1
Safety
Warning
and
Cautions
1.
Do not use this device if you have a cardiac pacemaker, implanted defibrillator, or other implanted
metallic or electronic device. Such use could cause
electric shock, burns, electrical interference, or
death
.2.If you are in the care of a physician, consult with your physician before using this device;
3.
Do not apply
stimu
lation
on your heart, head, mouth, pudendum or blemished skin areas;
4.
Do not apply stim
ulation across your chest because the introduction of electrical current into the
chest may cause rhythm disturbances to your heart, which could be lethal;
5.
Do not apply during pregnancy.
6.
Do not apply stimulation over painful areas.
If you have painful areas, you should consult with your
physician before using this device;
7.
Do not apply stimulation over open wounds or rashes, or over swollen, red, infected, or inflamed
areas or skin erupti
ons (e.g., phlebitis, thrombophlebitis, varicose veins);
8.
Do not apply stimulation over, or in proximity to, cancerous lesions;
9.
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;
10.
Do not apply stimulation when in the bath or shower;
11.
Do not apply stimulation while sleeping;
12.
Do not apply stimulation while driving, operating machinery, or during any activity in
which
electrical stimulation can put you at risk of injury;
13.
Do not use the device on children;
14.
Consult with your physician before using this device, because the device may cause lethal rhythm
disturbances to the heart in susceptible individuals; and
15.
Apply
stimulation only to normal, intact, clean, healthy skin;
16.
Do not use this device in high humidity areas such as a bathroom;
17.
Do not attempt to move the electrode heads while the device is operating; and
18.
Keep the device away from wet, high temperature and di
rect
sunshine
. Shady and dry place is good
for device stock.
1.
This device is not effective for pain of central origin, including headache;
2.
This device is not a substitute for pain medications and other pain management therapies;
3.
This device has no cura
tive value;
4.
This device is a symptomatic treatment and, as such, suppresses the sensation of pain that would
otherwise serve as a protective mechanism;
5.
The long
-
term effects of electrical stimulation are unknown;
6.
Since the effects of stimulation of the
brain are unknown, stimulation should not be applied across
your head, and electrodes should not be placed on opposite sides of your head;
2
7.
The safety of electrical stimulation during pregnancy has not been established;
8.
You may experience skin irritation
or hypersensitivity due to the electrical stimulation or electrical
conductive medium (gel);
9.
If you have suspected or diagnosed heart disease, you should follow precautions recommended by
your physician;
10.
If you have suspected or diagnosed epilepsy, you
should follow precautions recommended by your
physician;
11.
Use caution if you have a tendency to bleed internally, such as following an injury or fracture;
12.
Consult with your physician prior to using the device after a recent surgical procedure, because
stim
ulation may disrupt the healing process;
13.
Use caution if stimulation is applied over the menstruating uterus;
14.
Use caution if stimulation is applied over areas of skin that lack normal sensation
;
15.
Keep this device out of the reach of children;
16.
Turn off
the stimulator if the stimulation feels unpleasant or does not provide pain relief
;
17.
Use this device only with the leads, electrodes, and accessories recommended by the manufacturer.
Adverse Reactions
You may experience skin irritation and burns beneath the
stimulation electrodes applied to your
skin;
You may experience headache and other painful sensations during or following the application
of electrical stimulation near your eyes and to your head and face; and
You should stop using the device and should
consult with your physician if you experience
adverse reactions from the device.
To be used for temporary relief of pain associated with sore and aching
muscles in the shoulder,
waist, back, neck, upper extremities (arm), and lower extremities (leg) due to strain from exercise
or normal household work activities.
•••
Safety symbols
Type
B applied part
Attention, see operating manual for use
Indications for Use
3
Intro
d
uction of PL009 Electron
i
c Pulse
Massager
Overview
The Device’s
Parts
How the
device
works:
T
he operational principle of
the
device is to generate small pulses of electrical current and deliver
the pulses to an ordinary user’s skin through electrode adhesiv
e pads such that the underlying
nerves are activated and the pain associated with sore and aching muscles is temporarily re
lieved.
