Precautions - Accelerated Care Plus OMNISTIM FX2 PRO User Manual

Electrotherapy system
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®
2
OMNISTIM
FX
PRO USER MANUAL
not permitted exercise, NMES therapy should be avoided. Generally, NMES over a DVT of six weeks or less
should be avoided altogether.
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 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.
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.
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.
COPYRIGHT © 2004 - 2017, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED

Precautions

State and federal survey and JCAHO require all equipment to be
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