Accelerated Care Plus Neuroprobe 500 Pro User manual

COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
NEUROPROBE®500 PRO
Electrotherapy / Infrared Therapy System
User Manual
REVISED 08.30.2017
PART NO. 72266 290NPRB Rev 4
This manual and all content therein is owned exclusively by Accelerated Care Plus ("ACP") and is protected by
copyright. This manual or any portion thereof may not be photocopied, reproduced or translated to another language
without the express prior written consent of ACP. This manual may only be used by entities that have purchased the
equipment or have implemented the ACP program and are covered by an executed lease agreement. This manual
may not be used for any other purpose.
Any additional copies of the Manual shall be ordered from ACP. No changes or modifications shall be made to the
Manual without prior review and written authorization from ACP. No authorization is given to market, sell, disclose,
or exploit this Manual except as for purposes of using the Equipment as contemplated by the Lease Agreement.
ACCELERATED CARE PLUS MAKES NO WARRANTY OF ANY KIND WITH REGARD TO THIS
MANUAL, INCLUDING, BUT NOT LIMITED TO, THE IMPLIED WARRANTIES OF MERCHANTABILITY
AND FITNESS FOR A PARTICULAR PURPOSE. Accelerated Care Plus shall not be liable for errors contained
herein or for incidental or consequential damages in connection with the furnishing, performance or use of this
Manual. The information contained in this document is subject to change without notice.

2 NEUROPROBE®500 PRO USER MANUAL
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
NEUROPROBE®500 PRO
Electrotherapy / Infrared Therapy System
ACP manufactures a premier line of rehabilitation technologies to assist health care professionals with improved
outcomes and quality-of-life for Patients. The ACP product line includes Pain Control Systems, Muscle Stimulators,
Interferential Therapy, Therapeutic Ultrasound, Pulsed Shortwave Diathermy devices, and advanced Therapeutic
Exercise Systems. Our MEGAPULSE®, NEUROPROBE®, OMNISTIM®, OMNISOUND®, OMNICYCLE®,
OMNIVR®, OMNISTAND®, OMNIVERSA®, OMNISWD®and SYNCHRONY®represent the most recent
worldwide advances available for therapeutic application of electromedical devices and other rehabilitation
technology.
ACP is internationally recognized for its contribution to research in the development of medical applications for
therapeutic rehabilitation. The Company sponsors and conducts research at leading health care institutions and major
universities throughout the world.

NEUROPROBE®500 PRO USER MANUAL 3
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
SYMBOLS ON THE PRODUCT
Symbol
Used for
Symbol
Used for
Serial number
Type BF medical device per:
IEC 60601
Date of manufacture
Manufacturer
Caution, consult accompanying
documents
Caution, electrical precautions
Remote Control connection
CE mark of confidence compliant
to MDD (93/42/EEC)
Connection Electrode Cable
IP2X
Classification against intrusion of
water, dust, accidental contact of
a body part.
Proper disposal required. Do not
dispose of with regular
household waste. Follow state
and/or local regulations.
Alternating current device.
Observe the user manual
Consult instructions for use
Protect the product from
humidity
ON / OFF push button

