CLASSify allows users to determine the correct EC Product Class (commonly referred to as CE Class or Class) of a medical device, quickly and accurately. Our service was developed with the knowledge of the European Commission but does not constitute an endorsement of the website opinions expressed by us or other users, further, the Class determined and referral to European Official text and does not constitute opinion or judgement by the European Commission.
CLASSify constitutes additional armamentarium to the regulatory professional seeking to determine, confirm or simply check the Class of a medical device to be placed on the Market. With added ease of viewing information in graphical and textual mode, plus the ability to search for the Class of precedent devices already CE Marked, our website will be your primary resource when classification or re-classification is necessary.
Using our unique, intelligent Classification Chart, we offer our members the ability to classify their medical devices in a way previously unheard of. The chart utilises knowledge of the classification rules according to Annex IX from Council Directive (93/42/EEC) to determine what EC Product Class your medical device belongs to. Once you complete the classification of your device, a Classification Report will be available for your device which you can download as PDF. Saving you time and effort, CLASSify will quickly become your primary resource when classification or re-classification is necessary.
- Saves you time, money and possibly improves the quality of your own research.
- CLASSify provides 24-hour, online access to a powerful classification portal.
- Efficient, cost-effective and affordable… Why not use CLASSify?