7E Wellness MYOLIFT MD User manual

WELLNESS
MYO MDLIFTTM
Operations Manual
Master Device

©2020 7E Wellness Corporation l All Rights Reserved
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MyoLift MD Operations Manual
No portion of this manual may be produced or transmitted in any form or by
any means, electronic or mechanical, including photocopying and recording,
without the written permission by an authorized 7E Corporate Ofcer.
MYO MD OPERATIONS MANUAL
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LIFT

Table of
Contents
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INSTRUCTIONS FOR THE USER OF MYOLIFT MD
INTRODUCTION
ACCESSORIES
TECHNICAL SPECIFICATIONS
INSTALLATION
CONTROL & FUNCTIONS
HOW TO OPERATE
CHANGE TIMER
TROUBLESHOOTING
MAINTENANCE
WARRANTY
01
05
07
08
09
14
17
19
23
24
25
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MyoLift MD Master Device | Operations Manual

General Safety Information
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The MyoLift MD is a FDA cleared Microcurrent device for the estheticians and
medical elds. It is the responsibility of all users to read this operations manual
thoroughly before using the device. It is unsafe to operate without thorough
comprehension of the device. Proper handling and precautions of the device is
detailed with step-by-step instructions on the following pages.
CAUTION: Only a licensed professional or a supervised technically trained
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individual are permitted to operate the MyoLift MD.
Improper handling or use of the device may result in serious injury.
Do not operate this unit in an environment where other devices are being
used that intentionally radiate electromagnetic energy in an unshielded
manner.
The microcurrent device should be routinely checked before each use to
determine that all controls function normally. Pay close attention to the
intensity control so that they are properly adjusted and the power output
mode is in a stable manner. Determine that the procedure time control
actually terminates the power output when the timer reaches zero.
Do not use sharp objects such as a pencil point or ballpoint pen to operate
the button on the touch screen.
This unit should be operated in temperatures between 17°C and 38°C,
transported and stored in temperatures between - 30°C and +60°C, with
relative humidity ranges from 30% to 60%.
Handle the double-tipped probes applicators with care. Inappropriate
handling may adversely affect its characteristics.
Before each use, inspect the double-tipped probes for cracks or other
abnormalities, which may allow the ingress of conductive uid.
Inspect all cables before each use for any frays or cut wires.
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The MyoLift MD system is not designed to prevent the ingress of water or
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INSTRUCTIONS FOR THE USER OF MYOLIFT MD MASTER DEVICE
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liquid. Ingress of water and liquid could cause malfunction of internal
components of the system and, therefore, create a risk of injury to the user.
To ensure the device is grounded, connect the device only to an electrical
service receptacle which conforms to the applicable national and local
electrical codes.
Potential adverse reactions may include, but are not limited to: probes
burns, skin irritation or redness. Hypersensitivity to brass may cause an allergic
reaction.
Battery Information
Danger
Batteries contain Class E corrosive materials. In the event of battery cell
rupture or leaks, wear neoprene or natural rubber gloves while handling
the battery pack. Contents of a ruptured or leaking battery can cause
respiratory irritation.
Contents of cell coming in contact with skin may result in irritation or
chemical burn.
Under NO circumstances, shall the battery pack or cells be opened at any
time.
Change the battery pack according to the instructions presented in this
manual.
Never attempt to charge the battery pack with any other charging
mechanism.
Do not reverse the polarity of the battery pack. Doing so can increase the
individual cell temperature and cause cell rupture or leakage.
Never dispose a battery pack in a re.
Never short circuit the battery.
The battery may explode, ignite, leak or get hot causing serious personal
injury.
Dispose of battery according to national and local codes & regulations.
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Indication for Use
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MYOLIFT MD is indicated to be used as microcurrent for:
Facial toning and rming;
Detoxication;
Edema Reduction;
Tightening and Toning of the neck and facial skin.
This device is not designed to be used on any other body part.
Contraindications
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The MYOLIFT MD should be applied only to healthy intact skin. All medical
conditions should be consulted and advised by a medical professional prior to
undergoing any microcurrent therapy. Use of device is contradicted for:
Pregnancy;
Swollen areas;
Infected and/or inamed areas;
Skin eruptions;
Skin that lack normal sensation;
Epilepsy-seizures;
Surgical implants in the facial areas;
Pacemaker;
Recent facial surgery;
Any active cancer;
Heart disease;
Irregular heart rate.
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Precautions
Headache and other painful sensation have been reported during or
following electrical stimulation to the face. Lowering the intensity may
reduce or eliminate these sensations.
Adverse Reaction
Skin irritations and burns under the probes are possible.
Some individuals may experience skin irritation or hypersensitivity due to the
electrical stimulation or electrical conductive medium. This irritation can
