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Thank you for selecting TRANSTEK arm type blood pressure Monitor 

(TMB-1018-A). The monitor features blood pressure measurement, pulse rate 

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

reliable service.

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:

140*36mm Digital LCD display

Maximum 60 records per user

Measuring during inflation technology

General Description

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

They are the requirement of standard and using.

Safety Information

Symbol for “THE OPERATION 

GUIDE MUST BE READ”

Symbol for “COMPLIES WITH

MDD 93/42/EEC REQUIREMENTS”

Symbol for “MANUFACTURER”

Symbol for “SERIAL NUMBER”

Symbol for “TYPE BF APPLIED 

PARTS”

Symbol for “DIRECT CURRENT”

Symbol for “ENVIRONMENT 

PROTECTION - Electrical waste  

products should not be disposed of 

with household waste. Please recycle 

where facilities exist. Check with your 

local authority or retailer for recycling 

advice”

Symbol for “Authorised Representative 

in the European Community

EC REP

Symbol for “MANUFACTURE 

DATE”

CAUTION

This device is intended for adult use only.

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.

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.

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.

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 /adapter and the patient simultaneously.

To avoid measurement errors, please avoid the condition of strong electromagnetic field 

radiated interference signal or electrical fast transient/burst signal.

The user must check that the equipment functions safely and see that it is in proper working 

condition before being used.

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.

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

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 sensization or irritation reaction.

Please use ACCESSORIES and detachable partes specified/ authorised by MANUFAC-

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

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.

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. 

Please report to Transtek if any unexpected operation or events occur.

Please use the soft cloth to clean the whole unit. Don’t use any abrasive or volatile cleaners. 

Caution: These notes must be observed 

to prevent any damage to the device

INTRODUCTION

INTRODUCTION

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Содержание TMB-1018-A

Страница 1: ...r selecting TRANSTEK Blood Pressure Monitor TMB 1018 A Please keep this manual well in order to reference in future Arm Type Version 1 0 EC REP Guangdong Transtek Medical Electronics Co Ltd Zone A No...

Страница 2: ...ON FOR USER 13 Tips for measurement Maintenances ABOUT BLOOD PRESSURE 15 What are systolic pressure and diastolic pressure What is the standard blood pressure classification Why does my blood pressure...

Страница 3: ...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 The equipment is not AP APG equipment and not...

Страница 4: ...ure 1kPa 7 5mmHg Low battery Batteries are low and need to be replaced Shocking reminding Shocking will result in inaccurate Average The average of blood pressure Recalling The records will be showed...

Страница 5: ...ery cover Install the batteries by matching the correct polarity as shown Replace the cover 1 Battery powered mode 6VDC 4 AAA batteries 2 AC adaptor powered mode 6V 1A Please only use the recommended...

Страница 6: ...he cuff should be snug but not too tight You should be able to insert one finger between the cuff and your arm 3 Sit comfortably with your tested arm resting on a flat surface 2 3cm 4 Repeat steps 2 a...

Страница 7: ...st CAUTION The order of the record date time will display alternately 1 When the monitor is off press the START STOP to turn on the monitor and it will finish the whole measurement Adjust the zero LCD...

Страница 8: ...3 If you don t want to delete the records press START STOP to escape If you did not get the correct measurement you can delete all results by following steps below Delete the Records 4 If there is no...

Страница 9: ...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 Th...

Страница 10: ...fer 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 AC adaptor is inserted incorrectly Inser...

Страница 11: ...00 240V 50 60Hz 400mA Output 6V 1A Type UE08WCP 060100SPA Conforms to UL certificate Contact Information For more information about our products please visit www transtek cn you can get customer servi...

Страница 12: ...ablishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Risk management Labeling User manual General Requirements for...

Страница 13: ...G Guidance and manufacturer s declaration 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 8...

Страница 14: ...the device as recommended below according to the maximum output power of the communications equipment Rated maximum output power of transmitter W Separation distance according to frequency of transmit...

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