4
Quick
Op
e
ration
Guide
IMPORTANT:
TIP:
.
The
following
steps are
used to
guide
the
device
operation
:
1
st
Step
:
T u r n b o t h k n o b s t o “ O F F ” , t h e n
i
nsert
4pcAAA batteries
into
the
device
2
n
d
Step
:
C
onnect
the
electrode
pads to
the
wire
and
thencon
nectthewire
to
the device.
3
rd
Step
:
Put
the
electrode
pads on
m
assage
-
needed
body area
4
th
Step
:
Rotate
the
switch
knobs
on both
sides to
turn
the
power “ON”
5
th
Step:S
elect
one
of auto
m
atic
stimulation
progra
ms6
th
Step
:
Gradually
adjust
themassage
intensity
7
th
Step:S
elect
one
of
m
assage
m
o
des
and
adj
ustthe
electr
o
nic
pulsesp
eed
8
th
Step:Startmassaging
9
th
Step
:
Rotate
the
switch
knobs
on both
sides to
turn
off the
device
For the
details
of operation,
please
see
the
following
operating
instructions.
Description
of
Operation
Diagram
1
st
Step
–
Turn both knob
s to “OFF”, then
i
nsert t
he4pc
AAA
batte
ri
es
into the
Battery
compartment
and
direction
Make
sure
both
the
power
knobs
on
both
sides
aretur
ned OFF.
To
insert the
batt
e
ry,
slide
the
com
partment
cover
d
o
wnward
until
theco
ver pops
off.
Insert 4
p
c
AAA
batteriesac
cording to
the
diagram in
the
battery
compart
m
ent,a
nd
then
close
the
cover.
Match
the
flat end
of
the
battery
to
the
negative “
-” ma
rk
and match
the
other
end to the positive mark
“+”.2
n
d
Step
-
Connect
the
electrode
pads
to
the
wire
and
then
con
n
ectthewire
to
the
device.
Electric
wire
insertion
Electric
wire
connection
to
the
electrode
pads
The device has two
identical ports for
connecting the two identical lead wires.
Each lead wire is coupled to a pair of
identical electrode pads. Connect the first
pair of
electro
depads
to the two terminals
of the first lead wire, and insert the first lead
wire’s other end
into the first port. Connect
the second pair of
electro
d
e pads to the two
terminals of the second lead wire, and insert
the second lead wire’s other end into the
second port.
One
channel
issu
ggested
for
the
first
time
use
3
rd
Step
- Put
the electrode
p
ads
onmassage
-
needed
body area.
5
2
pads
from
one
chan
nelare
placed
on
the
body
area
such
as
shoulder at
the
sa
me time.
Make sure
the
pads
stick
on
the
skin.
Do
not
place or
m
ove the
pads
when
the
device
is
on.
Keep
the
skin
clean
beforepla
cing
the pads
4thStep
-
Rotate
the
switch
knobs
on
both
sides to
m
ake
the
power “ON”.
Switch
Button
LCD display
shows
“P”
There
are
two identical
power
knobs
located on
the
device’s
upper left
and
upper
right
sides
respectively
.
To start use the device,
r
otate
the
switch knobs
to
turn
the
power
“ON”.
Afterwards, a
letter
“P”
willbeshowed
on the
LCD display.
You may use the two channels
simultaneously or separately.
If you decide to
use one channel only, you may
just
turn one
knob to “OFF”.
Do
not
rotate
the
switch
knob too
fast. This knob
is
also for
the
Intensity control.
5
th
Step
-
Select
o
neofauto
m
atic
stimulation
progra
ms5
auto
m
atic
sti
m
ulation
progra
ms+
repeat
Five
auto
m
atic
sti
m
ulation
progra
m
sforwaist,
shoulder,
joint,
hand/foot,
sole,plus
a “
repeat
”tosti
m
ulate the
same
area
again.
