Therabody TheraFace PRO User manual

TheraFace PRO

2
EN
Przegląd produktu
TheraFacePRO
Zaawansowane rozwiązanie do terapii twarzy.
TheraFace PRO to przenośne urządzenie 4 w 1, które w kompleksowy sposób pozwoli Ci zadbać o dobre
samopoczucie i zdrowy wygląd twarzy. Pomaga zmniejszyć napięcie, rozluźnić mięśnie twarzy i poprawić wygląd
skóry. Oferuje zabiegi mikroprądami, terapię światłem LED (niebieskim, czerwonym i czerwonym z podczerwienią)
oraz zabiegi oczyszczające. Z TheraFace PRO dostosujesz zabiegi do swoich aktualnych potrzeb. Użyj różnych
pierścieni, aby ujędrnić twarz i poprawić jej owal, a także zapewnić głębokie oczyszczenie i relaks.
Przeznaczenie
TheraFace PRO ma za zadanie pomóc zmniejszyć napięcie, rozluźnić mięśnie twarzy i poprawić wygląd skóry
poprzez delikatną stymulację twarzy. Pierścienie do różnorodnych zabiegowe mają mają działanie liftingujące,
tonizujące napięcie, odmładzające i oczyszczające.
Terapia perkusywna
Terapia perkusyjna dopasowana do potrzeb twarzy. Masaż zmniejsza napięcie i rozluźnia mięśnie twarzy.

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EN
Pierścień do mikroprądów
Mikroprądy ujędrniają i napinają skórę. Zabieg
poprawia napięcie mięśni i kontur twarzy/szyi
• Połączenie z urządzeniem przez magnes – łatwe do
rozłączenia przez pociągnięcie
•Zabieg mikroprądowy jest wykonywany dzięki
pierścieniowi do mikroprądów.
Pierścień oczyszczający
Oczyszczanie usuwa nagromadzone na twarzy
kosmetyki, sebum i zanieczyszczenia
•Magnetyczne połączenie z urządzeniem – łatwe do
rozłączenia przez pociągnięcie
•Oczyszczanie jest uzyskiwane dzięki pierścieniowi
oczyszczającemu.
Żel bazowy do stosowania z
urządzeniem TheraFace PRO. Należy
nałożyć go na twarz przed rozpoczęciem
zabiegu mikroprądami, aby skuteczną i
bezpieczną terapię.
Żel przewodzący
TheraOneTM ConductiveGel

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EN
Pierścień LED:
światło niebieskie/ czerwone/
czerwone + podczerwień Spłyca zmarszczki wokół oczu i zapewnia
terapeutyczne rozgrzewanie, dzięki czemu
zmniejsza napięcie i uczucie dyskomfortu.
Pierścień LED: światło czerwone
Światło czerwone redukuje zmarszczki wokół
oczu.
Światło niebieskie pomaga w redukcji
trądziku (od małego do umiarkowanego)
* Światło niebieskie nie jest przeznaczone do leczenia
ani łagodzenia silnych zmian trądzikowych.
Zmarszczki wokół oczu
Łagod ny trądzik Umiarko wany trą d zik
Silne zmiany trądzikowe *
• Magnetyczne połączenie z urządzeniem –
łatwe do rozłączenia przez pociągnięcie
• Terapia światłem przed pierścień LED
Pierścień LED: światło niebieskie
Pierścień LED: światło
czerwone + podczerwine

EN Poznaj swoje urządzenie TheraFacePRO
Przyciskzasilania
Włącza / wyłącza urządzenie
Przycisk terapii perkusywnej
Kontroluje pracę końcówek perkusywnych
Przycisk pierścienia
Kontroluje pracę pierścienia
Attachment Ring
0Magnetic connection to thedevice and
can be removed by pulling
0Allthe Attachment Ringshaveonlyone
correctposition
Percussive Therapy Attachments
0Magneticconnection to the deviceand
can be removed bypulling
0Allthe Attachment Ringshaveonlyone
correctposition
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Flat - General use for the entire
face, neck and chest
Cone - More precisetreatment
fortargeted areassuchasaround
the eyes, nasolabial lines and
pressurepoints
Micro-point - Maximize
circulationforlargerareassuchas
the forehead,cheeks and chest
Hotand Cold Rings
(sold separately)
0Magnetic connection to the device
and can be removed by pulling
0Delivers the option of 3 Cold and
3Hot settings

