Officers and regulatory representatives of KiiltoClean Oy
HALENIUS Heidi
Responsible for verifying the compliance of medical devices with the requirements of the MDR and the Quality Management System, including compliance with company procedures.
Hidden
LOIMARANTA Laura
Responsible for preparing and updating the technical documentation and the Declaration of conformity, performing post-market surveillance for MD II and I products and in the case of investigational devices issuing the statement referred to in Annex XV, Chapter II, Section 4.1. Vigilance reporting.