Central African Republic medical device regulations
Official sources linkedMinistère de la Santé et de la Population 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 |
|---|---|---|---|---|
| Liste nationale, édition 2017 | Liste nationale des médicaments essentiels et dispositifs médicaux de la RCA 2017 Complete fifty-page national essential-medicines and medical-devices list preserved by WHO. It identifies products and levels of care/use. It is retained as an original national normative list, not as a substitute for a medical-device marketing-authorisation law. The separate pharmacy law of June 2020 and the import-declaration order of 17 May 2010 remain national legal-source gaps. | 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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