a declaration by the manufacturer that the product meets all the appropriate provisions of the relevant legislation implementing certain European Directives
a European marking of conformity that indicates that a product complies with the essential requirements of the applicable European laws or Directives with respect to safety, health, environment and consumer protection
The mark which may be applied to a product to demonstrate that it conforms to the requirements of a European Directive. The CE marking must be applied to all medical devices sold within the EU after June 13, 1998 to demonstrate that the device conforms to the essential requirements of the MDD.
Means the mandatory marking affixed to a product to indicate compliance with the procedures and requirements of relevant EU member state regulations (directives)
Approval marking for products being shipped into the 15 countries of the European Union
A mandatory mark for about 70% of the products sold on the European Free Trade Association (EFTA) and European Union (EU) markets. CE Marking is sometimes called "CE Mark" and referred to as the "Trade Passport to Europe " for non-EU products.
A label used to show that the Sound Level Meter conforms to the specification of a European Directive
Marking that is put on products that meet the requirements of current European standards. For Q-Med's products this means conformity with MDD, the EU directive.
