Theragun 2AU6T-THED Smart Goggles User Manual

: June 9, 2024
: THERAGUN

Table of Contents

Recommendation of Use
Device Description
Trouble Shooting
Service
Environment
Safety, EMC
Manufacturer Information
LIMITED WARRANTY
Read User Manual Online (PDF format)
Download This Manual (PDF format)

User Manual

Document Name	User Manual	Document No.	Smart Goggle-001
Model	SmartGoggles	Rev	1

Revision History

Modification date	Change description	Rev	Modified by
3/19/2022	Initial release.	1	Team

Recommendation of Use

1.1 CAUTION
The battery used in this device may present a risk of fire or chemical burn if mistreated. Do no disassemble, heat above 100 C or incinerate.
Dispose of used battery promptly. Keep away from children. Do not disassemble and do not dispose of in fire.
PLEASE DO NOT USE THE VENOM, OR ANY VIBRATION HIGH-INTENSITY EXERCISE DEVICE WITHOUT FIRST OBTAINING APPROVAL FROM YOUR DOCTOR IF ANY OF
THE FOLLOWING APPLY:
Pregnancy, diabetes with complications such as neuropathy or retinal damage, wear of pace-makers, recent surgery, epilepsy or migraines, herniated disks, spondylolisthesis, spondylolysis, or spondylosis, recent joint replacements or metal pins or plates or any concerns about your physical health. Frail individuals and children should be accompanied by an adult when using any vibration device. These contra indications do not mean that you are not able to use a vibration or exercise device but we do advise you to consult a doctor first.

DANGER
TO REDUCE THE RISK OF ELECTRIC SHOCK:

Do not reach for an appliance that has fallen into water.
Do not use while bathing or in a shower.
Do not place or store appliance where it can fall or be pulled into a tub or sink. Do not place in or drop into water or other liquid.

1.2 Warnings
BEFORE USING OR CHARGING THE Smart Goggle, READ ALL THE INSTRUCTIONS AND CAUTIONARY MARKINGS IN THIS MANUAL TO REDUCE THE RISK OF BURNS, FIRE, ELECTRIC SHOCK, OR INJURY TO PERSONS:
Do not operate under blanket or pillow. Excessive heating can occur and cause fire, electric shock, or injury to persons.

Close supervision is necessary when this appliance is used by, on, or near children, invalids, or disabled persons.
Use this appliance only for its intended use as described in this manual. Do not use attachments not recommended by the manufacturer.
Never operate this appliance if it has a damaged cord or plug, if it is not working properly, if it has been dropped or damaged, or dropped into water. Return the appliance to a service center for examination and repair.
Do not carry this appliance by supply cord or use cord as a handle.
Do not operate where aerosol (spray) products are being used or where oxygen is being administered.
Do not immerse unit in water. Keep liquids away from ventilation ports, buttons and charging port.
Do not remove screws or attempt to disassemble.
Unplug the unit after charging or prior to use.
This is not a toy. For adult use only. Do not use if injured. Consult your doctor before using this product.

FCC Caution:
Any Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.
This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.

IMPORTANT NOTE:
Note: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:

Reorient or relocate the receiving antenna.
Increase the separation between the equipment and receiver.
Connect the equipment into an outlet on a circuit different from that to which the receiver is connected.
Consult the dealer or an experienced radio/TV technician for help.

FCC Radiation Exposure Statement:
This equipment complies with FCC radiation exposure limits set forth for an uncontrolled environment.

ISEDC Warning
This device complies with Innovation, Science, and Economic Development Canada licence-exempt RSS standard(s). Operation is subject to the following two conditions:
(1) this device may not cause interference, and
(2) this device must accept any interference, including interference that may cause undesired operation of the device.
The device is compliance with RF exposure guidelines, users can obtain Canadian information on RF exposure and compliance.

1.3 Label & Symbols
The following labels and symbols appear on Wave Duo:

| Read instructions before use
---|---
| Level of protection type BF applied part
**| Direct current
| Manufacturer’s name and address
| Separate collection for waste electrical and electronic equipment
Note: For more information about disposal of equipment, its parts and accessories, please contact your local distributor.
**| In accordance with Directive 2014/35/EU electrical equipment designed for use within certain voltage limits, and Directive 2014/30/EU electromagnetic compatibility

Device Description

operation description

POWER long press power button to turn on/off;
POWER under device on situation, press power button again to chose mode and start function.
HEAT short press heat button to chose heating levels, long press heating button to turn heating function off.
VIBRATION VIBRATION short press vibration button to choose vibration levels, long press vibration button to turn vibration function off, long press to turn on vibration again.
3（SmartRelax） when chose smart mode (smart relax), the heart rate detection will turn on (only smart mode will turn on HR function, able to use fingers to put on HR window and red color LED will on and start heart rate exam)
15 working time: 15mins;
LED charging situation: OBG LED will show breathing situation and show match color to certain power level, no function on when charging.

Trouble Shooting

In the event that the device fails to perform as intended, the following notes will help to identify potential problems with the device and its setup.

Problem	Solution
Device turns off automatically	Maybe reach the set time or low power
Device cannot turn on	Maybe battery is in low power and you should recharge

batteries. .
Device shuts off in mid-treatment or only after few treatments| Check and recharge batteries.

if the device breaks or quits working, and you cannot fix the problem, please contact us.

