JOHARI DIGITAL Myolift QT User manual

Instruction Manual
Myolift QT

Myolift QT Instruction Manual
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Precautionary instructions
The precautionary instructions found in this section and throughout this manual are
indicated by specific symbols. Understand these symbols and their definitions before
operating this equipment. The definitions of these symbols are as follows:
CAUTION - Text with a “CAUTION” indicator will explain possible Safety infractions that could have the
potentialtocauseminortomoderateinjuryordamagetoequipment.
WARNING - Textwitha “WARNING” indicatorwillexplain possibleSafetyinfractionsthat will
potentiallycauseseriousinjuryandequipmentdamage.
DANGER - Text with a “DANGER” indicator will explain possible safety infractions that are imminently
hazardoussituationsthatwouldresultindeathorseriousinjury.
NOTE: Throughout this manual, “NOTE” may be found. These NOTEs are helpful
information to aid in the particular area or function being described.

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Table of Content
1. INSTRUCTION FOR THE USER.........................................................................................................................4
1.1 WARNINGS .............................................................................................................................................4
1.2 CAUTIONS...............................................................................................................................................4
1.3 CONTRAINDICATION ............................................................................................................................4
1.4 PRECAUTIONS ........................................................................................................................................5
1.5 ADVERSE REACTIONS............................................................................................................................5
2. INTRODUCTION TO MICROCURRENT..........................................................................................................5
3. How Does It Work? .......................................................................................................................................6
4. DEVICE INTRODUCTION ...............................................................................................................................6
5. DESCRIPTION .................................................................................................................................................6
6. Intended Use.................................................................................................................................................7
7. ACCESSORIES................................................................................................................................................7
8. SPECIFICATION..............................................................................................................................................7
8.1 DEVICE SPECIFICATIONS.......................................................................................................................7
8.2 TECHNICAL SPECIFICATIONS................................................................................................................8
8.3 GUIDANCE AND MANUFACTURIN'S DECLARATION..........................................................................8
9. CONTROLS & FUNCTIONS ..........................................................................................................................11
10. How to Operate Device........................................................................................................................12
10.1 DEVICE ON...........................................................................................................................................12
10.2 HOW TO ESTABLISH CREDENTIAL WITH APP ......................................................................................12
10.3 HOW TO CONNECT THE DEVICE WITH MOBILE ................................................................................14
10.4 DEVICE OPERATE RUN TIME................................................................................................................14
11. Applicator Overview..............................................................................................................................15
12. Device Operation Setting .....................................................................................................................15
12.1 FOR TREATING EYE AREA AND LIP AREA...........................................................................................15
12.2 FOR TREATING FACE LIFT.....................................................................................................................16
12.3 TREATING YOUR OWN TREATMENT ....................................................................................................17
13. DEVICe TREATMENT ................................................................................................................................17
14. TROUBLESHOOTING ................................................................................................................................18
15. MAINTENANCE ........................................................................................................................................18
15.1 CLEANING ............................................................................................................................................18
15.2 STORAGE ..............................................................................................................................................19
15.3 LIP & EYE MASK CABLES......................................................................................................................19
15.4 CARE FOR LIP & EYE mask..................................................................................................................19
15.5 SKIN CARE ............................................................................................................................................19

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16. WARRANTY...............................................................................................................................................19
16.1. WARRANTY COVERAGE...........................................................................................................19
16.2. WARRANTY DISCLAIMERS.........................................................................................................20
16.3. LEGAL REMEDIES .......................................................................................................................20
16.4. WARRANTY PERFORMANCE ....................................................................................................20
16.5. CUSTOMER SERVICE..................................................................................................................20
16.6. OUT OF WARRANTY SERVICE ...................................................................................................20

