Triple
T18842096
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Regulation (EU) 2017/746 on in vitro diagnostic medical devices |
E460822
|
entity |
| Predicate | shortName |
P43
|
FINISHED |
| Object | In Vitro Diagnostic Medical Devices Regulation |
—
|
NE NERFINISHED |
How this triple was built (2 steps)
Every LLM step that produced this triple, in pipeline order — named-entity classification, the disambiguation choices (the exact options shown, with the pick highlighted), and the generated description. The batch + timestamp of each is in the Provenance table below.
NER
Named-entity recognition
gpt-5-mini
Instruction
Given a phrase, classify it is english named entity (e.g., persons, organizations, works of art) in Latin script, or not (e.g., literals, dates, URLs, verbose phrases). For disambiguation, the statement where the phrase occurs as object is also given. Please return a JSON object with `phrase` (string, the phrase being analyzed) and `is_ne` (boolean, indicating whether the phrase is a Named Entity).
Input
Phrase: In Vitro Diagnostic Medical Devices Regulation | Statement: [Regulation (EU) 2017/746 on in vitro diagnostic medical devices, shortName, In Vitro Diagnostic Medical Devices Regulation]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: In Vitro Diagnostic Medical Devices Regulation Context triple: [Regulation (EU) 2017/746 on in vitro diagnostic medical devices, shortName, In Vitro Diagnostic Medical Devices Regulation]
-
A.
Regulation (EU) 2017/746 on in vitro diagnostic medical devices
chosen
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.
-
B.
Directive 98/79/EC on in vitro diagnostic medical devices
Directive 98/79/EC on in vitro diagnostic medical devices was an EU legal framework that set safety, performance, and conformity requirements for in vitro diagnostic medical devices placed on the European market.
-
C.
Regulation (EU) 2017/745
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.
-
D.
Council Directive 93/42/EEC on medical devices
Council Directive 93/42/EEC on medical devices was a key European Union legislative framework that set essential safety and performance requirements for medical devices marketed within the EU.
-
E.
European Union medical device regulations
European Union medical device regulations are a comprehensive set of legal and technical requirements governing the safety, performance, quality management, and market approval of medical devices within EU member states.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Provenance (2 batches)
The batch behind each pipeline step, in order, with when it ran. Timestamps are batch-level — stages were processed in waves, so the object chain (NER → NED1 → NEDg → NED2) reads in order, but predicate / elicitation batches can sit in a different wave.
| Step | Stage | Batch ID | Status | When |
|---|---|---|---|---|
| creating | Elicitation | batch_69d8dcfa11e4819090ab1ef5bdcd2b2e |
completed | April 10, 2026, 11:20 a.m. |
| NER | Named-entity recognition | batch_69e5b8eb32548190b2313e877f6ff179 |
completed | April 20, 2026, 5:26 a.m. |
Created at: April 10, 2026, 11:56 a.m.