HINGMED Q06 User manual

Upper arm blood pressure monitor
User manual
(Apply to：Q06、Q06B)
Edit：2020-11-22
Version: A/0

About this manual
The manual mainly introduces the installation and application method of upper
arm blood pressure monitor.Users should read carefully before application
(include warnings, contraindications and notes).
Manufacturer
Shenzhen Hingmed Medical Instrument Co., Ltd.
Manufacturing address: 4th Floor, Zhonghangfeixiang Building, NO. 371,
Guangshen Road, Baoan District, Shenzhen, People’s Republic of China
Tel: [phone]
Fax: [phone]
Post code: 518102
After-sales service
Company: Shenzhen Hingmed Instruments Co., Ltd.
Address: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road,
Baoan District, Shenzhen, People’s Republic of China
Tel: [phone]
Fax: [phone]
Post code: 518102
European Representative
Company Name:Wellkang Ltd
Company Address: Enterprise Hub, NW Business Complex,
1 Beraghmore Road,Derry, BT48 8SE, Northern Ireland,UK.
Tel: [phone]
Fax: [phone]
Web:www.wellkang.ltd.uk & www.CE-marking.eu
Email: [e-mail]
Version Information
This manual may upgrade due to software upgrading. User will not be notified further.
■ Version: A/0
■ Issue date: Nov. 2020
Software version:V1
Shenzhen Hingmed Medical Instruments Co., Ltd. owns and reserves the copyright.

Table of Content
1.Introduction ..................................................................................................................................................4
1.1product feature ..................................................................................................................................... 4
1.2Safety Instructions ............................................................................................................................... 4
1.3Intended Use ........................................................................................................................................ 4
1.4Important Information ....................................................................................................................... 4
1.5 Consist of blood pressure monitor ................................................................................................ 4
2 Important safety information ........................................................................................................................ 5
2.1Warning ...............................................................................................................................................5
2.2Caution ............................................................................................................................................... 5
3. Product structure and operation principle .....................................................................................................8
3.1The component of product ...................................................................................................................8
3.2Name and description of each part ...................................................................................................... 8
3.3 Display .............................................................................................................................................8
3.4Mark content and meaning ............................................................................................................ 8
4.Blood pressure measurement ....................................................................................................................... 9
4.1prepration ............................................................................................................................................ 9
4.2 Taking a measurement(Apply to Q06B & Q06) ................................................................................9
4.3Taking a measurement by the App (Apply to Q06B) .........................................................................10
6.maintenance ................................................................................................................................................. 11
7.Disposal........................................................................................................................................................12
8、Component replacement list ..................................................................................................................... 12
9、Warranty Card .........................................................................................................................................13
10 EMC information ..................................................................................................................................... 14

1.Introduction
1.1product feature
Thank you for purchasing the HINGMED upper arm blood pressure monitor.This monitor
can be used by multiple users,This blood Pressure monitor use the oscillometric method of
blood pressure measurement.It has some functions that measure the blood pressure and
display the result.When measuring the blood pressure,the user need to wear the cuff on the
upper arm.
1.2Safety Instructions
This instruction manual provides you with important information about the HINGMED upper
arm blood pressure monitor.To ensure the safe and proper use of this monitor,Read and
UNDERSTAND all of these instructions,If you do not understand these instructions or have
any questions,contact [phone] before attempting to use this monitor,For specific information
about your own blood pressure ,consult with your physician.
1.3Intended Use
This device is a digital monitor intended for use in measuring blood pressure(SYS and DIA)
and pulse rate.
Environments of use:home healthcare environment
Patient population:Adult
1.4Important Information
Read the Important safety Information in this instruction manual before using this
monitor.Follow this Instruction manual thoroughly for your safety. Keep for future
reference.For specifies information about your own blood pressure,consult with your
physician.
1.5 Consist of blood pressure monitor
The upper arm blood pressure monitor consist of main body,cuff,USB wire
Note:The cuff do not replace.
1.5.1 Difference of model
model
Bluetooth
Q06
×
Q06B
√
1.5.2 Performance
Item
Type

