beurer BM100B Upper Arm Electronic Blood Pressure Monitor Instruction Manual

Blood Pressure Monitor
Instruction Manual

Name: Upper Arm Electronic Blood Pressure Monitor
Model: BM100-EN/BM100B
Customer Service Information. Please Read!
For questions regarding this device, please contact us at Manufacturer. CONMO ELECTRONIC COMPANY LIMITED Address: 3rd Floor of No.4 Standard Workshop, Chengnan Industrial Park, Chengguan Town, Xincheng County, Laibin City, Guangxi Province
THESE INSTRUCTIONS CONTAIN IMPORTANT AND USEFUL INFORMATION ABOUT THIS DEVICE’S OPERATION. PLESE READ INSTRUCTIONS THOROUGHLY TO ENSURE THAT YOU HAVE THE FULL BENEFIT OF ALL THE DEVICE’S. KEEP THESE INSTRUCTIONS HANDY FOR FUTURE REFERENCE.

Please read this section carefully to familiarize yourself with features and operations before using the device.

• The warning signs and samples icons shown here are listed in order for you to use this device safely and correctly as well as to prevent device damage.
• Risk and injury to you and others; the icons and meaning are as follows:

PRECAUTION NOTICES| Indicates the proper conditions to use the device and to prevent damage, risk, and injury.
---|---
IMPORTANT NOTICE TO USERS| Indicates important notices users should read before using the device.
SCARE AND MAINTENANCE| This indicates the possibility of damage that may occur as a result of incorrect handling and improper maintenance.

INTENDED USE

The Upper Ann Electronic Blood Pressure Monitor is intended to measure the blood pressure and pulse rate of adults at a household or medical center.(Not suitable for neonate, pregnancy)

PRECAUTION NOTICES

• Do not use this device on other body parts, only use it on the upper arm.
• Do not disassemble the device as incorrect handling may cause injury.
• Keep the device from radiation equipment, as radiation may interfere with the proper device operation.

IMPORTANT NOTICES TO USERS

• This device is used for adults only.
• Make sure to use only the type of battery recommended(See Section “Preparation before use”)
• Do not use it on pregnant women. The result is inaccurate and the effects on the fetus are unknown.

Device Description:

Picture

Prepare before using

Insert batteries
This device operates on 4 “AA” batteries (Included).
Remove any plastic wrap from the batteries before installation.
Place the batteries into the battery compartment according to the “+” and “-” polarity symbols at the bottom of the compartment as shown below. If you do not intend to use this device for a prolonged time, it is advisable to remove the batteries before storing the device.

The direction of the 4 AA batteries

Tips: Please replace batteries when the device display

Battery instructions Warning

• Do not swallow the battery or battery fluid and place the battery and the product where it is not easily accessible to children. If a child or someone else swallows the battery or battery fluid, immediately call the hospital hotline.
• If the battery leaks and comes into contact with your eyes or skin, rinse immediately with plenty of water and immediately dial the hospital hotline.
• The battery cannot be recharged or regenerated for other uses.

Caution
If the battery leaks, please do not touch the battery liquid and touch the eyes. Wearing protective gloves, clean the battery compartment with a dry cloth.

Safety instructions

• Please use the specified battery size and battery model.
• Cannot be used with rechargeable batteries, as the device is not capable of charging the batteries.
• Replace batteries before they are completely dead. Replace batteries when the batteries indicate insufficient power.
• Leaky batteries may damage equipment. If you do not use this product for a long time, please remove the battery from the battery box before storage.
• To avoid power loss, please do not place any heavy objects on the product when not in use. (When the product is not in use, please do not place heavy objects on it.)
• Please replace the battery cover carefully.
• When the power is too low, the device will shut down automatically. This indicates its time to replace the 4 AA batteries.

Time/Date setting

• When the device is off, press and hold the  key to enter the year setting interface. Press the key can be increased from the default value to 99. Each time you press the value, it will increase once, and the adjustment to the required year key will be confirmed.

• Enter the month setting interface, the month will flash, each time you press the   key, the value will 0 increase once, and adjust to the required month, then press the
  key to confirm.

• To enter the data setting interface, the data will flash, each time you press the key, the value will increase once, and adjust to the required date and press the key to confirm.

• Enter the time interface, the default 24-hour time system will flash, the can switch between the 24-hour and 12-hour time system, confirm the required time and press them to confirm.

• Enter the time setting interface, and the clock will flash, the value will increase once every time the  key is pressed. After the correct time is confirmed, the minute will flash. Each time the is pressed, the value will increase once. After adjusting to the correct minute, press the key to confirm.

