ERA reviewing Category 8 & 9 for RoHS Directive
ERA has been awarded a contract by the European Commission to carry out a review of Directive 2002/95/EC. The main aim is to provide the data needed to determine if Category 8 (medical devices) and Category 9 (monitoring and control instruments) products can be brought within the scope of the Directive.
ERA would be pleased to hear from any stakeholders who would like to contribute to this review and in particular manufacturers of equipment that contain restricted substances that cannot currently be replaced by other materials or by a design change. |