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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.