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The redesigned Theragun Mini is smaller, lighter and more travel-friendly than ever. Scientifically proven to relieve aches and pains, ease tension and reduce stress, Theragun Mini makes it easy to get the relief you need anytime, anywhere. Comfortably treat different areas of the body with a new, more secure grip made for all hand sizes and 3 attachments scientifically designed to target specific pain points. And unlike other massage guns, Theragun Mini is made with a quiet, anti-stall motor, so you can massage even the toughest knots without stopping your treatment. Perfect for long flights and daily commutes, lunch breaks or a round of golf — Theragun Mini tucks right into your travel bag for quick, effective relief wherever life takes you.
Intended Use
The Theragun Mini's percussive massage therapy is intended to relieve minor daily aches and pains, reduce muscle tension, tightness, and stress, and ease painful knots.
Figure 2. QR code to download the app
If you currently have the Therabody app, proceed to step 4.
Figure 3. Corresponding pictures/diagrams of the device
The device comes with three attachments scientifically designed to target aches, pains, and tension all over the body.
Dampener
For tender or sensitive muscles.
The Dampener attachment is specifically designed for use on tender or sensitive muscles. With lower density foam and a wide base that maximizes contact with the body, this attachment delivers a soothing, low-impact treatment to effectively reduces aches and pains and keep you feeling your best.
Standard Ball
For large & small muscle groups.
The Standard Ball attachment is specifically designed for all-over use on both large and small muscle groups. This attachment offers a more targeted percussive therapy treatment with a firm, smaller surface area and medium impact level. Perfect for quick re-activation and easing soreness, the Standard Ball is your go-to during a workout, delivering effective relief while keeping you moving.
Thumb
For lower back and trigger points.
The Thumb attachment is specifically designed to deliver the precision of a human thumb, making it ideal for trigger point therapy and targeting the lower back.
Designed with a higher impact level and a shape that mimics the feel of an actual thumb, this attachment offers a dense, focused treatment for those stubborn areas. Perfect for anywhere you'd use a real thumb, the Thumb attachment provides the deep, targeted relief you need, all from the comfort of your home.
*Attachments can be used across other Theragun Mini device models.
It is recommended that you swap out the attachments if you start to notice signs of wear.
The following maintenance instructions are important to ensure that your device continues to work as it was designed. Failure to follow these instructions may cause your device to stop working.
Read the following instructions carefully before cleaning the device to ensure longevity of the device and its components. For the most hygienic device experience, sanitize it after each use.
Note: This device is not waterproof. Only clean with a damp cloth or alcohol-free cleansing wipe by wiping the device. Do not submerge the device in water or clean it under running water. Do not allow the device to come into contact with corrosive solutions, which can damage the device's appearance and function.
The battery life of the device is up to 120 minutes, depending on the attachment and treatment intensity used.
**Note: If using a charger from a third party, ensure that it is from a certified manufacturer and has not suffered any structural damage. Do not try to use the device while charging.
SCENARIO | ERROR CODE DISPLAYED | POTENTIAL CAUSE | POTENTIAL SOLUTIONS |
The motor stops working | The power button LED indicator blinks orange 10 times and then turns off | The device is not charged | Use a power adapter and charging cable to connect to the device to a power outlet to charge. |
The power button LED indicator blinks orange, blue, and green | The battery pack has overheated during charging or use | Ensure the device is powered off, remove from charger, and let the device rest for 60 minutes. | |
The 3 speed LED lights blink white 5 times then turn off | The motor has overheated | Ensure the device is powered off, remove from charger, and let the device rest for 60 minutes. | |
If the issue still persists after verifying all of the above, the device may be damaged. Contact Therabody for further assistance. Visit https://www.therabody.com/us/en-us/support/support.html for the available contact methods. | |||
Cannot charge the device | N/A | The power adapter cable is not well connected to the adapter socket on the console | Verify that the power adapter cable is well connected to the adapter socket on the console, and the power adapter is connected to the 100-240 Volt power outlet. If this doesn't work, contact Therabody for further assistance. Visit https://www.therabody.com/us/en-us/support/support.html for the available contact methods. |
The power outlet connected is beyond the range of 100-240 Volt | |||
The device is charging very slowly | Slow charging or incompletely charging | There may be an adapter issue, or the adapter power is too low | Ensure you are using the USB-C to USB-C cable provided, or one from a certified manufacturer. |
If the issue still persists, Contact Therabody for further assistance. Visit https://www.therabody.com/us/en-us/support/support.html for the available contact methods. | |||
Mechanical noise | There is a rattling noise when the device is turned on | Internal malfunction | Contact Therabody for further assistance. Visit https://www.therabody.com/us/en-us/support/support.html for the available contact methods. |
Bluetooth connectivity issue | Cannot connect to the app or the device isn't working properly once connected | The firmware is not updated to the latest version | Update the device firmware and try to connect to Bluetooth again. |
The phone version or system cannot support the connectivity | Update your phone to the latest version. If this doesn't work, try to install the app on another phone device. |
Store and transport the device
Store and transport the device in the travel pouch. Store the device in a cool and dry place (Temperature: -20°C - 45°C. Relative humidity: 10~85% RH. Air Compression: 70 – 106 kPa). Do not store the device where temperatures may exceed 40°C/104°F, such as in direct sunlight or in a vehicle.
