Elo TouchSystems 2401LM user manual Medical and Healthcare Application Disclaimer

Caution

ƒPower cord is used as a disconnection device. To de-energize equipment, disconnect the power cord.

ƒThis unit must follow the national requirement and local state laws to dispose unit.

ƒBefore connecting the cables to your Elo Touchmonitor, make sure all components are powered OFF.

ƒOnly 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.

ƒFor 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.

ƒPlease do not touch the patient and the Touchmonitor output connecter at the same time.

Note:

ƒThis symbol alerts the user to important information concerning the operation and maintenance of this unit, which should be read carefully to avoid problems.

ƒ This symbol means DC Current.

ƒ 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.

	User Manual 2401LM
© 2013 Elo Touch Solutions, Inc. All rights reserved.	SW200127 Rev A - Page 4 of 32