Emsi Tens-6000 User manual

TENS-6000

INSTRUCTION

MANUAL

•El

TENS-6000

Pleaseread

the

instruction

manualbefore

u:

Caution: Federal

law

(USA) restricts this device

to

sell

by or on

the

order

of

a

phy

Contents

Chapter

Page

I

INTRODUCTION

I.

i

General

information

I

1.2

Indications

foruseI

1.3

Warnings

I

1.4

Precautions

2

1.5

AdverseReactions

3

PRODUCT

DESCRIPTIONS

2.1

Front

and

Rear

Panel

.4-6

STIMULATION

MODES

7-9

INSTRUCTIONS

FORUSE

4.1

Check

Battery

10

4.2

Connect

electrodes

to

leadwires

II

4.3

Connect

leadwires

to

unit

12

4.4

Place

electrodes

on

skin

13

4.5

Adjust

Output

13

4.6

Select

the

mode

14

Chapter

Page

4.7

Adjust

the

Pulse

Rate

14

4.8

Adjust

the

Pulse

Width

15

4.9

Adjust

Timer

15

4.10

AdjustChannelAmplitude

15

4.

II

Turn

Unit

Off

,

17

4.12

PatientCompliance

Timer

17

4.1

3

Portability

20

4.14

"

Low

Battery

"

indicator

, 20

4.15

Battery

21

4.16

Care

of

Electrodes

21

4.17

Care

of

Electrodecords

21

5

HANDLING

AND

STORAGE

22

6

SPECIFICATION

22

7

ACCESSORIES

23

8

TROUBLESHOOTING

24

/.

INTRODUCTION

I.I

Generalinformation:

ThisTENS

isa

lightweight

and

portable

medicaldevice,

which

can

help

to

reduce

the

pain

and

discomfort.

It

utilizes

the

low

electric-current

to

stimulatemuscle nerve

to

achieve

the

symptomaticrelief

of

chronicintractablepain,

post-traumatic

and

post-surgicalpain.

1.2.

Indications

for

use:

This

device

is

used

in

symptomaticrelief

of

chronicintractablepain,post-traumatic

and

post-surgicalpain.

1.3

Warnings:

1.3.1

The

long-term

effects

of

chronicelectricalstimulation

are

unknown.

1.3.2

Stimulation should

notbe

appliedover

the

carotid

sinus

nerves,particularly

in

patients

with

a

known

sensitivity

tothe

carotid

sinus

reflex.

1.3.3

Stimulation

should

notbe

appliedover

the

neck

or

mouth.

Severe

spasm

ofthe

laryngeal

and

pharyngeal

muscles

may

occur

andthe

contractions

may

occur

andthe

contractions

maybe

strong

enough

to

close

the

airway

or

cause

difficulty

in

breathing.

1.3.4

Stimulationshould

notbe

appliedtransthoracically

in

that

the

introduction

of

electricalcurrent

into

the

heart

may

cause

cardiacarrhythmias.

1.3.5

Stimulationshould

notbe

appliedoverswollen,infected,

or

inflamed

areas

or

skin

eruptions,

e.g.,

phlebitis,

thrombophlebitis,

varicoseveins,etc.

1.3.6

Stimulation

should

notbe

applied

over,

orin

proximity

to,

cancerous

lesions.

1.3.7

For

external

use

only.

1.3.8

Donotuse

TENS

ontheeye

area.

1.3.9

Thisdeviceshould

be

usedonlyunder

the

continuedsupervision

ofa

physician.

1.3.10

Safety

of

TENSdevices

foruse

during

pregnancy

or

delivery

hasnot

beenestablished.

1.3.11

Electronicequipment

such

asECG

monitors

andECG

alarms

maynot

operate

properly

whenTENS

isin

use.

1.3.12

Apply

the

electrodes

to

clean,

dryand

unbrokenskinonly.

