Directive 2010/53/EU
E624793
Directive 2010/53/EU is a European Union law that sets common standards for the quality and safety of human organs intended for transplantation across EU member states.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Directive 2010/53/EU canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T6769666 — resolving that mention is where its identity was fixed. The disambiguator weighed these candidate entities and picked the highlighted one (or “None”, minting a new entity). This is how homonymy is resolved: the same surface form can point to different entities.
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Directive 2010/53/EU Context triple: [EU Organ Donation Directive, shortName, Directive 2010/53/EU]
-
A.
Directive 2009/147/EC
Directive 2009/147/EC is a key European Union law on the conservation of wild birds, forming one of the main legal pillars of the Natura 2000 protected areas network.
-
B.
Directive 2006/17/EC
Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
-
C.
Directive 2004/23/EC
Directive 2004/23/EC is a key European Union law that sets quality and safety standards for the donation, procurement, testing, processing, preservation, storage, and distribution of human tissues and cells for medical use.
-
D.
Directive 2003/41/EC
Directive 2003/41/EC was the original EU framework setting prudential and supervision rules for institutions for occupational retirement provision (IORPs) before being updated and replaced by the IORP II Directive.
-
E.
Directive 2004/24/EC
Directive 2004/24/EC is a European Union law that created a simplified registration and regulatory framework for traditional herbal medicinal products across EU member states.
- F. None of above. chosen
- G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: Directive 2010/53/EU Target entity description: Directive 2010/53/EU is a European Union law that sets common standards for the quality and safety of human organs intended for transplantation across EU member states.
-
A.
Directive 2009/147/EC
Directive 2009/147/EC is a key European Union law on the conservation of wild birds, forming one of the main legal pillars of the Natura 2000 protected areas network.
-
B.
Directive 2006/17/EC
Directive 2006/17/EC is a European Union measure that sets technical requirements for the donation, procurement, and testing of human tissues and cells used for medical purposes.
-
C.
Directive 2004/23/EC
Directive 2004/23/EC is a key European Union law that sets quality and safety standards for the donation, procurement, testing, processing, preservation, storage, and distribution of human tissues and cells for medical use.
-
D.
Directive 2003/41/EC
Directive 2003/41/EC was the original EU framework setting prudential and supervision rules for institutions for occupational retirement provision (IORPs) before being updated and replaced by the IORP II Directive.
-
E.
Directive 2004/24/EC
Directive 2004/24/EC is a European Union law that created a simplified registration and regulatory framework for traditional herbal medicinal products across EU member states.
- F. None of above. chosen
Statements (46)
| Predicate | Object |
|---|---|
| instanceOf | European Union directive ⓘ |
| adoptedBy |
Council of the European Union
ⓘ
European Parliament ⓘ European Parliament and Council of the European Union ⓘ |
| aimsTo |
ensure a high level of human health protection in organ transplantation
ⓘ
facilitate cross‑border exchange of organs within the EU ⓘ set common quality and safety standards for human organs ⓘ |
| appliesTo |
EU Member States
ⓘ
linked to:
Member States of the European Union
|
| concerns | human organs intended for transplantation ⓘ |
| contains |
provisions on data protection in the context of organ donation and transplantation
ⓘ
provisions on inspections and control measures by competent authorities ⓘ provisions on quality and safety requirements for organ characterisation ⓘ |
| excludes | tissues and cells regulated by Directive 2004/23/EC ⓘ |
| geographicalScope | European Union ⓘ |
| implementedBy | national transposition measures of EU Member States ⓘ |
| language | binding in all official languages of the European Union ⓘ |
| legalBasis | Article 168 of the Treaty on the Functioning of the European Union ⓘ |
| legalNature | binding legislative act ⓘ |
| policyArea |
health and safety
ⓘ
organ transplantation ⓘ public health ⓘ |
| principle |
non‑commercialisation of the human body and its parts
ⓘ
respect for donor and recipient anonymity, subject to national law ⓘ voluntary and unpaid organ donation ⓘ |
| regulates |
donation of human organs for transplantation
ⓘ
preservation of human organs for transplantation ⓘ procurement of human organs for transplantation ⓘ testing of human organs for transplantation ⓘ transplantation of human organs ⓘ transport of human organs for transplantation ⓘ |
| relationship |
complements national legislation on organ transplantation
ⓘ
forms part of the EU acquis in the field of health ⓘ |
| requires |
authorization of organ procurement organisations and transplant centres
ⓘ
designation of competent authorities in each Member State ⓘ establishment of national quality programmes for organ donation and transplantation ⓘ information to donors and their families in accordance with national law ⓘ protection of deceased donors ⓘ protection of living donors ⓘ reporting and management of serious adverse events and reactions ⓘ systems for traceability of organs from donor to recipient and vice versa ⓘ training of personnel involved in organ donation and transplantation ⓘ |
| scope | quality and safety of human organs intended for transplantation ⓘ |
| subjectMatter |
conditions for the donation, procurement, testing, preservation, transport and transplantation of human organs
ⓘ
reporting of serious adverse events and reactions related to organ transplantation ⓘ standards of quality and safety for human organs intended for transplantation ⓘ traceability of human organs ⓘ |
How these facts were elicited
The pipeline generated the facts above by prompting gpt-5.1 with this entity's name + description and the instruction below.
Instruction
You are a knowledge base construction expert. Given a subject entity and a description of it, return factual statements that you know for the subject as a JSON list of dictionaries(triples), where keys must be "subject", "predicate" and "object". The number of facts may be very high, between 25 to 50 or more, for very popular subjects. For less popular subjects, the number of facts can be very low, like 5 or 10. # Requirements - If you don't know the subject at all, return an empty list. - If the subject is not a named entity, return an empty list. - Include at least one triple where predicate is "instanceOf". - Do not get too wordy. - Separate several objects into multiple triples with one object.
Input
Subject: Directive 2010/53/EU Description of subject: Directive 2010/53/EU is a European Union law that sets common standards for the quality and safety of human organs intended for transplantation across EU member states.
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.