Dirigeants et représentants réglementaires de Spermosens AB
KITSON-PARKER Callum
ensuring the conformity of the devices is appropriately checked, in accordance with the QMS, before a device is released;
the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date; the post-market surveillance obligations are complied with in accordance with Article 10(9);
the reporting obligations referred to in Articles 82 to 86 are fulfilled;