CE Marking Logo Looking for an EU/EC European Authorised/Authorized Representative? Register/Notify your MD-Medical Devices and IVD-In Vitro Diagnostic Medical Devices in Europe by CE Marking Specialists based in London/UK. Click here to get FREE Guide Now! The CE conformity marking (logo) shall consist of the initials "CE " in the form shown below; If the CE marking is reduced or enlarged the proportions given in the above graduated drawing must be respected. - The various components of the CE marking must have substantially the same vertical dimension, which may not be less than 5 mm; The affixing of markings on the products which are likely to deceive third parties as to the meaning and form of the CE marking shall be prohibited. Any other marking may be affixed to the products or the data plate provided that the visibility and legibility of the CE marking is not thereby reduced; Attention: It should be noted that the C and E are not formed by perfect semi-circles, i.e. the top and bottom arms extend one square beyond the semi-circles, and the middle arm of the E stops one square short. Why do you need a representative in Europe? Why must the manufactures of medical devices appoint a EU Authorized Representative? Why is the Authorized Representative different from the importer/distributor ? Why choose Wellkang? How can Wellkang help you? What are included in Wellkangs EU Authorized Representative Service? 11 benefits by appointing Wellkang as your EU Authorized Representative? 3 unique benefits offered by Wellkang that are not available from others? Is Wellkang Group part of the U.S. government or EU authorities? How much does it cost? Competitive Price List! How to contact Wellkang? About Medical Devices Medical device CE Marking procedures Steps to obtain CE Marking for your Medical Devices Legal basis for medical devices Why must a medical device manufacture appoint a European Authorized Representative? Why must inform the Competent Authority? Who should apply/register with the Competent Authority? Changes to registered details? Is my product a Medical Device? How to classify Medical Devices? Class I (including Is & Im) medical devices CE Marking procedures Class IIa medical devices CE Marking procedures Class IIb medical devices CE Marking procedures Class III medical devices CE Marking procedures About CE Marking: What is CE marking? The CE marking logo What is a manufacturer? Why is CE marking called "European passport"? Does my product need CE Marking for the European Market? How to obtain CE Marking for my product? Where can I find CE marking related publications & guidelines? How to distinguish EU directives? Where can I find CE marking testing labs nearest to my location