INTRODUCTION................................................................................................................
Safety Information
LCD Display Signal
Monitor Components
BEFORE YOU START.......................................................................................................
The Choice of Power Source
Setting Date, Time and Measurement Unit
Install App and Pair-Up
START MEASUREMENT...................................................................................................
Apply the Cuff
Start Measurement
DATA MANAGEMENT.......................................................................................................
Recall the Records
Delete the Records
Data Transmission
INFORMATION FOR USER...............................................................................................
Tips for measurement
Maintenance
ABOUT BLOOD PRESSURE ............................................................................................
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Why does my blood pressure fluctuate throughout the day?
Why is the blood pressure I get from the hospital different from home?
Will I get the same result if I measure on the right wrist?
TROUBLESHOOTING.......................................................................................................
SPECIFICATIONS..............................................................................................................
AUTHORIZED COMPONENTS.........................................................................................
COMPLIED EUROPEAN STANDARDS LIST.....................................................................
EMC GUIDANCE...............................................................................................................
APPENDIX.........................................................................................................................
1
4
8
10
12
14
16
17
18
18
19
23
CATALOGUE
INTRODUCTION
1
The below signs might appear in the user manual, labeling or other component.
Safety information
T1A/250V Φ3.6*10CCC
F1
Thank you for selecting the Actiiv Blood Pressure Monitor (Digital Sleeve ACMMD002).
The monitor features blood pressure measurement, pulse rate measurement and the
storage of results. Readings taken by the ACMMD002 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 instruction for using this product.
Read the manual thoroughly before using this product.
Features:
For indoor use only
128mm x 50mm Blue LCD display with white backlight
Up to 60 records stored for each user
Measure-during-inflating technology
Symbol for “TYPE BF
APPLIED PARTS”
Symbol for “DIRECT
CURRENT”
CAUTION
The Bluetooth Combination
Mark
Symbol for “THE OPERATION
GUIDE MUST BE READ”
Please read this user manual carefully and thoroughly before use.
This device is intended for adult use in the home/domestic environment 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 upper 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. Please start or end medical treatment based solely on a physician’s treatment advice.
If you are taking medication, consult your physician to determine the most appropriate time for
your measurement. Never change a prescribed medication without your physician’s consent.
This unit is not suitable for continuous monitoring during medical emergencies or operations.
If the pressure of the cuff exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should
the cuff not deflate when its pressure exceeds 40 kPa (300 mmHg), detach the cuff from the upper
arm and press the homologous button to stop inflation.
Do not use the monitor in strong electromagnetic field conditions (e.g. mobile) that radiate
interference signals or electrical fast transient / burst signals.
The device is not AP/APG equipment. It is not suitable for use in the presence of a flammable
anesthetic mixture with air (or oxygen, nitrous oxide).
Please keep the unit out of reach of infants or children, since inhalation or swallowing of small
parts is dangerous or even fatal.
Please use ACCESSORIES and detachable parts specified / authorised by MANUFACTURER.
Otherwise, it may cause damage to the unit or danger to the user / patient.
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.
Please make sure the unit functions safely and it is in proper working condition before use.
