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Ss Lab-Agar™

EUDAMED

Class A (EU MDR)

Ref PP 0029

by BioMaxima Spółka Akcyjna

Identity

Trade Name
SS LAB-AGAR™ EUDAMED
Device Name
SS LAB-AGAR™ EUDAMED
Salmonella Shigella LAB-AGAR™ EUDAMED
Model / Reference
PP 0029 EUDAMED

Identifiers

Primary DI / UDI-DI
05902643930476 EUDAMED
Basic UDI-DI
59026439APSASHPF EUDAMED
59026439ASSASHQG EUDAMED
EMDN Code
W0104010405 NON-CHROMOGENIC MEDIA (PLATES) 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

Ss 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 (2)

  • EUDAMED 54b03fc2-694d-4d0b-a7fa-233ab351118c 61 fields · synced Jun 18, 2026
  • EUDAMED 212091aa-0e9d-4f0e-911b-9d444370c50a 61 fields · synced Jun 18, 2026