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Mannitol Salt Agar

EUDAMED

Class A (EU MDR)

Ref CB0085G

by Oxoid Ltd

Identity

Trade Name
MANNITOL SALT AGAR EUDAMED
Device Name
MANNITOL SALT AGAR EUDAMED
Model / Reference
CB0085G EUDAMED

Identifiers

Primary DI / UDI-DI
05032384134809 EUDAMED
Basic UDI-DI
5032384ManSaltAgrOLLL EUDAMED
EMDN Code
W0104010101 DEHYDRATED CULTURE MEDIA (DCM) 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

Mannitol Salt 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 dd597c4c-e21e-49ef-91f8-c5a506990bb3 61 fields · synced Jul 17, 2026