OMNISTIM
®
FX
2
PORTABLE PENS PATIENT USER MANUAL
- 5 -
COPYRIGHT © 2008 - 2021, ACCELERATED CARE PLUS CORP., ALL RIGHTS RESERVED
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Stimulation should not be applied directly over external stimulator systems with lead wires
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Neuromuscular electrical stimulation (NMES) should not be applied directly over or in
close proximity to Deep Vein Thrombosis (DVT), as it activates the muscle and causes
muscle contractions. This should be avoided in tissue following an acute DVT when the
thrombosis is not completely resolved. Therapists should follow the guidelines provided
by the referring physician on recommended activity level and modality use. If the patient
is not permitted exercise, NMES therapy should be avoided. Generally, NMES over a
DVT of six weeks or less should be avoided altogether.
Precautions
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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.
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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.
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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. 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.
Summary of Contents for OMNISTIM FX2
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