5. Unit setting
Enter the unit conversion interface, and the left arrow indicates the default unit is mmHg, and the key can switch between mmHg and Kpa, adjust to the required unit system and press the key to confirm.

6. Voice on/off/volume setting

Enter the voice broadcast switch interface, the default voice broadcast is ON, and the key can switch between the voice broadcast ON and the voice broadcast OFF. After adjusting to the required state, press the key to confirm. Enter the volume setting interface, press the key to increase. The value will increase once, increase from 0-30 volume, adjust to the appropriate volume, and press the  key to confirm.

Measure operation

1. Before the measuring

• Rest 5-10 minutes before measuring blood pressure.
• Avoid drinking alcohol, coffee, black tea, bathing, smoking, and exercising for 1 hour before measuring.
• Blood pressure rises when urination is urgent, so excrete urine before measurement.
• For patients with arteriosclerosis, diabetes, liver disease, high blood pressure, and end-to-end vascular circulation, please follow the instructions to use this product.
• High blood pressure can cause many serious diseases. If the doctor diagnoses high blood pressure, it is very important to do “basic blood pressure”.

2. Start measure

• Place the cuff flat on the table and make the Adhesive cloth down, Put the end of the cuff through the metal ring, circle it in a ring; The Adhesive cloth of the cuff should face outward. As shown in Pic1-2 (If the cuff has been looped beforehand, please ignore this step.)
• Put the cuff onto the measuring arm and point the hose to the arm, As shown in Pic3.
• Place the cuff on the arm, making sure that the lower edge of the cuff p is at 2-3 cm from the elbow joint, As shown in Pic4.
• Tighten the free edge of the cuff and stick the Adhesive cloth, As shown in Pic5-6.
• Make sure that the Adhesive cloth of the cuff is to be attached comfortably to prevent over-tightening and place the lower arm flat on the table and palm up. So that the cuff and the heart are at the same height. Also, please note that the cuff tube cannot be folded or bent. As shown in Pic 7-8.

Note l: If you are unable to use the left arm measurement, please use the right arm for the measurement, but in any case, all measurements must be made on the same side of the arm for measurement comparison.

Press the user button or or , the Display screen flashes the initial page and sends out a voice prompt. “Attention please, please keep silent and relax, keep the cuff and heart level. The motor Rotation and Pressure commence after the voice broadcast.

Note 2: By pressing or or , the operator can choose to measure user or user . Measurement results will be saved. If choose user key is selected, measurement results will not be saved.

• When pressurized, the pressure indicator bar changes accordingly. When the pressure reaches a stable value, the motor stops, and the pressure in the cuff begins to deflate at a constant rate. (If the pressure is insufficient and cannot be stabilized, Er4 appears on the screen and needs to be re-measured.)
• When an irregular pulse is detected, the screen appears icon and flashing.
• When the measurement is completed, the cuff is deflated, the systolic pressure, diastolic pressure, and pulse is displayed on the LCD, and the system compares the result with the international standard of blood pressure. The voice broadcast of the measurement results allows the user to know whether the blood pressure measurement is normal. (The voice settings will not be broadcast when they are turned off.)
• In the absence of any operation, the machine will automatically shut down after about 30 seconds.

Note3: When you choose to be in mmHg, the pressurization and measurement will be displayed in mmHg. When you choose to be in KPa, the pressurization and measurement will be displayed in KPa.

3. Memory rollback In the off state, Long time means pressing the key for greater than three seconds Short time means momentarily depressing the key.

• Press or for a long time queries the historical data of the corresponding user.

4. Memory delete

• Pressa or for a long time enters the historical data interface of the corresponding user. Press or select historical data, press appear DEL prompt to delete. Press to delete. Press and for a long time to delete all data.
• In the User history data interface to press for a long time shut down.

Note: If for some reason (for example, the user feels uncomfortable, etc.) and it is necessary to interrupt the measurement, please press the measurement key selected by the user at any time, the device will immediately reduce the pressure of the cuff.

