TRANSTEK TMB-2266 Blood Pressure Monitor User Manual
Version 1.0
Manufactured by: Guangdong Transtek Medical Electronics Co., Ltd.
Address: Zone A, No.105, Dongli Road, Torch Development District, 528437 Zhongshan, Guangdong, China
Thank you for selecting the TRANSTEK Blood Pressure Monitor TMB-2266. Please read this user manual carefully to ensure safe usage and keep it for future reference.
Introduction
General Description
The TRANSTEK Blood Pressure Monitor (TMB-2266) features blood pressure measurement, pulse rate measurement, and result storage, designed for reliable service. Readings are equivalent to those obtained by a trained observer using a stethoscope. This manual provides safety, care, and step-by-step usage instructions.
Features:
- 71mm x 82mm Digital LCD display with white backlight
- Maximum 199 records per user
- Measuring during inflation technology
Indications for Use
Intended for measuring blood pressure and heartbeat rate for adults with arm circumference ranging from 22cm to 32cm, 22cm to 42cm, or 22cm to 45cm. For indoor use only.
Contraindications
- Not suitable for pregnant women.
- Not suitable for patients with implanted electrical devices, such as cardiac pacemakers or defibrillators.
Measurement Principle
Uses the Oscillometric Measuring method. It establishes a 'zero pressure' equivalent to atmospheric pressure, then inflates the cuff and detects pressure oscillations generated by pulsatile blood flow to determine systolic pressure, diastolic pressure, and pulse rate.
Safety Information
The following symbols may appear on the device or in the manual:
- [i] Refer to instruction manual/booklet: Signifies that the manual must be read.
- [BF] Type BF applied part: Indicates the type of protection against electric shock.
- [DC] Direct Current: Indicates the power source.
- [SN] Serial Number: Device serial number.
- [MFG] Date and Country of manufacture: Manufacturing details.
- [MFR] Manufacturer: Manufacturer information.
- [Recycle] Recyclable: Indicates the product should be sent for separate collection facilities.
- [Indoor Use] For indoor use only: Specifies the usage environment.
- [Class II] Symbol for "Class II Equipment": Indicates electrical safety classification.
- [MR Unsafe] MR Unsafe: Identifies items posing risks in an MR environment.
- [Caution] Caution: Indicates necessary operator awareness or action to avoid undesirable consequences.
General Cautions:
- Intended for indoor, home use only.
- Not for public use or during patient transport.
- Not suitable for continuous monitoring during medical emergencies or operations.
- For non-invasive measuring and monitoring of arterial blood pressure on the arm only.
- For adult use; not for neonates, infants, or children unless instructed by a medical professional.
- Do not use on pregnant women or patients with implanted electrical devices.
- Effectiveness not established for users with common arrhythmias, peripheral arterial disease, or AV shunts. Consult a medical professional before use.
- Do not use for diagnosis or treatment. Consult a physician for any medical concerns.
- Consult a physician regarding medication timing for blood pressure measurement.
- Manufacturer is not liable for damages caused by misuse or abuse.
- Report any unexpected operations or events.
- Do not apply cuff on an arm with an intravenous drip or blood transfusion.
- Warning: Do not kink, fold, stretch, compress, or deform the tube during measurement.
- Warning: Frequent measurements can disrupt blood circulation.
- Warning: Do not apply cuff to delicate or damaged skin. Check cuff site for irritation.
- Warning: Do not place cuff on arms undergoing medical treatment (e.g., intra-vascular access, AV shunt).
- Warning: Avoid using on the same side as a mastectomy, especially if lymph nodes were removed; use the unaffected side.
- Warning: Do not use with other monitoring devices on the same arm.
- Check for prolonged impairment of blood circulation.
- Warning: In case of cuff over-inflation fault, remove cuff immediately. Prolonged high pressure can cause bruising.
- Warning: Do not use with high-frequency surgical equipment simultaneously.
