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NSAI and EU Directives

As the appointed Notified Body, NSAI actively oversees the implementation of the following EU Directives on behalf of the Irish Government:

  • MDR - Medical Device Directives
  • MDD - Medical Devices
  • IVD - In-Vitro Diagnostic Medical Devices
  • AIMD - Active Implantable Medical Devices
  • TSE - Medical Devices Utilising Tissue of Animal Origin
  • Medical Devices Incorporating Stable Derivatives of Human Blood or Human Plasma
  • Motor Vehicles and their Trailers
  • Non-Automatic Weighing Machines
  • Construction Products
  • EUETS - Green House Gas Directive
  • Road Speed Limiters
  • Digital and Analogue Tachographs
  • Plating of Vehicles
  • ATP Refrigeration Containers
  • ADR - Carriage of Dangerous Goods by Road.

In the future, NSAI is likely to assume new responsibilities for EU Directives. This web page will be updated as further changes occur.