Directive 2003/12/EC
E1342269
UNEXPLORED
Directive 2003/12/EC is a European Union legislative act that updates and refines the regulatory framework for medical devices established under Council Directive 93/42/EEC.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Directive 2003/12/EC canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T18750451 — 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 2003/12/EC Context triple: [Council Directive 93/42/EEC, amendedBy, Directive 2003/12/EC]
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A.
Directive 2003/4/EC
Directive 2003/4/EC is a European Union law that guarantees public access to environmental information held by public authorities, implementing the Aarhus Convention’s access-to-information pillar.
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B.
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.
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C.
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setting prudential and supervision rules for institutions for occupational retirement provision (IORPs) before being updated and replaced by the IORP II Directive.
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D.
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.
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E.
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.
- 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 2003/12/EC Target entity description: Directive 2003/12/EC is a European Union legislative act that updates and refines the regulatory framework for medical devices established under Council Directive 93/42/EEC.
-
A.
Directive 2003/4/EC
Directive 2003/4/EC is a European Union law that guarantees public access to environmental information held by public authorities, implementing the Aarhus Convention’s access-to-information pillar.
-
B.
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.
-
C.
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.
-
D.
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.
-
E.
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.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.
subject linked to:
Council Directive 93/42/EEC on medical devices