Regulation (EU) 2017/745
E1341291
UNEXPLORED
Regulation (EU) 2017/745 is the European Union’s comprehensive Medical Device Regulation that modernizes and strengthens the regulatory framework for medical devices across EU member states.
All labels observed (3)
| Label | Occurrences |
|---|---|
| Regulation (EU) 2017/745 on medical devices | 3 |
| Regulation (EU) 2017/745 canonical | 2 |
| Medical Devices Regulation (EU) 2017/745 | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T18750456 — 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: Regulation (EU) 2017/745 Context triple: [Council Directive 93/42/EEC, repealedBy, Regulation (EU) 2017/745]
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A.
Regulation (EU) 2019/942
Regulation (EU) 2019/942 is an EU legislative act that establishes and governs the mandate, powers, and functioning of the Agency for the Cooperation of Energy Regulators (ACER) within the internal energy market.
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B.
Regulation (EU) 2017/746 on in vitro diagnostic medical devices
Regulation (EU) 2017/746 on in vitro diagnostic medical devices is the European Union’s comprehensive legal framework governing the safety, performance, and market access of in vitro diagnostic medical devices.
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C.
Regulation (EU) No 536/2014
Regulation (EU) No 536/2014 is the European Union’s main legal framework governing the conduct, authorization, and oversight of clinical trials on medicinal products for human use.
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D.
Regulation (EU) No 1025/2012
Regulation (EU) No 1025/2012 is an EU legal framework that governs European standardization activities, defining how standards are developed, adopted, and used to support EU policies and the internal market.
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E.
Regulation (EU) No 1307/2013
Regulation (EU) No 1307/2013 is a key European Union law that lays down rules for direct payments to farmers under the Common Agricultural Policy, including the structure and conditions of the Basic Payment Scheme.
- 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: Regulation (EU) 2017/745 Target entity description: Regulation (EU) 2017/745 is the European Union’s comprehensive Medical Device Regulation that modernizes and strengthens the regulatory framework for medical devices across EU member states.
-
A.
Regulation (EU) 2019/942
Regulation (EU) 2019/942 is an EU legislative act that establishes and governs the mandate, powers, and functioning of the Agency for the Cooperation of Energy Regulators (ACER) within the internal energy market.
-
B.
Regulation (EU) 2017/746 on in vitro diagnostic medical devices
Regulation (EU) 2017/746 on in vitro diagnostic medical devices is the European Union’s comprehensive legal framework governing the safety, performance, and market access of in vitro diagnostic medical devices.
-
C.
Regulation (EU) No 536/2014
Regulation (EU) No 536/2014 is the European Union’s main legal framework governing the conduct, authorization, and oversight of clinical trials on medicinal products for human use.
-
D.
Regulation (EU) No 1025/2012
Regulation (EU) No 1025/2012 is an EU legal framework that governs European standardization activities, defining how standards are developed, adopted, and used to support EU policies and the internal market.
-
E.
Regulation (EU) No 1307/2013
Regulation (EU) No 1307/2013 is a key European Union law that lays down rules for direct payments to farmers under the Common Agricultural Policy, including the structure and conditions of the Basic Payment Scheme.
- F. None of above. chosen
Referenced by (6)
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
subject linked to:
Council Directive 93/42/EEC on medical devices
linked to: Regulation (EU) 2017/745
linked to: Regulation (EU) 2017/745
Regulation (EU) 2017/746 on in vitro diagnostic medical devices
→
relatedTo
→
Regulation (EU) 2017/745 on medical devices
ⓘ
linked to: Regulation (EU) 2017/745
subject linked to:
Council Directive 90/385/EEC on active implantable medical devices
linked to: Regulation (EU) 2017/745