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version:1.0 User Manual Blood Pressure Monitor TMB-2079 Arm Type Guangdong Transtek Medical Electronics Co., Ltd. Zone B, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China Thank you very much for selecting TRANSTEK Blood Pressure Monitor TMB-2079 Please do read the user manual carefully and thoroughtly so as to ensure the safe usage of this product, and keep the manual well for further reference in case you have problems. Table of Contents INTRODUCTION..................................................................................................................2 CATALOGUE BEFORE YOU START..........................................................................................................9 General Description Indications for Use Contraindications Measurement Principle Safety Information LCD Display Signal Monitor Components List The Choice of Power Supply Installing and Replacing the Batteries Setting Date, Time,the trends time Select the user ID Install the App and Pair-Up Search your Test Information Tie the Cuff Start the Measurement Recall the Records Delete the Records Tips for measurement Maintenances MEASUREMENT................................................................................................................17 DATA MANAGEMENT........................................................................................................20 INFORMATION FOR USER..............................................................................................24 ABOUT BLOOD PRESSURE.............................................................................................26 What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Irregular heartbeat detector Why does my blood pressure fluctuate throughout the day?
Why do I get a different blood pressure at home compared to the hospital?
Is the result the same if measuring on the right arm?
TROUBLE SHOOTING.......................................................................................................28 SPECIFICATIONS..............................................................................................................29 AUTHORIZED COMPONENT ...........................................................................................30 CONTACT INFORMATION.................................................................................................30 FCC STATEMENT...............................................................................................................31 COMPLIED STANDARDS LIST..........................................................................................32 EMC GUIDANCE................................................................................................................33 1 INTRODUCTION INTRODUCTION Safety Information The signs below might be in the user manual, labeling or other component. They are the requirement of standard and using. Symbol for THE OPERATION GUIDE MUST BE READ Symbol for TYPE BF APPLIED PARTS Symbol for Recycle Symbol for MANUFACTURER SN Symbol for SERIAL NUMBER Symbol for DIRECT CURRENT Symbol for MANUFACTURE DATE F1 T1A/250V 3.6*10CCC Symbol for ENVIRONMENT PROTECTION - Electrical waste products should not be disposed of with household waste. Please recycle where facilities exist. Check with your local authority or retailer for recycling advice For indoor use only Symbol for Class II Equipment Caution: These notes must be observed to prevent any damage to the device. General Description Thank you for selecting TRANSTEK arm type blood pressure monitor
(TMB-2079). The monitor features blood pressure measurement, pulse rate measurement and the result storage. The design provides you with two years of reliable service. Readings taken by the TMB-2079 are equivalent to those obtained by a trained observer using the cuff and stethoscope auscultation method. This manual contains important safety and care information, and provides step by step instructions for using the product. Read the manual thoroughly before using the product. Features:
72.8 mm74.2 mm Digital LCD display Maximum 120 records per each user 3rd technonoly: Measuring during inflation
(The updated technology in the world) Indications for Use The Transtek Blood Pressure Monitor is digital monitors intended for use in measuring blood pressure and heartbeat rate with arm circumference ranging from 22 cm to 32 cm ( about 8-12 ) , 22cm to 42cm(about 8-16). 22 cm to 45cm(about 8-17), It is intended for adult indoor use only. Contraindications 1.The device is not suitable for use on may be pregnant women or pregnant women. 2.The device is not suitable for use on patients with implanted,electrical devices, such as cardiac pacemakers, defibrillators. Measurement Principle This product uses the Oscillometric Measuring method to detect blood pressure. Before every measurement, the unit establishes a zero pressure equivalent to the atmospheric pressure. Then it starts inflating the arm cuff, meanwhile, the unit detects pressure oscillations generated by beat-to-beat pulsatile, which is used to determine the systolic and diastolic pressure, and also pulse rate. 2 3 INTRODUCTION CAUTION
* This device is intended for adult use in homes only.
* The device is not suitable for use on neonatal patients, pregnant women,patients with implanted, electronical devices, patients with pre-eclampsia, premature ventricular beats, atrial fibrillation, peripheral, arterial disease and patients undergoing intravascular therapy or arterio-venous shunt or people who received a mastectomy. Please consult your doctor prior to using the unit if you suffer from illnesses.
* The device is not suitable for measuring the blood pressure of children. Ask your doctor before using it on older children.
* The device is not intended for patient transport outside a healthcare facility.
* The device is not intended for public use.
* This device is intended for no-invasive measuring and monitoring of arterial blood pressure.It is not intended for use on extremities other than the arm or for functions other than obtaining a blood pressure measurement.
* Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood pressure.Do not begin or end medical treatment without asking a physician for treatment advice.
* If you are taking medication,consult your physician to determine the most appropriate time to measure your blood pressure. Never change a prescribed medication without consulting your physician.
* Do not take any therapeutic measures on the basis of a self measurement. Never alter the dose of a medicine prescribed by a doctor. Consult your doctor if you have any question about your blood pressure.
* When the device was used to measure patients who have common arrhythmias such as atrial or ventricular premature beats or atrial fibrillation, the best result may occur with deviation. Please consult your physician about the result.
* Don't kink the connection tube during use, otherwise, the cuff pressure may continuously increase which can prevent blood flow and result in harmful injury to the PATIENT.
