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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

ANTIBIOGO — IVDD — General IVDD by La Fondation Médecins…

MD Atlas
La Fondation Médecins Sans Frontières

EUDAMED last updated this device on Jun 11, 2025

ANTIBIOGO

B-FR-MF-00002487556

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: La Fondation Médecins Sans Frontières
UDI-DI code: D-FR-MF-00002487556
Reference / catalog number: ANTIBIOGO

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Manufacturer information

Organization name: La Fondation Médecins Sans Frontières
SRN: FR-MF-000024875
Manufacturer status: Active

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: D-FR-MF-00002487556
Basic UDI-DI: B-FR-MF-00002487556
Reference / catalog number: ANTIBIOGO
Issuing entity: EUDAMED

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Antibiogo is an aid to diagnosis stand-alone mobile device software intended to support laboratory tech- nicians measuring inhibition zone diameters (IZD) and interpreting antibiotic susceptibility tests (AST) from processed bacterial cultures from clinical samples. Antibiogo is intended to be used by trained laboratory technicians, non-expert in microbiology, operating in microbiology laboratories in Low and Middle Income Countries (LMIC).
Additional information URL: https://www.antibiogo.org/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W02039092VARIOUS MICROBIOLOGY INSTRUMENTS - IVD MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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Software identification

Related devices

This device is not currently linked to any other device.

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.