Implantable medical devices, active implantable medical devices and class III devices must be subject to clinical investigations, unless the use of existing clinical data can be duly justified.
Home | French Legislation Articles | Part five: Health products | Book II: Medical devices, in vitro diagnostic medical devices and other products and articles regulated in the interests of public health | Title I: Medical devices | Chapter I: Legal status of medical devices | Section 6: Conformity certification procedures | Subsection 3: Procedure for medical devices subject to evaluation of clinical data or clinical investigations. | Paragraph 2: Clinical investigations | Article R5211-36-2 of the French Public Health Code
Implantable medical devices, active implantable medical devices and class III devices must be subject to clinical investigations, unless the use of existing clinical data can be duly justified.
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is a Registered Trademark of
PETROFF LAW FIRM (SELARL LEGASTRAT)
182, rue de Rivoli
75001, Paris France
RCS Paris n°814433470
Paris Bar Registration n° (Toque) C2396
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