The new directive 2011/65/EU (ROHS 2.0) replaces the 2002/95/EC directive and will come into effect 20 days later, on July 21, 2011. (Attention! This

New RoHS Certificate Template 2011/65/EU Directive CE Certificate Template

The term 'effectiveness' referred to here refers to the implementation of the RoHS 2.0 directive in all EU member states starting from July 21, 2011. Each member state must complete the process of converting the RoHS 2.0 directive into its internal regulations within the period from July 21, 2011 to January 2, 2013! During the transition period from July 21, 2011 to January 2, 2013, companies still only need to comply with Directive 2002/95/EC. ）

1. Background

Directive 2002/95/EC will be repealed from January 3, 2013, and allied countries must update Directive 2011/65/EU to local law by January 2, 2013. The main content of the 2011/65/EU is summarized as follows: 1. The product scope clarifies the scope of the directive control and related definitions, expanding the scope of controlled products to all electronic and electrical equipment except for special exemptions, including Class 8 medical equipment and Class 9 monitoring equipment exempted by 2002/95/EC; - Class 11 products: all other electronic and electrical equipment, including cables and other components, not covered by Class 1-10 products. Although no new restricted substances have been added, four toxic and harmful substances (HBCDD, DEHP, DBP, and BBP) have been selected as candidates for restricted substances. 3. CE marking requirements include ROHS compliance of electronic and electrical equipment in the CE marking requirements. Producers should ensure that their products comply with ROHS and prepare corresponding declarations and technical documents when affixing the CE mark. 4. In order to provide sufficient time for manufacturers of products newly included in ROHS 2.0 control to comply with the directive requirements, ROHS 2.0 has established a control transition period for related products.

2 Origins

Medical equipment and monitoring devices, as well as their components, shall comply with ROHS2.0 from July 22, 2014; - In vitro diagnostic medical equipment and its components shall comply with ROHS2.0 from July 22, 2016; Industrial monitoring equipment and its components shall comply with ROHS2.0 from July 22, 2017; - Other products newly included in ROHS2.0 control shall comply with ROHS2.0 from July 22, 2019; 5. The exemption mechanism adopts existing exemption clauses and proposes 20 new exemptions for medical and monitoring equipment, while setting different exemptions for product categories with the longest validity period: the exemption validity period for the 8 major categories of products and the 11th category of products previously controlled by 2002/95/EC is 5 years; The exemption period for Class 8 and Class 9 products is as long as 7 years. 6. Add market supervision clauses and introduce unified product conformity assessment requirements and market supervision mechanisms. By implementing strict and unified market supervision to reduce the number of non compliant products in the market, the directive objectives can be effectively achieved. Relevant manufacturers should have a deep understanding of the directive requirements and take timely measures to ensure that their products comply with the new requirements proposed by ROHS2.0.

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