Dirigeants et représentants réglementaires de VUP Medical, a.s.
KÖNIGSMARKOVÁ Kristýna
MDR - Article 15, 3. (a) Responsible for 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.
Masqué
VALEŠOVÁ Eva
MDR - Article 15, 3. (d) Responsible for the reporting obligations referred to in Articles 87 to 91 are fulfilled;
MDR - Article 15, 3. (e) Responsible for ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
Masqué
BÁTLOVÁ Ivana
MDR - Article 15, 3. (b) Responsible for ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date.
Masqué
CEJPEK Kamil
MDR - Article 15, 3. (c) Responsible for ensuring that the post-market surveillance obligations are complied with in accordance with Article 10(10).