Q110576697

Summary

Q110576697 is an implementing regulation^[1].

Key Facts

• Q110576697 is in the country of Sweden^[2].
• Q110576697's instance of is recorded as implementing regulation^[3].
• Q110576697's instance of is recorded as Swedish government ordinance^[4].
• Q110576697's language of work or name is recorded as Swedish^[5].
• Q110576697's publication date is recorded as +2021-06-17T00:00:00Z^[6].
• Q110576697's work available at URL is recorded as https://www.riksdagen.se/sv/dokument-lagar/dokument/_sfs-2021-631^[7].
• Q110576697's work available at URL is recorded as http://data.riksdagen.se/dokument/sfs-2021-631^[8].
• Q110576697's applies to jurisdiction is recorded as Sweden^[9].
• Q110576697's legal citation of this text is recorded as SFS 2021:631^[10].
• Q110576697's published in is recorded as Swedish Code of Statutes 2021^[11].
• Q110576697's title is recorded as Förordning (2021:631) med kompletterande bestämmelser till EU:s förordning om medicintekniska produkter^[12].
• Q110576697's cites work is recorded as Act (2021:600) with supplementary provisions to the EU's regulations on medical devices^[13].
• Q110576697's repeals is recorded as Q100593878^[14].
• Q110576697's repeals is recorded as Q100588753^[15].
• Q110576697's on focus list of Wikimedia project is recorded as WikiProject Health Data Space^[16].
• Q110576697's maintained by WikiProject is recorded as Project Riksdagen's documents^[17].
• Q110576697's copyright status is recorded as public domain^[18].
• Q110576697's Swedish Riksdag document ID is recorded as sfs-2021-631^[19].