1.3.13

Thisdeviceshould

notbe

used

while driving,operatingmachinery,

or

during

any

activity

in

which

involuntary musclecontractions

mayputthe

user

at

undue risk

of

injury.

1.3.14

Thisdeviceshould

be

kept

outofthe

reach

of

children.

1.4

Precautions:

1.4.1

Cautionshould

be

used

for

patients

with

suspected

or

diagnosedheartproblems.

1.4.2

Cautionshould

be

used

for

patients

with

suspected

or

diagnosed

epilepsy.

1.4.3

Cautionshould

be

used

inthe

presence

ofthe

following:

(a)When

there

isa

tendency

to

hemorrhage

following

acutetrauma

or

fracture;

(b)Following

recent

surgicalprocedureswhenmuscle

contraction

may

disrupt

the

healingprocess.

(c)Over

the

menstruating

or

pregnantuterus;

and

(d)Over

areas

ofthe

skinwhich

lack

normalsensation.

1.4.4

Somepatients

may

experienceskin

irritation

of

hypersensitivity

duetothe

electricalstimulation

or

electrical

conductivemedium.

The

irritation

can

usually

be

reduced

by

using

an

alternateconductivemedium,

or

alternate

electrode

placement.

1.4.5

Electrodeplacement

and

stimulationsettingsshould

be

based

onthe

guidance

ofthe

prescribing

practitioner.

1.4.6

Thisdeviceshould

be

used

only

with

the

leads

and

electrodesrecommended

forusebythe

manufacturer.

1

.4.7

Isolated

cases

of

skin

irritation

may

occur

atthe

site

ofthe

electrodeplacement

following

long-term

application.

1.4.8

Effectiveness

is

highlydependentuponpatient

selection

bya

personqualified

inthe

management

of

pain

patients.

1.4.9

Ifthe

stimulation

levels

are

uncomfortable

or

becomeuncomfortable,reduce

the

stimulationamplitude

toa

comfortable

level

and

contact

your

physician

if

problemspersist.

1.5

Adverse

Reactions:

1.5.1

Possible

skin

irritation

or

electrode

burn

under

the

electrodes

may

occur.

1.5.2

Possible

allergicskinreaction

to

tape

orgelmay

occur.

3

2.

PRODUCT

DESCR/PT/ONS

Z.I

none

ana

ncnr

pnnci,

'|0p

View

""—

">

Knob

Cover

Channl

1

On/Off

and.

Channl

2

On/Off

and

Front

View

j

jB

1^1

\

Knob

Cover

Channl

1

Output

^

R^lde""™'

^s^

Receptacle

Kecepiacie

Amplitude

Knob

^^K^^^^^

Battery

Indicator

Mode-.

'

yA

Back

View

Knob

Cover

Channl

Output

—

^^j-vMiaiMHJtt

Pulse

Rate

.__£^1,

A

i

^~~

clip

Decrease

Button

^

//

^"

\t

Button

-/

^

Mode

Button

*

Lid

Cover

' ' j

;

"

1

Battery

Cover

it

nil""

i"

—

"

—

1

Knob

Cover:

An

acrylic

knob

cover

can

protect

from

touching

Amplitude

Controls

when

the

unit

is

used.

After

adjusting

the

output,

remember

to

have

the

coverclosed.

Lid

Cover:

A

panelcovers

the

controls

for

Mode,Set,INCREASE

and

DECREASE

Adjusting.Yourmedicalprofessional

mayask

toset

these

controls

foryouand

request

that

you

leave

the

cover

in

place.

Amplitude

Controls:

It

controls

the

"INTENSTITY"

level

of

stimulating

pulses.

Thesecontrolslocated

atthetopofthe

unit

regulate

the

amplitude,

or

intensity,

ofthe

stimulation

andarethe

ON/OFF

CONTROL

TheON

indicator

light

will

stay

litas

long

asthe

unit

is

working,

and

mimics

the

output

ofthe

electricalpulse.

