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Treoir 2001/95/CE maidir le sábháilteacht ghinearálta táirgí
Directive 2001/95/EC on general product safety
Treoir 2001/95/CE maidir le sábháilteacht ghinearálta táirgí
Directive 2001/95/EC on general product safety
Le Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí [4], bunaíodh rialacha chun sábháilteacht táirgí tomhaltóirí a áirithiú.
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety [4] established rules to ensure the safety of consumer products.
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí.
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety.
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí [54]
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety [54]
Ag féachaint do Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí, agus go háirithe Airteagal 4(1), pointe (a), de,
Having regard to Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety, and in particular Article 4(1), point (a), thereof,
Sa togra seo, déantar na rialacha maidir le faireachas margaidh i dTreoir 2001/95/CE maidir le sábháilteacht ghinearálta táirgí[5], Rialachán (CE) Uimh. 765/2008 ó Pharlaimint na hEorpa agus ón gComhairle lena leagtar amach na ceanglais maidir le creidiúnú agus maidir le faireachas margaidh a bhaineann le táirgí a mhargú[6] agus reachtaíocht um chomhchuibhiú a bhaineann le hearnálacha sainiúla a chumasc d’fhonn feabhas a chur ar a éifeachtaí atá gníomhaíochtaí faireachais mhargaidh san Aontas.
This proposal merges the rules on market surveillance of Directive 2001/95/EC on general product safety[5], Regulation (EC) No 765/2008 of the European Parliament and of the Council setting out the requirements for accreditation and market surveillance relating to the marketing of products[6] and of sector-specific harmonisation legislation in order to increase the effectiveness of market surveillance activities within the Union.
Sa togra comhcheanglaítear na rialacha a bhaineann le faireachas margaidh atá i dTreoir 2001/95/CE i dtaca le sábháilteacht ghinearálta táirgí[5], le Rialachán (CE) 765/2008 ó Pharlaimint na hEorpa agus ón gComhairle an 9 Iúil 2008 ina leagtar amach na ceanglais atá ag teastáil do chreidiúnú agus d’fhaireachas margaidh a bhaineann le margú táirgí[6] agus le reachtaíocht chomhchuibhithe a bhaineann go sonrach le hearnáil faoi leith chun éifeachtacht an fhaireachais mhargaidh laistigh den Aontas a mhéadú.
The proposal merges the rules on market surveillance of Directive 2001/95/EC on general product safety[5], Regulation (EC) 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance relating to the marketing of products[6] and of sector-specific harmonisation legislation in order to increase the effectiveness of market surveillance activities within the Union.
Dá réir sin, is gá cosaint do sceithirí a thabhairt isteach i ndáil leis na ceanglais sábháilteachta is infheidhme maidir le táirgí a rialaítear le reachtaíocht an Aontais um chomhchuibhiú a leagtar amach in Iarscríbhinní I agus II a ghabhann le Rialachán (AE) 2019/1020 ó Pharlaimint na hEorpa agus ón gComhairle, agus i ndáil leis na ceanglais ghinearálta sábháilteachta i gcomhair táirgí a leagtar amach i dTreoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle.
Accordingly, there is a need to introduce whistleblower protection in relation to the safety requirements applicable to products regulated by the Union harmonisation legislation as set out in Annexes I and II to Regulation (EU) 2019/1020 of the European Parliament and of the Council, and in relation to the general product safety requirements as set out in Directive 2001/95/EC of the European Parliament and of the Council.
Dá bhrí sin, áirithítear comhsheasmhacht agus comhlántacht le tionscnaimh eile an Choimisiúin atá ar bun nó atá beartaithe a bhfuil sé d’aidhm acu aghaidh a thabhairt ar na fadhbanna sin, lena n‑áirítear athbhreithniú ar reachtaíocht earnála táirgí (e.g. an Treoir maidir le hInnealra, an Treoir maidir le Sábháilteacht Ghinearálta Táirgí) agus tionscnaimh lena dtugtar aghaidh ar shaincheisteanna dliteanais a bhaineann le teicneolaíochtaí nua, lena n‑áirítear córais intleachta saorga.
Consistency and complementarity is therefore ensured with other ongoing or planned initiatives of the Commission that also aim to address those problems, including the revision of sectoral product legislation (e.g. the Machinery Directive, the General Product Safety Directive) and initiatives that address liability issues related to new technologies, including AI systems.
