necessary purchased a new one.

（3） Confirm the cuff is wrapped up

correctly (ref 4), retake the measurement

Er 2

Weak Signal or cuff is too loose

Cuff too loose，Confirm the cuff is wrapped up correctly（ref 4.2）retake the measurement

Er 3

Heavy shock during the

measurement.

Remain still, retake the measurement (ref

4.1）

Er 5

Bad Signal，moving or talking during the measurement

Remain still, retake the measurement (ref

4.1）

Er7

Measurement abnormal.

Please retake the measurement.

Low battery power, cannot inflate

Change battery（ref 3.1）

Abnormal

How to correct

After batteries installation, power

（1） Check batteries polarity。

The internal memory can hold up to 90 readings.

1) Memory Review

a) With monitor power off, hold the 【M】button to enter the memory mode. b) The unit will display the most recent 3 set of data average c) When holding the【M】button the user can view the data from the most recent date to the

oldest date. When holding the【S】button the user can view vice versa.

Caution: Continuous holding the 【M】button will delete all the memory.

2) Delete memory data

a) Enter into the memory mode. b) Press and hold the memory button until the “---” displayed, all the memory data will be

deleted

c) The unit will only delete the present set of memory data; the other set of memory data

will not be affected.

d) The device is not capable of deleting a single data entry e) Press the 【ON/OFF】 button exit the memory mode and turn off.

5. Error Indication

List of Error code.

6. Trouble Shooting

When the unit encounters malfunction during the use, refer to table below:

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on, no display.

（2） If still cannot power on, reinstall the batteries or

change new batteries

Measured value are abnormally high or low

（1） Confirm the cuff is wrapped up correctly。

（2） If the user clothing restricts the normal flow, please

remove the obstructing clothing and retake the measurement

（3） Relax, place the elbow on the desk with palm facing

up; cuff should align with heart level. Retake the measurement

Cuff inflation rate is too low or does not inflate

（1） Reconnect the air tube connector with the main unit （2） Cuff or bladder leakage, if necessary purchased a

new one.

Cuff deflates too quickly.

（1） Cuff too loose，confirm the cuff is wrapped up

correctly。

Measure value is different from the hospital or the value is inconsistent

（1） Blood pressure value is varied during the day which

also will affect by the human emotional and physical condition

（2） Record the variance and consult to the doctor

*If the above suggestion doesn’t remediable, please dial Pyle Technical Support: 718-535-1800

Description

Arm automatic blood pressure monitor

Model

PHBPB16TL

Display

LCD Digital Display

Measuring principle

Oscillometric Method

Measurement Range

Pressure: 0mmHg~280mmHg

（0kPa~37.3kPa）

Pulse: 40 pulse/min ~180 pulse/min

Accuracy

Pressure : ±3mmHg （±0.4kPa） Pulse: ±5%

Memory

90 sets memory of measurement values.

Automatic power off

Unattended 3 minutes

Power source

4 AAA Alkaline battery AC Adapter（AC 100~240 V）

Battery Life

Approx 200 measurements

Protection against electric shock

Type BF

IP classification

IP21

Operating Environment

Temperature：+41F～+104F； Humidity：≤93% Pressure: 70.0kPa～106.0kPa Altitude: ≤ 3 000 m

Storage and transport Environment

Temperature：-13F～+150F； Humidity：10%～95% Pressure:50.0kPa～106.0kPa

ext: 279 for help.

7. Specification

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Weight

270g（Without batteries）

Size

6.3"×3"×1.5"

Life time (Body)

Body

five years or 10000 times

Contents

·Cuff(Applicable arm circumference:

8.6" to 14" inches)

·AC Adapter（Optional）

·4 A AA alkaline batteries

·Storage case (Optional)

·Instruction Manual

·Guarantee Card

Cuff

10000 times

AC Adapter

50000 hours

This unit is intended for home use and the specification may be changed without prior notice.

Guidance and manufacturer’s declaration – electromagnetic emissions

The [EQUIPMENT or SYSTEM] is intended for use in the electromagnetic environment specified below. The customer or the user of the [EQUIPMENT or SYSTEM] should assure that it is used in such an environment.