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EN
Getting Started
Powering on the TheraFace PRO device
Push and hold the ON/OFF button to power on the
device and the OLED screen will turn on. 1. Start with aclean, dry face
2. Select and attachyourdesired
attachmentring
3. Turnon the device
4. Choose yoursettings
5. Get started
Basic getting started steps:
Switching Off
Push and hold the ON/OFF button again to switchthe
device off and the OLED screen will be off.
AutomaticShut Off
If the device is not manually powered off by pressing the Power button, the
device will automatically shut off after 10 minutes of inactivity.
Note: Make sure you turn off
the power on the device before
removing the rings.

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ENUsing theTheraFace PRO B. LED Treatment
1. The LED ring has 3 light therapy wavelength options: red,blue and
red+infrared.
To startusing the LED therapy mode, attach the LED ring to the
TheraFace PRO device.
Turn ON the TheraFace PRO device by pressing the Power Button
for 2 seconds.
Then, turn ON the LED ring by pressing the Attachment Ring button.
To toggle between light options (blue, red and red+infrared), press
the Attachment Ring button again.
The TheraFace PRO LED ring has a proximity sensor system, and will
only reach full light intensity (brightness) once the device is placed at
the right distance from your face (0.5 inches),reducing glare in the
interim. Avoid direct skin contact.
To turn off the LED ring, toggle to the Red+IR light mode and
press the Attachment Ring Button one more time or power off the
TheraFace PRO device by pressing the Power Button for 2 seconds.
Warning: Do not placetheLED Ring directly ontheskin. Keep theLED
Ring approximately0.5 inchesaway from theskin.
2.
3.
4.
5.
6.
7.
Start by washingyourface completely andrinse twice to remove residue.
Allowskin to dry completely before starting treatment. Be sure to visit
therabody.comfortreatment protocolsandinstructional videos.
A. Percussive Therapy Feature
1.
2.
3.
4.
5.
Select and attach the desired percussive therapy attachment
Once attached to the TheraFace PRO, turn ON the TheraFace PRO
device by pressing the Power Button for 2 seconds.
Turn on the percussive feature by pressing the percussive button once.
To toggle between the 3 speed options (1750, 2100 and 2400 rpm), press
the percussive button again.
To stop the percussive treatment, press the percussive button a third time.
Note: •Can be combined with Hot and ColdRings* - (*Hotand Cold Rings sold separately)
•Cannot be combined with the Microcurrent attachment or with the LED ring
Note:The TheraFace PRO device
will make abeeping sound every15
seconds.This will help you trackthe
timewithin each treatment and will
also inform you if a treatment has
been disconnected or iscompleted.
•1beep =timed feedback every 15sec so you
can timetheir protocolsbetter
•2 beeps =the LED, Microcurrent, Hot, or Cold
treatment has been accidentally disconnected
•3 beeps =the LED, Microcurrent,Hot, or Cold
treatmentis over