- Warning: Not AP/APG equipment; do not use where flammable anesthetics are present.
- Avoid measurements near strong electromagnetic fields or electrical fast transient/burst signals.
- Keep wireless communication devices (mobile phones, etc.) at least 30 cm (1 foot) away during measurement.
- Device may require up to 30 minutes to warm up/cool down from storage temperatures.
- Warning: Excessive cuff tube length could cause strangulation.
- Warning: Do not touch batteries/adapter output and user simultaneously.
- Adapter is specified as part of ME EQUIPMENT.
- Warning: Power cord is the disconnect device; ensure it is accessible.
- Monitor, adapter, and cuff are suitable for patient environment.
- Warning: Do not use if allergic to polyester, nylon, or plastic.
- Warning: Use only manufacturer-approved accessories.
- Warning: If discomfort occurs (pain), press the Power button to release air.
- No calibration required within two years.
- Do not attempt self-repair; use authorized service centers.
- Circuit diagrams, part lists, etc., available upon request from authorized personnel.
- Performance checks recommended every two years.
- Warning: Do not use while under maintenance or being serviced.
- Store in a clean, dry place, protected from moisture, heat, lint, dust, and direct sunlight.
- Ensure cuff tube is not squeezed, stretched, or kinked during storage.
- Warning: Keep device, cuff, and batteries away from children.
- Clean with a soft, dry cloth; use a dampened cloth with mild detergent if necessary. Do not use alcohol or harsh chemicals.
- Do not wash the cuff in a washing machine or dishwasher.
- Cuff service life is approximately 10,000 times.
- Dispose of accessories and device according to local guidelines.
LCD Display Signal
The LCD displays various information:
SYMBOL | DESCRIPTION | EXPLANATION |
---|---|---|
Systolic blood pressure | High pressure result | |
Diastolic blood pressure | Low pressure result | |
Pulse display | Pulse in beats per minute | |
Blood pressure level | Indicates blood pressure level | |
User ID | User 1/2/Guest | |
Current Time | Time (year:month:day:hour:minute) | |
Heartbeat | Heartbeat detection during measurement | |
Hand shaking | Hand shaking makes results inaccurate | |
Battery Indicator | Indicates the current battery level | |
Irregular heartbeat | Irregular heartbeat detected | |
Data transmitting | Data is transmitting | |
Memory Query | Indicates memory mode and group number | |
Cuff wearing | The cuff is secured | |
Bluetooth icon | Indicates Bluetooth is working | |
Voice Broadcast | Indicates Voice Broadcast is off | |
Triple Mode | Continuous measurement for three times, displays average result |
Monitor Components
The monitor consists of the following parts:
- CUFF
- AIR CONNECTOR PLUG
- AIR HOSE
- LCD DISPLAY
- DC POWER SOCKET
- USER SWITCH
- TRIPLE MODE BUTTON
- USER BUTTON
- START/STOP BUTTON
- MEMORY BUTTON
- BATTERY COMPARTMENT
Component list of the pressure measuring system:
- 1. Cuff
- 2. Air Hose
- 3. PCBA
- 4. Pump
- 5. Valve
List of Included Items
- 1. Blood Pressure Monitor (TMB-2266)
- 2. Cuff (Type BF applied part) with sizes: 22cm-32cm, 22cm-42cm, or 22cm-45cm
- 3. 4 x AAA batteries
- 4. User manual
Before You Start
The Choice of Power Supply
The device can be powered by:
- Battery powered mode: 6VDC 4 x AAA batteries.
- AC adaptor powered mode: 5V 1A (Use only the recommended AC adaptor model).
Please unplug the adaptor when not using utility power.
CAUTION: Use the correct batteries and the manufacturer-recommended AC adapter for best performance and to protect the monitor.
Installing and Replacing the Batteries
- Open the battery cover.
- Install batteries, ensuring correct polarity.
- Replace the battery cover.
