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31 results in 18 documents

  1. #629086

    Gaireas d'íomháú athshondais mhaighnéadaigh

    Magnetic resonance imaging apparatus

    REGULATION (EU) No 374/2014 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 16 April 2014 on the reduction or elimination of customs duties on goods originating in Ukraine

  2. #1650997

    íomháú athshondais mhaighnéadaigh

    magnetic resonance imaging

    Regulation (EU) No 388/2012 of the European Parliament and of the Council of 19 April 2012 amending Council Regulation (EC) No 428/2009 setting up a Community regime for the control of exports, transfer, brokering and transit of dual-use items

  3. #1748585

    íomháú athshondais mhaighnéadaigh

    magnetic resonance imaging

    Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL setting up a Union regime for the control of exports, transfer, brokering, technical assistance and transit of dual-use items (recast)

  4. #2054344

    Íomháú Athshondais Mhaighnéadaigh

    Magnetic Resonance Imaging

    Regulation (EU) 2021/821 of the European Parliament and of the Council of 20 May 2021 setting up a Union regime for the control of exports, brokering, technical assistance, transit and transfer of dual-use items (recast)

  5. #2229282

    Ní áirítear córais íomháithe athshondais mhaighnéadaigh núicléach ná córais tomagrafaíochta athshondais mhaighnéadaigh faoin raon feidhme seo.

    Nuclear magnetic resonance imaging and magnetic resonance tomography systems are not included in this scope.

    Commission Implementing Decision (EU) 2022/180 of 8 February 2022 amending Decision 2006/771/EC as regards the update of harmonised technical conditions in the area of radio spectrum use for short-range devices (notified under document C(2022) 644) (Text with EEA relevance)

  6. #2271821

    Íomháú Athshondais Mhaighnéadaigh

    Magnetic Resonance Imaging

    Commission Delegated Regulation (EU) 2022/1 of 20 October 2021 amending Regulation (EU) 2021/821 of the European Parliament and of the Council as regards the list of dual-use items

  7. #2549272

    Gléasra íomháithe athshondais mhaighnéadaigh

    Magnetic resonance imaging apparatus

    Commission Implementing Regulation (EU) 2022/1998 of 20 September 2022 amending Annex I to Council Regulation (EEC) No 2658/87 on the tariff and statistical nomenclature and on the Common Customs Tariff

  8. #2569431

    idirghníomhaithe féideartha le réimse maighnéadach, (mar shampla, téamh a bhaineann le híomháú athshondais mhaighnéadaigh);

    potential interactions with magnetic field, (for example heating related to magnetic resonance imaging);

    Commission Implementing Regulation (EU) 2022/2346 of 1 December 2022 laying down common specifications for the groups of products without an intended medical purpose listed in Annex XVI to Regulation (EU) 2017/745 of the European Parliament and of the Council on medical devices (Text with EEA relevance)

  9. #2695560

    Íomháú Athshondais Mhaighnéadaigh

    Magnetic Resonance Imaging

    Commission Delegated Regulation (EU) 2023/66 of 21 October 2022 amending Regulation (EU) 2021/821 of the European Parliament and of the Council as regards the list of dual-use items

  10. #2820679

    Íomháú Athshondais Mhaighnéadaigh

    Magnetic Resonance Imaging

    Commission Delegated Regulation (EU) 2023/996 of 23 February 2023 amending Regulation (EU) 2021/821 of the European Parliament and of the Council as regards the list of dual-use items

  11. #3018918

    Gléasra íomháithe athshondais mhaighnéadaigh

    Magnetic resonance imaging apparatus

    Commission Implementing Regulation (EU) 2023/2364 of 26 September 2023 amending Annex I to Council Regulation (EEC) No 2658/87 on the tariff and statistical nomenclature and on the Common Customs Tariff

  12. #3079176

    Gléasra íomháithe athshondais mhaighnéadaigh

    Magnetic resonance imaging apparatus

    22024A0022

  13. #3117419

    Ní rialaítear le X.A.I.001.k, leictreamaighnéid nó solanóidigh ‘fhorsheoltacha’ atá deartha lena n-úsáid i dtrealamh leighis um Íomháú Athshondais Mhaighnéadaigh.

    does not control “superconductive” electromagnets or solenoids designed for Magnetic Resonance Imaging (MRI) medical equipment.

    Council Regulation (EU) 2023/1214 of 23 June 2023 amending Regulation (EU) No 833/2014 concerning restrictive measures in view of Russia’s actions destabilising the situation in Ukraine

  14. #1655154

    Ní rialaítear le 3A001.e.3. leictreamaighdéid nó solanóidigh “fhorsheoltacha” atá saindeartha le húsáid i dtrealamh míochaine um Íomháú Athshonadais Mhaighnéadaigh (ÍAM).

