Officers and regulatory representatives of Podologie Oss
CLEUTJENS Rob
- 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;
- the technical documentation and the EU declaration of conformity are drawn up and kept upto-date;
- the post-market surveillance obligations are complied with in accordance with Article 10;
- the reporting obligations regarding vigilance are fulfilled