The list of semi-controlled medical materials and products and the terms and conditions for their circulation shall be determined by a decision of the Chairman or his delegate, in coordination with the Ministry, the Competent Health Authorities and other concerned parties, provided that their movement within the State is monitored through the electronic system stipulated under the provisions of Federal Decree-Law No. (30) of 2021 referred to.
Interpretation and application must be checked against the official text and current version.