{"id":3816,"date":"2009-01-08T12:33:00","date_gmt":"2009-01-08T04:33:00","guid":{"rendered":"https:\/\/li-on.biz\/?p=3816"},"modified":"2024-04-02T08:56:10","modified_gmt":"2024-04-02T00:56:10","slug":"%e6%ad%90%e7%9b%9frohs%e6%96%b0%e4%bf%ae%e8%a8%82%e8%8d%89%e6%a1%88-%e5%95%8f%e7%ad%94%e9%9b%86%e5%bd%99%e6%95%b4-no-43-2008","status":"publish","type":"post","link":"https:\/\/li-on.biz\/en\/%e6%ad%90%e7%9b%9frohs%e6%96%b0%e4%bf%ae%e8%a8%82%e8%8d%89%e6%a1%88-%e5%95%8f%e7%ad%94%e9%9b%86%e5%bd%99%e6%95%b4-no-43-2008\/","title":{"rendered":"EU RoHS New Revised Draft \u2013 Q&amp;A Collection NO.43\/2008"},"content":{"rendered":"<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>EU RoHS New Revised Draft \u2013 Q&amp;A Collection NO.43\/2008<\/strong><\/td><\/tr><tr><td><\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p>On December 3, 2008, the European Commission published a report proposing amendments to the existing RoHS Directive, along with a Q&amp;A document explaining the content and rationale for the amendments. The Q&amp;A document is summarized below:<\/p>\n\n\n\n<p class=\"translation-block\"><strong>A. Scope and Definitions<br>Proposal Content (What is proposed?)<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>Two new appendices have been added to describe the scope of the directives. Appendix I describes the specific product categories, and Appendix II, revised by the committee, provides a list of products in each category.<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>Medical devices and monitoring and control instruments will be included in the regulatory scope in stages.<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>New definitions have been added, such as \"medical devices\" and \"homogeneous materials\".<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p class=\"translation-block\"><strong>B. Prohibited Substances<br>Proposal Content<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>The list of prohibited substances and maximum concentration values \u200b\u200bfor the existing directives have been moved to Annex IV and will be revised by the Committee in accordance with the working procedures (comitology).<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>The list of prohibited substances remains unchanged; however, four substances (HBCDD, DEHP, BBP, and DBP) have been identified as priority for assessment and may be added to the list of prohibited substances in the future.<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>Allowing the use of components that do not comply with the directive will help bring equipment containing exclusionary items to market.<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>A new appendix on exclusions for medical devices and monitoring and control instruments has been added to address special circumstances where no viable alternatives exist at present.<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>The new prohibited substances will be consistent with the REACH directive assessment methodology to ensure consistency of chemical regulations and maximum synergistic effect.<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p class=\"translation-block\"><strong>C. Exclusion<br>Proposal Content<\/strong><\/p>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>The previous requirement for exclusionary programs to be reviewed every four years has been changed to a maximum validity period of four years for exclusionary programs.<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>The new criteria for exclusionary programs require feasible and reliable alternatives and must cover socioeconomic effects.<\/td><\/tr><tr><td><img decoding=\"async\" height=\"10\" width=\"13\" alt=\"\" src=\"wlmailhtml:{B1772447-9EA2-410B-8F5B-460E197404F6}mid:\/\/00000033\/!x-usc:http:\/\/newsletter.sgs.com\/eNewsletterPro\/uploadedimages\/000064\/orange_bullet_small.gif\"><\/td><td>The committee must establish detailed exclusion criteria to serve as a legal basis for decisions when economic operators make updated requests to the committee.<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p class=\"translation-block\"><strong>D. Product Conformity Assessment Requirements and Market Surveillance Mechanisms<br>Proposed Content<\/strong><br>New Clause Articles 7-17 introduce product conformity assessment requirements and market surveillance mechanisms consistent with \"Product Marketing\" (based on the general framework for product marketing as per Executive Committee Decision 768\/2008\/EC).<\/p>\n\n\n\n<p>The above translation is for reference only; please refer to the original text for accuracy.<\/p>\n\n\n\n<p><strong>source<\/strong> <a href=\"http:\/\/newsletter.sgs.com\/eNewsletterPro\/t.aspx?S=39&amp;ID=3409&amp;NL=347&amp;N=7308&amp;SI=132709&amp;URL=http%3a%2f%2feuropa.eu%2frapid%2fpressReleasesAction.do%3freference%3dMEMO%2f08%2f763%26format%3dHTML%26aged%3d0%26language%3dEN%26guiLanguage%3den\" target=\"_blank\" rel=\"noreferrer noopener\">Original text of the EU RoHS II Q&amp;A<\/a><\/p>\n\n\n\n<p><\/p>","protected":false},"excerpt":{"rendered":"<p>\u6b50\u76dfRoHS\u65b0\u4fee\u8a02\u8349\u6848 &#8211; 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