CLC/TC 111X/WG 06 - WEEE Recycling Standards
To study the WEEELABEX documents to investigate the possibility to have some EN standards based on WEEELABEX documents, giving some detailed recommendations on the matter. Possible Standardisation requests from the Recast of the WEEE Directive should be considered.
WEEE Recycling Standards
To study the WEEELABEX documents to investigate the possibility to have some EN standards based on WEEELABEX documents, giving some detailed recommendations on the matter. Possible Standardisation requests from the Recast of the WEEE Directive should be considered.
General Information
This document is applicable to the processes relating to the preparing for re-use of WEEE. NOTE 1 This document covers the preparing for re-use of WEEE arising from electrical and electronic equipment as listed in Annex I and Annex III of Directive 2012/19/EU. This document is applicable to preparing for re-use operators only and does not cover activities connected with used or second-hand equipment that have not become waste. It applies to all preparing for re-use operators, no matter their size or main focus of activity. This document assists in quantifying re-use, recycling and recovery rates in conjunction with EN 50625 1. In case of treatment operations (including the collection and logistics of WEEE) other than preparing for re-use, the EN 50625 series applies. Preparing for re-use processes includes the removal of whole components or parts where they are intended to either be used in the repair of faulty equipment or sold as re-use parts. The following EEE are not in the scope of this document: - industrial monitoring and control instruments; - in vitro diagnostic medical devices, medical devices or active implantable devices. NOTE 2 Examples of industrial monitoring and control instruments include equipment intended for use in potentially explosive atmospheres, and monitoring and control equipment that performs a safety function as part of industrial control system. NOTE 3 in vitro diagnostic medical devices, medical devices and active implantable devices have the capacity to collect and harbour pathogens, depending on the environment in which they operated. It is essential to follow clinically proven means for decontamination. Relevant Directives are 93/42/EEC and 98/79/EC.
- Standard38 pagesEnglish languagesale 10% offe-Library read for1 day
- Standard – translation37 pagesSlovenian languagesale 10% offe-Library read for1 day
This Technical Specification is intended to be used in conjunction with the WEEE Treatment Standard for temperature exchange equipment, EN 50625-2-3, and the Technical Specification for de-pollution, CLC/TS 50625 3-1.
- Technical specification60 pagesEnglish languagesale 10% offe-Library read for1 day
EN 50574:2012 gives the responsible take-back parties the task of defining target values. This Technical Specification provides applicable target values, characteristic numbers; sampling and analysis procedures, as well as monitoring and reporting requirements. Furthermore, this Technical Specification provides validation methodologies for tests and the daily business of the treatment plants as defined in EN 50574:2012.
- Technical specification32 pagesEnglish languagesale 10% offe-Library read for1 day