Tá an faireachas margaidh i mBallstáit i leith táirgí a chumhdaítear leis an Rialachán seo faoi réir Rialachán (CE) Uimh. 765/2008 ó Pharlaimint na hEorpa agus ón gComhairle an 9 Iúil 2008 lena leagtar amach na ceanglais maidir le creidiúnú agus maidir le faireachas margaidh a bhaineann le táirgí a mhargú [6] agus faoi réir Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí [7].
The market surveillance in Member States of products covered by this Regulation is subject to Regulation (EC) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance relating to the marketing of products [6] and Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety [7].
I gcás, i gcomhréir leis an dara fomhír d'Airteagal 1(8) nó leis an dara fomhír d'Airteagal 1(9) de Rialachán (AE) 2017/745 ó Pharlaimint na hEorpa agus ón gComhairle ina bhfuil táirge faoi réir na Treorach seo, beidh i sainchomhad an údaraithe margaíochta, má tá siad ar fáil, torthaí an mheasúnaithe ar chomhréireacht na comhpháirte feiste le ceanglais ghinearálta sábháilteachta agus feidhmíochta ábhartha Iarscríbhinn I a ghabhann leis an Rialachán sin atá i ndearbhú comhréireachta AE a thug an monaróir, sin nó an dearbhú ábhartha arna eisiúint ag comhlacht dá dtugtar fógra lena gceadaítear don mhonaróir an mharcáil CE a ghreamú den fheiste leighis.
Where, in accordance with the second subparagraph of Article 1(8) or the second subparagraph of Article 1(9) of Regulation (EU) 2017/745 of the European Parliament and of the Council, a product is governed by this Directive, the marketing authorisation dossier shall include, where available, the results of the assessment of the conformity of the device part with the relevant general safety and performance requirements set out in Annex I to that Regulation contained in the manufacturer's EU declaration of conformity or the relevant certificate issued by a notified body allowing the manufacturer to affix a CE marking to the medical device.
I dTreoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle leagtar síos na ceanglais sábháilteachta ginearálta atá ar gach táirge tomhaltais agus foráiltear maidir le hoibleagáidí agus cumhachtaí sonracha de chuid na mBallstát maidir le táirgí contúirteacha mar aon le malartú faisnéise chuige sin tríd an gCóras Mear-Mhalartú Faisnéise (RAPEX).
Directive 2001/95/EC of the European Parliament and of the Council lays down the general safety requirements for all consumer products and provides for specific obligations and powers of the Member States in relation to dangerous products as well as for the exchange of information to that effect through the Rapid Information Exchange System (RAPEX).
Cinneadh 2010/376/AE ón gCoimisiún an 2 Iúil 2010 maidir leis na ceanglais sábháilteachta atá le comhlíonadh ag caighdeáin Eorpacha le haghaidh táirgí áirithe i dtimpeallacht chodlata leanaí de bhun Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle maidir le sábháilteacht ghinearálta táirgí (IO L 170, 6.7.2010, lch. 39).
Commission Decision 2010/376/EU of 2 July 2010 on the safety requirements to be met by European standards for certain products in the sleep environment of children pursuant to Directive 2001/95/EC of the European Parliament and of the Council on general product safety (OJ L 170, 6.7.2010, p. 39).
Treoir 2001/83/CE ó Pharlaimint na hEorpa agus ón gComhairle maidir leis an gcód Comhphobail a bhaineann le táirgí míochaine lena n-úsáid ag an duine [12], Rialachán (CE) Uimh. 178/2002 ó Pharlaimint na hEorpa agus ón gComhairle an 28 Eanáir 2002 lena leagtar síos prionsabail agus ceanglais ghinearálta dhlí an bhia, lena mbunaítear an tÚdarás Eorpach um Shábháilteacht Bia agus lena leagtar síos nósanna imeachta i gcúrsaí sábháilteachta bia [13] agus Rialachán (CE) Uimh. 1831/2003 ó Pharlaimint na hEorpa agus ón gComhairle an 22 Meán Fómhair 2003 maidir le breiseáin lena n-úsáid i gcothú ainmhithe
Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use [12], Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety [13] and Regulation (EC) No 1831/2003 of the European Parliament and of the Council of 22 September 2003 on additives for use in animal nutrition
Le Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí [4] sonraítear nach féidir ach táirgí sábháilte a chur ar an margadh agus leagtar síos oibleagáidí na dtáirgeoirí agus na ndáileoirí maidir le sábháilteacht na dtáirgí.
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety [4] specifies that only safe products may be placed on the market and lays down the obligations of producers and distributors with respect to the safety of products.
