Note regarding validity of EC Certificate
The Medical Device Directive (MDD) 93/42/EEC has been replaced by the EU Medical Device Regulation (MDR) EU 2017/745.
Qualisys applies the transitional provisions outlined in Article 120 of the EU MDR 2017/745. Qualisys fulfils the requirements for the extended transitional period set out in EU Regulation 2023/607. Therefore, the attached EC Certificate remains valid until 31st December 2028 according to Article 120 Paragraph 3(b).
Please do not hesitate to contact us if you have any questions regarding regulatory compliance of Qualisys products: https://www.qualisys.com/about/contact-us/