Rohs2.0测试报告样本
ROHS2.0有害物质测试计划表
配方变更时/ 抽样5PCS委 托第三方测
同一供应商（由 物料供应商提供 有效的有害物质
2011/65/EU（ROHS 2.0）十项检测
同一供应商（由 物料供应商提供 有效的有害物质
USB HUB IC
料
试
检测报告）
检测报告）
主控IC
DDR
EMMC
1.新供应商供货物料、供应商新供货物料、或供应商物料材质出现变更时，进料检验时，必须实施以上环保检测项目,OK后能正式入库。 备注 2.供应商首次交货时需做RoHS检测，根据检验结果与所提供之第三方检测报告比对确认；
托第三方测 有效的有害物质
试
检测报告）
2011/65/EU（ROHS 2.0）十项检测
二次/半年/ 同一供应商（由 物料供应商提供 有效的有害物质
检测报告）
二三级管
功放IC
Байду номын сангаас
电源IC
串口IC
VGAIC
低
新供方/公司 一次/1年/
1次/1年/
I C 类
高清切换IC USB切换IC
风 险 进
1次/年
1次/年
3.进料依合格供应商名录对供应商材料或物料进行检测时,以不同材质及表面处理为类别进行抽检同一规格即可;
制表：
审核：
核准：
表单编号：xx-xxxx-xx A0
送检 单位
材料类别/站别
PCB
插 头
线 材 接 线 端 子
IQC
制造 物料
覆铜板 HDMI座 VGA座 串口座 网口座 USB座 耳机座
AV座 电池座 高频头座 SD卡座 SD卡座 2P接线母座 4P接线母座 6P接线母座 8P接线母座 9P接线母座 10P接线母座 屏线座子
欧盟工厂级RoHS2.0测试仪器的测试标准、规范及原理
随着ROHS2.0的实施，又有一大批产品因被检出不符合相关法规，而且这次全是ROHS新增加管理的项目：邻苯和REACH中的部分管理项目，因此，当这些产品投放到市场前，如不加以检测是否符合相关基准要求，其潜在的危害是巨大的，甚至有可能对消费者的生命、财产安全或环境造成损害。
骏辉腾科技的“X+1”计划助力工厂应对RoHS2.0法规2019年7月22日，RoHS2.0指令正式生效，具体指令需要管控的物质及限值如下:工厂级RoHS2.0一站式管控，需要简单，方便，快速，高效的管理手段；2006年7月1日生效以来，众多工厂已购XRF（X荧光光谱仪），术名：能量色散光谱仪，俗称：RoHS测试仪，或者RoHS+无卤测试仪，主要是用于检测有害物质中的元素分析应对RoHS指令；辅助合金分析，镀层分析等等功能；2019年7月22日强制执行的RoHS2.0新增了四项邻苯有害物质测试，已购的XRF已无法满足测试需求，需要配备对应的色谱仪器；骏辉腾科技借助专业的服务为广大客户提出了“X+1”计划，助力不同厂家，不同型号的X（X 荧光光谱仪）加上骏辉腾科技推出的LC-2800 有机物综合测试仪，并针对性设计出专业的工厂级实验室“既测试，又展示”的完善解决工厂级RoHS2.0十项检测。
并且同时可扩充测试PAHs,AZO,DMF,BPA等相关有机物，提出一站式服务解决了行业痛点及客户关心的重点；通过多年努力，现骏辉腾科技产品成功与各种品牌及型号的XRF进行了互补，让客户有更广阔的选择空间并为用户提供了便捷的服务；欧盟RoHS 2.0指令：2015年6月4日，欧盟在其官方公报上发布指令(EU) 2015/863对RoHS2.0(2011/65/EU) 附录II进行修订，正式将四种邻苯二甲酸酯(DEHP、BBP、DBP、DIBP) 列入RoHS2.0附录II中，到2016年12月31日止，欧盟成员国必须将此指令转为各国的法规并执行。
RoHS 2.0 调和标准及均质材料示例
Material Data Form (材質成分表)
IEC 62321
文件相關調和標準
IEC 62474
佐證技術文件10年備存
Overview : Homogeneous Materials example
IC:
Die ,Die attach ,wire ,Mold compound ,Lead frame, Plating…etc.
Surface finish(OSP , Immersion Gold…etc)
Solder mask Ink(Silk screen)
copper foil
Thin core (Pregpreg +copper foil)
Pregpreg (Epoxy resin + Glass Fiber+ Flame retardant)
Overview : Homogeneous Materials example
機構材質
需要依照機構圖面,才能確定最終完整材質
MHale Waihona Puke lar(銘板):PC,背膠,油墨…etc.
包裝材料
紙箱:
紙箱本體,油墨,白膠,鋼釘…etc
Overview : Homogeneous Materials example
Connector:
塑膠粒,pin 腳,鍍層(or PCB 板)
Overview : Homogeneous Materials example
PCB 空板:
Laminate基材,PREGPREG,COPPER FOIL, Solder mask ,Surface finish OSP …etc.
ROHS2.0联络报告
深圳市创亿欣精密电子股份有限公司 编号：
联络报告共 1 页 ， 第 1 页
各厂商负责人：
你们好！
2011年7月1日，欧盟议会和理事会在欧盟官方公报上发布指令 2011/65/EU（ROHS 2.0）以取代2002/95/EC ，新指令在2011年7月21日生效，2013年1月3日起指令2002/95/EC 将会被废除。
2011/65/EU RoHS2.0主要增加HBCDD、DEHP、DBP和BBP四项管控物质，即原来RoHS主要管控六项有害物质，现管控十项有害物质。
请各厂商自查交“深圳市创亿欣精密电子股份有限公司”物料是否含有最新增加的四项管控物质，因此请各厂商在2012年提交给“深圳市创亿欣精密电子股份有限公司”的物料SGS 报告，需要有此四项物质的测试项目及结果（金属类材料除外），另重申我司只接受SGS、CTI、ITS三家第三方检测公司的报告。
以上，谢谢各厂商的配合！并请在2012年1月13号前签回。
祝：新年快乐！。
欧盟ROHS2.0标准及检测方法
欧盟ROHS2.0标准及检测方法欧盟ROHS2.0标准欧盟公报(OJ)发布RoHS2.0修订指令(EU)2015/863，欧盟RoHS2.0更新终于尘埃落定，由原来的六项管控物质：铅（Pb）、汞（Hg）、镉（Cd）、六价铬（Cr VI）、多溴联苯（PBB）、多溴二苯醚（PBDE），变为十项管控物质，新增邻苯二甲酸二（2-乙基己基）酯（DEHP）、邻苯二甲酸甲苯基丁酯（BBP）、邻苯二甲酸二丁基酯（DBP）、邻苯二甲酸二异丁酯（DIBP）（简称邻苯4P），此前曾在ROHS2.0中被优先列为评估物质的六溴环十二烷（HBCCD）未被正式列入限制物质清单。
该十项管控物质管控的限量均为0.1%和0.01%。
此修订指令发布后，欧盟各成员国需在2016年12月31日前将此指令转为各国的法规并执行。
且2019年7月22日起所有输欧电子电器产品(除医疗和监控设备)均需满足该限制要求,;2021年7月22日起，医疗设备(包括体外医疗设备)和监控设备(包括工业监控设备)也将纳入该管控范围。
此外，已属REACH附件XVII第51条邻苯管控的玩具产品将不受此指令中DEHP、BBP、DBP的管控。
指令编辑欧盟议会及欧盟委员会于2003年2月13日在其《公报》上发布了《废旧电子电气设备指令》（简称《WEEE指令》）和《电子电气设备中限制使用某些有害物质指令》（简称《RoHS 指令》）《RoHS指令》和《WEEE指令》规定纳入有害物质限制管理和报废回收管理的有十大类102种产品，前七类产品都是我国主要的出口电器产品。
包括大型家用电器、小型家用电器、信息和通讯设备、消费类产品、照明设备、电器电子工具、玩具、休闲和运动设备、医用设备（被植入或被感染的产品除外）、监测和控制仪器、自动售卖机。
2008年12月3日，欧盟发布了WEEE指令（2002/96/EC）和RoHS指令（2002/95/EC）的修订提案。
本次提案的目的是创造更好的法规环境，即简单、易懂、有效和可执行的法规。
RoHS 2.0欧洲议会报告-20100615
RR\430424EN.docPE430.424v05-00EN United in diversityENEUROPEAN PARLIAMENT2009 - 2014Session documentA7-0196/201015.6.2010***IREPORTon the proposal for a directive of the European Parliament and of the Council on the restriction of the use of certain hazardous substances in electrical and electronic equipment (recast)(COM(2008)0809 – C6-0471/2008 – 2008/0240(COD)) Committee on the Environment, Public Health and Food Safety Rapporteur: Jill Evans(Recast - Rule 87 of the Rules of Procedure)PR_COD_1RecastingamSymbols for procedures* Consultation proceduremajority of the votes cast**I Cooperation procedure (first reading)majority of the votes cast**II Cooperation procedure (second reading)majority of the votes cast, to approve the common positionmajority of Parliament’s component Members, to reject or amendthe common position*** Assent proceduremajority of Parliament’s component Members except in casescovered by Articles 105, 107, 161 and 300 of the EC Treaty andArticle 7 of the EU Treaty***I Codecision procedure (first reading)majority of the votes cast***II Codecision procedure (second reading)majority of the votes cast, to approve the common positionmajority of Parliament’s component Members, to reject or amendthe common position***III Codecision procedure (third reading)majority of the votes cast, to approve the joint text(The type of procedure depends on the legal basis proposed by theCommission.)Amendments to a legislative textIn amendments by Parliament, amended text is highlighted in bold italics. Inthe case of amending acts, passages in an existing provision that theCommission has left unchanged, but that Parliament wishes to amend, arehighlighted in bold. Any deletions that Parliament wishes to make inpassages of this kind are indicated thus: [...]. Highlighting in normal italics isan indication for the relevant departments showing parts of the legislativetext for which a correction is proposed, to assist preparation of the final text(for instance, obvious errors or omissions in a given language version).Suggested corrections of this kind are subject to the agreement of thedepartments concerned.PE430.424v05-00 2/80 RR\430424EN.doc ENCONTENTSPage DRAFT EUROPEAN PARLIAMENT LEGISLATIVE RESOLUTION (5)EXPLANATORY STATEMENT (71)ANNEX: LETTER FROM THE COMMITTEE ON LEGAL AFFAIRS (76)ANNEX: OPINION OF THE CONSULTATIVE WORKING PARTY OF THE LEGAL SERVICES OF THE EUROPEAN PARLIAMENT, THE COUNCIL AND THE COMMISSION (78)PROCEDURE (80)RR\430424EN.doc 3/80 PE430.424v05-00ENPE430.424v05-00 4/80 RR\430424EN.doc ENRR\430424EN.doc 5/80 PE430.424v05-00ENDRAFT EUROPEAN PARLIAMENT LEGISLATIVE RESOLUTIONon the proposal for a directive of the European Parliament and of the Council on the restriction of the use of certain hazardous substances in electrical and electronic equipment (recast)(COM(2008)0809 – C6-0471/2008 – 2008/0240(COD)) (Ordinary legislative procedure: first reading - recast) The European Parliament ,− having regard to the Commission proposal to Parliament and the Council(COM(2008)0809),− having regard to Article 251(2) and Article 95 of the EC Treaty, pursuant to which theCommission submitted the proposal to Parliament (C6-0471/2008), – having regard to the Commission communication to Parliament and the Council entitled: 'Consequences of the entry into force of the Treaty of Lisbon for ongoing interinstitutional decision-making procedures' (COM)2009)0665), – having regard to Article 294(3) and Article 114 of the Treaty on the functioning of the EU, − having regard to the opinion of the European Economic and Social Committee of 16December 20091, − having regard to the opinion of the Committee of the Regions of 29 May 20102, − having regard to Rules 87 and 55 of its Rules of Procedure,− having regard to the report of the Committee on the Environment, Public Health andFood Safety (A7-0196/2010), 1. Adopts its position at first reading hereinafter set out, taking into account therecommendations of the Consultative Working Party of the legal services of the European Parliament, the Council and the Commission; 2. Calls on the Commission to refer the matter to Parliament again if it intends to amend theproposal substantially or replace it with another text; 3. Instructs its President to forward its position to the Council and the Commission and tothe national parliaments.1OJ C 306, 16.12.2009, p. 36–382OJ C 141, 29.5.2010, p. 55–64PE430.424v05-006/80RR\430424EN.docENAmendment 1Proposal for a directive Recital 3 a (new)Text proposed by the Commission Amendment(3a) Directive 2008/98/EC of theEuropean Parliament and of the Council of 19 November 2008 gives first priority to prevention in waste legislation. Prevention is defined inter alia as measures that reduce the content of harmful substances in materials and products.JustificationThe recast of RoHS should be put into the context of the waste hierarchy established in the waste framework directive in 2008. Prevention is the top priority in the binding waste hierarchy. Prevention includes measures to reduce the content of harmful substances in materials and products. The recast of RoHS recast is therefore an important opportunity to translate this obligation into concrete action, all the more that electrical and electronic equipment (EEE) continues to create numerous problems during waste treatment. Amendment 2Proposal for a directive Recital 3 b (new)Text proposed by the Commission Amendment(3b) The Council Resolution of 25 January 1988 on a Community