Terma Sp. z o.o.

a) checking the conformity of products in accordance with the quality management system in which these products are manufactured, before releasing the product, b) preparation and current updating of technical documentation and EU declaration of conformity, c) compliance with post-market surveillance obligations, d) fulfillment of obligations regarding the notification of medical devices, e) adding and managing Basic UDI-s and UDI-DI-s for the Manufacturer's devices.