Aaren Scientific, Inc.

(a) the conformity of the devices is appropriately checked (b) the technical documentation and the EU declaration of conformity are drawn up and kept up to date. (c) post-market surveillance obligations are complied with in accordance with Article 10(10) of the EU MDR 2017/745. (d) the reporting obligations referred to in Articles 87 to 91 of the EU MDR 2017/745 are fulfilled.