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Mueller Hinton II

EUDAMED

Class A (EU MDR)

Ref UM-MH-020Model Mueller Hinton II

by Bruker Daltonics GmbH & Co. KG

Identity

Trade Name
Mueller Hinton II EUDAMED
Device Name
Mueller Hinton II EUDAMED
Model / Reference
Mueller Hinton II EUDAMED
UM-MH-020 EUDAMED

Identifiers

Primary DI / UDI-DI
04251204327141 EUDAMED
Basic UDI-DI
425120430200001024FL EUDAMED
EMDN Code
W0104010206 MEDIA IN TUBES (SOLID & LIQUID) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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 II by Bruker Daltonics GmbH & Co. KG — 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
DE-MF-000024392

Sources (1)

  • EUDAMED 1fed6647-ccf3-455f-bcb7-5929ceee62f0 61 fields · synced Jul 16, 2026