Kinetik Wellbeing penny pad User manual

Applicable
Lower Back
Back Pain
Sciatica
Knee Pain
Menstrual Pain
Migraine
TENSTENS
How to operate your PennyPad
1. Ensure baery has been properly inserted into device
2. Remove blue protective film from gel pads
3. Place gel pads over correct position on back of TENS
Machine
4. Remove clear protective film from gel pads, do not
remove gel pads from device
5. Place the PennyPad onto treatment area
6. Press and hold + to turn PennyPad on and activate
Smart Contact Detection*
7. Press + again to
activate stimulation**
8. Use +/- to adjust
stimulation level
9. Automatic power
off after 20 minutes
10. Replace baery
when PennyPad
can’t be started up
Baery Replacement
Please replace baery when:
1. Power off during
stimulation and can't be
powered on again, or
2. Can't be powered on after
a long period of storage.
Note:
After Use
Always place protective
film back to
electrode after use.
Assemble your PennyPad
There are only few steps of assembly required and it
works as easy as the layout.
TM
against
daily
pain
One Piece Self-Adhesive
Electric Pain Reliever
One Piece Self-Adhesive
Electric Pain Reliever
3. Insert Baery
(CR2032 only)
1. Open baery cover
with a coin.
2. Flip open baery cover
with a pin with care.
4. Close and lock baery cover. 5. Place gel pads accordingly
and ready to use.
Thank you for choose the Kinetik Wellbeing
PennyPad. Please read these instructions for use
carefully and keep them for further use.
What is PennyPad?
The PennyPad is an innovative, One Piece
Self-Adhesive electronic pain reliever. Utilizing
TENS technology to target specific pain gates.
Elegantly designed by medical grade silicone, ultra
thin, flexible uni-body construction which perfectly
matches the contour of contacting surfaces. High
tech circuitry conserves energy by providing 20
minutes per treatment and up to 20 sessions per
baery life. The Kinetik Wellbeing TENS machine is
a safe and easy pain management option, bringing
people a brand new experience and changing the
world of pain.
What is TENS?
TENS, transcutaneous electric nerve stimulation,
means electrical stimulation of nerves through the
skin. TENS is recognised as a clinically proven,
effective, non-medication method of treating pain
from certain causes. It manages pain through
stopping the pain to prevent pain signals being
transmied to the brain. It also helps to release
endorphins which sooth the treatment area by
stimulating nerves. The PennyPad is free from
side-effects when used properly, and can be used as
a simple means of self-treatment. The method is
scientifically underpinned and medically approved.
Product Specification
Power CR2032 Lithium 3V
Pulse Rate 70Hz
Pulse Width 200µs
Output Voltage Max. 65 Vpp, based on 500 Ω load ±-10%
Treatment Time 20 minutes; auto-off
Pulse Strength 0 ~ 15 stages adjustable
Operation Environmen 10 ~ 40oC, 30 ~ 85% Relative Humidity
Storage Environment -10 ~ 50oC, 10 ~ 95% Relative Humidity
Tranporation Environment -10 ~ 50oC, 35 ~ 85% Relative Humidity
Size 112 x 72 x 10mm
Program modulation
Cycle Mode Pulse Width Pulse Rate On-time
1 Constant 200 70Hz 120s
2 Burst 200 70Hz 120s
If you need longer treatment, please repeat operating procedure.
1. There is no serviceable part content in this product.
2. Replace baery when necessary.
Read before you use
Pennypad should never be
used to mask or relieve
undiagnosed pain. Before
treating any symptoms of
pain, it is mandatory to
diagnose cause of pain by a
doctor.
All rights reserved MADE IN CHINA
HIVOX BIOTEK INC. 5F, No.123, Shingde Rd.,
Sanchong District 241, New Taipei City, Taiwan R.O.C.
HIVOX BIOTEK B.V.
De Run 4428, 5503 LR
Veldhoven, Netherlands
40°C 85%
10°C
Operating
30%
50°C 95%
-10°C
Storage
10%
50°C 85%
-10°C
Transport
35%
PennyPad
Note:
* Smart Contact Detection
automatically detect
connection. Audible alarm
will triggered when
improper contacted
between 2 electrodes.
** When power on,
stimulation level is set to 0
for safety purposes. One
more press will enter
stimulation mode. Press 3 sec to
power on;
intensity increase Press 3 sec to
power off;
intensity decrease
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By cmlam at 4:11 pm, May 31, 2019

