Bioptik Technology, Inc.

1. check of the conformity of the devices in accordance with the quality management system 2. drawing up and keeping up to date of the technical documentation and the EU declaration of conformity of devices 3. fulfillment of the post-market surveillance obligations 4. fulfillment of reporting obligations 5. 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.