标题: 做CE認證時捆綁ROHS問題 [打印本页] 作者: inbornqiu 时间: 2013-8-21 10:28 标题: 做CE認證時捆綁ROHS問題 去年就有聽說後續做CE認證可能會要求捆綁一起做ROHS的測試，各位大俠有沒有哪位知道具體的實施日期。。。作者: jjlamshushushu 时间: 2013-8-21 10:31
已经实施好久了作者: zhangrui110 时间: 2013-8-21 11:49
有这个要求的。以后可能还要加一个能效。作者: hancun 时间: 2013-8-21 11:53
DIRECTIVE 2011/65/EU 里面有，不同产品有不同的时间。 8 }' h# G( O1 G9 W* L7 R; v7 O3. Paragraph 1 shall apply to medical devices and monitoring and control instruments which are placed on the market from 22 July 2014, to in vitro diagnostic medical devices which are placed on the market from 22 July 2016 and to industrial monitoring and control instruments which are placed on the market from 22 July 2017.1 E: d9 A t% k" t5 e7 a: _# Q3 ]
4. Paragraph 1 shall not apply to cables or spare parts for the repair, the reuse, the updating of functionalities or upgrading of capacity of the following:+ `2 ~& q7 s$ u9 [ {" I
(a) EEE placed on the market before 1 July 2006;' R- n' V3 j% n
(b) medical devices placed on the market before 22 July 2014; R7 h% a' q7 {& O/ J. c(c) in vitro diagnostic medical devices placed on the market before 22 July 2016; % s2 P& A8 i% v0 `(d) monitoring and control instruments placed on the market before 22 July 2014;% K- f7 C8 ?8 c; Q$ n8 W0 q
(e) industrial monitoring and control instruments placed on the market before 22 July 2017; 2 Y H& G. ~# D- {* k; T(f) EEE which benefited from an exemption and which was placed on the market before that exemption expired as far as that specific exemption is concerned.作者: inbornqiu 时间: 2013-8-21 15:06
感謝各位，受教了。我說我們的產品怎麼就沒有強制要求實施呢。。。