* When using this device, please pay attention to the following situation which may interrupt blood flow and influence blood circulation of the patient, thus cause harmful injury to the patient: connection tubing kinking too frequent and consecutive multiple measurements; the application of the cuff and its pressurization on any arm where intravascular access or therapy, or an arterio-venous (A-V) shunt, is present; inflating the cuff on the side of a mastectomy.
* Warning: Do not apply the cuff over a wound;otherwise it can cause further injury.
*Do not inflate the cuff on the same limb which other monitoring ME equipment is applied around simultaneously, because this could cause temporary loss of function of those simultaneously-used monitoring ME equipment.
*On the rare occasion of a fault causing the cuff to remain fully inflated during measurement, open the cuff immediately. Prolonged high pressure (cuff pressure 300mmHg or constant pressure 15mmHg for more than 3 minutes) applied to the arm may lead to an ecchymosis.
*Please check that operation of the device does not result in prolonged impairment of patient blood circulation.+
* When measurement, please avoid compression or restriction of the connection tubing. INTRODUCTION CAUTION
* The device cannot be used with HF surgical equipment at the same time.
* The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER was clinically investigated according to the requirements of ISO 81060-2:2013.
* To verify the calibration of the AUTOMATED SPHYGMOMANOMETER, please contact the manufacturer.
* This device is contraindicated for any female who may be suspected of, or is pregnant. Besides providing inaccurate readings, the effects of this device on the fetus are unknown.
* Too frequent and consecutive measurements could cause disturbances in blood circulation and injuries.
* This unit is not suitable for continuous monitoring during medical emergencies or operations.Otherwise, the patients arm and fingers will become anaesthetic, swollen and even purple due to a lack of blood.
* When not in use, store the device with the adapter in a dry room and protect it against extreme moisture, heat, lint, dust and direct sunlight. Never place any heavy objects on the storage case.
* This device may be used only for the purpose described in this booklet. The manufacturer cannot be held liable for damage caused by incorrect application.
*This device comprises sensitive components and must be treated with caution. Observe the storage and operating conditions described in this booklet.
* The equipment is not AP/APG equipment and not suitable for use in the presence of a flammable anesthetic mixture with air of with oxygen or nitrous oxide.
* Warning: No servicing/maintenance while the ME equipment is in use.
* The patient is an intended operator.
* The patient can measure ,transmit data and change batteries under normal circumstances and maintain the device and its accessories according to the user manual.
* To avoid measurement errors, please avoid the condition of strong electromagnetic field radiated interference signal or electrical fast transient/burst signal.
*The blood pressure monitor, its adaptor, and the cuff are suitable for use within the patient environment. If you are allergic to polyester, nylon or plastic, please don't use this device.
* During use, the patient will be in contact with the cuff. The materials of the cuff have been tested and found to comply with requirements of ISO 10993-5:2009 and ISO 10993-10:2010. It will not cause any potential sensization or irritation reaction.
* Adaptor is specified as a part of ME EQUIPMENT.
* If you experience discomfort during a measurement, such as pain in the arm or other complaints, press the START/STOP button to release the air immediately from the cuff. Loosen the cuff and remove it from your arm.
* If the cuff pressure reaches 40 kPa (300 mmHg), the unit will automatically deflate. Should the cuff not deflate when pressures reaches 40 kPa (300 mmHg), detach the cuff from the arm and press the START/STOP button to stop inflation.
* Before use, make sure the device functions safely and is in proper working condition. Check the device, do not use the device if it is damaged in any way. The continuous use of a damaged unit may cause injury, improper results, or serious danger.
* Do not wash the cuff in a washing machine or dishwasher!
4 5 INTRODUCTION CAUTION
* The service life of the cuff may vary by the frequency of washing, skin condition, and storage state. The typical service life is 10000 times.
* It is recommended that the performance should be checked every 2 years and after maintenance and repair, by retesting at least the requirements in limits of the error of the cuff pressure indication and air leakage (testing at least at 50mmHg and 200mmHg).
* Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the local guidelines.
* Manufacturer will make available on request circuit diagrams, component part lists, descriptions, calibration instructions,etc., to assist to service personnel in parts repair.
* The plug/adapter plug pins insulates the device from the main supply. Do not position the device in a position where it is difficult to disconnect from the supply mains to safely terminate operation of ME equipment.
* The operator shall not touch output of batteries /adapter and the patient simultaneously.
* Cleaning :Dust environment may affect the performance of the unit. Please use the soft cloth to clean the whole unit before and after use. Dont use any abrasive or volatile cleaners.
* The device doesnt need to be calibrated within two years of reliable service.
* If you have any problems with this device, such as setting up, maintaining or using, please contact the SERVICE PERSONNEL of Transtek. Dont open or repair the device by yourself in the event of malfunctions. The device must only be serviced, repaired and opened by individuals at authorized sales/service centers.
* Please report to Transtek if any unexpected operation or events occur.
* Keep the unit out of reach of infants, young children or pets to avoid inhalation or swallowing of small parts. It is dangerous or even fatal.
* Be careful to strangulation due to cables and hoses, particularly due to excessive length.
* At least 30 min required for ME equipment to warm from the minimum storage temperature between uses until it is ready for intended use. At least 30 min required for ME equipment to cool from the maximum storage temperature between uses until it is ready for intended use.
