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Guangdong Transtek Medical Electronics Co., Ltd.
Zone A, No.105 ,Dongli Road, Torch Development District,
Zhongshan,528437,Guangdong,China
EC REP
User Manual
Blood Pressure Monitor
Model No: TMB-1490-BS
Thank you very much for selecting V.max-MX707 Blood Pressure Monitor
TMB-1490-BS.
Please read the user's manual carefully and thoroughly so as to ensure
the safe usage of this product. Keep the manual well for further reference
in case you have problems.
version:1.0
V.MAX-MX707
Arm Type
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Table of Contents
Related Manuals for TRANSTEK V.MAX-MX707
Summary of Contents for TRANSTEK V.MAX-MX707
- Page 1 Blood Pressure Monitor V.MAX-MX707 Model No: TMB-1490-BS Arm Type Thank you very much for selecting V.max-MX707 Blood Pressure Monitor TMB-1490-BS. Guangdong Transtek Medical Electronics Co., Ltd. Please read the user’s manual carefully and thoroughly so as to ensure Zone A, No.105 ,Dongli Road, Torch Development District, Zhongshan,528437,Guangdong,China the safe usage of this product.
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Page 2: Table Of Contents
CATALOGUE Table of Contents INTRODUCTION........................2 General Description Indications for Use Measurement Principle Safety Information LCD Display Signal Monitor Components List BEFORE YOU START......................9 The Choice of Power Supply Installing and Replacing the Batteries Setting Date, Time MEASUREMENT........................13 Tie the Cuff Start the Measurement DATA MANAGEMENT......................16 Recall the Records... -
Page 3: Introduction
Caution: These notes must be observed to prevent any damage to the device. The V.MAX-MX707 Blood Pressure Monitor is a digital monitor intended to measure blood pressure and heartbeat rate with arm circumference ranging from 22cm to 42cm(about 8¾˝-16½˝). It is intended for adult indoor use only. - Page 4 INTRODUCTION INTRODUCTION CAUTION CAUTION * When measurement, please avoid compression or restriction of the connection tubing. * This device is intended for adult use in homes only. * The device cannot be used with HF surgical equipment at the same time. * The device is not suitable for use on neonatal patients, pregnant women, patients with * The ACCOMPANYING DOCUMENT shall disclose that the SPHYGMOMANOMETER implanted electronical devices, patients with pre-eclampsia, premature ventricular beats,...
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Page 5: Lcd Display Signal
INTRODUCTION INTRODUCTION CAUTION LCD display signal * Do not wash the cuff in a washing machine or dishwasher! * 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). -
Page 6: Monitor Components
BEFORE YOU START INTRODUCTION The Choice of Power Supply Monitor Components 1.Battery powered mode: 6VDC 4×AAA batteries 2.AC adaptor powered mode: Component list of CUFF pressure measuring 1A (Not included) (Please only use the recommended AC system AIR TUBE adaptor model). 1 Cuff 2 Air tube Please unplug the adaptor to depart from... -
Page 7: Setting Date, Time
BEFORE YOU START BEFORE YOU START Setting Date and time (SETUP) 3.When you get the right year, press “START/STOP” It is important to set the time clock before using your blood button to set down and turn pressure monitor, so that a time stamp can be assigned to each to next step. -
Page 8: Measurement
BEFORE YOU START MEASUREMENT Tie the cuff 6.Repeat steps 2 and 3 to set the [HOUR] and [MINUTE]. 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. -
Page 9: Start The Measurement
Select “My Devices”, then “Add New”. monitor, and it will finish the whole measurement, save and transmit “V.MAX-MX707” will show up, select it the measurement data for the desired user. (Take User A for and then press “Add to My Devices”. Go example.) -
Page 10: Recall The Records
DATA MANAGEMENT DATA MANAGEMENT Delete the Records Recall the Records If you did not get the correct measurement, you can delete all 1. When the monitor is off, results for the selected user by following steps below. please press the “MEM”, it will display the latest record first when the records are less than three groups. -
Page 11: Information For User
INFORMATION FOR USER INFORMATION FOR USER Maintenance Tips for Measurement In order to get the best performance, please follow the Measurements may be inaccurate if taken in the following instructions below. circumstances. Avoid touching water, Put in a dry place and clean it with a dry cloth in case. -
Page 12: About Blood Pressure
ABOUT BLOOD PRESSURE ABOUT BLOOD PRESSURE What are systolic pressure and diastolic pressure? Why does my blood pressure When ventricles contract and pump blood out of the Systolic Diastolic fluctuate throughout the heart, the blood pressure reaches its maximum value blood entering blood discharging vein... -
Page 13: Troubleshooting
TROUBLESHOOTING SPECIFICATIONS This section includes a list of error messages and frequently Battery powered mode: 6VDC 4×AAA batteries asked questions for problems you may encounter with your blood AC adaptor powered mode: (Not included) pressure monitor. If the products not operating as you think it Power supply (Please only use the recommended AC should, check here before arranging for servicing. -
Page 14: Authorized Component
EN 1060-4:2004 Non-invasive sphygmomanometers - Part 4: Test Manufactured by: Guangdong Transtek Medical Electronics Co., Ltd. procedures to determine the overall system accuracy of automated Clinical investigation Company: Guangdong Transtek Medical Electronics Co., Ltd. -
Page 15: Emc Guidance
EMC GUIDANCE EMC GUIDANCE Table 2 EMC Guidance Guidance and manufacturer’s declaration – electromagnetic immunity 1)This product needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided, 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. - Page 16 EMC GUIDANCE EMC GUIDANCE Table 4 Table 3 Recommended separation distances between portable and mobile RF communications Guidance and manufacturer’s declaration – electromagnetic immunity equipment and the device. 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.
- Page 17 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. IMMUNITY Radiated RF Test...
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