4 NEUROPROBE®500 PRO USER MANUAL
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
TABLE OF CONTENTS
SYMBOLS ON THE PRODUCT .....................................................................................3
ELECTROTHERAPY/INFRARED INDICATIONS & CONTRAINDICATIONS ...................................5
Indications.......................................................................................................................................................5
Contraindications ............................................................................................................................................5
ELECTROTHERAPY/INFRARED WARNINGS & PRECAUTIONS ...................................................6
Electrotherapy Warnings.................................................................................................................................6
Infrared Therapy Warnings .............................................................................................................................7
Electrotherapy Precautions..............................................................................................................................7
Infrared Precautions ........................................................................................................................................8
THE NEUROPROBE®500 PRO..........................................................................................................9
Delivery of the Neuroprobe®500 Pro .............................................................................................................9
Introduction.....................................................................................................................................................9
Controls and Functions..................................................................................................................................10
Factory Settings.............................................................................................................................................11
Power Supply Operation ...............................................................................................................................12
OPERATIONAL SEQUENCE............................................................................................................12
Infrared Therapy with SLD Pads...................................................................................................................12
IFC Therapy with Pad Electrodes..................................................................................................................13
Combination Therapy with IFC and SLD Infrared Pads...............................................................................14
Probe Mode POINT STIMULATION (Optional).........................................................................................15
TREATMENT GUIDELINES ..............................................................................................................16
Introduction to Medium Frequency Currents ................................................................................................16
Electrode Application Techniques ................................................................................................................17
SLD Infrared Pad Application Techniques ...................................................................................................19
Treatment Preparation...................................................................................................................................19
INFECTION CONTROL EQUIPMENT AND PRINCIPLES OF USE.................................................21
Definitions.....................................................................................................................................................21
Universal Precautions - Body Substance Isolation........................................................................................21
Cleaning / Disinfecting of the Neuroprobe®500 Pro....................................................................................21
Cleaning and Low Level Disinfection...........................................................................................................21
Intermediate Level Disinfection....................................................................................................................22
Use of Barriers - Intermediate Level Disinfection ........................................................................................23
Neuroprobe®500 Pro Program Menu.............................................................................................25
Infrared..........................................................................................................................................................25
Sensory - Motor.............................................................................................................................................25
Probe Noxious...............................................................................................................................................28
Nerve Block...................................................................................................................................................28
TROUBLESHOOTING.......................................................................................................................30
Service Center ...............................................................................................................................................32
SPECIFICATIONS .............................................................................................................................34
STANDARD AND OPTIONAL ACCESSORIES................................................................................36
SLD Infrared Pads.........................................................................................................................................37
Electrodes......................................................................................................................................................37
Infection Control Supplies.............................................................................................................................38
STANDARD LIMITED PRODUCT WARRANTY...............................................................................39
Warranty Coverage .......................................................................................................................................39
Warranty Exclusion.......................................................................................................................................39
Warranty Period ............................................................................................................................................39
Warranty Validation......................................................................................................................................39
Return of Defective Equipment.....................................................................................................................40

NEUROPROBE®500 PRO USER MANUAL 5
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
ELECTROTHERAPY/INFRARED INDICATIONS & CONTRAINDICATIONS
CAUTION: Federal law restricts this device for sale or use by or on the order of a Practitioner
licensed by the laws of the state in which he/she practices to use or order the use of the device.
Please notice that Accelerated Care Plus cannot provide medical advice. If you have specific
medical questions, please contact your healthcare professional.
Indications
Electrotherapy:
Transcutaneous Electrical Nerve Stimulation (TENS) –Interferential Current (IFC)
Symptomatic relief and management of chronic intractable pain and as an adjunctive treatment in the
management of acute pain, post-surgical pain and pain associated with post-traumatic injury.
Infrared:
Super Luminous Diode (SLD) Infrared Therapy
The SLD Infrared Therapy Pads are indicated for emitting energy in the infrared spectrum to provide topical heating
for the purpose of elevating tissue temperature for:
Temporary relief of minor muscle and joint pains.
Minor arthritis pain and muscle spasm.
Relieving stiffness.
Promoting the relaxation of muscle tissue.
Temporarily increase of local blood circulation.
Contraindications
Electrotherapy:
Transcutaneous Electrical Nerve Stimulation (TENS) –Interferential Current (IFC)
Transcutaneous electrical stimulation, or powered muscle stimulators should not be used on patients with
cardiac demand pacemakers and/or implanted defibrillators.
Never connect lead wires to the power line or electro-surgery equipment. Use only the lead wires
recommended or approved by the manufacturer.
NOTE: There is no contraindication to the application of Transcutaneous Electrical Stimulation over metal
implants.
Infrared:
Super Luminous Diode (SLD) Infrared Therapy
None.
NOTE: The SLD Infrared Pads may be used on patients with implanted Pacemakers and electronic devices, as
the Infrared therapy will not affect their operations. There is no contraindication to the application of SLD
Infrared Pads over metal implants.

