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Users Manual EN-18
MINI 3D SOUND BAR & SUBWOOFER
Regulatory Information
CE compliance
This product is CE marked in compliance with the essential requirements
and other relevant provisions of Directive 1999/5/EC. Responsible for CE
marking is Toshiba Europe GmbH, Hammfelddamm 8, 41460 Neuss,
Germany. A copy of the official Declaration of Conformity can be obtained
from following website:
http://epps.toshiba-teg.com
.
This product and the original options are designed to observe the related
EMC (Electromagnetic Compatibility) and safety standards. However,
TOSHIBA cannot guarantee that this product still observes these EMC
standards if other units or cables not produced by TOSHIBA are connected.
In this case the persons who have connected those other units/cables have
to provide assurance that the system (sound bar plus options/cables) still
fulfills the required standards. To avoid general EMC problems, the
following guidance should be noted:
Only CE marked options should be connected/implemented
Only best shielded cables should be connected
Working Environment
The Electromagnetic Compliance (EMC) of this product has been verified
typically for this product category. Your product is not intended for industrial
use, but for personal use only. Any other working environment has not been
verified by TOSHIBA and the use of this product in these working
environments is maybe restricted or cannot be recommended. Possible
consequences of the use of this product in non verified working
environments can be:
Disturbances of other products or of this product in the nearby surrounding
area with temporarily malfunction or data loss/corruption as result.
Example of non verified working environments and related advices:
Industrial environment (e.g. where 3-phase 380V mains is being used
mainly): Danger of disturbances of this product due to possible strong
electromagnetic fields especially near to big machinery or power units.
Medical environment: The compliance to the Medical Product Directive has
not been verified by Toshiba, therefore this product cannot be used as a
medical product without further verification. The use in usual office
environments e.g. in hospitals should be no problem if there is no restriction
by the responsible administration.
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