Caution:

If the

stimulation

levels

are

uncomfortable

or

become uncomfortable, reduce

the

stimulation

intensity

to a

comfortable

level

and

contact

your

physician

if

problems

persist.

"INCREASE"

increace

control

button

(using

a

triangle-button)

This

button

will

carry

the

increasecharacter

to

increase

the

pulse

width

from

50~300us,

andto

increase

the

pulse

rate

from

2 to

ISOHz,

andto

increase

the

timer

from

5 to90

mins

to

continuousmode.

"DECREASE"

decrease

control

button

(using

a

invertedtriangle-button)

This

button

will

carry

the

decrease

character

to

decrease

the

pulse

width

from

300~50us,

andto

decrease

the

pulse

rate

from

ISO

to

2Hz,

andto

decrease

the

timer

from

continuous mode

to90to5

min.

"MODE"

button

(using

a

round-button

onthe

right

side

ofthe

control

panel)

This

button

willcarry

the

character

to

select

fora

Stimulation-Mode.

It

offers

the

modestatus

from

fivetype

of

stimulationmodes,which

are

Burst,

Normal,

MRW(Modulated

Rate

and

Width),

SD(Strengh

Duration)

and

Bi-Pulse.

"SET"

button

(using

a

round-button

onthe

middle

ofthe

control

panel)

This

button

will

carry

the

character

tosetthe

rate,

width

and

timer.Users

press

the

"SET"

button

to

enter

a

parametersettingmodeincludingrate,width

and

timer.

LCD

screen

This

LCD

will

be

utilized

to

display

stimulating

mode/

pulse

width/

pulse

rate

andto

display

timer.

The

channel

output

will

be

indicated

onthe

leftside(Channel

I)

and

right

side

(Channel

2)oftheLCD

screen.

The

modes

will

be

showed

onthetopoftheLCD

panel.

The

pulse

rate

and

width

will

be

showed

onthe

middle-right

ofthe

screen.

The

timer

and

clocksymbol

are

showed

onthe

middle-right

ofthe

screen,

the

clocksymbol

will

flash

in

final

5

min.

Battery

compartment

9

Voltage

battery-

I pc

3.STJ/V1ULAT/ON

MODES

The

stimulationmodeoffers

a

variety

of

stimulationmodes.

The

button

is

locatedunder

the

front

lid

cover

andis

adjusted

by

pressing

onthe

"MODE"

control

button.

Be

sure

that

whenadjustingthesestimulationmodes,

control

functionsthat

the

intensity(Amplitude),

output

controls

aresettothe

minimum

output

positions.

3.1

BURST

Mode:

The

burst

modeprovides

a

"burst"

of

sevenpulses.There

aretwo

bursts

that

are

delivered

per

second.Positivepulse

and

negative

pulse

iterative

continuously

at

fixed

100

Hz.

Pulse

width

from

50~300us.

3.2

NORMAL

Mode:

The

Normal

modeproduces

a

continuoustrain

of

impulses.

The

stimulation

parameters

arenot

automatically

interrupted

nor

varied

inany

way.

In

thismode,

the

pulserate

(from

2 to

150Hz),

pulse

width

(from

50to

300us)

are

fully

adjustable.

The

normal mode

is

quiteversatile

because

itmaybe

applied

with

a

variety

of

rate

and

width

settings.

3.3

MRW

(Modulated

Rate

and

Width)

Mode:

The

pulse

rate

and

width

are

automaticallyvaried

ina

cycle

to

produce

a

pleasant,

massage-like

sensation.It'sbelievedthatnervescanbecomeaccustomedto,or

"accommodated

"

tothe

same

electricalstimulusafter

a

period

of

time

and

thus

wouldrequireincreasing

the

intensity

to

further

"block"

the

pain.

