Triple

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).

Phrase: Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices | Statement: [Council Directive 90/385/EEC, fullName, Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices]

Target entity: Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices
Context triple: [Council Directive 90/385/EEC, fullName, Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices]

• A. Council Directive 90/385/EEC on active implantable medical devices chosen
  Council Directive 90/385/EEC on active implantable medical devices was an EU legal framework that set essential safety and performance requirements for active implantable medical devices such as pacemakers and implantable defibrillators.
• B. 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.
• C. 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.
• D. 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.
• E. 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.
• F. None of above.
• G. Unsure - the case is ambiguous/there is not enough information to decide.