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On the 26th May 2021, the Medical Device Directive (MDD) 93/42/EEC was replaced by the EU Medical Device Regulation (MDR) EU 2017/745. 

The original Vero EU Declaration of Conformity and CE Certification (see the following links) continue to be valid for placing products on the EU Market until December 31, 2028, taking advantage of the extended transitional period granted by regulation (EU) 2023/607. In addition, and as required, Vicon holds an ongoing contract with its EU Notified Body, allowing the continued sale of the Vero product in said period.

Vicon Motion Systems Ltd remains committed to complying with the transitional provisions outlined in Article 120 of the EU MDR 2017/745.

For additional inquiries, please contact Vicon’s Compliance team at compliance@vicon.com.