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Mueller Hinton Broth

EUDAMED

Class A (EU MDR)

Ref BT 5055.01

by BioMaxima Spółka Akcyjna

Identity

Trade Name
Mueller Hinton Broth EUDAMED
Device Name
Mueller Hinton Broth EUDAMED
Model / Reference
BT 5055.01 EUDAMED

Identifiers

Primary DI / UDI-DI
05902643947559 EUDAMED
Basic UDI-DI
59026439ABMHBRHF EUDAMED
59026439ASMHBRPA EUDAMED
EMDN Code
W0104010306 CULTURE MEDIA IN BOTTLES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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 Broth 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 (2)

  • EUDAMED ed0c4259-8c93-4a5d-9b81-ef21f47ca45e 61 fields · synced Oct 6, 2026
  • EUDAMED a28c4d6a-b83c-42e5-9f27-1574336370a7 61 fields · synced Oct 6, 2026