Arm Automatic Blood Pressure Monitor

(Electronic Sphygmomanometer)

User Manual

Thank your for purchasing our product.

Please read this manual carefully before using the product.

Please keep the manual appropriately for future reference.

This User Manual is suitable to the following models: FT-C21Y, FT-C22Y, FT-C23Y,

FT-C24Y, FTC11B, FT-C12B, FT-C21Y-V, FT-C22Y-V, FTC23Y-V, FT-C24Y-V,

FT-C11B-V, FT-C12B-V, FT-C11B-UR and FT-C11B-BT.

Table of Contents

(I) General Information

(II) Precaution for Use and Maintenance

(III) Name of Each Part

(IV) Measure Procedure

(V) Troubleshooting

(VI) Model List

I. General Information

Intended Use

Fudakang Arm Automatic Blood Pressure Monitor is intended for use by medical professionals or at home to monitor and display diastolic, systolic blood pressure and pulse rate on adult each time, with an air cuff buckled around one's arm according to the instruction in the user's guide manual.

Indications For Use

Fudakang Arm Automatic Blood Pressure Monitor is for use by medical professionals or at home and is a non-invasive blood pressure measurement system intended to measure the diastolic and systolic blood pressures and pulse rate of an adult individual by using a non-invasive technique in which an inflatable cuff is wrapped around the arm. The cuff circumference is limited to 8.7 inches to 12.6 inches.

Specification

Product Name

Applied Models

Arm Automatic Blood Pressure

FT-C21Y, FT-C22Y, FT-C23Y, FT-C24Y, FTC11B,

FT-C12B, FT-C21Y-V, FT-C22Y-V, FTC23Y-V,

FT-C24Y-V, FT-C11B-V, FT-C12B-V, FT-C11B-UR and FT-C11B-BT.

Measurement Principle Oscillography

Bluetooth Version

Bluetooth 4.0 BLE

Bluetooth Modulation Type GFSK

Cuff

Soft cuff, Cuff size 480mm × 140mm (+/- 5mm)

18.89 × 5.51 inch (+/- 0.19 inch)

Measurable Arm

Circumference Range

About 220~360mm (8.6 6~ 14.17 inch)

Measurement Range

Accuracy

Pressure: 0~280mmHg

Pulse: 30~160 times/minute

Pressure: ±3mmHg

Pulse: ±5%

Power Supply 4 x 1.5V AA Alkaline batteries 6V

Battery Life Approx. 250 times (180mmHg, 1 time/day, 22°C) ；

E ach measurement takes around 60 seconds, and each memory checking takes about 1 second

Protection against electric shock Type BF Cuff

IP classification IP21

Working Environment

Transport and storage

Environment

Temperature: 10~40°C

Humidity: ≤ 85% RH

Pressure: 86~106 kPa

Temperature: -20~60°C

Humidity: ≤ 85% RH

Pressure: 86~106 kPa

Electric Shock Protection Internal power unit

Memory Capacity

Inflation

2 Memory sets ; each 90 reading of data including date and time

Automatic Inflation by internal pump

Deflation

Display

Color Backlight display on

LCD (Optional)

Switch

Life Time

Contents

Automatic speed deflation system controlled by internal electromagnetic valve.

LCD digital display ; It can show Pressure, Pulse,

Date, Time

White backlight display when power on

Green backlight display when result is normal

Red backlight display when result is abnormal

3(ON/OFF, Memory, SET)

Machine : 5 years or 10000 times

Cuff : 10000 times

AC Adapter: 50000 hours

-Cuff

-4 x1.5V AA alkaline batteries 6V (Optional)

-Carrying bag(Optional)

-Instruction Manual

Note:

These specification may be changed without prior notice.

Contraindications:

1. Heart disease

2. High blood pressure or other circulatory disease

3. Arm injury

Patient Populations:

The device is intended to use for adults. DO NOT use this device on infants or small children..

Cleaning Information:

1. If the device is very dirty, wipe it clean with a cloth moistened with sterilizing alcohol or a neutral detergent. Then wipe it with a dry cloth.

