Officers and regulatory representatives of Pixee Medical
GIRAUD Stéphane
Responsible for the following parts of MDR 2017/745 article 15, §3:
(a) 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
(d) the reporting obligations referred to in Articles 87 to 91 are fulfilled
(e) 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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PECHEUR Lucie
Responsible for the following parts of MDR 2017/745 article 15, §3:
(b) the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date
(c) the post-market surveillance obligations are complied with in accordance with Article 10(10)