Officers and regulatory representatives of 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.
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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.
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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.
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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).