3EC International a.s. notified body has finished the certification audit at RITM OKB ZAO. The Certificate No. 2017-MDD/QS-014 was issued. The comprehensive audit has confirmed the compliance of our products with the European directive for medical products.

The personal (CHANS-SCENAR), professional (SCENAR-NT) devices and add-on electrodes were again approved for distribution in the EU territory. The CE marking was legally enacted in 1993. It is a mandatory conformity mark for products placed on the market in the European Economic Area/Union (EEA/EEC). The CE marking means that the product meets the EU basic quality and safety requirements for the consumer.