CNSP / MSP/P/AS DécretDécret n°2025-149/P/CNSP/MSP/P/AS
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
Décret n°2025-149/P/CNSP/MSP/P/AS is the official CNSP / MSP/P/AS identifier for “Modalités d'application de la loi n°2022-34 du 11 juillet 2022 — dispositions relatives aux dispositifs médicaux”. Décret n°2025-149/P/CNSP/MSP/P/AS is the official identifier CNSP / MSP/P/AS uses for this instrument.
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Modalités d'application de la loi n°2022-34 du 11 juillet 2022 — dispositions relatives aux dispositifs médicaux
Selected original physical pages 1, 71–73 and 143 of the 143-page official ampliation of Decree 2025-149 of 18 March 2025. Articles 353–358 include devices in other-health-product authorization, establishment, good-practice, inspection and AMM provisions; Article 365 provides device declaration, a ministerial homologation list and essential-requirement assessment. Operative comparison with already registered Order 633 and annex confirms device declaration, homologation, dossier and essential-requirement rules, while the actual homologation list and Annex V declaration form remain unverified. Order 377 Article 7 expressly implements the responsible pharmacist authority, resources and QMS duty in parent Article 92, separately read on original physical page 30. This does not turn the five-page published expression into a full 143-page transcription. Transitional actor wording and general repeal remain as printed; Gazette publication and later currentness remain unverified.
Décret n°2025-149/P/CNSP/MSP/P/AS is the official identifier CNSP / MSP/P/AS uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.