Disposal Instructions - natus Protektor32 Pods Manual Del Usuario

Storage Conditions:
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Temperature: -40°C to +70°C (-40°F to +158°F)
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Relative Humidity: 10% to 100%
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Atmospheric Pressure: 500 hPa to 1060 hPa
Compliance Standards:
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ISO 10993-1: 2018 Biological evaluation of medical devices — Part 1: Evaluation and testing within a
risk management process

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 DBA Excel-Tech Ltd. (Xltek) 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 DBA Excel-Tech Ltd. (Xltek) 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.
natus.com.
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