Service

Operation Instruction has no parts you can fix. Do not try to repair it. If servicing is required, please contact the selling retailer. All returned units to the manufacturer for repair, including Warranty repair and Out-Of-Warranty repair, must include the following:
During Warranty Period with proof of Purchase (store receipt).
Package the item securely and return it prepaid/insured – along with proof of purchase to:
Therabody, Inc.
6100 Wilshire Blvd. Suite 200 Los Angeles, CA 90048-5107, USA

Environment

Basic Unit Characteristics

Indicator Light| YES
Housing Materials| PC
Additional Features
Environment for

operation

| Temperature: 0 ~ 40° C

Relative humidity: <95% RH

Environment for

storage

| Temperature: -10° C ~ 40° C

Relative humidity: 10~95% RH

Use atmospheric

pressure

| 70-106Kpa
Software version| V1.0

Safety, EMC

This device is Class II equipment with type BF applied. It complies with Medical Electrical Safety Standards (IEC 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: 2007. These limits are designed to provide reasonable protection against harmful interference in a typical medical installation.
CAUTION:
Do not apply the device near any devices with Electromagnetic Interference (EMI), such as cell phones, Magnetic Resonance Imaging (MRI), computerized axial tomography (CT), diathermy, Radio Frequency Identification (RFID), etc. or MR environment. EMI, RF devices or MR environment may affect the normal function of the device or would cause user injury.
The patient is an intended operator. The ME EQUIPMENT shall not be serviced or maintained while in use with a patient.
Manufacturer’s declaration – electromagnetic immunity

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 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 of this equipment could result in increased electromagnetic emissions or decreased electromagnetic immunity of this equipment and result in improper operation.”
3* WARNING: Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the ME EQUIPMENT, including cables specified by the manufacturer. Otherwise, degradation of the performance of this equipment could result.”
Do not apply stimulation in the presence of electronic monitoring equipment (e.g., cardiac monitors, ECG alarms), which may not operate properly when the electrical stimulation device is in use.
Simultaneous connection of a user to a high frequency surgical ME equipment may result in burns at the site of the simulator electrodes and possible damage to the simulator.
Operation in close proximity (e.g. 1 m) to a shortwave or microwave therapy ME equipment may produce instability in the simulator output

Table 1

declaration – electromagnetic emission

Emissions test| Compliance
RF emissions

CISPR 11

| Group 1
RF emissions
CISPR 11| Class B
Harmonic emissions

IEC 61000-3-2

| Not applicable
Voltage fluctuations/ flicker emissions IEC 61000-3-3| Not applicable

Table 2

declaration – electromagnetic immunity

IEC 61000-4-5

short

70 % UT; 25/30 cycles

Table 3

declaration – electromagnetic immunity

Immunity test| IEC 60601 test

level

| Compliance level
Conducted| 3 V| Not applicable
RF| |
| 0.15 MHz to 80|
IEC 61000-4-| MHz|
6|

6 V in ISM bands

|
| between 0.15|
| MHz and 80|
| MHz|
Radiated RF| 10V/m| 10V/m
IEC 61000-4-| 80 MHz to 2.7|
3| GHz|

Table 4

declaration – IMMUNITY to proximity fields from RF wireless communications equipment

Immunity test| IEC60601 test level| Compliance level
Test frequency| Modulation| Maximum

power

| Immunity level
Radiated| 385 MHz| **Pulse| 1.8W| 27 V/m| 27 V/m
RF| | Modulation:| | |
IEC 61000-4-

3

| | 18Hz| | |
450 MHz| *FM+ 5Hz

deviation: 1kHz sine

| 2 W| 28 V/m| 28 V/m
| 710 MHz| **Pulse| 0.2 W| 9 V/m| 9 V/m
| 745 MHz| Modulation:

217Hz

| | |
| 780 MHz| | | |
| 810 MHz| **Pulse| 2 W| 28 V/m| 28 V/m
| 870 MHz| Modulation:

18Hz

| | |
| 930 MHz| | | |
| 1720| Pulse| 2 W| 28 V/m| 28 V/m
| MHz| Modulation:| | |
| 1845| 217Hz| | |
| MHz| | | |
| 1970| | | |
| MHz| | | |
| 2450| Pulse| 2 W| 28 V/m| 28 V/m
| MHz| Modulation:| | |
| | 217Hz| | |
| 5240| **Pulse| 0.2 W| 9 V/m| 9 V/m
| MHz| Modulation:| | |
| 5500| 217Hz| | |
| MHz| | | |
| 5785| | | |
| MHz| | | |

**Note* – As an alternative to FM modulation, 50 % pulse modulation at 18 Hz may be used because while it does not represent actual modulation, it would be the worst case.
Note**** – The carrier shall be modulated using a 50 % duty cycle square wave signal.

Manufacturer Information

Theragun, Inc.
6100 Wilshire Blvd. Suite 200 Los Angeles, CA 90048-5107, USA

LIMITED WARRANTY

For full warranty information, please visit www.therabody.com/warranty. To request a copy of the warranty by mail, you may send a request to the following address:
Therabody – Warranty
Attn: Customer Service
Therabody, Inc.
6100 Wilshire Blvd. Suite 200 Los Angeles, CA 90048-5107, USA
Please note, this is not a return address or a retail location. No Theragun Products or packages will be accepted at this location.