Therabody products are designed to unlock the body's natural ability to achieve health and well-being. Through science and technology, the Therabody portfolio of products allows people to access the therapeutic benefits of different natural phenomena to meet both their needs and preferences. There will be times when it is advisable to modify how devices are used (precautions) or times when it is not appropriate to use certain devices (contraindications). Read the following safety information for the Theragun Mini in its entirety prior to use.
General Device Use
Read the full Warnings and Guidance prior to using the device.
This device is intended for use by people in good health. This device is contraindicated against and should not be used by or on anyone with a history of epilepsy, seizures or cardiopathy.
The device is not recommended for anyone with an electronic implanted device (such as a pacemaker), cardiac arrhythmia, tumors, or acute episodes of inflammatory diseases. The device is not recommended for those who have arteriosclerosis, thromboses, or implants in the body region being treated.
Please consult your physician prior to using the device if you are pregnant and/or nursing. Immediately stop using the device at the first sign of discomfort. If you have any medical considerations, please consult your doctor before using the device.
These recommendations are derived from consultation with medical experts and published research regarding precautions and contraindications as of the printing date. For up-to-date information, please visit us online at https://www.therabody.com/us/en-us/ precautions-and-contraindictions.html.
Precautions:
Due care is required in these circumstances and device use may need to be modified. Consult with a medical professional if you currently have or suspect you may have any of the following conditions or if you have any questions.
Contraindications:
The following are circumstances where the potential risks may outweigh the benefits.
Consult a medical professional before use.
For full warranty information, please visit www.therabody.com/warranty. Customers who are in need of product support should visit https://www.therabody.com/ us/en-us/support/support.html for the available contact methods.
FDA-Registered
Limited Warranty Only With Authorized Retailer Purchase
Patents at www.therabody.com/patents
Manufactured and Distributed by:
Therabody, Inc.
1640 S Sepulveda, Suite 300
Los Angeles, CA 90025
USA
In the Australian market, the Therabody Theragun Mini device warranty is 1 year. For Australian Market Only: The purchase of this device is accompanied by a limited warranty. For complete details about the rights afforded to you under this warranty, visit https://therabody.com/anz/en-au/warranty-support/.
Importers:
Therabody Australia Pty Ltd
Waterman Business Centre 175 Maroondah Highway Suite 16, C307, Level 3
Ringwood Vic 3134 Australia
Therabody International Limited
5th Floor, 40 Mespil Road,
DO4C2N4 Dublin, Ireland
Therabody UK Limited
Portsoken House 155-157 The Minorities, London,
United Kingdom, EC3N1LJ
Capacity: 1200mah
Chemistry: Li-Ion
Weight of the battery: 90.5 g/0.20lbs
READ ALL INSTRUCTIONS AND CAUTIONARY MARKINGS IN THIS MANUAL, ON THE CHARGER, AND ON THE DEVICE BEFORE USING OR CHARGING THE DEVICE AND ITS ACCESSORIES.
When using the device, the following precautions should always be adhered to:
MedWatch is the Food and Drug Administration's (FDA) program for reporting serious reactions, product quality problems, therapeutic inequivalence/failure, and product use errors with human medical products, including drugs, biologic products, medical devices, dietary supplements, infant formula, and cosmetics.
If you think you or someone in your family has experienced a serious reaction to a medical product, you are encouraged to take the reporting form to your doctor. Your health care provider can provide clinical information based on your medical record that can help the FDA evaluate your report. However, we understand that for a variety of reasons, you may not wish to have the form filled out by your healthcare provider, or your health care provider may choose not to complete the form. Your health care provider is not required to report to the FDA. In these situations, you may complete the Online Reporting Form yourself. You will receive an acknowledgement from the FDA when your report is received. Reports are reviewed by FDA staff. You will be personally contacted only if we need additional information.
Use one of the methods below to submit voluntary adverse event reports to the FDA:
1*
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*
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*
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.