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1. INSTRUCTION FOR THE USER
1.1 WARNINGS
• Do not use over swollen, infected, or inflamed areas or skin eruptions, e.g., phlebitis, thrombophlebitis, broken
capillaries, varicose veins etc.
• Do not use in the eye area (circular muscle within the orbital rim), on the temples, on the mid-line of the neck
(bone of neck) or in the chest or groin area.
• Do not apply stimulation across your chest as the introduction of electrical current into the chest may cause
rhythmic disturbances to your heart, which could be lethal.
• Do not use while driving, operating machinery or during any activity in which involuntary muscle contractions
may put the user at undue risk of injury.
• Do not use the device when it is plugged in.
• Use of controls or adjustments, or the performance of procedures other than those specified herein, may result
in injury.
• Keep the device away from water (including baths, showers, and sinks).
• If the device begins to overheat, turn off immediately.
• Stop using the device immediately if you suspect the device to be malfunctioning, or not operating properly.
• Do not disassemble the device as this may cause damage, malfunction, electrical shock, fire or injury. There are
no user-serviceable parts inside the device.
1.2 CAUTIONS
• Not for patients with suspected or diagnosed heart problems.
• Not for patients with suspected or diagnosed epilepsy.
• Not to use with condition when there is a tendency to haemorrhage following acute trauma or fracture.
• Not use over areas of the skin which lack normal sensation.
1.3 CONTRAINDICATION
The Myolift QT Microcurrent device are contraindicated for the following health conditions:
Do not use:
• If you have a history of epilepsy or seizures.
• If you have had a recent facial surgery or other surgical procedure — consult with your doctor.
• If you have an electronic implanted device such as a defibrillator, neurostimulator, pacemaker or ECG Monitor.
If you use a body-worn medical device, such as an insulin pump consult with your doctor prior to use.
• If you have any active cancer or over any suspicious or cancerous lesion - consult your doctor.
• If you are pregnant.
• On infants and children below the age of 18, and keep device and attachments out of the reach of children.
• If you have Cochlear (ear) implants.
• If you have any Heart conditions or diabetes – consult your doctor.

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Always seek the advice of your physician or other qualified health provider with any questions you may have
regarding the medical condition.
1.4 PRECAUTIONS
The QT device is designed for cosmetic use only and for individuals in good health. If this is not the case for you,
please consult with your doctor before use.
• When you use the device and in between, you feel any discomfort stop the device immediately.
• If you suspect that you have had any side effect on the skin by using the device, consult with your doctor
immediately.
• A slight tingling sensation may occur while using the device. Lowering the intensity may reduce or eliminate
this sensation.
• There may be a perception of flashing lights during the use of your device, resulting from the stimulation of
your optic nerve. If you notice this condition constantly without the use of your device, consult with your doctor.
• When you use the device the electronic monitoring equipment’s, such as ECG monitors and ECG alarms, may
not operate properly.
•Do not store the device in the sunlight or on a hot surface. High temperatures may be damaging the device.
• The device should be operated, transported and stored in the manner specified in this manual.
1.5 ADVERSE REACTIONS
• Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical
conductive medium. The irritation can usually be reduced by using an alternate conductive medium.
• Skin irritation and burns beneath the applicator may be caused by use of other powered muscle stimulators. If
you experience skin irritation or burning, discontinue the use of the device immediately.
• If you experience a persistent headache and/or other persistent painful sensations during the use of the device,
you should stop using the device and consult with your doctor.
2. INTRODUCTION TO MICROCURRENT
Non-invasive facial treatments have grown in popularity over the last 20 years because of their results and ease-
of-use in the day & medical spas. Microcurrent, for the face, is another example of a procedure that began as a
medical treatment but, has now been adapted for use in the cosmetic marketplace. It is the only effective
aesthetic treatment available for facial toning and long-lasting results without the aid of a medical device.
The Myolift QT skin treatment uses microcurrent technology. The use of microcurrent treatments, in your skin
therapy regimen, will establish visible results. This gentle, non-aggressive, non-invasive, and progressive
treatment results in skin tightening, toning and firming. In fact, the results from microcurrent facial toning are so
dramatic that they are often referred to as "non-surgical facelifts.
With age, the muscles lose ATP (Adenosine Triphosphate) which is the energy of the skin cells and muscle tissue.
The skin starts to fall and expression lines begin to develop, as the furrow between the eyebrows. On the other
hand, the muscles on our face that are not used often begin to atrophy, which leads to sagging. Sagging around
the jawlines, chins, and neck are some of the examples where muscle definition is lost as we age. Microcurrent
is considered to be an all-natural solution to anti-aging.

