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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 II: In vitro diagnostic medical devices | Chapter I: Legal status of in vitro diagnostic medical devices | Section 6: Conformity certification procedures | Subsection 2: Applicable procedures. | Article R5221-20 of the French Public Health Code

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 II: In vitro diagnostic medical devices
    - Chapter I: Legal status of in vitro diagnostic medical devices
      - Section 6: Conformity certification procedures
        Subsection 2: Applicable procedures.

Article R5221-20 of the French Public Health Code

Article R5221-20 of the French Public Health Code

November 1, 2023
1:09 pm

The manufacturer may instruct his authorised representative to initiate the procedures mentioned in 1°, 2°, 4° and 5° of article R. 5221-19.

Original in French 🇫🇷

Article R5221-20

Le fabricant peut charger son mandataire d’engager les procédures mentionnées aux 1°, 2°, 4° et 5° de l’article R. 5221-19.

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