6. Important information
10
RoHS
Directive 2011/65/EC on the restriction of certain hazardous substances in electrical and electronic equip-
ment.
According to what declared by our components suppliers, this product is RoHS compliant.
6.3
Biological hazard and returns
Overview
The structure and the speci
fi
cations of this device as well as the materials used for manufacturing makes
it easy to wipe and clean and therefore suitable to be used for various applications in hospitals and other
medical environments, where procedures for frequent cleaning are speci
fi
ed.
However, normal use shall exclude biological contaminated environments, to prevent spreading of infec-
tions.
Therefore use of this device in such environments is at the exclusive risk of Customer. In case this device
is used where potential biological contamination cannot be excluded.
Customer shall implement the decontamination process as de
fi
ned in the latest edition of the ANSI/AAMI
ST35 standard on each single failed Product that is returned for servicing, repair, reworking or failure
investigation to Seller (or to the Authorized Service Provider). At least one adhesive yellow label shall be
attached on the top site of the package of returned Product and accompanied by a declaration statement
proving the Product has been successfully decontaminated.
Returned Products that are not provided with such external decontamination label, and/or whenever such
declaration is missing, can be rejected by Seller (or by the Authorized Service Provider) and shipped back
at Customer expenses.
6.4
Regulatory compliance information
Indications for use
This device is intended to be used in operation rooms, to display images from endoscopic cameras, room
and boom cameras, ultrasound, cardiology, PACS, anesthesiology and patient information. It is not in-
tended for diagnosis.
Manufacturing country
The manufacturing country of the product is indicated on the product label (
“Made in …”
).
Importers contact information
To
fi
nd your local importer, contact one of Barco’s regional of
fi
ces via the contact information provided on
our website (
www.barco.com
).
FCC Class A
This equipment has been tested and found to comply with the limits of a class A digital device, pursuant
to Part 15 of the FCC rules. These limits are designed to provide reasonable protection against harmful
interference when the equipment is operated in a commercial environment. This equipment generates,
uses and can radiate radio frequency energy and, if not installed and used in accordance with the instruc-
30
(451920612552) K5902150 MDSC-8358 28/11/2017
Summary of Contents for MDSC-8358 RL
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Page 20: ...4 Daily operation 18 451920612552 K5902150 MDSC 8358 28 11 2017 ...
Page 26: ...5 Advanced operation 24 451920612552 K5902150 MDSC 8358 28 11 2017 ...
Page 42: ...6 Important information 40 451920612552 K5902150 MDSC 8358 28 11 2017 ...
