Nivalit Spółka z ograniczoną odpowiedzialnością

Checking the compliance of devices with the quality management system in which the devices are manufactured, before a device is released; Preparation and ongoing updating of technical documentation and EU declaration of conformity; Compliance with post-market surveillance obligations in accordance with Art. 10 (10 ) MDR; Fulfilling the reporting obligations referred to in Art. 87-91 MDR; In the case of test devices, issue of the statement referred to in Section 4.1 of Chapter II of Annex XV MDR.