6 NEUROPROBE®500 PRO USER MANUAL
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
ELECTROTHERAPY/INFRARED WARNINGS & PRECAUTIONS
CAUTION: Federal law restricts this device for sale or use by, or on the order of, a Practitioner
licensed by the laws of the state in which he/she practices to use or order the use of the device.
Please note that Accelerated Care Plus cannot provide medical advice. If you have specific
medical questions, please contact your healthcare professional.
Electrotherapy Warnings
The long-term effects of electrical stimulation are unknown;
Do not apply stimulation over the patient’s neck because this could cause severe muscle spasms resulting in
closure of the airway, difficulty in breathing, or adverse effects on heart rhythm or blood pressure
Do not apply stimulation across the patient’s chest because the introduction of electrical current into the chest
may cause rhythm disturbances to the patient’s heart, which could be lethal. Stimulation should not be applied
transthoracically in the vicinity of the heart, as introduction of electrical current into the heart may cause cardiac
arrhythmias.
Do not apply stimulation when the patient is in the bath or shower
Do not apply stimulation while the patient is sleeping; and
Do not apply stimulation while the patient is driving, operating machinery, or during any activity in which
electrical stimulation can put the patient at risk of injury.
Consult with the patient’s physician before using this device because the device may cause lethal rhythm
disturbances to the heart in susceptible individuals
Apply stimulation only to normal, intact, clean, healthy skin.
Do not operate this device until the User Manual, including all Indications for Use, Contraindications, Warnings
and Precautions, have been carefully read and understood.
Operation of this device or placement of lead wires, probes, pads and electrodes in close proximity (less than 5
feet) to an operating shortwave or microwave diathermy unit may produce instability in the device output or
burns at the treatment site. Lead wires and device can pick up the magnetic field output of the diathermy and
through induction convert it into an electrical field, transmit the energy into the patient increasing the current
density at the electrodes of applicators. Since the patient may not feel the 27 MHz frequency, they lack the
protective sensation and tissue burns could result. Short-wave field could potentially damage or reset medical
devices in close proximity to the drum applicator.
Treatment should not be applied over the carotid sinus nerves, (located in the anterior neck triangle), including,
stellate ganglion, vagus nerve, or laryngeal or pharyngeal muscle. Particular care should be taken for patients
with a known sensitivity to the carotid sinus reflex, as carotid sinus stimulation may alter blood pressure and
cardiac contractility.
Do not apply treatment over testes, heart or eyes. Electrical stimulation may affect organ function.
Do not apply over or in close proximity to active cancer (except in terminal / palliative / hospice care), as
therapy may increase blood flow to the tumor.
Treatment should not be applied when high fever is present over swollen, severe infection (osteomyelitis,
sepsis, tuberculosis, etc.) or inflamed areas/skin eruptions (phlebitis, thrombophlebitis, varicose veins, etc.).
Do not apply over the lumbar or abdominal region, or over the uterus during pregnancy (to prevent uterine
contraction), or during menstruation as therapy may temporarily increase menstrual flow.
Treatment should not be applied transcranially. Since the effects of stimulation of the brain are unknown,
stimulation should not be applied across the head, and electrodes should not be placed on opposite sides of the
head;
Stimulation should not be applied to patients connected to patient monitoring equipment, as the stimulation may
have an effect on the proper operation of the monitoring equipment.
Stimulation should not be applied directly over external stimulator systems with lead wires