2. NEVER clean the blood pressure monitor with thinners or benzene, as they may damage it.

3. To clean the cuff, wipe it with a moist cloth. Avoid hard rubbing as this will cause air leakages. Take care also not to get water into the air hose.

Maintenance:

This product is designed for use over an extended period of time; however, it is generally recommended that it be inspected every five years to ensure proper function and performance. The device doesn’t need to be calibrated in five years of reliable service.

Modification of this equipment is allowed except change the batteries.

Protect the Nature Environment:

Please help to protect natural environment by respecting national and/or local recycling regulations when disposing of the battery and the product at the end of their useful live.

II. PRECAUTION FOR USE AND MAINTENANCE

Precautions for Use:

1. If you suffer from heart disease, high blood pressure or other circulatory disease, consult your physician before using the device. It is intended for adult indoor use only. The device is not suitable for public use.

2. The patient is an intended operator. The patient can measure, transmit data and charge battery under normal circumstances and maintain the device and its accessories according to the user manual.

3. If the cuff pressure feels abnormal or you experience any other irregularity while using the cuff, reduce the pressure immediately by pressing the “ON/OFF” switch and then consult the sales outlet where you purchased the device.

4. If you think the measurement is abnormal or if measurement makes you feel unwell, discontinue use and consult your physician.

5. Blood pressure measurement may not be possible for anyone with a weak pulse or arrhythmia.

6. Repeated blood pressure measurement may cause problems such as congestion or swelling in some people.

7. Frequently repeated blood pressure measurements will not give accurate results.

Allow an interval of about 3 minutes between measurements.

8. If you suffer from a severe problem with blood circulation in your arms, consult your physician before using the device. Failure to do so could be hazardous to your health.

9. Measurement may not be possible for anyone with insufficient blood flow to the area where measurements will be taken or who suffers from a frequent irregular heartbeat.

Consult your physician for advice on whether to use the device.

10. DO NOT wrap the cuff around an elbow. DO NOT wrap over a wound.

11. DO NOT wrap the arm cuff around an elbow in which a drip (intravenous infusion) is inserted or which is being used for blood transfusion as part of medical treatment.

Doing so could result in an injury or a serious accident.

12. DO NOT wrap the cuff on the arm on the side of a mastectomy.

13. DO NOT use the device in the vicinity of flammable gases such as those used for anesthesia. Doing so could ignite the gases and cause an explosion.

14. DO NOT use the device in enriched oxygen environments such as a hospital’s hyperbaric chamber or oxygen tent. Doing so could ignite the oxygen and cause a fire.

15. DO NOT use mobile phones near the device as this could result in a malfunction.

DO NOT use the device with hf surgical equipment.

16. If you use a cardiac pacemaker, consult your physician before using the device.

17. Be sure to use this device only for measuring blood pressure. DO NOT use it for any other purpose.

18. DO NOT use this device on infants, pregnant women or pre-eclamptic patients.

19. DO NOT use this device for patients that transport outside a healthcare facility.

20. Blood pressure measurement may not be possible for anyone with common arrhythmias such as arterial or ventricular premature beats or arterial fibrillation.

21. Be careful to strangulation due to cables and hoses, particularly due to excessive length. It will not cause any potential alergic reaction or contact injury. If you are allergic to dacron or plastic, please don’t use this device

Precautions for Maintenance:

1. DO NOT store the blood pressure monitor in locations exposed to direct sunlight, high temperatures (over 60°C), low temperatures (below -20°C), high relative humidity

(over 85%) or excessive amounts of dust.

2. DO NOT drop the blood pressure monitor or subject it to other shocks or vibration.

3. Remove the batteries if the device will be left unused for a long period.

4. DO NOT attempt to disassemble the device. User can open battery cover for new battery installation.

DO NOT bend the cuff or air hose excessively.