action programme to combat environmental pollution by cadmium 1 invites theCommission to pursue without delay the development of specific measures for such a programme. Human health also has to be protected and an overall strategy that in particular restricts the use of cadmium and stimulates research into substitutes should therefore be implemented. That Resolution stresses that the use ofcadmium should be limited to cases where such use is suitable and where safer alternatives do not exist.1OJ C 30, 4.2.1988, p. 1.RR\430424EN.doc7/80PE430.424v05-00ENJustificationThe reference to the Council Resolution of 1988 (Recital 4 of current RoHS) should bereinstated as it is the political reference for combating environmental pollution by cadmium.Amendment 3Proposal for a directive Recital 3 c (new)Text proposed by the Commission Amendment(3c) The European Parliament, in its resolution of 14 November 1996 on the communication from the Commission on the review of the Community Strategy on Waste Management and the draft Council resolution on waste policy 1, asked the Commission to present proposals for directives on a number of priority waste streams, including electrical and electronic waste. The European Parliament, in the same resolution, requested the Council and theCommission to put forward proposals to reduce the presence of hazardous substances in waste such as chlorine, mercury, polyvinyl chloride (PVC), cadmium and other heavy metals.1OJ C 362, 2.12.1996, p. 241.JustificationThe reference to the Parliament Resolution of 1996 (Recital 4 of current RoHS) should be inserted as an important reminder that Parliament already asked for concrete restrictions on PVC back in 1996. Amendment 4Proposal for a directive Recital 3 d (new)Text proposed by the Commission Amendment(3d) Regulation (EC) No 850/2004 of the European Parliament and of the Council of 29 April 2004 on persistent organic pollutants and amending DirectivePE430.424v05-008/80RR\430424EN.docEN79/117/EEC 1 recalls that the objective of protecting the environment and human health from persistent organic pollutants cannot be sufficiently achieved by the Member States, owing to thetransboundary effects of those pollutants, and can therefore be better achieved at Union level. Pursuant to that Regulation, releases of persistent organic pollutants, such as dioxins and furans, which are unintentional by-products of industrial processes, should be identified and reduced as soon as possible with the ultimate aim of elimination, where feasible. Thermal treatment oruncontrolled disposal of waste electrical and electronic equipment containinghalogenated flame retardants or PVC can contribute significantly to the formation of dioxins and furans.1OJ L 158, 30.4.2004, p. 7.JustificationThe RoHS recast needs to be put into the context of the EU’s international obligations to reduce total releases of dioxins and furans, with the goal of their continuing minimization and, where feasible, ultimate elimination. The final destiny of large quantities of WEEE remains unclear. High-temperature incineration remains the exception. Sub-standardtreatment of WEEE – in the EU or in third countries - risks remaining a reality for significant amounts. Emissions of dioxins and furans can only be addressed via material choices at design stage. Amendment 5Proposal for a directive Recital 3e (new)Text proposed by the Commission Amendment(3e) The study commissioned by theCommission on hazardous substances in electrical and electronic equipment highly recommended a phase-out oforganobromines and organochlorines due to their potential to form polybrominated and polychlorinated dioxins and furans in waste treatment operations, and gave priority to the phase-out of PVC overselective risk management options toguarantee a reduced release of PVC, of itsadditives and of hazardous combustionproducts. It also recommends thelabelling of beryllium metal and berylliumoxide and the voluntary phase-outcombined with market surveillance ofseveral other examined substances.JustificationThe recommendations of the Öko-Institut with its different options should be referred to,reflecting that the suggestions go beyond the recommendation to include substances intoAnnex IV.Amendment 6Proposal for a directiveRecital 3f (new)Text proposed by the Commission Amendment(3f) There is scientific uncertainty aboutthe safety of nanomaterials for humanhealth and the environment, nointernationally agreed definition of ananomaterial and no internationallyagreed test guidelines. The Commission'sScientific Committee on Emerging andNewly Identified Health Risks(SCENIHR) adopted on 28-29 September2005 an opinion on nanotechnologieswhich concluded that there were "majorgaps in the knowledge necessary for riskassessment and concluded that "existingtoxicological and eco-toxicologicalmethods may not be sufficient to addressall of the issues arising in relation tonanoparticles". There is increasingscientific evidence that some carbonnanotubes may behave like asbestos fibresand thus have severe impact on humanhealth. The same applies to nanosilverparticles which may end up in theenvironment and may have severe impactson soil, aquatic and terrestrial organisms.RR\430424EN.doc 9/80 PE430.424v05-00ENPE430.424v05-0010/80RR\430424EN.docENJustificationA 2009 research project on emerging nanotechnologies found that about 807 products are available on the market containing nanomaterials, some of which are EEE. There is acommon agreement amongst nanotoxicologists that risks of severe impacts on health and the environment are real, precautious measures are therefore warranted in regards tonanomaterials. This amendment is linked to the amendment of Art. 4 (1) b new, suggesting a labelling for nanosilver and carbon nanotubes.Amendment 7Proposal for a directive Recital 6Text proposed by the Commission Amendment(6) The substances covered by thisDirective are scientifically well researched and evaluated and have been subject to different measures both at Community and at national level.(6) The substances covered by this Directive should be scientifically well researched and evaluated prior toestablishing restrictions and becoming subject to different measures both at Union and at national level. Substances listed in Annex III should be scientifically well researched and evaluated prior to establishing restrictions.JustificationThe assessment of substances listed in annex III has not yet been completed. The substances listed in annex III are scheduled for assessment, which should be done thoroughly; however, this work has not yet been finished.Amendment 8Proposal for a directive Recital 7Text proposed by the Commission Amendment(7) The measures provided for in this Directive take into account existing international guidelines andrecommendations and are based on an assessment of available scientific and technical information. The measures are necessary to achieve the chosen level of protection of human and animal health and(7) The measures provided for in this Directive take into account existing international guidelines andrecommendations and are based on an assessment of available scientific and technical information. The measures are necessary to achieve the chosen level of protection of human and animal health andthe environment, having regard to the risks which the absence of measures would be likely to create in the Community. The measures should be kept under review and, if necessary, adjusted to take account of available technical and scientific information. the environment, having regard to the risks which the absence of measures would be likely to create in the Union. The measures should be kept under review and, if necessary, adjusted to take account of available technical and scientific information. In particular, the risks to human health and the environment arising from the use of substances listed in Annex XIV of Regulation (EC) No 1907/2006 with special attention to Hexabromocyclododecane (HBCDD), Bis (2-ethylhexyl) phthalate, Butyl benzyl phthalate (BBP) and Dibutylphthalate (DBP) should be considered as a priority.JustificationSubstances about which some concern has been expressed by various bodies.Amendment 9Proposal for a directiveRecital 8Text proposed by the Commission Amendment(8) This Directive supplements the general Community waste management legislation, such as Directive 2008/[…]/EC of the European Parliament and of the Council on waste. (8) This Directive supplements the general EU waste management legislation, such as Directive 2008/[…]/EC of the European Parliament and of the Council on waste as well as Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)1.1 OJ L 396, 30.12.2006, p. 1.JustificationIt should be stated specifically that RoHS supplements REACH. RoHS and REACH have different objectives, scope, timelines, and outreach. RoHS was created to address the specific problems of a fast-growing waste stream, REACH addresses chemical substances at a general level, with no special