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8 results in 4 documents

  1. #2915012

    An Raideolaíocht dhiagnóiseach

    Diagnostic radiology

    Commission Delegated Decision (EU) 2023/2383 of 23 May 2023 amending and correcting Directive 2005/36/EC of the European Parliament and of the Council as regards the evidence of formal qualifications and the titles of training courses (notified under document C(2023) 3276)

  2. #2915031

    An Raideolaíocht

    Radiology

    Commission Delegated Decision (EU) 2023/2383 of 23 May 2023 amending and correcting Directive 2005/36/EC of the European Parliament and of the Council as regards the evidence of formal qualifications and the titles of training courses (notified under document C(2023) 3276)

  3. #3067756

    trealamh atá le húsáid chun críocha raideolaíochta nó leighis;

    equipment for use for radiology or medical purposes;

    22024A0022

  4. #744626

    Tá feistí gníomhacha a beartaíodh le radaíocht ianúcháin a astú agus a beartaíodh don raideolaíocht dhiagnóiseach nó theiripeach, lena n-áirítear feistí don raideolaíocht idirghabhálach agus feistí lena rialaítear feistí den sórt sin nó lena ndéantar faireachán orthu, nó a bhfuil tionchar díreach acu ar a bhfeidhmíocht aicmithe mar aicme IIb.

    Active devices intended to emit ionizing radiation and intended for diagnostic or therapeutic radiology, including interventional radiology devices and devices which control or monitor such devices, or which directly influence their performance, are classified as class IIb.

    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

  5. #744007

    Áirítear ar fheistí inchumraithe córais tomagrafaíochta ríomhairithe (TR), córais ultrafhuaime, córais ainéistéise, córais Faireacháin fiseolaíoch, córais faisnéise raideolaíochta (CFR).

    Configurable devices include computed tomography (CT) systems, ultrasound systems, anaesthesia systems, physiological Monitoring systems, radiology information systems (RIS).

    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

  6. #743654

    Feistí a astaíonn radaíocht agus a beartaíodh lena n-úsáid sa raideolaíocht dhiagnóiseach, déanfar iad a dhearadh agus a mhonarú sa chaoi go mbeidh cáilíocht na híomhá agus/nó an aschuir iomchuí don úsáid leighis a beartaíodh dóibh agus san am céanna go laghdófar a oiread is féidir an méid radaíochta a nochtar an t-othar agus an t-úsáideoir dó.

    Devices emitting ionising radiation intended for diagnostic radiology shall be designed and manufactured in such a way as to achieve an image and/or output quality that are appropriate to the intended medical purpose whilst minimising radiation exposure of the patient and user.

    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

  7. #743655

    Feistí a astaíonn radaíocht ianúcháin agus a beartaíodh lena n-úsáid sa raideolaíocht theiripeach, dearfar agus monarófar iad sa chaoi go bhféadfar faireachán agus rialú iontaofa a dhéanamh ar an dáileog atáthar a thabhairt, ar chineál an léis, ar fhuinneamh léis agus, i gcás inarb iomchuí, ar cháilíocht na radaíochta.

    Devices that emit ionising radiation and are intended for therapeutic radiology shall be designed and manufactured in such a way as to enable reliable monitoring and control of the delivered dose, the beam type, energy and, where appropriate, the quality of radiation.

    Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance. )

  8. #1335193

    (b) beirt daoine eile a cheapfaidh Coláiste Ríoga na Máinleá in Éirinn, a gceapfar duine acu mar ionadaí do speisialtachtaí na máinliachta, agus a gceapfar an duine eile mar ionadaí do speisialtachtaí na n-anaestéiseachtaí agus na raideolaíochta le chéile;

    ( b ) two other persons appointed by the Royal College of Surgeons in Ireland, of whom one shall be appointed to represent the surgical specialties, and the other shall be appointed to represent jointly the specialties of anaesthetics and radiology;

    Number 4 of 1978: MEDICAL PRACTITIONERS ACT, 1978