* This equipment needs to be installed and put into service in accordance with the information provided in the ACCOMPANYING DOCUMENTS;
* 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 adistance d away from the equipment. The distance d is calculated by the MANUFACTURER from the 80MHz to 5.8 GHz column of Table 4 and Table 9 of IEC 60601-1-2:2014, as appropriate.
* Please use ACCESSORIES and detachable partes specified/ authorised by MANUFAC-
TURE. Otherwise, it may cause damage to the unit or danger to the user/patients.
* There is no 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.
* Please use the device under the environment which was provided in the user manual. Otherwise, the performance and lifetime of the device will be impacted and reduced.
* Adaptor is specified as a part of ME EQUIPMENT. 6 INTRODUCTION LCD display signal N SYMBOL SYMBOL DESCRIPTION DESCRIPTION EXPLANATION EXPLANATION Systolic blood pressure High pressure result Diastolic blood pressure Low pressure result mmHg Measurement Unit of the blood pressure Cuff wearing The cuff is secured Pulse User ID Pulse/minute User 1/2 Current Time Time(year:month:day:hour:minute) Heartbeat Heartbeat dectetion during measurement Hand shaking Hand shaking makes results inaccurate Battery Indicator Indicate the current battery Irregular heartbeat Irregular heartbeat Data transmitting Data is transmitting Memory Query Indicate it is in the memory mode and which group of memory it is. Blood pressure level Indicate blood pressure level Bluetooth icon The bluetooth icon blinks when the bluetooth is working Average value The average value of the latest three groups bood pressure value Trends name Indicate the picture of week or picture of day Blood pressre trend chart for days or weeks. Indicate the blood pressure trends for seven days or seven weeks, the X-axis of the trend chart represents time, from righ to left(data from the latest records to the earliest records), the Y-axis of the trend chart represents the high and low pressure values, when the systolic pressure is greater than or equal to 130mmHg,the top horizontal line will be light up, when the diastolic pressure is lower than 85mmg, the lower horizontal line will be light up. 7 INTRODUCTION Monitor Components CUFF AIR HOSE AIR CONNECTOR PLUG BEFORE YOU START The Choice of Power Supply 1.Battery powered mode:
6VDC 4AAA batteries 2.AC adaptor powered mode:
5V 1A
(Please only use the recommended AC adaptor model). Please unplug the adaptor to depart from the using utility power. CAUTION Component list of pressure measuring system 1 Cuff 2 Air pipe 3 PCBA 4 Pump 5 Valve LCD DISPLAY In order to get the best effect and protect your monitor,please use the the right batteries and special power adapter which complies with local safety standard. AC adaptor USER BUTTON USB POWER SOCKET Installing and Replacing the Batteries MEM BUTTON START/STOP BUTTON BATTERY COMPARTMENT Open the battery cover. Install the batteries by matching the correct polarity, as shown. Replace the battery cover. List 1.Blood Pressure Monitor
(TMB-2079) 2.Cuff (Type BF applied part)
(22cm~32cm or 22cm~42cm, 22cm~45cm) 3. 4AAA batteries 4.User manual 5. AC Adaptor
(BLJ06L060100P-V BLJ06L060100P-S BLJ06L060100P-B BLJ06L060100P-U) Replace the batteries whenever the below happen The shows The display is dim. The display does not light up CAUTION Do not use new and used batteries together. Do not use different types of batteries together. Do not dispose the batteries in fire. Batteries may explode or leak. Remove batteries if the device is not likely to be used for some time. Worn batteries are harmful to the environment. Do not dispose with daily garbage. Remove the old batteries from the device following your local recycling guidelines. 8 9 It is important to set the clock before using your blood pressure monitor, so that a time stamp can be assigned to each record that is stored in the memory. (The setting range of the year :20202099 time format:24H) BEFORE YOU START Setting Date, Time 1.When the monitor is off, Long press MEMbutton,it will display the time.Then press MEM or USER button to enter the mode for year setting. BEFORE YOU START 4.Repeat steps 2 and 3 to set the [MONTH] and [DAY]. 5
.Repeat steps 2 and 3 to set the [HOUR] and [MINUTE]. 2.Press MEM or USER button change the [YEAR]. Press MEM button will increase one year, press USER button will decrease one year. 3.When you get the right year, press START/STOP button to set down and then turn to next step [MONTH] and [DAY] setting. 6. After hour and minute are set,the LCD will display do nE and then turn off. 10 11 BEFORE YOU START Select the User ID Before you start the measurement, please select the desired user ID first. 1. When the monitor is off, hold press START/STOP button or press USER button, the user ID will show. Then press USER button to switch the user ID between user 1 and user 2. BEFORE YOU START Setting the trends time 1
.When the monitor is off, press MEM button to enter memory mode, press both USER and MEM buttons at the same time,it will display right picture, you could set the trends start time, press MEM button will increase time, pressUSER button will decrease time. 2.Press the START/STOP button to confrim the trends strat time, then set trends end time. 3. After the trends start time and end time are set, the LCD will disply do nE and then it will turn off. 2. Press START/STOP button to confirm user ID (If no any operation after two seconds), then the blood pressure will begin measure-
ment. 12 13 BEFORE YOU START BEFORE YOU START Install the App and Pair-Up Download the MedM Health app from APP Store or Google Play. Install the APP, and register an account. Search your test information After binding the app, back to the beginning page and click Blood Pressure to search your test information. Click My setting, choose the device and then bind the device and app 14 15 BEFORE YOU START MEASUREMENT RF Frequency Range: 2402 MHz to 2480 MHz Maximum output power: 2.7dBm Supply Voltage: 1.8-4.5 V Transmitting Distance: 10 meters List of compatible devices For iOS devices:
The operating system must be iOS 11.0 or more. For Android devices The operating system must be Android 8.0 or more CAUTION Interference may occur in the vicinity of equipment marked with the following symbol . And TMB-2079 may interfering vicinity electrical equipment. Sensitive people, including pregnant women pre-eclamptic and those who implanted medical electronic instruments, should avoid using the unit whenever possible. Keep the monitor at least 20 centimeters away from the human body
(especially the head) when the data transmission is proceeding after measurement. To enable the data transmission function, this product should be paired to Bluetooth end at 2.4 GHz. How to mitigate possible interference?
