The List has been confirmed during the Directive 94/9/EC ATEX Working Group meeting on 10 July 2013
Note that the list is not complete, it only clarifies some common inquires and provide examples of products within or outside the scope of the ATEX Directive 94/9/EC.
The List does not replace the vital risk assessment of each product and in addition ignition sources and explosion hazards related to the use of all the products shall also always be considered.
Gli standard internazionali hanno reso il test di usabilità un obbligo. Nella prospettiva, sui mercati internazionali in cui si stanno aggiornando l...
ID 26489 | Update news 24 Luglio 2026
In GU L 2026/1744 del 24.07.2026 pubblicato il:
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Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 ...
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