7E Wellness MYOLIFT MD User manual

7e Wellness Corporation,
5858 Dryden Place, #201 Carlsbad, CA 92008
Tel: 888-412-3160, Fax: 858-366-9831
Email: [email protected]
Website: www.7eWellness.com
Version 1.18
WELLNESS
MYO MDLIFTTM
Operations Manual
Master Device

©2017-2018 7E Wellness Corporation l All Rights Reserved
tm
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 corporation ofcer.
MYO MD OPERATIONS MANUAL
TM
LIFT

Table of
Contents
TM
INSTRUCTIONS FOR THE USER OF MYOLIFT MD
INTRODUCTION
ACCESSORIES
TECHNICAL SPECIFICATIONS
INSTALLATION
CONTROL & FUNCTIONS
HOW TO OPERATE
TROUBLESHOOTING
MAINTENANCE
WARRANTY
CHANGE TIMER
01
07
10
12
17
22
26
30
31
32
34
INSTRUCTIONS FOR THE
TM
USER OF MYOLIFT MD
MASTER DEVICE
CHAPTER KEY POINTS
General Safety Information
Battery Information
Indication for use
Contraindications
Precautions
Adverse Reaction
MyoLift MD Master Device | Operations Manual
1
MyoLift MD Master Device | Operations Manual

tm
The MyoLift MD Master Device is an FDA cleared Microcurrent
device for the aesthetics 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 individual are permitted to operate the
tm
MyoLift MD Master Device.
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 radiates electro-
magnetic 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 is that they are properly
adjusted and the power output mode is in a stable manner.
Verify that Also determine that the procedure time control
actually terminate 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
2 3
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 probe electrode with care,
ina ppro pria te hand ling m ay adv erse ly affe ct i t s
characteristics.
Before each use, inspect the double tipped electrode 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.
tm
The MyoLift MD Master Device system is not designated to
prevent the ingress of water or 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 reaction may include, but not limited to:
Electrode burns, skin irritation or redness. Hypersensitivity to
nickel may cause allergic pulmonary asthma.
BATTERY INFORMATION
Danger
Batteries contain Class E corrosive materials. In the event of
battery cell rupture or leaks, wear neoprene or natural rubber
GENERAL SAFETY INFORMATION
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual

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 on 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 of battery pack in the 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
and regulations.
INDICATION FOR USE
TM
MYOLIFT MD is indicated to be used as microcurrent for:
Facial toning and rming.
Detoxication.
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
TM
The MYOLIFT MD should be applied only to healthy intact skin.
All medical conditions such, any severe medical illness should be
consulted & advised by a medical professional prior undergoing
any microcurrent therapy. Use of device is contradicted for:
Pregnancy.
Swollen areas.
Infected and/or inamed areas.
Skin eruptions.
Skin that lack normal sensation.
Epilepsy-seizures.
Surgical implants in the facial areas.
Pace maker or heart rate balancer.
Recent facial surgery.
Cancerous lesions.
Undergoing cancer treatments.
4 5
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual

Severe heart disease.
Irregular hear rate.
Asthma-Flu or upset stomach.
Any other serious illness/disease not yet listed above.
PRECAUTIONS
Caution should be used for patient with suspected or
diagnosed heart problems.
MYOLIFT MD device is designed for use on healthy faces, if
TM
this is not the case for you, please consult your doctor before
use.
Headache and other painful sensation have been reported
during or following electrical stimulation to the head and
face. Lowering the intensity may reduce or eliminate these
sensations.
ADVERSE REACTION
Skin irritation and burn under the probes are possible adverse
reaction.
Some individuals may experience skin irritation or hyper-
sensitivity due to the electrical stimulation or electrical
conductive medium. This irritation can usually be reduced by
using an alternative conductive medium.
6 7
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
INTRODUCTION
CHAPTER KEY POINTS
Overview
Introduction to Microcurrent
Features