The range between the device and BT end should be reasonably close, from 1 meter to 10 meters. Please ensure no obstacles between the device and BT end so as to obtain quality connection and to lower the RF output range. To avoid interference, other electronic devices (particularly those with wireless transmission / Transmitter) should be kept at least 1 meter away from the monitor. 1. 2. Tie the cuff 1. 2. 3. Remove all jewelry, such as watches and bracelets from your left arm. Note: If your doctor has diagnosed you with poor circulation in your left arm, use your right arm. Roll or push up your sleeve to expose the skin. Make sure your sleeve is not too tight. Hold your arm with your palm facing up and tie the cuff on your upper arm, then position the tube off-center toward the inner side of arm in line with the little finger. Or position the artery mark over the main artery (on the inside of your arm). Note: Locate the main artery by pressing with 2 fingers approximately 2 cm above the bend of your elbow on the inside of your left arm. Identify where the pulse can be felt the strongest. This is your main artery. 4. The cuff should be snug but not too tight. You should be able to insert one finger between the cuff and your arm. 5. Sit comfortably with your tested arm resting on a flat surface. Place your elbow on a table so that the cuff is at the same level as your heart. Turn your palm upwards. Sit upright in a chair, and take 5-6 deep breaths. 6. Helpful tips for Patients, especially for Patients with Hypertension:
Rest for 5 minutes before first measuring. Wait at least 3 minutes between measurements. This allows your blood circulation to recover. Take the measurement in a silent room. The patient must relax as much as possible and do not move and talk during the measurement procedure. The cuff should maintain at the same level as the right atrium of the heart. Please sit comfortably. Do not cross your legs and keep your feet flat on the ground. Keep your back against the backrest of the chair. For a meaningful comparison, try to measure under similar conditions. For example, take daily measurements at approximately the same time, on the same arm, or as directed by a physician. 2~3cm 16 17 MEASUREMENT MEASUREMENT Start the Measurement Before you start the measurement,Download the Transtek Health app from APP Store or Google Play,and turn on the Bluetooth. Install the APP, and register an account. Then set your personal information (Gender, Birthday, Height, Weight, Name and so on). 1.Please switch the User button to select the user between User 1 and User 2. When you choose User 1,press the START/STOP button to confirm and then it will finish the whole measurement automatically, save and transmit the measurement data for the desired user. (Take User 1 for example.) LCD display Adjust the zero. N Inflating and measuring. Display and save the measurement result. 2.After the measurement was finished, the symbol will start blinking, and the data will start transmitting. ( Please connect the app during the transmission ) 3. If the data transmits successful, the symbol and symblo will disappear, and then the monitor will turn off. 4. If the data transmition fails, the monitor will turn off automatically.
(the symbol will be show in next measurement) 5.Press the START/STOP button to power off,otherwise it will turn off after 1 minute. Tips: Maximum 120 records are both for User 1 and User 2. 18 19 DATA MANAGEMENT Recall the Records 1. 1 When the monitor is off, please press MEM button,it will display the average value of all the recods in trends time. DATA MANAGEMENT Recall the Records 3. Then show the latest measurement records, you can press the MEM or SET button to get the record you want. N 2. Each press MEM button will show next record,there are seven average trends from the latest records to the earliest records. N N Date, Time, Year will display alternately. The current No. is No 2. The corresponding yeat is 2020. The corresponding date is January 1 .st The corresponding time is A.M. 06:00. Tips. Long press the MEM button will switch DAY trends to WEEK trends. Tips: Long pressUSER button to switch another User. CAUTION The most recent record (1) is shown first. Each new measurement is assigned to the first (1) record. All other records are pushed back one digit (e.g., 2 becomes 3, and so on), and the last record (120) is dropped from the list. 20 21 DATA MANAGEMENT DATA MANAGEMENT 4.If there is no record, when you pressMEM button to check the record, the following display will be shown. Delete the Records If you did not get the correct measurement, you can delete all results for the selected user by following steps. (Take User 1 for example.) 1. Long press MEM button, when the monitor is in the memory recall mode(Not in the trends chart),the display will show dE LE no + User ID. 2. Hold press USER or MEM button to switch dE LE YES,the display will show dE LE YES + User ID. N 3.Press START/STOP button to confrim deleting, the LCD will display do nE and then turn off. 22 23 INFORMATION FOR USER INFORMATION FOR USER Tips for Measurement Measurements may be inaccurate if taken in the following circumstances. Maintenance instructions below. In order to get the best performance, please follow the 18 Within 1 hour after dinner or drinking Immediate measurement after tea, coffee, smoking Put in a dry place and avoid the sunshine Avoid touching water, clean it with a dry cloth in case. Within 20 minutes after taking a bath When talking or moving your fingers Avoid intense shaking and collisions Avoid dusty and unstable temperature environment Using wet cloths to remove dirt Do not attempt to clean the reusable cuff with water and never immerse the cuff in water. In a very cold environment When you want to discharge urine 24 25 ABOUT BLOOD PRESSURE ABOUT BLOOD PRESSURE What are systolic pressure and diastolic pressure?
