Country: Slovak Republic
Title: Application for registration / notification of the manufacturer of medical devices in accordance with the Act on Medicines and Medical Devices
Description: The service will enable a natural person or legal entity to apply for a marketing authorization for the treatment of designated substances of category 2 and 3, their repair, designation of validity, change or cancellation pursuant to Act No. 362/2011 on medicines and medical devices and on amendments and supplements to certain acts. Applications can be submitted through a form available on the ŠÚKL web site in paper form, as well as fully electronically via a form published on the Central Public Administration Portal ( For electronic submission to it is necessary to use eID (electronic identity card) and KEP (Qualified Electronic Signature).
Category: Healthcare