{"answer_id":"praxikon:eu:ai-act:answer:zorg-medische-ai","canonical_page":"https://www.praxikon.com/en/antwoord/zorg-medische-ai","query":"We use AI in healthcare. Which AI Act rules apply there?","lang":"en","view":"full","mode":"scenario","question":"We use AI in healthcare. Which AI Act rules apply there?","situation":"AI in a healthcare context, from triage and administrative support to AI in or around medical devices.","likely_role":"Deployer (healthcare organisation)","note":"Healthcare has two routes: AI under the medical device rules follows Annex I (from 2 August 2028), other use cases such as emergency call triage fall under Annex III (from 2 December 2027). AI literacy for healthcare staff applies now.","matched_terms":[],"dataset":{"id":"praxikon:sys:registry:dataset:ai-act-implementation-graph","version":"2.2.0","schema_version":"1.5.0","effective_at":"2026-08-08T00:00:00.000Z","known_at":"2026-09-06T00:00:00.000Z","last_reviewed_at":"2026-08-08T00:00:00.000Z","licence":"https://www.praxikon.com/nl/legal/terms","canonical_url":"https://www.praxikon.com/api/v1/entities"},"obligations":[{"slug":"article-26-deployer-obligations","label":"Article 26: obligations of deployers of high-risk AI systems","summary":"Twelve paragraphs governing day-to-day use: use in line with the instructions, human oversight by competent people, input data, monitoring and notification, log retention, informing workers before deployment, registration by public authorities and informing the people about whom decisions are made.","legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","high_risk_regime_from":null,"human_page":"https://www.praxikon.com/en/verplichtingen/article-26-deployer-obligations","api":"https://www.praxikon.com/api/v1/obligations?lang=en","official_source":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","citations":[{"kind":"official_fact","statement":"Article 26 imposes twelve paragraphs on deployers of high-risk AI systems. Paragraph 1 requires appropriate technical and organisational measures to ensure use in accordance with the accompanying instructions for use. Paragraph 2 requires assigning human oversight to natural persons who have the necessary competence, training and authority, as well as the necessary support. Paragraph 3 leaves other obligations and the freedom to organise one's own resources unaffected. Paragraph 4 requires, to the extent the deployer exercises control over the input data, that such data is relevant and sufficiently representative in view of the intended purpose. Paragraph 5 requires monitoring on the basis of the instructions for use and informing the provider in accordance with Article 72; where there is reason to consider that use may result in a risk within the meaning of Article 79(1), the deployer shall without undue delay inform the provider or distributor and the relevant market surveillance authority and suspend use, and upon identifying a serious incident shall immediately inform first the provider and then the importer or distributor and the market surveillance authorities. Paragraph 6 requires keeping the automatically generated logs under the deployer's control for a period appropriate to the intended purpose and of at least six months, unless Union or national law provides otherwise. Paragraph 7 requires deployers who are employers to inform workers' representatives and the affected workers, before putting into service or using the system at the workplace, that they will be subject to its use. Paragraph 8 imposes the registration obligations of Article 49 on public authorities and Union institutions, bodies, offices and agencies and prohibits use of a system not registered in the EU database referred to in Article 71. Paragraph 9 links the information provided under Article 13 to the data protection impact assessment under Article 35 of Regulation (EU) 2016/679. Paragraph 10 sets additional conditions for post-remote biometric identification in law enforcement. Paragraph 11 opens with the words without prejudice to Article 50 of this Regulation and requires deployers of Annex III systems that make or assist in making decisions related to natural persons to inform those persons that they are subject to the use of the system; for high-risk AI systems used for law enforcement purposes Article 13 of Directive (EU) 2016/680 applies. The transparency obligations of Article 50 have applied since 2 August 2026 and are separate from the date on which paragraph 11 starts to apply. Paragraph 12 requires cooperation with the competent authorities.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 26(1)-(12)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"kind":"editorial_interpretation","statement":"The 2 December 2027 date invites postponement, but two elements are preparation work today. Paragraph 7 requires you to inform workers' representatives and the affected workers before the system is put into service at the workplace, and that information is provided, where applicable, in line with existing rules and practice on informing workers. That touches employee participation, and such a process takes months rather than weeks in practice, so a system that must go live in 2027 is discussed in 2026. Paragraph 2 also connects to the human oversight that Article 14 imposes on system design: you must designate natural persons with competence, training, authority and support. That is emphatically not the same as the measures obligation in Article 4. Article 4 requires measures supporting AI literacy and does not require you to guarantee a particular level for individuals; Article 26(2) requires identifiable overseers with a mandate. Conflating the two leaves you believing a generic e-learning is enough while still having no overseer with room to decide. A third underestimated element is paragraph 11: informing the people about whom an Annex III system makes or helps make decisions is visible customer or candidate communication that you have to design across your own organisation.