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Motility LAB-AGAR™

EUDAMED

Class A (EU MDR)

Ref PS 525- 100

by BioMaxima Spółka Akcyjna

Identity

Trade Name
Motility LAB-AGAR™ EUDAMED
Device Name
Motility LAB-AGAR™ EUDAMED
Model / Reference
PS 525- 100 EUDAMED

Identifiers

Primary DI / UDI-DI
05902643920897 EUDAMED
Basic UDI-DI
59026439ASMOTMRR 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

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

Motility 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 9b840862-0c47-4e2f-91bd-519e72e3a765 61 fields · synced Jun 19, 2026