Empi Active Manual - page 3
EMPI Active User Guide
Dear Patient,
Welcome to Empi, the leader in home rehabilitation devices.
Your healthcare professional has prescribed an Empi device to aid in your reha-
bilitation and/or pain management program. It is our goal, in partnership with your
healthcare provider, to help you achieve the best possible outcome in the shortest
amount of time.
In the next several days, an Empi Patient Care Specialist will attempt to contact you to:
1) Assess your overall satisfaction with the Empi device;
2) Address questions you may have regarding the device; and
3) Provide you with information regarding your insurance
company’s coverage policy.
If your health insurance policy provides coverage for the device, we will submit a
claim to them on your behalf. In the unlikely event the device is not a covered benefit,
Empi will contact you to discuss available payment options. If you decline the self-pay
option, you will be asked to return the device within 10 days of notification. A conve-
nient, pre-paid postage return envelope is provided with the Empi device kit.
For immediate assistance or for answers to questions regarding your Empi device,
please contact Empi at 800.328.2536 and an Empi Patient Care Specialist will be avail-
able to help you. Operating hours are 7:30AM to 5:30PM CST, Monday through Friday.
As a partner with your healthcare provider, Empi is committed to helping you improve
your health and quality of life. Thank you for the opportunity to serve you and help
you “rediscover living”.
Sincerely,
Your Empi Team
CAUTION: Federal Law (USA) restricts this device to sale
by or on the order of a physician (or licensed practitioner).
The following symbols may be located on the back of the Empi Active device:
Type BF Applied Part
Lead wires comply with the Performance Standard for electrode lead wires
(21 CFR part 898)
Attention, consult accompanying documents
Electronic Testing Lab, indicates product meets US and Canadian product safety
standards. This device complies with UL Std. 60601-1 and is certified to CAN/CSA Std.
C22.2 No. 601.1.
Council Directive 2002/96/EC concerning Waste Electrical and Electronic
Equipment (WEEE). Indicates a requirement not to dispose of WEEE as municipal
waste. Contact your local distributor for information regarding disposal of the unit
and accessories.
Federal Law (USA) restricts this device to sale by or on the order of a physician
(or licensed practitioner).
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