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3. HOW DOES IT WORK?
The Myolift QT devices use low-levels of safe, painless electrical impulses to the muscles in the face and neck.
The overly-tightened muscles relax and under-worked muscles regain their strength. In essence, microcurrent
facial toning re-educates the facial muscles and restores them back almost to their original shape. When this
happens the visible results are quite dramatic and the face is lifted, firmed, and toned back to a much more
youthful appearance. At the same time, the microcurrent improves circulation that stimulates the production of
collagen, improves tone and texture, and improves or eliminates fine lines.
Myolift QT facial toning is cumulative, which means that the more treatments the client has, the more
improvement they will see in their face and for a longer period of time.
Myolift QT is for facial lifting, tightening, and toning is a great alternative to a facelift since it is non-invasive, does
not require any recovery time, gives instant results, and does not have the same potential for harmful
complications as surgery does.
4. DEVICE INTRODUCTION
The Myolift QT is a Microcurrent, handheld, and mobile application-based device, and easy to operate. The
application is used in this device to support both the type of users (iPhone®/Android™). The User has to download
the application via Google Play™ store (Android) /App Store® (iOS) and connect the device via Bluetooth of their
phone and make their profiles accordingly. Its outer case is made up of thermoplastic resin. The device comes
with an external Power Supply to recharge the lithium-ion battery of the device when not in use. The user will
charge the device via wall adaptor. The device is automatically closed if it is not connected via Bluetooth or not
operated for more than 10 seconds.
5. DESCRIPTION
The purpose of this device is for lifting and toning the face and neck muscles. It is a battery-powered device used
with conductive gel. The conductive gel is used to reduce the impedance between the lip and eye mask and the
skin of the user.
In Myolift QT there is one channel and two output ports. One output through the applicator ball and another
output through the lead wire via the USB port connected through the charging jacking point.
The Lead wire is connected to the device via C type connector. There are lip and eye mask that will connect
through the lead wire to give skin treatment to the user.
The round shape applicator balls made up of stainless steel in this device are designed to gently roll over the skin
to deliver low-level electrical impulses in the face and neck. This device delivers approximately maximum 310
microamperes and low 160 microampere current.
Note: Both the output ports will not work at the same time.

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This device gives the user a unique combination of erases and educates waveforms, due to that the user will get
an effective skincare treatment. This skin treatment reprograms the muscle into a relaxing state to lengthen the
muscle and minimize the fine lines and wrinkles on the skin and gives the user a glowing face.
There are three different LEDs on the device as below:
•Blue: Indicates the device is ON/OFF (Blink) and when the device is connected with Bluetooth (Steady light).
•Red: Indicates the device battery is low.
•Green: Indicates that the device is charging up. And it will show the intensity (Low or high).
Note: - At the time of treatment steady green light will be shown on device.
6. INTENDED USE
The intended use of the device for face and neck muscle stimulation for cosmetic purposes.
7. ACCESSORIES
Myolift QT comes with the necessary components. Below is a list of items that are included:
S. No.
Particular
Quantity
1
User Manual
1
2
Lead Wire with C type connector 1.5 Meter
1
3
Eye mask
1
4
Lip mask
1
8. SPECIFICATION
8.1 DEVICE SPECIFICATIONS
Length : 168mm
Width : 39.7mm
Height : 46.4mm
Net Weight : Approx. 94 gram
Power Input : 110 - 220 VAC, 50/60 Hz
Electrical Class : CLASS II
Electrotherapy Electrical Class : TYPE BF
Operating Temperatures : Between 0°C to +40°C
Storage Temperatures : Between -30°C to +60°C