5. NEVER clean the blood pressure monitor with thinners or benzene, as they may damage it.

6. DO NOT hard rub when clean the cuff. Take care not to get water into the air hose.

7. DO keep the device out of reach of children, pets and insects.

III. Name of Each Part

Figure 1 - Appearance

MEMORY” Button /Clock Setting

Memory Button /Measured Result recall/ Clock Number

Adjusting

“ON/OFF” Button

LCD Display

Systolic Indicator

Diastolic Indicator

Pulse Indicator

Figure 2 – Display of LCD

Note for LCD display:

(1) Date: Month - Day

(2) Time: Hour – Minute

(3) Systolic Blood Pressure (unit: mmHg)

(4) Diastolic Blood Pressure (unit: mmHg)

(5) Pulse Rate(unit: beat/minute)

(6) WHO Blood Pressure Classification Indicator

(7) Inflation / Deflation Indicator

(8) Blood Pressure Measurement Unit

(9) Battery Symbol

(10) Irregular heartbeat Indicator

(11) Memory Record Number

* Back light display function is optional.

IV. Measure Procedure

Battery Loading

Remove the battery compartment cover by gently pushing down on arrow and sliding cover forward.

Place batteries with positive “+” and negative “-“ terminals into compartment and make sure they match the indicated terminals in the compartment.

Close the battery cover by gently sliding it into the compartment and pressing it into place.. See Figure 3.

Note ：

When the LCD display shows “Low Battery” signal ,the batteries must be replaced for accurate readings. See Figure 4

Do not use rechargeable batteries (voltage 1.2V). They are not suitable for this product, can damage the monitor and will cause inaccurate readings to be obtained.

Remove the batteries if the monitor will not be used for six month or longer to avoid damage from the possibility of leaking batteries.

All the measurements will remain in the memory should the batteries become drained, removed, or replaced.

Figure 3 Figure 4

NOTE: AC adapter is optional for power supply. Only use the adapter provided by manufacturer, that is complying with EC60601-1 standard requirements. Do not touch the AC adapter with wet hand while it is working. Do not tangle the power cords of the adapter during measuring process. The adapter is part of the blood pressure monitor. Unplug the AC adapter from power outlet to isolate the device from supply mains

Clock Adjusting and Unit Change

Press the “SET” button for 5 seconds during the device is turned off, the number of the

YEAR will begin to blink on the LCD display. Press the “” ” button to advance the YEAR displayed. When you have reached the correct date, press the “SET” button and release.

(Don't keep on clicking on the 'SET' button without being released during programming.)

When the “SET” button is

pressed and released, the YEAR will stop blinking and the MONTH will begin to blink.

Press and release the “ ” button until the desired month is reached.

See Figure 5.

Repeat this process to set the DAY, HOUR, MINUTES.

After you change the batteries, you have to readjust the date and time. Time is maintained using a 24 HOUR clock. AM/PM is not displayed.

NOTE: When the number that you wish to set – i.e. YEAR, MONTH, DAY, HOUR,

MINUTE - is blinking, each time you press and release the “ ” button, the number will increase by one. ***Time is displayed using a 24 hour clock. AM/PM are not displayed.

Figure 5

For the unit change, you can select the mmHg or Kpa; and the mmHg is the definition unit.

When the machine is turned off, press the button “ON/OFF” more than about 10 seconds till LCD blinks ,then press Memory button to switch between mmHg and Kpa .

Arm Cuff Connecting

★ The cuff should be snug but not too tight. You should be able to insert two fingers between the cuff and your arm.

★ Place the cuff around the left bare arm ½” to ¾”’ above the elbow joint. The air tube should be oriented to run down the center of the inside of your arm. (Refer to diagram on cuff for proper placement. )

★ Keep the cuff at approximately the same level as your heart.

★ Unless your physician recommends otherwise, always use the left arm to measure

your blood pressure.

See Figure 6

★ Arm cuff connecting should make arm feel no much tension. Don’t connect too tense

(otherwise the measurement will be not precise).

★ Keep up right position on the same height of heart.

★ Do not bend with the cuff or the air tube. Do not inflate before fitting the cuff.

★ When the cuff is dirty, detach it from the equipment, wash the cuff by hand with proper detergent and rinse it in the enough cold water, dry in air. Never iron it.

★ Only use the manufacturer cuff with the main unit to ensure accurate measurement.

NOTE:

★ REFER TO THE DIAGRAM PRINTED ON THE CUFF FOR PROPER PLACEMENT.

★ FOR ACCURATE READINGS, THE CUFF/PRESSURE MUST BE ORIENTED

CORRECTLY AND ALIGNED WITH THE ARTERY.

