natus otometrics HI-PRO 2, Руководство по установке

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USA Code of Federal Regulations. 21 CFR Part 801. §
801.109(b)(1)
UL recognized component for Canada and the United
States.
Electronic equipment covered by the Directive
2002/96/EC on waste electrical and electronic equipment
(WEEE).
All electrical and electronic products, batteries, and accu-
mulators 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 Otometrics,
or to any Otometrics supplier. You can also contact your
local authorities for advice on disposal.
6.2 HI-PRO 2 Warning notes
When connecting equipment to the USB connector, the following
must be considered:
• Equipment must be certified to relevant EN/IEC safety stand-
ards, e.g. EN/IEC 60950.
• Use of connected equipment in a patient environment, see
Note 1.
Ensure that the electro-medical system complies with the require-
ments of IEC 60601-1:2005+AMD1:2012 and EN 60601-
1:2006+A1:2013.
1. The HI-PRO 2 is a part of an electromedical system. When assembling an elec-
tromedical system, the person carrying out the assembly must take into account
that connecting other equipment that does not comply with the same safety
requirements as the HI-PRO 2 may lead to a reduction in the overall safety level
of the system.
The HI-PRO 2 is designed to ensure compliance with requirements in IEC 60601-
1:2005+AMD1:2012 and EN 60601-1:2006+A1:2013 when the PC, printer, etc.
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