Replace batteries when:
- The [Low Battery] symbol (bAt Lo) shows.
- The display is dim.
- The display does not light up.
CAUTION: Do not mix new and used batteries, or different battery types. Do not dispose of batteries in fire. Remove batteries if the device will not be used for an extended period. Dispose of used batteries responsibly.
Setting Date, Time and Voice
Setting the clock is important for time-stamping records. The year range is 2022-2052, and the time format can be 12H or 24H.
- With the monitor off, press and hold the [USER] button. The Bluetooth symbol [Bluetooth] will appear. Then press the [START/STOP] button to enter the year setting. Use the [USER] or [MEMORY] button to change the year. Hold [USER] to advance years quickly; hold [MEMORY] to go back quickly.
- Press [START/STOP] to confirm the year. The date format will flash. Use [USER] or [MEMORY] to switch between [month/day] and [day/month] formats.
- Press [START/STOP] to confirm the date format. The month will flash. Repeat the process to set the month, day, time format, hour, and minute.
- After setting the minute, the voice setting will appear. It will speak "Voice on" or "Voice off". Use [USER] or [MEMORY] to adjust the voice volume (2, OFF, 1, 2...).
- Press [START/STOP] to confirm the voice setting. The display will show "do nE" before turning off.
Pair a smart device with the monitor
You can save and send measurement data to a smart device via Bluetooth.
- Turn on Bluetooth and the app on your smart device.
- When the monitor is off, press and hold the [START/STOP] button to start pairing. The Bluetooth symbol [Bluetooth] will flash.
- If pairing is successful, the Bluetooth symbol will stop flashing, and the monitor will shut off automatically. The date and time will be set automatically from the smart device.
If pairing is unsuccessful within 60 seconds, it will time out and shut off.
Technical Specifications for Bluetooth:
- RF Frequency Range: 2402 MHz to 2480 MHz
- Output Power Range: -1.57dBm
- Supply Voltage: 1.8-3.6 V
- Transmitting Distance: 10 meters
Compatible Devices:
- iOS devices: Operating system must be iOS 13.0 or higher.
- Android devices: Operating system must be Android 5.0 or higher.
CAUTION regarding Bluetooth and Interference:
- Interference may occur near equipment with the [RF Interference] symbol.
- Sensitive individuals, pregnant women, and those with implanted medical devices should avoid using the unit if possible.
- Keep the monitor at least 20 cm (approx. 8 inches) away from the human body during data transmission.
- Pairing requires Bluetooth at 2.4 GHz.
How to mitigate possible interference:
- Keep the device and BT end reasonably close (1-10 meters) with no obstacles for a quality connection.
- Keep other electronic devices (especially wireless transmitters) at least 1 meter away from the monitor.
Setting a user ID
There are 3 user IDs available: [User 1], [User 2] (each with 199 memory spaces), and [Guest] (no memory space).
- When the monitor is off, press the [USER] button to display the current user ID. Press [USER] again to switch between [User 1], [User 2], and [Guest].
- Press [START/STOP] to confirm the selected user ID. The User ID will stop flashing, and the monitor will enter measurement mode.
Measurement
Applying the cuff
- Remove jewelry (watches, bracelets) from the arm. If advised by a doctor due to poor circulation, use the right arm.
- Roll up or push up the sleeve to expose the skin. Ensure the sleeve is not too tight.
- With palm facing up, tie the cuff on the upper arm. Align the [Artery Indicator] with the main artery on the inside of the arm. (Locate the artery by pressing about 2 cm above the elbow bend on the inside of the arm; feel for the strongest pulse).
- Ensure the bottom edge of the cuff is 2-3 cm above the inside elbow. Wrap the cuff snugly but not too tightly; one finger should fit between the cuff and the arm.
- Sit upright in a comfortable chair with your back supported. Keep feet flat and legs uncrossed. Rest your arm on a flat table, with the cuff at the same level as your right atrium.
