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Mueller Hinton E Agar

EUDAMED

Class B (EU MDR)

Ref 541963

by bioMérieux SA

Identity

Trade Name
Mueller Hinton E Agar EUDAMED
Device Name
Mueller Hinton E Agar EUDAMED
Model / Reference
541963 EUDAMED

Identifiers

Primary DI / UDI-DI
03573026597672 EUDAMED
Basic UDI-DI
357302BUDI000030SK EUDAMED
Unit of Use DI
03573026597689 EUDAMED
EMDN Code
W0104010403 SUSCEPTIBILITY TEST MEDIA (PLATES) EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Mueller Hinton E Agar by Biomerieux Sa — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
bioMérieux SA
EUDAMED SRN
FR-MF-000004436

Sources (1)

  • EUDAMED 9fdc2bba-f9ca-4979-9f7e-aabac8e06037 61 fields · synced Jul 31, 2026