Cleaning and maintenance

The device is not delivered sterile and has no degradable components, therefore, the shelf-life is not applicable. Please Pay Attention to the maintenance:

• Avoid impact, dampness, dust, and keep the device away from chemicals, places with high-temperature fluctuations, and heat sources. (For example, fireplace, heating, etc.) Otherwise, the product may be damaged.
• Do not use strong solvents, detergents, detergents, or other chemically enhanced items to clean the product.
• Do not immerse the product in water or liquid; otherwise, the liquid immersed in the product will damage it.
• Do not put this product in the washing machine, dishwasher, or dryer.
• Don’t press the button too hard or with sharp objects.
• Do not attempt to repair or debug the product by yourself; otherwise, it will cause damage to the product. If the product is damaged due to misuse, it is not covered by our warranty. If repair is required, please return the product to the local distributor within the warranty period. If the product is out of the warranty period, please contact our customer service. Please read the relevant terms of the warranty service carefully and know what is within the scope of the warranty and what is not. Before submitting complaints and suggestions, please first check whether batteries need to be replaced.
• Do not disassemble or change the parts of the product. Unauthorized disassembly or change of the parts of the product will affect the device’s normal use.
• Please clean the product regularly with a dry cloth.
• Place the product in a dry place to avoid sun exposure, extreme heat, extreme cold, or humidity.
• Before storage, please dry it and place it in a place that is not easily accessible to children. Please do not expose the product to strong vibrations, such as dropping it on the floor. Follow the instructions in this operation guide, and use the product correctly.
• If the original parts are replaced with parts supplied by a non-manufacturer, measurement errors may occur.
• Daily maintenance: It is recommended to use a soft dry cloth to clean the device every month.
• The device is a measurement device, it is recommended to calibrate it every year at the manufacturer or qualified third party.

Management

• The toxic substances contained in batteries are harmful to the environment. Please dispose of the batteries in strict accordance with the local battery use specifications. Please do not dispose of batteries with ordinary household waste.
• Please follow the local laws and regulations on material recycling and properly dispose of the product per the local laws and regulations.

Operational instructions

Warning

• Packaging materials are fatal to children and may cause asphyxia. Please remove packaging immediately and keep the children away.
• Prevent the product from falling, or objects from falling onto the product.
• This device cannot be used for medical diagnosis. For medical advice, consult a professional doctor. In case of emergency, please call the hospital hotline immediately.
• This device is not a toy. Please put it in a place that is not easily accessible to children.

Caution

• If the battery leaks, please avoid contact with the skin (e.g., wearable protective gloves) and wipe the battery box clean with a dry cloth.
• Do not disassemble the product; otherwise, you may be injured.
• Do not insert your finger into the product or any clamping slot.

Technical Data

• Blood pressure range:0∼2951runhg;
• Pressure accuracy:th3nunHg;
• Pulse:40∼180 bmp;
• Pulse accuracy: ±5%
• Product size: 150,113*80nun;
• Ann circumference:22∼32cm;
• Memory user number:99;
• Working temperature: 10°C ∼40°C
• Working humidity:15%∼85%
• Working atmosphere pressure: 80kPa∼105kPa
• Storage temperature: -20°C∼+55°C
• Storage humidity: 15%∼85%, Non-condensing
• Storage atmosphere pressure: 80kPa∼105kPa

Error symbol explanation

measurement is serious
Er7| Pressure over 300mmHg| Er8| Abnormal calibration data or abnormal memory IC
Er9| IC error| |

Problem shooting

Why are blood pressure measurements higher in hospitals than at home?

• Some people feel nervous in hospital clinics. This white-coated hypertension is reflected in blood pressure.
• People taking blood pressure drugs have normal blood pressure changes, which is the effect of drugs.
• After sleeping all night, before waking up in the morning, the body’s metabolic activity is in a low state, and the blood pressure measured at this time is inaccurate.

Better measurement conditions.

• In a warm and comfortable room, sit upright in a chair.
• Measure at the same time every day.
• Take several deep breaths to relax.

Symbol explanation

| Read instruction manual before use
---|---
| Type B is applicable.
IP21| Use the device in dry conditions
| The device should not be treated as unclassified municipal refuse but should be classified and treated specially.

Accessories

• Blood pressure monitor………….1pcs
• Cuff ……………………………………….1pcs
• Batteries………………………………….4pcs
• Instruction manual……………….. 1pcs