- Take 5-6 deep breaths and relax before starting.
Helpful tips for measurement:
- Measure in a silent room.
- Rest for 5 minutes before measurement.
- Wait at least 3 minutes between measurements for circulation to recover.
- Remain relaxed, do not move or talk during measurement.
- For consistent comparison, measure under similar conditions (e.g., same time, same arm).
Start the Measurement
A. Single measurement
Press the [START/STOP] button when the monitor is OFF. The measurement will proceed automatically, saving and transmitting data.
- The display shows the latest measurement record.
- It adjusts to zero, indicating "starting measurement, please remain still and quiet".
- [O] symbol flashes for cuff wrap detection.
- Cuff wrap is confirmed ([O] is solid), inflating and measuring.
- The result is displayed, saved, and read out (e.g., "your blood pressure is 116 over 78, pulse is 80").
B. Triple mode measurement
Press the [TRIPLE MODE] button when the monitor is OFF. The monitor performs three measurements automatically, saving and transmitting data. The average of the three results is displayed.
- The display shows the latest measurement record.
- It adjusts to zero, indicating "starting measurement, please remain still and quiet".
- [O] symbol flashes for cuff wrap detection.
- Cuff wrap is confirmed ([O] is solid), inflating and measuring.
After the second measurement, the second measurement (60 seconds countdown) is displayed. After the third measurement, the third measurement (60 seconds countdown) is displayed.
The final result is displayed, saved, and read out (e.g., "your blood pressure is 120 over 80, pulse is 90").
After measurement, the Bluetooth symbol [Bluetooth] blinks as data transmission begins. If successful, the symbol stops blinking and disappears. The monitor turns off automatically after about 1 minute. If unsuccessful within 60 seconds, it times out and shuts off.
Press [START/STOP] to turn off the device manually; otherwise, it turns off automatically.
Notes:
- Press [START/STOP] anytime to stop the measurement.
- If a user has previous records, the last measurement will be displayed before starting a new one.
- Irregular heartbeat [ ] and excessive body motion [ ] detection: If an irregular heartbeat is detected, the [ ] symbol appears with the result. If excessive body motion is detected, the [ ] symbol flashes for 5 seconds. If motion persists, the [ ] symbol will be displayed with the final result. Note: Readings may be inaccurate if these symbols are displayed.
Data Management
Recall the Records
- When the monitor is off, press the [MEMORY] button. The user ID will blink. Use [USER] or [MEMORY] to switch between user IDs ([User 1], [User 2], [Guest]).
- Press [START/STOP] to confirm the selected user ID. The latest record for that user will be displayed.
- Press [USER] or [MEMORY] to display the next record.
When voice is on, the monitor will read the memory values aloud (e.g., "memory 1, your blood pressure is 120 over 80, pulse is 80").
The display alternates between Date/Time/Year and the current record group.
Note: The most recent record is shown first (Record 1). New measurements are assigned to Record 1, pushing older records back. The oldest record (199) is dropped.
Delete the Records
A: To delete a single measurement:
- Enter memory recall mode (as described in 'Recall the Records').
- Select the measurement to erase using [USER] or [MEMORY].
- Press and hold the [MEMORY] button for about 5 seconds until "dEL y" blinks.
- Use [USER] or [MEMORY] to switch between "dEL y" ([Delete Yes]) and "dEL no" ([Delete No]). Press [START/STOP] to confirm.
If "dEL y" is selected, the record is deleted, and subsequent records shift forward (e.g., 03 becomes 02). If "dEL no" is selected, deletion is cancelled.
B: To delete all measurements:
- Enter memory recall mode.
- Press and hold both [USER] and [MEMORY] buttons for 5 seconds. "dEL AL" will blink along with the user ID.
- Use [USER] or [MEMORY] to switch between "dEL AL" ([Delete All]) and "dEL no" ([Delete No]). Press [START/STOP] to confirm.
