Barco High Bright MDSC-2326 DDIH, Руководство пользователя

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6. Important information
在中国大
陆销
售的相
应电
子信息
产
品（
EIP
）都必
须
遵照中国大
陆
《
电
子
电
气
产
品有害物
质
限制使用
标识
要求》
标
准
贴
上
环
保使用期限（
EFUP
）
标签
。
Barco
产
品所采用的
EFUP
标签
（
请
参
阅实
例，徽
标
内部的
编
号使用于指定
产
品）基于中国大
陆
的《
电
子信息
产
品
环
保使用期限通
则
》
标
准。
All Electronic Information Products (EIP) that are sold within Chinese Mainland must comply with the
“Marking for the restriction of the use of hazardous substances in electrical and electronic product” of Chi-
nese Mainland, marked with the Environmental Friendly Use Period (EFUP) logo. The number inside the
EFUP logo that Barco uses (please refer to the photo) is based on the “General guidelines of environ-
ment-friendly use period of electronic information products” of Chinese Mainland.
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 …” ).
56 K5902135 (451920612562) MDSC-2326 01/12/2017