Model
Q06B /Q06
Measuring method
Oscillometric method
Range
From 0 to 289mmHg
Pulse range
40-200bpm
Resolution ratio
1mmHg
Accuracy
±3mmHg (pulse rate ±3bpm or ±3% whichever is grater)
Power
DC 3.7V Li-ion
Cuff size
22cm-41cm or 22cm-36cm
Size
L:116*W:58*H:17.8
Operating conditions
T: 5 ℃-40 ℃; RH: 10%-95%; non-condensing,atmospheric
pressure(70KPa-106Kpa)
Transport and storage
conditions
under the condition of temperature (-20℃- 55℃), RH (no more than 90%)
non-condensing and atmospheric pressure (70KPa-106Kpa)
Expected service life
Five years
2Important safety information
2.1Warning
Do not service and maintenance while the ME equipment is in use
Do not modify this equipment without authorization of the manufacturer.
Always consult with your doctor.self-diagnosis of measurement results and self-treatment are
dangerous.
People with sever blood flow problems or blood disorders,should consult a doctor before using the
device as cuff inflation can cause internal bleeding.
Do not disassemble the device and arm cuff
*******************************************
* Please do not measure the arm that is being injected with an intravenous drip or a blood
transfusion, otherwise it could cause an accident.
2.2Caution
*The patient is a intended operator
*All of the function of the medical device can safety use.
*Do not use a mobile phone or other devices that emit electromagnetic
fields,near the medical device,this may result in incorrect operation of the
medical device.
* if the device will not be used for three month,please recharge every three
month
*If the device will not be used for six month or more ,please remove the battery.

*please use the adapter which output DC 5V 2A to charge the device
When the device start inflating may have a little uncomfortable.
Do not leave the device unattended with infants or person who can express
their consent.
Do not apply strong shocks and vibrations to or drop the device and arm cuff.
Do not take measurements after bathing,drinking alcohol,smoking,exercising
or eating.
Do not wash the arm cuff or immerse it in water.
Do not connect this device with other device,it maybe cause a potential
damage.
*Three hundreds of discharge cycles after which a rechargeable battery needs to be replaced
**********************************************************
Please use the machine in the following use environment and storage place, if it is stored or
used outside the specified temperature and humidity range (storage conditions: temperature
-20 ℃~ +55 ℃, relative humidity no more than 90%;Operating conditions: Temperature
+5 ℃~ +40 ℃, relative humidity 10%-95%), the system may not achieve the claimed
performance specifications.
* Places that don't splash water
* Do not put in hot, humid, direct sunlight places, places with less dust, do not put in places
containing salt and sulfur, etc.
* Place in a stable place where there is no tilt, vibration, impact (including handling), etc
* Patients with anticoagulants or with blood clotting disorders may get blood clots in the cuff
even if it is worn in the correct position during blood pressure measurements.
* If the cuff fails to inflate within two and a half minutes, instruct the patient to remove the
cuff manually. Prolonged excessive inflation may lead to blood obstruction and make the
patient feel uncomfortable.
* When there is a common arrhythmia, the device fails to meet the claimed performance
requirements
* Any blood pressure measurement is influenced by the subject's posture and his/her physical
condition
* If you move or speak while taking a measurement, your arms are not in the right position,
the machine is not on the level, or the machine shakes
* For accurate measurements, keep your back straight and sit correctly.
Please relax and keep quiet.

