1. The conformity of devices is appropriately checked, in accordance with the SQ Innovation Quality Management System (QMS), before release.
2. The post-market surveillance (PMS) obligations are complied with in accordance with Article 10(10) of the (EU) MDR 2017/745.
3. The Technical Tocumentation and EU declarations of conformity are drawn up and maintained up to date.
4. The reporting obligations referred to in Articles 87 - 91 of the (EU) MDR 2017/745 are fulfilled.