The
LCD display will
show
atim
erof15mi
nutes when you choose
one
of
the
m.6
th
Step
-
Gradually
increa
sethemassage
inten
s
itytoa
com
f
ortable
lev
e
l
Intensity
adjust
m
ent
The
beginning
intensity
level
should
start
from
1.Adjust
the
power/i
nten
sity
to a
comfortable level
during
the
treat
m
ent
by
tuning the power knobs
. The
lowest
level
is1and
the
strongest
level is
10.
7thStep
-
Select
oneofm
assage
m
odes
and
adju
stelectro
nic
pulse
speed
Massage
m
odes
and
Speed
Themanual
p
rogra
m
s
for
M
ASSAGE
,
BEAT
,
and
KNEAD can be selected by
pressing the corresponding button
.
Speed
program
is
available
for
them.
Find
suitable
speed
by tuning
“Speed
+”
or “Speed
–
”.
Note:
Important:
6
8
th
Step
-St
art
m
assaging
After
these
tting
of device,
it
is
working
.
The
pads c
anbecovered
with clothing.
Turn
off the
device
if
necessary
or
whenever you don’t feel comfortable.
9
th
Step
-Rotate
the
switch
knobs on both
sides to
turn
off the
device.
The
best
treat
m
enttimeis
~15
minutes
each
session
.
Disconnect
the
wires and
electrode
pads after
themassaging.
Take
the
batteries
outifnot
used frequently.
Put
the
device
inadry and
s
h
ady
place.
Please
m
ake
sure every
part
of
device
and
accessories
in
good conditions
before
the
use of the
device.
Ask for
replace
m
entincase
of any
breaking,
cracking and
scratching.
Important:
7
Performance Specifications
Power Source
6V
Battery
Number
of Output
Modes
3Num
berofAlternating
Output
Channels
2Timer
Range
(minutes)
15 minW
eight
8.21 oz.
(battery
and
wire
included)
Dim
ensions
(in.)[Wx H x D]
2.24 x
7.80 x 0.91
W
avefo
r
m
Monophasic
Shape
Rectangular
Maxi
mum
Output
V
oltage
12.8V@50
0
?
51V@ 2 k
?
368V@10
k
?
Maxi
mum
Output
Current
15
m
A
@50
0?3.2
mA@2k?0.6
m
A
@10
k?Duration
of pri
m
ary
(depolarizing)
phase
40
m
sec
Pulse
Duration
100
—
680 µsec
Frequency
1
-
100Hz
Net
Cha
r
ge
18000µC@50
0
?
Maxi
mum
Phase Cha
r
ge
23 µC @50
0
?
Maxi
mum
Current
Density
1.4mA
/cm
²
@500
?
Maxi
mumAverage
Current
18mA
@50
0
?
Maxi
mumAverage
Power Density
0.23
W
/cm
²
@50
0
?
Burst
Mode (Pulses per
burst)
1
(Bursts per
second)
25
(Burst
duration)
0.2
-
1 sec
(Duty Cycle)
5
-25ONTi
me1 sec
OFF
T
ime
1 sec
84.5.
Quality A
s
surance Tests
Key function test
LCD chec
k
Program s
t
ability te
s
t
How
to
clean
the
Electronic Pulse Massager
Maintaining
the
Elec
t
ronic Pulse Massager
How to store the Electronic Pulse Massager
The
test
res
u
lt
of each
step
should
meet
the
following
pass criteria.
Other
w
ise,itis considered
failed
and
you should
contact
P
rospera
Corporation
for a
repair
or replace
m
ent.
:
W
hen
the
functional
keys are
pressed
step
by step,
the
outputs
of the device
should
be
identical
to
the
following
description:
1.When
the
left
or rig
h
t
ON/OFF knob at
the
o
f
f condition
is
turned
on, the
device
is
turned
on
but
no output
at
the
mom
ent.
2.When
the
function
keys (such as knead
and
massage)
are
pressed,
the
corresponding output
willbegenerated
on the
turned
-
on
side.