When ventricles contract and pump blood out of the heart, the blood pressure reaches its maximum value in the cycle, which is called systolic pressure. When the ventricles relax, the blood pressure reaches its minimum value in the cycle, which is called diastolic pressure. Systolic blood discharging artery Diastolic blood entering vein press relax What is the standard blood pressure classification?
The chart on the right is the standard blood pressure classifi-
cation published by American Heart Association (AHA). This chart reflects blood pressure categories defined by American Heart Association. Blood Pressure Category Systolic mmHg (upper#) Diastolic mmHg (lower#) Normal Elevated less than 120 and less than 80 120-129 and less than 80 High Blood Pressure
(Hypertension) Stage 1 High Blood Pressure
(Hypertension) Stage 2 130-139 80-89 or or 140 or higher 90 or higher Hypertensive Crisis
(Consult your doctor immediately) Higher than 180 and/or Higher than 120 CAUTION Please consult a physician if your measuring result falls outside the range. Please note that only a physician can tell whether your blood pressure value has reached a dangerous point. Irregular Heartbeat Detector An irregular heartbeat is detected when a heartbeat rhythm varies while the unit is measuring the systolic and diastolic blood pressure.During each measurement, the monitor records all the pulse intervals and calculate the average ; if there are two or more pulse intervals ,the difference between each interval and the average is more than the average value of 25% , or there are four or more pulse intervals ,the difference between each interval and the average is more than the average value of 15%,the irregular heartbeat symbol appears on the display when the measurement results are appeared. CAUTION The appearance of the IHB icon indicates that a pulse irregularity consistent with an irregular heart-beat was detected during measurement. Usually this is NOT a cause for concern. However, if the symbol appears often, we recommend you seek medical advice. Please note that the device does not replace a cardiac examination, but serves to detect pulse irregularities at an early stage. 26 Why does my blood pressure fluctuate throughout the day?
1. Individual blood pressure varies multiple times everyday. It is also affected by the way you tie your cuff and your measurement position, so please take the measurement under the same conditions. 2.If the person takes medicine, the pressure will vary more. 3.Wait at least 3 minutes for another measurement. Why do I get a different blood pressure at home compared to the hospital?
The blood pressure is different even throughout the day due to weather, emotion, exercise etc, Also, there is the white coat effect, which means blood pressure usually increases in clinical settings. What you need to pay attention to when you measure your blood pressure at home:
If the cuff is tied properly. If the cuff is too tight or too loose. If the cuff is tied on the upper arm. If you feel anxious. Taking 2-3 deep breaths before beginning will be better for measuring. Advice: Relax yourself for 4-5 minutes until you calm down. Is the result the same if measuring on the right arm?
It is ok for both arms, but there will be some different results for different people. We suggest you measure the same arm every time. 27 TROUBLE SHOOTING SPECIFICATIONS This section includes a list of error messages and frequently asked questions for problems you may encounter with your blood pressure monitor. If the products not operating as you think it should, check here before arranging for servicing. Power supply Battery powered mode:
AC adaptor powered mode:
(Please only use the recommended AC adaptor model). 5V 1A 6VDC 4AAA batteries Display mode Digital LCD V.A.72.8mm 74.2mm PROBLEM SYMPTOM CHECK THIS REMEDY Measurement mode No power Display will not light up. Low batteries show Display is dim or Batteries are exhausted. Replace with new batteries Batteries are inserted incorrectly. Insert the batteries correctly AC adaptor is inserted incorrectly. Insert the AC adaptor tightly Batteries are low. Replace with new batteries Measurement range Accuracy E 1 shows The cuff is too tight or too loose. Refasten the cuff and then measure again. Normal working condition Oscillographic testing mode Rated cuff pressure:
0mmHg~299mmHg(0kPa ~ 39.9kPa) Measurement pressure:
SYS: 60mmHg~230mmHg (8.0kPa~30.7kPa) DIA: 40mmHg~130mmHg (5.3kPa~17.3kPa) Pulse value: (40-199)beat/minute Pressure:
5-40within3mmHg(0.4kPa) Pulse value:5%
A temperature range of :+5C to +40C A relative humidity range of 15% to 90%, non-condensing, but not requiring a water vapour partial pressure greater than 50 hPa An atmospheric pressure range of :
