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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
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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,
i n a p p r o p r i a t e h a n d l i n g m a y a d v e r s e l y a f f e c t 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.
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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