focus on waste. REACH is a regional law still in its infancy, RoHS is already setting a global standard. Key problems with WEEE are due to polymers, which are exempted from REACH. RoHS should be further developed to address the specificRR\430424EN.doc 11/80 PE430.424v05-00problems of the recovery and disposal of WEEE at the origin.Amendment 10Proposal for a directiveRecital 11Text proposed by the Commission Amendment(11) The technical development of electrical and electronic equipment without heavy metals, PBDE and PBB should be taken into account. (11) The technical development of electrical and electronic equipment without heavy metals, brominated flame retardants, chlorinated flame retardants, PVC and its hazardous plasticisers should be taken into account.JustificationThe electronics industry is well-advanced in its global initiative to phase out the use of brominated/chlorinated flame retardants and PVC. Major electronics companies have already phased out the use of these substances in some/all of their products (e.g. 50% of all new mobile phones are already low halogen). Almost all major electronics companies have committed to do so for consumer products (e.g. market share of low-halogen personal computers will be at over 40% in the next 1-2 years). Similar action has already been undertaken by some manufacturers of ‘white goods’ in the past.Amendment 11Proposal for a directiveRecital 12Text proposed by the Commission Amendment(12) As soon as scientific evidence is available and taking into account the precautionary principle, the prohibition of other hazardous substances and their substitution by more environmentally friendly alternatives which ensure at least the same level of protection of consumers should be examined, paying attention to coherency with other Community legislation, and in particular to Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH). Specific account should be taken of the (12) Periodically, and as soon as scientific evidence is available, and taking into account the precautionary principle, the prohibition of other hazardous substances and their substitution by more environmentally friendly alternative substances or technologies which ensure at least the same level of protection of consumers should be examined.To this end, the Commission should study the negative impacts of other hazardous substances and the feasibility of substituting them, in particular at the end of life of electrical and electronic equipment, with a view to making legislative proposals to strengthen thePE430.424v05-00 12/80 RR\430424EN.docpotential impact on SMEs.provisions of this Directive on a regularbasis. This examination should include afull impact assessment with consultationof relevant stakeholders. The examinationshould also pay attention to coherencewith other EU legislation and maximisesynergies with the work carried out underRegulation (EC) No 1907/2006. Specificaccount should be taken of the potentialimpact on SMEs.JustificationAmendment 12Proposal for a directiveRecital 12 a (new)Text proposed by the Commission Amendment(12a) The development of renewableforms of energy is one of the Union’s keyobjectives, and the contribution made byrenewable energy sources toenvironmental and climate objectives iscrucial. Directive 2009/28/EC of 23 April2009 on the promotion of the use ofenergy from renewable sources andamending and subsequently repealingDirectives 2001/77/EC and 2003/30/EC1recalls that there should be coherencebetween those objectives and theremainder of the Union’s environmentallegislation. Consequently, this Directiveshould not prevent the development ofrenewable energy technologies thatpresent no danger to the environment andthat are sustainable and economicallyviable, such as photovoltaic solar panels,which should be excluded from the scopeof this Directive. Independent impactassessment studies requested by theCommission also recommend theexclusion of photovoltaic solar panelsfrom the scope of this Directive.RR\430424EN.doc 13/80 PE430.424v05-001 OJ L 140, 05.06.2009, p. 16.JustificationThe revision of the RoHS Directive should be coherent with the EU’s climate change objectives and should allow the development of sustainable, economically viable forms of energy. It is therefore essential to allow specific exclusions from the scope of this Directive in order to help the EU attain its broader objectives as regards environmental protection, security of energy supply and combating climate change.Amendment 13Proposal for a directiveRecital 13Text proposed by the Commission Amendment(13) Exemptions from the substitution requirement should be permitted if substitution is not possible from the scientific and technical point of view , taking specific account of the situation of SMEs or if the negative environmental, health or socio-economic impacts caused by substitution are likely to outweigh the health, environmental or socio-economic benefits of the substitution or the availability and reliability of substitutes is not ensured.Substitution of the hazardous substances in electrical and electronic equipment should also be carried out in a way so as to be compatible with the health and safety of users of electrical and electronic equipment. The placing on the market of medical devices requires a conformity assessment procedure, according to Directives 93/42/EC and98/79/EC, which could require the involvement of a notified body designated by Competent Authorities of Member States. If such a notified body certifies that the safety of the potential substitute for the intended use in medical devices or in vitro medical devices is not demonstrated, this will be viewed as a clear negative socio-economic, health and consumer safety impact. It should be possible to apply for (13) Exemptions from the substitution requirement should be permitted if substitution is not possible from a scientific and technical point of view, taking specific account of the situation of SMEs or if the negative environmental and health impacts caused by substitution are likely to outweigh the health and environmental benefits of the substitution. Substitution of the hazardous substances in electrical and electronic equipment should also be carried out in a way so as to be compatible with the health and safety of users of electrical and electronic equipment. Socio-economic considerations should be taken into account when deciding on the duration of an exemption. It should be possible to grant a grace period after expiry of an exemption in case more time is required to ensure adequate availability of substitutes, including for reasons of intellectual property restrictions. The placing on the market of medical devices requires a conformity assessment procedure, according to Directives 93/42/EC and98/79/EC, which could require the involvement of a notified body designated by Competent Authorities of Member States. If such a notified body certifies thatPE430.424v05-00 14/80 RR\430424EN.docexemptions of equipment coming under the scope of this Directive from the date of its entry into force, even when that is before the actual inclusion in the scope of that equipment. the safety of the potential substitute for the intended use in medical devices or in vitro medical devices is not demonstrated, this will be viewed as a clear negative socio-economic, health and consumer safety impact. It should be possible to apply for exemptions of equipment coming under the scope of this Directive from the date of its entry into force, even when that is before the actual inclusion in the scope of that equipment.Amendment 14Proposal for a directiveRecital 14Text proposed by the Commission Amendment(14) Exemptions from the prohibition for certain specific materials or components should be limited in their scope, in order to achieve a gradual phase-out of hazardous substances in electrical and electronic equipment, given that the use of those substances in such applications should become avoidable.(14) Exemptions from the prohibition for certain specific materials or components should be adopted on a case-by-case basis and should be limited in their scope and duration, in order to achieve a gradual phase-out of hazardous substances in electrical and electronic equipment, given that the use of those substances in such applications should become avoidable.Amendment 15Proposal for a directiveRecital 14 a (new)Text proposed by the Commission Amendment(14a)The use of nanomaterials inelectrical and electronic equipment mayincrease with the further development oftechnology. There is inadequateinformation about the use ofnanomaterials other than nanosilver andcertain carbon nanotubes in electrical andelectronic equipment and the risksRR\430424EN.doc 15/80 PE430.424v05-00associated with such use. In order toenable the Commission to assess thesafety of nanomaterials in electrical andelectronic equipment, economic operatorsshould notify the use of nanomaterials inelectrical and electronic equipment andprovide all relevant data with regard totheir safety for human health and theenvironment. The Commission shouldassess the information received and comeforward with a legislative proposal foradequate risk management, if necessary.Producers should label electrical andelectronic equipment that containsnanomaterials that can lead to exposureof consumers, in order to enableconsumers to make an informed choice.Amendment 16Proposal for a directiveRecital 19Text proposed by the Commission Amendmentdeleted(19) The measures necessary for theimplementation of this Directive should beadopted in accordance with CouncilDecision 1999/468/EC of 28 June 1999laying down the procedures for theexercise of implementing powersconferred on the Commission.