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•  Consider the electromagnetic compatibility of the device (ex. power disturbance, radio 

frequency interference etc.) Please use it indoor only.

•  Over high frequency measurements may result in blood flow interference, which is 

likely to cause uncomfortable sensations, such as partial subcutaneous hemorrhage, 
or temporary numbness to your arm. In general, these symptoms should not last long. 
However, if you do not recover in time, please seek your medical practitioners for help.

•  Rest at least 5 - 10 minutes before taking a measurement.
•  To allow your blood vessels to return to the condition prior to taking the 

measurement, please wait at least 3 - 5 minutes in between measurements. You may 
need to adjust the wait time according to your personal physiological situation.

•  We recommend you using the same arm (preferably the left arm) and measuring 

around the same time each day.

•  Perform measurements in a quiet and relaxed environment at room temperature.
•  DO NOT move or shake the device during a measurement. Please keep quiet and do 

not talk during measurements.

•  This product is not suitable for: 

Pregnant women 
People with arrhythmias 
Undergoing intravenous injection on any limb 
Currently in a dialysis treatment 
In pre-eclampsia condition

•  For those who have had a mastectomy or lymph node clearance, it is recommended to 

take a measurement on the unaffected side.

•  When used among medical electronic equipment on the same limb, pressurization of 

the cuff may cause temporarily malfunction to other devices.

•  If you have one of the circulatory problems as arteriosclerosis, diabetes, liver disease, 

kidney disease, severe hypertension, peripheral circulation, please consult your 
healthcare professional before using the device.

•  Blood pressure measurements taken with this device are equivalent to those obtained 

by a trained observer using the cuff / stethoscope auscultation method and are within 
the accuracy limits prescribed by the Standard of EN 1060-4.

•  If the cuff is worn incorrectly, or the shape of the upper arm is special (for example, the 

circumference of the upper arm differs largely from the circumference of the forearm), 
excessive gap might occur between the arm cuff and the arm, and it might lead to 
measurement errors or inaccuracies. If you have any question about the condition of 
cuff wearing and/or measurement result, please consult your healthcare professional.

•  The applied part is cuff.
•  DO NOT use the device on infants, children, or those who cannot express their own 

intention.

•  To avoid accidental strangulation, keep this product away from children and DO NOT 

drape tube around neck.

•  The medical device should not used adjacent to or stacked with other equipment. In 

case adjacent or stacked use is necessary. The medical device should be observed to 
verify normal operation in the configuration in which it will be used.

DEVICE OVERVIEW

PART NAMES AND PRODUCT COMPONENTS

UNIT DISPLAY

4 AAA “LR03” (1.5V)

Alkaline Batteries

Arm cuff with tube

Month / Date

Hour : Minute

Systolic pressure

BP category indicator

Excessive body

motion detector

Cuff fitness detection

Diastolic pressure

Average of last 3 measurements

Blood pressure unit

Low battery symbol

Pulse symbol

Heart rate detector

Heart rate

Arm cuff hole

Set button

Memory

button

5 V 1A AC/DC

adapter (optional)

LCD Display

BP Category 

indicator

START / STOP button

Summary of Contents for 16994

Page 1: ...1 Upper Arm Blood Pressure Monitor with Voice Broadcast Technology Instruction Manual Model HL858A2 LT Item 16994 Manual Version 001 Issue Date XX ...

Page 2: ...curate idea of your blood pressure MEASUREMENT METHOD HL858A2 LTAutomatic Upper Arm Blood Pressure Monitor measures blood pressure and heart rate by oscillometric method meaning the fluctuations in pressure are measured Once the cuff is wrapped around your upper arm just turn on the monitor and inflation automatically starts The inflation of the cuff creates pressure around the arteries inside upp...

Page 3: ...osis diabetes liver disease kidney disease severe hypertension peripheral circulation please consult your healthcare professional before using the device Blood pressure measurements taken with this device are equivalent to those obtained by a trained observer using the cuff stethoscope auscultation method and are within the accuracy limits prescribed by the Standard of EN 1060 4 If the cuff is wor...

Page 4: ...perly BP Category Indicator The arrowhead points out the specific BP Category that your measurement reading fits in Average of Last 3 Measurements ThissymbolappearswhenLCDdisplaysaverage value of last3readings IRREGULAR HEARTBEAT DETECTOR The symbol will appear on screen indicating a certain heartbeat irregularity was detected during measurement The heartbeat rhythm that is more than or less than ...

Page 5: ... Insert 4 new AAA 1 5 V LR03 alkaline batteries into the compartment as shown Make sure the polazrities and align with the symbols inside the compartment 3 Replace the batteries when The low battery icon appears The display is dim or does not turn on Do not mix new and used batteries Do not mix alkaline standard carbon zinc or rechargeable cadmium batteries Such action may shorten the battery life...

Page 6: ...uff inanyway MEMORY FUNCTION 1 Themonitorfeaturesmemorystoragewithdateandtimestampsfortwo 2 users saving 120recordsperuser 240total 2 Aftereachmeasurement thesystolicanddiastolicpressure heartrateandBPCategory Indicator IrregularHeartbeatDetectorandExcessivebodymotiondetector if any withthe dateandtimewillbeautomaticallystored Eachnewreadingwillreplacetheoldest TAKING THE MEASUREMENT 1 With the cu...

Page 7: ...ol The cuff was wrapped incorrectly for example too loosely or too tightly Please reference applying the Cuff section to wrap the cuff correctly Note If EP appears on the display just return the device to your local distributor or importer RECALLING DATA 1 Press buttontoselectUser1or2 2 PressM buttontoenterMemoryMode If thereisnodatastored nothing exceptmonth date andtime willappearonthedisplay If...

Page 8: ...hthelimitsforaClassBdigital device pursuanttoPart15of theFCCRules Theselimitsaredesignedtoprovidereasonable protectionagainstharmfulinterferenceinaresidentialinstallation Thisequipmentgenerates usesandcanradiateradiofrequencyenergyand if notinstalledandusedinaccordancewith theinstructions maycauseharmfulinterferencetoradiocommunications However there isnoguaranteethatinterferencewillnotoccurinapar...

Page 9: ...15kV air discharge In the case of air discharge testing the climatic conditions shall be within the following ranges AmbientTemperature 15 C 35 C Relative Humidity 30 60 Power frequency 50 or 60Hz magnetic eld IEC 61000 4 8 30A m 50 or 60Hz 30A m 50 or 60Hz Powerfrequency magnetic eldsshouldbeatlevels characteristicof atypical locationinatypicalcommercial orhospitalenvironment Electrical fast tran...

Page 10: ...ed by an electromagnetic site survey a should be less than the compliance level in each frequency range b Interference may occur in the vicinity of equipment marked with the following symbol NOTE 1 At 80MHz and 800MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures object...

Page 11: ...399 8 30 am 5 00 pm EST Monday Friday or contact us at info stareliteinc com Our customer service will be happy to assist you 2021 Sunbeam Products Inc All rights reserved Distributed by Star Elite Inc Montreal Canada H3B 3X9 SE005 080621 Upper Arm Blood Pressure Monitor Model HL858A2 LT Printed in China ...

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