Sunlight Medical, Inc.

To ensure 1) the conformity of the devices is appropriately checked; 2) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; 3) the post-market surveillance obligations are complied with in accordance with Article 10(10); 4) the reporting obligations referred to in Articles 87 to 91 are fulfilled; 5) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.