Aithris 35
Recital 35
(35) Ba cheart a áireamh ar shonraí pearsanta a bhaineann leis an tsláinte na sonraí uile i ndáil le stádas sláinte ábhair sonraí, ar sonraí iad lena nochtar faisnéis a bhaineann le stádas sláinte coirp nó meabhrach an duine is ábhar de na sonraí, mar atá ag an am, mar a bhí nó mar a bheidh.
Áirítear ar an méid sin faisnéis faoin duine nádúrtha a bailíodh le linn an chláraithe le haghaidh seirbhísí cúraim sláinte nó le linn sholáthar na seirbhísí sin amhail dá dtagraítear i dTreoir 2011/24/AE ó Pharlaimint na hEorpa agus ón gComhairle (9) don duine nádúrtha sin; uimhir, siombal nó mír eolais a shanntar do dhuine nádúrtha le go ndéanfar an duine nádúrtha a shainaithint go huathúil chun críocha sláinte; faisnéis a fhaightear de bharr tástáil nó scrúdú a dhéanamh ar chuid den chorp nó ar shubstaint de chuid an choirp, lena n-áirítear de bharr sonraí géiniteacha agus samplaí bitheolaíocha; agus aon fhaisnéis faoi ghalar, mar shampla, nó faoi mhíchumas, baol galair, stair liachta, cóir chliniciúil, nó staid fhiseolaíoch nó bhithleighis an ábhair sonraí, beag beann ar an bhfoinse as a dtagann sí, mar shampla ó dhochtúir nó ó ghairmí cúram sláinte eile, ó ospidéal, ó fheiste míochaine nó ó thástáil in vitro diagnóiseach.
(35) Personal data concerning health should include all data pertaining to the health status of a data subject which reveal information relating to the past, current or future physical or mental health status of the data subject.
This includes information about the natural person collected in the course of the registration for, or the provision of, health care services as referred to in Directive 2011/24/EU of the European Parliament and of the Council [9] to that natural person; a number, symbol or particular assigned to a natural person to uniquely identify the natural person for health purposes; information derived from the testing or examination of a body part or bodily substance, including from genetic data and biological samples; and any information on, for example, a disease, disability, disease risk, medical history, clinical treatment or the physiological or biomedical state of the data subject independent of its source, for example from a physician or other health professional, a hospital, a medical device or an in vitro diagnostic test.
(9) Treoir 2011/24/AE ó Pharlaimint na hEorpa agus ón gComhairle an 9 Márta 2011 maidir le cearta othar i gcúram sláinte trasteorann a chur i bhfeidhm (IO L 88, 4.4.2011, lch. 45). https://eur-lex.europa.eu/legal-content/EN/AUTO/?uri=OJ:L:2011:088:TOC
[9] Directive 2011/24/EU of the European Parliament and of the Council of 9 March 2011 on the application of patients’ rights in cross-border healthcare (OJ L 88, 4.4.2011, p. 45). https://eur-lex.europa.eu/legal-content/EN/AUTO/?uri=OJ:L:2011:088:TOC
The latest consolidated version of the Regulation with corrections by Corrigendum, OJ L 127, 23.5.2018, p. 2 ((EU) 2016/679). Source: EUR-lex.