Devices class IIa, IIb, III

In order to place the CE making on a class IIa, IIb or III medical device and launch it on the market the manufacturer must contact a notified body which will provide a CE certificate after checking they conform with the procedures laid down by the regulation.

Contact :

Federal Agency for Medicines and Health Products 
Health Products Division 
Eurostation II
Place Victor Horta, 40 box 40
1060 Brussels

Fax : +32 (0)2 524 81 20

Email : meddev@afmps.be

 

Last updated on 05/12/2016