OVERVIEW
MYOLIFT MD is, FDA-cleared anti-aging device is safe and easy
TM
to use facial therapy. The device is designed to diminish wrinkles,
tone the skin and re-educate the muscles, improve the skin's
elasticity minimizes ne lines, reduce redness and broken veins,
and destroy pore-clogging bacteria. The unique double tipped
probe hand piece applicator has been designed for optimal
contact for facial structures of all shapes and size. With electrical
current which continually alternate between the positive and
negative spheres, it is guaranteed to provide the optium current
needed for each individual.
For sufcient conductivity of the device, a conductive solution is
utilized. Therefore, it is vitally important to apply 7E conductive gel
to the skin area to be treated prior to the application of the
treatment. The probe sphere is glided over the skin, following the
natural contours of face, for an instant visible face lift.
INTRODUCTION TO MICROCURRENT
The microcurrent facial therapy is one of the latest procedures in
anti- aging protocols and is a non-invasive and comfortable
alternative to facial surgery, Botox, Thermage, dermabrasion,
chemical peels and other anti-aging approaches that either
treat only the local area or are damaging to the skin. The
microcurrent facial can take years off the face and neck, with no
risk or side effects and with rapid and lasting results.
8 9
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
Microcurrent therapies constitutes the delivery of tiny
electrical impulses which mirror the body's own natural bio
electrical eld. The low-level waveform-shaped electrical
impulses are transmitted through dual tipped probes with the
aid of a water-based conductive gel.
Microcurrent facial therapy involves the gentle electrical current
re-educattion to the underlying muscles & improves circulation,
texture, tone, and minimizes ne lines.
In most cases, treatment is virtually sub-sensory, with just a slight
electrical tingling sensation may be felt by the client.
FEATURES
Non Invasive.
Progressive not Aggressive.
Anti-aging benets without down time.
Results are accumulative.
FDA cleared over the counter microcurrent device.
Touch screen: simple one touch selection of stimulating
programs.

ACCESSORIES
10 11
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ACCESSORIES
TM
MYOLIFT MD comes with the complete set of accessories
needed for the treatment. List of accessories is as follow:
Ball Tipped Electrodes
Adaptor with AC Cord
INPUT: 100-240V AC, 50/60Hz
OUTPUT: 24V DC (02.5A)
Operations Manual
Conductivity Treatment Gel
Particulars
S.No. Quantity
1
1
1
1
1
2
3
4

TECHNICAL
SPECIFICATIONS
CHAPTER KEY POINTS
Device Specication
Waveform Specications
12 13
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
DEVICE SPECIFICATION
TM
Power (MYOLIFT MD Unit)
Input
Electric Class
System Specication
TM
Length MYOLIFT MD Unit
TM
Width MYOLIFT MD Unit
TM
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

WAVEFORM SPECIFICATIONS
Waveform
Frequency
Polarity
Max. Intensity
Default Starting Value
Synergic
20Hz
Alternating
800μA (at 500 Ω Load)
300μA
Circulation Mode
Waveform
Frequency
Polarity
Max. Intensity
Default Starting Value
Ramp
300 Hz
Direct
800μA (at 500 Ω Load)
500μA
Lymphatic Drainage
14 15
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
Waveform
Frequency
Polarity
Max. Intensity
Default Starting Value
Square
10Hz
Direct
800μA (at 500 Ω Load)
200μA
Light Lift
Waveform
Frequency
Polarity
Max. Intensity
Default Starting Value
Rectangular
0.8 Hz
Direct
800μA (at 500 Ω Load)
300μA
Deep Lift
Waveform
Frequency
Polarity
Max. Intensity
Default Starting Value
Synergetic
500Hz
Alternating
800μA (at 500 Ω Load)
500μA
Firming Mode
Waveform
Frequency
Max. Intensity
Default Starting Value
Symmetrical Biphasic Square
0.9 Hz
800μA (at 500 Ω Load)
400μA
Educate

Waveform
Frequency
Polarity
Max. Intensity
Default Starting Value
Synergetic
30Hz
Alternating
650μA (at 500 Ω Load)
500μA
Iontophoresis Mode
Waveform
Frequency
Max. Intensity
Default Starting Value
Symmetrical Biphasic Square
0.625 Hz
800μA (at 500 Ω Load)
300μA
Erase
16 17
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
INSTALLATION
CHAPTER KEY POINTS
Starting the Device
Replacement of Battery