(This amendment is linked to the replacement of the former "regulatory procedure with scrutiny" by the new procedure of delegated acts under Article 290 of the Treaty on the Functioning of the European Union.)JustificationRecital 20 as modified covers the necessary provisions.Amendment 17PE430.424v05-00 16/80 RR\430424EN.docProposal for a directiveRecital 20Text proposed by the Commission Amendment(20) In particular the Commission should be empowered to adapt Annexes II, III, IV,V and VI to technical and scientific progress and to adopt other necessary implementing measures. Since those measures are of general scope and are designed to amend non-essential elements of Directive 2002/95/EC, they must be adopted in accordance with the regulatory procedure with scrutiny provided for in Article 5a of Decision 1999/468/EC. (20) In order to allow the provisions of this Directive to be adapted to technical and scientific progress and to adopt other necessary measures, the Commission should be empowered to adopt delegated acts in accordance with Article 290 of the Treaty on the functioning of the European Union (TFEU) in respect of the adaptation of Annexes V, VI,VIa and VIb, the adoption of a format for applications for exemptions, detailed rules for compliance with maximum concentration values, on sampling and inspection, the definition of nanomaterials, standards for the detection of nanomaterials, the application of the labelling of nanomaterials and adaptations to REACH.Amendment 18Proposal for a directiveRecital 23 a (new)Text proposed by the Commission Amendment(23a) A thorough analysis of the addedvalue of the RoHS Directive should becarried out in the context of the upcomingreview of Regulation (EC) No 1907/2006.RR\430424EN.doc 17/80 PE430.424v05-00Amendment 19Proposal for a directiveArticle 1Text proposed by the Commission AmendmentThis Directive lays down rules on the restriction of use of hazardous substances in electric and electronic equipment with a view to contribute to the protection of human health and the environmentally sound recovery and disposal of waste electrical and electronic equipment. This Directive lays down rules on the restriction of use of hazardous substances in electric and electronic equipment with a view to contribute to the protection of human health, the environment, and the environmentally sound recovery and disposal of waste electrical and electronic equipment.JustificationThe subject matter should reflect the content of the recitals. Recital 4 says: “even if WEEE were collected separately and submitted to recycling processes, its content of mercury, cadmium, would be likely to pose risk to health and the environment”. Recital 5 then states that “the most effective way of ensuring the significant reduction of risks to health and the environment relating to those substances … is the substitution”. Thus the phase-out of hazardous substances contributes to the protection of the environment as such, not just via environmentally sound recovery and disposal.Amendment 20Proposal for a directiveArticle 2 - paragraph 1Text proposed by the Commission Amendment1. This Directive shall apply to electrical and electronic equipment falling under the categories set out in Annex I as specified in Annex II . 1. This Directive shall apply to electrical and electronic equipment, including cables, consumables and accessories, falling under the categories set out in Annex I.PE430.424v05-00 18/80 RR\430424EN.doc。
供应商ROHS 2.0环保要求调查表及供应商ROHS 2.0环保声明书
Company (公司名称)：
Address (地址)﹕
供应商ROHS 2.0环保要求调查表及供应商ROHS 2.0环保声明书
供应商ROHS 2.0环保要求调查表
供货商名称Supplier Name::
地址Address:
签名Signature:
公章Company Stamp:
日期Date:
NO
ROHS原有6项有害物质substance
1
镉及其化合物Cadmium and its compounds（Cd）
6
十溴联苯醚Polybrominated Diphenyl ether（PBDE）
ROHS 2.0新增四项有害物质substance
1
Hexabromocyclododecane and all major diastereoisomers identified
六溴环十二烷（HBCDD）
2
Bis (2-ethyl(hexyl)phthalate)邻苯二甲酸二(2-乙基己基)（DEHP）
<1000ppm
邻苯二甲酸二(2-乙基己基)
<1000ppm
邻苯二甲酸丁苄酯（BBP）
<1000ppm
邻苯二甲酸二丁酯（DBP)
<1000ppm
详细内容请参照歐盟RoHS2.0指令
我司已理解并执行环保（RoHS2.0指令等）要求， 并郑重承诺：所提供的产品，元器件，原材料， 辅料等符合环保要求。如有任何原料更改,均须重新提交所更改材料后的RoHS2.0测试报告,待XX公司确认OK后方可更换.
Is there anyROHS 2.0testReport
以下rohs2.0中管控的邻苯测试项目
ROHS指令(2002/95/EC) 资料下称ROHS1.0从 2006 年 7 月 1 日起，欧盟对电子电气产品禁用六种危险物质进行了管控，已被纳入管控的物质包括铅、镉、汞、六价铬、多溴联苯、多溴联苯醚（PBBs）以及多溴联苯醚、其中最为关注的是铅、镉、汞等重金属。
为了进一步降低电子电气产品对环境的污染，以及人体长期接触后可能对人体健康造成的潜在危害，欧盟于 2011 年 7 月 1 日颁布了ROHS2.0指令(2011/65/EU)，并于 2013 年7 月 22 日起正式实施。
和 ROHS1.0相比，ROHS2.0 扩大了管控的物质范围，并对标准进行了更新，特别是在多溴联苯、多溴联苯醚等卤代阻燃剂的使用上做了明确的规定。
ROHS2.0对于管控的物质增加了四种物质，即邻苯二甲酸、邻苯二甲酸二丁酯、邻苯二甲酸二辛酯和邻苯二甲酸二十二烷酯。
以下将对 ROHS2.0中新增管控的邻苯测试项目进行详细介绍。
1. 邻苯二甲酸含量测试为了确定电子电气产品中邻苯二甲酸的含量是否符合 ROHS2.0标准的要求，需要进行相应的化学测试。
通过合适的实验方法和仪器设备，可以准确地测定出产品中邻苯二甲酸的含量，从而判断其是否符合欧盟的相关法规要求。
这一测试项目是 ROHS2.0中对邻苯的管控要求的重要组成部分，也是保障产品质量和安全的重要手段之一。
2. 邻苯二甲酸二丁酯含量测试邻苯二甲酸二丁酯是一种常见的可塑剂，在电子电气产品的制造中被广泛使用。
然而，过量的邻苯二甲酸二丁酯对人体健康和环境都可能造成危害。
根据 ROHS2.0 的要求，需要对产品中邻苯二甲酸二丁酯的含量进行测试，确保其符合相关的管控标准。
通过专业的实验室和技术人员进行测试，可以准确判定产品中邻苯二甲酸二丁酯的含量是否符合法规要求。
3. 邻苯二甲酸二辛酯含量测试邻苯二甲酸二辛酯是一种常见的增塑剂，也被广泛用于电子电气产品的制造中。
然而，过量的邻苯二甲酸二辛酯对人体和环境都可能构成危害。
新版RoHS2.0指令介绍及如何解读 RoHS检测报告
新版 RoHS 2.0 的重要含义 2011/65/EU
8
RoHS 2.0 与旧版RoHS主要区别 --- RoHS2 Vs RoHS1
CE 标识及配套支撑性技术文档的要求
CE marking and Technical Documentation Files (TDF) required to show RoHS2 compliance
Large-scale fixed installations Transportation (i.e. cars, trains, airplanes, etc… Non-road B2B )
mobile machinery (i.e. forklift)
Active implanted medical devices Photovoltaic panels (professionally installed) R&D equipment
www.interte k.co m
11
RoHS 2.0不管制的产品
RoHS2 – Exclusions
Military Equipment Equipment designed to be sent into space Large-scale
stationary industrial tools
2000chromateconversioncoatingszinccadmiumaluminiumzincalloyszincaluminiumalloystestmethods锌镉铝锌合金以及锌铝合金上铬酸盐涂层测试方法epa3060aalkalinedigestionhexavalentchromium六价铬的碱式消解法epa7196achromiumhexavalentcolorimetric六价铬比色法rohsiec62321主要包含的内容7gcms检测聚合物中的pbb和pbderohs筛选测试方法就是用能?散射x射线荧光光谱仪edxrf或波长散射x射线荧光光谱仪wdxrf装置对样品中目标物质进?初步半定?的一种测试手段运用多种分析方法来分析有机材??属材?无机非?属材?以及专用电子材?中受限物质的浓?iec62321rohsiec62321rohsiec62321rohsiec623218金属样品中无色及有色铬酸盐镀层中含六价铬的测试类似于iso36139显色法测试聚合物和电子元件中六价铬类似于usepa3060arohsiec62321104样品前处理1043微波消解类似于usepa305211423密闭体系的酸消解法类似于usepa3052rohsiec623211342王水消解类似usepa3050b1343微波消解类似usepa3052rohsastmf9632003icpaesaasen711994iso81241997icpaesaasrohsrohs测试报告的解读需要包含以下信息测试报告的唯一编号比如序列号或报告号而且每一页都有此编号页码也是报告的一部分可用来辨识报告的结束
rohs检测报告模板
rohs检测报告模板篇一：SGS RoHS测试报告模板Test ReportNo. CANEC13Date: 12 May 20XXPagel of 5 Co.,LTD.SHANGMEILIN District .ShenzhenThe following sample was/were submitted and identified on behalf of the clients as : SGS Job No :Date of SampleReceived :Testing Period :Test Requested :Test Method :Test Results :Conclusion :CP13-- GZ09 May 20XX09 May 20XX -12 May 20XXSelected test as requested by clientPlease refer to next pagePlease refer to next pageBased on the performed tests on submitted samples, the results of Lead, Mercury, Cadmium, Hexavalent chromium, Polybrominated biphenyls , Polybrominated diphenyl ethers xxply with the limits as set by RoHS Directive20XX/65/EU Annex II; recasting 20XX/95/ECSigned for and on behalf of SGS-CSTC Ltd.MErry Lv Approved SignatoryTest ReportTest Results :No. CANEC13Date: 12 May 20XXPage 2 of 5Specimen Sample IDDescription1CAN13- Green fluidRemarks : 1 mg/kg = 1 ppm= %MDL= Method Detection Limit ND = Not Detected "-" = Not RegulatedRoHS Directive 20XX/65/EUTest Method :With reference to IEC 62321:20XX:Determination of Cadmium by ICP-OES.Determination of Lead by ICP-OES. Determination of Mercury by ICP-OES.Determination of Hexavalent Chromium by Colorimetric Method using UV-Vis. Determination of PBBs / PBDEs content by GC-MS.Test ItemCadmium Lead Mercury Hexavalent Chromium Sum of PBBsMonobromobiphenylDibromobiphenylTribromobipheny ITetrabromobiphenylPentabromobiphenylHexabromobiphe nylHeptabromobiphenylOctabromobiphenylNonabromobiph enyl DecabromobiphenylSum of PBDEsMonobromodiphenyl etherLimitlOO 1,000 1,000 1,000 1,000 --------------- 1,000 -Unitmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgmg/kgMDL2 2 2 2 - 5 5 5 5 5 5 5 5 5 5 - 5002ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND ND NDTest ReportTest ItemDibromodiphenyl etherTribromodiphenyl etherTetrabromodiphenyl etherPentabromodiphenyl etherHexabromodiphenyl etherHeptabromodiphenyl etherOctabromodiphenyl etherNonabromodiphenyl etherDecabromodiphenyl etherNotes :No. CANEC13Date: 12 May 20XXPage 3 of 5Limit- --------------- -- -Unitmg/kg5 mg/kg5 mg/kg5 mg/kg5mg/kg5 mg/kg5 mg/kg5 mg/kg5 mg/kg5NDND ND ND ND ND ND ND NDThe maximum permissible limit is quoted from the directive20XX/65/EU, Annex IINote: the results shown for the content of totalweight in wet sample..Test ReportATTACHMENTSNo. CANEC13Date: 12 May 20XXPage 4 of 5RoHS Testing Flow Chart1) Nameof the person who made testing : Michael Tso / Cutey Yu / Dayi Zhan 2) Name of the person in charge of testing : Adams Yu / Yolanda Wei3) These samples were dissolved totally by pre -conditioning method according to below flow chart .Sample PreparationTest ReportSample photo:No. CANEC13Date: 12 May 20XXPage 5 of 5SGSauthenticate the photo on original report only*** End of Report ***篇二：rohs检测认证,rohs检测标准,rohs检测报告rohs检测认证，rohs检测标准，rohs检测报告ROHS检测方法将相关产品送往专业实验室进行检测，要将产品拆分为单一材质既均一材质后进行测试，其中铅、镉、汞、六价铬、多溴联苯、多溴二苯醚等六种有害物质是否符合RoHS指令要求，若符合就可获得RoHS合格报告和证书，若不符合，就得另找符合要求的产品进行替代。