The

Modulation

mode

was

produced

to

offer

a

variety

of

differentelectricalstimulation,thus

preventingnerveaccommodation

so

that

less

intensity

is

required

for

long

and

'

7

H

£

effective

treatment.

In

thismode,during

the

beginning

of0.5

sec.period,

the

WIDTH

decreased

to

50%

ofits

original

setting

and

then

during

the

sec.

period,

the

RATE

is

decreased

to50%ofits

original

setting.Therefore,

the

total

cycle

time

isI

second.

0.5

sec

Set

Rate

O.Ssec

Set

Width

50%ofSet

Width

50%ofSet

Rate

6

seconds

3.4

SD

(Strength

Duration)

Mode:

Strength-Durationmodulation

consists

of

alternatingmodulatedintensity

and

pulse

width,

so

that

the

intensity

is

always

increasing

while

the

pulse

width

is

decreasing

and

vice-versa.

The

stimulationintensitymodulate

to

62.5%maximum

of

setting

(width

equal

to

setting).

The

pulse

width

modulate

to67%of

setting

(intensity

equal

to

setting).Total

cycle

time

is6

seconds.

Rate

(from

2~l50Hz),

width

(from

50~300us)

are

fully

adjustable.

3.5

Bi-Pulse

Mode:

Delivers

4

pulses

per

second

to

Channel

I

(i.e.

the

pulse

rate

of

Channel

I is

fixed

at

4 Hz)

while delivering

100

pulses

per

second

to

Channel2(i.e.

the

pulserate

of

Channel

2 is

fixed

at

100

Hz).Stimulation

is

burst

onfor

1.0

second,then

offfor

1.0

second.

There

illustration

each

pulse

as a

verticalline.

Pulse

width

(from

50~300us)

is

fully

adjustable.

NOTE:

Always

read this

instruction

manual beforeuse.

1sec.

(sec.

1sec.

4.

INSTRUCTIONS

FOR USE

PREPARATION

FORUSE

4.1

CheckBattery:

Proceed

to

insert

a fresh9V

alkaline

or

rechargeable

battery

into

the

batterycompartment.Makesure

that

youare

installing

the

batteriesproperly.

The

battery

is

inserted

inthe

casing

onthe

back

ofthe

stimulator

unit.

BE

SURE

TO

MATCH

THE

POSITIVE

AND

NEGATIVE ENDS

OFTHE

BATTERY

TOTHE

MARKINGS

INTHE

BATTERY

COMPARTMENT

OF

UNIT.

To

remove

the

batterycover,

press

andtugit

following

the

direction

ofthe

arrow

indicated

onthe

batterycover.

Note:

Please

install

batteries

according

to

their

positive(+)

and

negative

(-)

ends

correctly

V

CONNECTING

THE

STIMULATOR

4.2

Connect

electrodes

to

lead

wires:

Insert

the

lead

wire

connector

into

electrodes

connector

(standard

0.08inchfemale

connection).

MAKE

SURE

THAT

NO

BAREMETAL

OFTHE

PINS

IS

EXPOSE.

Caution:

f.

Always

use

electrodes

whose

measure

of

area

is

more

than

16

cm1

2.

Always

use

electrodes

which

are

legally

marketed

in the US

under

SlO(k)

procedure.

•••»•%*.

4.3

Connect

lead

wires

to

unit:

Before

proceeding

to

this step,

be

sure

the

unit

is

completely

turned

OFF.

Holding

the

insulated

portion

ofthe

lead

wire

connector,

insert

the

angled-"L"

plug

into

the

receptacle

onthetopofthe

main

unit.

Please

ensure

the

leads

are

inserted

correctly.

The

unit

hastwo

output

receptacles

which

are

controlled

by

Channel

I and

Channel

2

Amplitude

Control

knobs

at

thetopofthe

unit.

Youmay

choose

touseone

channel

with

one

pair

of

lead

wires

or

both

channels

with

two

pairs

of

lead

wires.

