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ABMed HO-LD-0003,

HO-LD-0003, version 1

Autorisation d’utilisation d’urgence des produits de santé
BeninAgence béninoise du Médicament et des autres produits de SantéRegistrationEffective 2025-11-03
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What this code is

HO-LD-0003, version 1 is the official ABMed identifier for “Autorisation d’utilisation d’urgence des produits de santé”. HO-LD-0003, version 1 is the official identifier ABMed uses for this instrument.

Instrument
HO-LD-0003,
Full name
HO-LD-0003, 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

Autorisation d’utilisation d’urgence des produits de santé

Official 22-page emergency-use-authorisation guideline, version 1, with the stated application date 3 November 2025. The defined health products expressly include medical devices; the request-letter template specifically includes DMDIV information. Preserves the final annex and reference pages. Section 6.1 names a pre-submission meeting form without reproducing that form, so the guide alone does not supply every referenced application form.

HO-LD-0003, 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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