usually be reduced by using an alternative conductive medium.
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Overview
MYOLIFT MD is a FDA-cleared anti-aging device that is safe and easy-to-use for
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facial therapy. The device is designed to diminish wrinkles, tone the skin, re-
educate the muscles, improve the skin's elasticity, minimize ne lines, reduce
redness and broken veins, and destroy pore-clogging bacteria. The unique
double-tipped probes have been designed for optimal contact for facial
structures of all shapes and sizes. With electrical current, which continually
alternates between the positive and negative spheres, it is guaranteed to
provide the optium current needed for each individual.
For sufcient conductivity of the device, a conductive gel is utilized. Therefore,
it is very important to apply 7E Conductive Tx Gel to the skin area to be treated
prior to the application of the treatment. The probes glide over the skin, following
the natural contours of face, for an instant and visible facelift.
Introduction to Microcurrent
The microcurrent facial therapy is one of the latest procedures in anti-aging
protocols and is a non-invasive, comfortable alternative to facial surgery, Botox
and other anti-aging modalities. The microcurrent facial can take years off the
face and neck, with no risk or side effects and with rapid and lasting results.
Microcurrent therapies constitutes the delivery of tiny electrical impulses which
mirror the body's own natural bioelectrical eld. The low-level waveform shaped
electrical impulses are transmitted through double-tipped probes with the aid
of a water-based conductive gel.
Microcurrent facial therapy involves gentle electrical current re-education to
the underlying muscles and improves circulation, texture, tone, and minimizes
ne lines.
In most cases, treatment is virtually sub-sensory and a slight electrical tingling
sensation may be felt by the client.
INTRODUCTION
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Features
Non Invasive;
Progressive not Aggressive;
Anti-aging benets without down time;
Results are cumulative;
FDA cleared over the counter microcurrent device;
Touch screen: simple one touch selection of stimulating programs.
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MYOLIFT MD comes with a complete set of accessories needed for the
treatment. List of accessories is as follows:
Classic Applicator Probes
Adaptor with AC Cord
INPUT: 100-240V AC, 50/60Hz
OUTPUT: 24V DC (02.5A)
Operations Manual
Conductivity Tx Gel
Particulars
S.No. Quantity
1
1
1
1
1
2
3
4
ACCESSORIES
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Device Specication
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Power (MYOLIFT MD Unit)
Input
Electric Class
System Specication
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Length MYOLIFT MD Unit
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Width MYOLIFT MD Unit
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Height MYOLIFT MD Unit
Standard Weight
Electrical Type
Microcurrent
Operating Temperature
Storage Temperature
+24Volts DC, 2.5A
Class II
365mm
325mm
365mm
Approx 3.5 kg (5.5lbs)
TYPE BF
Between 17°C to 38°C
Between -30°C to 60°C
TECHNICAL SPECIFICATIONS
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Starting the Device
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Keep the MYOLIFT MD Master Device on a stable surface.
Connect the adaptor's AC Cord into a grounded wall outlet that has 110-220
VAC,50/60Hz. Your power supply must match the voltage requirements.
To open the back cover, turn the device so the back is in view.
To open, pull the cover up and out from bottom side.
INSTALLATION
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The USB Connectors are located on the back side of the Enclosure
Insert adaptor's pin into DC Adaptor Power Input on the back of the device.
Press the Rocker Switch to Switch ON on the side of the device.
If the device is being operated on battery, rst press the Rocker Switch,
followed by the Power Button to Switch ON the device.
DC Input Socket
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Remove the Battery by unplugging the Connector
Replacement of Battery
Ensure the device is unplugged.
Unscrew Battery Cover located on the bottom of the device with a
screwdriver as shown.
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Replace the Battery pack
Insert Battery Connector
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Tighten the battery cover with screwdriver properly
WARNING: Battery should be as per manufacturer specications
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Device Description
As we rotate the Intensity Control Knob to the right, the intensity increases and
is displayed on the screen.
ON/OFF Switch
Timer and Intensity
Control Knob
LCD Display
USB Connectors
(Not for User)
DC Input
Socket
DC Adaptor
Power Input
Back View of Device
Front View of Device
CONTROL AND FUNCTIONS
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LCD Screen Description
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MYOLIFT MD is an innovative touch screen desktop device providing
microcurrent stimulation through probes.
When the “READY”
icon is Red, this
indicates that the
microcurrent
output is ready
for treatment.
Intensity Selected Button
Pause Button
When the
“RUNNING” icon
is Green, this
indicates the
output is currently
running and
conducting.
Stop Button
Timer is enabled
now and it is
running.
Running
Ready
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When the
“RUNNING” icon
is Red, this
indicates the
output is currently
running but not
conducting.
Intensity Selected Button
Pause Button
Stop Button
Timer is enabled
now and it is
running.
Running
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