* In case of equipment failure, the error code will be displayed in the format of "EC XX", see
the section on Common Failures for details.
* State that the blood pressure measured should be explained by a professional.
The product is not intended for newborns.
*The specifications and labels of this product meet the requirements of EN1060-1 and
EN1060-3
*Frequent inflating can lead to blood clots and discomfort
*Too Frequent measurements may result poor circulation or bruising
*Do not put the cuff over a wound, and it will cause further injury
*If there are arterial or venous shunt tubes on the arm, please follow the doctor's instructions
before use, otherwise it may cause physical discomfort
*People who have had mastectomies may be unwell or have mismeasured results
*Do not use other medical electrical equipment on the blood pressure measuring arm
*Please confirm (for example, by observation of the relevant limb) whether this product is
available No lasting damage to the patient's blood circulation.Suffering from blood
circulation disorder,For patients with blood diseases, please use under the guidance of a
doctor.Acute internal bleeding may result from compression of the arm during measurement.
*While in use with a patient,Do not service and maintain the device.
* The device compliance with IEC 60601-1-2,keep away other HF device.
*Please assure that connect The part’s voltage of input or output compliance with
IEC60601-1 the requirement of safe extra low voltage,and the part of input or output forbid
connecting other device.
* The manufacturer responsible for After service ,the people with unauthorized do not
repair calibration the device.
*the time from switching “ON” until the device is ready for NORMAL USE ,That time less
10s.
*when the ambient temperature is 20 °C ,the time that the device to warm from the
minimum storage temperature between uses until the device is ready for its intend use need
one hour;
*when the ambient temperature is 20 °C,the time that the device to cool from the maximum
storage temperature between uses until the device is ready for its intend use need one hour

*Three hundreds of discharge cycles after which a rechargeable battery needs to be replaced
* Please put the device keep away the children and pet
The list of device that can potentially cause interference problem,eg. Microwave oven;
3. Product structure and operation principle
3.1The component of product
No.
Compment
Count
size
1
Main body
1pcs
2
USB wire
1pcs
1M
3
Cuff
1pcs
22-41cm or 22-36cm
4
User Manual
1pcs
3.2Name and description of each part
3.3 Display
3.4Mark content and meaning
NO.
description
NO.
description
A
Cuff
C
Start/Stop Button
B
USB inlet
D &E
The button of View the record
Symbol
Description
Symbol
Description
A
B
C
D
E
Systolic pressure monitor
diastolic pressure monitor
Bluetooth function
Battery indicator
Pulse rate

4.Blood pressure measurement
4.1prepration
(1) Sit on a chair with your feet flat on the floor,place your arm on the
table so the cuff level of your heart,keep still and do not talk during
measurement.
(2) Please press the "start/stop" button to wake up the device and
the time is displayed .
(3) Wear the cuff ,refer to the right picture.
4.2 Taking a measurement(Apply to Q06B & Q06)
CF type applied part
Series number
Manufacturer
Valid date
Keep dry
This way up
Fragile
Complying with WEEE
standard
Stacking limit by
number
Temperature limitation
Refer to user manual
Date of manufacture
General warning sign
General Prohibition sign
General Mandatory
action sign
IP22
2：protect against solid foreign
Protected against solid foreign
objects of 1 2,5 mm
and greater
2：Protection against vertically
falling water drops when
Enclosure tilted up to 15°
Atmospheric pressure
limitation

(1)press the "start/stop" button,the cuff start to inflate automatically,increasing number on the
display ,remain still and do not move your arm and until the measurement process is
complete.
(2) When the measurement is complete,your cuff completely defeat, your blood pressure and
pulse rate are displayed and broadcast.
4.3Taking a measurement by the App (Apply to Q06B)
(1)Login the APP,press the "start/stop" button on the Main page,,the cuff start to inflate
automatically,increasing number on the display and APP ,remain still and do not move your
arm and until the measurement process is complete.
(2)When the measurement is complete,your cuff completely defeat, your blood pressure and
pulse rate are broadcast and displayed on the device and the APP .
Notice: To stop the inflation or measurement push the Start/Stop button,the monitor will stop
inflating and start deflating ,and will turn off .
5.Error message
When an error occurs, the screen will display the following error code:
Error code
Cause
Remedy
EC01
Cuff not applied correctly
Remove the cuff ,read “taking a measurement”
Wait 2-3minutes
Take another measurement
EC04
Weak signals, which can be measured when
the pulse is too weak or when the cuff is too
loose
Make sure that the measured part is in good
contact with the cuff and that the arm
circumference is within the measured range
EC06
Excessive motion may be measured when
the signal contains motion spurious or too
much interference
Pay attention to avoid talking, fidgeting and
measuring again during measurement
EC07
Overpressure was measured, with cuff
pressure exceeding 290mmHg in adult
mode
Wait 2-3minutes
Take another measurement

