While most EC directives require products to carrying the “CE” mark, products certified under the Marine Equipment Directive carry the “wheel mark”.
The MED sets out performance and testing standards to be met by marine equipment placed on board an EU ship.
As of 18 September 2016 the only applicable MED is Directive 2014/90/EU of the European Parliament and of the Council of 23 July 2014 on marine equipment (and repealing Council Directive 96/98/EC).
The directive covers types of marine equipment that fall under following International Conventions developed by the International Maritime Organization (IMO):
Design, construction and performance requirements and testing standards for marine equipment is provided in the Annex to Commission Implementing Regulation (EU) 2017/306, which was published in the Official Journal of the European Union on the 24 February 2017.
This Regulation entered into force on the 16 March 2017 and became directly applicable.
All manufacturers producing equipment to comply with the MED require involvement of UDICER/NAUTITEST to assess products to the MED.
We offer certification for the EC Type Examination (Module B), Unit Verification (Module G), Product Verification (Module F) and the production-control phase (Modules D or E) of the following categories of equipment:
Scope of the Directive: Applicable also to the equipment placed on board.
An adequate analysis and assessment of the risk(s): Technical documentation shall include an adequate analysis and assessment of the risk(s).
Wheelmark: Wheelmark to be followed by the identification number of the notified body involved in the production control phase, and the year in which the mark is affixed.
Electronic Tag: Introduction of the possibility of marking equipment with an electronic tagging in addition to or instead of the Wheelmark.
Obligation of economic operators: Introduction of definitions and responsibilities of economic operators (manufacturer, authorised representative, importer and distributor). Manufacturers not located in the EU are required to appoint, by written mandate, an authorised representative within the EU.
Authorised representative: Must be appointed by a manufacturer who is not located in the territory of at least one Member State.
The Declaration of Conformity should: