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Label & Symbols
The following labels and symbols appear on Theragun PRO PLUS
No.
Icon
1
Muscles
CE Mark
2
NOM Mark
Separate collection for waste electrical and electronic equipment.
3
Muscles
Note: For more information about disposal of equipment, its parts and
accessories, please contact your local distributor.
IP Classification: The first number 2: Protected against access to hazardous
parts with a finger, and the jointed test finger of 12 mm Ф, 80 mm length,
IP22
4
shall have adequate clearance from hazardous parts, and protected
against solid foreign objects of 12.5 mm Ф and greater.
5
Please read the user manual before use.
6
Type BF apply part
Joints + Mus-
7
Manufacturer information
cles
8
UKCA Mark for UK
Troubleshooting
Issue
Solution
Device turns off automat-
1. Battery level is low
ically or Device does not
2. Device still does not turn on
turn on
Device shuts off
1. Check and recharge batteries.
mid-treatment or
2. Motor or connection have been
Vibration motor does not
damaged
turn on
1. The ambient temperature is too high
or too low
Battery will not charge
2. Possible defective charging cable
3. Possible defective battery
Descripton
Corrective Action
1. Charge the battery
2. Contact Therabody
Try charging the device fully, removing
the charging cable and then pressing left
button for 3 seconds. If problem persists,
contact Therabody
1. Charge the device when the ambient
temperature is between 5° C and 35° C
2. Try using a different USB-C cable and
adapter
3. Contact Therabody
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
comply 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 equip-
ment 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 electro-
magnetic 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 performance of this equipment could result
Guidance and manufacturer´s declaration – electromagnetic emission –
for all EQUIPMENT AND SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic emission
The Theragun PRO PLUS is intended for use in the electromagnetic environment
specified below. The customer or the user of Theragun PRO PLUS should assure that it
is used in such an environment.
Emissions test
Compliance
RF emissions
Group 1
CISPR 11
RF emissions
Class B
CISPR 11
Harmonic emissions
Not applicable
IEC 61000-3-2
Voltage fluctuations
flicker emissions
Not applicable
IEC 61000-3-3
Electromagnetic environment - guidance
The Theragun PRO PLUS 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.
The Theragun PRO PLUS suitable for use in all
establishments, including domestic establishments and
those directly connected to the public low-voltage power
supply network that supplies buildings used for domestic
purposes.
EN
5
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