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 26(1)-(12)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"kind":"recommended_action","statement":"Draw up now a list of the systems likely to qualify as high-risk from 2 December 2027 and add three columns: who exercises human oversight and with what mandate, when you will inform the works council and the affected workers, and how the persons concerned will receive the notice under paragraph 11. Plan the employee participation process a year ahead.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 26(1)-(12)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}]},{"slug":"article-4-ai-literacy","label":"Article 4: AI literacy","summary":"Providers and deployers take measures that support the development of AI literacy.","legal_status":"applicable","deadline_at":"2025-02-02T00:00:00.000Z","high_risk_regime_from":null,"human_page":"https://www.praxikon.com/en/verplichtingen/article-4-ai-literacy","api":"https://www.praxikon.com/api/v1/obligations?lang=en","official_source":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","citations":[{"kind":"official_fact","statement":"Since 27 July 2026, providers and deployers must take measures supporting the development of AI literacy. The provision does not require a guaranteed individual level.","source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amendment of Article 4; entry into force 27 July 2026","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"kind":"editorial_interpretation","statement":"Evidence is primarily a proportionate record of measures by role and context, not one prescribed course or certificate.","source_id":"praxikon:eu:ai-act:source:commission-ai-literacy-qa","source_locator":"Questions on measures, formats, certificates and records","source_url":"https://digital-strategy.ec.europa.eu/en/faqs/ai-literacy-questions-answers","eli":null},{"kind":"recommended_action","statement":"Inventory roles and AI systems, select appropriate measures and record the choice, implementation and periodic review.","source_id":"praxikon:eu:ai-act:source:commission-ai-literacy-qa","source_locator":"Implementation examples and evidence guidance","source_url":"https://digital-strategy.ec.europa.eu/en/faqs/ai-literacy-questions-answers","eli":null}]},{"slug":"annex-iii-high-risk","label":"Annex III: high-risk AI","summary":"Classification route for standalone high-risk AI systems under Article 6(2) and Annex III.","legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","high_risk_regime_from":null,"human_page":"https://www.praxikon.com/en/verplichtingen/annex-iii-high-risk","api":"https://www.praxikon.com/api/v1/obligations?lang=en","official_source":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","citations":[{"kind":"official_fact","statement":"The core rules in Chapter III, Sections 1 to 3, for systems under Article 6(2) and Annex III become applicable on 2 December 2027.","source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 113, Article 6(2) and Annex III application date","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"kind":"editorial_interpretation","statement":"The later application date does not remove the classification question. An early classification record avoids design and procurement decisions without evidence.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 6 and Annex III","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"kind":"recommended_action","statement":"Document now the intended purpose, Annex III point, Article 6(3) assessment, profiling and selected registration path.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 6(2)-(4), Article 49 and Annex III","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}]},{"slug":"article-18-document-retention","label":"Article 18: documentation keeping","summary":"The provider of a high-risk AI system keeps the technical documentation, the quality management system documentation, the changes approved by notified bodies and the decisions they issued, and the EU declaration of conformity at the disposal of the national competent authorities for a period ending ten years after the system has been placed on the market or put into service.","legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","high_risk_regime_from":null,"human_page":"https://www.praxikon.com/en/verplichtingen/article-18-document-retention","api":"https://www.praxikon.com/api/v1/obligations?lang=en","official_source":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","citations":[{"kind":"official_fact","statement":"Paragraph 1 provides that the provider shall, for a period ending 10 years after the high-risk AI system has been placed on the market or put into service, keep at the disposal of the national competent authorities: (a) the technical documentation referred to in Article 11; (b) the documentation concerning the quality management system referred to in Article 17; (c) the documentation concerning the changes approved by notified bodies, where applicable; (d) the decisions and other documents issued by the notified bodies, where applicable; (e) the EU declaration of conformity referred to in Article 47. Paragraph 2 provides that each Member State shall determine conditions under which that documentation remains at the disposal of the national competent authorities for the period indicated for the cases when a provider or its authorised representative established on its territory goes bankrupt or ceases its activity prior to the end of that period. Paragraph 3 provides that providers that are financial institutions subject to requirements regarding their internal governance, arrangements or processes under Union financial services law shall maintain the technical documentation as part of the documentation kept under the relevant Union financial services law.