ROHs2
ROHs2.0管理控制规定符合RoHS2.0指令的声明函等作为RoHS2.0符合性依据。
5.2原材料采购5.2.1采购部负责对RoHS2.0原材料进行采购，并要求供应商提供RoHS2.0认证报告或第三方检测报告或符合RoHS2.0指令的声明函等作为RoHS2.0符合性依据。
5.2.2采购部门应对RoHS2.0原材料进行记录，包括RoHS2.0认证报告或第三方检测报告或符合RoHS2.0指令的声明函等。
5.3仓库管理5.3.1仓库负责对RoHS2.0与非RoHS2.0物料的区域划分，环保物料隔离与标识。
5.3.2RoHS2.0物料的来料入库、储存、发料和产品出入库应严格按照ROHS2.0标准操作。
5.4生产管理5.4.1生产部门负责RoHS2.0产品的生产、测试、维修、包装等操作。
5.4.2生产部门应对在线RoHS2.0物料、成品、工装夹具设备等进行标识和管理。
5.5质量控制5.5.1质量部门负责对原材料、半成品、成品之环保确认，并对整个有环保要求的产品的品质进行监控。
5.5.2质量部门应对RoHS2.0产品进行记录，包括RoHS2.0认证报告或第三方检测报告或符合RoHS2.0指令的声明函等。
6.0文件控制6.1本程序由环保部门负责审核、批准并发布，环保部门对本程序进行修订时，应及时通知相关部门。
6.2本程序应定期进行审核，如有需要，应及时修订并重新发布。
6.3本程序的有效性应在实际操作中进行验证，并进行记录。
7.0附录7.1RoHS2.0认证报告样本7.2第三方检测报告样本7.3符合RoHS2.0指令的声明函样本5.1.3 公司应对供应商提交的符合RoHS2.0指令的声明函等资料进行抽样检验，确保检验结果为合格品。
5.1.4 采购部应组织研发部和质量部对供应商进行现场检查，检查内容包括：a。
供应商是否有文件化的RoHS2.0产品控制程序，控制原材料的采购和整个生产流程中原材料的控制，确保不掺入任何不符合RoHS2.0标准的原材料和产品；在加工过程中进行全程监控并标识；b。
关於ROHS2.0 测试报告
供應商名稱Supplier Name::
地址Address:
簽名Signature:
公章Company Stamp:
日期Date:
NO
ROHS 原有6項有害物質substance
1
鎘及其化合物Cadmium and its compounds（Cd）
2
鉛及其化合物Lead and its compounds（Pb）
3
l butyl phthalate 邻苯二甲酸丁苄酯（BBP）
4
Dibutyl phthalate 邻苯二甲酸二丁酯（DBP)
請確認貴司產品是否有ROHS2.0測試報告List out ROHS2.0testreportofproduct
產品名稱Product Name
XX料號
PN
是否有ROHS 2.0測試報告
Is there anyROHS 2.0testReport
計畫提交日期
Sumbit date
備注
Remark
備註：如果有ROHS 2.0測試報告，請提交報告并在以上表格填寫產品型號；如果沒有，請告知哪些產品計畫在何時提交報告,謝謝~
Remark：If you havethe ROHS2.0testreport,pleasesubmitand list out the PN; If you don’t haveit, please let us know which datewhich productyou will submitreport，tks!
3
汞及其化合物Mercury and its compounds（Hg）
4
六價鉻及其化合物Hexavalent Chromium and its compounds（Cr6+）
SGS RoHS测试报告模板
SGS RoHS测试报告模板No. CANEC13 Date: 12 May 2013Page1 of 5Test ReportCo.,LTD.SHANGMEILIN District .ShenzhenThe following sample(s) was/were submitted and identified on behalf of the clients as : SGS Job No :CP13- - GZDate of Sample 09 May 2013Received :09 May 2013 - 12 May 2013Testing Period :Selected test(s) as requested by clientTest Requested :Please refer to next page(s)Test Method :Please refer to next page(s)Test Results :Based on the performed tests on submitted samples, the results of Lead, Conclusion :Mercury, Cadmium, Hexavalent chromium, Polybrominated biphenyls (PBB),Polybrominated diphenyl ethers (PBDE) comply with the limits as set by RoHSDirective 2011/65/EU Annex II; recasting 2002/95/ECSigned for and on behalf ofSGS-CSTC Ltd.MErry LvApproved SignatoryNo. CANEC13 Date: 12 May 2013Page 2 of 5Test Report Test Results :Test Part Description :Specimen No.SGS Sample IDDescription1CAN13- Green fluidRemarks :(1) 1 mg/kg = 1 ppm = 0.0001%(2) MDL = Method Detection Limit(3) ND = Not Detected ( < MDL )(4) "-" = Not RegulatedRoHS Directive 2011/65/EUTest Method :With reference to IEC 62321:2008:(1) Determination of Cadmium by ICP-OES.(2) Determination of Lead by ICP-OES.(3) Determination of Mercury by ICP-OES.(4) Determination of Hexavalent Chromium by Colorimetric Methodusing UV-Vis.(5) Determination of PBBs / PBDEs content by GC-MS.Test Item(s)LimitUnitMDL002Cadmium (Cd)100 mg/kg2 ND Lead (Pb)1,000 mg/kg2 ND Mercury (Hg)1,000 mg/kg2 ND Hexavalent Chromium (CrVI)1,000 mg/kg2 ND Sum of PBBs1,000 mg/kg- ND Monobromobiphenyl- mg/kg5 ND Dibromobiphenyl- mg/kg5 ND Tribromobiphenyl- mg/kg5 ND Tetrabromobiphenyl- mg/kg5 ND Pentabromobiphenyl- mg/kg5 ND Hexabromobiphenyl- mg/kg5 ND Heptabromobiphenyl- mg/kg5 ND - mg/kg5 ND OctabromobiphenylNonabromobiphenyl - mg/kg5 ND Decabromobiphenyl- 5 mg/kgND Sum of PBDEs 1,000 mg/kg- ND Monobromodiphenyl ether- mg/kg5 NDNo. CANEC13 Date: 12 May 2013Page 3 of 5Test Report002Test Item(s)LimitUnitMDL5 ND Dibromodiphenyl ether- mg/kgTribromodiphenyl ether- mg/kg5 ND Tetrabromodiphenyl ether- mg/kg5 ND5 Pentabromodiphenyl ether- mg/kgND5 ND Hexabromodiphenyl ether- mg/kgHeptabromodiphenyl ether- mg/kg5 ND Octabromodiphenyl ether- mg/kg5 ND Nonabromodiphenyl ether- mg/kg5 ND Decabromodiphenyl ether- mg/kg5 NDNotes :(1) The maximum permissible limit is quoted from the directive2011/65/EU, Annex IINote: the results shown for the content of total weight in wet sample. .No. CANEC13 Date: 12 May 2013Page 4 of 5Test ReportATTACHMENTSRoHS Testing Flow Chart1) Name of the person who made testing,Michael Tso / Cutey Yu / Dayi Zhan 2) Name of the person in charge of testing,Adams Yu / Yolanda Wei3) These samples were dissolved totally by pre -conditioning method according to below flow chart(Cr6+ and PBBs/PBDEs test method excluded).Sample PreparationNo. CANEC13 Date: 12 May 2013Page 5 of 5Test Report Sample photo:CANEC13CAN13-SGS authenticate the photo on original report only *** End of Report ***。
ROHS2.0(草案).pdf
Brussels, 3 September 2009 THE EUROPEA U IO12847/09Interinstitutional File:2008/0240 (COD)E V 537MI 308CODEC 1053OTEfrom : General Secretariatto : DelegationsNo. prev. doc. : 10977/09 ENV 434 MI 244 CODEC 846No. Cion prop. : 17333/08 ENV 1019 MI 553 CODEC 1859 - COM(2008) 809 finalSubject : Proposal for a Directive of the European Parliament and of the Council on the restriction of the use of certain hazardous substances in electrical and electronicequipment (RoHS) - (recast)Delegations will find attached a compromise text on the Articles and Annexes of the above-mentioned proposal (bold underline). Following the WPE discussions, the Presidency has, in particular, introduced an important change in the scope of the proposal, which is now covering all EEEs unless specifically excluded. Annexes I and II (categories and positive lists) have been deleted from the text. The exclusions from the scope, as a consequence, need to be further refined and the Presidency would welcome contributions from delegations on the impact of this change as well as any suggestions on the nature of such exclusions.Articles 4(7) and 5 are also revised, keeping in mind that the relationship with REACH should be clarified further. The changes in Article 3 points (b) to (kb) and in Articles 7 to 17 have beendiscussed previously and appear in the text as simple underlining._________________________A EXProposal for aDIRECTIVE OF THE EUROPEA PARLIAME T A D OF THE COU CILon the restriction of the use of certain hazardous substances in electrical and electronicequipment ∗p.m. recitalsArticle 1Subject matter[...]This Directive lays down rules on the restriction of use of hazardous substances in electrical and electronic equipment with a view to contribute to the protection of human health and the environmentally sound recovery and disposal of waste electrical and electronic equipment.Article 2Scope1. This Directive shall apply to electrical and electronic equipment. [...]2. This Directive shall apply without prejudice to requirements of ∗∗ Community legislation onsafety and health, on chemicals, in particular Regulation (EC) 1907/2006, as well as ofspecific Community waste management legislation.∗Some editorial changes (suggestions already circulated) have been incorporated into this text. ∗∗Consultative Committee Opinion.3. This Directive does not apply to [...]:(a)equipment which is necessary for the protection of the essential interests of thesecurity of Member States, including arms, munitions and war material intended forspecifically military purposes;(b)equipment which is specifically designed as part of another type of equipment thatdoes not fall within the scope of this Directive and can fulfill its function only if it ispart of that equipment;(c) equipment which is not intended to be placed on the market as a single functional orcommercial unit;(ca) large-scale stationary industrial tools;(cb) musical pipe organs.Article 3DefinitionsFor the purposes of this Directive, the following definitions shall apply:(a) "electrical and electronic equipment" (hereinafter ∗ ‘EEE’) means equipment which isdependent on electric currents or electromagnetic fields in order to work properly andequipment for the generation, transfer and measurement of such currents and fields [...] and designed for use with a voltage rating not exceeding 1000 volts for alternating current and 1500 volts for direct current;[...](b) "manufacturer" means any natural or legal person who manufactures EEE or who has EEEdesigned or manufactured, and markets it under his name or trademark;∗Consultative Committee Opinion.