Fillauer Motion Control Internal Li-Ion Battery Set User manual

MC Internal Li-Ion Battery Set
User Guide

MC Internal Li-Ion Battery Set
User Guide
Introduction
Your prosthesis contains a Motion Control Internal Li-Ion Battery and charging system. Lithium Ion presents
the longest battery life in a small, lightweight package. Motion Control has built in safeguards and protections
to ensure the battery operates safely and eciently. Please follow the instructions in this guide. Failure to do
so could result in shorter usage time, shorter battery life, accidental re, or possible explosion.
Special Precautions
MC Battery Charger
Use only the Motion Control battery charger and wall adapter with Motion Control batteries. If a
replacement charger is needed, contact Motion Control.
Remove the prosthesis before charging
Do not wear the prosthesis while charging. Always remove the prosthesis before plugging the charger
into the charging port.
Do not alter
Do not alter the wiring or circuits in the battery in any way. Do not cross the power leads anywhere in
the system. This will cause a short circuit in the system that could lead to re or explosion and will void
the warranty.
Keep the battery system dry
Do not allow the battery system to get wet.
Charging
The charger consists of three parts -
the wall adapter, automotive adapter,
and the charger. Plug the wall adapter
(or automotive adapter) into the
charger, then plug the charger into
the charging port (Figure 2).
To charge the battery, plug the wall
adaptor into the wall, and the plug
into the charger. The yellow “Fault”
light should illuminate. Then plug the
cable from the charger into the charging port on the prosthesis. The red “Charging” light should illuminate. The
red light will stay illuminated until the battery is fully charged, then the green “Complete” light will illuminate.
This usually takes 2-3 hours.
If the yellow Fault light does not change to the red charging light, re-check all the connections. If the red light
continues to be illuminated, return the prosthesis and charger to your prosthetist. If the battery takes longer
than 3-4 hours to charge or never reaches a “complete” charge (green Light), return the prosthesis and charger
to your prosthetist.
Charging Port
Charger
Wall
Adapter
Auto
Adapter
Connect battery to charger as shown
3

Power On/O
If your prosthesis does not have an electric wrist rotator, the
switch on the terminal device (hand or ETD) is adequate to turn
the system o.
If your prosthesis has an electric wrist rotator, the system needs
to be either plugged into the charger, or powered o when not
in use. To power o the system, insert the (provided) interrupter
plug into the charging port, and the system is o. This plug is
attached to a convenient key fob.
Interrupter Plug
Limited Warranty
Seller warrants to Buyer that the equipment delivered hereunder will be free from defects in materials
and manufacturing workmanship, that it will be of the kind and quality described and that it will perform
as specied in Seller’s written quotation. The limited warranties shall apply only to failures to meet said
warranties that appear within the eective period of this Agreement. The eective period shall be one year
(12 months) from the date of delivery to the tting center that has purchased the components. Refer to the
shipping receipt for the date of shipment.
For more information regarding the Limited Warranty, see the MC FACT SHEET - Limited Warranty.
Return Policy
Returns are accepted for a full refund (not including any repairs that may be required) for up to 30 days from
date of shipment.
Returns 31-60 days from date of shipment will be accepted, subject to a 10% restocking fee.
Returns 61-90 days from date of shipment will be accepted, subject to a 15% restocking fee.
Beyond 90 days, returns are not accepted. Returns must be in re-saleable condition.
Technical Specications
Operating Temperature: -5° to 60° C (23° to 140° F)
Transport & Storage Temperature: -20° to 50° C (-4° to 122° F)
Battery: Lithium-Ion, 1150 mAh
Voltage: 7.2 Vdc
Declaration of Conformity
The product herewith complies with the Medical Device Directive 93/42/EEC guidelines, and is registered with
the United States Food and Drug Administration (Registration No. 1723997).
© 2018 Motion Control, Inc. 1910077 Rev B 09-06-2018 F
Motion Control, Inc.
115 N Wright Brothers Drive
Salt Lake City, UT 84116
801.326.3434
Fax [phone]
www.UtahArm.com