3.When
the
left
or right
intensity
-
adjust
knob is
gradually
turned,
the
intensity
of the
output
on
the
corresponding
side
will
be
adjusted
to
the
level
showed on the
knob.
4.When
the
increase/
d
ecrease
speed
keys are
pressed, the
speed
of the
outputs
on both le
ftand
right
sides will
b
e
adju
sted
to
the
level
displayed
on the
LCD screen.
:
The
information
displayed
on the
LCDscreen
should
be
identical
to
the following
descriptio
n:1.
When the
ON/OFF knob is
turned on
to
start
the
device,
the
LCD screen
displays
a
letter
“P”.2.When a button of “Massage”, “Beat” or “Knead” is selected, the
LCDscreen
d
i
splays an icon
corresponding to
the selected button.
3.
When a button of “Waist”, “Shoulder”, “Joint”, “Hand
-
Foot” or “Sole” is selected, the
LCDscreen
d
i
splays a dot on a position in a human figure icon corresponding to
the selected
button.
When t
he speed + adjustment key is pressed, the
LCDscreen
d
i
splays a
speed bar comprising
of
squares
which are moving faster
.
When the speed
-
adjustment key is pressed, the L
CD
screen
d
i
splays a speed bar comprising
of squares which are moving slower.
:
The
program
should
work consistently
and
identically
as
designed
duringmultiple
test
s.
Use da
mpcloth
or water
to
clean
the
device.
Do not
let
the
sticky
side
of the
pad
touch anything,
including
the
greasy
finger
tips.
Clean
the
pads, if
necessary,
with
a
soft damp cloth.
1.
The
device
uses 4pc
A
AA batteries.
To
replace
the
battery,
m
ake
sure both
switch knobs are
turned
“OFF”. Slide
the
compart
m
ent
cover
open.
Rem
ove
the
old
batteries. Insert
4pc
AAA
batteries
according
to
the
diagram.
And finally
close
the
cover.
2.Besure t
heelectrode
p
ads
aresu
itable
sticky.
R
eplace
the
p
adsifthe
following situ
a
tions
oc
cur:a)
can
notsense the
stimulation;
b) the
stimulation
is
weaker;
c)
cannot stick
the
pads
on the
skin;
d)
electrode
pads
are
oily
, wet,
or
their
cover
s
having breaking or worn
out.
Recommend
to
use Prospera’s electrode
pads.
3.
Change
a
new wire
if
it
is
too
old
or broken.
Recommend
to
use
Prospera’s wire.
Environ
m
ental
condition
for transport
and
storage
9
Easily
fragile
product
.
Keep
the
product
in
the
dry place.
Be
away
from
water
and
rain.
Product
package
should
be
recycled.
Stacked
up 4 cartons
at
most
.
Te
m
perature
range:
0oCto48
o
C
Humi
dity:
1
0% to
85%
A
tmospheric
pressure:
400hpa
to
1060pha
The
electrode
pads co
ming
with
the
device
are
disposable,
and
should
be
replaced
when their
adhe
si
veness
becom
es
worse. Contact
Prospera
for re
placements.
Do not
letth
e sticky
side
of the
pad
touch
anything,
includ
ingthe
greasy
finger
tips.
Clean
the
pads, if necessary,
with
a
soft
damp
cloth.
Contact
Prospera
toorderreplacement
parts.
Be
sure to
use
only
Prospera’s Electro
n
ic Pulse
Massager
Check
the
Prospera website
at
www.prosperacorp.com
for additional Product
infor
m
ation.
Electronic
P
ulse
Massager
---
Part
# PL009
Electrode
Pads
---
Part #
P
L009
-
P
Electric
Wire
----
Part
# PL009
-
W
1. The
PL009
Electronic
Pulse
Massager is
compliance
with:
Medical
electrical
equip
m
ent-Part1:General
require
m
ents
for safety.
