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Mueller Hinton 2 LAB-AGAR™

EUDAMED

Class A (EU MDR)

Ref PS 79- 500

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- 500 EUDAMED

Identifiers

Primary DI / UDI-DI
05902643907515 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 f7d3c074-7e0d-4c65-8422-d8d7c77e93e8 61 fields · synced Jun 19, 2026