Telemon certification
Telemon is certified as Class IIa Digital Medical Device (EU QUALITY MANAGEMENT SYSTEM CERTIFICATE No. 2024-MDR/QS-028)
Telemon Quality Management System is certified under EN ISO 13485:2016
It has also received registration in ŠÚKL (The Slovak State Institute for Drug Control) and an American FDA (Food and Drug Administration),
which are responsible for the protection of public health and the safety of pharmaceuticals and medical devices.