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Mueller Hinton 2 LAB-AGAR™

EUDAMED

Class A (EU MDR)

Ref PS 79- 100

by BioMaxima Spółka Akcyjna

Identity

Trade Name
Mueller Hinton 2 LAB-AGAR™ EUDAMED
Device Name
Mueller Hinton 2 LAB-AGAR™ EUDAMED
Model / Reference
PS 79- 100 EUDAMED

Identifiers

Primary DI / UDI-DI
05902643917514 EUDAMED
Basic UDI-DI
59026439ASMHR6 EUDAMED
EMDN Code
W0104010101 DEHYDRATED CULTURE MEDIA (DCM) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

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 2 LAB-AGAR™ by BioMaxima Spółka Akcyjna — Class A — 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

EUDAMED SRN
PL-MF-000039473

Sources (1)

  • EUDAMED b9023c17-677c-40a8-a4f4-3277f7f3d8dc 61 fields · synced Jun 18, 2026