NEUROPROBE®500 PRO USER MANUAL 7
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
Infrared Therapy Warnings
Avoid looking directly into the SLD Infrared Pads. High intensity light may have the potential for retinal
damage with prolonged exposure.
Do not apply to patients with photo dermatitis due to a condition (e.g. systemic lupus) or medication.
Do not apply on persons using immune suppressant drugs, or those taking steroid injections.
Electrotherapy Precautions
The safety of electrical stimulation during pregnancy has not been established;
Some patients may experience skin irritation or hypersensitivity due to the electrical stimulation or electrical
conductive medium. The irritation can usually be reduced by using an alternate conductive medium, or alternate
electrode placement.
Application site and settings should be based on the guidance of the prescribing practitioner.
All equipment and accessories should be kept out of the reach of children or unqualified persons.
Do not connect this device to any wall outlet that has not been properly grounded, or to any electrically non-
isolated medical device Powered muscle stimulators should be used only with the leads and electrodes
recommended for use by the manufacturer. Use this device only with the leads, electrodes, and accessories
recommended by the manufacturer. Use only ACP specified accessories and/or supplies with ACP devices. Do
not use any power cords, or power supplies, other than the ones provided or specified for this device. Use of any
other power supply could seriously damage the device and will void the warranty.
The use of conductive mediums other than specifically approved pre-gelled or self-adhering electrodes such as
ultrasound gel or lotion, hand or body lotion, electrolyte spray mist, paper towels, non-approved reusable or
disposable pre-gelled or self-adhering electrodes—are not advised for use with OmniVersa, Omnistim Systems.
When cleaning the device, never immerse them or wash them with water. See the infection control section in
this manual for cleaning instructions. Devices should not be submerged in water or other liquids.
Failure to follow the manufacturer’s prescribed maintenance for this device may lead to device failure and
transient or unreliable performance. State and federal survey and JCAHO require all equipment to be
maintained and calibrated according to the manufacturer recommended schedules.
A potential electric shock hazard exists once the device outer casing has been in part, or fully, removed. Only
qualified service personnel should perform Service and repairs. Warranty will be voided if the outer casing has
been removed or tampered with.
Use caution when the patient has a tendency to bleed internally, such as following an injury or fracture. Do not
apply over areas of hemorrhage or active bleeding.
Inspect and cleanse the skin prior to application. Following treatment check the skin for evidence of irritation
or burns, and if present, treat as appropriate. If the patient has, or complains of, skin irritation following
treatment; shorten the treatment time on the next treatment session, or use an alternative type of therapy or
electrode placement.
Gradually increase the output intensity/power to required dose or patient tolerance while monitoring the device
display.
Caution should be taken with patient exhibiting psychological or physical hypersensitivity to the therapeutic
treatment. Several attempts should be made to place them at ease so that their confidence and cooperation can
be gained during the treatment.
The treatment area should be checked from time to time, and if there is evidence of, or if the patient complains
of, pain during treatment, adjust the output downward until it is tolerated by the patient. If the patient continues
to complain of pain, discontinue the treatment and shorten the treatment time on the next treatment session, or
use an alternative type of therapy or electrode placement.