★ CONTINUOUS CUFF PRESSURE MAY EFFECT BLOOD FLOW AND CAUSE

HARMFUL INJURY

Figure 6

Note: The cuff is “ TYPE BF APPLIED PART”

Measuring Process

POSTURE FOR TAKING BLOOD PRESSURE MONITOR

★ Make yourself comfortable and sit-up straight, legs uncrossed, feet flat on the floor

★ Place your arm with cuff in front of you on the table with your palm facing up.

★ Cuff should be at the same height as your heart.

TIPS FOR BLOOD PRESSURE MONITORING

★ Relax for about 5 minutes before measurement.

★ Do not smoke or ingest caffeine at least 30 minutes prior to measurement.

★ Remove any constricting clothing and place the cuff on a bare arm.

★ Keep still and do not talk until the measurement is complete.

★ The cuff must be neither too tight nor too loose. Using a little force, you should be

able to place two fingers between the cuff and your arm.

Figure 7

After you are in a comfortable position, press the “ON/OFF” button. The device will perform a self verification/check. During this verification/check the LCD will display all

“8’s”. At the conclusion of the verification/check the LCD will display “00”. See Figure 8.

If the device has voice function, it will speak out the displayed blood pressure, heart rate.

If an irregular heartbeat is detected, the IRREGULAR HEARTBEAT symbol will appear and blink in the display screen. See Figure9.

NOTE:

★ Do not self-diagnosis according to measured result. Consult with your physician for further diagnosis.

★ If the device cause any discomfort during measuring process or fail to perform as indicated ,please turn off the power or discontinue use.

★ If cuff inflates up to 300 mmHg (40kPa) doesn’t stop, please remove the cuff or turn off the device immediately.

Reading Memory Results

READING AN AVERAGE OF THE LATEST THREE MEASUREMENTS (AVg)

★ When the monitor is turned off, press and release the “ or ” button. LCD will display “ AVg ” in the upper corner of the LCD Display. The result that is first displayed and the result that is first announced – if in “TALKING” mode – is the average of your latest three measurements.

★ To review the results that are in memory – PRESS the “ or ” button to scroll through previous measurements. Each time you press and release the “ or ” button the next oldest result will be displayed. If the “TALKING” function is turned “ON” each result will be verbally announced,

Figure 8 Figure 9

2-PERSON MEASUREMENT SETTING FUNCTION

This model has 2-Person memory banks and 90 memories storage for each. Press and release ‘SET’ button can prompt to P1 (Person 1) or P2 (Person 2) as your ID to access the measurement for the first time operation when the device is turned off. Each time, before taking measurement or check memory from the storage, please be sure you have advanced to the correct ID (P1 or P2) which you already set forth prior to turning on the device.

Assessing High Blood Pressure for Adults

The follow standards for assessing high blood pressure (without regard to age or gender) have been established as a guide line according to WHO (World Health Organization) standard. See Figure 10. Please note that other risk factors (e.g. diabetes, obesity, smoking, etc.) need to be taken into consideration and may affect these figures. Consult with your physician for accurate assessment.

Figure 10

From the above figure, we can see the classification of blood pressure for adults is as below. The WHO BP Classification Indicating Bar would show out the blood pressure level by the color indicator .

Blood Pressure

Classification

SBP (mmHg) DBP (mmHg) COLOR INDICATOR

Optimal <120 <80

Normal 120-129 80-84

GREEN

High-Normal 130-139 85-89

Stage 1 Hypertension 140-159 90-99 YELLOW

Stage 2 Hypertension 160-179

Stage 3 Hypertension ≧ 180

Note:

100-109

≧ 110

ORANGE

RED

The graph is not exact, but may be used as a guide in understanding non-invasive blood pressure measurements. The device is only intended for use with adults.

Delete for all Memories

★ Press and hold the “ or ” BUTTON until all numbers change to “ZERO”.. All results in memory are now deleted. LCD will show the Figure 11 for two seconds.

Note : Date and time settings are not changed by using the memory delete function.

Figure 11

Shut Down

After measurement, press button “ON/OFF” to turn off the device. The device will be automatically power off after 1 minute of none use.

