Q100698261
Swedish law from 1993
Press Enter · cited answer in seconds
0 sources
Q100698261
Summary
Q100698261 is a statute[1].
Key Facts
- Q100698261 is in the country of Sweden[2].
- Q100698261's instance of is recorded as statute[3].
- Q100698261's language of work or name is recorded as Swedish[4].
- Q100698261's publication date is recorded as +1993-06-03T00:00:00Z[5].
- Q100698261's work available at URL is recorded as https://www.riksdagen.se/sv/dokument-lagar/dokument/_sfs-1993-584[6].
- Q100698261's work available at URL is recorded as http://data.riksdagen.se/dokument/sfs-1993-584[7].
- Q100698261's applies to jurisdiction is recorded as Sweden[8].
- Q100698261's legal citation of this text is recorded as SFS 1993:584[9].
- Q100698261's published in is recorded as Swedish Code of Statutes 1993[10].
- Q100698261's title is recorded as Lag (1993:584) om medicintekniska produkter[11].
- Q100698261's repealed by is recorded as Act (2021:600) with supplementary provisions to the EU's regulations on medical devices[12].
- Q100698261's repeals is recorded as Q100700456[13].
- Q100698261's maintained by WikiProject is recorded as Project Riksdagen's documents[14].
- Q100698261's copyright status is recorded as public domain[15].
- Q100698261's effective date is recorded as +1993-07-01T00:00:00Z[16].
- Q100698261's Swedish Riksdag document ID is recorded as sfs-1993-584[17].