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a Synapse electroceutical technology

General Instructions for Use

In addition, see product packaging for instructions specific to your device.

Electroceutical treatment for complex wounds 

Accel-Heal® is a Class IIa registered medical device designed to accelerate healing in complex wounds using proprietary 
electroceutical programs.

The Accel-Heal

®

 treatment uses 6 single use devices used consecutively to deliver 12 days of treatment and is intended for use for 

the treatment of complex wounds. The units may be used during sleep.

1. 

Clean the skin surrounding the wound with the alcohol 

wipes included in the pack. 

  Attach the Accel-Heal® Unit to the electrode pads by 

connecting the cables from the Accel-Heal® Unit to the 

electrical leads from the electrode pads. 

 

  Do this by pushing the electrode connectors at the end 

of the cables leading from the Accel-Heal® Unit into the 

electrode receptors at the end of the electrical leads 

leading from the electrode pads. 

2. 

Press and hold button for 2 seconds to activate device.

Activating the Program

 

When your 

fi

nger is released the program will com-

mence its operation and the green LED will 

fl

ash once 

every two seconds. The program runs its speci

fi

sequence after which time the device will turn itself 

o

ff

. That’s it, it is that simple.

Connect the electrical leads from the electrode pads to

the cable ends from the Accel-Heal® Unit.

3. 

Flashing green light indicates activation. 

Device will now run for 48 hours.

Stopping the Program Part-Way Through

 

If you wish to cease a program part-way through, the 

device may be switched o

ff

 by pressing and holding 

down the on/o

ff

 button for 2 seconds. When the de-

vice is re-started a new program will start from 

the beginning.

  The following rules should be adhered to when using 

a Synapse Electroceutical device.

Treatment Discomfort

 

Synapse Electroceutical treatments should be pain 

free and sub-sensory (without feeling). However a 

tingling sensation may be felt by some users and 

is normal. If discomfort is experienced the device 

should be switched o

ff

 and the electrodes removed 

immediately. Therefore, if in the unlikely event you do 

feel increased pain or discomfort following use of the 

device, please cease using it immediately and contact 

your referring clinician. We strongly advise that the 

electroceutical treatments will be more e

ff

ective if you 

are well hydrated, in addition, ensure the skin is clean 

and dry before pad placement.

Skin Irritation 

 

In the unlikely event that skin irritation develops 

please stop using the Synapse Electroceutical device 

and contact your clinician. Please do ensure that the 

pads are clean prior to use.

Contra-indications Hazards 

Your clinician should have explained the few con-

tra-indications for using the device; these are:

Heart Conditions 

Consult your physician before using the Synapse Elec-

troceutical device if you have a heart condition and/or 

have an implanted cardiac pacemaker.

%

95%

  The program will now run its 48 hour sequence after 

which time the unit will turn itself o

ff

.  At this time 

you should apply the next unit following the same 

directions as above until the full course of treatment is 

completed.

Attach the electrodes either side of wound or dressing

area.

Trouble Shooting

 

Problem

: When there is poor contact between the 

conducting electrode pads and the skin, the green ‘ON’ 

light/LED 

fl

ashes more quickly at a rate of twice per 

second.

  Remedy

: Clean the skin and reapply or use fresh pads.

  Problem

: The green ‘ON’ light will not light.

  Remedy

: The device has completed its treatment 

course. Please return the device via the instructions 

below.

Returning the Devices

  Please dispose of used and decontaminated 

devices in your organisation’s Waste Electrical and 

Electronics Equipment (WEEE) disposal facility. Al-

ternatively, please contact Synapse Electroceutical 

Ltd. on 01959 569433 to obtain a return envelope. 

The devices will then be disposed of in an environ-

mentally sound manner. These devices are medical 

electrical devices and should not be disposed of 

with general waste. Devices will only be accepted 

if accompanied with a decontamination certi

fi

cate 

or statement of decontamination. Devices can be 

decontaminated by wiping them gently with 70% 

isopropyl alcohol.

General Advice

 

The Synapse Electroceutical devices have been 

developed as a result of signi

fi

cant medical and sci-

enti

fi

c research and they are intended to be used/

recommended for use by a medical or healthcare 

clinician/practitioner following a consultation. 

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