    3A001.e.3. does not control “superconductive” electromagnets or solenoids specially designed for Magnetic Resonance Imaging (MRI) medical equipment.

    Regulation (EU) No 388/2012 of the European Parliament and of the Council of 19 April 2012 amending Council Regulation (EC) No 428/2009 setting up a Community regime for the control of exports, transfer, brokering and transit of dual-use items

  15. #1749649

    Nóta:Ní rialaítear le 3A001.e.3. leictreamaighnéid nó solanóidigh "fhorsheoltacha" atá saindeartha le húsáid i dtrealamh míochaine um Íomháú Athshondais Mhaighnéadaigh (ÍAM).

    Note:3A001.e.3. does not control "superconductive" electromagnets or solenoids specially designed for Magnetic Resonance Imaging (MRI) medical equipment.

    Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL setting up a Union regime for the control of exports, transfer, brokering, technical assistance and transit of dual-use items (recast)

  16. #2056624

    Ní rialaítear le 3A001.e.3. leictreamaighnéid nó solanóidigh ‘fhorsheoltacha’ atá saindeartha lena n-úsáid i dtrealamh leighis um Íomháú Athshondais Mhaighnéadaigh (MRI).

    3A001.e.3. does not control "superconductive" electromagnets or solenoids specially designed for Magnetic Resonance Imaging (MRI) medical equipment.

    Regulation (EU) 2021/821 of the European Parliament and of the Council of 20 May 2021 setting up a Union regime for the control of exports, brokering, technical assistance, transit and transfer of dual-use items (recast)

  17. #2274331

    Ní rialaítear le 3A001.e.3. leictreamaighnéid nó solanóidigh ‘fhorsheoltacha’ atá saindeartha lena n-úsáid i dtrealamh leighis um Íomháú Athshondais Mhaighnéadaigh (MRI).

    3A001.e.3. does not control "superconductive" electromagnets or solenoids specially designed for Magnetic Resonance Imaging (MRI) medical equipment.

    Commission Delegated Regulation (EU) 2022/1 of 20 October 2021 amending Regulation (EU) 2021/821 of the European Parliament and of the Council as regards the list of dual-use items

  18. #2548385

    Leictreamaighnéid de chineál nach n-úsáidtear ach amháin le haghaidh gléasra don íomháú athshondais mhaighnéadaigh seachas leictreamaighnéid atá faoi cheannteideal 9018

    Electromagnets of a kind used solely or principally for magnetic resonance imaging apparatus other than electromagnets of heading 9018

    Commission Implementing Regulation (EU) 2022/1998 of 20 September 2022 amending Annex I to Council Regulation (EEC) No 2658/87 on the tariff and statistical nomenclature and on the Common Customs Tariff

  19. #2563863

    Ciallaíonn “aonaid íomháithe athshondais mhaighnéadaigh (MRI)” meaisíní a bhfuil teicníc íomháithe acu atá deartha chun struchtúir inmheánacha an choirp a amharcléiriú lena n-úsáidtear réimsí maighnéadacha agus leictreamaighnéadacha a mbíonn éifeacht athshondais de adaimh hidrigine mar thoradh orthu.

    ‘Magnetic resonance imaging (MRI) units’ means machines with an imaging technique designed to visualise internal structures of the body using magnetic and electromagnetic fields which induce a resonance effect of hydrogen atoms.

    Commission Regulation (EU) 2022/2294 of 23 November 2022 implementing Regulation (EC) No 1338/2008 of the European Parliament and of the Council as regards statistics on healthcare facilities, healthcare human resources and healthcare utilisation (Text with EEA relevance)

  20. #2698151

    Ní rialaítear le 3A001.e.3. leictreamaighnéid nó solanóidigh ‘fhorsheoltacha’ atá saindeartha lena n-úsáid i dtrealamh leighis um Íomháú Athshondais Mhaighnéadaigh (MRI).

    3A001.e.3. does not control "superconductive" electromagnets or solenoids specially designed for Magnetic Resonance Imaging (MRI) medical equipment.

    Commission Delegated Regulation (EU) 2023/66 of 21 October 2022 amending Regulation (EU) 2021/821 of the European Parliament and of the Council as regards the list of dual-use items

  21. #2823260

    Ní rialaítear le 3A001.e.3. leictreamaighnéid nó solanóidigh ‘fhorsheoltacha’ atá saindeartha lena n-úsáid i dtrealamh leighis um Íomháú Athshondais Mhaighnéadaigh (MRI).

    3A001.e.3. does not control "superconductive" electromagnets or solenoids specially designed for Magnetic Resonance Imaging (MRI) medical equipment.

