EEA-Lex

With EEA-Lex you can find information about proposed EU legal acts with possible EEA relevance, adopted EU acts under consideration for incorporation into the EEA Agreement, and acts that have already been incorporated into the Agreement.

Searching in English gives the widest results. You can refine your research results by using the categories in the right-hand column.

Advanced Search

Commission Decision of 7 October 2013 authorising Germany to maintain the limit values for antimony, arsenic, barium, lead and mercury beyond the entry into application of the limit values for chemical substances according to Article 55, 2nd sentence of Directive 2009/48/EC of the European Parliament and of the Council on the safety of toys in application of the Order of the President of the General Court of 15 May 2013 (T-198/12R)
Beschluss der Kommission vom 7. Oktober 2013 zur Ermächtigung Deutschlands, die Grenzwerte für Antimon, Arsen, Barium, Blei und Quecksilber nach Anwendungsbeginn der Grenzwerte für chemische Stoffe gemäß Artikel 55 Satz 2 der Richtlinie 2009/48/EG des Europäischen Parlaments und...
Commission Implementing Decision 2013/431/EU of 12 August 2013 allowing Member States to extend provisional authorisations granted for the active substances benalaxyl-M and valifenalate (notified under document C(2013) 5184)
Durchführungsbeschluss der Kommission vom 12. August 2013 zur Ermächtigung der Mitgliedstaaten, vorläufige Zulassungen betreffend die Wirkstoffe Benalaxyl-M und Valifenalat zu verlängern (2013/431/EU)
Framkvæmdarákvörðun framkvæmdastjórnarinnar frá 12. ágúst 2013 um að heimila aðildarríkjum að framlengja bráðabirgðaleyfi sem voru veitt fyrir nýju, virku efnunum benalaxýli-M og valífenalati (tilkynnt með númeri C(2013) 5184) (2013/431/ESB)
Kommisjonens gjennomføringsbeslutning av 12. august 2013 om tillatelse for medlemsstatene til å forlenge midlertidige godkjenninger gitt for de aktive stoffene benalaksyl-M og valifenalat (2013/431/EU)
Commission Decision 2013/204/EU of 25 April 2013 concerning the non-inclusion of formaldehyde for product-type 20 in Annex I, IA or IB to Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market (notified under document C(2013) 2284)
Beschluss der Kommission vom 25. April 2013 über die Nichtaufnahme von Formaldehyd in Anhang I, IA oder IB der Richtlinie 98/8/EG des Europäischen Parlaments und des Rates über das Inverkehrbringen von Biozid-Produkten für die Produktart 20 (2013/204/EU)
Ákvörðun framkvæmdastjórnarinnar frá 25. apríl 2013 um að færa formaldehýð ekki á skrá í vöruflokk 20 í I. viðauka, I. viðauka A eða I. viðauka B við tilskipun Evrópuþingsins og ráðsins 98/8/EB um markaðssetningu sæfiefna (2013/204/ESB)
Kommisjonsbeslutning av 25. april 2013 om at formaldehyd for produkttype 20 ikke skal oppføres i vedlegg I, IA eller IB til europaparlaments- og rådsdirektiv 98/8/EF om markedsføring av biocidprodukter
Commission Implementing Decision 2013/205/EU of 25 April 2013 allowing Member States to extend provisional authorisations granted for the new active substances acequinocyl, aminopyralid, ascorbic acid, flubendiamide, gamma-cyhalothrin, ipconazole, metaflumizone, orthosulfamuron, Pseudomonas sp. strain DSMZ 13134, pyridalil, pyroxsulam, spiromesifen, thiencarbazone and topramezone (notified under document C(2013) 2246)
Durchführungsbeschluss der Kommission vom 25. April 2013 zur Ermächtigung der Mitgliedstaaten, vorläufige Zulassungen für die neuen Wirkstoffe Acequinocyl, Aminopyralid, Ascorbinsäure, Flubendiamid, gamma-Cyhalothrin, Ipconazol, Metaflumizon, Orthosulfamuron, Pseudomonas sp....
Framkvæmdarákvörðun framkvæmdastjórnarinnar frá 25. apríl 2013 um að heimila aðildarríkjum að framlengja bráðabirgðaleyfi sem voru veitt fyrir nýju, virku efnunum asekínósýli, amínópýralíði, askorbínsýru, flúbendíamíði, gammasýhalótríni, ipkónasóli, metaflúmísóni,...
Kommisjonens gjennomføringsbeslutning av 25. april 2013 om tillatelse for medlemsstatene til å forlenge midlertidige godkjenninger gitt for de nye aktive stoffene acekinocyl, aminopyralid, askorbinsyre, flubendiamid, gammacyhalothrin, ipkonazol, metaflumizon, ortosulfamuron,...
Commission Implementing Decision of 19 February 2013 approving restrictions of authorisations of biocidal products containing difenacoum notified by Germany in accordance with Directive 98/8/EC of the European Parliament and of the Council (notified under document C(2013) 772)
Durchführungsbeschluss der Kommission vom 19. Februar 2013 zur Genehmigung der von Deutschland gemäß der Richtlinie 98/8/EG des Europäischen Parlaments und des Rates gemeldeten Beschränkungen der Zulassungen von difenacoumhaltigen Biozid-Produkten (2013/95/EU)
Commission Implementing Decision of 19 February 2013 regarding restrictions of authorisations of biocidal products containing difenacoum notified by Germany in accordance with Directive 98/8/EC of the European Parliament and of the Council (notified under document C(2013) 780)
Durchführungsbeschluss der Kommission vom 19. Februar 2013 über die von Deutschland gemäß der Richtlinie 98/8/EG des Europäischen Parlaments und des Rates gemeldeten Beschränkungen der Zulassung von difenacoumhaltigen Biozid-Produkten (2013/96/EU)
Commission Decision, 2013/85/EU, of 14 February 2013 concerning the non-inclusion of certain substances in Annex I, IA or IB to Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market (notified under document C(2013) 670)
Beschluss der Kommission vom 14. Februar 2013 über die Nichtaufnahme bestimmter Wirkstoffe in Anhang I, IA oder IB der Richtlinie 98/8/EG des Europäischen Parlaments und des Rates über das Inverkehrbringen von Biozid-Produkten (2013/85/EU)
Ákvörðun framkvæmdastjórnarinnar frá 14. febrúar 2013 um að færa tiltekin efni ekki á skrá í I. viðauka, I. viðauka A eða I. viðauka B við tilskipun Evrópuþingsins og ráðsins 98/8/EB um markaðssetningu sæfiefna (tilkynnt með númeri C(2013) 670) (2013/85/ESB)
Kommisjonsbeslutning av 14. februar 2013 om at visse stoffer ikke skal oppføres i vedlegg I, IA eller IB til europaparlaments- og rådsdirektiv 98/8/EF om markedsføring av biocidprodukter
Commission Implementing Decision 2013/38/EU of 18 January 2013 allowing Member States to extend provisional authorisations granted for the new active substances emamectin and maltodextrin (notified under document C(2013) 51)
Durchführungsbeschluss der Kommission vom 18. Januar 2013 zur Ermächtigung der Mitgliedstaaten, die vorläufigen Zulassungen für die neuen Wirkstoffe Emamectin und Maltodextrin zu verlängern (2013/38/EU)
Framkvæmdarákvörðun framkvæmdastjórnarinnar frá 18. janúar 2013 um að heimila aðildarríkjum að framlengja bráðabirgðaleyfi sem voru veitt fyrir nýju, virku efnunum emamektíni og maltódextríni (tilkynnt með númeri C(2013) 51) (2013/38/ESB)
Kommisjonens gjennomføringsbeslutning av 18. januar 2013 om tillatelse for medlemsstatene til å forlenge midlertidige godkjenninger gitt for de nye aktive stoffene emamektin og maltdekstrin (2013/38/EU)

Disclaimer: EEA-Lex is provided for information purposes only. The information is not guaranteed or promised to be current or complete and is not intended to replace any applicable legal sources.

Seminar on the European Economic Area - EEA - Brussels 15 September 2020