” The Member States shall notify the Commission and other Member States of the bodies which they have designated for carrying out the tasks pertaining to the procedures referred to in Article XYZ [Conformity Assessment Procedures]and the specific tasks for which the bodies have been designated. The Commission shall assign identification numbers to these bodies, hereinafter referred to as ‘notified bodies’.“
With some 75 Notified Bodies available to a medical device manufacturer for product Conformity Assessment and CE-Marking, the identification of the most appropriate Notified Body can be an overwhelming task. We have generated a working tool to be able to narrow-down the field.
Simply click the appropriate photo below. We are available to you as a local resource to support you in your selection process.
