a) the conformity of the devices is appropriately checked, in accordance with the QMS under which the devices are manufactured, before a device is released
(b) the TD and the EU DoC are drawn up and kept up-to-date
(c) the post-market surveillance obligations are complied with in accordance with Art. 10
(d) the reporting obligations referred to in Art. 87-91 are fulfilled
(e) in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.