700 hPa to 1060 hPa Temperature:-20C to +60C A relative humidity range of 93%, non-condensing, at a water vapour pressure up to 50hPa Storage & transportation condition Measurement perimeter of the upper arm About 22 cm to 32 cm, 22cm to 42cm, 22cm~45cm Weight Approx.230g(Excluding the batteries and cuff) External dimensions Attachment Mode of operation Degree of protection Protection against ingress of water Device Classification Approx.134.8mm100.2mm64.8mm 4AAA batteries,user manual,AC adapter Continuous operation Type BF applied part IP21 It means the device could protected against solid foreign objects of 12.5mm and greater, and protect against vertically falling water drops. 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. 29 E 2 shows E 3 shows Error message The monitor detected motion or talking during measuring. Movement can affect the measurement.Relax for a moment and then measure again. The measurement process does not detect the pulse signal. Loosen the clothing on the arm and then measure again. E 4 shows The treatment of the measurement failed. Relax for a moment and then measure again. Warning message OUT shows Out of measurement range Relax for a moment. Refasten the cuff and then measure again. If the problem persists, contact your physician. 28 AUTHORIZED COMPONENT Authorized Component 1.please use the TRANSTEK authorized adapter. Adapter ModelBLJ06L060100P-V BLJ06L060100P-S BLJ06L060100P-B BLJ06L060100P-U InputAC 100-240V 50/60Hz 0.2A Max Output5V 1000mA Contact Information For more information about our products, please visit www.transtek.cn.you can get customer service, usual problems and customer download, transtek will serve you anytime. Manufactured by:
Company:
Address:
Guangdong Transtek Medical Electronics Co., Ltd. Guangdong Transtek Medical Electronics Co., Ltd. Zone B, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China FCC STATEMENT FCC Statement contains FCC IDOU9TMB2079-B This device complies with Part 15 of the FCC Rules. Operation is subject to the 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. Caution: The user is cautioned that changes or modifications not expressly approved by the party responsible for compliance 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 Radiation Exposure Statement:
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. 30 31 COMPLIED STANDARDS LIST Complied Standards List Risk management EN ISO 14971:2012 / ISO 14971:2007 Medical devices -
Application of risk management to medical devices Labeling User manual General Requirements for Safety Electromagnetic compatibility Performance requirements EN ISO 15223-1:2016 / ISO 15223-1:2016 Medical devices. Symbols to be used with medical device labels, labelling and information to be supplied. Part 1 : General requirements EN 1041:2008 +A1:2013 Information supplied by the manufacturer of medical devices EN 60601-1:2006+A1:2013/ IEC 60601-1:2005+A1:2012 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance EN 60601-1-11:2015/ IEC 60601-1-11:2015 Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment EN 60601-1-2:2015/ IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic disturbances - Requirements and tests EN ISO 81060-1:2012 Non-invasive sphygmomanometers - Part 1:
Requirements and test methods for non-automated measurement type Clinical investigation Usability Software life-cycle processes Bio-compatibility 32 EN 1060-4:2004 Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers ISO 81060-2:2018 Non-invasive sphygmomanometers - Part 2:
Clinical validation of intermittent automated measurement type EN 60601-1-6:2010+A1:2015/IEC 60601-1-6:2010+A1:2013 Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability IEC 62366-1:2015 Medical devices - Part 1: Application of usability engineering to medical devices EN 62304:2006/AC: 2008 / IEC 62304: 2006+A1:2015 Medical device software - Software life-cycle processes ISO 10993-1:2018 Biological evaluation of medical devices- Part 1: Evaluation and testing within a risk management process ISO 10993-5:2009 Biological evaluation of medical devices -
Part 5: Tests for in vitro cytotoxicity ISO 10993-10:2010 Biological evaluation of medical devices -
Part 10: Tests for irritation and skin sensitization EMC GUIDANCE EMC Guidance The ME EQUIPMENT or ME SYSTEM is suitable for home healthcare environments WarningDont near active HF surgical equipment and the RF shielded room of an ME system for magnetic resonance imaging, where the intensity of EM disturbances is high. Warning Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally. Warning: Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation. WarningPortable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the equipment TMB-2079, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result. Technical description 1all necessary instructions for maintaining BASIC SAFETY and ESSENTIAL PERFORMANCE with regard to electromagnetic disturbances for the excepted service life. 2Guidance and manufacturers declaration -electromagnetic emissions and Immunity Guidance and manufacturers declaration - electromagnetic emissions Emissions test Compliance RF emissions CISPR 11 RF emissions CISPR 11 Harmonic emissions IEC 61000-3-2 Voltage fluctuations/
flicker emissions IEC 61000-3-3 Group 1 Class [ B ]
Class A Comply 33 IEC 80601-2-30:2018 Medical electrical equipment- Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers Table 1 Guidance and manufacturers declaration electromagnetic Immunity Guidance and manufacturers declaration - electromagnetic Immunity Immunity Test IEC 60601-1-2 Test level Electrostatic discharge (ESD) IEC 61000-4-2 8 kV contact 2 kV, 4kV, 8 kV, 15 kV air Compliance level 8 kV contact 2 kV, 4kV, 8 kV, 15 kV air Test Frequency
(MHz) Band
(MHz) 385 380-390 TETRA 400 Service Modulation Distance (m) IMMUNITY Modulation