Please scan QR code for a copy of the Declaration of Conformity under Regulation (EU) 2019/1020
Meanings of symbols
No. | Icon | Descripton | Location of Label |
1 | ![]() | CE Mark | On rating label |
2 | ![]() | Please read the user manual before use. | In packaging |
3 | ![]() | 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. | On rating label |
4 | IP22 | 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, shall have adequate clearance from hazardous parts, and protected against solid foreign objects of 12.5 mm Ф and greater. | On rating label |
5 | ![]() | RCM Mark | On rating label and packaging |
6 | ![]() | Type BF apply part | On rating label |
7 | ![]() | Manufacturer information | On rating label |
8 | ![]() | UKCA Mark for UK | On rating label |
9 | ![]() | Bluetooth | On packaging |
10 | ![]() | IC Canada | On rating label |
11 | ![]() (01) 00840295405810 (10) 0000 (21) 00000 | Unique Device Identification (UDI) | On rating label and packaging |
12 | ![]() (01) 00840295405810 (10) 0000 (21) 00000 | Date of Manufacture | On rating label |
GUIDANCE AND MANUFACTURER´S DECLARATION – ELECTROMAGNETIC EMISSION – FOR ALL EQUIPMENT AND SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic emission | ||
The Theragun Mini is intended for use in the electromagnetic environment specified below. The customer or the user of Theragun Mini should assure that it is used in such an environment. | ||
EMISSIONS TEST | COMPLIANCE | ELECTROMAGNETIC ENVIRONMENT - GUIDANCE |
RF emissions CISPR 11 | Group 1 | The Theragun Mini 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. |
RF emissions CISPR 11 | Class B | The Theragun Mini 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. |
Harmonic emissions IEC 61000-3-2 | Not applicable | |
Voltage function / flicker emissions IEC 61000-3-3 | Not applicable |
GUIDANCE AND MANUFACTURER'S DECLARATION – ELECTROMAGNETIC IMMUNITY – FOR ALL EQUIPMENT AND SYSTEMS
Guidance and manufacturer´s declaration – electromagnetic immunity | |||
The Theragun Mini is intended for use in the electromagnetic environment specified below. The customer or the user of the Theragun Mini should assure that it is used in such an environment. | |||
IMMUNITY TEST | IEC 60601 TEST LEVEL | COMPLIANCE LEVEL | ELECTROMAGNETIC ENVIRONMENT - GUIDANCE |
Electrostatic discharge (ESD) IEC 61000-4-2 | ± 8 kV contact ± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air | ± 8 kV contact ± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air | Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. |
Electrostatic transient / burst IEC 61000-4-4 | ± 2 kV for power supply lines ± 1 kV for input/output lines | N/A | Mains power quality should be that of a typical commercial or hospital environment. |
Surge IEC 61000-4-5 | ±1kV differential mode ±2kV common mode | N/A | Mains power quality should be that of a typical commercial or hospital environment. |
Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11 | 0% UT; 0,5 cycle g) At 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315° 0% UT; 1 cycle and 70% UT; 25/30 cycles Single phase: at 0° 0% UT; 250/300 cycle 0% UT; 250/300 cycle | N/A | Mains power quality should be that of a typical commercial or hospital environment. If the user of the Theragun Mini requires continued operation during power mains interruptions, it is recommended that the Theragun Mini be powered from an uninterruptible power supply or a battery. |
Power frequency (50/60 Hz magnetic field IEC 61000-4-8 | 30 A/m | 30 A/m | Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. |
|
Guidance and manufacturer´s declaration – electromagnetic immunity – for EQUIPMENT and SYSTEM
Guidance and manufacturer´s declaration – electromagnetic immunity | |||
The Theragun Mini is intended for use in the electromagnetic environment specified below. The customer or the user of the Theragun Mini should assure that it is used in such an environment. | |||
IMMUNITY TEST | IEC 60601 TEST LEVEL | COMPLIANCE LEVEL | ELECTROMAGNETIC ENVIRONMENT - GUIDANCE |
Conducted RF IEC 61000-4-6 Radiated RF IEC 61000-4-3 | 3 Vrms 150kHz to 80MHz 6 V in ISM and amateur radio bands between 0,15 MHz and 80 MHz 10 V/m 80MHz to 2.7GHz 385MHz-5785MHz Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communication equipment (Refer to table 9 of IEC 60601-1-2:2014) | N/A 10 V/m 80MHz to 2.7GHz 385MHz-5785MHz Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless communication equipment (Refer to table 9 of IEC 60601-1-2:2014) | Portable and mobile RF communications equipment should be used no closer to any part of the Theragun Mini, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance:![]() where p is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m).b Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey,a should be less than the compliance level in each frequency range.b Interference may occur in the vicinity of equipment marked with the following symbol: ![]() |
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Recommended separation distances between portable and mobile RF communications equipment and the EQUIPMENT or SYSTEM - for EQUIPMENT and SYSTEMS
Recommended separation distances between portable and mobile RF communications equipment and the Theragun Mini
The Theragun Mini is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Theragun Mini can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Theragun Mini as recommended below, according to the maximum output power of the communications equipment | ||||
Rated maximum output of transmitter W | Separation distance according to frequency of transmitter m | |||
150 kHz to 80 MHz outside ISM and amateur radio bands![]() | 150 kHz to 80 MHz in ISM and amateur radio bands![]() | 80 MHz to 800 MHz![]() | 80 MHz to 800 MHz![]() | |
0.01 | 0.12 | 0.20 | 0.035 | 0.07 |
0.1 | 0.38 | 0.63 | 0.11 | 0.22 |
1 | 1.2 | 2.00 | 0.35 | 0.70 |
10 | 3.8 | 6.32 | 1.10 | 2.21 |
100 | 12 | 20.00 | 35 | 70 |
For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
Here you can download full pdf version of manual, it may contain additional safety instructions, warranty information, FCC rules, etc.
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