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C. Microcurrent Treatment
1. Remove any percussive therapy attachment before attaching the
Microcurrent Ring.
Prior to starting the microcurrent treatment, apply the TheraOne™
Conductive Gel to your clean, dry face or treatment area to ensure
the treatmentis delivered correctly.
Attach the Microcurrent Ring to the TheraFace PRO device.
Once attached to the TheraFace PRO, turn ON the TheraFace PRO
device bypressing the PowerButton for 2 seconds.
Turnon the microcurrenttreatmentby pressing the ring button once.
To adjust the intensity level toyour comfort, press the ring button once
to toggle between the3intensity options.
To stopthe microcurrenttreatment, pressthe ring button athirdtime.
2.
3.
4.
5.
6.
7.
PRO Tip:When using the Microcurrent Ring, slowly glide the device using light
to medium pressure, keeping both spheres on the face at once. A microcurrent
protocol of 5-8 minutes can be completed once per 24-hour period. Be sure to
visittherabody.com fortreatmentprotocolsandinstructional videos.
1.
2.
3.
Note: •Thereisa preset shutoff timeof8 minutes
•Cannot be combined with the percussive therapy attachments
•While the Microcurrent Ring will work with any conductive gel, we
recommendtheTheraOne™Conductive Gel if available in your market.
Warning: When using the TheraFace PRO with the Microcurrent Ring, a
microcurrent primeris required. DoNOT use theMicrocurrent Ring onthemidline
oftheneck oreye area.
D. Microcurrent Primer: TheraOne Conductive Gel
The TheraOne™Conductive Gel isa primerintended to be used with the
TheraFace PRO device prior to startingthe microcurrent treatment to ensure
the treatment is delivered safelyand effectively.
Directions:
Start with a clean, dry face.
Apply a mask-like layer of the conductive gel to all treatment areas
of the face and neck.
Following treatment with the microcurrent ring, rinse off and apply
your favorite moisturizer.
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EN Warnings:Use onlyas directed. Avoid eye contact. Do NOT usetheonthemidline
ofthe neck. Prior tostarting themicrocurrent treatment,testbyapplyinga small
amountof theTheraOneConductiveGelonasmallpatchofskin first.Skinmay
absorb gel during microcurrent session; reapply if neededtoensure even glide of
deviceontheskin.
1. Tone: Use one cotton pad with toner applied sweeping gently
across the face,avoiding the eye area and concentrating on the
nose, nasal fold, and chin
Serum: Apply serum
Moisturizer: Apply moisturizer
SPF: Apply SPF only in the morning or daytime hours
2.
3.
4.
Ifyoualready useatoner,serum,moisturizer,and/orSPF,thenapplyin
thisorderfollowingthecompletionofanyTheraFacePRO protocol:
After Skin Treatment
Clean your face with a warm, damp washcloth.
Device Maintenance
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.
Care and Cleaning
Visually inspectthe TheraFace PRO device andattachment ringsforanyobvious
signsof debrisbuild-up. Wipe your deviceandattachmentringsdownwithadamp
clothoralcohol-freecleansing wipe. Aftercleaning,allowthedeviceandattachment
ringstodry thoroughly beforestoringor beginninganothertreatmentprotocol.A
properly cleaneddeviceshouldhaveno visiblesignsof debrisormoisture.
Note: This product is not waterproof, only clean with a damp cloth or alcohol-free cleansing
wipe by wiping the device and attachment rings. Do not submerge the device in water or clean
it under running water (other than the Cleaning Ring). Do not allow the device to come into
contact with any corrosive solutions, which would damage appearance and function. Store
the device in a cool and dry place (Temperature:0°C/32°F - 40°C/104°F Relative humidity:
10~95%RH).Do not store the device or battery where temperatures may exceed 40°C/104°F,
such as in direct sunlight or in a vehicle.
TheraFacePRO Device After Care &Cleaning

EN
ImportantSafetyInformation
General TheraFace PRO Use
Read the fullWarningsand Guidance priorto usingthe TheraFace PRO.
This device is contraindicated against and should not be used by or on anyone with a history
of epilepsy, seizures or cardiopathy. The TheraFace PRO is not recommended for anyone
with an electronic implanted device (such as a pacemaker), cardiac arrhythmia, tumors, or
acuteepisodes of inflammatory diseases.The device is not recommended for those who have
arteriosclerosis, thromboses or implants in the body region being treated. Dental implants
should be firmlyanchored before using the device.Do not use the device on the eyes, eyelids,
or the areaimmediately surrounding the eye (Periorbita area). The device should not be used
ifyou have dark brown or black spots,such as large freckles, birthmarks, moles or warts, on the
areato be treated.The device is not recommended ifyou have eczema, psoriasis,lesions, open
wounds or active infections other than mild to moderate acne, such as cold sores,in the areato
be treated.Wait for the infected area toheal before using the device. Thedevice should not be
used ifyou have abnormalskin conditions caused by diabetes orother systemicor metabolic
diseases. It is not recommended to use this device ifyou havea historyof herpesoutbreaks
inthe areaof treatment,unless you have consulted with your physicianand have received
preventivetreatmentbefore using the device. Please consult your physician prior to use if you
arepregnant and/or nursing.
Pleaseconsultyourphysicianprior touse ifyou are pregnantand/ornursing.
Immediately stop using the deviceat the first sign of discomfort.
The device is not recommended for anyone under the age of 18 without adult supervision
and should be kept out of reach of children. If you have any medical concerns, are taking
any medications that cause light sensitivity, or have had any facial surgery or other surgical
procedures, please consult your doctor before using the device.
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Chargingthe TheraFace PRO
•TheTheraFacePRO is USB-C enabled with the connector at the bottom of the
device.
•TheTheraFace PRO includes aUSB-C toUSB-A cable.
•You can plug the deviceinto anystandardUSB adapter.
•TheTheraFace PRO allows for fast-charging if charged withaUSB-C adapter.
Note: Make sure the charger is from a certified manufacturer and it hasn’t suffered any
structural damage. The TheraFace PRO device will not work while charging.
TheraFace PRO Warnings andGuidance
(Precautions andContraindications)
Background
This device is intended to be used on the face, neck,and upper chest regions of
the body. If you have any specific medical conditions or concerns,please consult
your physician before using this product. There will be times when it is advisable
to modify how devices are used (precautions) ortimes when it is not appropriateto
use certain devices (contraindications). The following document highlights these
for each modality or treatment attachment included with the TheraFace PRO
device as of the date of printing. For up-to-date information, please visit usonline.