Important Information Regarding
Electro Magnetic Compatibility (Emc)
Guidance And Manufacturer’s
Declaration - Electromagnetic Emissions:
This device is intended for use in the electromagnetic environment specified below. The user
of this device should make sure it is used in such an environment.
The use of PennyPad other than those specified by Kinetik
Wellbeing, with the exception of accessories sold by
Kinetik Wellbeing as replacement parts for internal
components, may result in increased emission or
decreased immunity of the device.
PennyPad should not be used adjacent to or stacked with
other equipment. In case adjacent or stacked use is
necessary, PennyPad should be observed to verify normal
operation in the configuration in which it will be used.
Refer to further guidance below regarding the EMC
environment in which the device should be used.
•
•
Emissions Test Compliance Electromagnetic environment - guidance
RF emissions CISPR 11
RF emissions CISPR 11
Harmonic emissions IEC61000-3-2
Voltage fluctuations /Flicker
emissions IEC61000-3-3
The device uses RF energyonlyfor its internal function.
Therefore,its RF emissions are verylow andare not
likelyto cause anyinterference in nearbyelectronic.
Baery operated device.
Just need test Radiated Emission of CISPR 11 equipment.
SEM44 is suitable for use in all establishments,
including domestic establishments and those directly
connected to the public low-voltage power supply.
Group1
Class B
Not applicable
Not applicable
Guidance And Manufacturer’s
Declaration - Electromagnetic Immunity:
This device is intended for use in the electromagnetic environment specified below. The user
of this device should make sure it is used in such an environment. (IEC 60601-1-2, Table 2)
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance
Electrostatic
discharge
(ESD) IEC
61000-4-2
±6kV contact
±8kV air
±6kV contact
±8kV air
Floors should be wood, concrete or ceramic tile. If
floors are covered with synthetic material, the
relative humidity should be at least 30%.
Portable and mobile RF communications
equipment should be used no closer to any part of
SEM44 than the recommended separation distance
calculated from the equation applicable to the
frequency of the transmier.
Recommended Separation Distances Between Portable And
Mobile Rf Communications Equipment And This Device:
This device is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of this device can help prevent
electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmiers) and this device as recommended
below, according to the maximum output power of the communications equipment. IEC
60601-1-2, Table 6
Rated maximum
output power
of transmier (W)
Separation distance according to frequency of transmier (m)
0.01
0.1
1
10
100
Not applicable
Not applicable
Not applicable
Not applicable
Not applicable
0.16
0.368
1.16
3.7
12
0.233
0.736
2.33
7.4
23
150 kHz to 80 MHz
Not applicable
80 MHz to 800 MHz 800 MHz to 2.5 GHz
Electrical fast
transient/burst
IEC 61000-4-4
±2kV for
power supply line
±1kV for
input/out line
Not Applicable
Not applicable for baery operated device.
Surge
IEC 61000-4-5
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
Not Applicable
Not applicable for baery operated device.
Voltage dips,
short
interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
<5 % UT (>95 % dip
in UT) for 0.5 cycle
40 % UT (60 % dip
in UT) for 5 cycles
70 % UT (30 % dip
in UT) for 25 cycles
<5 % UT (>95 % dip
in UT) for 5 sec
Not Applicable
Not applicable for baery operated device.
Power frequency
(50Hz/60Hz)
magnetic field
IEC 61000-4-8
3 A/m 3 A/m
Power frequency magnetic fields should be at
levels characteristic of a typical location in a
typical commercial or hospital environment.
Note: Ut Is The A.C. Mains Voltage Prior To The Application Of The Test Level.
P
E
d





=
1
5.3
P
E
d





=
1
7
or transmiers rated at a maximum output power not listed above, the recommended separation distance d in meters (m)
can be estimated using the equation applicable to the frequency of the transmier, where P is the maximum output
power rating of the transmier in was (W) according to the transmier 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.
Applications:
• Back pain
• Joint pain (e.g. knee joint, hip joint, shoulder)
• Neuralgia
• Headache
• Menstrual Pain
• Pain after injuries to musculoskeletal system
• Pain with circulatory problems
• Chronic pain through various causes
Warnings
● Never use this unit near
the heart, around the mouth,
or on diseased skin.
● Do not use this unit in
places with high humidity
such as the bathroom.
● May need to use under the
supervision of a physical
therapist.
● For external use only.
● Long-term stimulation at
the same site may cause skin
discomfort. Consult a
dermatologist if skin
discomfort persists.
● Do not use Pennypad
during the first 12 weeks of
pregnancy.
● Consult a doctor before
you use this device if you
receive other medical
treatments.
● Do not disassemble or
remodel this unit.
● Do not use this unit while
sleeping, driving or bathing.
● Prevent any metal object,
such as belt buckle or
necklace coming into contact
with PennyPad.
● Supervision and medical
consultancy recommended if
you are under age 16.
Maintenence &
Damage
● If the unit is not
functioning properly or
causes discomfort, stop using
it immediately.
● Pause the PennyPad before
removing/moving the
stimulation region.
● Use only for the specific
pain problem diagnosed by
professionals.
● Consult your local
authorities for proper baery
disposal.
● Remove baery from
baery chamber if you are
not going to use it for a
longer period.
Knee Flexors
Adductors
Qudriceps
Ankle
Pectoral Muscles
Deltoid
Large Dorsals
Biceps
Elbow
Wrist
Abdominal Muscles
Sore Shoulder
PMS
Neck Pain
Trapezium
Lumbar Region
External
Abdominal Obligue
Deltoid
Triceps
Large Dorsals
Plantar Flexors
Buttocks
Hamstrings
(Biceps Femoris)
Upper Back Pain
Sciatica
Sciatica
Body Maps
With the increased number of electronic devices such as
computers and mobile (cellular) telephones, medical devices in
use may be susceptible to electromagnetic interference from other
devices. Electromagnetic interference may result in incorrect
operation of the medical device and create a potentially unsafe
situation. Medical devices should also not interfere with other
devices. In order to regulate the requirements for EMC (Electro
Magnetic Compatibility) with the aim to prevent unsafe product
situations, This device complies with European standards
EN60601-1 and EN60601-1-2 (In accordance with IEC 61000-4-2,
IEC 61000-4-3, IEC 61000-4-4, IEC 61000-4-5, IEC 61000-4-6, IEC
610004-8 and IEC610004-11) and is subject to special precautionary
measures with regard to electromagnetic compatiblity.
Please note that portable and mobile HF communication systems
may interfere with this unit.
Kinetik pennypad UK IB 20190530
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