Directive 93/42/EEC
E1345430
UNEXPLORED
Directive 93/42/EEC is a key European Union legislative act that established harmonized safety and performance requirements for medical devices placed on the EU market.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Directive 93/42/EEC canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T18842174 — 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 93/42/EEC Context triple: [Council Directive 90/385/EEC, amendedBy, Directive 93/42/EEC]
-
A.
Directive 94/45/EC
Directive 94/45/EC is a European Union directive that established the framework for setting up European Works Councils to ensure employees are informed and consulted in companies operating in multiple EU member states.
-
B.
Council Directive 92/43/EEC
Council Directive 92/43/EEC is a key European Union law on the conservation of natural habitats and wild fauna and flora, forming one of the main pillars of EU nature protection policy.
-
C.
Council Directive 79/409/EEC
Council Directive 79/409/EEC was the original European Union legislation establishing comprehensive protection and conservation measures for all wild bird species and their habitats across member states.
-
D.
Directive 98/79/EC
Directive 98/79/EC is a European Union directive that sets regulatory requirements for in vitro diagnostic medical devices to ensure their safety, performance, and free movement within the EU market.
-
E.
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.
- 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 93/42/EEC Target entity description: Directive 93/42/EEC is a key European Union legislative act that established harmonized safety and performance requirements for medical devices placed on the EU market.
-
A.
Directive 94/45/EC
Directive 94/45/EC is a European Union directive that established the framework for setting up European Works Councils to ensure employees are informed and consulted in companies operating in multiple EU member states.
-
B.
Council Directive 92/43/EEC
Council Directive 92/43/EEC is a key European Union law on the conservation of natural habitats and wild fauna and flora, forming one of the main pillars of EU nature protection policy.
-
C.
Council Directive 79/409/EEC
Council Directive 79/409/EEC was the original European Union legislation establishing comprehensive protection and conservation measures for all wild bird species and their habitats across member states.
-
D.
Directive 98/79/EC
Directive 98/79/EC is a European Union directive that sets regulatory requirements for in vitro diagnostic medical devices to ensure their safety, performance, and free movement within the EU market.
-
E.
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.
- 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 90/385/EEC on active implantable medical devices