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Cled Agar

EUDAMED

Class A (EU MDR)

Ref PO0120A

by Oxoid Ltd

Identity

Trade Name
CLED AGAR EUDAMED
Device Name
C L E D MEDIUM EUDAMED
Model / Reference
PO0120A EUDAMED

Identifiers

Primary DI / UDI-DI
05032384017584 EUDAMED
Basic UDI-DI
5032384CLEDOLKP EUDAMED
EMDN Code
W0104010405 NON-CHROMOGENIC MEDIA (PLATES) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

EUDAMED

Reagent

Yes

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

Cled Agar by Oxoid Ltd — 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

Manufacturer
Oxoid Ltd
EUDAMED SRN
GB-MF-000016914
Authorised Representative
Thermo Fisher Diagnostics B.V. NL-AR-000013157

Sources (1)

  • EUDAMED c18580c5-32bc-43ca-b6f0-eee7058f1c59 61 fields · synced Jul 31, 2026