EU AUTHORISED REPRESENTATIVE

Under the current European legislation for Medical Devices, Personnel Protective Equipment’s, Electrical Equipment’s, and many other products, the European Authorized Representative is assigned a pivotal role in the CE Marking process. If you don’t have one, you can simply not sell your products within the European Union.

The EU authorities will not correspond with non-European manufacturers directly. All contacts and correspondence with regards to your company and your products will go via your European AuthorisedRepresentative.

The name and address of your European Authorized Representative must be shown on your labeling, packaging or instructions for use. As a result, various parties from all over Europe will contact us, when they have queries or questions regarding your devices. This means, we will be in constant communication with your distributors, end-users, customers, etc.

Certlink Certification Services will support all necessary reporting, registration and communication with European authorities and bodies – to the right person at the right time, every time. European Regulations also require that the European Authorized Representative holds a copy of the manufacturers Declaration of Conformity and Technical File and a register of product complaints in Europe.