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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.

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 81060-2:2018.

* 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 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 adapter, 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 sensitization or irritation reaction.

* Adapter 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!

INTRODUCTION

INTRODUCTION

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Содержание TMB-1491-BHJ

Страница 1: ...onitor Please read the user manual carefully and thoroughly so as to ensure the safe usage of this product Keep this manual for further reference in case any issues arise Version 1 0 Guangdong Transte...

Страница 2: ...the Records Delete the Records INFORMATION FOR USER 21 Tips for measurement Maintenance ABOUT BLOOD PRESSURE 23 What are systolic pressure and diastolic pressure What is the standard blood pressure c...

Страница 3: ...such as cardiac pacemakers de brillators Contraindications This product uses the Oscillometric Measuring method to detect blood pressure Before every measurement the unit establishes a zero pressure...

Страница 4: ...f patient blood circulation When measurement please avoid compression or restriction of the connection tubing CAUTION The device cannot be used with HF surgical equipment at the same time The ACCOMPAN...

Страница 5: ...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 prov...

Страница 6: ...the measurement 6V 1A Do not use new and used ba eries together Do not use di erent types of ba eries together Do not dispose the ba eries in re Ba eries may explode or leak Remove ba eries if the dev...

Страница 7: ...EM bu on will increase the number by one in a cycling manner When you get the right year press SET bu on to con rm the entry The screen will then show a blinking number represen ng the MONTH It is imp...

Страница 8: ...between user 1 user 2 and USER G guest 1 Press SET bu on to ensure your choice it will show User ID and donE and then turn o 2 7 A er the UNIT is set the LCD will display donE rst then display all th...

Страница 9: ...ment Sensi ve people including pregnant women pre eclamp c and those who implanted medical electronic instruments should avoid using the unit whenever possible Keep the monitor at least 20 cen meters...

Страница 10: ...eep breaths Rest for 5 minutes before rst measuring Wait at least 3 minutes between measurements This allows your blood circula on to recover The pa ent must relax as much as possible and do not move...

Страница 11: ...1 is shown rst Each new measurement is assigned to the rst 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 from the list 2 Each press M...

Страница 12: ...can delete all results for the selected user by following steps Take User 1 for example If there is no record when you press MEM bu on to check the record the right display will be shown 3 Tips for Me...

Страница 13: ...n 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 o en we recommend yo...

Страница 14: ...during use please check the following points PROBLEM SYMPTOM CHECK THIS REMEDY No power Low batteries Error message Display will not light up Ba eries are exhausted Replace with new ba eries Insert th...

Страница 15: ...ery Powered Mode Internally Powered ME Equipment AC Adapter Powered Mode Class II ME Equipment A temperature range of 5 C to 40 C A rela ve humidity range of 15 to 90 non condensing but not requiring...

Страница 16: ...ses Bio compatibility 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...

Страница 17: ...anufacturer s declaration electromagnetic emissions RF emissions CISPR 11 RF emissions CISPR 11 Group 1 Class B Class A Comply Compliance Harmonic emissions IEC 61000 3 2 Voltage fluctuations flicker...

Страница 18: ...3 Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communicati ons equipment Band MHz Modulation W Distance m IMMUNITY TEST LEVEL V m TETRA 400 Pulse modulation b 18 Hz GMRS 460 FRS 460...

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