Voice Function

The device with voice function can speak out in the following state:

The device will speak out the prompt that “keep silence to take a cuff at the same height with your heart ” when the measure begin.

The device will speak out the displayed blood pressure (systolic and diastolic pressure), heart rate after each measurement finish.

The device will speak out the last time displayed memory blood pressure (systolic and diastolic pressure), and heart rate when reading memory result.

Note: The voice function is ONLY for models FT-C21Y-V, FT-C22Y-V, FT-C23Y-V,

FT-C24Y-V, FT-C11B-V, FT-C12B-V.

UART connection and Blue Tooth Function

The UART connection model is FT-C11B-UR

Operation Method:

★ Install the APK accordance with the communication protocol into the signal receiving device such as mobile phone.

★ Use cable to connect receiving device with the blood pressure monitor which with

UART port .

★ Activate the receiving device and let it be in stand- by status for blood pressure measuring.

★ Activate the blood pressure monitor which with UART port and start testing according to the normal blood pressure monitor operation method.

★ After testing the result including systolic pressure , diastolic pressure and pulse will display on LCD , press the SEND button to send these data to the receiving device such as mobile phone .

The Blue Tooth function model is FT-C11B-BT.

Operation Method:

★ Install the APK accordance with the communication protocol into the blue tooth signal receiving device such as mobile phone.

★ Activate the receiving device and let it be in stand- by status for blood pressure measuring.

★ Activate the blood pressure monitor which with blue tooth function and start testing according to the normal blood pressure monitor operation method.

★ After testing the result displayed on LCD including systolic pressure ,diastolic pressure and pulse will be automatically sent to the blue tooth receiving device such as mobile phone .

The additional function of this model blood pressure monitor is that transmit the test result to the APK in the receiving device via blue tooth technology.

The above two models have all function as old ones have but they have different “result output “method.

V. Troubleshooting

Abnormality

LCD shows Low Battery icon

Shows abnormal result

Reason Checkout

Batteries are low.

Cuff is not tightened properly or its position is incorrect.

The arm is moved during measuring.

Irregular heartbeat

Change new batteries.

Tighten cuff correctly and refer to

“Arm Cuff Connecting”.

Stay calm, arm remains steady. Do not move during measuring.

You can test again for light irregular heartbeat patients. It is inappropriate for serious irregular heartbeat patients to use this

Shows abnormal result

After power on ,no display on LCD

Cuff inflation rate is too low or does not inflate

Cuff deflates too quickly

Measure result is different from the hospital or value is inconsistent

LCD shows “Er U”

LCD shows “Er H”

LCD shows “Er 1”

LCD shows “Er 2” device.

Speaking, frightened nervous or excited measurement

Do not speak, take deep breath

2~3 times to relax yourself.

Wrong position

Adjust position; refer to “Arm Cuff

Swathing”.

Some interference in inflation or wrong operation during measuring

Refer to the inflation step in

“Measuring process”.

Battery problem or wrong battery polarity

Install battery correctly or replace new battery; If the device is still not activated, then stop using it.

Air tube not connected with main device properly; Cuff or bladder inside the cuff leakage air

Cuff has been applied too loose.

This is normal

Insufficient inflation

Reconnect the air tube;

Purchase a new cuff

Make sure cuff is wrapped up correctly

Blood pressure value is varying during the day and will also be affected by emotional and physical condition

Measure again.

Inflation over 305 mmHg Measure again

Undetectable the pulse Measure again

Radiation interference Away the radiation source

LCD shows “Er 3” Measured result wrong Measure again

Note: If you cannot resolve the problem, you can contact manufacturer or its service agent for replacement policy.

STATEMENTS AND DECLARATIONS:

1. MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in the ACCOMPANYING DOCUMENTS

2. Wireless communications equipment such as wireless home network devices, mobile phones, cordless telephones and their base stations, walkie-talkies can affect this equipment and should be kept at least a distance d = 3,3 m away from the equipment.

(Note. As indicated in Table 6 of IEC 60601-1-2:2007 for ME EQUIPMENT, a typical cell phone with a maximum output power of 2 W yields d = 3,3 m at an IMMUNITY LEVEL of

3 V/m)

3. The manufacturer are available for request of circuit diagrams, component part lists, descriptions ,calibration instructions ,or other information that will assist service personnel to repair those parts of the device

4. Changes or modifications not expressly approved by the party responsible for compliance 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.