(c) "distributor" means any natural or legal person in the supply chain, other than themanufacturer or the importer, who makes EEE available on the market;(d) "importer" means any natural or legal person established within the Community, who placesEEE from a third country on the Community market;(da) "authorised representative" means any natural or legal person established within the Community who has received a written mandate from a manufacturer to act on his behalf in relation to specified tasks;(db) "economic operators" mean the manufacturer, the authorised representative, the importer and the distributor;(e) "making available on the market" means any supply of EEE for distribution, consumption oruse on the Community market in the course of a commercial activity, whether in return for payment or free of charge;(f) "placing on the market" means the first making available of EEE on the Community market;(g) "harmonised standard" means a standard adopted by one of the European standardisationbodies listed in Annex I to Directive 98/34/EC on the basis of a request made by theCommission in accordance with Article 6 of Directive 98/34/EC;(ga) "technical specification" means a document that prescribes technical requirements to be fulfilled by a product, process or service;[…](i) "CE marking" means a marking by which the manufacturer indicates that the product is inconformity with the applicable requirements set out in Community harmonization legislation providing for its affixing;(j) "conformity assessment" means the process demonstrating whether the requirements of the present Directive relating to EEE, are met;(k) "market surveillance" means the activities carried out and measures taken by public authorities to ensure that EEE complies with the requirements set out in this Directive and do not endanger health, safety or other issues of public interest protection ;(ka) "recall" means any measure aimed at achieving the return of a product that has already been made available to the end user;(kb) "withdrawal" means any measure aimed at preventing a product in the supply chain from being made available on the market;(l) "homogeneous material" means a material of uniform composition throughout that can not be mechanically disjointed into different materials, meaning that the materials can not, inprinciple, be separated by mechanical actions such as unscrewing, cutting, crushing,grinding and abrasive processes;(m) "medical device" means a medical device within the meaning of point (a) of Article 1(2) of Directive 93/42/EC;(n) "in vitro diagnostic medical device" means an in vitro diagnostic medical device within the meaning of point (b) of Article 1(2) of Directive 98/79/EC;(o) "active implantable medical device" means any active implantable medical device within the meaning of point (c) of Article 1(2) of Directive 90/385/EEC;(p) "industrial monitoring and control instruments" mean monitoring and control instruments designed for exclusively industrial or professional use.Article 4Prevention1. Member States shall ensure that EEE, including spare parts for its repair or its reuse placed ∗on the market, does not contain the substances listed in Annex IV.∗Consultative Committee Opinion.2. For the purposes of this Directive, the maximum concentration value by weight inhomogeneous materials as specified in Annex IV shall be tolerated [...].3. Paragraph 1 shall apply to medical devices and monitoring and control instruments whichare placed on the market from 1st January 2014, to in vitro medical devices which are placed on the market from 1st January 2016 and to industrial monitoring and control instrumentswhich are placed on the market from 1st January 2017.4. Paragraph 1 shall not apply to spare parts for the repair or to the reuse of the following:(a) EEE placed on the market before 1 July 2006.(b) Medical devices placed on the market before 1st January 2014.(c) In vitro diagnostic medical devices placed on the market before 1st January 2016.(d) Monitoring and control instruments placed on the market before 1st January 2014.(e) Industrial monitoring and control instruments placed on the market before1st January 2017.(f) EEE which benefited from an exemption and was placed on the market before thatexemption expired.5. Paragraph 1 shall not apply to active implantable medical devices. By 2020 the Commissionshall review the exclusion of active implantable medical devices with a view to proposeinclusion.6. Paragraph 1 shall not apply to the applications listed in Annexes V and VI.[...]7. […] 1The Commission shall adopt a methodology for the review of Annex IV, based on the process set out in Articles 69 to 72 of Regulation (EC) o 1907/2006 and the soundrecovery and disposal of waste electrical and electronic equipment. This measure,designed to amend non essential elements of this Directive, shall be adopted inaccordance with the regulatory procedure with scrutiny referred to in Article 18(2).7a.The list of prohibited substances in Annex IV shall be reviewed according to the methodology referred to in paragraph (7) and, if necessary, amended, following thesubmission of a request by the Commission or a Member State if it is considered that the use of a substance in EEE, or the waste derived from it, poses a hazard to humanhealth or the environment that is not adequately controlled and needs to be addressed on a Community-wide basis. Those measures, designed to amend non essentialelements of this Directive shall be adopted in accordance with the regulatoryprocedure with scrutiny referred to in Article 18(2).Article 5Adaptation of the Annexes to scientific and technical progress1. The Commission shall, for the purposes of adapting the annexes to scientific and technicalprogress, adopt the following measures:(a) […]1It is proposed to delete Annex III, replacing it by the mention of the priority substances concerned in Recital 7 as follows:"(7) The measures provided for in this Directive take into account existing internationalguidelines and recommendations and are based on an assessment of available scientific and technical information. The measures are necessary to achieve the chosen level of protection of human and animal health and the environment, having regard to the risks which the absence of measures would be likely to create in the Community. The measures should be kept under review and, if necessary, adjusted to take account of available technical and scientificinformation. In particular, the risks to human health and the environment arising from the use of Hexabromocyclododecane (HBCDD), Bis (2-ethylhexyl) phthalate (DEHP), Butyl benzyl phthalate (BBP) and Dibutylphthalate (DBP) should be considered as a priority. "[...](b) Inclusion of materials and components of EEE in Annexes V and VI where either ofthe following conditions is fulfilled:–their elimination or substitution via design changes or materials andcomponents which do not require any of the materials or substances referred toin Article 4(1) is scientifically or technically impracticable;–the availability and reliability of substitutes is not ensured or the negativesocio economic impacts caused by substitution are disproportionatecompared to the environmental, health, consumer safety or socio economicbenefits thereof;–the negative environmental, health, consumer safety […] impacts caused by substitution are likely to outweigh the environmental, health or consumersafety […] benefits thereof;[...](c) deletion of materials and components of EEE from Annexes V and VI where theconditions set out in point (b) are no longer fulfilled.Those measures designed to amend non essential elements of this Directive shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 18(2).2. Measures adopted in accordance with point (b) of paragraph 1 shall have a maximumvalidity period of four years and may be renewed. The Commission shall decide in due time on any application for renewal that is submitted no later than 18 months before anexemption expires.3. Before Annexes are amended [...], the Commission shall inter alia consult producers ofelectrical and electronic equipment, recyclers, treatment operators, environmentalorganisations and employee and consumer associations. [...]4. As long as materials or components are included in Annexes V and VI to this Directive, onthe basis of Article 5(1)(b) of this Directive, those applications shall also be consideredexempted from the authorisation requirements set out in Article 58(2) of the regulation (EC) No 1907/2006. 