EN Microcurrent RingAttachment
These recommendations are derived from consultation with
medical experts and the published research in regards to
precautions and contraindications and are as of the date of
printing.For up-to-date information, please visit us online.
When using the device with the microcurrent treatment,
a microcurrent conductive gel primer is required. Prior to
starting the microcurrent treatment, test by applying a small
amount of the conductive gel on a small patch of skin.
Precautions
•Recent injury, surgery, or facial treatment such as neurotoxin,
dermal filler, microneedling, laser, and/or chemical peel until
skinhasfullyhealed
•Do notuseduringa breakoutfromHerpesSimplexVirus
•Do not use over facial hair; facial hair must be shaved prior to
use as haircaninterferewiththeconductivity
•Do notuseifyousufferfrom anyheartcondition
•Do notusedirectlyover centerofneck(bone), specifically
avoidingthethyroid
•Do notuse onbreast area
•Do notuse acrossyour chest
•Do notuse on groinarea
•Do notusedirectlyontheeyes,eyelids,ortheareaimmediately
surroundingtheeye (Periorbitaarea).
•Do not applytobrokenskin
•Do notuse on children
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Contraindications
The following are circumstances where the potential risks
may outweigh the benefits. Consult a medical professional
before use.
•Skinrash,openwounds,blisters,localtissueinflammation,
infections,bruises, ortumors
•Pacemakerorotherimplantedelectronicdevices
•Epilepsy
•Pregnancy
•Cancer/tumors
•Thrombosis
•Phlebitis
•Metalplatesorpinsintheapplicationarea
•Implanted defibrillators/ stimulators
LED RingAttachment (Red
LED, Red+IRLED, and Blue LED
Therapies)
These recommendations are derived from consultation with
medical experts and the published research in regards to
precautions and contraindications as of the date of printing.
For up-to-date information, please visit us online.
Precautions
•Recent injury, surgery,orfacialtreatment suchas neurotoxin,
dermalfiller,microneedling,laser,and/orchemical peeluntilskin
has fullyhealed.
•CurrentbreakoutfromHerpesSimplexVirus
•Forfacial hair: Use LED over facial hair, followingthe patternof
hairgrowth(typicallyina downwardmotion)
•Do notapplydirectlytotheeyeball/eyelid
•Do not applytobrokenskin
•Do not applyretinolbeforeuse of redLED light
Contraindications
The following are circumstances where the potential risks may
outweighthebenefits. Consultamedicalprofessionalbeforeuse.
•Skinrash,openwounds,blisters,localtissueinflammation,
infections,bruises,or tumors
•Pregnancy/nursing
•Abnormalsensations(ex.numbness)
•Cancer/tumors
•Epilepsy
•Cardiopathy(heartdisease)
•Photo allergyordisorder(ex.Lupus, porphyria)
•Medicationsthat causelightsensitivity
•Medicationsforsevereacne
•Extremesensitivityto light
•Melasmaorhyperpigmentation(especiallyifexacerbatedby
mildwarmth)
•Suspiciouslesionsorskincancer–pleasevisityourphysician
•Iftakingorusinganyretinolor sun-sensitivemedicationsor
productsorbenzoylperoxidedonotuseinfraredlight