Medical
electrical
equip
m
ent
-Part1-2:
General
require
m
ents
for saf
ety
CollateralSt
anda
rd"-Ele
ctrom
agnetic
compatibility
-
Require
m
ents
and
test
s.Medical
electrical
equip
m
ent-Part2:Particular
require
m
ents
for the
safety
of nerve
andmuscle
sti
m
ulators.
2. The
electro
depadiscompliance
with:
Biological
Evaluation
of Medical
Devices-
Part5:Tests
for In
Vitro
Cytot
o
xicity
.
Biological
evaluation
of
m
edical
d
evices
-
Part10:Tests
for
irritation
a
nddelaye
d-type
hyperse
n
sitivity.
When to order new pads
Part Replacement
.
Conformity to Standards
IEC60601
-
1
IEC60601
-1-
2
IEC 60601
-
2-10
EN ISO 10993
-
5
EN ISO 10993
-
10
•••••
10
Trouble Sho
o
ting
If the
device
is
not
operating
properly,
please
check
it
for the
following
proble
m
s
or conditions.
If
the
recom
m
ended
action
does not
s
o
lve
the
proble
m,please
return
it
to
the authorized
d
ealer
for
the
replace
m
ent/repair
of the
device.
MALFUNCTION
CAUSE
SOLUTION
Stimulation
is
weak
or not
existent
Are the
electrode
heads
in
close
cont
act
withth
eskin?Do the
electrode
heads
touch
eachot
her?
Are the
wires connected
to
the
electro
deheads
and
the
m
ain
device
properly?
Are the
batteries
dead?Rem
ove,
clean
and
place
back
on the
skin.
If so then
separate.
Disconnect,
clean
and
reconnect
all
the
parts.
Replace
the
dead
batteries.
Skin
turns red
Is treat
m
enttim
e
too
long?
Treat
another
area.
Skin
feels
numbAre electro
deheads
dirty?
Do the
electrode
heads
touch
the
skin
closely?
Clean
withdam
p
cloth.
Remove
and
place
a
g
ain
on
the
skin.Device
does not
turnonBatteries
installed
correctly?
Are batteries
dea
d?Rem
ove
and
install
batteries.
Replace
the
dead
batteries.
Pads are
not
sticky
Pads get
d
e
teriorative
Contact
Prospera for
replace
m
ents.
11
Consumer
Warranty
Prospera offers a
90-day
standard
warranty
to
the
m
assage
products.
Labor
and
parts
are included
during
warranty
period.
Consu
m
ers
are
required
to
provide
m
odelnum
ber
and dated
proof of
purchase
(sa
lesreceipt)
when contacting
P
rospera
for the
w
arranty service.
Non
-
warranty
servi
ceis
provided
on a
“perin
cident”basis.Th
e
consu
merwillve
rify that
the
product
has failed
and
provide
infor
m
ation
for servicing
the
unit.
All
applica
b
le repairs,
parts,
shipping,
handling,
local
tax
and
“per
incident”
fees
willbe
charged
for non
-
warranty
repairs
and
support calls.
12
Positions
\
\
W ais t
S ho uld er
Jo ints
Sole
of
Foot
v
Hand
or
Foot
(
(
n
13
Warranty
C
ard
Warranty Registration Form
Product
Name:
Product
Model:
Date
of Purchase:
First
Na
m
e:
Address:
Purchase
Price:
Retailer:
Last
Name:
City:
Phone:
Signature
and
date:
State:
E
m
ail:
Zip:
Please
m
ail
to:
Prospera Corporation
405 Boulder
Ct,
Ste
500
Pleasanton,
CA 94566
Telephone:
925-225-0888
Fax:
925-225-0660
E
m
ail:
sales@
p
rosperacorp.com
Manufact
u
rer’s Cont
a
ct Information
Prospera Corporation
(
U
.S.)
405 Boulder
Court,
Suite
500
Pleasanton,
CA 94566
Tel:
925-225-0888
Fax:
925-225
-
0660
E
m
ail:
jane@prosper
ac
orp.com
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