STARTING THE DEVICE
TM
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 back cover, turn the device so the back is in view.
To open, pull the cover up and out from bottom side.
The Connectors are located on the back side of the Enclosure
18 19
Insert adaptor's pin into DC input socket on the back of the
device.
Press the Rocker Switch to Switch ON 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.
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual

20 21
Remove the Battery by unplugging the Connector
Replace the Battery pack
Insert Battery Connector
Tighten the battery cover with screwdriver properly
WARNING: Battery should be as per manufactures specications
REPLACEMENT OF BATTERY
Ensure the device is unplugged.
Unscrew Battery Cover located on the bottom of the device
with screwdriver as shown.
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual

DEVICE DESCRIPTION
As we rotate the intensity control Knob, the intensity keeps on
increasing value of which is display on the screen.
ON/OFF Switch
USB
(Not for User)
Microcurrent
Output
Power Button &
Intensity Control
Knob
LCD Display
DC Adaptor
Power Input
CONTROL AND
FUNCTIONS
CHAPTER KEY POINTS
Device Description
LCD Screen Description
22 23
Back View of Device
Front View of Device
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual

LCD SCREEN DESCRIPTION
TM
MYOLIFT MD Master Device is an innovative touch screen
desktop device providing microcurrent stimulation through
probe electrodes.
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 enable
now and it is
running
24 25
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
Running
Intensity
Selected
Button
Pause
Button
When the
“RUNNING” icon
is Red, this
indicates the
output is currently
running but not
conducting
Stop Button
Timer is enable
now and it is
running
Ready
Running

PREPARE SKIN FOR TREATMENT
Remove makeup and jewelry.
Cleanse the face skin with appropriate cleansing product.
Tone the skin using skin toner.
Apply the appropriate 7E Conductivity Tx Gel. With a mask
brush, apply a thick layer all over the face including the neck,
eyebrow and upper lip and apply gel to facial probes
electrodes.
MICROCURRENT TREATMENT
Connect the applicator, AC Cord and switch on the device
using Rocker Switch provided on the left side.
Insert Twin Ball Probe into device’s output plug.
The device will display Home Screen with Facial Therapies,
Setting and Help options as Follow:
26 27
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
HOW TO OPERATE
CHAPTER KEY POINTS
Prepare Skin For Treatment
Microcurrent Treatment

28 29
The device will display the facial therapies page showing
all facial therapies.
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual
Press the Facial Therapies icon.