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EN
PercussiveTherapyAttachments
(Flat, Cone, Micro-point)
These recommendations are derived from consultation with
medical experts and the published research in regards to
precautions and contraindications as of the date of printing.
For up-to-date information, please visit us online.
Precautions
Due care is required in these circumstances and the use of the
devices may need to be modified (such as attachment used,
the force applied, the position of the body,avoidance of use in
direct contact with an area, etc.).Where appropriate or if you
have any concerns, seek the advice of a medical professional
•Recent injury,surgery, or facial treatment such as neurotoxin,
dermal filler, microneedling, laser, and/or chemical peel until
skinhasfullyhealed.
•CurrentbreakoutfromHerpesSimplexVirus
•Hypertension(controlled)
•Abnormalsensations(e.g.,numbness)
•Sensitivityto pressure
•Medicationsthat mayaltersensations
•Do notapplydirectlytotheeyeball/eyelid
•Do not applytobrokenskin
Contraindications
The following are circumstances where the potential risks may
outweighthe benefits. Consult a medical professionalbefore use.
•Skinrash,open wounds,blisters,localtissue inflammation,
infections,bruises,ortumors
•Activeacne breakout
•Bone fracture ormyositis ossificans
•Hypertension(uncontrolled)
•Acute orseverecardiac,liver,orkidneydisease
•Neurologicconditionsresultinginlossoraltered sensation
•Directapplicationto theeyesorthroat
•Bleedingdisorders
•Recentsurgeryorinjury
•Connectivetissuedisorders
•Peripheralvascularinsufficiencyordisease
•Medicationsthatthinthe blood oraltersensations
•Directpressureoversurgicalsiteor hardware
•Extremediscomfortor pain
•Pacemaker,ICD, orhistoryofembolism
CleansingRingAttachment
These recommendations are derived from consultation with
medical experts and the published research in regards to
precautions and contraindications as of the date of printing.
For up-to-date information, please visit us online.
Precautions
•Recent injury, surgery, or facial treatment such as neurotoxin,
dermal filler, microneedling, laser, and/or chemical peel until skin
has fullyhealed.
•CurrentbreakoutfromHerpesSimplexVirus
•If youhave facial hair, usethe cleansingringfollowing the pattern
ofhairgrowth(typicallya downward motion) and/ormakesmall
circularmotionsifcomfortable
•Do notapplydirectlytotheeyeball/eyelid
•Do not applytobrokenskin
Contraindications
The following are circumstances where the potential risks may
outweighthebenefits. Consulta medicalprofessionalbeforeuse.
•Skinrash,open wounds,blisters,localtissueinflammation,
infections,bruises,or tumors
Hot RingAttachment
These recommendations are derived from consultation with
medical experts and the published research in regards to
precautions and contraindications as of the date of printing.For
up-to-date information, please visit us online.
Precautions
•Recent injury, surgery,orfacialtreatmentsuchasneurotoxin,

