Disposal Instructions - natus Nicolet EDX UB4 Bedienungsanleitung

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IEC 60601-1:2005+A1:2012 - General Safety Ed. 3.1
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IEC 60601-1-2:2014 – EMC Fourth Edition
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IEC 60601-2-40:2016 – Particular requirements for the basic safety and essential performance of
electromyography and evoked response equipment
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IEC 60601-1-6:2013 – Collateral Usability

Disposal Instructions:

Natus is committed to meeting the requirements of the European Union WEEE (Waste Electrical and
Electronic Equipment) Regulations 2014. These regulations state that electrical and electronic waste
must be separately collected for the proper treatment and recovery to ensure that WEEE is reused or
recycled safely. In line with that commitment Natus may pass along the obligation for take back and
recycling to the end user, unless other arrangements have been made. Please contact us for details on
the collection and recovery systems available to you in your region at
Electrical and electronic equipment (EEE) contains materials, components and substances that may be
hazardous and present a risk to human health and the environment when WEEE is not handled correctly.
Therefore, end users also have a role to play in ensuring that WEEE is reused and recycled safely. Users
of electrical and electronic equipment must not discard WEEE together with other wastes. Users must use
the municipal collection schemes or the producer/importers take-back obligation or licensed waste
carriers to reduce adverse environmental impacts in connection with disposal of waste electrical and
electronic equipment and to increase opportunities for reuse, recycling and recovery of waste electrical
and electronic equipment.
Equipment marked with the below crossed-out wheeled bin is electrical and electronic equipment. The
crossed-out wheeled bin symbol indicates that waste electrical and electronic equipment should not be
discarded together with unseparated waste but must be collected separately.
Disclaimer:
Natus Medical Incorporated is not responsible for injury, infection or other damage resulting from the use
of this product.
Any serious incident that has occurred in relation to the device should be reported to Natus Medical
Incorporated and the competent authority of the Member State in which the user and/or patient is
established.
Refer to the Natus website for an electronic copy of this document.
Instructions to Access the eIFU:
A copy of the Instructions for Use in PDF format is in the associated product area:
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Neurology: https://neuro.natus.com/neuro-support
Search for "Nicolet EDX UB4 Cart and Cart Grounding Kit IFU" (refer to the Product Part Numbers) and
choose the version for your local language for the instructions to use.
The files can be printed, saved, or searched using Adobe Reader. A copy of Adobe Reader can be
downloaded directly from Adobe Systems (www.adobe.com).
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