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"kind":"official_fact","statement":"The amended application dates for Chapter III, Sections 1, 2 and 3, with the exception of Article 6(5), are 2 December 2027 for the standalone Annex III route and 2 August 2028 for high-risk AI in products covered by the Annex I harmonisation legislation.","source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 113 application dates","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"kind":"editorial_interpretation","statement":"Four things here are our reading and not the text. First the application date: Regulation (EU) 2026/1744 does not name Article 18 separately, so the fact that this duty moves with 2 December 2027 and 2 August 2028 follows from its placement in Chapter III, Section 3, and not from an explicit provision. Second the starting moment. Paragraph 1 names the placing on the market and the putting into service side by side without choosing, and for a system where both moments occur that is years of difference at the end of the period. Counting from the later moment is the only count that falls short under neither reading, and that is what we would advise a provider. The other reading is defensible: in Union product law the placing on the market is usually the moment that counts, and then the period ends earlier. Third a substantially modified version: the text is silent, and it is equally defensible that every version gets its own period as that the original one continues. Fourth the reach of paragraph 3: it names only the technical documentation, so we keep points (b) to (e) under the general regime until the contrary is settled. Paragraph 2, finally, is addressed to the Member State and not to you. The Netherlands has not yet determined those conditions, so what happens to your file on insolvency or cessation of activity currently follows from contract and not from law.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"kind":"recommended_action","statement":"Designate per high-risk system one place of retention where the five components of paragraph 1 come together. Record side by side when the system was placed on the market and when it was put into service, and calculate the end date from the later of those two moments, so that you do not fall short under either reading. Set that end date as a commitment in a system that survives a change of staff, and keep the Article 19 logs separately with their own period. If you work with an authorised representative, record who holds which copy, because Article 22(3)(b) places the same availability on them as well. When procuring a high-risk system, put in the contract what happens to the documentation if the supplier stops or goes bankrupt, because paragraph 2 leaves that arrangement to national law that does not yet exist in the Netherlands.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 18(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}]},{"slug":"article-13-instructions","label":"Article 13: transparency towards deployers","summary":"Comprehensible instructions for use and system information so deployers can operate the system correctly.","legal_status":"upcoming","deadline_at":"2027-12-02T00:00:00.000Z","high_risk_regime_from":null,"human_page":"https://www.praxikon.com/en/verplichtingen/article-13-instructions","api":"https://www.praxikon.com/api/v1/obligations?lang=en","official_source":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","citations":[{"kind":"official_fact","statement":"Article 13 requires high-risk systems to be designed transparently enough for deployers to interpret and use the output, with instructions covering purpose, accuracy, limitations, human oversight and maintenance.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 13(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"kind":"official_fact","statement":"For the Annex III route this requirement applies from 2 December 2027; for high-risk AI in regulated products (Annex I) from 2 August 2028.","source_id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","source_locator":"Amended Article 113 application dates","source_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj"},{"kind":"editorial_interpretation","statement":"The instructions are the hinge between provider and deployer duties: what the provider fails to supply here, the deployer cannot deliver under Article 26. Ask for it explicitly at procurement.