Tar éis ghlacadh Rialachán (CE) Uimh. 178/2002 ó Pharlaimint na hEorpa agus ón gComhairle an 28 Eanáir 2002 lena leagtar síos prionsabail agus ceanglais ghinearálta dhlí an bhia, lena mbunaítear an tÚdarás Eorpach um Shábháilteacht Bia agus lena leagtar síos nósanna imeachta in ábhair a bhaineann le sábháilteacht bia [9] a bhfuil feidhm aige maidir le gach céim den phróiseas táirgthe, próiseála agus leithdháilte bia agus beatha ar leibhéal an Aontais agus ar an leibhéal náisiúnta, tá forálacha ginearálta Aontais maidir le bia-ábhair infheidhme go díreach ar na táirgí a chumhdaítear le Treoir 1999/4/CE, le Treoir 2000/36/CE, le Treoir 2001/111/CE, le Treoir 2001/113/CE agus le Treoir 2001/114/CE.
Following the adoption of Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety [9], which applies to all stages of production, processing and distribution of food and feed at Union and national level, general Union provisions on foodstuffs apply directly to the products covered by Directives 1999/4/EC, 2000/36/EC, 2001/111/EC, 2001/113/EC and 2001/114/EC.
Treoir Uimh. 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Le Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council, of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4);
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4);
Le Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
De thoradh ghlacadh Rialachán (CE) Uimh. 178/2002 ó Pharlaimint na hEorpa agus ón gComhairle an 28 Eanáir 2002 lena leagtar síos prionsabail agus ceanglais ghinearálta dlí an bhia, lena mbunaítear an tÚdarás Eorpach um Shábháilteacht Bia agus lena leagtar síos nósanna imeachta maidir le sábháilteacht bia[10], ar rialachán é a bhfuil feidhm aige maidir le gach céim den phróiseas táirgthe, próiseála agus leithdháilte bia agus beatha ar leibhéal an Aontais agus ar an leibhéal náisiúnta, tá forálacha ginearálta an Aontais maidir le bia‑ábhair infheidhme go díreach ar na táirgí atá cumhdaithe le Treoracha 1999/4/CE, 2000/36/CE, 2001/111/CE, 2001/113/CE agus 2001/114/CE.
Following the adoption of Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety[10], which applies to all stages of production, processing and distribution of food and feed at Union and national level, general Union provisions on foodstuffs apply directly to the products covered by Directives 1999/4/EC, 2000/36/EC, 2001/111/EC, 2001/113/EC and 2001/114/EC.
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4): Airteagail 3 agus 5.
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4): Articles 3 and 5.
cuirfidh an tAontas faisnéis roghnaithe ar fáil don Ríocht Aontaithe óna chóras rabhaidh RAPEX, nó óna chomharba, dá dtagraítear i dTreoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí, nó a comharba;
the Union is to provide the United Kingdom with selected information from its RAPEX alert system, or its successor, as referred to in Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety, or its successor;
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Agus measúnú an Aontais ar a mhéid a chomhlíonann an córas náisiúnta ábhartha an Treoir maidir le Sábháilteacht Ghinearálta Táirgí mar bhonn leis, pléifidh na páirtithe na céimeanna a d’fhéadfaí a leanúint agus iad ag dul i gcomhar lena chéile.
Based on EU’s assessment of the compliance of the respective national system with the General Product Safety Directive, the parties will discuss the possible steps to be followed in their cooperation.
Ag féachaint do Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí, agus go háirithe an chéad fhomhír d’Airteagal 4(2) de,
Having regard to Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety, and in particular the first subparagraph of Article 4(2) thereof,
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4), arna leasú go deireanach le Rialachán (CE) Uimh. 596/2009 ó Pharlaimint na hEorpa agus ón gComhairle (IO L 188, 18.7.2009, lch. 14).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety, OJ L 11, 15.1.2002, p. 4, as last amended by Regulation (EC) No 596/2009 of the European Parliament and of the Council (OJ L 188, 18.7.2009, p. 14).