    Commission Delegated Regulation (EU) 2023/996 of 23 February 2023 amending Regulation (EU) 2021/821 of the European Parliament and of the Council as regards the list of dual-use items

  22. #3018110

    Leictreamaighnéid de chineál nach n-úsáidtear ach amháin le haghaidh gléasra don íomháú athshondais mhaighnéadaigh seachas leictreamaighnéid atá faoi cheannteideal 9018

    Electromagnets of a kind used solely or principally for magnetic resonance imaging apparatus other than electromagnets of heading 9018

    Commission Implementing Regulation (EU) 2023/2364 of 26 September 2023 amending Annex I to Council Regulation (EEC) No 2658/87 on the tariff and statistical nomenclature and on the Common Customs Tariff

  23. #3078472

    Leictreamaighnéid de chineál nach n-úsáidtear ach amháin le haghaidh gléasra don íomháú athshondais mhaighnéadaigh seachas leictreamaighnéid atá faoi cheannteideal 9018

    Electromagnets of a kind used solely or principally for magnetic resonance imaging apparatus other than electromagnets of heading 9018

    22024A0022

  24. #2002758

    lena leasaítear, chun í a chur in oiriúint don dul chun cinn teicniúil agus eolaíoch, Iarscríbhinn IV a ghabhann le Treoir 2011/65/AE ó Pharlaimint na hEorpa agus ón gComhairle a mhéid a bhaineann le díolúine i leith úsáid bios(2-eitilheicsil) taláite (DEHP) i gcomhpháirteanna plaisteacha i gcornaí brathadóra íomháithe athshondais mhaighnéadaigh (MRI)

    amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of bis(2-ethylhexyl) phthalate (DEHP) in plastic components in magnetic resonance imaging (MRI) detector coils

    Commission Delegated Directive (EU) 2021/1979 of 11 August 2021 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of bis(2-ethylhexyl) phthalate (DEHP) in plastic components in magnetic resonance imaging (MRI) detector coils (Text with EEA relevance)

  25. #2002769

    An 12 Meán Fómhair 2018 agus an 2 Deireadh Fómhair 2019, fuair an Coimisiún iarratais arna ndéanamh i gcomhréir le hAirteagal 5(3) de Threoir 2011/65/AE maidir le díolúine a liostú in Iarscríbhinn IV a ghabhann leis an Treoir sin, i leith úsáid DEHP i gcomhpháirteanna plaisteacha i gcornaí brathadóra íomháithe athshondais mhaighnéadaigh (MRI) (“an díolúine a iarradh”)

    On 12 September 2018 and 2 October 2019, the Commission received applications made in accordance with Article 5(3) of Directive 2011/65/EU for an exemption to be listed in Annex IV to that Directive, for the use of DEHP in plastic components in magnetic resonance imaging (MRI) detector coils (‘the requested exemption’).

    Commission Delegated Directive (EU) 2021/1979 of 11 August 2021 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of bis(2-ethylhexyl) phthalate (DEHP) in plastic components in magnetic resonance imaging (MRI) detector coils (Text with EEA relevance)

  26. #2377527

    Treoir Tharmligthe (AE) 2021/1979 ón gCoimisiún an 11 Lúnasa 2021 lena leasaítear, chun í a chur in oiriúint don dul chun cinn eolaíoch agus teicniúil, Iarscríbhinn IV a ghabhann le Treoir 2011/65/AE ó Pharlaimint na hEorpa agus ón gComhairle a mhéid a bhaineann le díolúine i leith úsáid bios(2-eitilheicsil) taláite (DEHP) i gcomhpháirteanna plaisteacha i gcornaí brathadóra íomháithe athshondais mhaighnéadaigh (MRI), tá sí le hionchorprú i gComhaontú LEE.

    Commission Delegated Directive (EU) 2021/1979 of 11 August 2021 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of bis(2-ethylhexyl) phthalate (DEHP) in plastic components in magnetic resonance imaging (MRI) detector coils is to be incorporated into the EEA Agreement.

    Decision of the EEA Joint Committee No 122/2022 of 29 April 2022 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2022/1566]

  27. #2439881

    lena leasaítear, chun í a chur in oiriúint don dul chun cinn teicniúil agus eolaíoch, Iarscríbhinn IV a ghabhann le Treoir 2011/65/AE ó Pharlaimint na hEorpa agus ón gComhairle a mhéid a bhaineann le díolúine i leith úsáid luaidhe i bhfeistí íomháithe athshondais mhaighnéadaigh áirithe

    amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of lead in certain magnetic resonance imaging devices

    Commission Delegated Directive (EU) 2022/1632 of 12 May 2022 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of lead in certain magnetic resonance imaging devices (Text with EEA relevance)

  28. #2439891

    Le Treoir Tharmligthe 2014/7/AE, dheonaigh an Coimisiún díolúine i leith úsáid luaidhe i sádair, bratuithe foircinn de chomhpháirteanna leictreacha agus leictreonacha agus cláir ciorcad phriontáilte, naisc de shreanga leictreacha, sciatha agus nascóirí iata a úsáidtear i dtrealamh leighis íomháithe athshondais mhaighnéadaigh áirithe (“an díolúine”), trí na feidhmeanna sin a áireamh in Iarscríbhinn IV a ghabhann le Treoir 2011/65/AE.

