National Standards Authority Of Ireland

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EU Directive


 

NSAI has been appointed Notified Body or are active in respect of the following EU Directives:

  • Simple Pressure Vessels
  • Gas Appliances
  • Toys
  • Telecommunications Terminal Equipment
  • Machinery
  • Medical Devices
  • IVD - In-Vitro Diagnostic Medical Devices
  • AIMD - Active Implantable Medical Devices
  • TSE - Medical Devices Utilising Tissue of Animal Origin
  • Active Implantable Medical Devices
  • Medical Devices incorporating stable derivatives of human blood or human plasma
  • Personal Protective Equipment
  • Motor Vehicles and their Trailers
  • Low Voltage
  • Non-automated Weighing Machines
  • Lifts Directive
  • Pressure Equipment
  • Construction Products
  • EUETS - Green House Gas Directive
  • Solvents Directive
  • Road Speed Limiters
  • Digital and Analogue Tackograph
  • Plating of Vehicles
  • ATP Refrigeration containers
  • ADR - Carriage of dangerous goods by road

Further appointments are expected.

As the body in Ireland responsible for Certification of products to Irish and European standards, NSAI is well placed to advise manufacturers on the requirements to be met in order to enable them to place the CE Marking on their products in accordance with relevant EU Directives.

CE Marking, which indicates that a product complies with harmonised EU requirements for safety and health, based on Directives, will become increasingly important, as CE Marking is mandatory for trading throughout the EU.

"10 Steps to CE marking"

Step 1: Identify the Directive/s that are applicable to your product. You can download these directives free of charge from the EU website: www.newapproach.org/

Step 2: Identify the conformity assessment procedure that must be taken. This could be self-declaration, involve testing, inspection or quality system assessment from a Notified Body or a combination of these. The conformity assessment procedure will differ depending on your product and the Directive in respect of which you will be CE marking. If you are unsure about which procedure to take please contact NSAI for advice.

Step 3: Determine the dates by which you must take action. This will be the date that the Directive comes into force. The majority of directives are already in force. In these cases, it is an offence to place a product on the market without CE marking because it indicates a presumption of conformity with all relevant Legislation.

Step 4: Identify if there are any Harmonised European Standards applicable to your product. These are not always mandatory for manufacturers although there is a presumption that conformity to these standards will give conformity with the relevant part of the Directive. Whenever possible or appropriate, manufacturers should follow harmonised standards.

Step 5: Ensure the product complies with all the essential requirements of the Directive(s). Take appropriate measures to comply or identify existing data and test reports.

Step 6: Identify whether independent assessment of your conformity to the Directive, or some aspects of it, is required from a Notified Body. This will be stated in the directive and is dependent upon the product you are CE marking. You must not affix CE marking to your product until all necessary certifications have been obtained from the Notified Body.

Step 7: Maintain Technical Documentation required by the Directive(s). Your technical documentation should support your compliance with the requirements of the Directive. It is essential to retain this documentation.

Step 8: Prepare the Declaration of Conformity and the required supporting evidence. The Declaration of Conformity along with the Technical Documentation should be available to Competent Authorities (EU Members) upon request.

Step 9: Check that no other purely national requirements exist in the countries where the product will be sold. These may include national standards, labeling or packaging requirements.

Step 10: Affix CE marking on your product and/or it’s packaging and accompanying literature as stated in the directive.

For more information, see link below:

http://europa.eu.int/comm/enterprise/regulation/goods/index_en.htm

FOB Rev. 10




Last Updated - [31 Aug 2007 @ 16:36:51]

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Email: nsai@nsai.ie

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