lena leasaítear Cinneadh Cur Chun Feidhme (AE) 2019/417 ón gCoimisiún lena leagtar síos treoirlínte maidir le bainistíocht a dhéanamh ar Chóras an Aontais Eorpaigh um Mearfhaisnéis ‘RAPEX’ a bunaíodh faoi Airteagal 12 de Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle maidir le sábháilteacht ghinearálta táirgí agus a chóras fógartha
amending Commission Implementing Decision (EU) 2019/417 laying down guidelines for the management of the European Union Rapid Information System ‘RAPEX’ established under Article 12 of Directive 2001/95/EC of the European Parliament and of the Council on general product safety and its notification system
Ag féachaint do Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí, agus go háirithe an tríú fomhír d’Airteagal 11(1) agus pointe 8 den Iarscríbhinn II a ghabhann léi de,
Having regard to Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety, and in particular Article 11(1), the third subparagraph, thereof and point 8 of Annex II thereto,
Cinneadh Cur Chun Feidhme (AE) 2019/417 ón gCoimisiún an 8 Samhain 2018 lena leagtar síos treoirlínte maidir le bainistíocht a dhéanamh ar Chóras an Aontais Eorpaigh um Mearfhaisnéis ‘RAPEX’ a bunaíodh faoi Airteagal 12 de Threoir 2001/95/CE maidir le sábháilteacht ghinearálta táirgí agus a chóras fógartha ( IO L 73, 15.3.2019, lch. 121).
Commission Implementing Decision (EU) 2019/417 of 8 November 2018 laying down guidelines for the management of the European Union Rapid Information System ‘RAPEX’ established under Article 12 of Directive 2001/95/EC on general product safety and its notification system ( OJ L 73, 15.3.2019, p. 121).
AN RIALAITHEOIREACHT CHOMHPHÁIRTEACH MAIDIR LE CÓRAS AN AONTAIS EORPAIGH UM MEARFHAISNÉIS ‘RAPEX’ A BUNAÍODH FAOI AIRTEAGAL 12 DE THREOIR 2001/95/CE Ó PHARLAIMINT Ó PHARLAIMINT NA hEORPA AGUS ÓN gCOMHAIRLE (AN TREOIR MAIDIR LE SÁBHÁILTEACHT GHINEARÁLTA TÁIRGÍ)
JOINT CONTROLLERSHIP OF THE EUROPEAN UNION RAPID INFORMATION SYSTEM ‘RAPEX’ ESTABLISHED UNDER ARTICLE 12 OF DIRECTIVE 2001/95/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL (THE GENERAL PRODUCT SAFETY DIRECTIVE)
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Ní mór a áirithiú leis na ceanglais sin go ndéanfaidh táirgí atá i gcomhréir leis na caighdeáin sin an ceanglas ginearálta sábháilteachta a leagtar amach in Airteagal 3 de Threoir 2001/95/CE a chomhlíonadh.
Those requirements need to ensure that products which conform to those standards satisfy the general safety requirement set out in Article 3 of Directive 2001/95/EC.
Cinneadh 2010/9/AE ón gCoimisiún an 6 Eanáir 2010 maidir leis na ceanglais sábháilteachta atá le comhlíonadh ag caighdeáin Eorpacha le haghaidh fáinní folctha, áiseanna folctha agus tobáin folctha agus seastáin folctha do leanaí agus do pháistí óga de bhun Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle maidir le sábháilteacht ghinearálta táirgí (IO L 3, 7.1.2010, lch. 23).
Commission Decision 2010/9/EU of 6 January 2010 on the safety requirements to be met by European standards for bath rings, bathing aids and bath tubs and stands for infants and young children pursuant to Directive 2001/95/EC of the European Parliament and of the Council on general product safety (OJ L 3, 7.1.2010, p. 23).
Cinneadh 2013/121/AE ón gCoimisiún an 7 Márta 2013 maidir leis na ceanglais sábháilteachta atá le comhlíonadh ag caighdeáin Eorpacha le haghaidh suíocháin áirithe do leanaí de bhun Threoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle maidir le sábháilteacht ghinearálta táirgí (IO L 65, 8.3.2013, lch. 23).
Commission Decision 2013/121/EU of 7 March 2013 on the safety requirements to be met by European standards for certain seats for children pursuant to Directive 2001/95/EC of the European Parliament and of the Council on general product safety (OJ L 65, 8.3.2013, p. 23).
Beartaítear leis na ceanglais sin a áirithiú go gcomhlíonfaidh táirgí atá i gcomhréir leis na caighdeáin sin an ceanglas ginearálta sábháilteachta a leagtar amach in Airteagal 3(1) de Threoir 2001/95/CE.