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8.2 TECHNICAL SPECIFICATIONS
Antenna Specification
•Maximum Transmitted Power (dBm) - 0
•Average Gain (dBi typ.) - -0.5
8.3 GUIDANCE AND MANUFACTURIN'S DECLARATION
ELECTROMAGNETIC COMPATIBILITY
Myolift QT complies with the requirements of IEC 60601-1-2:2014 (EMC Collateral standard) including the
E-field susceptibility requirements at a 3 V/m, at frequencies from 80 MHz to 2.7 GHz. However, even at
this level of device immunity, certain transmitting devices (cellular phones, two-way radios, cordless
phones, paging transmitters, RFID devices etc.) emit radio frequencies that could interrupt equipment
operation if operated in a range too close to the equipment. User should be aware of possible radio
frequency interference if hand held device is operated in close proximity to the equipment. Portable and
mobile RF communications equipment may affect the normal function of the Myolift QT.
Do not use cables or accessories other than those provided with the Myolift QT system, as this may result
in increased electromagnetic emissions or decreased immunity to such emissions.
If the Myolift QT system is used adjacent to or stacked with other equipment, observe and verify normal
operation of the system in the configuration in which it will be used prior to using it.
Hand held and mobile RF communications equipment may affect the normal function of the
Myolift QT.
Do not use cables or accessories other than those provided with the Myolift QT system, as this
may result in increased electromagnetic emissions or decreased immunity to such emissions.
If the Myolift QT system is used adjacent to or stacked with other equipment, observe and
verify normal operation of the system in the configuration in which it will be used prior to using
it.
Test
Electrical Safety environment –guidance
IEC 60601-1:2005+AMD1:2012
Medical Electrical Equipment Safety standards,
IEC 60601-2-10:2012+AMD1:2016
Part 2: Particular requirements for the safety of nerve and muscle
stimulators
IEC 60601-1-11:2015
Part 1-11: General requirements for basic safety and essential
performance —Collateral standard: Requirements for medical
electrical equipment and medical electrical systems used in the
home healthcare environment
Guidance and manufacturing's declaration –electromagnetic emissions
Mode
Waveform
Level /Intensity
Pulse Width
Frequency
Output (Vpp)
Educate
Symmetrical
Biphasic Sq.
Wave
Level 1 (Low)
60 m sec
0.9 Hz;
0.08 V
Level 2 (High)
60 m sec
0.694 Hz;
0.155 V
Erase
Level 1 (Low)
400 m sec
0.625 Hz
0.08 V
Level 2 (High)
400 m sec
0.625 Hz
0.155 V

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The Model Myolift QT is intended for use in the electromagnetic environment specified below. The
customer or the user of the Model Myolift QT should assure that it is used in such an environment
Emission test
Compliance
Electromagnetic environment –guidance
RF emission CISPR 11
Group 1
The Model Myolift QT uses RF energy only for its
internal function. Therefore its RF emissions are very
low and are not likely to cause ant interference in
nearby electronic equipment.
RF emissions CISPR 11
Class A
The Model Myolift QT is suitable for use in all
establishments, including domestic establishment and
those directly connected to the public low –voltage
power supply network that supplies building used for
domestic purposes.
Harmonic emission IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions IEC61000-3-3
Complies
Radiated RF
IEC 61000-4-3
Group 1
Guidance and manufacturing's declaration –electromagnetic Immunity
The Model Myolift QT is tended for use in the electromagnetic environment specified below. The
customer or the user of the model Myolift QT 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 floors are covered
width synthetic material, the relative
humidity should be at least 30%.
Electric fast transient /
burst IEC 61000-4-4
± 2.0 kV/100 kHz
(AC Power port )
± 2.0 kV/100
kHz (AC Power
port )
Mains power quality should be that
of a typical commercial or hospital
environment
Surge IEC
61000-4-5
0.5, 1 kV (Differential
mode) Line to Line
0.5, 1, 2 kV (Common
mode) Line to Gnd
Phase Angle:
0°,90°,270°
± 1kV differential
mode
± 2kV common
mode
Mains power quality should be that
of a typical commercial or hospital
environment.
Conducted RF
IEC 61000-4-3
ISM band between
0.15 - 80MHz: 6V rms,
ISM band between
0.15 - 80MHz: 6V
rms,
Mains power quality should be that
of a typical commercial or hospital
environment. If the user of the
Model Myolift QT requires
continued operation during power
mains interruptions
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 s
<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 s
Mains power quality should be that
of a typical commercial or hospital
environment. If the user of the Model
Myolift QT requires continued
operation during power mains
interruptions, it is recommended that
the Model Myolift QT be powered
from an uninterruptible power
supply.