Using

both

channelsgive

the

user

the

advantage

of

stimulating

two

different

areas

atthe

same

time.

Angle"L"-shape

plug

Self-adhesive

ElectrodesPads

4.4

Placeelectrodes

on

skin:

Apply

electrodes

to the

exact

site

indicated

by

your

physician

following

the

instructionincluded

with

the

electrodeslabeling.Makesure that

the

electrodes

are

placed

firmly

to

skin

and

make

goodcontactbetween

the

skin

andthe

electrodes.Before

applying

electrodes,

be

sure

that

the

applied

skin

surface

is

thoroughly

cleaned

and

dried.

Place

the

electrodes

over

the

skin,

attach themproperly,

firmly

and

evenly.

ADJUSTING

THE

CONTROLS

4.5

Adjust

Output:

TurnAmplitude

Control

knob

for

Channel

I or2

clockwise.Then

you

will

hear

a

"

Bl!"

sound.Before

you

increase

the

Amplitude,

you

must

select

the

mode,

rate

and

width.

jp

4.6

Select

the

mode:

Press

"MODE"

button

tosetthe

stimulationmoderecommended

by

your

physician

or

therapist.

For

details

aboutstimulatingwaveform

and

sequences,

please

refer

to

Sec.

3

"StimulationModesdescriptions".

Caution:

Please consult

physicians

for

your

suitable

stimulation

mode.

4.7

Adjust

the

PulseRate:

The

pulses

rate

are

adjustable

2~l50Hz.

2Hz~20

Hz

inI Hz

increment

and

20~

ISO

Hzin5 Hz

increment.

Press

SET

button

to

enter

the

Pulse

Rate

set

function,then

press

INCREASE

or

DECREASE

button

to

adjust

Pulse

Rate

tothe

setting

recommended

by

your

medical

professional.

*

4.8

Adjust

the

Pulse

Width:

The

pulse

width

is

adjustable

50~300us

in

lOus

increment.

Press

SET

button

to

enter

the

Pulse

Width

set

function,

then

pressINCREASE

or

DECREASE

button

to

adjustPulse

Width

tothe

setting

recommended

by

your

medicalprofessional.

4.9

Adjust

Timer:

The

timer

is

adjustable

5~90minutes

or

continuous

in5

minutes

increment.

Continuous

option

is

just

the

to90

minutes,

i.e.

from

5-90

minutes

to

continuous

and

then

to5

minutes

isa

cycle.

During

5

minutes'

final

count

down,

the

clock

symbol

will

flashonce

every

one

second.

0

4.10

Adjust

Channel

Amplitude:

Turn

Channel

I or2

clockwise.

The

output

indication

will

be

showed

onthe

left

side

(Channel

I)

and

right

side

(Channel

2)oftheLCD

screen

as

long

asthe

unit

isin

operation.

Slowly

turn

the

Channel

Amplitude

control

until

you

reach

the

setting

recommended

by

your

medical

professional.Repeat

forthe

other

channel,

if

both

channels

are

tobe

used.

Caution:

Ifthe

stimulation

levels

ore

uncomfortable

or

become uncomfortable, reduce

the

stimulation

intensity

toa

comfortable

level

and

contact your physic/on

if

problems persist.

Operation Procedure Chart:

Press

"MODE"button

Burst

Mode

^'

Press

"MODE"button

Normal

Mode

Press

"MODE"button

MRVVMode

1

'

Press

"MODE"button

SO

Mode

1f

Press

"MODE"button

Bi-Pu/se

Mode

Adjust

(I)

Pulse

Width

(2)

Timer

by

"SET"

&

"

INCREASE/DECREASE"

button.

Adjust

(I)

Pulse

Rate

(2)

Pulse

Width

(3)

Timer

by

"SET"

&

"

INCREASE/DECREASE"

button.

Adjust

(I)

PulseRate

(2)

Pulse

Width

(3)

Timer

by

"SET"

&

"

INCREASE/DECREASE"

button.

