Please be advised that Oko Institute, have been appointed as the external consultant to review the June 2025 batch of EU RoHS exemption pack renewals or refusals. If any of these Annex III or Annex IV exemptions are applicable see the table for interested registrants. MedTech Europe usually coordinate responses for the European MD/IVD market. Note that there will need to be similar work conducted in the GB RoHS to renew exemption packs under Annex III and Annex IV, however there is no umbrella project coordinating for Annex III submissions and no MD/IVD co-ordination at this time.
The annex III exemptions include specialist Mercury lamps. If these are applicable, and you are not submitting evidence to MedTech Europe, you should contact Lighting Europe, and if they agree, provide your evidence to be included in their submission.
