CE marking is a mandatory conformity mark for products placed on the market in the European Economic Area (EEA). With the CE marking on a product the manufacturer ensures that the product conforms with the essential requirements of the applicable EC directives.
      The Ce marking certifies that SCAGEL is a medical device. The Medical Device Directive (93/42/EEC and 2007/47/EC) defines the medical device is ”any instrument, object or other similar article which is used for medical purposes in patients, in diagnosis, therapy or surgery”.
      The letters "CE" stand for "Conformité Européenne" ("European Conformity").