(W) 1.8 0.3 EMC GUIDANCE Table 2 Electrical fast transient/burst IEC 61000-4-4 Surge IEC61000-4-5 Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 Power frequency magnetic field IEC 61000-4-8 Conduced RF IEC61000-4-6 2 kV for power supply lines 1 kV signal input/output 100 kHz repetition frequency 2 kV for power supply lines 1 kV signal input/output 100 kHz repetition frequency 0.5 kV, 1 kV differential mode 0.5 kV, 1 kV differential mode 0.5 kV, 1 kV,2 kV common mode 0.5 kV, 1 kV,2 kV common mode 0 % UT; 0,5 cycle. At 0, 45, 90, 135, 180, 225, 270 and 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 and 315. 0 % UT; 1 cycle and 70 % UT;
25/30 cycles; Single phase: at 0. 0 % UT; 250/300 cycle 30 A/m 50Hz/60Hz 30 A/m 50Hz/60Hz 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 Radiated RF IEC61000-4-3
(Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communica-
tions equipment) EMC GUIDANCE TEST LEVEL
(V/m) 27 28 9 28 0.3 0.3 0.3 0.3 28 0.3 28 430-470 704-787 800-960 1700-
1990 Pulse modulation b) 18Hz FM c) 5kHz deviation 1kHz sine GMRS 460 FRS 460 LTE Band 13, 17 Pulse modulation b) 217Hz Pulse modulation b) 18Hz Pulse modulation b) 217Hz GSM 800/900, TETRA 800, iDEN 820, CDMA 850, LTE Band 5 GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1, 3, 4,25; UMTS Bluetooth, WLAN, 802.11 b/g/n, RFID 2450, LTE Band 7 2 0.2 2 2 2 2450 2400-
2570 Pulse modulation 217 Hz 450 710 745 780 810 870 930 1720 1845 1970 5240 5500 5785 5100-
5800 WLAN 802.11 a/n Pulse modulation 217 Hz 0.2 0.3 9 34 35
1 | Label and Label Location | ID Label/Location Info | 1017.91 KiB | January 17 2021 |
Label TMB-2079 Dimension49.7 X 17.3mm Material80GMS art paper with glue 80g+
Colourblack text with white background Pantone Reflex Blue C TMB-2079 Model Rating:Battery powered mode: 4x AAA size batteries,6V AC adaptor powered mode: 5V 1A
(Please use the AC adaptor which authorized by the manufacturer!) FCC ID: OU9TMB2079-B Guangdong Transtek Medical Electronics Co., Ltd. Zone B , No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China IP Classification:IP21 SN 2018XXXXXXXXXXXXX 2020-12 FCC Statement 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. 2020-12 IP Classification:IP21 2018X X X X X X X X X X X X X S N
(Please use the A C adaptor w hich authorized by the m anufacturer!) This device co m plies with P art 15 of the F C C R ules. O peration is subject to the follo wing tw o conditions: (1) this device m ay not cause harmfulinterference, and (2) this device m ust accept R atin g:B attery po w ered m ode: 4x A A A size batteries,6 V any interference received, including interference that m ay cause undesired operation. Zone B , N o.105 ,D ongli R oad, Torch D evelop m ent District, G uangdong Transtek M edical Electronics C o., Ltd. A C adaptor po w ered m ode: 5 V 1 A Zhongshan,528437,G uangdong,C hina F C C State m ent T M B-2079 M o del
1 | Authorization Letter | Cover Letter(s) | 176.78 KiB | January 17 2021 |
Guangdong Transtek Medical Electronics Co.,Ltd Date: 2020-12-24 Federal Communications Commission 7435 Oakland Mills Road Columbia MD 21046 To whom it may concern:
I, the undersigned, hereby authorize UL Verification Services Inc. to act on our behalf in all manners relating to application for equipment authorization, including signing of all documents relating to these matters. Any and all acts carried out by UL Verification Services Inc. on our behalf shall have the same effect as acts of our own. I, the undersigned, hereby certify that we are not subject to a denial of federal benefits, that includes FCC benefits, pursuant to Section 5301 of the Anti-Drug Abuse Act of 1988, 21 U.S.C. 853(a). In authorizing UL Verification Services Inc. as our representative, we still recognize that we are responsible to:
a) comply with the relevant provisions of the certification program;
b) c) d) e) f) make all necessary arrangements for the conduct of the evaluation, including provision for examining documentation and access to all areas, records (including internal audit reports) and personnel for the purposes of evaluation (e.g. testing, inspection, assessment, surveillance, reassessment) and resolution of complaints;
make claims regarding certification only in respect of the scope for which certification has been granted;
do not use our product certification in such a manner as to bring the Certification Division into disrepute and not make any statement regarding our product certification which the Certification Division may consider misleading or unauthorized;
upon suspension or cancellation of certification, discontinue use of all advertising matter that contains any reference thereto and return any certification documents as required by the Certification Division;
use certification only to indicate the products are certified as being in conformity with specified standards;
g) h) i) j) endeavor to ensure that no certificate or report nor any part thereof is used in a misleading manner;
ensure that any reference to our product certification in communication media such as documents, brochures or advertising, complies with the requirements of the Certification Division;
keep a record of all complaints made known to us relating to the products compliance with requirements of the relevant standard and to make these records available to the when requested;
take appropriate action with respect to such complaints and any deficiencies found in products or services that affect compliance with the requirements for certification;
