Accelerated Care Plus OMNISOUND 3000C PRO User manual

COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
OMNISOUND®3000C PRO
Ultrasound Therapy System
User Manual
REVISED 08.22.2017
PART NO.32223…2903000C REV 3
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.

OMNISOUND®3000C PRO USER MANUAL 1
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
OMNISOUND®3000C PRO
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®, OMNIBAND®,
OMNITEST®, OMNICYCLE®,and OMNIVR®represent the most recent world wide 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.

2 OMNISOUND®3000C PRO USER MANUAL
COPYRIGHT © 2001 - 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

OMNISOUND®3000C PRO USER MANUAL 3
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
TABLE OF CONTENTS
SYMBOLS ON THE PRODUCT...............................................................................................................................2
ULTRASOUND INDICATIONS & CONTRAINDICATIONS..............................................................................4
Indications ..........................................................................................................................................................4
Contraindications................................................................................................................................................4
ULTRASOUND WARNINGS & PRECAUTIONS..................................................................................................5
Warnings ............................................................................................................................................................5
Precautions .........................................................................................................................................................5
THE OMNISOUND®3000C PRO .............................................................................................................................7
Delivery of the Omnisound®3000C Pro ...........................................................................................................7
Introduction ........................................................................................................................................................7
Controls and Functions.......................................................................................................................................8
Default Operating Screen .................................................................................................................................10
Factory Settings................................................................................................................................................10
Power Supply Operation...................................................................................................................................11
Operational Sequence.......................................................................................................................................11
Application Techniques....................................................................................................................................13
Connection for Combination Therapy..............................................................................................................14
INFECTION CONTROL EQUIPMENT AND PRINCIPLES OF USE ..............................................................15
Definitions........................................................................................................................................................15
Universal Precautions –Body Substance Isolation ..........................................................................................15
Cleaning / Disinfecting of the Omnisound®3000C Pro...................................................................................15
Cleaning and Low Level Disinfection..............................................................................................................15
Intermediate Level Disinfection.......................................................................................................................15
Use of Barriers - Intermediate Level Disinfection............................................................................................17
MODES OF OPERATION.......................................................................................................................................18
History..............................................................................................................................................................18
Theory of Operation .........................................................................................................................................18
Temporal Variation of Ultrasonic Output.........................................................................................................19
Beam Characteristics, Power, and Intensity Measurement...............................................................................21
Temperature Mode of Operation / Delta T Mode.............................................................................................24
TROUBLESHOOTING............................................................................................................................................25
Calibration........................................................................................................................................................26
Service Center ..................................................................................................................................................26
TECHNICAL SPECIFICATIONS ..........................................................................................................................27
OMNISOUND®3000C PRO STANDARD AND OPTIONAL ACCESSORIES.................................................30
Infection Control Supplies................................................................................................................................31
STANDARD LIMITED PRODUCT WARRANTY...............................................................................................32
Warranty Coverage...........................................................................................................................................32
Warranty Exclusion..........................................................................................................................................32
Warranty Period ...............................................................................................................................................32
Warranty Validation.........................................................................................................................................32
Return of Defective Equipment........................................................................................................................33

4 OMNISOUND®3000C PRO USER MANUAL
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
ULTRASOUND 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
The Omnisound Pro is indicated for:
Relieving pain
Decreases joint stiffness and contractures
Reduction of muscle spasm
Increases local circulation
Relief of pain, muscle spasms, and joint contractures that may be associated with: adhesive capsulitis,
bursitis with slight calcification, myositis, soft tissue injuries, shortened tendons due to past injuries and
scar tissues
Relief of sub-chronic, chronic pain and joint contractures resulting from: capsular tightness, capsular scaring
Contraindications
Patients with an implanted medical device other than a pacemaker.
Near brain, cervical ganglia, spine, laminectomy sites (can cause spinal-cord heating)
Near the reproductive organs
Total hip arthroplasties with methylmethacrylate or high density polyethylene
Arthroplasties—the effect on bony ingrowth arthroplasties is not well defined; for this reason the most
prudent course is avoiding ultrasonic therapy over these areas
Note: There is no contraindication to the application of Ultrasound over metal implants.
Over or near bone growth centers until bone growth is complete
Over the thoracic area if the patient is using a cardiac pacemaker
In an area of the body where a malignancy is known to be present
In an area of the body where infectious disease is present
Blood vessels in poor condition should not be treated as the vessel walls may rupture as a result of the
exposure
Patients suffering from cardiac disease should not receive treatment over the cervical ganglia, the stellate
ganglion, the thorax in the region of the heart, or the vagus nerve, as a reflex coronary vasospasm might
result. Only low intensities and short treatment times should be used if these patients are treated in other
areas since the stimulation of practically any afferent autonomic nerve (especially the vagus nerve) in the
body may cause a change in cardiac rate
Patients with thrombophlebitis or other potentially thromboembolic diseases (such as DVT) should not be
treated since a partially disintegrated clot could result in an obstruction of the arterial supply to the brain,
heart or lungs
Over a healing fracture
Over the eye
Over the pregnant uterus

