Handleiding easy@Home EBP-095 Bloeddrukmeter

Handleiding

2 3

INTRODUCTION INTRODUCTION

Thank you for selecting arm type blood pressure Monitor

(EBP-095). The monitor features blood pressure measurement, pulse rate

measurement and the result storage. The design provides you with two

years of reliable service.

Readings taken by the EBP-095 are equivalent to those obtained by a

trained 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.

The signs below might be in the user manual, labeling or other component.

They are the requirement of standard and using.

Safety Information

Features:

60mm*80mm Digital LCD display

Maximum 60 records

Measuring during inflation technology

General Description

This device is intended for adult 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 wrist 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.

If the cuff pressure exceeds 40 kPa (300 mmHg),the unit will automatically deflate. Should the cuff

not deflate when pressures exceeds 40 kPa (300 mmHg),detach the cuff from the arm and press

the START/STOP button to stop inflation.

To avoid measurement errors, carefully read this manual before using the product.

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.

The operator shall not touch output of batteries/AC adapter and the patient simultaneously.

Do not wind air tube in the neck.

CAUTION

This device may provide contradictory results for any female subject who may be suspected of, or

is pregnant. Besides providing inaccurate readings, the effects of this device on the fetus are

unknown.

The device has been evaluated clinically using manual cuff/stethoscope auscultation as the

reference. Blood pressure measurements determined with this device are equivalent to those

obtained by a trained observer using the cuff/stethoscope auscultatory method, within the limits

prescribed by the American National Standard, Manual, electronic, or automated

sphygmomanometers.”

If you have any problems with this device, such as setting up, maintaining or using, please

contact the SERVICE PERSONNEL of . Don’t open or repair the device by yourself.

Please use ACCESSORIES and detachable partes specified/ authorised by MANUFACTURE.

Otherwise, it may cause damage to the unit or danger to the user/patients.

Please note that Luer lock connectors are not used on the product and please DO NOT change

any provided connectors.

Manufacturer will make available on request circuit diagrams, component parts list etc.

WARNING: No modifications of this equipment is allowed.

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.

Please use the device under the environment which was provided in the user manual. Otherwise,

the performance and lifetime of the device will be impacted and reduced.

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 alergic reaction or contact injury.

The device doesn’t need to be calibrated within the two years of reliable service.

Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the

local guidelines.

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.

T1A/250V Φ3.6*10CCC

F1

For indoor use only

Symbol for “MANUFACTURER”

Symbol for “SERIAL NUMBER”

Symbol for “TYPE B APPLIED

PARTS”

Symbol for “ENVIRONMENT

PROTECTION – Electrical waste

products should not be disposed of

with household waste. Please follow

local guidelines.”

Symbol for “DIRECT CURRENT”

Symbol for “Class II Equipment”

Symbol for “THE OPERATION

GUIDE MUST BE READ”

Symbol for “MANUFACTURE

DATE”

Please report to if any unexpected operation or events occur.

Beoordeling

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