If "dEL AL" is selected, the unit displays "dEL do nE" + User ID, deletes all records for that user, and then displays "---". If "dEL no" is selected, deletion is cancelled.
Information for User
Tips for Measurement
Measurements may be inaccurate in the following circumstances:
- Within 1 hour after dinner or drinking.
- Immediate measurement after tea, coffee, or smoking.
- Within 20 minutes after taking a bath.
- While talking or moving fingers.
- In a very cold environment.
- When needing to discharge urine.
(Visuals showing these scenarios with 'X' marks are described here)
Maintenance
Follow these instructions for best performance:
- Store in a dry place, away from direct sunlight.
- Avoid touching water; clean with a dry cloth.
- Avoid intense shaking and collisions.
- Avoid dusty and unstable temperature environments.
- Use damp cloths with mild detergent to remove dirt.
- Do not clean the reusable cuff with water or immerse it in water.
About Blood Pressure
What are systolic pressure and diastolic pressure?
Systolic pressure is the maximum blood pressure when the heart's ventricles contract and pump blood. Diastolic pressure is the minimum blood pressure when the ventricles relax.
What is the standard blood pressure classification?
According to the World Health Organization (WHO) and International Society of Hypertension (ISH) classification (1999):
Level | Systolic blood pressure (mmHg) | Diastolic blood pressure (mmHg) |
---|---|---|
Optimal Blood Pressure | <120 | <80 |
Normal Blood Pressure | 120-129 | 80-84 |
High-normal Blood Pressure | 130-139 | 85-89 |
Grade 1 hypertension (mild) | 140-159 | 90-99 |
Grade 2 hypertension (moderate) | 160-179 | 100-109 |
Grade 3 hypertension (severe) | ≥180 | ≥110 |
CAUTION: Only a physician can determine your normal BP range and assess if your blood pressure has reached a dangerous point.
Irregular Heartbeat Detector
The monitor detects an irregular heartbeat rhythm during measurement. If there are two or more pulse intervals where the difference from the average is more than ±25%, or four or more intervals where the difference is more than ±15%, the irregular heartbeat symbol [ ] will appear.
CAUTION: The [ ] symbol indicates a detected pulse irregularity. While usually not a cause for concern, frequent appearance warrants medical advice. This device detects irregularities but does not replace a cardiac examination.
Why does my blood pressure fluctuate throughout the day?
- Blood pressure varies daily due to factors like cuff application, measurement position, emotions, and exercise.
- Medication can also affect blood pressure.
- Wait at least 3 minutes between measurements.
Why do I get a different blood pressure at home compared to the hospital?
Blood pressure can vary due to daily changes and the 'white coat' effect (increased BP in clinical settings). Pay attention to proper cuff tying, tightness, arm position, and relaxation before measurement.
Tips for home measurement:
- Ensure the cuff is tied properly.
- Check cuff tightness (not too tight, not too loose).
- Ensure the cuff is on the upper arm.
- Relax before measuring. Take 2-3 deep breaths. Relax for 4-5 minutes until calm.
Is the result the same if measuring on the right arm?
Both arms can be used, but results may differ slightly. It is recommended to measure on the same arm each time for consistency.
Troubleshooting
If abnormalities occur, check the following:
PROBLEM SYMPTOM | CHECK THIS | REMEDY |
---|---|---|
No power / Display can not light up. | Batteries are depleted. Batteries are inserted incorrectly. Adapter is inserted incorrectly. | Replace with new batteries. Insert batteries correctly. Insert AC adapter correctly. |
High Battery (bAt H shows) | The battery is too high. | Replace with the correct DC plug. |
Low Battery (bAt Lo& shows) | The battery is too low. | Replace with new batteries. |
Error E1 shows | The cuff is not wrapped or wrapped incorrectly, or the cuff air plug is loose. | Refasten the cuff and insert air tube plug correctly, then measure again. |
Error E2 or [ ] shows | Excessive body motion (shaking of the arm with the cuff on) or weak pulse detected. | Relax for 5 minutes, then keep still and measure again. |
Error E3 shows | Pulse is not detected during measuring. | Loosen clothing on the arm and measure again. |
Error E4 shows | The measurement failed. | Relax for 5 minutes and measure again. |
Error EExx shows | A calibration error occurred (XX indicates error code). | Retake measurement. If problem persists, contact retailer or customer service. Refer to warranty for contact information. |
Warning message (out shows) | Out of measurement range. | Relax for a moment and measure again. If problem persists, contact your physician. |
NOTE: If the product still does not work, contact Customer Service. Do not disassemble or attempt self-repair.
