Officers and regulatory representatives of OHST Medizintechnik AG
SCHLEUSS Torsten
ensuring that the post-market surveillance obligations are complied with in accordance with Article 10(10)
ensuring that in the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued
Hidden
SCHEDLO Chris
ensuring that 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
ensuring that the reporting obligations referred to in Articles 87 to 91 are fulfilled,
ensuring that the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date