5. Guidance and manufacturer’s delclaration

Guidance and manufacture’s declaration – electromagnetic emission

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

Emission test Compliance Electromagnetic environment – guidance

RF emissions

CISPR 11

Group 1

Class B

The

[EQUIPMENT or SYSTEM] use 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 emission

CISPR 11

Harmonic emissions

IEC 61000-3-2

Voltage fluctuations/ flicker emissions

IEC 61000-3-3

Not applicable

Not applicable

Guidance and manufacture’s declaration – electromagnetic immunity

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

Immunity test IEC 60601 test level Compliance level

Electromagnetic environment - guidance

Electrostatic discharge (ESD)

IEC 61000-4-2

Electrical transient/burst

IEC 61000-4-4

Surge

IEC 61000-4-5 fast

±6 kV contact

±8 kV air

±2 kV for power supply lines

±1 kV for input/output lines

±1 kV differential mode. ±2 kV common mode

±6 kV contact

±8 kV air

Not applicable

Not applicable

Floors should be wood, concrete or ceramic tile. If floor 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.

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

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

Voltage dips, short interruptions and voltage variations on power supply input lines

IEC 61000-4-11

<5% U

T

(>95% dip in U

T

) for 0.5 cycle

40% U

T

(60% dip in U

T

) for 5 cycles

70% U

T

(30% dip in U

T for 25 cycles

)

<5% U

T

(>95% dip in U

T

) for 5 sec

Not applicable Mains power quality should be that of a typical commercial or hospital environment. If the user of the TL-100D requires continued operation during power mains interruptions, it is recommended that the

TL-100D be powered from an uninterruptible power supply or a battery.

Power frequency

(50Hz) magnetic field IEC 61000-4-8

3A/m 3A/m

NOTE U

T

is the a.c. mains voltage prior to application of the test level.

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

Guidance and manufacture’s declaration – electromagnetic immunity

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

Immunity test

IEC 60601 test level

Compliance level

Electromagnetic environment - guidance

Portable and mobile RF communications equipment should be used no closer to any part of the [EQUIPMENT or SYSTEM] , including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended separation distance

Conducted RF

IEC 61000-4-6

3 V rms

150 kHz to 80 MHz

Not applicable d

=

1 .

167 P

Radiated RF

IEC 61000-4-3

3 V/m

80 MHz to 2.5 GHz

3 V/m d

=

1 .

167 d

=

2 .

333

P

80 MHz to 800 MHz

P 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 metres

(m).

Field strengths from fixed RF transmitters, as determined by an 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.

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 [EQUIPMENT or

SYSTEM] is used exceeds the applicable RF compliance level above, the [EQUIPMENT or SYSTEM] should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the [EQUIPMENT or SYSTEM] . b

Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

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

The [EQUIPMENT or SYSTEM] i s 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

(W)

Separation distance according to frequency of transmitter

(m)

150 KHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz

0.01

0.1

1

10

100 d

=

1 .

167

0.117

0.369

1.167

3.689

11.667

P d

=

1 .

167

0.117

0.369

1.167

3.689

11.667

P d

=

2 .

333

0.233

0.738

2.333

7.379

23.333

P

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 is affected by absorption and reflection from structures, objects and people.

FCC ID: 2ADNQFTC11BBT

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

Explanation of Symbols:

LOT

Symbol for batch code Symbol for manufacturer

Symbol for ‘CE”

Symbol for “electrical and electronic equipment”

Symbol for “TYPE BF APPLIED PART”

Symbol for “Follow operating instructions”

IP21

Symbol for “the IP classification”

Symbol for “ RF transmitters”

Manufacturer: FUDAKANG INDUSTRIAL CO.,LTD

Address :No.8 Yinghe Road, Yuanjiangyuan Management Zone, Changping Town,

Dongguan, Guangdong China.

Tel: 86-769-81098181 Fax: 86-769-81098187 Website: www.fudakang.com

Software Version1.3

Manual Version:V2.0