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 13(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"},{"kind":"recommended_action","statement":"Translate received instructions per system into internal work instructions per role and record who received them.","source_id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","source_locator":"Article 13(1)-(3)","source_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj"}]}],"conditional":[{"slug":"article-61-informed-consent","id":"praxikon:eu:ai-act:obligation:article-61-informed-consent","label":"Article 61: informed consent of test subjects for testing in real world conditions","status":"possibly_applies","source_locator":"Article 60(4), point (i), with Article 61(1)","addressee":"reader","human_page":"https://www.praxikon.com/en/verplichtingen/article-61-informed-consent"}],"sources":[{"id":"praxikon:eu:ai-act:source:reg-eu-2024-1689","title":"EU Artificial Intelligence Act 2024/1689","publisher":"European Parliament and Council","canonical_url":"https://eur-lex.europa.eu/eli/reg/2024/1689/oj","eli":"http://data.europa.eu/eli/reg/2024/1689/oj","source_version":"original-oj-2024-07-12","verified_at":"2026-08-08T00:00:00.000Z"},{"id":"praxikon:eu:ai-act:source:reg-eu-2026-1744","title":"Digital Omnibus on AI 2026/1744","publisher":"European Parliament and Council","canonical_url":"https://eur-lex.europa.eu/eli/reg/2026/1744/oj","eli":"http://data.europa.eu/eli/reg/2026/1744/oj","source_version":"official-journal-2026-07-24","verified_at":"2026-08-08T00:00:00.000Z"},{"id":"praxikon:eu:ai-act:source:commission-ai-literacy-qa","title":"AI literacy questions and answers","publisher":"European Commission","canonical_url":"https://digital-strategy.ec.europa.eu/en/faqs/ai-literacy-questions-answers","eli":null,"source_version":"updated-2026-07-27","verified_at":"2026-08-08T00:00:00.000Z"},{"id":"praxikon:eu:ai-act:source:commission-draft-high-risk-classification-guidelines","title":"Draft guidelines on the classification of high-risk AI systems","publisher":"European Commission (AI Office)","canonical_url":"https://digital-strategy.ec.europa.eu/en/library/draft-commission-guidelines-classification-high-risk-ai-systems","eli":null,"source_version":"draft-for-consultation-2026-05-19","verified_at":"2026-08-08T00:00:00.000Z"},{"id":"praxikon:eu:ai-act:source:iso-iec-jtc1-sc42","title":"ISO/IEC JTC 1/SC 42: international standards for artificial intelligence","publisher":"ISO/IEC JTC 1/SC 42","canonical_url":"https://www.iso.org/committee/6794475.html","eli":null,"source_version":"catalogue-checked-2026-08-08","verified_at":"2026-08-08T00:00:00.000Z"}],"first_actions":[{"label":"Assign human oversight and give those people a mandate","summary":"Name, per high-risk system, who exercises oversight, and ensure that person has the competence, training, authority and support to actually set the output aside."},{"label":"Take role- and context-specific AI literacy measures","summary":"Determine for each role, system and context which combination of instruction, guidance, practice or training is appropriate."},{"label":"Justify the Article 6(3) exception against each individual condition","summary":"Name which of the four Article 6(3) conditions you invoke, with facts, and separately justify why the system poses no significant risk of harm to health, safety or fundamental rights and does not materially influence the outcome of decision making."}],"evidence":[{"label":"Deployment dossier: logs, worker information and information to affected persons","summary":"The dossier that shows you retain the logs, that you informed workers and their representatives in time, and that the people about whom decisions are made are aware of it.","url":null},{"label":"AI literacy measures record","summary":"Versioned record of roles, context, measures, participation or instruction and review moments.","url":null},{"label":"Article 49(2) registration record for the system assessed as not high-risk","summary":"Proof that the system for which you invoke the Article 6(3) exception is registered as Article 49(2) requires, with the registration number linked to the underlying assessment.","url":null}],"guidance":[{"label":"No mandatory course format, no certificate, no exam and no AI officer","statement":"The Commission Q&A on AI literacy states that there is no one size fits all when it comes to AI literacy and that no strict requirements or mandatory trainings are imposed. On certification, the Q&A states literally that there is no need for a certificate and that organisations can keep an internal record of trainings or other guiding initiatives. On assessment, it states that Article 4 of the AI Act does not entail an obligation to measure the AI knowledge of employees. On governance, it states that no specific governance structure is mandated to comply with Article 4, so that unlike the data protection officer under the GDPR, no AI officer needs to be appointed. On the level, the Q&A states that following the Digital Omnibus amendment AI literacy remains an obligation for providers and deployers of AI systems, but that no specific or sufficient level is mandated and that the Regulation does not require guaranteeing any specific level of AI literacy of any individual. Against that, the Q&A states that simply relying on the AI systems' instructions for use or asking staff to read them might be ineffective, and that organisations should take into account general AI understanding within the organisation, whether they are a provider or a deployer, the risks associated with the systems deployed, staff knowledge gaps considering technical knowledge, experience, education and training, and contextual factors such as sector, purpose and affected populations. The Q&A further states that organisations may implement different levels of training or learning