OMNISOUND®3000C PRO USER MANUAL 5
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
Over ischemic tissues in individuals with vascular disease where the blood supply would be unable to
follow the increase in metabolic demand
Over areas of recent bleeding or hemorrhage
Over areas of active tuberculosis
ULTRASOUND 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 notice that Accelerated Care Plus cannot provide medical advice. If you have specific
medical questions, please contact your healthcare professional.
Warnings
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. 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 heart. Thermal/sub-thermal treatment may affect organ function.
Treatment should not be applied when high fever is present.
Do not apply over the lumbar or abdominal region, or over the uterus during menstruation as therapy may
temporarily increase menstrual flow.
Treatment should not be applied directly over external stimulator systems.
The treatment head should be moved continuously during treatment to avoid discomfort and burns.
An appropriate coupling medium should be employed in order to ensure energy transmission to the tissue.
Precautions
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.
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.
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.

6 OMNISOUND®3000C PRO USER MANUAL
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
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.
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
applicator 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 or overheating during treatment, adjust the output downward until it is tolerated by the patient. If the
patient continues to complain of pain or overheating, discontinue the treatment and shorten the treatment time
on the next treatment session, or use an alternative type of therapy or applicator placement.
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.
Treatment should not follow the application of medicated patches, salves, or creams. The presence of electrical
stimulation may be altered by the presence of these materials on the patient’s skin. Some medications can alter the
patient’s sensation. Heat can also increase the absorption of medication and may be contraindicated. If there is a
medical necessityto performsuchtreatments, these patients should be monitored diligently during application.
Caution should be used when applying thermal ultrasound 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.
Do not connect this device to any electro medical equipment for combination therapy except the Omnistim®
family of electro stimulators.
Do not immerse any part of the operator’s body into the water bath during underwater techniques since the
long-term biophysical effects of ultrasonic energy exposure have not been evaluated.
Over acute skin conditions such as eczema, dermatitis, etc.

OMNISOUND®3000C PRO USER MANUAL 7
COPYRIGHT © 2001 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
THE OMNISOUND®3000C PRO
Delivery of the Omnisound®3000C Pro
Upon receipt of your Omnisound®3000C 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.
NOTE: The purpose of this manual is to acquaint you with the Omnisound®operating features and functions.
In order to avoid any misunderstanding, please read the manual carefully before attempting to assemble or
operate the Omnisound®. If questions remain unanswered, contact your ACP sales representative or call 1-800-
350-1100 or internationally call 1-775-685-4000.
Introduction
Welcome to the Omnisound®3000C Pro, the system that redefines therapeutic ultrasound. While conceiving and
designing the Omnisound®3000C Pro, ACP set out to overcome the limitations of ordinary ultrasound devices.
Here are just a few of the functions we developed that make the Omnisound®3000C Pro truly the future of
ultrasound therapy:
Controlled Depth of Penetration - The Omnisound®3000C Pro enables you to treat soft tissue injuries,
superficially with 3 MHz and instantly at the push of a button, treat deeper injuries with 1 MHz - without
switching transducers.
Two Transducer Sizes - Our 2cm2and 5cm2heads offer optimum flexibility in treatment and are automatically
enabled as you change from one to the other.
Fully Adjustable Transducer Head - A comfortable, consistent contact can be maintained during any surface
or underwater application because the transducer head rotates to any degree angle from 0 to 3600.
Microprocessor Controlled Digital Screen - Easy-to-read digital screen offers accurate indications of all
treatment parameters plus the calibration date, assist screens, automatic self-test, Effective Radiating Area
(ERA) and Beam Non-uniformed Ratio (BNR).
Continuous and Pulsed Modes - Variable duty factors offer a choice between 5, 10, 20, 25, 33, 50 and 100%
applications for optimum flexibility in all phases of treatment.
Delta T Temperature Mode - Automatic dose control system helps to assure consistent tissue heating.
Finger Tip Control - You no longer have to return to the ultrasound unit to alter output intensity. Just push the
switch on the transducer.
Combination Therapy - Interconnect port allows combination therapy with the Omnistim®family of
electrostimulators.
Excellent BNR and ERA - Our superior BNR and ERA makes for highly uniform and comfortable
applications.
Over Heating Temperature Sensing Monitor - A coupling monitor indicates when the transducer head is
overheated and the power is shut down automatically.
Automatic Self-Test with Problem Identification - Allows accurate evaluation and documentation of unit
functionality . . . before you begin treatment.