Officers and regulatory representatives of Metrum Cryoflex Sp. z o.o.
JURASZ Henryk
a) ensuring 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;
b) ensuring the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date;
c) ensuring the post-market surveillance obligations are complied with in accordance with Article 10(10) MDR;
d) ensuring the reporting obligations referred to in Articles 87 to 91 (MDR) are fulfilled;