Slovak Republic Regulations on In Vitro Diagnostic Devices

Label	Title
No. 56/2018 Coll., as amended	Act on Product Conformity Assessment, Making a Designated Product Available on the Market, and on Amendments to Certain Acts / April 1, 2018 repeals Act No. 264/1999 Coll. on technical requirements for products and on conformity assessment / amendment by Act No. 351/2022 Coll. applies from June 28, 2025
No. 569/2001 Coll. current version repealed	Regulation of the Government of the Slovak Republic laying down details on technical requirements and conformity assessment procedures for in vitro diagnostic medical devices
(EU) 2017/746 in PDF format as of January 10, 2026, including amendment (EU) 2024/1860	Regulation of the European Parliament and of the Council on in vitro d iagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU // Amendment (EU) 2024/1860 applies from July 9, 2024