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Urea Indol Broth

EUDAMED

Class A (EU MDR)

Ref BT 5061.01

by BioMaxima Spółka Akcyjna

Identity

Trade Name
Urea Indol Broth EUDAMED
Device Name
Urea Indol Broth EUDAMED
Model / Reference
BT 5061.01 EUDAMED

Identifiers

Primary DI / UDI-DI
05902643949805 EUDAMED
Basic UDI-DI
59026439ABURINM6 EUDAMED
59026439ASURINSZ 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

EUDAMEDEUDAMED

Microbial Substances

No

EUDAMEDEUDAMED

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

Urea Indol 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 3af2e459-2780-48a2-96a8-9c13b357f1ac 61 fields · synced Oct 5, 2026
  • EUDAMED dd0151d9-7589-41f3-b889-d6febc9e6da2 61 fields · synced Oct 5, 2026