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C.l.e.d / Staph-Strep Biplate

EUDAMED

Class A (EU MDR)

Ref PB1228E

by Oxoid Ltd

Identity

Trade Name
C.L.E.D / STAPH-STREP BIPLATE EUDAMED
Device Name
C.L.E.D / STAPH-STREP BIPLATE EUDAMED
Model / Reference
PB1228E EUDAMED

Identifiers

Primary DI / UDI-DI
05032384279746 EUDAMED
Basic UDI-DI
5032384CLEDStaphStrepS8 EUDAMED
EMDN Code
W0104010407 BI-PLATES - INCLUDING NON-CHROMOGENIC & CHROMOGENIC MEDIA COMBINATION 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

C.l.e.d / Staph-Strep Biplate 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 58227d7e-c32f-483e-9a29-1a4b6d43038e 61 fields · synced Jun 18, 2026