A notified body is an organisation designated by an EU Member State (or by other countries under specific agreements) to assess the conformity of certain products before being placed on the market.. These bodies are entitled to carry out tasks related to conformity assessment procedures set out in the applicable legislation when the intervention of a third party is required.. The Notified Bodies must be designated by a national supervisory authority and notified by the EU Commission. The independence of the Notified Bodies is ensured by the notification system, which provides for continuous surveillance and regular re-designation by the supervisory authorities. TÜV SÜD's international expertise. TÜV SÜD is one.

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Notified Bodies and Certificates module. Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) establish that Notified Bodies (NB) should register in EUDAMED any information regarding certificates issued (including amendments and supplements), suspended, reinstated.. Notified Bodies are also designated by European Economic Area (EEA) countries, as well as by other countries (e.g. Switzerland or Turkey) with specific agreements with the EU. A list of all official notified bodies under the construction products regulation is available in the NANDO-CPR database.