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AMMPS Réf.

Réf. DE ER DM/01, édition 9

Checklist d'enregistrement des dispositifs médicaux
MoroccoDivision Enregistrement des Médicaments et des Produits de Santé, AMMPSRegistration
What this code is

Réf. DE ER DM/01, édition 9 is the official AMMPS identifier for “Checklist d'enregistrement des dispositifs médicaux”. Réf. DE ER DM/01, édition 9 is the official identifier AMMPS uses for this instrument.

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Réf.
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Réf. DE ER DM/01, édition 9
Category
Registration
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French
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
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About this regulation

Checklist d'enregistrement des dispositifs médicaux

Checklist d'enregistrement des dispositifs médicaux, Réf. DE ER DM/01, édition 9 — the form a device registration file is checked against. Three parts: Partie A, what the applicant fills in (the object of the application, the type of device, its status and its risk class); the part reserved for the administration, which lists the pieces of the file in paper form and marks each one received, not applicable, missing or observed; and the notes and referrals, which state that every piece must be dated, signed and stamped by the Moroccan establishment's legal representative and that a change to the nature of the device requires a fresh application. It is the operational checklist for the same registration the device law establishes. The document's own two pages disagree with each other: page 1 carries "Edition : 9 / Date d'application : 30/01/2025" while page 2 still carries "Edition : 8 / Date d'application : 10/08/2020". The edition the cover states is recorded on this row and both are visible in the extract.

Réf. DE ER DM/01, édition 9 is the official identifier AMMPS uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.