Smart Meter iBloodPressure SMBP802-GS-001 Скачать руководство пользователя страница 4

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*  This device may be used only for the purpose described in this booklet. The manufacturer 

and Smart Meter cannot be held liable for damage caused by an incorrect application.

INTENDED USERS AND USES CAUTIONS

*  This device is intended for adult home use only.

*  This device is intended for non-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.

*  The device is not suitable for use on neonatal patients, pregnant women, patients with 

implanted electronic devices, patients with pre-eclampsia, premature ventricular beats, 

atrial fibrillation, peripheral arterial disease, patients undergoing intravascular therapy, 

patients with an arterio-venous shunt, or mastectomy patients. Please consult your doctor 

before using the unit if you suffer from these or other illnesses.

*  The device is not suitable for measuring the blood pressure of children. Ask your doctor 

before using it on older children.

*  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.

*  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 prescribed medication without consulting 

your physician.

*  Consult your doctor if you have any questions about your blood pressure.

*  When the device is 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.

*  Do not apply the cuff on an arm that has other medical devices, an intravenous drip, or a 

blood transfusion attached.

*  Warning: Do not apply the cuff over a wound as it can cause further injury.

*  This device was clinically investigated according to the requirements of ISO 81060-2:2013.

USE ENVIRONMENT CAUTIONS

*  Please use the device in the environment described in this manual. Otherwise, the 

performance and lifetime of the device will be reduced.

*  The device is intended for indoor home use.

*  The device is not intended for use during patient transport.

*  The device is not intended for public use.

*  The device cannot be used with HF surgical equipment at the same time.

*  The device is not AP/APG equipment and not suitable for use in the presence of a 

flammable anesthetic mixture with air of oxygen or nitrous oxide.

*  This unit is not suitable for continuous monitoring during medical emergencies or 

operations.

INTRODUCTION

INTRODUCTION

*  To avoid measurement errors, avoid electromagnetic field radiated interference signals or 

electrical fast transient/burst signals.

*  Wireless communications equipment such as wireless home network devices, mobile 

phones, cordless telephones and their base stations, and walkie-talkies may affect this 

equipment and should be kept at least 13 feet away from the device during use. The 

distance of 13 feet is calculated by the manufacturer from the 80 MHz to 5.8 GHz column 

of Table 4 and Table 9 of IEC 60601-1-2:2014, as appropriate.

*  At least 30 minutes is required for the device to warm from the minimum storage 

temperature until it is ready for use. At least 30 minutes is required for the device to cool 

from the maximum storage temperature until it is ready for use.

*  The blood pressure monitor and the cuff are suitable for use within the home 

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. The cuff should not cause irritation.

USE CAUTIONS

*  Too frequent and consecutive measurements could cause disturbances in blood 

circulation and injuries.

*  When using this device, please pay attention to the following situations which may 

interrupt blood flow and influence blood circulation and cause injury: connection tube 

kinking, too frequent and multiple consecutive measurements, the application of the cuff 

and pressurization on any arm with intravascular access therapy, where an arterio-

venous (A-V) shunt is present, and inflating the cuff on the side of a mastectomy.

*  Don't compress, restrict, or kink the connection tube during use, otherwise, the cuff 

pressure may continuously increase which can prevent blood flow and result in injury.

*  Please check that operation of the device does not result in prolonged impairment of 

blood circulation.

*  If you experience discomfort during measurement, such as pain in the arm, press any 

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 the pressure reaches 40 kPa (300 mmHg), detach the 

cuff from the arm immediately and press any button to stop inflation. Prolonged high 

pressure (cuff pressure 

 300 mmHg or constant pressure 

 15 mmHg for more than 3 

minutes) applied to the arm may lead to an ecchymosis.

*  The operator should not touch the power supply and the patient simultaneously.

CAUTION

CAUTION

Содержание iBloodPressure SMBP802-GS-001

Страница 1: ...Model SMBP802 GS 001 User Manual To use the monitor correctly and safely please read the manual thoroughly Please keep this manual in order to reference in future Manufactured for Smart Meter LLC 201...

Страница 2: ...a Measurement INFORMATION FOR USER 14 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 16 What are systolic pressure and diastolic pressure What is the standard blood pressure classification Ir...

Страница 3: ...revent any damage to the device SN Symbol for MANUFACTURE DATE General Description The iBloodPressure monitor features blood pressure measurement pulse rate measurement and cellular result transmissio...

Страница 4: ...presence of a flammable anesthetic mixture with air of oxygen or nitrous oxide This unit is not suitable for continuous monitoring during medical emergencies or operations INTRODUCTION INTRODUCTION T...

Страница 5: ...onments may affect the performance of the unit Please use a soft cloth to clean the whole unit before and after use Don t use abrasive or volatile cleaners Do not wash the cuff in a washing machine or...

Страница 6: ...ims The display does not light up 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 Remove...

Страница 7: ...so that the tube exits towards the hand Place your arm through the cuff loop with your palm facing up Position the cuff s edge about an inch 2 3 cm above the elbow Align the marker located to the rig...

Страница 8: ...links on the LCD indicates data is transmitting Taking a Measurement Transmitting results Tip You can press START STOP button at any time to stop measuring during the process 3 If the data is successf...

Страница 9: ...y place and avoid the sunshine Avoid intense shaking and dropping Use a damp cloth to remove dirt Avoid contact with water clean exterior with a dry cloth Avoid dusty places and unstable temperatures...

Страница 10: ...t the day due to weather emotion exercise etc Also there is the white coat effect which means blood pressure usually increases in clinical settings It is okay to measure on either arm however there ma...

Страница 11: ...is allowed Power supply Display mode Measurement mode Oscillographic testing mode Measurement range Measurement perimeter of the upper arm Weight External dimensions Attachment Mode of operation Cont...

Страница 12: ...device labels labelling and information to be supplied Part 1 General requirements IEC 80601 2 30 2018 Medical electrical equipment Part 2 30 Particular requirements for the basic safety and essential...

Страница 13: ...d amateur radio bands between 0 15 MHz and 80 MHz 6V For AC power port 3 Vrms 6 Vrms in ISM and amateur radio bands 80 AM at 1 KHz 10 V m 80 MHz 2 7 GHz 80 AM at 1 kHz 10 V m 80 MHz 2 7 GHz 80 AM at 1...

Страница 14: ...Rules These limits are designed to provide reasonable protection against harmful interference in a residential installation This equipment generates uses and can radiate radio frequency energy and if...

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