Elo TouchSystems Blood Glucose Meter Elo Touch Solutions Touch Monitor User Manual

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© 2013 Elo Touch Solutions, Inc. All rights reserved.
User Manual 2401LM
SW200127 Rev A - Page 4 of 32
Caution
Power cord is used as a disconnection device. To de-energize equipment, disconnect
the power cord.
This unit must follow the national requirement and local state laws to dispose unit.
Before connecting the cables to your Elo Touchmonitor, make sure all components
are powered OFF.
Only approved components complying with IEC60601-1 series can be connected to
2401LM touch monitor for Healthcare Applications in Patient Environment. The use of
ACCESSORY equipment not complying with the equivalent safety requirements of this
equipment may lead to a reduced safety of the resulting system. Consideration relating
to the choices of accessory equipment should include: Use of accessory in the patient
environment.· Evidence that the safety certification of the accessory has been
performed in accordance to the appropriate IEC 60601-1 and/or IEC 60601-1-1
harmonized national standard.
For continued safety
- This unit only complies to the above standards if used with a medical grade power
cord.
- A medical grade power supply, such as the one specified, is required for use in a
medical application.
Please do not touch the patient and the Touchmonitor output connecter at the same
time.
Note:
This symbol alerts the user to important information concerning the operation and
maintenance of this unit, which should be read carefully to avoid problems.
This symbol means DC Current.
This symbol means ON/OFF stand-by switch.
Medical and Healthcare Application Disclaimer:
It is the sole responsibility of any person intending to commercialize, market or use any of Elo
Touch Solutions, Inc. or its family of companies ("Elo") products for medical or healthcare
applications to ensure that such product is adequate and appropriate for the person's
intended use and complies with all applicable laws, regulations, codes and standards
including but not limited to the European Union Medical Device Directive, United States
Federal Food, Drug, and Cosmetic Act, regulations of the United States Food and Drug
Administration (FDA), and for obtaining and maintaining any required regulatory approvals
including but not limited to any required market clearances. Elo has not sought nor received
any rulings from the FDA or any other federal, state, or local government agency or notified
body as to the safety, effectiveness or appropriateness of its product for such applications.
Persons intending to evaluate or use Elo's product for medical or healthcare purposes must
rely on their own medical and legal judgment without any representation on the part of Elo.

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