Eketromagnetle compatibility

• The BMI00-EN/BM10013 upper arm electronic blood pressure monitor meets the national standard 1EC60601-1-2 electromagnetic compatibility requirements.
• Portable and mobile RF communication equipment may affect the performance of BM100-EN/BM10013 upper arm electronic blood pressure monitor, and avoid strong electromagnetic interference when using it, such as near mobile phones, microwave ovens, etc.
• The essential performance of the equipment is to measure the body blood pressure and pulse on define pressure and pulse range, under the pressure range, the accuracy is ± 3nunHg for pressure and ±5% for a pulse; the pressure and pulse accuracy may be degraded due to the equipment disturbances.
• The equipment should not be used close to or stacked with other equipment. If it must be used close to or stacked, it should be observed to verify that it can operate normally in the configuration in which it is used.
• Use of accessories, transducers and cables other than those specified or provided by the manufacturer of the equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.
• Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30cm (12 inches) to any part of the BM100-EN/BM100B upper arm electronic blood pressure monitor, otherwise, degradation of the performance of the equipment could result.
• The user should use this equipment with the electromagnetic compatibility information provided by the accompanying document.
• Guidelines and manufacturer declarations are detailed in the attachment.

Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless

communications equipment:

Test frequency
(MHz)

| Band (MHz)| Service| Modulation| Maximum power(m)| Distance(rn)| IMMUNITY TEST LEVEL(V/m )
---|---|---|---|---|---|---
385| 380-390| TETRA 400| Pulse modulation 18HZ| 1.8| 0.3| 27

450

| 430-470| GMRS 460, FRS 460| FM ±5 kHz deviation 1 kHz sine| 2| 0.3|

28

710| 704-787| LTE Band 13, 17| Pulse modulation 217HZ| 0.2|

0.3

| 9
745
780
810| 800-960| GSM 800/900,TETRA 800,
iDEN 820,CDMA850, LTE Band 5| Pulse modulation 18HZ| 2| 0.3|

28

870
930
1720| 1700-l999| GSM 1800,CDMA1900,
GSM 1900,DECT,LTE
Band 1,3,4,25, UMTS| Pulse modulation 2 l7HZ| 2| 0.3|

28

1845
1970

2450

|

2400- 2570

| Bluetooth WLAN, 802.11 b/g/n,
RFID 2450,LTE Band 7| Pulsc modulation 217HZ| 2| 0.3| 28
5240|

5100- 5800

| WLAN 802.1 l a/n| Pulse modulation 217HZ| 0.2| 0.3| 9
5500
5785

Warning: MR-unsafe

Do not expose the device to a magnetic resonance (MR) environment.

• The device may present a risk of projectile injury due to the presence of ferromagnetic materials that can be attracted by the MR magnet core.
• Thermal injury and bums may occur due to the metal components of the device that can heat during MR scanning.
• The device may generate artifacts in the MR image.

The device may not function properly due to the strong magnetic and radiofrequency fields generated by the MR scanner.

Guidance and manufacturer’s declaration — electromagnetic emission

The BM100-EN/BMI00B upper arm electronic blood pressure monitor is intended for use in the electromagnetic environment specified below. The customer or the user of the BMI00-EN/BM100B upper arm electronic blood pressure monitor should assure that it is used in such an environment.

Emissions test| Compliance| Electromagnetic environment – guidance
---|---|---
RF emissions CISPR 11| Group l|

The BM100-EN/BMl00B upper arm electronic blood pressure monitor 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|

The BM 100-EN/BMl00B upper arm electronic blood pressure monitors are 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.

Harmonic emissions IEC 61000-3-2| Not applicable
Voltage fluctuations flicker emissions IEC 61000-3-3| Not applicable

Guidance and manufacturer’s declaration — electromagnetic immunity

The BM100-EN/BM l00B upper arm electronic blood pressure monitor is intended for use in the electromagnetic environment specified below. The customer or the user of the BM100-EN/BMl00B upper arm electronic blood pressure monitor should assure that it is used in such an environment.

Electrostatic
discharge (ESD)
IEC 61000-4-2Power frequency
(50/60 Hz)
magnetic field
IEC   61000-4-8Conducted RFIEC 61000-4-6

Radiated RF

IEC 61000-4-3

| ± 8 kV contact
± 2 kV, ± 4 kV, ± 8 kV,
± 15 kV air30 A/ir10Vrms150 kHz to 80 MHz 6v in ISM and amateur radio bands between
0,15 MHz and 80 MHz 10 V/m

80 MHz to 2.7 GHz

385MHz-5785MHz Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communication equipment (Refer to table 9 of IEC 60601-1-2:2014)

| ±8 kV contact
± 2 kV, ± 4 kV, ± 8 kV,
± 15 kV air30 A/mN/A10 V/m

80 MHz to 2.7 GHz
385MHz-5785MHz Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communication equipment (Refer to table 9 of IEC 60601- l-2:2014)

Electromagnetic environment – guidance

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.
Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.
Portable and mobile RF communications equipment should be used no closer to any part of the BM100-EN/BM100B upper arm electronic blood pressure monitor, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.

