Omron Avail PM601 User manual

For questions call: 1-800-634-4350
Pads are for Single Patient Use Only.
OmronHealthcare.com 3125420-0E

1
TABLE OF CONTENTS
Introduction ...............................................................................................2
Safety Instructions .............................................................................. 2
Intended Use........................................................................................ 2
Contraindication.................................................................................. 3
Receiving and Inspection....................................................................3
Symbols Glossary...................................................................................... 4
Important Safety Information ................................................................... 5
Warnings .............................................................................................5
Cautions............................................................................................... 7
Adverse Reactions...............................................................................9
How the Device Works............................................................................ 10
Know Your Device 11
Package Contents .............................................................................. 11
Part Names And Functions on the Device........................................ 12
Usage of Storage Case And Pad Holder ........................................... 13
Part Names And Functions of the Omron TENS App ..................... 14
Operating Instructions 16
Preparing for Use .............................................................................. 16
Get Started with Your Therapy......................................................... 19
Other App Features ........................................................................... 28
How to Control And Reduce Your Pain............................................ 29
After Daily Use 30
Storage And Removing.....................................................................30
Cleaning And Disposal ..................................................................... 31
Appendix 32
Reset the Device................................................................................ 32
Troubleshooting................................................................................. 33
Accessories........................................................................................ 37
Specications .................................................................................... 39
Limited Warranty.............................................................................. 40
Regulatory Compliance Information 42
FCC Statement .................................................................................. 42
Important Information Regarding Electro Magnetic
Compatibility (EMC) ........................................................................ 43

2
INTRODUCTION
Thank you for purchasing the Omron®AvailTM.
Avail is a wireless, independent dual channel wearable electrotherapy
device that is designed to alleviate chronic muscle and joint pain on
multiple body locations. It delivers TENS (Transcutaneous Electrical
Nerve Stimulation) technology and microcurrent therapy through the
simple, convenient control of the Omron TENS iOS or Android app.
Premium, contouring pads allow for discreet and convenient placement
on multiple pain locations on the body.
TENS is a safe and drug-free treatment for pain that has been used for
over 30 years by medical professionals such as physical therapists and
chiropractors.
Notes:
•Keep this instruction manual in a convenient place or store with the
device for future reference.
•Register your product online at www.register-omron.com. You can
also register your product via the Omron app.
•Keep your purchase receipt as proof of purchase for warranty
coverage.
•The illustrations used in this manual are images.
SAFETY INSTRUCTIONS
This instruction manual provides you with important information about
this device. To ensure the safe and proper use of this device, read and
understand all of the safety and operating instructions. If you do not
understand these instructions or have any questions, contact 1-800-
634-4350 before attempting to use this device.
INTENDED USE
The AvailTM is intended for the relief of pain associated with sore or
aching muscles of the lower back, arms, legs, shoulders or feet due to
strain from exercise or normal household work activities.
When used for the symptomatic relief and management of chronic,
intractable pain and relief of pain associated with arthritis, use the Tap,
Shoulder, Arm or Leg mode of stimulation.
Environment of Use: Clinic, hospital and home environments.
Patient Population: Adult

3
SAVE THESE INSTRUCTIONS
INTRODUCTION
CONTRAINDICATION
Do not use this device if you have a cardiac pacemaker, implanted
defibrillator or other implanted metallic or electronic device. Such
use could cause electric shock, burns, electrical interference or
death.
RECEIVING AND INSPECTION
Remove this device from the packaging and inspect all package
contents for damage. If there is any damage, DO NOT USE and
contact Omron Healthcare Customer Service at 1-800-634-4350.

4
SYMBOLS GLOSSARY
For symbol information, visit: OmronHealthcare.com/symbols-glossary
WARNING Indicates a potentially hazardous situation which, if not avoided, could result in death or serious injury.
CAUTION Indicates a potentially hazardous situation which, if not avoided, may result in minor or moderate injury to the user or patient or damage to
the equipment or other property.
Type BF applied part. (Pads)
Class II equipment.
Catalogue number.
Consult instructions for use.
This product should not be used by persons with medical implants, e.g. heart pacemakers, artificial heart, lung or other electronic life support
systems.
IP classification is degrees of protection provided by enclosures in accordance with IEC 60529. This device is protected against solid foreign
objects of diameter 12 mm such as a finger and greater, and against vertically falling water drops which may cause issues during a normal
operation.
IP classification is degrees of protection provided by enclosures in accordance with IEC 60529. This device is protected against solid foreign
objects of diameter 12 mm such as a finger and greater, and against oblique falling water drops which gives trouble to normal operation.
Tested to comply with FCC (Federal Communications Commission) standards.

5
IMPORTANT SAFETY INFORMATION
WARNINGS
Keep this device and the pads out of the reach of infants, toddlers and
children.
Keep out of the reach of young children because the AC adapter cord
could cause strangulation.
Consult with your physician before using this device, because
the device may cause lethal rhythm disturbances to the heart in
susceptible individuals.
If you have had medical or physical treatment for your pain, consult
with your physician before using this device.
If you are in the care of a physician, consult with your physician
before using this device.
If your pain does not improve, becomes more than mild, or continues
for more than five days, stop using the device and consult with your
physician.
Do not place this device across your chest or near your heart because
the introduction of electrical current into the chest may cause rhythm
disturbances to your heart, which could be lethal.
Do not place the pads near or on cancerous lesions, diseased skin,
open wounds, rashes, swollen, red, infected or inflamed areas or skin
eruptions such as phlebitis, thrombophlebitis and varicose veins.
Do not place the pads over your neck because this could cause severe
muscle spasms resulting in closure of your airway, difficulty in
breathing, or adverse effects on heart rhythm or blood pressure.
Do not place the pads on or near the head, mouth, face, heart or
genitals.
Do not use this device when bathing, showering, sleeping, during
exercise, while sweating or in high humidity.
Do not apply stimulation while driving, operating machinery, or
during any activity in which electrical stimulation can put you at risk
of injury.
Do not use this device on infants, toddlers, children, pregnant
women, persons incapable of expressing their thoughts or on persons
unable to operate the device by themselves.
Do not use this device while using another TENS device.

