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CAUTION

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 samb 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.

* 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 

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 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 data 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 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.

* 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!

* 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 operator shall not touch output of batteries 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. Don’t use any abrasive or volatile cleaners.

* The device doesn’t 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. Don’t 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.

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INTRODUCTION

INTRODUCTION

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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