Version:1.0 User Manual Blood Pressure Monitor TMB-1872-B 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-1872-B. Please read the user manual carefully and thoroughtly so as to ensure the safe usage of this product, Keep the manual well for further reference in case you have problems.
CATALOGUE CATALOGUE Table of Contents INTRODUCTION...................................................................................................................2 General Description Indications for Use Contraindications Measurement Principle Safety Information LCD Display Signal Monitor Components List BEFORE YOU START...........................................................................................................
INTRODUCTION General Description Thank you for selecting TRANSTEK arm type blood pressure monitor (TMB-1872-B). 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-1872-B are equivalent to those obtained by a trained observer using the cuff and stethoscope auscultation method.
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.
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).
INTRODUCTION BEFORE YOU START Monitor Components The Choice of Power Supply 1.Battery powered mode: CUFF 6VDC 4*AAA batteries 2.
BEFORE YOU START Setting Date, Time 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 :2018—2058 time:24H/12 H) 1.When the monitor is off, presse “SET” button shortly it will display the time.Then press “SET” button for 3 seconds to enter the mode for year setting. 2.Press “MEM” button to change the [YEAR].
BEFORE YOU START BEFORE YOU START Select the User 1. When the monitor is off, press and hold “MEM ”button to enter user setting mode. The user ID will blink. Pair-up the Blood Pressure Monitor with Your Device 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.Turn on Bluetooth and the app.
MEASUREMENT BEFORE YOU START List of compatible devices: For iOS devices: The operating system must be iOS 8 or more, such as iPhone 4S, iPhone 5/5C/5S, iPhone 6/6 Plus and so on. For Android devices: The operating system must be 4.3 or more. CAUTION Interference may occur in the vicinity of equipment marked with the following symbol . And TMB-1872-B may interfering vicinity electrical equipment.
MEASUREMENT MEASUREMENT If the data transmission fails, the Bluetooth symbol blinks all the time , and it will diaplay symbol “ + ” then turns off. Start the Measurement 1.When the monitor is off, press “Start/Stop” button to turn on the monitor, and it will finish the whole measurement . ( Take user 1 for example.) LCD display START STOP Adjust the zero. If the data transmission succeeds, the Bluetooth symbol will not blink then the device will turn off. Inflating and measuring.
DATA MANAGEMENT DATA MANAGEMENT Delete the Records Recall the Records If you did not get the correct measurement, you can delete results by following steps below. 1. When the monitor is off, please press “MEM” button to show the recent record. A: Delete one record If the records are less than 3 groups, it will display the latest record instead. ( Take user 1 for example.) 1.
DATA MANAGEMENT INFORMATION FOR USER Tips for Measurement B: Delete all records 1.Hold pressing “MEM” button for 3 seconds when the monitor is in the memory recall mode, the flash display “dEL ALL+User ID” will show. Measurements may be inaccurate if taken in the following circumstances. 2.Press and hold “Start/stop” button to confirm deleting and the monitor will display “dEL donE+USER ID” and then turn off.
INFORMATION FOR USER ABOUT BLOOD PRESSURE Maintenance What are systolic pressure and diastolic pressure? Please calibrate the blood pressure monitor in specific institute once every two years to ensure the precise measurement. In order to get the best performance, please follow the instructions below for storage. 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.
SPECIFICATIONS AUTHORIZED COMPONENTS TROUBLESHOOTING ABOUT BLOOD PRESSURE Why does my blood pressure fluctuate throughout the day? 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. 1. Individual blood pressure varies multiple times everyday.
SPECIFICATIONS AUTHORIZED COMPONENT Battery powered mode: 6VDC 4*AAA batteries Power supply AC adaptor powered mode: 5V 1A (Please only use the recommended AC Authorized Components 1.please use the TRANSTEK authorized adapter. adaptor model).
COMPLIED STANDARDS LIST FCC STATEMENT FCC Statement FCC ID：OU9TMB1872BS 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.
EMC GUIDANCE EMC GUIDANCE Table 2 EMC Guidance 1)This product needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided, and this unit can be affected by portable and mobile RF communications equipment. 2)* Do not use a mobile phone or other devices that emit electromagnetic fields, near the unit. This may result in incorrect operation of the unit.
EMC GUIDANCE EMC GUIDANCE Table 4 Table 3 Guidance and manufacturer’s declaration – electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment.
EMC GUIDANCE Table 5 Guidance and manufacturer’s declaration - electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device, should assure that it is used in such an environment. Radiated RF Test Band a) Service a) Modulation b) Modulation b) IEC61000-4-3 Frequency (MHz) (W) (Test (MHz) specifications 1.
