Guinea medical device regulations
Official sources linkedDNPM rules and guidance for medical device market access, registration, and lifecycle compliance. Each code opens a metadata page with the official source and readable HTML when available.
| Code | Regulation | Category | Effective | Provenance |
|---|---|---|---|---|
| Loi L/2018/024/AN du 20 juin 2018 | Loi relative aux médicaments, produits de santé et à l’exercice de la profession de pharmacien Complete 43-page signed national law preserved in WHO’s policy-document repository. It expressly defines and regulates medical devices, including the device provisions in Articles 25–32. OCR transcribes the signed publication in its original French; this is not a third-party regulatory summary. | General | — | Official |
Exports carry source + retrieval dateWhat these codes are
Each row above represents one regulatory instrument. Its code is the authority’s identifier. A regulation page collects the metadata and official source; when readable HTML is available, article links can open and highlight the exact cited passage.
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