Hyaltech Ltd.

• The conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released; • The post-market surveillance obligations are complied with in accordance with Article 10(10); • The reporting obligations referred to in Articles 87 to 91 are fulfilled;

• The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; • In the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.