← Back to catalogue

SS LAB-AGAR™ / Chromogenic Salmonella LAB-AGAR™

EUDAMED

Class A (EU MDR)

Ref PD 020

by BioMaxima Spółka Akcyjna

Identity

Device Name
SS LAB-AGAR™ / Chromogenic Salmonella LAB-AGAR™ EUDAMED
Model / Reference
PD 020 EUDAMED

Identifiers

Primary DI / UDI-DI
05902643931008 EUDAMED
Basic UDI-DI
59026439APD020D8 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

Yes

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™ / Chromogenic Salmonella 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
PL-MF-000039473

Sources (1)

  • EUDAMED 68e9db01-dbdc-4317-b507-2666fd01a05a 61 fields · synced Jul 8, 2026