Natera, Inc.

Post Market Surveillance (Primary): the post-market surveillance obligations are complied with in accordance with Article 10(9);

Design Control/Product Release (Primary): 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

Design Control/Product Release (Deputy): 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 Post Market Surveillance (Deputy): the post-market surveillance obligations are complied with in accordance with Article 10(9);

Technical Documentation (Primary): the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date

Technical Documentation (Deputy): the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date Reporting Obligations (Primary): the reporting obligations referred to in Articles 82 to 86 are fulfilled Clinical Performance Studies (Primary): In the case of devices for performance studies intended to be used in the context of interventional clinical performance studies or other performance studies involving risks for the subjects

Reporting Obligations (Deputy): the reporting obligations referred to in Articles 82 to 86 are fulfilled