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RE: EU Ross Directive Insert Date Dear Insert Name, Smiths Medical has initiated a program to review and reconfigure its electrical and electronic products and their components to eliminate materials
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01
Read and understand the requirements of the RE EU RoHS Directive.
02
Identify the products or components that fall under the scope of the directive.
03
Determine the substance restrictions and maximum concentration limits specified in the directive.
04
Conduct testing or obtain test reports to verify the compliance of products or components.
05
Implement necessary changes in the manufacturing or supply chain processes to ensure compliance.
06
Maintain records and documentation to demonstrate compliance with the directive.
07
Regularly review and update compliance procedures to stay aligned with any amendments to the directive.

Who needs re eu rohs directive?

01
Manufacturers of electrical and electronic equipment (EEE) or their authorized representatives.
02
Importers of EEE into the European Union market.
03
Distributors and retailers selling EEE within the European Union market.
04
Certain categories of components and spare parts providers.
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The RE EU RoHS Directive restricts the use of certain hazardous substances in electrical and electronic equipment.
Manufacturers, importers, and distributors of electrical and electronic equipment are required to file RE EU RoHS Directive.
To fill out RE EU RoHS Directive, companies need to ensure their products comply with the restricted substances and provide a Declaration of Conformity.
The purpose of RE EU RoHS Directive is to protect human health and the environment by reducing the amount of hazardous substances in electronic products.
Companies must report the list of restricted substances used in their products, as well as provide information on compliance and testing.
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