Emissions test

Compliance

Electromagnetic environment - guidance

RF emissions CISPR 11

Group 1

The [EQUIPMENT or SYSTEM] uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions CISPR 11

Class B

Harmonic emissions IEC 61000-3-2

Not applicable

Voltage fluctuations/flicker

Not applicable

Important information regarding Electro Magnetic Compatibility (EMC)

With the increased number of electronic devices such as PC’s and mobile (cellular) telephones, medical devices in use may be susceptible to electromagnetic interference from other devices. Electromagnetic interference may result in incorrect operation of the medical device and create a potentially unsafe situation. In order to regulate the requirements for EMC (Electro Magnetic Compatibility) with the aim to prevent unsafe product situation, the IEC60601-1-2 standard has been implemented. This standard defines the levels of immunity to electromagnetic interferences as well as maximum levels of electromagnetic emissions for medical devices. This medical device manufactured by pump conforms to this IEC60601-1-2:2007 standard for both immunity and emissions. Nevertheless, special precautions need to be observed:

·Do not use mobile (cellular) telephones and other devices, which generate strong electrical or electromagnetic fields, near the medical device. This may result in incorrect operation of the unit and create a potentially unsafe situation. Recommendation is to keep a minimum distance of 7 m. Verify correct operation of the device in case the distance is shorter. Further documentation in accordance with IEC60601-1-2:2007 is available at pump at the address mentioned in this user manual.

Please dispose of the batteries according to local regulations.

Guidance and manufacturer’s declaration

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emissions IEC 61000-3-3

Guidance and manufacturer’s declaration – electromagnetic immunity

Immunity

test

IEC 60601 test

level

Compliance

level

Electromagnetic environment -

guidance

Electrostatic discharge (ESD) IEC 61000-4-2

±6 kV contact ±8 kV air

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. If ESD interfere with the operation of equipment, counter measurements such as wrist strap, grounding shall be considered.

Electrical fast transient/burst IEC 61000-4-4

±2 kV for power supply lines ± 1 kV for input/output lines

Not applicable

Mains power quality should be that of a typical commercial or hospital environment.

Surge IEC 61000-4-5

± 1 kV differential mode ± 2 kV common mode

Not applicable

Mains power quality should be that of a typical commercial or hospital environment.

Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11

< 5% UT (>95% dip in UT) for 0.5 cycle

40% UT (60% dip in UT) for 5 cycles 70% UT (30% dip in UT) for 25 cycles < 5% UT

(>95% dip in UT) for 5 sec

Not applicable

Mains power quality should be that of a typical commercial or hospital environment. If the user of the [equipment or system] requires continued operation during power mains interruptions, it is recommended that the [equipment or system] be powered from an uninterruptible power supply or a battery.

Power frequency (50/60 Hz) magnetic field IEC 61000-4-8

3 A/m

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

Guidance and manufacturer’s declaration – electromagnetic immunity

Immunity test

IEC 60601 test

level

Compliance

level

Electromagnetic environment -

guidance

Conducted RF IEC 61000-4-6

3 Vrms 150 kHz to 80 MHz

Portable and mobile RF communications equipment should be used no closer to any part of the

Guidance and manufacturer’s declaration – electromagnetic immunity –

for EQUIPMENT and SYSTEMS that are not LIFE – SUPPORTING

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Radiated RF IEC 61000-4-3

3 V/m 80 MHz to 2.5 GHz

3V/m

[EQUIPMENT or SYSTEM], including cables, than the recommended separation distance calculated from the equation applicable to the frequency or the transmitter. Recommended separation distance

d = 1.2

80 MHz to 800 MHz

d = 2.3

800 MHz to 2.5 GHz

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 meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, should be less than the compliance level in each frequency range. Interference may occur in the vicinity of equipment marked with the following symbol:

Recommended separation distances between portable and mobile

Recommended separation distances between portable and mobile RF communications equipment and the [EQUIPMENT or SYSTEM]

The [EQUIPMENT or SYSTEM] is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the [EQUIPMENT or SYSTEM] can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the [EQUIPMENT or SYSTEM] as recommended below, according to the maximum output power of the communications equipment.

Rated maximum

output power of

transmitter

Separation distance according to frequency of transmitter

150 kHz to 80 MHz

d = 1.16

80 MHz to 800 MHz

d = 1.16

800 MHz to2.5 GHz

d = 2.33

0.01

0.12

0.23

0.1

0.38

0.73

1.2

2.3

3.8

7.3

100

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (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.

RF communications equipment and the EQUIPMENT or SYSTEM –

For EQUIPMENT and SYSTEMS that are not LIFE – SUPPORTING

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NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

Pyle PHBPB16TL User guide

Specifications and Main Features

Frequently Asked Questions

User Manual