Specifications
- Power supply: Battery: 6VDC 4xAAA; AC Adaptor: 5V 1A (use recommended model).
- Display mode: Digital LCD V.A. 71mm x 82mm.
- Measurement mode: Oscillometric testing mode.
- Measurement range: Cuff pressure: 0-299 mmHg; Systolic: 60-230 mmHg; Diastolic: 40-130 mmHg; Pulse: 40-199 beats/minute.
- Accuracy: Pressure: ±3 mmHg; Pulse: ±5%.
- Normal working condition: Temperature: +5°C to +40°C; Humidity: 15% to 90% RH (non-condensing); Atmospheric pressure: 700 hPa to 1060 hPa.
- Storage & transportation condition: Temperature: -20°C to +60°C; Humidity: ≤93% RH (non-condensing).
- Measurement perimeter of the upper arm: 22 cm - 32 cm, 22cm - 42cm, 22cm - 45cm.
- Weight: Approx. 278g (excluding batteries and cuff).
- External dimensions: Approx. 100mm x 138mm x 51mm.
- Attachment: 4xAAA batteries, user manual, Type-C cable.
- Mode of operation: Continuous operation.
- Degree of protection: Type BF applied part.
- Protection against ingress of water: IP21 (Protected against solid objects >12.5mm and vertically falling water drops).
- Device Classification: Battery Powered Mode: Internally Powered ME Equipment; AC Adaptor Powered Mode: Class II ME Equipment.
- Software Version: A01.
WARNING: No modification of this equipment is allowed.
Authorized Component
Use only the TRANSTEK authorized adapter:
- Adapter Type: BLJ06L060100P-U
- Input: 100-240V, 50-60Hz, 0.2A max
- Output: 5V 1000 mA
Contact Information
For more information, visit www.transtekcorp.com.
Manufactured by: Guangdong Transtek Medical Electronics Co., Ltd.
Address: Zone A, No.105, Dongli Road, Torch Development District, 528437 Zhongshan, Guangdong, China.
EMC Guidance
This equipment is suitable for home healthcare environments.
Warnings:
- Avoid use near active HF surgical equipment or RF shielded rooms for MRI.
- Avoid stacking or using adjacent to other equipment; observe normal operation if necessary.
- Use of non-specified accessories may increase emissions or decrease immunity.
- Keep portable RF communications equipment (including antennas) at least 30 cm (12 inches) away from the TMB-2266.
Technical description:
- Instructions for maintaining basic safety and essential performance regarding electromagnetic disturbances.
- Guidance and manufacturer's declaration on electromagnetic emissions and immunity.