Adjust

(I)

Pulse

Rate

(2)

Pulse

Width

(3)

Timer

by

"SET"

&

"

INCREASE/DECREASE"

button.

Adjust

(I)

Pulse

Width

(2)

Timer

by

"SET"

&

"

INCREASE/DECREASE"

button.

4.1

I

Turn

Unit

Off:

Turn

both

channel

controls

to

"off".

Thenunplug

the

electrode

lead

wires, graspingthem

bythe

plug,

notthe

cord.

If

treatment

will

be

resumedshortly

the

electrodes

maybe

left

onthe

skin.

When

the

electrodes

are

removed,

clean

the

skin

andthe

electrodesthoroughly

with

mild

soap

and

water.

If

there

is

skin

irritation

from

tape

or

gel,consult

yourprescriber.

Caution:

When

the

therapy

time

is

completed,

ifthe

user doesn't turn

offthe

amplitude

knob,

the

unit

will have

"Bi-Bi"

sound every

10

seconds until

the

amplitude

knob

is

turn

off

completely.

4.12

Patient

Compliance

Timer:

The

patient

compliance

timer

can

memorize

60

sets

of

operationrecords;

the

totalrecordtime

is999

hours.

After

the

unit

is

turnedoff,

youcan

start

touse

patientcompliancetimer.First,

press

and

hold"Mode"

button

and

turn

onthe

either

one

amplitude knob

simultaneously

to

initiatepatientcompliancetimer.

Individual

treatment

time:

Press

"INCREASE"

button

(triangle

button)

or

"DECREASE"

button

(inverted

triangle

button)

tosee

nextrecord

of

treatmenttime

with

the

number

of

times

or

of

treatmenttime

with

the

number

of

times.

Press

and

hold"Set"

button

for3

seconds

to

delete

theon

showingrecord.

After

theon

showingrecord

is

deleted,

the

unitwill

sound

"Bi".

n

JU"

M

VI

un

iu

NOTE:

1.

Ifthe

treatment

time

is

under

one

minute,

it

will

notbe

recorded

For

example,

If

your

treatment

time

is

10

minutes

and30

seconds,

the

patient

compliance

timer

will

record

10

minutes,

not

11

minutes.

2. The

patient

compliance

timer

can

only

record

up to 999

minutes

for

each

treatment. Therefore,

if

you

keep

using

the

stimulator

for

over

999

minutes,

it

will

only

record

999

minutes

andthe

record

time

will

flash

to

mean

the

treatment time

is

over

999

minutes.

Cumulativetreatmenttime:

When

initiating

patient

compliance

timer,

press

"Mode"

to

shift

the

record

of

individual

treatmenttime

with

the

number

of

times

tothe

record

of

cumulative

treatmenttime.Whenshowing

the

record

of

cumulative

treatmenttime,there

will

bean

"M"

mark

flashing

onthe

upper

right

corner

of

middle-right

screen.

Press

and

hold"Mode"

&

"Set"button

simultaneously

for3

seconds

to

delete

all

the

records

including

individualtreatmenttimerecord

and

cumulativetreatment

timerecord.

%

The

patient

compliance timer will keep

the

records

even when

the

battery

has no

charge. Only when

users

press

and

hold

"

Set"

or

"Mode"

&

"Set",

the

recordswill

be

deleted.

H2

ICU

CARE

AND

MAINTENANCE

4.13

Portability:

Your

Unit

is

portable

andmaybe

clipped

toa

belt,shirtpocket,

braor

otherclothing.

4.14

"Low

Battery"

indicator:

When

thelow

powerindicator

flashes,

it

means

that

the

batteryshould

be

replaced

with

a newoneas

soon

as

possible.

However,

the

stimulatorwill

continue

to

operate

for

several

more

hours.

5.