2Article 6Implementing measuresThe Commission shall adopt detailed rules for:–applications for exemption including a format and types of information to be provided when introducing those applications, including analysis of the alternatives and, if suitablealternatives are available, substitution plans as referred to in Regulation (EC) 1907/2006;–complying with the maximum concentration values of Article 4(2);–the implementation of Article 5(2), taking into account the need for legal certainty for economic operators pending a Commission Decision on renewal of exemptions.Those measures designed to amend non essential elements of this Directive shall be adopted in accordance with the regulatory procedure with scrutiny referred to in Article 18(2).[...]Article 7Obligations of manufacturersMember States shall ensure that:1. When placing EEE on the market, manufacturers […] ensure that they have been designedand manufactured in accordance with the requirements set out in Article 4.2. Manufacturers […] draw up the required technical documentation and carry out the internalproduction control procedure set out in module A of Annex II to Decision No 768/2008/EC or have it carried out.2The link with REACH should be further discussed also in connection with Article 2(2).Where compliance of EEE with the applicable requirements has been demonstrated by that procedure, manufacturers […] draw up an EC declaration of conformity and affix the CEmarking.3. Manufacturers […] keep the technical documentation and the EC declaration of conformityfor ten years after the EEE has been placed on the market.4. Manufacturers […] ensure that procedures are in place for series production to remain inconformity. Changes in product design or characteristics and changes in the harmonisedstandards or in technical specifications by reference to which conformity of an EEE isdeclared shall be adequately taken into account.5. When deemed appropriate with regard to the risks presented by a product, manufacturers […],to protect the health and safety of consumers, carry out sample testing of marketed EEE,investigate, and, if necessary, keep a register of complaints, of non-conforming EEE andproduct recalls, and […] keep distributors informed of any such monitoring.6. Manufacturers […] ensure that their EEE bears a type, batch or serial number or otherelement allowing their identification, or, where the size or nature of the EEE does not allow it, that the required information is provided on the packaging or in a document accompanying the EEE.7. Manufacturers […] indicate their name, registered trade name or registered trade mark and theaddress at which they can be contacted on the EEE or, where that is not possible, on itspackaging or in a document accompanying the EEE. The address must indicate a single point at which the manufacturer can be contacted.8. Manufacturers who consider or have reason to believe that EEE which they have placed onthe market is not in conformity with […] this Directive […] immediately take the necessary corrective measures to bring that EEE into conformity, to withdraw it or recall it, ifappropriate. Furthermore, where the EEE presents a risk, manufacturers […] immediatelyinform the competent national authorities of the Member States in which they made the EEE available to that effect, giving details, in particular, of the non-compliance and of anycorrective measures taken.9. Manufacturers […], further to a reasoned request from a competent national authority,provide it with all the information and documentation necessary to demonstrate theconformity of the EEE, in a language which can be easily understood by that authority. They shall cooperate with that authority, at its request, on any action taken to eliminate the risks posed by EEE which they have placed on the market.Article 8Authorised representativesMember States shall ensure that:1. A manufacturer […] has the possibility to appoint an authorised representative by writtenmandate.The obligations laid down in Article 7(1) and the drawing up of technical documentation shall not form part of the authorised representative's mandate.2. An authorised representative […] perform s the tasks specified in the mandate received fromthe manufacturer. The mandate shall allow the authorised representative to do at least thefollowing:(a) keep the EC declaration of conformity and the technical documentation at the disposalof national surveillance authorities for ten years;(b) further to a reasoned request from a competent national authority, provide that authoritywith all the information and documentation necessary to demonstrate the conformity ofEEE;(c) cooperate with the competent national authorities, at their request, on any action takento eliminate the risks posed by EEE covered by their mandate.Article 9Obligations of importersMember States shall ensure that:1. Importers […] place only compliant products on the Community market.2. Before placing EEE on the market importers […] ensure that the appropriate conformityassessment procedure has been carried out by the manufacturer. […] Importers will further ensure that the manufacturer has drawn up the technical documentation, that the EEE bears the CE marking and is accompanied by the required documents, and that the manufacturer has complied with the requirements set out in Article 7(5) and (6).Where an importer considers or has reason to believe that EEE is not in conformity withArticle 4, he […] does not place the EEE on the market until it has been brought intoconformity. Furthermore, where the EEE presents a risk, the importer […] will inform themanufacturer and the market surveillance authorities to that effect.3. Importers […] indicate their name, registered trade name or registered trade mark and theaddress at which they can be contacted on the EEE or, where that is not possible, on itspackaging or in a document accompanying the EEE.4. Importers […] ensure that, while EEE is under their responsibility, storage or transportconditions do not jeopardise its compliance with the requirements set out in Article 4.5. When deemed appropriate with regard to the risks presented by EEE, importers […],to protect the health and safety of consumers, carry out sample testing of marketed EEE,investigate, and, if necessary, keep a register of complaints, of non-conforming EEE and EEE recalls, and […] keep distributors informed of such monitoring.6. Importers who consider or have reason to believe that an EEE which they have placed on themarket is not in conformity with this Directive […] immediately take the corrective measures necessary to bring that EEE into conformity, to withdraw it or recall it, if appropriate.Furthermore, where the EEE presents a risk, importers […] will immediately inform thecompetent national authorities of the Member States in which they made the EEE available to that effect, giving details, in particular, of the non-compliance and of any corrective measures taken.7. Importers […] keep, for ten years, a copy of the EC declaration of conformity at the disposalof the market surveillance authorities and ensure that the technical documentation can bemade available to those authorities, upon request.8. Importers […], further to a reasoned request from a competent national authority, provide itwith all the information and documentation necessary to demonstrate the conformity of EEE in a language which can be easily understood by that authority. They shall cooperate with that authority, at its request, on any action taken to eliminate the risks posed by EEE which they have placed on the market.Article 10Obligations of distributorsMember States shall ensure that:1. When making EEE available on the market distributors […] act with due care in relation tothe requirements applicable.2. Before making EEE available on the market distributors […] verify that the EEE bears the CEmarking, that it is accompanied by the required documents in a language which can be easily understood by consumers and other end-users in the Member State in which the EEE is to be made available on the market, and that the manufacturer and the importer have complied with the requirements set out in Article 7([…]6) and ([…]7) and Article 9(3).Where a distributor considers or has reason to believe that EEE is not in conformity withArticle 4, he […] does not make the EEE available on the market until it has been brought into conformity. Furthermore, where the EEE presents a risk, the distributor […] will inform the manufacturer or the importer to that effect as well as the market surveillance authorities.3. Distributors […] ensure that, while EEE is under their responsibility, storage or transportconditions do not jeopardise its compliance with the requirements set out in Article 4.4. Distributors who consider or have reason to believe that EEE which they have made availableon the market is not in conformity with this Directive […] make sure that the correctivemeasures necessary to bring that EEE into conformity, to withdraw it or recall it,if appropriate, are taken. Furthermore, where the EEE presents a risk, distributors […] will immediately inform the competent national authorities of the Member States in which they made the EEE available to that effect, giving details, in particular, of the non-compliance and of any corrective measures