Defined terms — Commission Delegated Directive 2014/15/EU of 18 October 2013 amending, for the purposes of adapting to technical progress, the Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for lead, cadmium and hexavalent chromium in reused spare parts, recovered from medical devices placed on the market before 22 July 2014 and used in category 8 equipment placed on the market before 22 July 2021 , provided that reuse takes place in auditable closed-loop business-to-business return systems, and that the reuse of parts is notified to the consumer Text with EEA relevance
European Union · 32014L0015 · 25 provisions
No defined terms have been extracted from this instrument yet. That is a limit of our reader rather than a statement that the act defines nothing: extraction reads the drafting constructions it has been taught, and coverage is uneven across legal traditions.