Can an authorized representative sign the EU Declaration of Conformity?

Jun 13, 2016 ... The RoHS Directive 2011/65/EU, or 'RoHS2' as it is sometimes called, is a CE marking Directive and is a European law. 7 Steps to CE Certification with Intertek · Determine which directive(s) are applicable to your product · Fulfill the essential requirements · Establish a ... Jan 31, 2023 ... In the case of a sterile device, the CE mark is placed on the package that keeps the device sterile. In the case of devices involving a notified ... What products need CE marking? · active implantable medical devices · appliances burning gaseous fuels · cableway installations designed to carry persons ... Sep 1, 2023 ... CE Mark Directives for Wireless Devices. For wireless devices, it's crucial to adhere to specific directives that regulate their functionality ... Feb 8, 2022 ... Devices in the Class IIa category are for short-term use (30 days or less), such as tubing intended for drug delivery, syringes, and surgical ... By preparing a Declaration of Conformity and affixing the CE marking, which is usually a “self-certification” process, the manufacturer declares that their ... Mar 13, 2025 ... Electronic products sold in the EU must have a CE Mark. Learn about the CE Mark requirements and compliance standards required for ... Dec 22, 2022 ... In this article, we will learn about the principal regulations for obtaining CE marking, followed by a step-by-step guide to getting a medical device's CE ... CE Marking indicates that your medical device complies with applicable EU regulations, and enables the commercialization of your products across all EU member ...