Those requirements intend to ensure that products which conform to those standards satisfy the general safety requirement set out in Article 3(1) of Directive 2001/95/EC.
maidir le sábháilteacht ghinearálta táirgí, lena leasaítear Rialachán (AE) Uimh. 1025/2012 ó Pharlaimint na hEorpa agus ón gComhairle agus Treoir (AE) 2020/1828 ó Pharlaimint na hEorpa agus ón gComhairle agus lena n-aisghairtear Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle agus Treoir 87/357/CEE ón gComhairle
on general product safety, amending Regulation (EU) No 1025/2012 of the European Parliament and of the Council and Directive (EU) 2020/1828 of the European Parliament and the Council, and repealing Directive 2001/95/EC of the European Parliament and of the Council and Council Directive 87/357/EEC
Rialachán (AE) 2023/988 ó Pharlaimint na hEorpa agus ón gComhairle an 10 Bealtaine 2023 maidir le sábháilteacht ghinearálta táirgí, lena leasaítear Rialachán (AE) Uimh. 1025/2012 ó Pharlaimint na hEorpa agus ón gComhairle agus Treoir (AE) 2020/1828 ó Pharlaimint na hEorpa agus ón gComhairle agus lena n-aisghairtear Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle agus Treoir 87/357/CEE ón gComhairle (IO L135,23.5.2023, lch.1).’.
Regulation (EU) 2023/988 of the European Parliament and of the Council of 10 May 2023 on general product safety, amending Regulation (EU) No 1025/2012 of the European Parliament and of the Council and Directive (EU) 2020/1828 of the European Parliament and the Council, and repealing Directive 2001/95/EC of the European Parliament and of the Council and Council Directive 87/357/EEC (OJ L 135, 23.5.2023, p. 1).’.
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).
Cinneadh Cur Chun Feidhme (AE) 2019/417 ón gCoimisiún an 8 Samhain 2018 lena leagtar síos treoirlínte maidir le bainistiú Chóras an Aontais um Mearfhaisnéis ‘RAPEX’ arna bhunú faoi Airteagal 12 de Threoir 2001/95/CE maidir le sábháilteacht ghinearálta táirgí agus a chóras fógartha ( IO L 73, 15.3.2019, lch. 121).
Commission Implementing Decision (EU) 2019/417 of 8 November 2018 laying down guidelines for the management of the European Union Rapid Information System ‘RAPEX’ established under Article 12 of Directive 2001/95/EC on general product safety and its notification system ( OJ L 73, 15.3.2019, p. 121).
Rialachán (AE) 2023/988 ó Pharlaimint na hEorpa agus ón gComhairle an 10 Bealtaine 2023 maidir le sábháilteacht ghinearálta táirgí, lena leasaítear Rialachán (AE) Uimh. 1025/2012 ó Pharlaimint na hEorpa agus ón gComhairle agus Treoir (AE) 2020/1828 ó Pharlaimint na hEorpa agus ón gComhairle agus lena n-aisghairtear Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle agus Treoir 87/357/CEE ón gComhairle (IO L 135, 23.5.2023, lch. 1).’;
Regulation (EU) 2023/988 of the European Parliament and of the Council of 10 May 2023 on general product safety, amending Regulation (EU) No 1025/2012 of the European Parliament and of the Council and Directive (EU) 2020/1828 of the European Parliament and the Council, and repealing Directive 2001/95/EC of the European Parliament and of the Council and Council Directive 87/357/EEC (OJ L 135, 23.5.2023, p. 1).’;
Ba cheart feidhm a bheith ag forálacha ginearálta an Rialacháin seo gan dochar do na ceanglais sábháilteachta agus chothabhála maidir le feistí gairmiúla íomháithe leighis agus feistí radaiteiripe mar a shainmhínítear i Rialachán (AE) 2017/745 ó Pharlaimint na hEorpa agus ón gComhairle agus maidir le feistí leighis diagnóiseacha in vitro mar a shainmhínítear i Rialachán (AE) 2017/746 ó Pharlaimint na hEorpa agus ón gComhairle, agus d’fhéadfaí iad a chomhlánú le ceanglais a leagtar síos le haghaidh táirgí áirithe a chumhachtaítear le ceallraí faoi bhearta cur chun feidhme faoi Threoir 2009/125/CE.
The general provisions of this Regulation should apply without prejudice to the safety and maintenance requirements for professional medical imaging and radiotherapy devices as defined in Regulation (EU) 2017/745 of the European Parliament and of the Council and for in vitro diagnostic medical devices as defined in Regulation (EU) 2017/746 of the European Parliament and of the Council, and could be complemented with requirements laid down for particular products powered by batteries under implementing measures under Directive 2009/125/EC.
Treoir 2001/95/CE ó Pharlaimint na hEorpa agus ón gComhairle an 3 Nollaig 2001 maidir le sábháilteacht ghinearálta táirgí (IO L 11, 15.1.2002, lch. 4).
Directive 2001/95/EC of the European Parliament and of the Council of 3 December 2001 on general product safety (OJ L 11, 15.1.2002, p. 4).