Directive 2000/70/EC
E1342268
UNEXPLORED
Directive 2000/70/EC is a European Union legislative act that updated and strengthened the regulatory framework for medical devices, particularly those incorporating stable derivatives of human blood or human plasma, within the scope of Council Directive 93/42/EEC.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Directive 2000/70/EC canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T18750449 — 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 2000/70/EC Context triple: [Council Directive 93/42/EEC, amendedBy, Directive 2000/70/EC]
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A.
Directive 2001/82/EC
Directive 2001/82/EC is a key European Union law that sets out the rules for the authorization, supervision, and pharmacovigilance of veterinary medicinal products across EU member states.
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B.
Directive 2002/58/EC
Directive 2002/58/EC is a European Union directive that sets out rules on privacy and data protection in the electronic communications sector, complementing the broader EU data protection framework.
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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 2007/64/EC
Directive 2007/64/EC is a European Union directive that established a harmonized legal framework for payment services within the EU, promoting competition, transparency, and consumer protection in the payments market.
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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 2000/70/EC Target entity description: Directive 2000/70/EC is a European Union legislative act that updated and strengthened the regulatory framework for medical devices, particularly those incorporating stable derivatives of human blood or human plasma, within the scope of Council Directive 93/42/EEC.
-
A.
Directive 2001/82/EC
Directive 2001/82/EC is a key European Union law that sets out the rules for the authorization, supervision, and pharmacovigilance of veterinary medicinal products across EU member states.
-
B.
Directive 2002/58/EC
Directive 2002/58/EC is a European Union directive that sets out rules on privacy and data protection in the electronic communications sector, complementing the broader EU data protection framework.
-
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 2007/64/EC
Directive 2007/64/EC is a European Union directive that established a harmonized legal framework for payment services within the EU, promoting competition, transparency, and consumer protection in the payments market.
-
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