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READ THE INTENDED USE AND SAFETY INSTRUCTIONS
CAREFULLY
INDICATIONS FOR USE
Mollii is intended for management and symptomatic relief of chronic intractable,
post-traumatic and post-surgical pain, as a transcutaneous electrical nerve stimula-
tion (TENS) device; and for muscle re-education, prevention or retardation of disuse
atrophy, increasing local blood circulation, maintaining or increasing range of mo-
tion, and relaxation of muscle spasms and as a neuromuscular electrical stimulation
as a neuromuscular electrical stimulation (NMES) device.
CONTRA INDICATIONS
Do not use:
- If the user has implanted electronic medical devices or equipment which can
be disrupted by magnets, for example, shunts
- Together with electronic life-support equipment or high-frequency operation
equipment
-Together with ECG-equipment.
There is a risk of Mollii disturbing the function of the above-mentioned types of
equipment .
All incorrect usage is at the user’s own risk.
WARNINGS
Do not modify Mollii without authorization of the manufacturer.
Use of this equipment adjacent to or stacked with other equipment should be
avoided because it could result in improper operation. If such use is necessary, this
equipment and the other equipment should be observed to verify that they are
operating normally.
Use of accessories, transducers and cables other than those specified or provided
by the manufacturer of Mollii could result in increased electromagnetic emissions
or decreased electromagnetic immunity of this equipment and result in improper
operation.
Do not use Mollii near a magnetic resonance imager.
Portable radio frequency communications equipment (including cell phones,
computers and peripherals such as antenna cables and external antennas) should
be used no closer than 30 cm (12 inches) to any part of the equipment, including
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