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Dermasel Agar

EUDAMED

Class A (EU MDR)

Ref PO0737A

by Oxoid Ltd

Identity

Trade Name
DERMASEL AGAR EUDAMED
Device Name
DERMASEL AGAR EUDAMED
Model / Reference
PO0737A EUDAMED

Identifiers

Primary DI / UDI-DI
05032384024506 EUDAMED
Basic UDI-DI
5032384DermaselAgrOLUS EUDAMED
EMDN Code
W0104030201 PPM FOR YEASTS AND FUNGI 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

Dermasel 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 d08468fa-4244-45d9-8983-ab6f9a9c71a3 61 fields · synced Jun 18, 2026