Report supply interruptions of medical devices

If a manufacturer expects that there will be interruptions in the supply of a medical device, it must report this to the competent authority in accordance with Article 10a of Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR).

You can find more information here: www.basg.gv.at/fuer-unternehmen/medizinprodukte/hersteller

Further inquiry note

medizinprodukte@basg.gv.at