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EN dermalfiller,microneedling,laser,and/orchemicalpeeluntil
skinhasfullyhealed.
•CurrentbreakoutfromHerpesSimplexVirus
•Do notapplydirectlyontheeyeball/eyelid
•Do not applytobrokenskin
Contraindications
The following are circumstances where the potential risks may
outweighthebenefits. Consulta medicalprofessionalbeforeuse.
•Skin rash, open wounds, bliszters,local tissue
inflammation, infections, bruises, ortumors
Cold RingAttachment
Theserecommendationsare derived from consultationwith
medical experts and the published research in regards to
precautionsand contraindications.
Precautions
•Recent injury, surgery, or facial treatment such as neurotoxin,
dermal filler, microneedling, laser, and/or chemical peel until
skinhasfullyhealed.
•CurrentbreakoutfromHerpesSimplex Virus
•Do notapplyon theeyeball/eyelid
•Do not applytobrokenskin
Contraindications
The following are circumstances where the potential risks may
outweighthebenefits. Consulta medicalprofessionalbeforeuse.
•Skinrash,open wounds,blisters,localtissueinflammation,
infections,bruises,or tumors
•Cold hypersensitivity/Coldurticaria
•Circulatoryinsufficiency
Additional Unit Warnings
When using the device, these basic precautions should
always be followed:
1. USEONLY AS INSTRUCTED. Usethe device as described
inthe device User Manualonly.Only usethe recommended
attachments, accessories, and replacementparts.Do not carry
out any maintenance onyourown.
2. NOT FOR CHILDREN. The device is not intended for use by
young children or persons with reduced physical, sensory, or
reasoning capabilities, or lack of experience and knowledge
withhow the deviceshould beoperated, unlesstheyhave
•Forfacial hairuseCold Ring asnotedinstandard protocol been givensupervisionorinstructionbya responsibleperson.
Do not allowthe device to beused asatoy.Children shouldbe
supervisedto ensurethattheydo not playwiththe device.
3. CHARGING LOCATIONS. The device should be charged
indoorsinawellventilated,drylocation. Donot chargethe
deviceoutdoors, ina bathroom,orwithin 10feet (3.1meters)
of abathtub or pool.Do not usethe device orchargeronwet
surfaces anddo not expose the charger tomoisture,rain,orsnow.
Do not usethe device inthe presenceof explosiveatmospheres
(gaseous fumes, dust, or flammable materials). Sparks may be
generated,possiblycausing afire.
4.DO NOT OVERCHARGE. Do not leave the battery in the
Chargerfor more than 1hourafter the battery hasbeen fully
charged. Thebattery includesa TheragunProtectionsystem
toavoidthe risk of overcharging.However,overchargingmay
reduce its lifeover time
5.DO N OT BU RN OR INCINERATE THE DEVICE OR ITS
BATTERIES.Thebatterymay explode,causingpersonalinjury
ordamage. Toxicfumesandmaterialsare createdwhenthe
batteryisburned.
6.DO N OTCRUSH, DRO P,OR DAMAGE THEDEVICE
BATTERIESOR CHARGER. Donot usea chargerthathas
receiveda sharpblow,been dropped, runover,ordamaged in
any way.
7. BATTERY CHEMICALS C AU SE SERIOUS BURNS. Never allow
theinternalbattery to come into contact with the skin, eyes, or

14
15.THERMAL LIMITER.Thedevice hasan automaticresetthermal EN
mouth.Ifa damaged batteryleakschemicals,use rubberor
neopreneglovestodisposeof it.If skinisexposedto battery
fluids,wash with soapand waterand rinse withvinegar. Ifeyes
are exposedto batterychemicals,immediatelyflush with
waterfor20 minutesand seekmedicalattention.Remove and
disposeof contaminated clothing.
objectmakesa connection between the positive andnegative
contactson the battery orthe 16V connector.Do not place a
battery nearanythingthatmay causea shortcircuit,suchas
coins, keys, or nails in your pocket. A short circuited battery
may causefire and personalinjury.
9.DO NOTOPERATE UND ER BLANKET AND PILLOW OR
BETWEENCOUCH CUSHIONS.Excessiveheatingcanoccur
andcause fire,electricshock,or injury.
10.STORINGTHE DEVICE &BATTERY.Storeinacool,dryplace.
Only charge the device when the ambient temperature is
between 0°C/32°F- 40°C/104°F.Donot storethedeviceor
batterieswheretemperaturesmayexceed40°C/104°F, suchas in
directsunlightorinavehicle.
11.DISPOSING OF BATTERIES.TheTheraFacePRO lithium-ion
batteries for the device are more environmentally friendly
thansome other typesof batteries. Always disposeof device
batteries according to federal, state, and local regulations.
Contactarecyclingagencyinyourareafor recyclinglocations.
Even discharged batteries contain some energy. Before
disposing, use electrical tape to cover the device’s 16V
connector/terminals to prevent the battery from shorting,
which could causea fireor explosion.
8. DO NOT SHORT CIRCUIT.A battery willshortcircuit ifametal 12.DO NOT DISASSEMBLE. Disassembly orincorrectreassembly
may result in the risk of electric shock, fire, or exposure to
battery chemicals. The warranty will be void if the device,
batteries, or charger are disassembled or if any parts have
been removed.
13.SERVICE.If the device, batteries, orchargerisnot working
properly,hasreceivedasharp blow,or has been dropped,
it.Do not attempt to repairor disassemblethe devicewhich
may resultinan electricshock orfire.
14.DO NOTUSE WHILE BATHING OR IN THESHOWER,TUB,
ORSINK.Do not place orstorethe deviceor batteries where
itcan fall orbe pulled intoa tub orsink.Do not place inor
drop intowaterorother liquid.Donot reach for anappliance
thathasfallen intoorcome intocontact withwater. Unplug
immediately.
damaged,leftoutdoors, ordropped intowater, then do not use Risk
limiterthatshuts off the deviceto preventoverheatingandfire.
16.POLARIZEDPLUG. To reduce the risk of electricshock,this
appliancehas a polarizedplug (onebladeis widerthanthe other).
This plug will fitinapolarizedoutletonlyone way.If the plug
does not fitfullyin the outlet,reversethe plug. If itstill doesnot
fit,contact a qualifiedelectrician toinstallthe Theragun Proper
outlet. Do not change the plug inanyway.
17. DO NOT OPERATE the device whereaerosol (spray)is being
used or whereoxygen is being administered.
SAVE THESE INSTRUCTIONS
1. Use the TheraFace PRO device and attachment rings only as
describedwithinthisUserManual.The risksanddangersofusing
theTheraFacePROdeviceandattachmentringsinanywayother
thanspecifiedintheprovidedUserManualareunknownandmay
resultinnegativesideeffects.
2. ThisTheraFacePROdevicewasnot testedforuseovertheeye
socketoreyelidso therisksareunknown.

