Optelec ClearView C HD User Manual page 35

Optelec
replacement of ClearView C modules. This warranty is valid only when
serviced in the country of original purchase, and with intact seals. For
additional warranty claims or service during or after warranty period, please
contact your Optelec distributor.
Optelec is not responsible for any uses of this device other than those
described in this manual.
WEEE Notice
The directive on Waste Electrical and Electronic Equipment (WEEE), which entered into force as
th
European law on 13
equipment at end-of-life.
The purpose of this Directive is, as a first priority, the prevention of WEEE, and in addition, to
promote the reuse, recycling and other forms of recovery of such wastes so as to reduce disposal.
The WEEE logo (shown at the left) on the product or its box indicates that this product
must not be disposed of or dumped with your other household waste. You are liable to
dispose of all your electronic or electrical waste equipment by relocating over to the
specified collection point for recycling of such hazardous waste. Isolated collection and
proper recovery of your electronic and electrical waste equipment at the time of
disposal will allow us to help conserving natural resources. Moreover, proper recycling of the
electronic and electrical waste equipment will ensure safety of human health and environment. For
more information about electronic and electrical waste equipment disposal, recovery, and
collection points, please contact your local city centre, household waste disposal service, shop
from where you purchased the equipment, or manufacturer of the equipment.
RoHS Compliance
This product is in compliance with Directive 2011/65/EU of the European Parliament and
of the Council of 1 July 2011, on the restriction of the use of certain hazardous substances
in electrical and electronic equipment (RoHS-II) and its amendments.
Compliance
This product is in conformity with the following directives:
Council directive 93/42/EEC of 14th June 1993 concerning medical devices
Class I / Annexe VII.
Electrical medical equipment requires special precaution with regard to EMC
(Electro Magnetic Compatibility) and must be installed and put into service
according to EMC guidelines.
WARNING: The use of accessories and cables other than those specified
and sold by the manufacturer of the ClearView C, as replacement parts for
components, may result in increased emissions or decreased functioning of
the ClearView C.
English
February 2003, resulted in a major change in the treatment of electrical
This device bears the CE, FCC and UL approval
mark.
ClearView C
35