8 NEUROPROBE®500 PRO USER MANUAL
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
Do not apply treatment directly over/under hot or cold packs. Caution is recommended when treatment follows
the application of hot or cold therapy, which may alter the patient’s sensation. Application of thermal agents
over areas of impaired circulation should be performed with caution as the circulation may be insufficient to
heat or cool the tissue, altering the patient’s perception of warmth and pain, and burns or tissue necrosis may
result from subsequent treatment.
Caution is recommended when treatment follows the application of medicated patches, salves, or creams which
may alter the patient’s sensation. If there is a medical necessity to perform such treatments, these patients
should be monitored diligently during application. The effect of electrical stimulation may be altered by the
presence of these materials on the patient’s skin.
Caution should be used over areas of body where circulation is impaired, or which lack normal sensation.
Absent or diminished sensation should be avoided or, if unavoidable, treated with caution. Establishment of
acceptable intensity levels for desensitized areas may be related to the intensity levels tolerated on normal skin
in opposite or related body parts.
Caution should be used in the presence of recent surgical procedures, fractures or healing bone and soft tissue
when muscle contraction may disrupt the healing process.
Caution should be used for patients with suspected or diagnosed epilepsy. Patients with suspected or diagnosed
epilepsy should follow precautions recommended by their physicians.
Electrodes should not be placed in direct contact or in close proximity (one inch or less) of each other during
treatment. Electrodes placed in contact or in close proximity can lead to high energy density and skin burns
under or between the electrodes.
Care should be used when removing electrodes after treatment, in order to minimize the potential for skin
tearing. Skin should be inspected after removal of electrodes for any signs of tearing or irritation.
Do not connect the stimulator to any electrical equipment for combination therapy except the Omnisound®
family of ultrasounds.
Infrared Precautions
Lay the SLD Infrared Pads flat whenever possible. Avoid excessive or unnecessary bending.
Do not apply SLD Infrared Pads to the body if wet. Dry the area thoroughly. The electronics in the pad may be
short circuited if wet.

NEUROPROBE®500 PRO USER MANUAL 9
COPYRIGHT © 2006 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
THE NEUROPROBE®500 PRO
Delivery of the Neuroprobe®500 Pro
Upon receipt of your Neuroprobe®500 Pro inspect the shipping container and contents for any obvious or concealed
damage. All ACP products are packaged carefully for rapid, safe delivery. We guarantee delivery in perfect
condition to the postal or delivery services; however, any damage or loss incurred during transportation or delivery
is the postal or Delivery Company’s responsibility. If damage or loss to the product and/or container is obvious or
suspected, appropriate notation must be made on the signed freight bill at the time of delivery. All damage claims
should be promptly filed with the delivering carrier and must be initiated by the addressee where the package was to
be delivered. Retain the original shipping container and inserts for validation of damage claim or use at a later date.
Unpack and check all accessories. A list of enclosed accessories is provided with each unit to assist you in
identifying the type and number of accessories.
NOTE: The purpose of this manual is to acquaint you with the Neuroprobe
®
500 Pro’s operating features and
functionality. Please read the manual carefully before attempting to operate the Neuroprobe
®
500 Pro. If
questions remain unanswered, contact your local ACP representative, or call 1-800-350-1100. Outside the
USA, call 1-775-685-4000.
Introduction
The Neuroprobe®500 Pro gives the clinician the option of using any combination of an Estim probe, Interferential Current
in bipolar or quadripolar modes, or Monochromatic Infrared Therapy to reduce pain and increase circulation.
Flexible neoprene pads deliver heat and Infrared therapy through multiple clusters of infrared and red visible super
luminous diodes (SLD). The SLD cluster pads are contoured and designed for fast set-up over key nerves, arteries
and acu/trigger points.
The Neuroprobe®500 Pro offers audio and visual detection of acu/trigger points and is designed to provide Infrared
therapy, sensory, motor, noxious, and nerve block stimulation techniques for advanced pain management. Its two
separate generators produce medium frequency 5000 Hz alternating currents in continuous or modulated modes.
Two isolated output circuits with independent intensity controls are provided. The output of each circuit is easily
determined in milliamps or micro amps through the display screen. A probe mode and point locator is built into the
system to detect areas of low skin resistance and trigger points. The digital timer allows the operator to select the
length of the total treatment time and to monitor the time remaining in minutes.
The Neuroprobe®500 Pro offers Full Field (FF) Interferential Current (IFC) therapy. An interferential vector
scanning mode can be turned off or on for stationary or continuous movement of the interferential field.
The Neuroprobe®500 Pro’s optional probe with fully adjustable parameters provides a wide variety of uses for pain
management with trigger point stimulation for pain control.
The Neuroprobe®500 Pro provides a nerve block mode through treatment pads with high output capable of sensory
nerve block, or through the optional probe to produce local trigger point anesthesia.