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ABMed HO-LD-0005,

HO-LD-0005, version 1

Refus, suspension et retrait d’AMM/AC au Bénin
BeninAgence béninoise du Médicament et des autres produits de SantéRegistrationEffective 2025-11-03
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What this code is

HO-LD-0005, version 1 is the official ABMed identifier for “Refus, suspension et retrait d’AMM/AC au Bénin”. HO-LD-0005, version 1 is the official identifier ABMed uses for this instrument.

Instrument
HO-LD-0005,
Full name
HO-LD-0005, version 1
Category
Registration
Source links
Source publication
French
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Dates
Published
—
Effective
2025-11-03
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About this regulation

Refus, suspension et retrait d’AMM/AC au Bénin

Complete eleven-page official guideline on refusal, suspension, withdrawal, cancellation and expiry of marketing or commercial authorisations, version 1, applied from 3 November 2025. The guideline's health-product definition expressly includes medical devices. Includes the final voluntary-withdrawal/suspension letter template; product-specific fields remain as written in the original.

HO-LD-0005, version 1 is the official identifier ABMed uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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