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This device is type BF applied equipment . It complies
with Medical Electrical Safety Standards (IE(60601-1).
This device also complies with Medical EMC Standard
(IEC 60601-1-2).The has been tested and found to com-
ply with the electromagnetic compatibility (EMC) limits
for medical devices to IEC 60601-1-2: 2014. These limits
are designed to provide reasonable protection against
harmful interference in atypical medical installation.
WARNING:
1* WARNING: 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
Guidance and manufacturer´s declaration – electromagnetic emission – for all EQUIPMENT AND SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic emission
The Theragun RELIEF is intended for use in the electromagnetic environment specified below. The cus-
tomer or the user of Theragun RELIEF should assure that it is used in such an environment.
Emissions test
RF emissions
CISPR 11
should be observed to verify that they are operating
normally.
2* WARNING: Use of accessories. transducers and
cables other than those specified or provided by the
manufacturer this equipment could result in increased
electromagnetic emissions or decreased electromag-
netic immunity of this equipment and result in proper
operation.
3* WARNING: Portable RF communications equipment
(including peripherals such as antenna cables) should
be used no closer than 30 cm (12 inches) to any part of
the ME EOUIPMENT, including cables specified by the
manufacturer. Otherwise, degradation of the perfor-
mance of this equipment could result
Compliance
Group 1
Electromagnetic environment -
guidance
The Theragun RELIEF uses RF energy only for
its internal function. There for, its RF emissions
are very low and are not likely to cause any
interference in nearby electronic equipment.
EN
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