The procedure to challenge the designation of a medical device or other product subject to the Classification Rules prescribed by Council Directive 93/42/EEC (as Amended) is through Judicial Review. The right to seek Judicial Review is permitted in the respective EU Member State and at the European Court of Justice.
CLASSify gather important Judicial Reviews which may help in researching the EC Product Class of your device. These are available below to download, free of charge.
If you know of a Judicial Review which you feel may be relevant to device classification, please contact us and we will review it for inclusion.