On the 26th of May 2021, the Medical Device Directive (MDD was repealed and ) 93/42/EEC was replaced by the EU Medical Device Regulation (MDR) EU ) 2017/745. Vicon’s
The original Vero EU Declaration of Conformity and CE Certification with expiry dates of the 17th of August 2023 may (see the following links) continue to be used to place valid for placing products on the EU Market under until December 31, 2028, taking advantage of the extended transitional period , as set out in granted by 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 . In addition, and as required, Vicon holds an ongoing contract with its EU Notified Body, enabling Vicon to continue to sell allowing the continued sale of 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) 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 any enquiresadditional inquiries, please contact Vicon’s Compliance team at compliance@vicon.com.
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