- Binding source for the four phthalates added to RoHS Annex II.
"amending Annex II to Directive 2011/65/EU"
RoHS restricts hazardous substances in electrical and electronic equipment at homogeneous-material level, with technical documentation, CE marking, supplier evidence, exemptions, and testing controls.
Use this EU RoHS Directive timeline page to turn RoHS dates, exemptions, substance amendments, and transition points into clear scope decisions, owner actions, evidence records, and source-linked next steps.
Structured answer sets in this page tree.
Cited legal and guidance references.
Timeline under EU RoHS Directive is a practical compliance question: decide scope, map the duty to the cited source, assign an owner, and keep evidence that can survive release reviews, procurement questions, and authority requests.
Use the Timeline as a decision tool, not only as a date list. For RoHS, the milestones visitors usually need are the directive history, the transposition deadline, the repeal date for RoHS 1, and the later substance transition dates for phthalates and other scope changes.
Key dates include: Directive 2011/65/EU was adopted on 8 June 2011 and published on 1 July 2011; Member States had to adopt national measures by 2 January 2013; Directive 2002/95/EC was repealed with effect from 3 January 2013; Commission Delegated Directive (EU) 2015/863 was published on 4 June 2015; the phthalates DEHP, BBP, DBP and DIBP applied from 22 July 2019 for most EEE and from 22 July 2021 for medical devices and monitoring and control instruments.
Keep evidence that a reviewer can follow without knowing the project history. The file should show what was assessed, what rule was applied, what was tested or reviewed, what changed, who approved it, and what still needs monitoring.
For RoHS, the core evidence set is BOM and material declarations, restricted-substance matrix, exemption register, supplier declarations, test plan, lab reports where needed, EN IEC 63000 technical file, EU declaration of conformity, and change-control records. Add a short assumptions note to explain assumptions, exclusions, and unresolved issues.
Turn this EU RoHS Directive page into a repeatable workflow for product, legal, quality, procurement, support, and engineering teams. Keep citations, owners, evidence, and review triggers together.
Treat the checklist as a decision workflow, not as a static policy. The goal is to get a documented yes/no/needs-escalation answer that product, legal, quality, regulatory, and support teams can reuse.
"amending Annex II to Directive 2011/65/EU"
"technical documentation required for assessing materials"
"restriction of the use of certain hazardous substances"
"Harmonised standards are European standards adopted on the basis of a request."
"Exemptions are limited in time"