6.maintenance
************************************************************
Note: * Sphygmomanometers and accessories need not be sterilized, but should be kept clean.
If there is pollution, it should be promptly cleaned before disinfection.
*Suggestion that clean the device by every month;
To protect the device from damage,please observe the following:
Do not subject the device to extreme temperature,humidity,moisture or direct sunlight.
Do not wash the arm cuff or immerse it in water.
The arm cuff of the device is not detachable
7.4.7(1) Before cleaning the sphygmomanometer (include cuff), it is necessary to turn off the
device
(2) Do not use volatile liquids to clean the main body,the main body should be clean with a
soft, dry cloth.
(3) use a soft, moistened cloth and soap to clean the cuff
(4) Do not carryout repair the device by yourself,if there is any breakdown ,please conduct
with your local authorised distributor or dealer .
Calibration
EC09
The measurement timeout, in adult mode,
exceeded 120 seconds
Wait 2-3minutes
Take another measurement
EC 11
Push the “start/stop” button to Stop
measuring
Push the “start/stop”button to take another
measurement
EC26
Battery is worn
Please recharge
If there is other error code ,please contact customer service.

The accuracy of this blood pressure monitor has been carefully tested and is designed for a
long service life.
It is generally recommend to have the device inspected every two years to ensure correct
functioning and accuracy.please consult your local authorised distributor or dealer.
Replace the battery
-Remove the setting screw as shown on the right
- Use the new battery to replace the old battery
-Place the positive electrode of the lithium battery in the battery slot consistent with the
positive electrode of the shell material display
7.Disposal
Disposal of this product and used batteries should be carried out in accordance with the
national regulations for the disposal of electronic products
8、Component replacement list
Caution:Please use the component supply by the manufacture ,otherwise might cause the
measurement error or injury
NO.
Component
Type
1
Battery
1020mAh，3.7V

9、Warranty Card
Warranty Card
Product model and SN code：Name：
Purchase Date：Address：
Dealer：Tel：
Postal Code：Dealer stamp：
The limited liability of guarantee
Hingmed provides the original purchaser the following limited warranty from the date of invoicing.
upper arm blood pressure monitor………………………………………… 12 months
Hingmed warrants each monitor to be free from defects in material and workmanship. Liability
under this warranty covers servicing of the returning monitor from customer prepaying to the
prospective factory (depending on location). Hingmed will repair any defective component(s) or
part(s) during the period of this limited warranty.
Should a defect become apparent, the original purchaser should notify Hingmed of the suspected
defect; the monitor should be carefully packaged and be prepaid shipped to:
Shenzhen Hingmed Medical Instrument Co., Ltd.
Address: 4th Floor, Zhonghangfeixiang Building, NO. 371, Guangshen Road, Bao’an District,
Shenzhen, People’s Republic of China
Tel: [phone]
Fax: [phone]
Postal code: 518102
Email: [e-mail]
The monitor will be repaired as soon as possible, and be returned by the same shipping method
as received by the factory if it is prepaid.
This limited warranty is invalid if the monitor has been damaged due to accidents, misuse,
negligence, or maintained by any person not authorized by Hingmed.
This limited warranty contains the entire obligations of Hingmed, exclude other expressed, implied
or regulated warranties. Representatives or employees without authorized by Hingmed will
assume any further liability or grant any further warranties except as set herein.
7.9.3.3*Hingmed will make available on request circuit diagrams, component part lists,
descriptions, calibration instructions, or other information that will assist service personnel to
repair those parts of ME equipment that are designated by Hingmed as repairable by after sale
SERVICE PERSONNEL .

