TRANSTEK TMB-1491 Скачать руководство пользователя | Manualshive

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User Manual

Blood Pressure Monitor

TMB-1491

Arm Type

Thank you very much for selecting TRANSTEK Blood Pressure Monitor

TMB-1491.
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.

EC REP

Guangdong Transtek Medical Electronics Co., Ltd.

Zone A, No.105 ,Dongli Road, Torch Development District,

Zhongshan,528437,Guangdong,China

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Содержание TMB-1491

Страница 1: ...tor TMB 1491 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 EC REP Guangdong Transtek Medical Electronics Co Ltd Zone A No 105 Dongli Road Torch Development District Zhongshan 528437 Guangdong China ...

Страница 2: ...he Records Delete the Records INFORMATION FOR USER 17 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 19 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 mea...

Страница 3: ...ained 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 60mm 40 5 mm Digital LCD Maximum 60 records per each user General Description 3rd technology Measuring during inflation The updated technology in the wor...

Страница 4: ...unit is not suitable for continuous monitoring during medical emergencies or operations Otherwise the patient s arm and fingers will become anaesthetic swollen and even purple due to a lack of blood When not in use store the device 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 ...

Страница 5: ...ween 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 co...

Страница 6: ...e display is dim The display does not light up Always select the authorized specified battery Four AAA size alkaline batteries Please use TRANSTEK authorized cuff The size of the actual cuff please refer to the label on the attached cuff 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 Rem...

Страница 7: ...tton shortly it will display the time Then hold pressing SET button to enter the mode for year setting 2 Press MEM button to to change the YEAR Each press will increase the numeral by one in a cycling manner 3 When you get the right year press SET button to set down and turn to next step 4 Repeat steps 2 and 3 to set the MONTH and DAY 5 Repeat steps 2 and 3 to set the HOUR and MINUTE 7 After the u...

Страница 8: ...art Turn your palm upwards Sit upright in a chair and take 5 6 deep breaths Rest for 5 minutes before first measuring Wait at least 3 minutes between measurements This allows your blood circulation to recover The patient must relax as much as possible and do not move and talk during the measurement procedure For a meaningful comparison try to measure under similar conditions For example take daily...

Страница 9: ... 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 60 is dropped The current No is No 2 The corresponding time is A M 8 18 The corresponding date is January 1st CAUTION DOWN UP The date and time of the record will be shown alternately Note If you want to check another user s records please turn off the blood pres...

Страница 10: ...following circumstances If you did not get the correct measurement you can delete all results by following steps below Delete the Records 2 Press SET to confirm deleting and the monitor will turn off 3 If you don t want to delete the records press START STOP to escape 4 If there is no record the right display will show START STOP 1 Hold pressing MEM and SET for 3 seconds when the monitor is in the...

Страница 11: ...c pressure What is the standard blood pressure classification The blood pressure classification published by World Health Organization WHO and International Society of Hypertension ISH in 1999 is as follows Irregular Heartbeat Detector 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 N...

Страница 12: ...ailer or our customer service department for further assistance Refer to the warranty for contact information and return instructions E21 shows The treatment of the measurement failed Relax for a moment and then measure again The monitor detected motion talking or the pluse is too poor while measuring Relax for a moment and then measure again 1 Individual blood pressure varies multiple times every...

Страница 13: ...bout our products please visit www transtek cn you can get customer service usual problems and customer download transtek will serve you anytime Authorized European Representative Manufactured by Company Address Company MDSS Medical Device Safety Service GmbH Address Schiffgraben 41 30175 Hannover Germany Guangdong Transtek Medical Electronics Co Ltd Zone A No 105 Dongli Road Torch Development Dis...

Страница 14: ...g and information to be supplied Part 1 General requirements IEC 80601 2 30 2013 Medical electrical equipment Part 2 30 Particular requirements for the basic safety and essential performance of automated non invasive sphygmomanometers ISO 81060 2 2013 Non invasive sphygmomanometers Part 2 Clinical validation of automated measurement type EN 60601 1 2 2007 IEC 60601 1 2 2007 Medical electrical equi...

Страница 15: ...eclaration electromagnetic immunity IMMUNITY test Not applicable 3 V m Compliance level IEC 60601 TEST LEVEL Conducted RF IEC 61000 4 6 Radiated RF IEC 61000 4 3 3 V m 80 MHz to 2 5 GHz 3 Vrms 150 kHz to 80 MHz Electromagnetic environment guidance Portable and mobile RF communications equipment should be used no closer to any part of the device including cables than the recommended separation dist...

Страница 16: ...ecommended below according to the maximum output power of the communications equipment Rated maximum output power of transmitter W Separation distance according to frequency of transmitter m For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres m can be estimated using the equation applicable to the frequency of the transmitter where P is...

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