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.
Federal Agency for Medicines and Health Products
Health Products Division
Place Victor Horta, 40 box 40
Fax : +32 (0)2 524 81 20
Email : firstname.lastname@example.org