NEXALIN ADI User manual

i
Bob
OPERATING INSTRUCTIONS
Nexalin®ADIDevice
Nexalin Support Center
1776 Yorktown Ave #550
Houston, TX 77056
Telephone: [phone]
Website: www.nexalintechnology.com
The Future of Brain-Based Health

ii
This document was, as much as possible, accurate at the time of release. However, changes may have
been made to the device it describes since that time. Late-breaking information may be supplied
separately in the form of Advisory Notices.
Nexalin® is a registered trademark of Nexalin Technology, Inc.
The Nexalin ADI Device is manufactured by Nexalin Technology, Inc. and marketed by Nexalin
Technology, Inc. for exclusive use at Nexalin Advanced Therapy Centers.
Document Number: IFU-7006-00
Part Number: KS09003, Rev 01
Copyright © July 2013 by Nexalin Technology, Inc.
1776 Yorktown Ave #550, Houston, TX 77056
All rights reserved. No part of this document may be reproduced by any means with - out the prior
written permission of Nexalin Technology, Inc.
Nexalin Support Center
Telephone: [phone]
Website: www.nexalintechnology.com

iii
Table of Contents
SECTION 1
The Nexalin ADI Device ..................................................................................................................5
Intended Use ..................................................................................................................................5
Contraindications ...........................................................................................................................5
Warnings and Limitations ..............................................................................................................5
Possible Adverse Side Effects ........................................................................................................6
Explanation of Symbols ..................................................................................................................7
SECTION 2
Nexalin ADI Device Specifications ..................................................................................................8
Applicable Standards .....................................................................................................................8
Electrical .........................................................................................................................................8
Environmental ...............................................................................................................................8
Mechanical .....................................................................................................................................8
SECTION 3
The Nexalin ADI System .................................................................................................................9
Nexalin Electrodes .........................................................................................................................9
Nexalin ADI Device Setup ...............................................................................................................9
SECTION 4
Nexalin ADI System Operations ...................................................................................................10
Instructions for the Patient ..........................................................................................................10
Powering On the Nexalin ADI Device............................................................................................10
Preparing the Patient ...................................................................................................................11
Applying the Nexalin Electrodes ..................................................................................................11
Attaching the Nexalin Electrode Clips ..........................................................................................12
The Nexalin ADI Therapy Session .................................................................................................12
Completing the Nexalin ADI Therapy Session ..............................................................................12
Pause Mode .................................................................................................................................12
Default Nexalin ADI Device Parameters .......................................................................................13
Nexalin ADI Device Status Indications .........................................................................................14
Check Electrode LED.....................................................................................................................14
Battery LED...................................................................................................................................15
System Error LED .........................................................................................................................16
Error Code 9 .................................................................................................................................16
All Other Error Codes....................................................................................................................17

iv
Table of Contents (continued)
SECTION 5
Service and Maintenance ............................................................................................................18
Cleaning the Nexalin ADI System .................................................................................................18
SECTION 6
Nexalin ADI Device Accessories ...................................................................................................19
SECTION 7
Limited Warranty and Expected Life ............................................................................................19
Nexalin ADI Device Returns .........................................................................................................19
Contact Information ....................................................................................................................20
Disposal of the Nexalin ADI System Products ..............................................................................20
(This Space Intentionally Left Blank)

1
SECTION 1
The Nexalin® ADI Device
The Nexalin® ADI Device is a FDA-cleared transcranial electrical stimulation (TES) or cranial electrotherapy
stimulation (CES) device manufactured by Nexalin Technology, Inc. It delivers a safe and effective electrical
stimulation to the patient that provides relief from the symptoms associated with anxiety, depression, and
insomnia.
The proper use of the Nexalin ADI Device includes the application of three external electrodes. One electrode
is placed on the patient's forehead and one is placed behind each ear over the mastoid area. These three
electrodes are specifically placed to enhance the performance of the Nexalin ADI Device. When the device is
activated, a mild current travels between the forehead electrode and each mastoid electrode. The level of
current and the duration of the Nexalin ADI Therapy session are preset to default parameters and cannot be
changed.
The Nexalin ADI Device includes several features that are designed to protect the patient during a Nexalin ADI
Therapy session. When followed properly, these operating Instructions will help to ensure that a safe and
effective treatment is administered.
Intended Use
The Nexalin ADI Device is classified as cranial electrotherapy stimulation (CES) device. Its intended use is for
relief from the symptoms associated with anxiety, depression, and insomnia.
The Nexalin ADI Device is intended for use by or on the order of a licensed healthcare practitioner. Only a
Nexalin Certified Technician (NCT) is qualified to operate and administer a Nexalin ADI Therapy Treatment
session.
Contraindications
Use of the Nexalin ADI Device is strictly prohibited if the patient has any of the following conditions:
History of seizures, epilepsy, hydrocephalus, or tumors of the central nervous system.
Acute brain injuries and infections.
Break in skin integrity at the areas of electrode placement.
Skin sensitivity to electrode gels or adhesives.
Presence of implanted electronic stimulators.
Pregnant or may be pregnant.
Children, ages 12 and under.
Warnings and Limitations
Use of the Nexalin ADI Device may have an increased or decreased effectiveness if the patient has any of the
following conditions:
Acute psychiatric disorders (not depression).
Presence of the pronounced habituation of morphine-like substances. Use of psychoactive drugs.