5. 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
5.3
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.
5.4
Regulatory information
Indications for use
The MDRC-1219 (TS) is intended to be used as a tool in displaying and viewing digital images (excluding
digital mammography) for review and analysis by trained medical practitioners. Caution (USA): Federal
law restricts this device to sale by or on the order of a physician. (Details & exemptions are in the Code
of Federal Regulations Title 21, 801 Part D).
FCC class B
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions:
(1) this device may not cause harmful interference, and (2) this device must accept any interference re-
ceived, including interference that may cause undesired operation.
This device has been tested and found to comply with the limits for a Class B digital device, pursuant to
Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful
interference in a residential installation. This device generates, uses and can radiate radio frequency
energy and, if not installed and used in accordance with the instructions, may cause harmful interference
K5902128 (451920612451) MDRC-1219 (TS) 03/11/2016
25