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EN Labels
NO.
SYMBOLS
DESCRIPTION
1CE mark
2the Restriction of Hazardous Substances
3“WEEE (Waste Electrical and Electronic Equipment)”.
The wasteproducts should be handledlegally.
4Keep dry
5FCC Federal Communications Commission
6Please read the user manual before use
7Type BF apply part.
Product Specifications
B
ASIC UNIT CHARACTERISTICS
P
ower Source
Use
r supplied USB-Aor USB-C adapter
Indica
tor Light
YES
Housing
Materials
PC
ADDI
TIONAL FEATURES
Environment for operation Temperature: 0 ~ 40°C
Relative humidity:
<93% RH
Environment for storage Temperature: -25°C ~ 50°
C Relative humidity:
10~95%RH
Use
atmospheric pressure
70
-106Kpa

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EN
Maximum
Output Current
420
μA -560μA @500 Ohm
400
μA -600μA @2k Ohm
4
75μA -520μA @10k Ohm
Pulse
Width
On
60ms / Off 60ms
Frequency
8.3Hz
Net
Charge
N/A
- Battery operated
Maximum
Current Density
1.65mA/cm^2
@500Ohm
Maximum
Power Density
F
OR LED TREATMENT
Light
wavelength
1.3
6125mW/cm² @500
IR+Red:830nm±10nm/633±10 nm
Blue light:415nm±10nm, Red light:633nm±10nm
For Microcurrent Treatment:
Stimula
ted site
F
ace and neck
Number
of modes
3
Output
Intensity Level
4
Indica
tor Light
Y
es , OLED display
Timer
Range
5
-8minutes per day for 6 weeks
Housing
Materials
Console:
PC plastic
OUTPUT
SPECIFICATION
Waveform
Pulsed
Biphasic
Operating
voltage
0
-15.5V
Maximum
power
24mW
Au
tomatic shut-down
Yes
Maximum
Output
Voltage(+/-
10%)
210-280mV @500 Ohm
0.8- 1.2V @ 2k Ohm
4.75-5.2V@ 10k Ohm
Powerof light
(mW//cm2) IR+Red70±5%/60±5%
Redlight 60±5%, Bluelight 45±5%
FOR PERCUSSIVE THERAPY
Percussive 1750,2100 and2400 rpm
Frequency 1750rpm:29.1Hz 2100rpm:35Hz 2400rpm:40Hz

1. Thisdevice is Class II equipment with type BF applied part. It complies with Medical
Electrical Safety Standards(IEC 60601-1).
2. Thisdevice is also compliant with Medical E M C Standard (IEC 60601-1-2).
3. All the user directly contracting materialsfor the main device housing and output
contacts in this device are biocompatible for its intended use. They comply with
biocompatibility standards ISO 10993-5 (Cytotoxicity) and ISO 10993-10 (Irritation
and Sensitization).
The TheraFace PRO has been tested and found to comply with the electromagnetic
compatibility (EMC) limits for medical device 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 deviceor would cause user injury.
17
EN Safety,EMC &Bio-compatibility FCC compliancestatement
This device complies with Part 15 of the F CC 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. Changes
or modifications not expressly approved by the party responsible for compliance could void the
user’s authority to operate the equipment.
This equipment has been tested and found to comply with the limits for a Class B digital device,
pursuant to Part 15 of the F CC Rules. These limits are designedto 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:
•Reorientor relocate the receiving antenna.
•Increasethe 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.

