On the 26th of May 2021, the MDD was repealed and replaced by the EU Medical Device Regulation (EU) 2017/745. Vicon’s Declaration of Conformity and CE Certification with expiry dates of the 17th of August 2023 may continue to be used to place products on the EU Market under the extended transitional period, as set out in regulation (EU) 2023/607 until the 31st of December 2028. During the extended transitional period, Vicon Motion Systems Ltd shall continue to comply with the transitional provisions of the (EU) MDR 2017/745, Article 120.
Vicon has a contract in place with its EU Notified Body, enabling Vicon to continue to sell the Vero product on the EU Market until 2028.
The following original Vero EU DoC and CE Certification remain applicable and relevant with respect to the aforementioned changes to MDD (Medical Device Directive) (93/42/EEC) and EU Medical Device Regulation (EU) 2017/745.
For any enquires, please contact Vicon’s Compliance team at compliance@vicon.com.
