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
Information
Type
Delegated directive
Regulated products
Medical Devices
Published
October 18, 2013
Last updated
October 18, 2013
Description
Commission Delegated Directive 2014/15/EU amends Directive 2011/65/EU regarding exemptions for lead, cadmium, and hexavalent chromium in reused spare parts from medical devices.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0