Mandatory requirements for placing a medical device into circulation within the Eurasian Economic Union include its registration and expert evaluation, which are conducted by the competent authority of the reference state. Identical requirements apply both to medical devices produced within the EAEU territory and to those imported from third countries into the customs territory of the Union. The registration procedure involves the issuance of official authorisation by the competent authority, granting the right to medical use and free circulation of the device across all EAEU member states.

Mandatory requirements for placing a medical device into circulation within the Eurasian Economic Union include its registration and expert evaluation, which are conducted by the competent authority of the reference state. Identical requirements apply both to medical devices produced within the EAEU territory and to those imported from third countries into the customs territory of the Union. The registration procedure involves the issuance of official authorisation by the competent authority, granting the right to medical use and free circulation of the device across all EAEU member states.

Biologically active additives (dietary supplements) are preparations that belong to specialized food products with bioactive substances of natural and /or identical to natural origin, as well as probiotic microorganisms in the composition. Dietary supplements are intended for consumption with food or introduction into the composition of food products.