What should teams do before a RoHS exemption expires?
Start with the legal entry, not with a supplier statement. RoHS exemptions are tied to a listed application in Annex III or Annex IV, and the Directive allows those lists to be adapted to scientific and technical progress.
For each product that depends on an exemption, record the Annex entry number, exact wording, EEE category, restricted substance, homogeneous material or component use, expiry date, renewal status, and technical-file evidence. If the application no longer matches the exemption wording, treat the product as needing a new compliance path.
Do not build a current-status table unless it is sourced from the current consolidated Directive, the official Commission exemptions list, or the delegated directive that changed the relevant entry.
- Assign one owner to verify the current Annex wording and expiry date against the official source.
- Confirm whether a renewal application was filed at least 18 months before the exemption expires.
- If no renewal is available or the renewal is rejected, prepare a redesign, substitution, qualification, or market-withdrawal decision before the transition period ends.
- Keep the expiry review with the EU declaration of conformity, technical documentation, supplier evidence, and change-control record.
Consolidated RoHS source for Article 5 exemptions, Annex III, Annex IV, renewal timing, and pending-decision validity.
Commission source for exemption procedure timing, current evaluation stages, renewal requests, and official exemption materials.
Amending directive that clarified maximum validity periods and pending renewal process details.