The CE marking (also known as CE mark) is a mandatory conformance mark on many products placed on the single market in the European Economic Area (EEA). The CE marking certifies that a product has met requirements of the applicable European Medical device derivative like active implantable medical device (AIMD) Directive 90/385/EEC and  medical device Directive 93/42/EEC and its further modifications.


Our experts and partners who are EU Authorized Representatives identify hazards, assess risks, carry out all applicable tests to determine the appropriate measures to meet with CE mark, CE marking, CE certification mark regulations.