10 EMC information
This product needs special precautions regarding EMC and needs to be installed and put into
service according to the EMC information provided, and this unit can be affected by portable and
mobile RF communications equipment.
Do not use a mobile phone or other devices that emit electromagnetic fields, near the unit.
This may result in incorrect operation of the unit.
Caution: This unit has been thoroughly tested and inspected to assure proper performance
and operation!
Caution: this machine should not be used adjacent to or stacked with other equipment and
that if adjacent or stacked use is necessary, this machine should be observed to verify normal
operation in the configuration in which it will be used
Guidance and manufacture’s declaration – electromagnetic emission
the device is intended for use in the electromagnetic environment specified below. The customer of the
user of the device should assure that it is used in such an environment.
Emission test
Compliance
Electromagnetic environment – guidance
RF emissions
CISPR 11
Group 1
the device use RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not likely to
cause any interference in nearby electronic
equipment.
RF emission
CISPR 11
Class B
the device is suitable for use in all
establishments, other than domestic and
those directly connected to the public
low-voltage power supply network that
supplies buildings used for domestic
purposes.
Harmonic emissions
IEC 61000-3-2
Not applicable
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Not applicable

Guidance and manufacture’s declaration – electromagnetic immunity
the device is intended for use in the electromagnetic environment specified below. The customer or the user ofdevice
should assure that it is used in such an environment.
Immunity test
IEC 60601 test level
Compliance level
Electromagnetic environment -
guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±8 kV contact
±15 kV air
±8 kV contact
±15 kV air
Floors should be wood, concrete
or ceramic tile. If floor are covered
with synthetic material, the
relative humidity should be at
least 30%.
Electrical fast
transient/burst
IEC 61000-4-4
±2 kV for power supply
lines
±1 kV for input/output
lines
Not applicable
Mains power quality should be
that of a typical commercial or
hospital environment.
Surge
IEC 61000-4-5
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
Not applicable
Mains power quality should be
that of a typical commercial or
hospital environment.
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
IEC 61000-4-11
<5% UT
(>95% dip in UT)
for 0.5 cycle
40% UT
(60% dip in UT)
for 5 cycles
70% UT
(30% dip in UT)
for 25 cycles
<5% UT
(>95% dip in UT)
for 5 sec
Not applicable
Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the device requires continued
operation during power mains
interruptions, it is recommended
that the device be powered from
an uninterruptible power supply or
a battery.
Power frequency
(50Hz/60Hz)
magnetic field IEC
61000-4-8
3 A/m
3 A/m
Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital

environment.
NOTE UTis the a.c. mains voltage prior to application of the test level.
Guidance and manufacture’s declaration – electromagnetic immunity
The device is intended for use in the electromagnetic environment specified below. The
customer or the user of the device should assure that it is used in such an environment.
Immunity
test
IEC 60601
test level
Compliance
level
Electromagnetic environment - guidance
Conducted
RF
IEC
61000-4-6
3 Vrms
150 kHz to 80
MHz
Not
applicable
Portable and mobile RF communications
equipment should be used no closer to any part of
the device, including cables, than the
recommended separation distance calculated from
the equation applicable to the frequency of the
transmitter.
Recommended separation distance
Where Pis the maximum output power rating of
the transmitter in watts (W) according to the
transmitter manufacturer and dis the
recommended separation distance in metres (m).
Field strengths from fixed RF transmitters, as
determined 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
Radiated RF
IEC
61000-4-3
3 V/m
80 MHz to 2.5
GHz
3 V/m

marked with the following symbol:
NOTE 1 At 80 MHz and 800 MHz, 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, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones
and land
mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theoretically
with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an
electromagnetic site
survey should be considered. If the measured field strength in the location in which the device is used
exceeds the applicable RF compliance level above, the device should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such as
re-orienting or relocating the device.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
Recommended separation distances between
portable and mobile RF communications equipment and the device .
the device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.
The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the device as
recommended below, according to the maximum output power of the communications equipment.
Rated maximum output
power of transmitter
Separation distance according to frequency of transmitter
(m)

(W)
150 KHz to 80 MHz
80 MHz to 800 MHz
800 MHz to 2.5 GHz
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in
metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for 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, objects and people.