k) document the actions taken. This authorization is valid until further written notice from the applicant. Sincerely Yours, Signed by:
Company Name: Guangdong Transtek Medical Electronics Co.,Ltd Contact Name: Kevin Tan Title of PersonR&D Director Address: Zone A, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China
1 | Confidentiality Letter | Cover Letter(s) | 119.32 KiB | January 17 2021 |
Guangdong Transtek Medical Electronics Co.,Ltd Federal Communications Commission 7435 Oakland Mills Road Columbia MD 21046 Subject:
Request for Confidentiality FCC ID:
OU9TMB2079-B To Whom It May Concern:
Schematic Diagram Block Diagram Theory of Operation Pursuant to the provisions of Sections 0.457 and 0.459 of the Commissions rules (47 CFR 0.457, 0.459), we are requesting the Commission to withhold the following attachments as confidential document from public disclosure indefinitely. Above mentioned document contains detailed system and equipment description are considered as proprietary information in operation of the equipment. The public disclosure of above documents might be harmful to our company and would give competitor an unfair advantage in the market. It is our understanding that all measurement test reports, FCC ID label format and correspondent during certification review process cannot be granted as confidential documents and those information will be available for public review once the grant of equipment authorization is issued. Best Regards Company Name: Guangdong Transtek Medical Electronics Co.,Ltd Contact Name: Kevin Tan Title of PersonR&D Director Address: Zone A, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China Date:2020-12-24
frequency | equipment class | purpose | ||
---|---|---|---|---|
1 | 2021-01-17 | 2402 ~ 2480 | DTS - Digital Transmission System | Original Equipment |
app s | Applicant Information | |||||
---|---|---|---|---|---|---|
1 | Effective |
2021-01-17
|
||||
1 | Applicant's complete, legal business name |
Guangdong Transtek Medical Electronics Co.,Ltd
|
||||
1 | FCC Registration Number (FRN) |
0021999248
|
||||
1 | Physical Address |
Zone A, No.105,Dongli Road Torch Development District
|
||||
1 |
Zone A, No.105,Dongli Road
|
|||||
1 |
Zhongshan, Guangdong, N/A
|
|||||
1 |
China
|
|||||
app s | TCB Information | |||||
1 | TCB Application Email Address |
L******@ul.com
|
||||
1 | TCB Scope |
A4: UNII devices & low power transmitters using spread spectrum techniques
|
||||
app s | FCC ID | |||||
1 | Grantee Code |
OU9
|
||||
1 | Equipment Product Code |
TMB2079-B
|
||||
app s | Person at the applicant's address to receive grant or for contact | |||||
1 | Name |
K******** T********
|
||||
1 | Title |
R&D Director
|
||||
1 | Telephone Number |
+86-7********
|
||||
1 | Fax Number |
+86-7********
|
||||
1 |
n******@transtekcorp.com
|
|||||
app s | Technical Contact | |||||
n/a | ||||||
app s | Non Technical Contact | |||||
n/a | ||||||
app s | Confidentiality (long or short term) | |||||
1 | Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?: | Yes | ||||
1 | Long-Term Confidentiality Does this application include a request for confidentiality for any portion(s) of the data contained in this application pursuant to 47 CFR § 0.459 of the Commission Rules?: | No | ||||
if no date is supplied, the release date will be set to 45 calendar days past the date of grant. | ||||||
app s | Cognitive Radio & Software Defined Radio, Class, etc | |||||
1 | Is this application for software defined/cognitive radio authorization? | No | ||||
1 | Equipment Class | DTS - Digital Transmission System | ||||
1 | Description of product as it is marketed: (NOTE: This text will appear below the equipment class on the grant) | Blood Pressure Monitor | ||||
1 | Related OET KnowledgeDataBase Inquiry: Is there a KDB inquiry associated with this application? | No | ||||
1 | Modular Equipment Type | Does not apply | ||||
1 | Purpose / Application is for | Original Equipment | ||||
1 | Composite Equipment: Is the equipment in this application a composite device subject to an additional equipment authorization? | No | ||||
1 | Related Equipment: Is the equipment in this application part of a system that operates with, or is marketed with, another device that requires an equipment authorization? | No | ||||
1 | Grant Comments | Listed output power is peak conducted. | ||||
1 | Is there an equipment authorization waiver associated with this application? | No | ||||
1 | If there is an equipment authorization waiver associated with this application, has the associated waiver been approved and all information uploaded? | No | ||||
app s | Test Firm Name and Contact Information | |||||
1 | Firm Name |
UL Verification Services (Guangzhou) Co., Ltd.
|
||||
1 | Name |
S**** G******
|
||||
1 | Telephone Number |
+86 0********
|
||||
1 |
S******@ul.com
|
|||||
Equipment Specifications | |||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Line | Rule Parts | Grant Notes | Lower Frequency | Upper Frequency | Power Output | Tolerance | Emission Designator | Microprocessor Number | |||||||||||||||||||||||||||||||||
1 | 1 | 15C | 2402.00000000 | 2480.00000000 | 0.0018600 |
some individual PII (Personally Identifiable Information) available on the public forms may be redacted, original source may include additional details
This product uses the FCC Data API but is not endorsed or certified by the FCC