TROUBLESHOOTING
Observation Possible Cause Remedy
None of the
displays are
lighting up after
switching on
the rocker switch
Internal Error Turn off the rocker
switch and inform
the supplier
Uncomfortable
stimulation
Lack of
conductive gel
Pause the stimula-
tion, Put more
conductive gel
and reposition the
probe electrodes
on the treatment
area. Then restart
treatment
Skin irritation at
probe electrode
placement site
Improper contact Wet or change
the electrode
Sudden high
Intensity while
increasing
intensity level
Increasing too
fast
Increase slowly
giving time for
client to adjust
comfort level
Weak stimulation
or no stimulation
even at maximum
intensity setting
Probe electrode
conduction is low,
lead wire is worn
out or damaged
Change
electrodes.
Change
electrode wires
MAINTENANCE
Cleaning/Sanitizing
Soiled unit is sanitized with an antiseptic
Hands should be sanitized and dry during the operation.
Sanitize the probe and applicator by spraying with antiseptic
on a damp cloth and wipe well.
Warning
Do not pull out hand held applicators from the cables.
All wires and cables should be kept loosely winded or
breakage may occur.
Storage
To keep the device free of dust when not in use, covered the
device with a drape or towel.
Do not store the device in a damp environment such as in
proximity of a facial steamer or hot towel cabi. Dampness will
affect the device and may cause rust.
30 31
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32 33
Warranty Duration:
This product warranty extends to the original consumer/
purchaser of the product. This product is covered by the initial
warranty to the original purchasing consumer for a period of two
years (24 months) from the original purchase date. An extended
Warranty of 3 years can be purchased. For more information,
contact 7E Wellness corporate ofce.
Warranty Coverage:
This product is warranted against defective materials or
workmanship. This warranty ceases if the product has been
damaged by accident, in shipment, unreasonable use, misuse,
neglect, improper service, commercial use, repair by
unauthorized personnel or cause not arising out of defect in
materials or workmanship. This warranty does not extend or cover
the following:
Units which are used in violation furnished by manufacturer.
Units which have been altered or modied.
Units that have been damaged or parts which have had the
serial number removed, altered, defaced, or rendered
illegible.
Removed, altered, defaced or rendered illegible.
Normal wear and tear.
Replacement of the adaptors, elastic, or elastic cord.
Warranty Disclaimers:
This warranty is in lieu of all warranties, expressed or implied. No
representative or person is authorized to assume for manu-
facturer/any other liable in connection with the sale of 7E
Wellness products. There shall be no claims for defects or failure of
performance or product failure, any theory of tort, contract or
commercial law including, but not limited in negligence, gross
negligence, and strict liability, breach of warranty and breach of
contract. Some states do not allow the exclusion or limitation of
implied warranties or consequential damage, therefore, the
above limitations may not apply to all. The manufacturer is not
responsible nor liable for indirect, special or consequential
damages arising out of or in connection with the performance of
the product or other damage with respect to loss of property or
loss revenues/prot.
Out of Warranty Service:
Purchaser will be advised appropriately of charges rendered for
repairs made to the product after the expiration date of the
aforesaid two (2) year warranty period has terminated. The
distributor cannot assume responsibility for loss or damage during
shipment. In returning the product for repairs, carefully pack for
shipment and insure the package with the shipping company.
Ensure that the unit and all accessories related to the problems
are returned. Send a copy of the sales receipt or other proof of
purchase to determine warranty status. Include the full return
address. C.O.D. shipments cannot be accepted.
WARRANTY
MyoLift MD Master Device | Operations Manual MyoLift MD Master Device | Operations Manual

CHANGE TIMER
The MyoLift MD Master Device operates with a default intensity
level and timer for each model. All modes have the treatment
time displayed along with the amount of time in minutes. Each
Mode has a “Total Treatment Time”. This Total Treatment Time is
made up of the total minutes of each sub-mode. At the
completion of each sub-mode treatment timing, the device is
programmed to sound a beep. Tap on the next displayed
highlighted sub-mode and its default timing is automatically
advanced for that sub-mode.
To customize the service, the treatment time can be changed
from the default timing with the assistance of the encoder during
or before the treatment. Only in the Custom Mode setting are the
8 sub-modes. Each sub-mode is in 10-minute defaults and the
ultimate range is 0-100 minutes. In the Custom Mode settings there
is no automatic advancement to the next sub-mode. The
Professional user is at liberty to select any mode and treatment
time range from 0-100 minutes. Its default treatment time is 10
minutes on GUI. The table below provides the range of time for
that treatment time from 0-30 minutes.
a. Circulation
b. Lymph Drainage
c. Light Lift
d. Deep Lift
e. Firming
f. Iontophoresis
2 min
10 min
16 min
9 min
10 min
3 min
0-30 min
0-30 min
0-30 min
0-30 min
0-30 min
0-30 min
S.No. Modes GUI display Range
Face Lifting (Total time 50 min)
a. Circulation
b. Lymph Drainage
c. Iontophoresis
2 min
10 min
3 min
0-30 min
0-30 min
0-30 min
1
Rejuvenation (Total time 15 minutes)
2
a. Circulation
b. Lymph Drainage
c. Erase
d. Educate
e. Firming
2 min
10 min
5 min
15 min
5 min
0-30 min
0-30 min
0-30 min
0-30 min
0-30 min
Wrinkle Reduction (Total time 37 minutes)
3
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34 35
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