Medical Devices Ordinance
E1538038
UNEXPLORED
The Medical Devices Ordinance is a Swiss legal framework that regulates the safety, performance, market approval, and post-market surveillance of medical devices in Switzerland.
All labels observed (1)
| Label | Occurrences |
|---|---|
| Medical Devices Ordinance canonical | 1 |
How this entity was disambiguated
This entity first appeared as the object of triple T22457974 — 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: Medical Devices Ordinance Context triple: [Swissmedic, appliesRegulation, Medical Devices Ordinance]
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A.
Medical Device Amendments of 1976
The Medical Device Amendments of 1976 are U.S. legislation that established a comprehensive regulatory framework for the safety and effectiveness of medical devices, including classification, premarket approval, and performance standards.
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B.
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.
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C.
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.
-
D.
Analytical, Diagnostic and Therapeutic Techniques and Equipment
Analytical, Diagnostic and Therapeutic Techniques and Equipment is a broad medical subject category encompassing the tools, procedures, and methods used to detect, analyze, and treat health conditions.
-
E.
MedTech
MedTech is Johnson & Johnson’s medical technology division, focused on developing and providing advanced devices and solutions for surgery, orthopedics, cardiovascular care, and other clinical specialties.
- 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: Medical Devices Ordinance Target entity description: The Medical Devices Ordinance is a Swiss legal framework that regulates the safety, performance, market approval, and post-market surveillance of medical devices in Switzerland.
-
A.
Medical Device Amendments of 1976
The Medical Device Amendments of 1976 are U.S. legislation that established a comprehensive regulatory framework for the safety and effectiveness of medical devices, including classification, premarket approval, and performance standards.
-
B.
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.
-
C.
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.
-
D.
Analytical, Diagnostic and Therapeutic Techniques and Equipment
Analytical, Diagnostic and Therapeutic Techniques and Equipment is a broad medical subject category encompassing the tools, procedures, and methods used to detect, analyze, and treat health conditions.
-
E.
MedTech
MedTech is Johnson & Johnson’s medical technology division, focused on developing and providing advanced devices and solutions for surgery, orthopedics, cardiovascular care, and other clinical specialties.
- F. None of above. chosen
Referenced by (1)
Full triples — surface form annotated when it differs from this entity's canonical label.