taken.5. Distributors […], further to a reasoned request from a competent national authority, provide itwith all the information and documentation necessary to demonstrate the conformity of EEE.They […] cooperate with that authority, at its request, on any action taken to eliminate the risks posed by EEE which they have made available on the market.Article 11Cases in which obligations of manufacturers apply to importers and distributors Member States shall ensure that an importer or distributor […] is considered a manufacturer for the purposes of this Directive and that he […] is subject to the obligations of the manufacturer under Article 7, where he places EEE on the market under his name or trademark or modifies EEE already placed on the market in such a way that compliance with the applicable requirements may be affected.Article 12Identification of economic operatorsMember States shall ensure that economic operators […], on request, identify the following to the market surveillance authorities, for ten years:(a) any economic operator who has supplied them with EEE;(b) any economic operator to whom they have supplied EEE.Article 13EC declaration of conformity1. The EC declaration of conformity shall state that the fulfilment of requirements specifiedin Article 4 has been demonstrated.2. The EC declaration of conformity shall have the model structure and shall contain theelements specified in Annex VII and shall be updated. It shall be translated into the language or languages required by the Member State in which market the product is placed or madeavailable.3. By drawing up the EC declaration of conformity, the manufacturer shall assume responsibilityfor the compliance of the EEE.Article 14General principles of the CE markingThe CE marking shall be subject to the general principles set out in Article 30 of Regulation (EC) No 765/2008.Article 15Rules and conditions for affixing the CE marking1. The CE marking shall be affixed visibly, legibly and indelibly to the EEE or to its data plate.Where that is not possible or not warranted on account of the nature of the EEE, it shall be affixed to the packaging and to the accompanying documents, where the legislation concerned provides for such documents.2. The CE marking shall be affixed before the EEE is placed on the market. It may be followedby a pictogram or any other mark indicating a special risk or use.3. […]4. Member States shall build upon existing mechanisms to ensure correct application of theregime governing the CE marking and take appropriate action in the event of improper use of the marking. Member States shall also provide for penalties for infringements, which mayinclude criminal sanctions for serious infringements. Those penalties shall be proportionate to the seriousness of the offence and constitute an effective deterrent against improper use.Article 16Presumption of conformityMember States shall presume electrical and electronic equipment bearing the CE markingas conforming to this Directive.EEE on which tests and measurements have been performed in accordance with harmonised standards, the references of which have been published in the Official Journal of the European Union, shall be presumed to comply with all the relevant requirements of this Directive to which such standards relate.Article 16aFormal objection to a harmonised standard1. When a Member State or the Commission considers that a harmonised standard does notentirely satisfy the requirements which it covers and which are set out in [Article 4], theCommission or the Member State concerned shall bring the matter before the Committee set up by Article 5 of Directive 98/34/EC, giving its arguments. The Committee shall, havingconsulted the relevant European standardisation bodies, deliver its opinion without delay.2. In the light of the Committee's opinion, the Commission shall decide to publish, not topublish, to publish with restriction, to maintain, to maintain with restriction or to withdraw the references to the harmonised standard concerned in or from the Official Journal of theEuropean Union.3. The Commission shall inform the European standardisation body concerned and, if necessary,request the revision of the harmonised standards concerned.Market surveillance and controls of EEE entering the Community market Member States shall carry out market surveillance, in accordance with Articles 15 – 29 of Regulation (EC) No 765/2008.Article 18Committee1. The Commission shall be assisted by the Committee set up by Article 18 of EuropeanParliament and Council Directive on waste 2006/12/EC of 5 April 2006 3 .2. Where reference is made to this paragraph, Article 5a(1) to (4) and Article 7 of Decision1999/468/EC shall apply, having regard to the provisions of Article 8 thereof.Article 19PenaltiesThe Member States shall lay down the rules on penalties applicable to infringements of the national provisions adopted pursuant to this Directive and shall take all measures necessary to ensure that they are implemented ∗. The penalties provided for must be effective, proportionate and dissuasive. The Member States shall notify those provisions to the Commission by the date specified in Article 20 at the latest and shall notify it without delay of any subsequent amendment affecting them. *3OJ L 114, 27.4.2006, p. 9.∗Consultative Committee Opinion.。
rohs2
rohs2.0十项有害物质限制浓度
以下是RoHS 2.0对十项有害物质的限制浓度要求（单位为百
分比）：
1. 镉（Cd）：限制浓度不超过0.01%（1000ppm）
2. 铅（Pb）：限制浓度不超过0.1%（1000ppm）
3. 汞（Hg）：限制浓度不超过0.1%（1000ppm）
4. 六价铬（Cr6+）：限制浓度不超过0.1%（1000ppm）
5. 多溴联苯（PBBs）：限制浓度不超过0.1%（1000ppm）
6. 多溴二苯醚（PBDEs）：限制浓度不超过0.1%（1000ppm）
7. 多溴邻苯三醚（PBDs）：限制浓度不超过0.1%（1000ppm）
8. 邻苯二甲酸酯（DEHP）：限制浓度不超过0.1%（1000ppm）
9. 苯并[α]芘（BBP）：限制浓度不超过0.1%（1000ppm）
10. 邻苯二甲酸酯（DBP）：限制浓度不超过0.1%（1000ppm）
需要注意的是，这些限制浓度指的是整个电子和电气设备中相关材料的重量百分比。
此外，RoHS 2.0还对这些物质的测量
方法和允许例外情况进行了更详细的规定。
Quanta_欧盟RoHS2.0符合性宣告表(模板)
廣達電腦股份有限公司333桃園市龜山區文化二路211號Quanta Computer Inc.No.211, Wen Hwa 2nd Rd.,Guishan Dist., Taoyuan City 333, Taiwan (R.O.C.)TEL: 886-3-327-2345Quanta declaration of EU RoHS 2.0 ConformityTo Whom It May Concern,______________________________________________________ (hereinafter ‘Company’), as a □supplier or□manufacturer of the products showing on this declarations and corresponding test reports to Quanta ComputerInc.(Quanta), Company hereby certify and guarantee that1. All component, assembly or product(s) has been designed and manufactured in comply with EU RoHS2.0(Directive 2011/65/EU) and new Directive (EU) 2015/863 to amend Annex II, restricted four phthalates substances in Electrical and electronic equipment, and phthalates requirements below:Bis(2-Ethylhexyl) phthalate (DEHP): threshold max 0.1%;Benzyl butyl phthalate (BBP): threshold max 0.1%;Dibutyl phthalate (DBP): threshold max 0.1%;Diisobutyl phthalate (DIBP): threshold max 0.1%.Note: The EU RoHS 2.0 Directive will be restricted four phthalates from 22 July 2019 for all electrical andelectronic equipment apart from Category 8 (medical devices) and Category 9 (monitoring and controlequipment) that will have an additional two years to comply by 22 July 2021.And meet the phase out of latest EU RoHS exemption expiration dates is advanced by 1 year for the Quanta.2. Company will always comply with the latest EU directive (as known as RoHS).In case of any discrepancies between the English version and Chinese version, the English version shall be governed.做為廣達電腦股份有限公司(下稱：廣達)之揭露於產品環保聲明書及其化學檢測報告上之□供應商或□製造商，本公司同意確認及擔保以下三點事項：1. 保證本公司設計及生產之零部件、配件或產品等符合歐盟Directive 2011/65/EU指令及(EU) 2015/863指令修訂要求四項鄰苯二甲酸鹽物質在電子電機設備中，如下:鄰苯二甲酸二(2-乙基己基)酯(DEHP) 限值0.1%鄰苯二甲酸丁酯苯甲酯(BBP) 限值0.1%鄰苯二甲酸二丁酯(DBP) 限值0.1%鄰苯二甲酸二異丁酯(DIBP) 限值0.1%備註: RoHS 2.0法規將於2019年7月22日開始執行禁用鄰苯二甲酸鹽物質四項物質於電子電機設備，而醫療設備和監控儀器禁用執行日為2021年7月22日。
ROHS_2.0标准
XXXXXXXXX有限公司环保标准(RoHS 2.0标准)Date:2014-5-26 项次环境管制物质限量标准1 Lead(Pb)/Lead Compounds铅及铅化合物塑胶(含橡胶)/涂料/墨水/焊锡:<800ppm(PVC及线材胶皮:<300ppm)合金类:钢材:<0.35% (3500ppm)铝合金:<0.4%(4000ppm)铜合金:<4% (40000ppm)2 Cadmium/cadmium compounds镉及镉化合物<75ppm不能使用于稳定剂、着色剂和表面覆涂处理（不能检测到）。
3 Mercury and mercury compounds汞及汞化合物不能检测到(ND)4 Hexavalent chromium compounds六价铬化合物<1000ppm5 Polybrominated biphenyls(PBB)多溴联苯PBB+PBDE<500ppm(并且十溴联苯醚不被豁免)6 Polybrominated diphenylethers(PBDE)多溴联苯醚7 Hexabromcyclododecane(HBCDD)六溴环十二烷＜1000ppm8 Bis(2-ethyl(hexyl)phthalate(DEHP)邻苯二甲酸二（2-乙基已基）酯<1000ppm9 Butyl benzyl phthalate(BBP)邻苯二甲酸丁苄脂<1000ppm10 Dibutyl phthalate(DBP)邻苯二甲酸二丁脂<1000ppm11PFOS全氟辛烷磺酸<50 ppm12 SVHC最新候选物质REACH<1000ppm13 Pb+Cd+Hg+Cr+6、PBB、PBDE(包装材料)Pb+Cd+Hg+Cr+6<80ppmPBB:不能检测到(ND)PBDE:不能检测到(ND)。
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《电子信息产品污染防治管理办法》规定，自2006年7月1日起，列入电子信息产品污染重点防治目录中的电子信息产品中不得含有铅、汞、镉、六价铬、聚合溴化联本醚和聚合溴化联本及其他有毒有害物质。
对于2006年7月1日以前的一段时间，要求电子信息产品制造商们实行有毒有害物质的减量化生产措施，并积极寻找可替代品。
同时，一个名为“电子信息产品污染防治标准工作组”的机构也已经开始筹备成立，该机构的主要任务是研究和建立符合中国国情的电子信息产品污染防治标准，开展与电子信息产品污染防治有关的标准研究和制定工作，特别是加快制定急需的材料、工艺、测试方法和实验方法的基础标准。
RoHS认证周期：七个工作日RoHS禁止有害物质的测试标准及方法（目前所用的测试方法是业界默认的方法，并非欧盟强制规定的）
今年针对非金属ROHS检测强制执行ROHS 2.0，也就是ROHS 10项检测，其中除了之前ROHS 6项中的铅，镉，汞，六价铬，多溴联本，多溴联本醚之外，还增加了邻苯二甲酸盐中的三项，和六溴环十二烷，一共增加了四项。
所以现在非金属检测ROHS 2.0的都是检测这10项，金属ROHS检测不变。