approaches depending on knowledge, experience, education and role, and that staff with a degree or experience in AI development are normally considered AI literate, while the organisation must still verify that those persons understand the specific AI systems of the organisation, know how to deal with them and are aware of all risks.","source_locator":"Commission Q&A on AI literacy, sections on required level, training formats, certificates, assessment of knowledge and governance structures (consulted 9 August 2026)"},{"label":"Article 4 reaches beyond your own staff, and the national supervisor enforces it","statement":"The Commission Q&A on AI literacy states that Article 4 applies to providers and deployers of AI systems and in addition to other persons dealing with the operation and use of AI systems on their behalf, covering persons broadly within the organisational remit, with a contractor, a service provider and a client given as examples. On clients, the Q&A states that they may need AI literacy depending on the specific risk, reasoning that affected persons should understand how decisions taken with the assistance of AI will have an impact on them. On geographic scope, the Q&A states that the AI Act's legal framework applies to both public and private actors inside and outside the EU as long as the AI system is placed on the Union market, used in the Union, or its use has an impact on people located in the EU. On supervision, the Q&A states that the supervision and enforcement of Article 4 is not with the AI Office but under the remit of national market surveillance authorities, and that supervision and enforcement began on 2 August 2026, while Article 4 itself entered into application on 2 February 2025. On sanctions, the Q&A states that national market surveillance authorities could impose penalties and other enforcement measures for infringements of Article 4, that this will be based on national laws that Member States were due to adopt by 2 August 2025, that any sanction must be proportionate and based on the individual case taking into account factors such as the nature and gravity of the infringement and its intentional or negligent character, and that sanctions are more likely if there is proof of an incident due to a lack of appropriate training and guidance. Article 4 is not listed in the enumeration in Article 99(4) of the AI Act, which covers only Articles 16, 22, 23, 24, 26, 31, 33(1), (3) and (4), 34 and 50, so the level of any penalty for Article 4 follows from national law rather than from the Regulation's own ceilings. The Q&A further states that Article 4 reinforces the transparency provisions of Article 13 and the human oversight provisions of Article 14 and indirectly contributes to the protection of affected persons, and that for deployers of high-risk systems the Article 26 obligation to ensure staff are trained to ensure human oversight is a distinct requirement; that requirement becomes applicable on 2 December 2027 for standalone Annex III systems and on 2 August 2028 for Annex I systems.","source_locator":"Commission Q&A on AI literacy, sections on target groups, geographic scope, supervision and enforcement, and sanctions (consulted 9 August 2026)"},{"label":"Article 6 has two separate routes to high-risk","statement":"The European Commission's draft guidelines on the classification of high-risk AI of 19 May 2026, which are expressly non-binding, state in paragraph (7) that an AI system is high-risk in two scenarios: first, where it is intended to be used as a safety component of a product, or is itself a product, covered by the Union harmonisation legislation listed in Annex I and required to undergo third-party conformity assessment; and second, where it falls within one of the use cases in the areas listed in Annex III. Paragraph (448) of those same draft guidelines notes that the Article 113 application dates have been postponed by the AI Omnibus to 2 December 2027 for the Article 6(2) route and 2 August 2028 for the Article 6(1) route.","source_locator":"Draft guidelines on high-risk AI classification (19 May 2026), General principles chapter, section II, paragraph (7); section V, paragraph (448)"},{"label":"Broadly positioned and general purpose AI systems: a disclaimer is not enough","statement":"According to the non-binding draft guidelines of 19 May 2026 on the classification of high-risk AI, paragraph (12) provides that where the instructions for use, contractual arrangements, terms of service, usage policy, promotional and sales materials or technical documentation present the AI system as broadly applicable across a generality of contexts and functions, and do not consistently limit its application or exclude high-risk uses, the system's intended purpose will be deemed to also encompass high-risk use cases and therefore qualify as high-risk. Under these draft guidelines this applies in particular where such uses are feasible and reasonably foreseeable given the system's functionalities and capabilities. The same paragraph states that merely asserting, for example in the terms of service, that high-risk uses are excluded is insufficient where the provider's overall presentation, examples or product positioning effectively provides for or promotes such uses, and that any limitations of use must be described clearly, concretely and coherently across all materials.","source_locator":"Draft guidelines on high-risk AI classification (19 May 2026), General principles chapter, section II.2, paragraph (12)"}],"examples":[{"label":"Lawyers learn the technology, developers learn the law","situation":"Dedalus Healthcare, which among other things supplies AI that predicts complications for hospital patients, trains its legal staff, data protection officer, compliance function and quality and regulatory affairs department on the technical side. Developers and engineers conversely receive training focused on the legal and compliance aspects of the AI Act. The executive committee received its own session tailored to its role.","outcome":"This practice was submitted by the organisation itself to the Commission living repository. The repository collects and shares practices; it does not approve them or set them as a standard.","lesson":"Look for knowledge deliberately outside a single discipline, because the repository names collaboration between industry and academia as one of the ways organisations build AI literacy.","source_locator":"Living repository of AI literacy practices, practice submitted by the organisation concerned","provenance":"official"},{"label":"Expert system that draws a conclusion from encoded knowledge","situation":"A hospital uses an older diagnostic support expert system in which physicians encoded knowledge, facts and rules. Based on the symptoms a doctor enters, the system independently draws a conclusion about possible conditions.","outcome":"The Commission guidelines on the definition of an AI system use this case to draw the line between software that does and does not fall under the regulation. The document is non-binding.","lesson":"Machine learning is not a requirement, so you cannot argue that your system merely applies rules encoded by experts; logic and knowledge based systems that draw conclusions on their own are covered too.","source_locator":"Commission Guidelines C(2025) 5053 final, 29.7.2025, borderline cases under the definition in Article 3(1)","provenance":"official"},{"label":"Chatbot answering factual questions from a benefits case handler","situation":"A chatbot answers a case handler's factual questions relating to the evaluation of a natural person's application for healthcare benefits, for instance the applicant's age. The case handler can grant or deny the benefits based on those answers.","outcome":"The Commission draft guidelines of 19 May 2026 address this case when determining whether an application falls under Annex III. The document is a consultation version: non-binding and not yet final.","lesson":"A chatbot that only returns existing facts in structured form falls under the exemption, but once it answers case-specific legal questions it steers the decision and is high-risk.","source_locator":"Draft guidelines on high-risk AI classification, 19 May 2026, annex on Annex III","provenance":"official"},{"label":"Emergency triage system: two routes to high risk","situation":"A hospital uses AI to prioritise incoming patients at the emergency department. The question is not whether the system is high-risk but by which route: as a medical device under product legislation, or directly under Annex III.","outcome":"The Commission draft guidelines of 19 May 2026 state that an emergency healthcare patient triage system may qualify as a medical device; where it then meets Article 6(1), it is high-risk via Annex I and sectoral rules apply. A triage system that is not a medical device is high-risk via Article 6(2) and point 5(d) of Annex III. The document is a consultation version: non-binding and not yet final.","lesson":"First establish whether your triage system is a medical device, because that question decides the whole route: via Annex I the assessment travels with the medical conformity assessment and its date, via Annex III the separate timeline of Article 6(2) applies. Either way the outcome is high-risk, so postponing that determination only creates uncertainty about which regime to set up.","source_locator":"Draft guidelines on high-risk AI classification, 19 May 2026, annex on Annex III, paragraphs (334) and (335)","provenance":"official"}],"standards":[{"label":"ISO/IEC 12792: transparency taxonomy of AI systems","summary":"The international taxonomy of transparency information elements, usable as a checklist for the Article 13 instructions for use.","statement":"ISO/IEC 12792:2025 (Information technology: Artificial intelligence: Transparency taxonomy of AI systems) was published in November 2025 by ISO/IEC JTC 1/SC 42. It specifies a taxonomy of information elements to help stakeholders identify and address transparency needs, and describes the semantics of those elements and their relevance to different stakeholders' objectives. The text was adopted as a European standard as EN ISO/IEC 12792:2025. It is not cited in the Official Journal and therefore confers no presumption of conformity under Article 40. For Article 13 the designated deliverable is prEN 18229-3."}],"definitions":[],"answer_page":"https://www.praxikon.com/en/antwoord/zorg-medische-ai","follow_up_questions":[{"question":"We use AI to monitor or evaluate employees. What applies?","url":"https://www.praxikon.com/en/antwoord/werknemers-monitoren"},{"question":"What are a deployer’s obligations under Article 26?","url":"https://www.praxikon.com/en/antwoord/artikel-26-deployer-plichten"},{"question":"How do we set up human oversight of AI?","url":"https://www.praxikon.com/en/antwoord/menselijk-toezicht"}],"disclaimer":"General interpretation, not legal advice. The official source remains authoritative.","methodology":"https://www.praxikon.com/en/methodologie"}