17
Definition of symbols
Electronic equipment covered by the Directive 2012/19/EU of the European Parliament and of the Coun-
cil of 4 July 2012 on waste electrical and electronic equipment (WEEE).
All electrical and electronic products, batteries, and accumulators must be taken to separate collection at
the end of their working life. This requirement applies in the European Union. Do not dispose of these
products as unsorted municipal waste.
You can return your device and accessories to Natus Medical Denmark ApS, or to any Natus
Medical Denmark ApS supplier. You can also contact your local authorities for advice on disposal.
Follow instructions for use
Follow instructions for use
Consult instructions for use
Indicates the need for the user to consult the instructions for use.
Complies with Type B requirements of IEC60601-1.
CE marking of conformity
Certification mark that indicates conformity with applicable regulations and directives for the European
Economic Area.
MEDICAL - General Medical Equipment as to electrical shock, fire and mechanical hazards only in accord-
ance with:
ANSI/AAMI ES60601-1:2005/(R)2012
IEC 60601-1-6
CAN/CSA-C22.2 No. 60601-1:14
CAN/CSA-C22.2 No. 60601-1-6
Used in error message dialogs if software program fails. See the detailed information in the dialog box.
18
Warning notes
This manual contains information and warnings, which must be followed to ensure the safe performance of the devices and
software covered by this manual. Local government rules and regulations, if applicable, should also be followed at all times.
Standards and safety-related issues relating to the MADSEN Astera² Audiometer Control Panel (ACP) are comprised by the
MADSEN Astera² symbols, standards and warning notes.
MADSEN Astera²
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17 Definition of symbols