    By Delegated Directive 2014/7/EU, the Commission granted an exemption for the use of lead in solders, termination coatings of electrical and electronic components and printed circuit boards, connections of electrical wires, shields and enclosed connectors that are used in certain medical magnetic resonance imaging (MRI) equipment (‘the exemption’), by including those applications in Annex IV to Directive 2011/65/EU.

    Commission Delegated Directive (EU) 2022/1632 of 12 May 2022 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of lead in certain magnetic resonance imaging devices (Text with EEA relevance)

  29. #2439933

    feistí íomháithe athshondais mhaighnéadaigh, lena n-áirítear cornaí comhtháite, a úsáidtear i réimsí maighnéadacha laistigh de gha 1 m thart timpeall ar isealár an mhaighnéid i dtrealamh leighis íomháithe athshondais mhaighnéadaigh, a eisiatar Dearbhú Comhréireachta ina leith den chéad uair roimh an 30 Meitheamh 2024.

    MRI devices including integrated coils, which are used in magnetic fields within the sphere of 1 m radius around the isocentre of the magnet in medical magnetic resonance imaging equipment, for which the Declaration of Conformity is issued for the first time before 30 June 2024.

    Commission Delegated Directive (EU) 2022/1632 of 12 May 2022 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of lead in certain magnetic resonance imaging devices (Text with EEA relevance)

  30. #2777897

    Treoir Tharmligthe (AE) 2022/1632 ón gCoimisiún an 12 Bealtaine 2022 lena leasaítear, chun í a chur in oiriúint don dul chun cinn teicniúil agus eolaíoch, Iarscríbhinn IV a ghabhann le Treoir 2011/65/AE ó Pharlaimint na hEorpa agus ón gComhairle a mhéid a bhaineann le díolúine i leith úsáid luaidhe i bhfeistí íomháithe athshondais mhaighnéadaigh áirithe, tá sé le hionchorprú i gComhaontú LEE.

    Commission Delegated Directive (EU) 2022/1632 of 12 May 2022 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of lead in certain magnetic resonance imaging devices is to be incorporated into the EEA Agreement.

    Decision of the EEA Joint Committee No 307/2022 of 9 December 2022 amending Annex II (Technical regulations, standards, testing and certification) to the EEA Agreement [2023/1249]

  31. #2439927

    Treoir Tharmligthe 2014/7/AE ón gCoimisiún an 18 Deireadh Fómhair 2013 lena leasaítear, chun í a chur in oiriúint don dul chun cinn teicniúil, Iarscríbhinn IV a ghabhann le Treoir 2011/65/AE ó Pharlaimint na hEorpa agus ón gComhairle a mhéid a bhaineann le díolúine i leith luaidhe i sádair, bratuithe foircinn de chomhpháirteanna leictreacha agus leictreonacha agus cláir ciorcad phriontáilte, naisc de shreanga leictreacha, sciatha agus nascóirí iata a úsáidtear i (a) réimsí maighnéadacha laistigh de gha 1 m thart timpeall ar isealár an mhaighnéid i dtrealamh leighis íomháithe athshondais mhaighnéadaigh, lena n-áirítear monatóirí othair a dheartar lena n-úsáid laistigh den gha sin, nó (b) i réimsí maighnéadacha laistigh de raon 1 m ó dhromchlaí seachtracha maighnéad cioglatróin, maighnéid le haghaidh bíomaí a iompar agus treoir bíomaí a rialú a chuirtear i bhfeidhm maidir le teiripe cáithníní (IO L 4, 9.1.2014, lch. 57).

    Commission Delegated Directive 2014/7/EU of 18 October 2013 amending, for the purposes of adapting to technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for lead in solders, termination coatings of electrical and electronic components and printed circuit boards, connections of electrical wires, shields and enclosed connectors which are used (a) in magnetic fields within the sphere of 1 m radius around the isocentre of the magnet in medical magnetic resonance imaging equipment, including patient monitors designed to be used within this sphere, or (b) in magnetic fields within 1 m distance from the external surfaces of cyclotron magnets, magnets for beam transport and beam direction control applied for particle therapy (OJ L 4, 9.1.2014, p. 57).

    Commission Delegated Directive (EU) 2022/1632 of 12 May 2022 amending, for the purposes of adapting to scientific and technical progress, Annex IV to Directive 2011/65/EU of the European Parliament and of the Council as regards an exemption for the use of lead in certain magnetic resonance imaging devices (Text with EEA relevance)