HANDLING

AND

STORAGE

4.1

5

Battery:

^

To

replace

the

battery,

remove

the

battery

cover

and

extract

the

battery.

Replace

ita

with

a 9 V

alkaline

or

similar

rechargeable

battery.

Notice

that

the

battery

is*

inserted

correctly.

'i^l

nk.

4.16

Care

of

Electrodes:

To

avoid

skin

irritation

and

ensure

good

contact

with

skin,

clean

silicone

rubber

electrodes

with

soap

and

water

frequently.

The

electrodes

must

be

dried

completely

before

using.

^

Ifyouare

using

self-adhesive

electrodes,

please

disregard

this

procedure.

%*.

The

user

shall

always

usethe

electrodes which

fulfill

the

local regulatory

requirements.

4.17

Care

of

Electrode

cords:

Clean

the

electrodecords

by

wipingthem

with

damp

cloth.

Coatingthemlightly

with

talcum

powder

will

reduce

tangles

and

prolong

the

life.

.-*

in

Keep

.this

device

into

the

handy

carrying

case

and

storage

at

room

temperature.

6.

SPECIFICATION

Channel

PowerSource:

Output

waveform;

Pulse

Width:

Pulse

Frequency:

Adjustable

Intensity

Levels:

Five

Massage

Modes:

PatientComplianceTimer

Operationambient:

Storage

&

transportation:

Timer:

Lead

wires:

Safety

standard

Dual,isolatedbetween

channels

9V

DC

square

shape

battery(alkalinebatteries

or

similar rechargeablecell)

Asymmetric

biphasicsquarepulse.

Variable,

50~300us

Variable,

2-150

Hz

0to40

Volcs(at

load=500

ohm)

Burst

Normal

MRW

SD

Bi-Pulse

Memorize

60

sets

of

operationrecords

Total

recordtime

is999

hours

temperaturerange:IO-35°C

humidityrange:

20-90%RH

temperature

Range:

0°C-70°C

humidity

Range:

20-90%RH

5~90Minutes

auto-shutoff

or

Continuous

male

connector

2.00+OJ

IEC

6060

1

-

1

,

IEC6060

1

-

1

-2(EMC

test),

IEC

6060

1

-2-

1

0(partly

applied)

8.

TROUBLESHOOTING

Stimulation

Modes descriptions

Mode

Pulse

Frequency

Pulse

Width

Cycle

Time

BURST

Fixed

lOOHz

50~300us

0.5

Sec.

NORMAL

2~

1

SOHz,

50~300us

Constant.

MRW

2-1

SOHz

50~300us

1

Sec.

SD

2~l50Hz

50~300us

6

Sec.

BI-PULSE

Channel

1

fixat

4Hz,Channel

2 fixat

1

OOHz

50~300us

2

Sec.

Unit:

Voltage

At

Load

SOOQ

*The

values

of

digital

settings

hove

±5%

tolerance.

7

ACCESSORIES

4

PCS.

1

PC.

2

PCS.

IPC.

If

yourunit

does

not

seem

tobe

operatingcorrectly,refer

tothe

chartbelow

to

determinewhat

maybe

wrong.

Should

none

of

these

measures

correct

the

problem,

the

unit

should

be

serviced.

Self-Adhesive

Electrodes

9

V

Battery

Lead

Wires

Instructional

Manual

•TheLCD

indicatorlights

upbut

unit

does

not

functionproperly.

1.

Check

all

control

settings.

Are

they

setto

values

prescribed

by

your

medical

professional

?

2.

Are

electrodes

in

proper

position?

3.

Check

lead

wires.

Be

sure

all

connectors

are

firmly

sealed.

4.

Replace

cord

set

withanother

to

check

for

broken

wires.

1

Low

Batteryindicator

flash.

.

Replace

battery

with

a new

one.

'

None

ofLCD

indicatorslights

up.

I.

Replace

battery

with

a new

one.

EMSI TENS-6000 User manual

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