6
IMPORTANT SAFETY INFORMATION
Do not apply stimulation in the presence of electric monitoring
equipment such as cardiac monitors and ECG alarms because the
equipment may not operate properly when the device is in use.
Never bend or fold the pads.
If you have any serious illness, consult with your physician before
using this device.
Apply the pads only to normal, intact, clean, healthy skin of adult
patients.
For Hospitals and Clinics: Operation in close proximity (e.g. 1 m)
to a shortwave or microwave therapy ME equipment may produce
instability to the stimulator output.
For Hospitals and Clinics: Simultaneous connection of a patient to high
frequency surgical equipment and this device may result in bums at the
site of the stimulator electrodes and possible damage to the stimulator.
Do not place the storage case within 2 inches (approx. 5 cm) to
any person who is using pacemakers or implantable cardioverter
debrillators(ICDs).Magnetsareembeddedinthestoragecaseso
thatmagnetismmayaectpacemakersorICDs.
Do not place the charger within 6 inches (approx. 15 cm) to any
person who is using pacemakers or implantable cardioverter
debrillators(ICDs).Thechargeremitselectromagneticelds,which
mayaectpacemakersorICDs.
Data Transmission/Remote Control
This product emits radio frequencies (RF) in the 2.4 GHz band. DO
NOT use this product in locations where RF is restricted, such as on
an aircraft. For further information on potential restrictions refer to
documentation on the Bluetooth usage by the FCC.
Battery Handling and Usage
Topreventtheriskofoverheating,reorexplosion:
•Do not puncture, crush, disassemble or modify the device.
•Do not throw the device into fire.
•Do not recharge, use, or leave the device in any high temperature
environment such as in a location near a fire or in direct sunlight.
The device contains a built-in rechargeable Lithium-Ion battery
which must be disposed of properly. Dispose of the device
according to applicable local government regulations.
Do not disassemble the device by yourself.

7
IMPORTANT SAFETY INFORMATION
CAUTIONS
TENS is not effective for pain of central origin, including headache.
TENS is not a substitute for pain medications and other pain
management therapies.
TENS devices have no curative value.
TENS is a symptomatic treatment and, as such, suppresses the
sensation of pain that would otherwise serve as a protective mechanism.
Effectiveness is highly dependent upon patient selection by a
practitioner qualified in the management of pain patients.
Do not use this device to treat one region for extended periods of
time. The long-term effects of electrical stimulation are unknown.
If you experience any skin irritation or redness after a session, do not
continue stimulation in that area of the skin.
If you have suspected or diagnosed heart disease, you should follow
precautions recommended by your physician.
If you have suspected or diagnosed epilepsy, you should follow
precautions recommended by your physician.
Use caution if you have a tendency to bleed internally, such as
following an injury or fracture.
Consult with your physician prior to using the device after a recent
surgical procedure because stimulation may disrupt the healing
process.
Use caution if stimulation is applied over the menstruating uterus.
Use caution if stimulation is applied over areas of skin that lack
normal sensation.
Use this device only with components provided in the AvailTM
packaging and accessories recommended by the manufacturer. (Refer
to page 11 and 37)
Place the pads at least 1 inch apart. Do not place the adhesive surface
of the pads on the spine.
Do not apply the pads with wet hands, and do not apply the pads that
are wet.
Pads are for Single Patient Use Only. Never share the pads with
another person.

8
IMPORTANT SAFETY INFORMATION
Do not overlap or put the pads on top of each other because therapy
may weaken or stop.
Do not leave the pads placed on the skin after treatment.
Do not apply any lotion, cream or ointment to the pads.
Never attempt to modify the device.
The pads should not touch any metal object such as a belt buckle or
necklace.
To avoid damage to the adhesive surface of the pads, only put the
pads on the skin or the plastic pad holder.
Always place clean pads in accordance with illustrations provided
(Refer to pages 20 - 24, Pad Placement).
If the device is not functioning properly or you feel discomfort,
immediately stop using the device.
Before use, inspect the cord for open wires or any damage. If
damaged, do not use and replace immediately.
Clean and dry affected area so it is free of all lotions, oils and sweat.
Clean or change the pad when it loses adhesion.
Do not put any metal object, such as coin, clip or other metal on the charger.
Do not put the pad on your body where it cannot be reached by your
own hand.
Do not place the storage case within 2 inches (approx. 5 cm) to any
magnetic memory devices such as key cards or credit cards. Magnets
are embedded in the storage case so that it may lose data stored on a
magnetic memory.
Data Transmission/Remote Control
Do not place integrated circuit cards, magnets, metal objects, or
other devices that emit electromagnetic fields near this device while
the device is controlled remotely. This may result in the incorrect
operation of your device and smartphone.

9
IMPORTANT SAFETY INFORMATION
ADVERSE REACTIONS
•You may experience skin irritation and burns beneath the stimulation
electrodes applied to your skin.
•You may experience headache and other painful sensations during or
following the application of electrical stimulation near your eyes and
to your head and face.
•You should stop using the device and should consult with your
physician if you experience adverse reactions from the device.