Table 1: Guidance and manufacturer's declaration - electromagnetic emissions
Emissions test | Compliance |
---|---|
RF emissions CISPR 11 | Group 1 |
RF emissions CISPR 11 | Class [B] |
Harmonic emissions IEC 61000-3-2 | Class A |
Voltage fluctuations / flicker emissions IEC 61000-3-3 | Comply |
Table 2: Guidance and manufacturer's declaration - electromagnetic Immunity
Immunity Test | IEC 60601-1-2 Test level | Compliance level |
---|---|---|
Electrostatic discharge (ESD) IEC 61000-4-2 | ±8 kV contact; ±2 kV, ±4 kV, ±8 kV, ±15 kV air | ±8 kV contact; ±2 kV, ±4 kV, ±8 kV, ±15 kV air |
Electrical fast transient/burst IEC 61000-4-4 | ±2 kV for power supply lines; ±1 kV signal input/output; 100 kHz repetition frequency | ±2 kV for power supply lines; Not applicable; 100 kHz repetition frequency |
Surge IEC61000-4-5 | ±0.5 kV, ±1 kV differential mode; ±0.5 kV, ±1 kV, ±2 kV common mode | ±0.5 kV, ±1 kV differential mode |
Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 | 0% UT; 0.5 cycle. At 0°, 45°, 90°, 135°, 180°, 225°, 270°, 315°. 0% UT; 1 cycle and 70% UT; 25/30 cycles; Single phase: at 0°. 0% UT; 250 / 300 cycle | 0% UT; 0.5 cycle. At 0°, 45°, 90°, 135°, 180°, 225°, 270°, 315°. 0% UT; 1 cycle and 70% UT; 25/30 cycles; Single phase: at 0°. 0% UT; 250 / 300 cycle |
Power frequency magnetic field IEC 61000-4-8 | 30 A/m; 50 Hz / 60 Hz | 30 A/m; 50 Hz / 60 Hz |
Conducted RF IEC61000-4-6 | 3 V; 0.15 MHz - 80 MHz; 6 V in ISM and amateur radio bands between 0.15 MHz and 80 MHz; 80% AM at 1 kHz | 3 V; 0.15 MHz - 80 MHz; 6 V in ISM and amateur radio bands between 0.15 MHz and 80 MHz; 80% AM at 1 kHz |
Radiated RF IEC61000-4-3 | 10 V/m; 80 MHz - 2.7 GHz; 80% AM at 1 kHz | 10 V/m; 80 MHz - 2.7 GHz; 80% AM at 1 kHz |
NOTE: UT is the a.c. mains voltage prior to application of the test level.
Table 3: Guidance and manufacturer's declaration - electromagnetic Immunity
Radiated RF Test Band (MHz) | Service Specifications for ENCLOSURE PORT IMMUNITY to RF wireless communications equipment) | Modulation | Maximum Power (W) | Distance (m) | IEC 60601-1-2 Test Level (V/m) | Compliance level (V/m) |
---|---|---|---|---|---|---|
380-390 | TETRA 400 | Pulse modulation 18 Hz | 1.8 | 0.3 | 27 | 27 |
430-470 | GMRS 460, FRS 460 | FM ± 5k Hz deviation; 1 kHz sine | 2 | 0.3 | 28 | 28 |
704-787 | LTE Band 13, 17 | Pulse modulation 217 Hz | 0.2 | 0.3 | 9 | 9 |
800-960 | GSM 800/900, TETRA 800, iDEN 820, CDMA 850, LTE Band 5 | Pulse modulation 18 Hz | 2 | 0.3 | 28 | 28 |
1700-1990 | GSM 1800; CDMA 1900; GSM 1900; DECT; LTE Band 1, 3, 4, 25; UMTS | Pulse modulation 217 Hz | 2 | 0.3 | 28 | 28 |
2400-2570 | Bluetooth, WLAN, 802.11 b/g/n, RFID, 2450, LTE Band 7 | Pulse modulation 217 Hz | 2 | 0.3 | 28 | 28 |
5100-5800 | WLAN 802.11 a/n | Pulse modulation 217 Hz | 0.2 | 0.3 | 9 | 9 |
FCC Statement
FCC ID: OU9-TMB-2266
FCC Regulatory Compliance: 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 causes 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.
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
- This device may not cause harmful interference, and
- This device must accept any interference received, including interference that may cause undesired operation.
RF Exposure Compliance: This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment. This transmitter must not be co-located or operating in conjunction with any other antenna or transmitter.