18
EN
MANUFACTURER’S DECLARATION –ELECTROMAGNETIC EMISSIONS
TheTheraFacePRO is intended for use in the electromagnetic environments specified below. The customer or the userof the TheraFacePRO should ensure that it is used insuch an environment.
EMISSIONS TEST COMPLIANCE ELECTROMAGNETICENVIRONMENT - GUIDANCE
RF emissions
CISPR 11 Group 1 The TheraFace PRO uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronicequipment.
RF emissions
CISPR 11 Class B The TheraFacePRO is 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 Class A
Voltage function / flicker emissions
IEC 61000-3-2 Complies

19
EN
The TheraFace PRO is intended for use inthe electromagnetic environmentspecifiedbelow. The customeror the user of the TheraFace PRO should ensure that it is used insuch an environment.
IMMUNITYTEST IEC 60601 TEST LEVEL COMPLIANCE LEVEL ELECTROMAGNETIC ENVIRONMENT- GUIDANCE
Electrostaticdischarge(ESD)
IEC 61000-4-2
±6kVcontact
±8kVair ±6kV contact ±8kVair Floors should be wood, concrete or ceramic tile.If floors are covered with synthetic material, the
relative humidity should be at least30%.
Electrostatic transient/ burst
IEC 61000-4-4
±2kV for power supplylines
±1kV for input/outputlines ±2kVfor power supply lines ±1kV for input/outputlines Mains power quality should be that of a typical commercial or hospital environment.
Surge
IEC 61000-4-5 ±1kVdifferentialmode ±2kVcommonmode ±1kV differentialmode ±2kVcommonmode Mains power quality should be that of a typical commercial or hospitalenvironment.
Voltage dips,short interruptions and
voltagevariationson power supply
inputlines
IEC 61000-4-11
<5%UT(>95%dip inUT)
for 5 sec <5% UT(>95%dipin UT) for 5 sec Mains power quality should be that of a typical commercial or hospitalenvironment.If the user of the TheraFace PRO requires continued operation during power mains interruptions, it is
recommendedthat the TheraFace PRO be powered from an uninterruptible power supply
or abattery.
Power frequency (50/60 Hz
magneticfield
IEC 61000-4-8
3 A/m 3 A/m Power frequency magnetic fields should be at levelscharacteristic of a typical location in a typical
commercialor hospital environment.
NOTE UTisthe a.c. mainsvoltage prior to application of the testlevel.
MANUFACTURER’S DECLARATION –ELECTROMAGNETIC IMMUNITY

20
IMMUNITY TEST IEC 60601 TEST LEVEL COMPLIANCE LEVEL ELECTROMAGNETIC ENVIRONMENT- GUIDANCE
EN
ConductedRF
IEC 61000-4-6
3 Vrms
150kHz to 80MHz 3V Portableand mobileRF communications equipment should be used no closer to any part of the
higi Station, including cables, than the recommended separation distance calculated from the
equationapplication to the frequency of the transmitter.
Recommended separation distance Where p is the maximum output power rating of the
transmitterin watts(W) according to the transmitter manufacturer and d isthe recommended
separation distance in metres(m).b
Field strengths form fixed RFtransmitters,as determined by an electromagnetic sitesurvey, a
should be less than the compliancelevel in each frequency range.b
Interferencemay occur in the vicinity of equipment marked with the following symbol:
RadiatedRF 3V/m
80MHz to 2.5GHz 3V/m NOTE 1At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic isaffected by absorption
and reflection from structures,objects and people.
Field strengths from transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted
theoretically with accuracy. To assessthe electromagnetic environment due to fixed RFtransmitters, an electromagnetic site survey should be considered. If the measured filed strength in the location in which the
TheraFace PRO is used exceeds the applicable RFcompliance level above. The TheraFace PRO should be observed to verifynormal operation. If abnormal performance is observed,additional measuresmay be
necessary, such asreorienting or relocating the higi Station.Overthe frequency range 150kHz to 80 MHz, filed strengths shouldbe less than 3V/m.