Recommended separation distance

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).b
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

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 is affected by absorption and reflection from structures, objects, and people.
a . The ISM {industrial, scientific and medical) bands between 150 kHz and 80 MHz are 765 MHz to 6,79d MHz; 13,553 MHz to t3,567 MHz; 26,9S7 MHz to 27,2B3 MHz; and 4ß,66 MHz to 40,70 MHz The ama r radio bands between 0,15 MHz end 80 MHz are t,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, S,3 MHz to 5,4 MHz, 7 MHz to 7,3 MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz æ 18,1 7 MHz, 21,0 MHz to 2 t,4 MHz, 24,89 MHz to 24,94 MHz, 28,0 MHz to 29,7 MHn and S0,0 MHz to 54,0 MHz
b. Field strengths from fixed transmitters. such ss 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 To assess the elœtromagnetic environment due to fixed RF transmitters, an electromagnetic siîe survey should be considered. If the measured field strength in the location in which the BM 100-ENfBM IOOB upper arm electronic b1øød pressure monitor is used exceeds the applicable RF compliance level above, the BM100-ENfØM IOOB upper arm electronic blood pressure monitor should be observed to verify normal operation. If abnormal performanœ is observed, additional measures may be necessary, such as reorienting or relocating the BM 100-EN/BM100B upper arm electronic blood pressure monitor.
c. Over the frequency range I ã0 kHz to 80 MHz, field strengths should be less than 3V/fn.

Recommended separation distances between portable and mobile RF communications equipment and the BlV1100-EN/BM100B upper arm electronic blood pressure monitor

The BM100-ENIBM100B upper arm electronic blood pressure monitor is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the BM100-EN/BM100B upper arm electronic blood pressure monitor can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the BM100-ENIBM100B upper arm electronic blood pressure monitor as
recommended below, according to the maximum output power of the communications equipment.

Separation distance according to the frequency of the transmitter (m)

Rated maximum output of
transmitter
W

| 150 kHz to 80 MHz outside ISM and amateur radio bands
| 150 kHz to 80 MHz in ISM and amateur radio bands
| 80 MHz to 800 MHz
| 800 MHz to 2.7 GHz

0.01

| 0.12| 0.20| 0.035|

0.07

0.1

| 0.38| 0.63| 0.11|

0.22

1

| 1.2| 2.00| 0.35|

0.70

10

| 3.8| 6.32| 1.10|

2.21

100

| 12| 20.00| 35|

70

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

Bluetooth
Blood Pressure Monitor
INSTRUCTIONS FOR US E

Download APP.
Scan the QR code below to directly download the APP or download and install it in the application market search “Common Health”

Android
http://down.conmo.net/| IOS
http://itunes.apple.com/cn/app/che-ling-ling-fu-wu-ban/id1530339511?mt=8
---|---

Enter the login page to log in/register a user account. Or select to skip, only the current measurement record can be seals and the historical record cannot be saved.

1. Turn on the Bluetooth function of the mobile phone. After wearing the cuff according to the dado/Instructions, click the blood pressure monitor page on the home page of mobile phone APP, and at the age time preaa or key of blood pressure monitor to start and pair with the mobile phone. After agreeing to pair, the measurement results are synchronized to the mobile phone APP.

Note: Press to start up, it will be unable to pair with the mobile phone.

4. If the Bluetooth blood pressure monitor device cannot be found, click the Bluetooth symbol at the upper left corner to refresh the
   

5. The trend icon in the upper right corner allows you to view the user’s blood pressure measurement trend/history.

CONMO ELECTRONIC COMPANY LIMITED

[Product Name] Upper Arm Electronic Blood Pressure Monitor
[Manufacturer]____  CONMO ELECTRONIC COMPANY LIMITED
[Residence]____  Floor 3 and LI, building LI, Chengnan Industrial Park, Chengguan Town, Xincheng County, Laibin City, Guangxi Province, China
[Production Address] __  Floor 3, building LI, Chengnan Industrial Park, Chengguan Town, Xincheng County, Laibin City, Guangxi Province, China
[After-sales Service Unit]  CONMO ELECTRONIC COMPANY LIMITED
[Contact] _____  0772-5513028

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.
NOTE: The manufacturer is not responsible for any radio or TV interference caused by unauthorized modifications or changes to this equipment. Such modifications or changes could void the user’s authority to operate the equipment.
NOTE: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be 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.

FCC Caution: Any changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate this equipment.

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